Abstract
There is increased scientific interest in the effects of nutrition on cognition and well-being. Plant sourced polysaccharides play multiple roles in the biological processes required for health and well-being. This study explored the subjective experiential reports of well-being following intake of a plant derived polysaccharide supplement. The study used a 12 week double-blind, placebo controlled polysaccharide supplementation design. 109 middle-aged adults (45–60 years) took a standardised teaspoon of a combination of plant polysaccharides or a placebo twice daily for 12 weeks (3.6 g per day), and completed three, open-ended interviews at weeks 4, 8 and 12. Participants who took the polysaccharide supplement reported significantly more perceived beneficial changes in both physical and psychological well-being, specifically at week 12, compared to those who received the placebo. This study provides a starting point for understanding the perceived beneficial impact of polysaccharide interventions on aspects of well-being. Importantly, as a health-related application of polysaccharide science, this research supports the relationship that is emerging between the properties and function of polysaccharides. It is essential that future research assesses the effects of polysaccharide intake on a range of physical and psychological well-being outcomes to further the understanding of structure-function relationships with the aim of enhancing the functional health and well-being of individuals.
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Introduction
The concept of well-being can be defined as anything that relates to an individual’s ability to function well, physically, mentally, emotionally and spiritually. Often replaced by terms such as quality of life, well-being encompasses feeling good physically and psychologically even in the presence of illness and disease (Schickler 2005). The ability of food components to affect well-being is attracting increasing research attention, with positive effects of nutrition reported for both physical and psychological well-being. For example, micro nutrients such as B vitamins (B1, B2 and B6) and iron have been shown to improve mood (Benton and Donohoe 1999; Kaplan et al. 2007). In addition, various nutrients such as omega-3 fatty acids have been associated with better physical health outcomes (Lee et al. 2009). Importantly, plausible biological mechanisms by which certain nutrients affect physical and psychological well-being are beginning to be understood.
One nutritional component that is emerging as a significant mediator of biological mechanisms that contribute to human health are polysaccharides. As a group, polysaccharides are complex carbohydrate compounds found primarily in plants (e.g., vegetables and fruit), algae and fungi (Warrand 2006).Traditionally, polysaccharides have been used as thickening, emulsifying and stabilising agents in food. However, for centuries a number of cultures have used polysaccharide-rich plants and fungi, such as aloe and mushrooms, for therapeutic effects. In general, saccharide compounds derived from natural sources are structurally diverse and can contain as much as ten different monosaccharide sugars, such as mannose, galactose, fucose, glucose and arabinose. Importantly, the diversity in the origins of polysaccharides and the structural size of the molecules suggests that the physiochemical properties of polysaccharides influence a broad range mechanisms that impact biological processes required for health, such as cell-to-cell signalling events (Leung et al. 2006; Stella et al. 2001). Thus, there is broad scope to determine potential, functional health outcomes of polysaccharides in terms of subjective changes in overall well-being, both physical and psychological.
At present, the biological properties and mechanisms of action of polysaccharides are being explored for their positive effect on human health and well-being. For example, saccharides are emerging as significant immune modulating molecules that are important for overall healthy function (Schepetkin and Quinn 2006). In addition, some of the physiological properties and health effects of polysaccharides have been shown to include ‘prebiotic’ activity, essential for gastrointestinal health (Mann et al. 2007; Marzorati et al. 2010). For brain health, saccharides have been shown to influence cellular responses within the brain, including cell function and neurotransmitter activity, with some plant sourced polysaccharides demonstrating neuroprotective effects (Chan et al. 2007; Chang and So 2008; Griessen et al. 1989; Hirano et al. 2003; Li et al. 2011; Matthies et al. 1996). In humans, one study showed improved health outcomes in terms of reduced severity of physical symptoms following 9 months of supplementation with plant sourced polysaccharides in patients with chronic fatigue syndrome (Dykman et al. 1998). Further studies are needed to investigate the impact of saccharides for physical health outcomes.
With regard to psychological well-being, to date two studies have shown that polysaccharide supplementation improves mood as assessed by the Profile of Mood States (POMS). Specifically, following 5 weeks of polysaccharide supplementation, there was a significant decrease in anger and significant increases in energy and positive outlook on life in a group of individuals diagnosed with alcoholism (Dykman and Briggs 1997). More recently, utilising the same measure, there was a significant reduction in overall hostility and irritability and a significant increase in overall positive outlook on life following 12 weeks of polysaccharide supplementation in a group of healthy, middle-aged adults (Best et al. 2010). Studies that examine mechanisms of effect suggest that saccharides may influence psychological well-being due to their involvement in the regulation of neurotransmitters (Backstrom et al. 1995; Martinowich and Lu 2008; Tate and Blakely 1994), such as serotonin, that are involved in the modulation of mood states, such as anxiety and depression.
Research into polysaccharide effects in humans is a novel area of investigation and little is known about the participants’ subjective experience of changes in well-being following polysaccharide supplementation. Understanding the effect of the supplementation from the participants’ perspective provides a rich source of information to corroborate the impact of an intervention (Leidy and Vernon 2008; Smith 2005). Throughout the aforementioned 12 week polysaccharide supplementation study in middle-aged adults (Best et al. 2010) participants were invited to provide anecdotal reports of their experience of well-being via semi-structured interviews. The present study sought to analyse these reports. Participants in the Best et al. (2010) study were randomly allocated to either a polysaccharide supplementation or a placebo condition, according to a double-blind, placebo controlled design. Information concerning perceived changes in well-being was collected at weeks 4, 8 and 12 of the study.
Examining perceived changes in well-being over these 4-week intervals enabled us to document any perceived supplementation effects over time. Because of the longer-term structural and functional role of polysaccharides in the human body and brain (Best et al. 2007; 2009), we predicted an increase in perceived changes in well-being across the three scheduled interviews in terms of overall frequency and number of reported changes across time. We also analysed the content of the reports.
Method
Participants
There were 109 middle-aged Caucasian adults (aged 45–60 years) who took part in the study. Participants who had a history of serious mood disorders or psychiatric conditions, or had experienced recent major surgery or health conditions were excluded. Participants were recruited from the Adelaide metropolitan community local newspaper and television media advertisements and through word of mouth,. The sample included 38 males and 71 females. The mean age was 53 years (SD = 4.4). Participants had on average experienced 13.5 years of education (SD = 3.32), and rated their overall perceived health as good (M = 3.5, SD = 1.06), on a 5-point scale ranging from 1 (= poor) to 5 (= excellent). Further detail regarding the sample, recruitment methods and participant retention can be found in Best et al. (2010).
Procedure
Supplements
Participants took two teaspoons (3.6 g dose) per day of either a polysaccharide supplement (Ambrotose®complex, a proprietary and patented blend of plant polysaccharides) or a placebo (rice flour starch powder) that were carefully matched for colour and texture. These materials were provided by Mannatech Inc (Coppell, Texas), and came in 75 g containers. Participants took one teaspoon of supplement in the morning and one in the evening by either mixing the amount in a small glass of water or juice, or swallowing the amount straight from the standardised teaspoon. Participants recorded whether they had taken both teaspoons each day on a chart. The amount not consumed by the end of the study was determined by the number of teaspoon amounts left in the container out of the possible 168 serves (2 serves per day for 84 days). The experimenter and participants were blind to the supplement condition each participant had been randomly allocated to over the 12 week supplementation and interview period.
Interviews
During the 12 week supplementation period, participants were contacted by telephone 3 times at regular 4-week intervals: at week 4, week 8 and week 12 to provide feedback on their perceptions of well-being. Each time participants were asked three, pre-determined, semi structured questions: 1) how are you going with the supplements (a general question concerning participants’ experience and progress in taking the supplement, 2) have there been any circumstances or events that have affected your present state of health and well-being, and 3) have you noticed any general changes in well-being over the last month? All three telephone calls were scheduled in advance in order to adequately capture the 4 week intervals for each participant.
At each time point, participants were informed that the interviewer was keeping brief notes on their progress and feedback. An open-ended, semi-structured interview style was used with summary statements utilised to reflect back to the participant the notes that had been taken. This was done to ensure that the interviewer had adequately captured the participant’s feedback. The interviewer was a doctorate trained psychologist, well-trained to conduct open-ended interviews and take notes on the anecdotal feedback. Participants often openly conversed about a variety of issues relating to their experience of taking the supplement, including taste of the supplement, method of taking the supplement, if they had missed any days and general information about the study. The interviewer took notes from the verbal anecdotal reports.
Results
Compliance and Consumption
Across the sample, compliance with the supplementation protocol was good with an average of 80 days out of 84 on which participants consumed the supplements. In addition, participants, on average, consumed 294 g of the possible 300 g of each supplement. Analyses of variance indicated that there were no significant differences between the polysaccharide and placebo groups in the number of days the supplement was consumed (F(1,88) = 0.05, p = .98): polysaccharide condition M = 81.12, SD = 10.20, placebo condition M = 80.22, SD = 6.11) or the percentage amount of supplement consumed across the 12 weeks (F(1,88) =0.32, p = 0.57): polysaccharide condition M = 98.32, SD = 4.28, placebo condition M = 97.66, SD = 5.15).
Number of Perceived Changes
Of the total sample, 58 participants (38 females and 20 males) anecdotally reported perceived beneficial changes across the 12 week supplementation period, yielding a response rate of 53%. Of these, 42 were in the polysaccharide condition and 16 were in the placebo condition. Additionally, 43 participants reported no perceived changes (12 in the polysaccharide condition, 31 in the placebo condition), and 8 reported a negative change (5 in the polysaccharide condition, 3 in the placebo condition). The latter included 7 reports of increased flatulence and feeling bloated, and 1 report of feeling thirsty.
Chi-square analysis was used to determine the level of association between supplement conditions and the presence of anecdotal reports of perceived beneficial change and no change. Due to cell counts of less than 5, reports of perceived negative change were grouped with reports of no change. There was a significant association between conditions and whether or not there was a report of perceived beneficial change, X 2 (1) = 16.69, p < 0.001. This represents, based on the odds ratio, that participants were 5.25 times more likely to report a perceived beneficial change if they were in the polysaccharide condition than if they were in the placebo condition. The results of the contingency table are presented in Table 1.
Content of Perceived Changes
The overall number of individual reports were grouped into different themes. Specifically, the interviewer established the description and content of each theme based on the terms used by participants. Across the supplement conditions individuals reported perceived beneficial changes in both physical and psychological well-being. As can be seen in Table 2, participants reported perceived beneficial changes primarily in energy, general sense of calmness, sleep quality, concentration and feeling clearheaded, as well as gastrointestinal health, reduced physical pain and improved skin condition. Example descriptions of each theme from participants in the polysaccharide condition are provided in Table 3. To categorise the reports by themes, the first and second author explored and described the themes individually to determine a measure of inter-rater reliability (r = 0.82).
Perceived Beneficial Changes Over Time
To investigate changes in the number of perceived beneficial reports over time, a mean score was calculated for the number of reports in each condition for each time point; week 4, week 8 and week 12. Differences between supplement conditions for the mean number of reports at each time point were examined with a 2 (group: polysaccharide and placebo) x 3 (time points: weeks 4, 8, 12) Analysis of Variance. There was a significant Group x Time interaction (F(2,112) = 3.45, p = 0.035). Post hoc comparisons showed that participants in the polysaccharide condition reported significantly more perceived beneficial changes than those in the placebo condition at week 12, (t(55) = 3.19, p = 0.002). However, there were no significant differences between groups at week 4 (t (56) = 0.12, p = .21) or week 8 (t(56) = 0.43, p = .67). Figure 1 shows the mean number of beneficial reports across time for each condition. There were no significant main effects of Group (F(1,56) = 1.29, p = 0.26) or Time (F(2,112) = 2.13, p = 0.12).
Discussion
To our knowledge, this study was the first to explore perceived changes in well-being following a polysaccharide supplementation intervention. The results show that participants in the polysaccharide condition reported significantly more changes than those who received the placebo. This finding is consistent with previous research that has demonstrated improvements in well-being following supplementation with polysaccharides on a standardised measure of mood (Best et al. 2010; Dykman and Briggs 1997). Specifically, following 12 weeks of supplementation, middle aged adults in the polysaccharide condition of the Best et al. study were significantly less tense, hostile and had a more positive outlook on life than those in the placebo condition. These same participants perceived beneficial changes of supplementation themselves, as reported here. Thus, the current findings indicate that polysaccharides have an effect on perceived changes in well-being that are consistent with the reported changes captured by standardised measures of mood.
The content of the reports revealed that participants perceived beneficial changes in both physical and psychological well-being, particularly in energy levels, quality of sleep, gastrointestinal health, and sense of calmness, concentration and clear-headedness. These themes are consistent with previous research of polysaccharide effects. For example, the reports of perceived change in gastrointestinal health are consistent with mechanistic studies in animals that demonstrate positive effects of polysaccharide intake on gut function (Marzorati et al. 2010; Matsumoto et al. 2008). Similarly, the reports of perceived improvement in the experience of arthritic pain lend support to the findings of saccharide involvement in arthritic conditions (Alavi and Axford 2008; Gelderman et al. 1998; Kossi et al. 1999; Lefkowitz et al. 1999). In addition, the perceived changes in psychological well-being are consistent with the role of polysaccharides within the brain that may influence the regulation of mood, namely cell interactions and neurotransmitter response (Chicoine and Bahr 2007; Hirano et al. 2003; Kleene and Schachner 2004; Krishnan and Nestler 2010; Martin 2002; Matthies et al. 1996).
The results of this study show that the number of perceived changes, when examined across time, was significantly higher for those in the polysaccharide condition in the last month of the study. This significant increase in the number of perceived reports from those in the polysaccharide condition towards the end of the study supports the hypothesised long-term effect of polysaccharides within the human body and brain. In particular, saccharides are thought to play a long-term structural and functional role in the brain, such as the development and function of neuronal membranes and synaptic junctions (Best et al. 2005). As a result, any saccharide effects on mechanisms that influence well-being are likely to become apparent following intake over longer periods of time.
This study, as a preliminary exploration of perceived changes following polysaccharide supplementation, has expanded our current knowledge of potential saccharide effects on well-being. Overall, this investigation may lead to further research with stronger methodology and measurement to capture and categorise the well-being changes that polysaccharides may offer. Indeed, research into the effects of polysaccharides on well-being is in the early stages and emerging research suggests direct, functional physiological roles for these bioactive carbohydrates (Alavi et al. 2011). Thus, future research should continue to investigate changes in well-being following polysaccharide supplementation with standardised measures and qualitative approaches that capture both physical and psychological effects.
References
Alavi, A., & Axford, J. S. (2008). Sweet and sour: the impact of sugars on disease. Rheumatology, 47(6), 760–770.
Alavi, A., Fraser, O., Tarelli, E., M, B., & Axford, J. (2011). An open-label dosing study to evaluate the safety and effects of a dietary plant-derived polysaccharide supplement on the N-glycosylation status of serum glycoproteins in healthy subjects. European Journal of Clinical Nutrition, 1–9.
Backstrom, J. R., Westphal, R. S., Canton, H., & Sanders-Bush, E. (1995). Identification of rat serotonin 5-HT2C receptors as glycoproteins containing N-Linked oligosaccharides. Molecular Brain Research, 33(2), 311–318.
Benton, D., & Donohoe, R. (1999). The effects of nutrients on mood. Public Health Nutrition, 2(3a), 403–409.
Best, T., Kemps, E., & Bryan, J. (2005). Effects of saccharides on brain function and cognitive performance. Nutrition Reviews, 63(12), 409–418.
Best, T., Kemps, E., & Bryan, J. (2007). A role for dietary saccharide intake in cognitive performance. Nutritional Neuroscience, 10(3–4), 113–120.
Best, T., Kemps, E., & Bryan, J. (2009). Association between dietary saccharide intake and self-reported cognition in middle-aged adults. British Journal of Nutrition, 101, 93–99.
Best, T., Kemps, E., & Bryan, J. (2010). Saccharide effects on cognition and well-being in middle-aged adults: A randomised controlled trial. Developmental Neuropsychology, 35, 66–80.
Chan, W. K., Law, H. K. W., Lin, Z.-B., Lau, Y. L., & Chan, G. C.-F. (2007). Response of human dendritic cells to different immunomodulatory polysaccharides derived from mushroom and barley. International Immunology, 19(7), 891–899.
Chang, R. C.-C., & So, K.-F. (2008). Use of anti-aging herbal medicine, lycium barbarum, against aging-associated diseases. What do we know so far? Cell Molecular Neurobiology, 28, 643–652.
Chicoine, L. M., & Bahr, B. A. (2007). Excitotoxic Protection by Polyanionic Polysaccharide: Evidence of a Cell Survival Pathway Involving AMPA Receptor–MAPK Interactions. Journal of Neuroscience Research, 85, 294–302.
Dykman, K. D., & Briggs, J. (1997). The effects of nutritional supplementation on alcoholics: Mood states and craving for alcohol. Journal of American Nutraceutical Association (supp 1), 8–11.
Dykman, K. D., Tone, C., Ford, C., & Dykman, R. A. (1998). The effects of nutritional supplements on the symptoms of fibromyalgia and chronic fatigue syndrome. Integrative Physiological and Behavioural Science, 33(1), 61–71.
Gelderman, M., Stuart, R., Vigerust, D., Fuhrmann, S., Lefkowitz, D. L., Allen, R. C., et al. (1998). Perpetuation of inflammation associated with experimental arthritis: the role of macrophage activation by neutrophilic myeloperoxidase. Mediators of Inflammation, 7(6), 381–389.
Griessen, M., Speich, P. V., Infante, F., Bartholdi, P., Cochet, B., Donath, A., et al. (1989). Effect of absorbable and nonabsorbable sugars on intestinal calcium absorption in humans. Gastroenterology, 96(3), 769–775.
Hirano, E., Saito, H., Ito, Y., Ishige, K., Edagawa, Y., Shimizu, N., et al. (2003). P B-2, a polysaccharide fraction from lichen Flavoparmelia baltimorensis, peripherally promotes the induction of long-term potentiation in the rat dentate gyrus in vivo. Brain Research, 963, 307–311.
Kaplan, B., Crawford, S., Field, C. J., Simpson, J., & Steven, A. (2007). Vitamins, minerals, and mood. Psychological Bulletin, 133(5), 747–760.
Kleene, R., & Schachner, M. (2004). Glycans and neural cell interactions. Nature Reviews Neuroscience, 5(3), 195–208.
Kossi, J., Peltonen, J., Ekfors, T., Niinikoski, J., & Laato, M. (1999). Effects of hexose sugars: Glucose, fructose, galactose and mannose on wound healing in the rat. European Surgical Research, 31(1), 74–82.
Krishnan, V., & Nestler, E. J. (2010). Linking molecules to mood: new insight into the biology of depression. American Journal of Psychiatry, 167(11), 1305–1320.
Lee, J. H., O'Keefe, J. H., Lavie, C. J., & Harris, W. S. (2009). Omega-3 fatty acids: cardiovascular benefits, sources and sustainability. Nature Reviews Cardiology, 6(12), 753–758.
Lefkowitz, D. L., Gelderman, M. P., Fuhrmann, S. R., Graham, S., Starnes, J. D., Lefkowitz, S. S., et al. (1999). Neutrophilic myeloperoxidase-macrophage interactions perpetuate chronic inflammation associated with experimental arthritis. Clinical Immunology, 91(2), 145–155.
Leidy, N. K., & Vernon, M. (2008). Perspectives on patient-reported outcomes: content validity and qualitative research in a changing clinical trial environment. PharmacoEconomics, 26(5), 363–370.
Leung, M. Y. K., Liu, C., Koon, J. C. M., & Fung, K. P. (2006). Polysaccharide biological response modifiers. Immunology Letters, 105, 101–114.
Li, S. Y., Yang, D., Yeung, C. M., Yu, W. Y., Chang, R. C. C., So, K. F., et al. (2011). Lycium barbarum polysaccharides reduce neuronal damage, blood-retinal barrier disruption and oxidative stress in retinal ischemia/reperfusion injury. PLoS ONE, 6(1), e16380. doi:16310.11371/journal.pone.0016380.
Mann, J., Cummings, J. H., Englyst, H. N., Key, T., Liu, S., Riccardi, G., et al. (2007). FAO/WHO scientific update on carbohydrates in human nutrition: conclusions. European Journal of Clinical Nutrition, 61(Suppl 1), S132–S137.
Martin, P. T. (2002). Glycobiology of the synapse. Glycobiology, 12(1), 1R–7R.
Martinowich, K., & Lu, B. (2008). Interaction between BDNF and serotonin: role in mood disorders. Neuropsychopharmacology, 33(1), 73–83.
Marzorati, M., Verhelst, A., Luta, G., Sinnott, R., Verstraete, W., Van de Wiele, T., et al. (2010). In vitro modulation of the human gastrointestinal microbial community by plant-derived polysaccharide-rich dietary supplements. International Journal of Food Microbiology, 139, 168–176.
Matsumoto, S., Hara, T., Nagaoka, M., Mike, A., Mitsuyama, K., Sako, T., et al. (2008). A component of polysaccharide peptidoglycan complex on Lactobacillus induced an improvement of murine model of inflammatory bowel disease and colitis-associated cancer. Immunology, 128, e170–e180.
Matthies, H., Staak, S., & Krug, M. (1996). Fucose and fucosyllactose enhance in-vitro hippocampal long-term potentiation. Brain Research, 725, 276–280.
Schepetkin, I. A., & Quinn, M. T. (2006). Botanical polysaccharides: Macrophage immunomodulation and therapeutic potential. International Immunopharmacology, 6, 317–333.
Schickler, P. (2005). Achieving health or achieving wellbeing? Learning in Health and Social Care, 4(4), 217–227.
Smith, A. (2005). The concept of well-being: relevance to nutrition research. British Journal of Nutrition, 93(Suppl 1), S1–S5.
Stella, H., Service, R., & Schurmi, P. (2001). Carbohydrates and glycobiology. Science, 291, 5512.
Tate, C. G., & Blakely, R. D. (1994). The effect of N-linked glycosylation on activity of the Na(+)- and Cl(− )-dependent serotonin transporter expressed using recombinant baculovirus in insect cells. Journal Biological Chemistry, 269(42), 26303–26310.
Warrand, J. (2006). Healthy polysaccharides: the next chapter in food products. Food Technology and Biotechnology, 44(3), 355–370.
Acknowledgements
To Mannatech, Inc (Coppell, Texas) for the provision of the supplements. This study was conducted independently and there are no undisclosed financial conflicts of interest of any of the authors. Author TB received a write-up stipend from Mannatech, Inc for this manuscript.
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Best, T., Kemps, E. & Bryan, J. Perceived Changes in Well-Being Following Polysaccharide Intake in Middle-Aged Adults. Applied Research Quality Life 7, 183–192 (2012). https://doi.org/10.1007/s11482-011-9158-2
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DOI: https://doi.org/10.1007/s11482-011-9158-2