Abstract
This book chapter summarizes selected scientific evidence on phytochemistry and pharmacological potential of Rumex hastatus. This herb is a bushy shrub and is an annual, biennial and perennial herb. The edible parts of the plant are young leaves and shoots (Padulosi 1999) belonging to the family Polygonaceae, and it is commonly known as khatimal. R. hastatus is commonly found in northern Pakistan, southwest of China and northeast Afghanistan. In India, it is widely distributed in western Himalayas, Himachal Pradesh, Jammu and Kashmir and Uttaranchal. It has been reported to possess a wide range of traditional medicinal uses including in asthma, cancer, rheumatism, diuretic, diarrhoea, dysentery, toothache, gum healing, jaundice, hepatitis, cough, fever, piles, carminative, purgative, fungal infection, lungs, bleeding and as a flavouring agent. Preliminary phytochemical screening showed that this plant is rich in various chemical constituents which are medicinally important such as flavonoids, anthraquinones, cardiac glycosides, alkaloids, terpenoids, tannins, saponins, phenolic compounds and coumarins. It has anti-nociceptive, antipyretic, anti-inflammatory, hepatic protective, anticholinesterase, antioxidant, antiradical, cytotoxic, anti-tumour, and angiogenic potential. The objective of the present current chapter is to collect all the relevant research articles which give information regarding traditional uses, phytochemistry and therapeutic potential of R. hastatus. R. hastatus has potential for curing various diseases and has been well studied for its phytochemical properties. However, further scientific studies are needed to explore mechanisms of actions, adverse effects of the extracts, toxicity and the therapeutic effect of major secondary metabolites.
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6.1 Introduction
An examination is required to characterize and portray the future errands of phytochemical research in the new millennium and not just of the present status of improvement of phytochemical research yet in addition to chemosynthetic pharmaceutical exploration. Both end up in a race to grow new prescriptions, with less or no reactions, for restorative and preventive application in illnesses for which casualty-based treatment has been nonexistent or blemished (Yaniv and Bachrach 2005). Use of plants as drugs has started between 4500–1600 BC and 2500–600 BC in Rig-Veda and Ayurveda, respectively. Apart from this, they have been used by Greeks and Arabs in the history, which saw its rise to India and Europe as well (Jan et al. 2011). Different plant species are developed and utilized as vegetables and food, throughout the globe; however huge numbers of these are ignored and underutilized. These are labelled “dismissed or underutilized” on the grounds that they remain ineffectively described and abandoned by examination and protection. Likewise, they have been maintained by social tendencies and conventional framework. Continuous negligence of these vegetables implies that their potential centrality will be underestimated, henceforth underestimated at this point, yet a large number of them are light and versatile and bear unfavourable climatic conditions more than the fascinating ones. Extraordinary danger of delayed hereditary eroding and vanishing is put on them, which could additionally prevent opportunity choices for the country occupants (Padulosi et al. 1999; Johns and Eyzaguirre 2006; Mal 2007; Ghane et al. 2010). A portion of these disregarded and underutilized crop species might be wild, yet their jobs are indispensable in food security and nourishment and financially assist the people living below the poverty line in the provincial territories of the emergent nations (Magbagbeola et al. 2010). Vital medicinally important constituents are present in herbs producing distinct physiological activity on the human body. Alkaloids, tannins, flavonoids, terpenoids, saponins and phenols include the significant ones. Due to their therapeutic significance and low poisonousness, drug specialists are concerned about their exploration (Inayatullah et al. 2012). Isolation of many such entities has been established from different plants with perhaps novel mechanism of actions and negligible poisonousness to the host cell (Ahmad and Aqil 2007).
6.1.1 Rumex and Polygonaceae
Ever since the time humans use plants and spices as cure against maladies and infirmities because of their healing benefits and different restorative focal points, Rumex L. (Dock) species have increased gigantic acknowledgement (Babulka 2004). Two huge clades were characterized after the atomic phylogenetic investigation by Navajas-Pérez et al. (2005) inside the variety Rumex, one framed by the species of subg. Rumex and the other made out of the species of subgenera Acetosa (includes Rumex hastatus), acetosella and platypodium. Various Rumex species have been customarily utilized in various places of the world which in history have verifiable foundation. Propensities to utilize plants for various purposes, for example, medication, food, pharmaceuticals and so forth, are inculcated on the basis of interrelationship among the past, the present and what’s to come, which is woven in human civilizations (Zhang et al. 2014). The two spheres of well-being which include ethnoveterinary and ethnomedicine are the main aspects in clinical practice where the plants have a great utility (Abbasi et al. 2013; Disler et al. 2014; Bartha et al. 2015; Hussain et al. 2015; Vogl et al. 2016). In the family Polygonaceae, Rumex is the second largest genus. It is widely distributed in most part of Europe, North America, Africa and Asia, predominantly in the northern half of the globe (Vasas et al. 2015). The family Polygonaceae generally known as the knotwood or smart weed family is a group of blooming or flowering plants (Uddin et al. 2014) and involves 56 plant genera with 5109 logical plant names of species, of these 1266 are acknowledged species names. A further of 1675 scientific plant names of intra-specific position for the family Polygonaceae are incorporated in the plant list (List 2010), among which Eriogonum (2410 species), Rumex (200 species), Coccoloba (120 species) and Persicaria (100 species) are the biggest ones (Uddin et al. 2014). Numerous types of this class are herbs; however some are bushes as well, and a couple are rhizomes. The genus Rumex is a commonly recognized name, represented by 25 perennial plant species in nations like Poland. In traditional medicine leaf, seeds, fresh plant juice, seeds, and aerial parts are the generally utilized. Rich hereditary diversity in a few wild plants of nutritional worth and potential therapeutic properties is mostly found in the West Himalayan biogeographic zone, which is known for it (Sinha and Sinha 2001; Singh et al. 2002). Asthma, bronchitis, cough, loose bowels, diarrhoea, dermatitis, ear infection, inflammatory conditions, jaundice, kidney disease, leprosy, toothache, ulcerative colitis and intestinal parasites are among the few medicinal properties credited to this family (Uddin et al. 2014).
6.1.2 Rumex hastatus D. Don
R. hastatus belongs to the family Polygonaceae and is commonly called as “Khatimal”. It is found in abundance in northern Pakistan, southwest China and northeast Afghanistan (Shinwari and Gilani 2003). The leaves and shoots are used in chutneys and pickles due to its pleasant acidic taste (Manan et al. 2007). It is reported that the whole plant is used as medicine. It is laxative, alterative and tonic (Shinwari and Gilani 2003) and used for treating sexually transmitted diseases like AIDS (Sahreen et al. 2011). The aqueous extract of the roots of Rumex is used traditionally for curing asthma (Abbasi et al. 2010, Abbasi et al. 2011). The leaves and young shoots are used as carminative, purgative, diuretic and in stomach problems (Murad et al. 2011). All the previous studies on R. hastatus leaves have proven them to be constituting righteous phenolic principles and are therefore verified antioxidant sources. (Zhang et al. 2009; Sahreen et al. 2011) reported seven phenolic compounds from R. hastatus roots by referring the use in Chinese herbal system. The R. hastatus has been evaluated for various activities like antioxidant (Sahreen et al. 2011); antifungal (Hussain et al. 2010); antifungal and anti-bacterial (Hussain et al. 2010); antidiarrhoeal (Shakuntala et al. 2011) and anti-viral (Taylor et al. 1996).
6.1.3 Review Methodology
There is no literature of review on R. hastatus that has been published yet; therefore the book chapter on the present topic was assembled with the goal of compiling the relevant data on the plant till date, this species being sparsely explored as compared to its other allies and species. The collection of selection of relevant data was made through a search using the keyword “Rumex,” “R. hastatus”. Pertinent data was collected from various major scientific databases including Medline, Scopus, ScienceDirect, Prota, SciFinder, PubMed, Google and Google Scholar, and plant taxonomy was validated by the databases Mansfeld’s Encyclopedia, The Plant List, and PFAF. Various publication sites like Taylor and Francis, Elsevier and Springer used to collect the literature. Additional information on traditional use and botany was obtained from published books and MSc dissertation. A total of about 250 papers and articles were compiled which were published in different journals until May 2020. Data was analysed from different perspectives. All the literature was searched with the aim of obtaining data from different parts of the world and not specifically a particular region, thereby covering a vast and imperative field of knowledge. This was done to obtain the necessary data and research on the pertaining topic, until the present time. On the basis of 161 references, the present review was designed to provide a survey of the current state of knowledge of the phytochemistry and isolation; morphology and anatomy; nutritional importance; ethnobotany; and pharmacological activities of R. hastatus, as well as its traditional uses which have been supported by pharmacological investigations in order to identify its relevance as food and potential therapeutic applications and to show further directions of research (Table 6.1).
6.2 Ethnobotany
R. hastatus is quite rampant across the globe, and it is known by a variety of names in different languages.
Synonyms
Rumex arifolius (List 2013)
Rumex dissectus (Abbasi et al. 2011)
Taxonomical Classification
Kingdom | Plantae |
---|---|
Subkingdom | Angiosperms |
Division | Flowering plants |
Class | Magnoliopsida |
Subclass | Caryophyllidae |
Order | Caryophyllales |
Family | Polygonaceae |
Genus | Rumex L. |
Species | Hastatus D. Don |
Conservation Status.
R. hastatus is included in IUCN Red List of threatened plants.
6.2.1 Habitat and Edible Part
Being a bushy shrub, R. hastatus is about 30–90 cm high (Singh et al. 2013a, b). The young shoots and leaves of this plant are edible (Sher et al. 2015; Seidemann 2005).
6.2.2 Ecology
6.2.2.1 Altitude
R. hastatus D. Don is mainly distributed at elevations of about 2400 m (Dutt et al. 2015). In Nepal, it however occurs at an elevation of 1000–2600 m (Manandhar 2002).
6.2.2.2 Climate, Soil, pH and Lifespan
R. hastatus can grow in semi-shade (light woodland) or no shade. It can grow in wasteland, dry slopes and rocks (Dutt et al. 2015), shady slopes or dry streambeds (Manandhar 2002). The soil which is suitable for its growth includes light (sandy), medium (loamy) and heavy (clayey) soils and preferably well-drained soil. R. hastatus is an annual, biennial and perennial herb belonging to the family Polygonaceae. The common perennial herbs which grow in sour and acidic soils are members of this family (Zabta et al. 2003).
6.2.3 Distribution
R. hastatus is widely distributed in northeast Afghanistan, in north of Pakistan and southwest of China at an altitude of 700–2500 m (Qaiser 2001). In India the Rumex is widely distributed in Kumaun, Himachal Pradesh, Uttarakhand, Chandigarh, western Himalayas and Jammu and Kashmir (Zabta et al. 2003; Seidemann 2005; Paul and Chowdhury 2019). In Himachal Pradesh, the plant is found in Hamirpur, Lahual Chamba, Kullu and Spiti (Singh et al. 2014). It is also found in Mongolia, Russia, Tajikistan,Kazakhstan, Kyrgyzstan, Europe (Paul and Chowdhury 2019), Muree and Gilgit/Baltistan (Hameed et al. 2010).
6.2.4 Phenology
Flowering time: May–June (Hameed et al. 2010).
Fruiting time: March–November (Singh et al. 2014).
6.2.5 Pollination
R. hastatus is a hermaphrodite (has both male and female organs), and it is mostly pollinated by wind.
6.2.6 Propagation
R. hastatus is propagated through seeds, which can be sown in spring. The seedlings are transferred in pots individually when they are large enough to handle and planted out in the summer. Division takes place in spring.
6.2.7 Morphology and Description
Stem: The stem is herbaceous above and woody below and is erect and branched (Abbasi et al. 2011). The branches are finely grooved, purple-brown; branchlets are green and glabrous and about 50–90 cm tall (Anjen et al. 2003).
Leaves: The colour of the leaves is pale green with simple lobes which are directed outwards (Abbasi et al. 2011). The central lobe is narrowly triangular and linear. Leaves are solitary or fascicled; the blade is 1.5–3 cm × 1.5–2 mm and the petiole is 1.5–3.5 cm; apex is acute; basal lobes are curved; pedicel is slender and articulate below the middle; ocrea is fugacious and membranous (Anjen et al. 2003).
Roots: The roots are cylindrical, 0.5–0.9 cm wide and 3.5–6.5 cm long. The roots have transverse fissures and dark brown colour on upper surface. The inner surface is brown in colour and the fracture is short and mealy (Singh et al. 2013a, b).
Flowers: The flowers are numerous, small, pinkish in terminal paniculate clusters (Abbasi et al. 2011). They are polygamous. The petals of the male flowers are nearly uniform. In the female flowers, however, the outer petals are elliptic, and the inner ones are enlarged in fruit. Achenes are brown, ovoid, trigonous and shiny, ca. 2 mm. The valves are membranous, pinkish, orbicular or reniform, nearly pellucid, with small tubercle at the base; base is deeply cordate, apex is obtuse, and the margin is nearly entire (Anjen et al. 2003).
Fruits: R. hastatus bears one-seeded nutlet and fruit is pinkish (Abbasi et al. 2011).
6.3 Ethnomedicinal Importance
Traditional folk medical practices are empirical in nature; several million people with limited access to organized modern health-care centres depend on traditional systems of medicine to cater their primary health-care needs. Traditional systems of medicine are widely acknowledged to be effective and safe without any side effects (Farnsworth 1988). It has been ethnomedicinally used for various ailments. Various parts of the R. hastatus like leaves, roots, and stem are used in therapy. Different forms of preparation of this medicinal plant are employed (Table 6.2).
6.4 Nutritional Importance
In outlining the nutritional facts, the food quality and figures should be one of the major areas. R. hastatus is notable for its therapeutic importance; it is additionally utilized as nourishment for people. Leaves which are sour in taste are eaten raw as salad or made into chutney (Singh and Thakur 2014; Bhatia et al. 2018). To be concluded as a nutritional source and functional food, several authors assessed the nutritional and dietary properties of the plant and proved it as such (Ahmad et al. 2019). Many studies suggested that R. hastatus contains ample nutritional constituents and is a vital source of secondary metabolites, which can prove to be important for production of energy, growth and other functions. This plant is rich source of carbohydrates and fibre. Protein, moisture content, ash content and fats were also recorded (Hameed and Dastagir 2009; Singh et al. 2013a, b). Mineral elements though usually form a small portion of total composition of plant materials; they are nevertheless of great physiological importance particularly in the body metabolism (Bamiro et al. 1995). The elemental analysis in different parts of plant was carried out, and the concentrations are shown in Table 6.3 (Hameed et al. 2008).
6.5 Contraindication
Significant levels of oxalic acid are present in the plants, which gives the leaves of numerous individuals from this variety an acidic lemon flavour. Though completely alright in little amounts, the leaves ought not be eaten in huge amounts since the oxalic acid can secure up different supplements in the food, particularly calcium, along these lines causing mineral inadequacies. When the plant is cooked, the concentration of oxalic acid gets, however, decreased. Therefore, individuals with a propensity to rheumatism, arthritis, gout, kidney stones, or hyperacidity should take particular alert if considering this plant for their eating regimen, since it can bother their condition (Bown 1995).
6.7 Phytochemistry
A comprehensive literature survey on phytochemical investigations of R. hastatus reveals that the chemical constituents reported from this plant are from different classes of secondary metabolites that include flavonoids, anthraquinones, phenolic compounds, naphthalenes and various other constituents given in Table 6.5 (Zhang et al. 2009; Sahreen et al. 2014).
R. hastatus is differentiated by the presence of various secondary phytoconstituents. There are over 20 compounds which have been isolated from this plant. In roots the most abundant phytoconstituents are the anthraquinones and their derivatives (Sharma et al. 2018). By UPLC-DAD method, various anthraquinone derivatives have been isolated from the methanol extract of aerial and root part. A phytochemical investigation on roots also led to the isolation of some naphthalenes by column chromatography as reported by Zhang et al. (2009). Apart from naphthalenes and anthraquinones, the other constituents isolated from R. hastatus are flavonoids. These are the polyphenolic compounds having potential antioxidant properties (Schlachterman et al. 2008). HPLC on the alcoholic extract of root and leaf and column chromatography of the root extract led to the isolation of some flavonoids (Zhang et al. 2009; Sahreen et al. 2011; Sahreen et al. 2014). Moreover, new fatty acid esters and phenolic glucosides were isolated and identified from the aerial parts of R. hastatus by column chromatography for the first time (Sultana et al. 2017). The isolated compounds and their nature are given in Tables 6.6 and 6.7, and their structures are shown in Figs. 6.2, 6.3, and 6.4.
6.8 Pharmacology
Plants are well-known excellent perspectives for the discovery of new therapeutical products. The World Health Organization (WHO) estimates that 65–80% of the population of the developing countries depends on medicinal plants for basic pharmaceutical care (Singh et al. 2013c). The fact the plants are prominent origins for new bioactive principles is established and hence has wide utility in therapeutics (Kinghorn et al. 2011). Different parts of the medicinal plants have been utilized for various therapeutic purposes in folk medicine. Indeed, many of the plants and their preparations have been recorded to be used to treat different maladies and promote healing (Sen et al. 2010).
6.8.1 Anti-Nociceptive
The occurrence of tissue damage to the body is informed by means of a warning system called as pain (Nickel et al. 2012). Since pain modulation is an intricate process involving many mediators and receptors at the peripheral and central levels, its management using the available analgesics could not completely thrive well. Nociceptive neuron sensitivity is adjusted by a large variety of mediators in the extracellular space which either include neurotransmitters or neuromodulators in turn activating a large number of receptors and therefore a cascade of events controlling the perception of pain (Julius and Basbaum 2001; Scholz and Woolf 2002; Lewin et al. 2004; Hucho and Levine 2007; List 2010). Identification of the components involved in the complex process is undertaken worldwide, and attempts are being made to develop new agents that act on these components (Bektas et al. 2015). Analgesic drugs such as opiates that are currently available are not useful in all the cases as their beneficial effects are superseded by their various adverse effects (Zendehdel et al. 2011). Therefore, there is an urgent need of new analgesic drugs with promising pharmacological actions. In addition, the revelation of plant-based drugs with high restorative viability, however less or, perhaps, no toxicity, may be beneficial as substitutions to customary analgesics like narcotics and NSAIDs (Sen et al. 2010). Singh et al. (2013a, b) evaluated the anti-nociceptive potential of R. hastatus. The study involved the use of acetic acid-induced writhing method, tail flick model and formalin-induced pain model in mice, for establishing anti-nociceptive activity of the ethanol and aqueous extract of stem and root, using standard drugs. The study revealed that the minimum (200 mg/kg) and maximum (400 mg/kg) doses of the aqueous and ethanol extract of root and stem showed significant inhibition in mice in acetic acid-induced abdominal constrictions. Maximum inhibition was shown by the ethanolic extract (400 mg/kg) of root in abdominal constrictions in mice induced by acetic acid, and the effect was comparable to that produced by indomethacin. Taken together, the above results indicated that peripheral and central analgesic activity is exhibited by aqueous and ethanol extracts of both root and stem of R. hastatus. However, out of aqueous and ethanolic extracts, the former is more active. Both phases of the formalin-induced pain are inhibited with a more pronounced effect on the second than the first phase. Both central and peripheral effects are confirmed from the study. The results observed from both tail flick test and acetic acid-induced abdominal constrictions were found to be significant.
6.8.2 Antipyretic
When the body reaches to a temperature above normal, the condition is called as fever or pyrexia. An antipyretic is a kind of drug that will forestall or decrease fever by bringing down internal heat level from a raised state. Nonetheless, the “normal” temperature can fluctuate from individual to individual inside specific boundaries. By and large, most non-steroidal anti-inflammatory drugs (NSAIDs) work by repressing prostaglandin synthetase inside the nerve centre (Deshpande et al. 2003). Most of the antipyretic drugs cause inhibition of prostaglandin E2 (PGE2) biosynthesis and Cox-2 expression which in turn causes reduction in elevated body temperatures. Most of these agents are toxic to the hepatic cells, cortex of brain, glomeruli, and heart muscles, but they have high selectivity to inhibit Cox-2 in an irreversible manner, while the selectivity is lower for the natural Cox-2 inhibitors but with lesser toxic effects (Bouldin et al. 1999). Microbes including bacteria and viruses are the causative agents of fever setting off the body’s defence system (Deshpande et al. 2003). Pain and pyrexia are frequently associated with infections and ailments. The drugs generally prescribed include the non-steroidal anti-inflammatory drugs (NSAIDs) which however have huge gastrointestinal side effects like peptic ulcer perforations, bleeding and obstructions restricting their uses in clinical settings (Ofman et al. 2002; Castellsague et al. 2012). Since there are fewer propensities for herbal drugs to cause any toxicity, therefore there is a huge demand of the same. Further there is an increase in the health-care costs which in turn influences people to find newer and natural low-cost alternatives (Bouldin et al. 1999).
Singh et al. (2013a, b) evaluated stem and roots of R. hastatus for its antipyretic activity using yeast-induced pyrexia in rats and was performed on the ethanolic and aqueous extracts of the plant. In hyperthermic rats, at the dosage of 400 mg/kg, the ethanolic extracts of both the parts produced a pronounced antipyretic effect in a dose-dependent manner when compared with untreated rats. The results were proportionate with the standard drug, paracetamol (150 mg/kg). This consequently confirmed that R. hastatus possessed significant antipyretic potential.
6.8.3 Anti-Inflammatory
The act of utilizing plants, their parts, or concentrates as anti-inflammatory mixture is known since ancient times (Khalifa 2004). When infectious microorganisms, for example, viruses, fungi or bacteria, attack the body, dwell specifically in tissues and additionally flow in the blood, inflammation takes place (Artis and Spits 2015; Isailovic et al. 2015; Pedraza-Alva et al. 2015). There are two principal classes of inflammatory substances: anti-inflammatory mediators and pro-inflammatory mediators. Moreover, some mediators possess both properties of anti- and pro-inflammation (Vignali and Kuchroo 2012). Cytokines (e.g. tumour necrosis factor, α interleukins and interferons), chemokines which include monocyte chemoattractant protein 1 and eicosanoids (e.g. leukotrienes and prostaglandins) are widely concentrated in relationship with the pathological states among the cellular pathways and inflammatory mediators. A significant pro-inflammatory cytokine which is discharged from different cells and applies numerous cell effects includes the tumour necrosis factor (TNF)-α, which is an effective inflammation-regulating transcription factor (Montgomery and Bowers 2012; Zelová and Hošek 2013). Nevertheless anti-inflammatory medications are frequently connected with serious toxic effects, for example, peptic ulcers and gastrointestinal bleeding (Alwashli et al. 2012). Many natural drugs isolated from medicinal plants are considered as successful and more secure for the treatment of different ailments including inflammation (Stevenson and Hurst 2007).
The aqueous and ethanol extracts of roots and stem of R. hastatus were evaluated for anti-inflammatory activity (Singh et al. 2013a, b). This in vivo study made use of two common models cotton pellet-induced granuloma and carrageenan-induced paw oedema method at a dose of 400 mg/kg; the ethanolic concentrates of both root and stem (400 mg/kg) of R. hastatus happened to show more critical mitigating action than the lesser 200 mg dosages, in experimenting animals, following 3 hours of medication treatment. Dose-dependent anti-inflammatory action was prominent, which was comparable to the standard drug indomethacin, following 6 hours of drug treatment. Further, inhibition in rise of dry weight of cotton pellet-induced granuloma was shown by stem as well as root extracts of R. hastatus in the second method used. However, ethanol extract of the root showed the greatest per cent inhibition at 400 mg/kg of drug treatment, with the ethanol extract of the stem at the same dose trailing behind and the aqueous extract being least effective. The carrageenan-induced paw oedema method was used to evaluate the acute inflammatory activity. Carrageenan (a sulphated polysaccharide belonging to the family Rhodophyceae) is obtained from a seaweed and is most widely used to produce biphasic acute inflammation. The liberation of serotonin and histamine marks the first phase (about 1 hour), while the liberation of prostaglandin, bradykinin, lysosome and protease marks the second phase, which exceeds 1 hour. The second accelerating phase of swelling relation is measured after 3 hours, wherein prostaglandins play the significant role (Hernández-Pérez and Rabanal 2002). This study reveals that R. hastatus extracts exhibited inhibition of oedema, through all the phases of inflammation; nonetheless the effectiveness in the proliferative phase of inflammation was confirmed by the prominent contraction of cotton pellet granuloma by all the extracts. The outcome of this study strongly indicates the anti-inflammatory potential of R. hastatus which however requires more exploration.
6.8.4 Antioxidant and Antiradical
Impressive consideration has been given to phenolics and flavonoids within enzymatic and non-enzymatic antioxidant components. Plants are expected to be a source of common antioxidant principles exhibiting significant antioxidant action and may assist with ensuring cells against the oxidative harm brought about by free radicals (Kähkönen et al. 1999). The hydroxyl and conjugated ring structures which are present in phenolic compounds have the ability of preventing oxidation through hydrogenation or complexing with oxidizing species and in turn scavenging free radicals (Shahidi et al. 1992). Along these lines, the medicinal plants have promising antioxidant compounds to be tried as antiradical drugs for the cure of illnesses arising because of oxidative pressure. The valuable impacts of antioxidant compounds have been confirmed in a few trial and epidemiological investigations (Ruch et al. 1989; Babu et al. 2001).
Sahreen et al. (2011) conducted a study to evaluate the antioxidant potential of different fractions of leaves of R. hastatus. The study found out that the ethyl acetate fraction of the plant contained high amount of total polyphenolics and exhibited promising potential of scavenging for ABTS radicals and hydroxyl radicals as well as prevention of β-carotene linoleic acid peroxidation, while butanolic fraction contained high flavonoid content and reflected most promising iron chelation, DPPH, and phospho-molybdate scavenging activity. However, scavenging of hydrogen peroxide by the chloroform fraction reflected its most potent antioxidant potential, although the antioxidant potential of methanolic and ethyl acetate fractions was found to be lower than that of standard.
Since no antioxidant studies had been conducted on the roots of R. hastatus, therefore (Sahreen et al. 2015) hypothesized that being an important ethnopharmacological part of the plant, the roots must have potential antioxidant activity, and henceforth designed an in vitro study on the same using different fractions. The results revealed that all the isolated fractions of the extract exhibited dose-dependent activity. The methanol and the butanol fractions showed the highest antioxidant potential, except hydrogen peroxide radical scavenging assay where highest scavenging activity was found in the chloroform fraction. Significant beta-carotene linoleic acid was found in the aqueous fraction, with the least potential shown by ethyl acetate and n-hexane fractions. Further analysis in both the studies carried on by Sahreen et al. on the ethyl acetate fraction suggested the presence of kaempferol, luteolin, rutin and luteolin-7-O-glucoside and vitex might probably be the source of antioxidant potential of the plant (Sahreen et al. 2011; Sahreen et al. 2015).
Similar findings were found by Ahmad et al. (2015), when their study on the antioxidant potential of R. hastatus revealed strong antioxidant capability of crude saponin and flavonoid extract obtained by fractionation of methanol extract of R. hastatus; ABTS free radical scavenging, DPPH, and hydrogen peroxide assays were used. Moreover the current study showed that the flavonoid fraction of the plant possessed highest antioxidant activity, and since the previous studies had revealed that the fractions exhibiting promising antioxidant potential contained flavonoids and phenols, it goes parallel with the fact that they may be credible for the drug possessing antioxidant potential, as reported (Sahreen et al. 2011; Afzal et al. 2014).
In one more investigational study executed by Ahmad et al. (2016a, b), the volatile oil of R. hastatus was put under surveillance, the results of which proved that the volatile oil of the plant was an antioxidant source in the free radical scavenging assay, which was significant and comparable with the positive control. Taken together, the results of all the studies clearly demonstrate the high antioxidant potential of R. hastatus, which after subjecting to development of new drug candidates can be helpful in numerous pathological states linked to oxidative stress and generation of free radicals.
6.8.5 Hepatic Protective Effect
The liver plays out an assortment of significant host safeguard and metabolic activities that incorporate gluconeogenesis, detoxification, production of acute phase proteins, expulsion of endogenous mediators, emission of favourable pro-inflammatory cytokines, etc. (Pastor et al. 1995). It is a remarkable organ because of the fact that the loss of liver cells due to medication toxicity or different abuse can be overwhelmed by recovery (Mehendale 2005). Numerous reports uncovered that the free radicals created during hepatic damage exhausted the levels of the enzyme and non-enzyme framework which are connected to liver wounds (Liu et al. 2006).
A study was designed by Sahreen et al. (2013) on the leaves of R. hastatus to analyse their hepatoprotective activity, using methanol and its fractioned extracts hexane, butanol, chloroform, ethyl acetate and aqueous extract against carbon tetrachloride (CCl4), the agent causing hepatotoxicity in rats. The glutathione reserves as well as the activity of enzymes involved in oxidation were depleted, while the lipid peroxides, DNA and histopathological injuries were elevated by administration of CCl4. Moreover the hepatic damage like necrosis, fatty changes, Kupffer cell infiltration and cellular hypertrophy was also caused. When the different fractions of leaves of R. hastatus (200 mg/kg body weight) were supplemented, attenuation in the toxicity was noted in the liver tissues as the numerous parameters like enzymatic, histological and serological were normalized. Per cent DNA fragmentation and ladder assay were performed which clearly indicated the amelioration of hepatic damage and oxidative stress induced by CCl4.
Another similar study was undertaken by Sahreen et al. (2017) in order to explore the hepatoprotective nature of R. hastatus roots, using methanol and ethyl acetate extracts. Again, CCl4 was used as the agent to trigger hepatotoxicity which was checked over by different liver function markers including alkaline phosphatase, γ-glutamyltransferase, aspartate transaminase, alanine transaminase and lactate dehydrogenase. Also lipid profile was assessed by the amount of triglycerides, HDL, LDL and serum TC. Furthermore DNA and cell damages and enzyme activities were also assessed. After the co-administration of the different extracts of roots of R. hastatus, the lipid profile, liver function markers and cellular and DNA damages were restored in rats. The oxidation status was also improved revealing that the roots of R. hastatus are a strong source of antioxidant activity and have the capacity to restore liver from the toxicity and fibrosis caused by CCl4. This is a clear indication that the plant reflects promising treatment of ailments regulated by markers controlling oxidation as well as free radical-mediated pathological states and hence is a good drug candidate to be explored for hepatic ailments due to its hepatoprotective potential.
6.8.6 Anticholinesterase
The most widely recognized neurological diseases are depression, Alzheimer’s disease, epilepsy, anxiety, madness, susto (fear), numbness, insomnia, migraine, headache, stress, Parkinson’s disease and so on (Bourbonnas-Spear et al. 2005; Aarsland et al. 2008). Depending on their traditional knowledge, large quantities of normal therapeutically active components have been extracted from different medicinal plants. For instance, the Ginkgo biloba was scientifically verified as anti-ageing and was customarily seen as memory enhancer, which however was established for treating Alzheimer’s disease (mild or moderate) (Burkard and Lehrl 1991; Kanowski et al. 1996; Le Bars et al. 1997). Essential oils are comprehended to possess major significance as they can neutralize free radicals, which are produced in the process of metabolism of oxygen (Ruberto and Baratta 2000). ROS are liable for many ailing conditions which include nervous diseases and oxidative pressure (Kumar et al. 2012). They are also known for their scavenging potential and effectiveness in many cognitive conditions. Among the psychological issues, the disease called Alzheimer’s disease (AD) is widely recognized in old individuals (Mukherjee et al. 2007). One helpful methodology for AD is to build the centralization of the synapse (acetylcholine) by hindering the protein (acetylcholinesterase) liable for its breakdown. Different medications of plant origin as well as chemical origin have been utilized for the regulation of Alzheimer’s and different apprehensive diseases (Small et al. 1997).
Ahmad et al. (2015) conducted a study aiming to investigate the potential of R. hastatus using various fractions, viz. chloroform, n-hexane, ethyl acetate, crude saponins, aqueous fraction, methanol extract and flavonoids for acetylcholinesterase and butyrylcholinesterase inhibition at various concentrations (125, 250, 500, 1000 μg/mL) in order to substantiate its traditional uses in neurological disorders, using Ellman’s spectrophotometric analysis. Concentration-dependent cholinesterase inhibition was shown by all the extracts with radical scavenging potentiality. Saponins and flavonoids reflected the highest potential inhibition, while moderate to high potential inhibition was reflected by the subsequent fractions. In the same manner, potential against butyrylcholinesterase inhibition of different plant extracts was also carried out. Therefore, the strong anticholinesterase potential of saponin and flavonoid extracts as well as the other fractions of R. hastatus confirmed claimed ethnomedicinal properties and established the potential of R. hastatus in the era of nervous disorders. Also the activity of extracts was comparable to that of positive control, galantamine. Furthermore, the study also revealed that the saponin and the flavonoid extracts exhibited the most prominent activity based on the enzyme (AChE, BChE) inhibition as well as radical scavenging potential, which also directed to the fact that the plant is a potent source of anticholinesterase compounds, which are most probably the saponins and flavonoids. This as well is supported by the fact that the saponins are also significant secondary metabolites, verified to be beneficial in different pharmacological activities. For example, traditional Chinese drugs are a source of saponins, demonstrating remarkable antioxidant potential (Xi et al. 2008). Also the saponins known as bacosides isolated from Bacopa monnieri and the flavonoids known as ginkgo flavon glycosides isolated from Ginkgo biloba possess the said activities (Das et al. 2002).
In another study conducted by Ahmad et al. (2016a, b), the isolation of essential oil from R. hastatus was done, which after assessment indicated that the plant is a potential source of significant volatile principles possessing anticholinesterase potential. The essential oil was subjected to the anticholinesterase assay performed against acetyl cholinesterase (AChE) and butyrylcholinesterase (BChE) at different concentrations (62.5–1000 μg/mL). The results were however comparable with the positive control taken as galanthamine. Results of the study strongly indicate the anticholinesterase potential of essential oil. A clear conclusion could be drawn that R. hastatus as an important source of constituents may perhaps result in therapy development and neutralize free radicals as well as rehabilitate neurodegenerative disorders. The most common constituents isolated from R. hastatus during the study include the following: palmitic acid, methyl palmitate, myristic acid, capric acid, pelargonic acid, drimenol, cetane, docosane, velleral, isolongifolol, neophytadiene, acetone, widdrol and levulinic acid. After exploring the different constituents of essential oil obtained, it was concluded that the significant anticholinesterase activity of the volatile oil was due to the presence of various phytoconstituents present. It was also found that the prominent activity of R. hastatus might be attributed to its hydrophobic nature due to its significant affinity towards the hydrophobic site of AChE, which is also the active site (Steinberg et al. 1975; Loizzo et al. 2008). Various phytoconstituents of volatile oil have also been brought to light by other investigators previously, possessing antiradical and anticholinesterase activities (Yi and Kim 1982; Stamatis et al. 1999; Decker et al. 2005; Mehendale et al. 2008; Öztürk et al. 2011; Sengupta and Ghosh 2012).
6.8.7 Anti-Tumour and Angiogenic Potential
Tumour is primarily described by unusual and unnecessary multiplication of cells, which dynamically disturb the cells in the neighbourhood. The formation of new blood vessels which is called the angiogenesis likewise happens alongside the multiplication of cells which happens in ordinary tissues very rarely, besides embryogenesis and wound repairing (Folkman 1992). It has been clearly showed that exorbitant angiogenesis prompts a few pathological states including ovarian cyst atherosclerosis, cancer, arthritis and osteomyelitis (Carmeliet and Jain 2000). Different chemotherapeutic substances are utilized against the pathophysiological conditions, which are angiogenesis dependent, particularly against tumour. Due to plenty of dangerous impacts of these agents, their use is discouraged, and the researchers are attempting to investigate bioactive substances obtained from medicinal plants which might be used in the management of tumour and other deadly disorders (Coats 1994; LaPoint et al. 2011; Ashton 2012). Plants, which are the most significant source of therapeutic substances, have been gaining substantially more consideration of the analysts for their great viability and low poisonousness (Shah et al. 2015). Potato tumour measure has been directed on a few plants of different families with remarkable outcomes (Haque et al. 2000; Hussain et al. 2007). High anti-angiogenic action has likewise been shown by a few species of plants using chorioallantoic membrane (CAM) assay (MiuRA et al. 2002; Wang et al. 2004). Numerous bioactive substances obtained from different plants have been assessed against tumour, showing great potential (Da Rocha et al. 2001).
Sahreen et al. (2015) conducted a study in order to evaluate the anti-tumour and anti-antigenic activities of different extracts of R. hastatus using potato tumour assay. The results simplified that the methanolic extract showed effective anti-tumour potential followed by n-butanol, aqueous and chloroform. Further ethyl acetate and n-hexane fraction showed the least potential. The outcome of this study was found to be in accordance to other studies (Fatima et al. 2009) establishing that it is the concentration of the samples on which the tumour inhibition rates depend upon. Findings of the study confirmed the preceding reports of (Islam et al. 2010; Ashraf et al. 2015) confirming that the anti-tumour potential is attributed to the bioactive principles of the plant as well as their strong solubility with appropriate solvent and also proving the statement of (Fatima et al. 2009) that tumour induction was changeable in case of different extracts of solvent.
In another study performed by Ahmad et al. (2016a, b), the anti-tumour and anti-antigenic potential of crude saponins, methanol extract and various fractions of R. hastatus were evaluated, using potato tumour assay. The study found that the extracts exhibited notable potential in the assay. However the chloroform and saponin fractions exhibited the most prominent activities which lead to the conclusion that these might probably be potential targets for the isolation of bioactive compounds possessing anti-neoplastic action. It was noted that the anti-tumour activity possessed by some extracts of R. hastatus is more prominent than some previously known instances from various plants (Haque et al. 2000; Hussain et al. 2007). Similarly, the anti-antigenic potential of the plant is comparable with different plants with strong antiangiogenic activities (Wang et al. 2004) as well as higher than the formerly reported daidzein and genistein (Krenn and Paper 2009). Furthermore it is evident from the above discourse that saponin and the chloroform extracts being the most active might be the potential sources of active compounds, which can strongly ameliorate metastasis and neo-vascularization.
6.8.8 Cytotoxic Activity
One of the most challenging diseases nowadays throughout the world is cancer which is one of the leading causes of mortality. A few variables have been accounted which cause hyperproliferation and malignancy (Borrego-Soto et al. 2015). The free radical-prompted lesions have been considered as one of the main sources of malignant growth (Valko et al. 2006). Different restorative systems are followed for the therapy of malignancy; however, chemotherapy has been considered as the most worthy and positive prognostic helpful methodology (Mohamed et al. 2015). Because of the useful and safe nature of all the medications from normal sources being biodegradable are favoured over the manufactured ones (Coats 1994). Different subsidiaries of natural anticancer medications are additionally being integrated and used against cancer (Jordan and Wilson 2004).
(Kamal et al. 2015) executed a study to establish the cytotoxic activity of crude saponins and methanolic extract as well as the subsequent fractions of R. hastatus against brine shrimps. Excellent activity was shown by the saponin extract at the concentration of 1000, 100 and 10 μg/mL. Among the fractions, the chloroform fraction also showed prominent cytotoxicity. However, ethyl acetate and crude methanol extract showed similar lethality as LC50 of 90 μg/mL. Further aqueous fraction and n-hexane fraction showed mediocre potential. The lethality caused in brine shrimps was notably highest in the case of the saponin extract, in which evidence is that anticancer properties might be attributed to these compounds. Moreover, it is also noted that the ethyl acetate and chloroform fraction showed remarkable cytotoxicity, which directs to the fact that the compounds (saponins and other components) responsible for the cytotoxicity are present in good amounts in these extracts. There is a positive correlation existing between the brine shrimp lethality assay and human nasopharyngeal carcinoma (KB cell line) as reported by Mclaughlin et al. (1998), Abdul et al. (2009), Fatima et al. (2009). All these results confirm the cytotoxic potential of different extracts of R. hastatus.
On the other hand, another study was conducted by Sahreen et al. (2015) to confirm the cytotoxic activities of R. hastatus roots, again using brine shrimp assay. Different fractions were evaluated for cytotoxicity, and the potential was found to be according to the following pattern: butanol > methanol > chloroform > aqueous > ethyl acetate > n-hexane. The earlier reports of (Hussain et al. 2010) were found in uniformity with the above findings, who also established that the methanol extracts of Rumex species showed prominent cytotoxic potential and the plant was highly active against larvae of brine shrimp.
A more explained study was done by Ahmad et al. (2016a, b), to evaluate cytotoxic potential of this plant against NIH/3T3 and HeLa cell lines using different extracts of R. hastatus. It was aimed to find out the most active fraction of the plant, as well as the identification of bioactive constituents, causing cytotoxicity. It was found that all the solvent fractions were active against both cell lines but the chloroform fraction was prominent in activity against both cell lines. Furthermore the noted IC50 values along with the GC-MS analysis of chloroform fraction confirmed the presence of most of the active constituents in this fraction only, which also indicated the fact that this fraction should perhaps be the target for isolation of components useful in cytotoxic therapy to a large extent. The analysis of the chloroform extract also revealed some of the compounds possessing anti-cancer activities in R. hastatus including dihydrojasmone, phytol, anthracenedione, eicosanol, silane, aristolone, nonivamide, ar-tumerone, ethyl α-d-glucopyranoside and sitostenone. (Komiya et al. 1999), for instance, reported that, in human lymphoid leukaemia Molt 4B cells, phytol has been known to induce programmed cell death. Similarly (Flescher 2005) reported dihydrojasmone, a new family of anticancer agents, which is also one of the member of jasmonate family. In nanoparticle-type drug delivery system, silane has been confirmed as a remarkable agent, for anticancer compounds. Apart from anticancer activity, nonivamide a skin permeation enhancer used in various ointments etc. is also present in the chloroform fraction of the plant (Fang et al. 2001). Also, C20 aliphatic alcohols have been found useful in the management of hyperproliferative skin disorders, and eicosanol, present in R. hastatus, is also a C20 alcohol. Pope et al. (2001) and Firestone and Sundar (2009) also reported two sesquiterpenes, aristolone and Ar-tumerone, which show the cytotoxic potential. Similarly vitamin E, a phenolic compound with prominent free radical scavenging and cytotoxic activity, has also been reported (Baldioli et al. 1996; Yu et al. 2009; Salvador et al. 2013). The steroids extracted from plant extract were used against cancer cells. Therefore it shows that sitostenone, a natural steroid found in the plant extract after analysis, might also be responsible for the cytotoxic activity. Compiling all the results, it is very much evident that the chloroform fraction of R. hastatus possessed the most prominent activity against the two types of cell lines. Concluding from the above discourse, it’s quite obvious that R. hastatus is a potent source of cytotoxic compounds, hence can be explored for the development of different drugs in this direction.
6.8.9 Antidiarrhoeal Activity
High death rate in developing nations is due to diarrhoea where more than 5,000,000 children under 5 die yearly from serious diarrhoeal infections (Heinrich et al. 2005). It is described by frequent recurrence of solid discharge, stomachache and wet stool (Maiti et al. 2007). Diarrhoeal ailment is a main source of mortality and bleakness, particularly in kids in developing nations (Mani et al. 2010). A dominant part of diarrhoeal cases are because of bacterial enteropathogens, diarrhoeagenic Escherichia coli being the most widely recognized reason in developing nations. The traveller’s diarrhoea is caused by two important bacterial classes of diarrhoeagenic E. coli, mostly enteroaggregative and enterotoxigenic (Adachi et al. 2001) and intrusive bacterial microorganisms like Campylobacter, Shigella and Salmonella (Hoge et al. 1998). Thusly, there is a pressing requirement for the increase of research into plants claiming medicinal value in diarrhoeal infections (Mohammed et al. 2009). For the management of diarrhoeal infections, a large population of developing nations largely depend on natural medications. Considering this reality the World Health Organization has established a diarrhoeal disease control program, which incorporates investigations of conventional therapeutic practices, increasing health education and avoidance of the disease (Shaphiullah et al. 2003).
Very less research has been reported regarding the antidiarrhoeal activity of R. hastatus, though a study was undertaken by Shakuntala et al. (2011) to confirm the same using the ethanolic extract of the roots of R. hastatus. In normal gastrointestinal models of rats at 100, 150 and 200 mg/kg body weight, castor oil-induced diarrhoea was followed. The incidence, severity and the typical parameters of diarrhoea were reported to decrease with the increase in the doses of the ethanolic extract of the plant at 100, 150 and 200 mg/kg body weight. The prominent anti-motility potential shown by the extract was comparable to the standard, atropine sulphate. This provides a basis to conclude that R. hastatus possesses some antidiarrhoeal potential, though more research and investigation are required in this direction.
6.8.10 Antimicrobial
Nowadays, most of the nations use plants as the main source of potent and effective drugs to treat various diseases and ailments (Srivastava et al. 1996). Different diseases and infections are treated by potent therapeutic agents isolated from plants (Uniyal et al. 2006). As an integrative system of medicine, plants are being accessed to confirm their antimicrobial potential for the management and protection against pathogens in recent years because the plant extracts possessing antimicrobial properties can be very vital. Potent natural compounds obtained from plants possess an important role in the defence mechanism of plants as well as their physiological actions in the human body (Sahreen et al. 2010). Resistance is the major drawback with the commercial antibiotics which are being used for various infections. Moreover, a bunch of toxic effects like hypersensitivity, immune suppression, etc. are connected with the use of these drugs. As a matter of fact, the plants are not only being widely used as drugs but as cosmetics and nutritional food as well, further evaluation of which by in vitro methods has confirmed their utility as antimicrobials and in other diseases as well (Krishnaiah et al. 2007).
Vast antimicrobial activity studies have been carried out on R. hastatus. In one of the study carried out by Sahreen et al. (2015) on methanol extract of the plant as well as its different fractionated extracts, numerous plant extracts reflected prominent antimicrobial potential, which is why they are being widely used in PHCs. All these results show that the plant has immense potential for antimicrobial activity.
6.8.10.1 Antifungal
Sahreen et al. (2015) designed a study on R. hastatus roots using agar tube dilution method against A. niger, A. flavus, A. fumigatus and F. solani. Inhibition of all the fungi was observed which reflects the antifungal potential of R. hastatus, although it requires further research and investigation.
6.8.10.2 Antibacterial Activity
Diverse antibacterial studies have been conducted on R. hastatus. Sahreen et al. (2015) performed a study on different root extracts of R. hastatus using agar well diffusion method. Crude methanol extract was fractioned with n-hexane, chloroform, n-butanol, ethyl acetate and residual aqueous fraction. Staphylococcus aureus which is a Gram-positive bacteria was inhibited by the extracts in the following order chloroform>n-hexane>methanol; however the other extracts had no effect on the growth of the respective bacteria. Besides, the chloroform fraction followed by methanol, butanol and ethyl acetate inhibited Bacillus subtilis, although the rest of the extracts didn’t inhibit the growth of the respective bacteria. Similarly, the Gram-negative bacteria Klebsiella pneumonia’s growth was inhibited in the order, viz. ethyl acetate, n-hexane>methanol, whereas other fractions did not inhibit its growth. Pseudomonas aeruginosa was also found to be inhibited by the plant. Moreover, growth of Salmonella typhi was inhibited in the order n-hexane>n-butanol>ethyl acetate, chloroform, methanol and aqueous. Furthermore, the growth of Enterobacter aerogenes was inhibited in the order aqueous>methanol and chloroform, and the remaining fractions did not show inhibition of the respective bacteria. Additionally, Micrococcus luteus and Escherichia coli reflected no antibacterial activity of any of the extracts. All the above results strongly indicate very potent activity of R. hastatus against different Gram-positive and Gram-negative bacteria.
Similar findings were found in the study conducted by Andleeb et al. (2018). Under this research, analysis of antibacterial potential of R. hastatus against various clinical pathogenic bacteria such as Serratia marcescens, Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, Streptococcus pyogenes, Staphylococcus epidermidis and Pseudomonas aeruginosa was performed using agar well diffusion method. The maximum inhibition of S. pyogenes was shown by the diethyl ether extract, while moderate inhibition was shown by chloroform fraction. Moderate inhibition of K. pneumonia and S. aureus was shown by diethyl ether and acetone fractions. Low or even no effect was shown by ethanol fraction on the growth of bacteria. Spot screening, TLC-bioautography and genomic DNA extraction (broth dilution method) also demonstrated the antibacterial effect of R. hastatus. Fine conclusion can be drawn from the above results that most of the extracts analysed were found to be promising source for the exploration of novel antimicrobials, thereby making it clear that R. hastatus could be successfully used as prominent antibacterial agent, as well as overcome the enigma of bacterial infections and multidrug-resistant microbial strains. (Ogram et al. 1987) further analysed the effect of the plant extracts on microbial DNA extracted from sediments and drew the same conclusion (Sahreen et al. 2011). The fall in DNA damages was exhibited by different root extracts of the plant. Lastly further establishment of the activity was reflected by spot screening results which is in accordance with the studies of (Oke and Hamburger 2002; Hussain et al. 2010).
One more study was conducted by Kamal et al. (2015) in the same direction. The analysis of crude flavonoids, saponins, crude methanolic extract and resultant fractions of R. hastatus by well diffusion method was carried out. The flavonoid fraction showed potent activity against all strains, which was however followed by the saponin extract, comparable to the positive control in the antibacterial assay. Similarly good zones of inhibition were shown by the ethyl acetate and chloroform fractions; the largest was however displayed by flavonoid extract against Bacillus cereus, while saponin was more effective against Escherichia coli. All the extracts were effective against Staphylococcus aureus, Klebsiella pneumoniae, Proteus mirabilis and Pseudomonas aeruginosa. Further analysis of various samples of R. hastatus revealed that this plant shows potent antibacterial activity; besides the flavonoid fraction was most active against different strains. It has already being established that this group of compounds is reported to possess remarkable anti-infective properties, and there are different compounds of flavonoids which have been discovered and identified, possessing potent antibacterial potential (Cushnie and Lamb 2005). Furthermore, it has been notified that synergistic effect is shown by numerous compounds of flavonoids when in combination, for instance, isorhamnetin-3-rutinoside, quercetin and rutin, present in the samples of Marrubium globosum, possess higher potential than the individual compound (Kimura and Yamada 1984). Moreover the saponins extracted from the plant also displayed prominent antibacterial potential against different bacterial strains which has also been reported by several investigators (Avato et al. 2006).
6.8.11 Antidiabetic Activity
Diabetes mellitus is a metabolic issue described by increment in blood glucose level. It can influence people at any phase of life, yet the recurrence of diabetes is extensively high among the corpulent and matured individuals (Mellitus 2005). Various restorative measures are utilized to reduce the indications of this ailment. One of the powerful helpful measures is to diminish the absorption of glucose from the digestive system. Hence, the retention of glucose from the digestive system can be diminished viably by α-glucosidase inhibition. Different plants have been accounted to have the α-glucosidase restraint potential (Ha et al. 2014). Diabetes mellitus is one of the regular metabolic issues with micro- and macrovascular complexities that cause noteworthy dismalness and death. It is considered as one of the five driving reasons for death on the planet (Vats et al. 2004; Kumar et al. 2006). In the present-day medication, no agreeable powerful treatment is as yet accessible to cure the disease (Ghosh and Suryawanshi 2001). There is expanding request by patients to utilize natural compounds with antidiabetic potential because of reactions and after-effects related with the utilization of insulin and oral hypoglycaemic agents (Holman and Turner 1991; Kameswrarao et al. 1997; Rao et al. 2001). These constraints have generally incited the investigation of the executives systems including the utilization of plant-based drugs which are as well low-cost antidiabetic drugs with less announced toxic symptoms (Atanasov et al. 2015).
This research was designed by Ahmad et al. (2019) on the different samples of R. hastatus for exploration of its in vitro antidiabetic activity. Further analysis of the extracts through GC (FID-MS) confirmed the presence of 120 compounds, among which, few antidiabetic agents were also identified, viz. guanidine, phytol, caryophyllene, anozol, nerolidol, ethylthreonine, butyl phthalate, indoline, myristic acid, dihydrobenzofuran and palmitic acid. It is a clear indication that the plant possesses antidiabetic potential. It may also be concluded that R. hastatus is among low-risk and nutritious plants based on the reported data. It can therefore be labelled as green functional food with antidiabetic activity, along with the source of different secondary metabolites. Growth, energy production and other vital functions of the body can be thereby met effectively along with the possible management of diabetes mellitus. Furthermore, when the traditional vegetables are unavailable, scarce or highly priced, it can also be used in this direction as well.
6.9 Conclusion
The medicinal plants are highest source of different phytoconstituents, possessing diverse pharmacological and ethnomedicinal activities. Medicinal plants have various properties for curing of various diseases for so many years. Currently an extensive research is going on worldwide to find novel phytoconstituents possessing novel pharmacological activities. In this book chapter, the facts reported are hard to clearly establish the structure-activity relationships and functionality regarding the pharmacological effects of various phytoconstituents.
In this chapter the data are collected from all the sources regarding ethnomedicinal uses, botanical description, pharmacology and phytochemistry of R. hastatus (Polygonaceae) a healing herb wildly grown in the areas of southwest China, northern Pakistan and northeast Afghanistan. Various phytoconstituents like quinones, terpenoids, coumarins, flavonoids, volatile oil and carotenoids have been reported in R. hastatus. It is noteworthy that R. hastatus has extensive medicinal uses, as ethnobotanical and ethnomedicinal data indicate. It exhibits several pharmacological activities such anti-inflammatory, hepatoprotective, antidiabetic and anti-tumour. It is potentially an important medicinal plant for mankind. So well-designed clinical trials are needed in order to change from traditional to a well-established use of R. hastatus medicinal plant preparations for the prevention and treatment of various ailments.
Abbreviations
- A. flavus :
-
Aspergillus flavus
- A. fumigatus :
-
Aspergillus fumigatus
- A. niger :
-
Aspergillus Niger
- ABTS:
-
2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)
- AChE:
-
Acetyl cholinesterase
- AD:
-
Alzheimer’s disease
- AIDS:
-
Autoimmuno deficiency disease
- BChE:
-
Butyrylcholinesterase
- ca.:
-
Circa (approx.)
- CAM:
-
Chorioallantoic membrane assay
- Cox-2:
-
Cyclooxygenase-2
- DNA:
-
Deoxyribonucleic acid
- DPPH:
-
Diphenyl-1-picrylhydrazyl
- E. coli :
-
Escherichia coli
- EtOH:
-
Ethanol
- F. solani :
-
Fusarium solani
- FID-MS:
-
Flame ionization detector with mass spectrometer
- H2O2:
-
Hydrogen peroxide
- HDL:
-
High-density lipoproteins
- IUCN:
-
International Union for Conservation Research
- LC50:
-
Lethal concentration
- LDL:
-
Low-density lipoproteins
- MeOH:
-
Methanol
- NSAIDs:
-
Non-steroidal anti-inflammatory drugs
- PFAF:
-
Plants for a future
- PHCs:
-
Primary health Centre
- R. hastatus :
-
Rumex hastatus
- STD:
-
Sexually transmitted disease
- TC:
-
Total cholesterol
- TLC:
-
Thin layer chromatography
- TNF:
-
Tumour necrosis factor
- Tsp:
-
Teaspoon
- UPLC-DAD:
-
Ultra-performance liquid chromatography method with diode array detection
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Hassan, I., Insha Mushtaq, Raja, W.Y., Bhat, Z.A. (2022). A Review on Ethnomedicinal, Phytochemistry and Pharmacological Activities of Rumex hastatus D. Don. In: Masoodi, M.H., Rehman, M.U. (eds) Edible Plants in Health and Diseases . Springer, Singapore. https://doi.org/10.1007/978-981-16-4959-2_6
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