Abstract
The hydrolysate of Oncorhynchus keta (chum salmon) milt was found to exhibit strong inhibitory activity against dipeptidyl peptidase-IV (DPP-IV), and the hypoglycaemic effect of these salmon milt peptides (SMPs) was confirmed using oral starch tolerance tests in Sprague–Dawley rats. Specifically, the oral administration of SMPs at a dose of 300 mg/kg body weight for 1 week resulted in a significant decrease in the blood glucose level of the rats 60 min after starch consumption compared with the control. The bioassay-guided separation of SMPs, using a combination of column chromatographic techniques, led to the identification of 12 active di-, tri- and tetrapeptides, including four novel DPP-IV inhibitory peptides, namely Phe-Pro-Val-Gly, Leu-Pro-Val-Leu, Val-Pro-Phe-Pro and Ile-Pro-Leu. Among these 12 peptides, Ile-Pro contributed the most (1.3%) to the total DPP-IV inhibitory activity of SMPs. Therefore, SMPs may have the potential to be used as a suppressor of postprandial hyperglycaemia and to be considered a promising functional food material for the prevention of type II diabetes.
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Introduction
Diabetes, which is caused by a lack of insulin action, is a metabolic disease that is characterised by chronic hyperglycaemia. Specifically, blood glucose control can not only suppress the onset of diabetes, but also hinder the development of related complications, such as retinopathy, nephropathy, neuropathy, myocardial infarction and cerebral infarction. It can also improve the quality of life and life expectancy of patients. In Japan, more than 95% of patients with diabetes are considered to have type II diabetes (non-insulin-dependent diabetes). Recently, dipeptidyl peptidase IV (DPP-IV) inhibitors, such as sitagliptin and alogliptin, have been approved as new type II diabetes drugs (Andukuri et al. 2009; Gallwitz 2007). Such compounds have attracted particular attention owing to their ability to control blood glucose levels with fewer side effects than other commonly used diabetes drugs. More specifically, DPP-IV degrades incretin, which is a gastrointestinal hormone with actions similar to those of gastric inhibitory polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) (Drucker 2003). These hormones act on pancreatic β-cells to promote the secretion of insulin in an inactive form. Therefore, DPP-IV inhibitors can maintain the activity of incretin and promote the secretion of insulin. Furthermore, DPP-IV is a serine protease that recognises and cleaves the second proline (Pro) or alanine (Ala) residue in the N-terminal of peptides, and it has been reported to act strongly on peptides possessing Pro and Ala at the second residue of the N-terminal as well on those possessing lysine (Lys) and arginine (Arg) as the N-terminal residue (Davy et al. 2000).
Although several compounds with the ability to inhibit DPP-IV have been obtained via chemical synthesis, these are associated with numerous safety issues and adverse side effects. Reports of DPP-IV inhibitors derived from natural products include peptides derived from whey protein hydrolysates (Lacroix et al. 2016; Nongonierma and FitzGerald 2013; Tulipano et al. 2011) and those derived from camel milk protein (Nongonierma et al. 2018), Porphyra dioica protein hydrolysates (Cermeño et al. 2019), peptides derived from Euphausia superba (Antarctic krill) protein (Ji et al. 2017a, b),and hydrolysates derived from gelatin extracted from salmon skin (Cheung and Li-Chan 2017; Jin et al. 2020; Li-Chan et al. 2012; Neves et al. 2017b) and muscle (Ketnawa et al. 2019; Neves et al. 2017a).
Our institution, a fishery company, is interested in developing new products by identifying novel functions of materials based on a range of fishery resources. In particular, the application of unused resources contributes to the effective utilisation of limited resources and to a reduction in environmental impact and has significance from a sustainable development goal perspective. In addition, to date the utilisation value of milt from seafood is lower than that of roe, with applications limited to fertiliser or feed. Additionally, salmon milt, which is relatively widely used in Japan, accounts for more than 10,000 tons of industrial waste annually. Thus, in this study, we investigated new salmon milt peptides (SMPs) that exhibit DPP-IV inhibitory activity and examined their ability to suppress postprandial hyperglycaemia. Additionally, we identified the peptides present in SMPs.
Material and methods
Materials
Milt of Oncorhynchus keta (chum salmon), a fishery processing by-product, was obtained from Peter Pan Seafoods Inc. (Valdez, AK, USA). All enzymes were purchased from Amano Enzyme Inc. (Aichi, Japan), and the reagents required for peptide synthesis were purchased from Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan). The DPP-IV inhibitory activity of the isolated SMPs was measured using a commercial in vitro enzymatic assay based on the DPP-IV Drug Discovery Kit (Enzo Life Sciences Inc., Enzo Biochem, Farmingdale, NY, USA), and acetonitrile (LC-MS grade), methanol (LC-MS grade), chloroform and formic acid were purchased from Kanto Chemicals (Tokyo, Japan).
Preparation of test substances
Enzyme selection
Minced chum salmon milt (8 g) was added to distilled water (15 mL) and the pH of the resulting solution was adjusted to ensure optimal pH conditions for the functioning of each enzyme using a 2 M NaOH or 1 M HCl solution. The enzymes and reaction conditions are listed in Table 1. After preincubation at the optimal temperature for 15 min, 2.0 mg (1% by dry weight) of each enzyme was added and the mixture was stirred for 4 h. Thereafter, the reaction solution was heated to 90 °C to inactivate the enzyme, and the solution was filtered through Celite. The filtrate was then lyophilised to obtain the hydrolysate, whose DPP-IV inhibitory activity was then evaluated.
Preparation of SMPs
Minced salmon milt (7.2 kg) was hydrolysed using protease (17.5 g; from Aspergillus melleus; Amano Enzyme Inc.) for > 5 h at 50 °C. Thereafter, the reaction mixture was heated to 90 °C and maintained at this temperature for 15 min to inactivate the enzyme. The reaction mixture was then filtered through Celite. The higher molecular weight components were then removed via ultrafiltration (Pellicon® 5K PLCC-C; MilliporeSigma, Burlington, MA, USA), whereas the lower molecular weight components were evaporated and dried to obtained SMPs.
DPP-IV inhibitory activity
The DPP-IV inhibitory activity of SMPs was measured using a commercial in vitro enzymatic assay that involved the use of the DPP-IV Drug Discovery Kit (Enzo Life Sciences Inc.), with a slight modification of the manufacturer’s instructions. Specifically, the assay was performed in 96-well plates using Ile-Pro-Ile (Diprotin A) as a positive control. Different concentrations of the test samples (10 μL) were pre-incubated with 50 mM Tris buffer (25 μL, pH 7.5) and 0.01 mM AMC (50 μL; H-Gly-Pro-amino-4-methylcoumarine, BML-P189-9090; Biomol GmbH, Hamburg, Germany) at 37 °C for 10 min. The assay was started after the addition of recombinant human DPP-IV (15 μL, 2 mU/mL). Plates were read at fluorescence wavelengths of 340 nm (excitation) and 460 nm (emission) using a microplate reader (GENio Pro; Tecan Co., Tecan Group Ltd., Männedorf, Switzerland) at 5-min intervals between 0 and 30 min. The recorded data were plotted against time, and the best-fit straight line was obtained in the time range over which the increase in relative fluorescence units was linear. The data were expressed as the percentage of remaining activity in the presence of the test sample versus the control (without sample). For each sample, three different assays were performed, and those curves showing the logarithmic regression of the dose–response curves were plotted to determine the 50% inhibitory concentration (IC50) values of the DPP-IV activity. In addition, the contribution ratio of each identified peptide to the DPP-IV inhibitory activity of SMPs was obtained using the following formula (Seki et al. 1996):
where Ap represents the proportion of the DPP-IV inhibitory peptide to SMPs (ppm), Ip represents the IC50 value of the inhibitory peptide (μg/mL) and Is represents the IC50 value of SMPs (μg/mL).
Evaluation of the postprandial hypoglycaemic effect of SMPs in Sprague–Dawley rats
Male Sprague–Dawley (SD) rats (SLC Inc., Shizuoka, Japan), aged 6 weeks, were used in this study. The rats, which were housed in a ventilated room maintained at 25 ± 3 °C with 50 ± 9% relative humidity, under an alternating 12 h/12 h light/dark cycle, were fed a solid diet (CRF-1; Oriental Yeast Co., Ltd., Tokyo, Japan) for 1 week. Thereafter, they were divided into three groups of ten rats, namely, the 0, 150, and 300 mg/kg SMPs-treated groups, respectively. After treatment for 1 week, the rats were fasted for 16 h, and 2 g starch per kilogram body weight (2 g/kg) was orally administered concurrently with 0, 150, or 300 mg/kg of SMPs. Blood samples were then taken from the tail at 0, 30, 60 and 120 min after treatment administration, and the blood glucose levels were measured using a blood glucose monitoring system (Freestyle Freedom™; NIPRO Corp., Osaka, Japan). The blood glucose levels were compared with those of the rats in the control group, which had not been exposed to SMPs. All experiments were carried out in accordance with the protocols and guidelines approved by the animal care committee of KAC Co., Ltd. Kyoto, Japan).
Bioassay-guided separation and analysis of SMPs
The SMPs separation process utilised in the present study is outlined in Fig. 1. Specifically, SMPs (50 g) were subjected to column chromatography using a DIAION HP20 column (650 g; Mitsubishi Chemicals, Mitsubishi Chemical Holdings Corp., Tokyo, Japan). After being charged in the column, the sample was eluted using a stepwise elution system as follows: 5 L of distilled water (fraction 1-1), 3 L of 50% (v/v) hydrous methanol (fraction 1-2) and 5 L of methanol (fraction 1-3). Each fraction was evaluated for its DPP-IV inhibitory activity, and fraction 1-2 (5.0 g), which showed the strongest inhibitory activity, was further separated using a silica gel chromatographic column (Hi Flash Column, 250 g, φ60 × 180 mm; Yamazen Corp., Osaka, Japan) with a stepwise solvent system consisting of chloroform/methanol/water (C/M/W). This fraction was further separated into eight fractions as follows: 2.5 L of C/M/W at 85/15/1 (fraction 2-1), 1 L of C/M/W at 65/16/2 (fraction 2-2), 1.5 L of C/M/W at 65/16/2 (fraction 2-3), 0.4 L of C/M/W at 65/25/4 (fraction 2-4), 2.1 L of C/M/W at 65/25/4 (fraction 2-5), 2.5 L of C/M/W at 6/4/1 (fraction 2-6), 2.5 L of C/M/W at 4/6/1 (fraction 2-7) and 2.5 L of methanol/2.5 M NH3 aqueous solution at 1/1 (fraction 2-8).
Given that fractions 2-3 and 2-4 exhibited the strongest DPP-IV inhibitory activities, fraction 2-3 (45 mg) was further fractionated using hydrous methanol in an ODS silica gel chromatographic column (Hi Flash Column, 14 g, φ20 × 65 mm; Yamazen Corp.). The column was eluted and fractionated using a stepwise solvent system, and ten fractions were obtained: 300 mL of water (fraction 3-1), 150 mL of 5% methanol (fraction 3-2), 150 mL of 5% methanol (fraction 3-3), 150 mL of 5% methanol (fraction 3-4), 150 mL of 10% methanol (fraction 3-5), 150 mL of 10% methanol (fraction 3-6), 150 mL of 10% methanol (fraction 3-7), 150 mL of 20% methanol (fraction 3-8), 150 mL of 40% methanol (fraction 3-9) and 150 mL of methanol (fraction 3-10). Additionally, fraction 2-4 (247 mg) was fractionated using hydrous methanol in an ODS chromatographic column (Hi Flash Column, 14 g, Φ20 × 65 mm; Yamazen Corp.). After elution, this fraction was again divided into the following fractions: 300 mL of water (fraction 4-1), 150 mL of 5% methanol (fraction 4-2), 150 mL of 10% methanol (fraction 4-3), 150 mL of 20% methanol (fraction 4-4), 150 mL of 40% methanol (fraction 4-5), 150 mL of 60% methanol (fraction 4-6) and 150 mL of methanol (fraction 4-7).
Peptide synthesis
The synthetic peptides were prepared using the conventional Fmoc-solid-phase synthesis method with a peptide synthesiser (SyroI; Biotage Uppsala, Sweden). Fmoc-amino acid resin (HMP preloaded, 40 mmol) was used to synthesise the C-terminal, and Fmoc-amino acid (1 mmol) was used to realise the extension of the peptide chain. The synthesised peptide resin was cleaved using a mixture of TFA/triethylsilane/water (2 mL, 95/3/2) for a duration of > 2 h, after which it was filtered and the filtrate subsequently evaporated. The obtained residue was eluted from the resin using 10% (v/v) acetic acid (2 mL), following which dichloromethane (2 mL) was added. After stirring, the organic layer was removed by pipetting, and the same procedure was repeated three times. Following the subsequent evaporation of the aqueous layer, the residue was purified using an ODS silica gel chromatographic column (Sep Pak Vac 6 cc [1 g] C18 cartridge; Waters Corp., Milford, MA, USA) with different concentrations of methanol and 0.1% (v/v) aqueous trifluoroacetic acid (TFA).
Spectral analysis
The various fractions and the synthesised peptides were analysed using LCMS-IT-TOF (combined liquid chromatography [LC] system and high-performance ion trap/time-of-flight [IT-TOF] mass spectrometry [MS]). Chromatographic separations were performed on an XTerra MS C18 column (2.1 × 100 mm, 3.5 μm particle size; Waters Corp.). Further, a gradient programme was employed with a mobile phase combining solvent A (0.1% TFA in water) and solvent B (methanol) as follows: 3% B (0–15 min), 3–60% (15–45 min) and 60% (45–50 min). The flow rate was 0.1 mL/min, and the column and sample temperature were maintained at 40 and 15 °C, respectively. Mass spectrometric detection was performed on an LCMS-IT-TOF spectrometer (Shimadzu Corp., Kyoto, Japan) with an electrospray ionisation (ESI) source.
Quantitative analysis of SMPs
The quantitative determination of the concentrations of the inhibitory peptides in the SMPs was carried out by LC–MS/MS. Specifically, chromatographic separation was performed on an ACQUITY HSS PFP column (2.1 × 150 mm, 1.8 μm particle size; Waters Corp.). A gradient programme with a mobile phase combining solvent A (0.1% formic acid in water) and solvent B (methanol) was employed as follows: 20–72% B (0–15 min). The flow rate was 0.2 mL/min and the injection volume was 2 μL; the column and sample temperatures were maintained at 40 and 15 °C, respectively.
Mass spectrometric detection was realised using a Xevo TQD triple quadruple mass spectrometer equipped with an ESI source in the positive mode (Waters Corp.). The quantitative analysis of the inhibitory peptides was performed using the multiple reaction monitoring (MRM) method. The dwell time was set to 25 ms for each MRM transition, and the MRM transition channels (Q1/Q3) and the cone/collision energies (CE) of the inhibitory peptides were set as follows: Ile-Pro, 229.1/86.0 (8/16 V); Leu-Pro, 229.1/116.0 (4/12 V); Phe-Pro, 263.1/116.0 (28/14 V); Val-Pro-Ile, 328.2/229.1 (4/28 V); Val-Pro-Leu, 328.2/229.1 (32/16 V); Ile-Pro-Ile, 342.1/229.1 (4/18 V); Leu-Pro-Leu, 342.1/229.1 (32/16 V); Ile-Pro-Leu, 342.2/229.1 (34/18 V); Leu-Pro-Phe, 376.1/263.2 (36/18 V); Phe-Pro-Val-Gly, 419.2/120.0 (40/38 V); Leu-Pro-Val-Leu, 441.3/169.1 (42/32 V); and Val-Pro-Phe-Pro, 459.2/197.1 (42/24 V). Further, the optimal MS parameters were: capillary voltage, 3.15 kV; desolvation temperature, 50 °C. Data acquisition and processing were performed using Analyst software (MassLynx; Waters Corp.).
Statistical analysis
All assays were performed at least in triplicate. Each data point is presented as the mean of results corresponding to three samples that had been subjected to analysis of variance followed by Dunnett’s test. p < 0.05 were considered to indicate statistically significant differences, and all analyses were performed using SPSS software (ver. 27; IBM Corp., Armonk, NY, USA).
Results
Enzyme selection
Food-grade enzymes were selected based on their DPP-IV inhibitory activity and yield (Table 1). Among these, Protease P “Amano” 3SD, which was derived from Aspergillus melleus, exhibited the strongest DPP-IV inhibitory activity (59.2% at a concentration of 300 μg/mL), and its yield from wet salmon milt was 4.6% w/w.
Postprandial hypoglycaemic effect of SMPs
To clarify the postprandial hypoglycaemic effect of SMPs, the oral starch tolerance test was performed in SD rats. Specifically, SMPs were administered to the SD rats at doses of 0, 150, and 300 mg/kg body weight. The blood glucose concentrations as well as the area under the curve (AUC) at the different measurement times are shown in Table 2. In the 300 mg/kg SMPs group, the blood glucose level at 30 and 60 min after SMPs administration was lower and significantly lower than that in the control group, respectively. Additionally, the AUC of the 300 mg/kg SMPs group was significantly lower than that of the control group.
Separation and identification of DPP-IV inhibitory peptides in SMPs
The DPP-IV inhibitory activity of SMPs at a concentration of 300 μg/mL was found to be 37.1%. After the initial column separation on the Diaion HP20 column, fraction 1-2, which was eluted with 50% hydrous methanol, with a yield of 7.3 g, showed the strongest inhibitory activity (63.2%). Further fractionation of this fraction by silica gel column chromatography using a stepwise solvent system consisting of C/M/W resulted in eight fractions. Fractions 2-3 (yield 60.5 mg) and 2-4 (yield 290.6 mg) were found to exhibit a strong DPP-IV inhibitory activity (at a concentration of 200 μg/mL, 68.7% for fraction 2-3 and 91.0% for fraction 2-4), and each of these fractions was further separated by ODS column chromatography. All of the isolated fractions were evaluated for their DPP-IV inhibitory activities, and LC-MS analysis was performed on the more active fractions. The amino acid composition of the peptide in each fraction was estimated based on the mass number detected through LC-MS analysis. Subsequently, the predicted peptide was synthesised and analysed using LC-TOF-MS, and the peptides in SMPs were identified by comparing the retention time and the specific mass number. In this way, a total of 12 active DPP-IV inhibitory peptides were identified from SMPs, as shown in Table 3.
The contribution ratios of the identified peptides were calculated from their respective IC50 values and contents as previously described (Seki et al. 1996). Further, the identified peptides were quantified via MS using a Xevo TQD triple quadrupole mass spectrometer equipped with a positive-mode ESI source. The contribution ratio of each dipeptide against SMPs with respect to the inhibition of DPP-IV activity is shown in Table 4. Among the identified peptides, Val-Pro-Ile and Ile-Pro-Ile showed the strongest DPP-IV inhibitory activities, with IC50 values of 1.0 μg/mL. The newly identified compounds, namely Ile-Pro-Leu, Phe-Pro-Val-Gly, Leu-Pro-Val-Leu and Val-Pro-Phe-Pro, also showed low IC50 values (9.0, 17.2, 20.4, and 10.0 μg/mL, respectively). Thus, the major peptides in the SMPs sample were found to be dipeptides, namely Leu-Pro, Ile-Pro and Phe-Pro (527, 360 and 246 ppm, respectively). These peptides had low IC50 values whereas their high content resulted in a high contribution.
Discussion
The prevalence of metabolic syndromes, including glucose intolerance, is a serious health problem that requires the development of effective preventive and therapeutic methods. Additionally, in the context of diabetes, impaired glucose tolerance is associated with an impaired action of insulin (insulin resistance) or the prevention of insulin secretion from pancreatic β-cells. GLP-1 is a gastrointestinal hormone produced by gastrointestinal secretory cells (L cells) that are abundant in the ileum and large intestine. This hormone exerts various effects, such as promoting insulin secretion from pancreatic β-cells and the proliferation of pancreatic β-cells and inhibiting apoptosis, and has been reported to also exhibits anorexigenic effects and to be rapidly cleaved at the N-terminal residues by DPP-IV in the blood, resulting in its inactive form. Thus, its half-life can be as short as approximately 2 min (Hansen et al. 1999). Additionally, given that the inhibition of blood DPP-IV prolongs the half-life of GLP-1, thereby allowing the effect of insulin to persist and enabling the decrease in blood glucose levels, DPP-IV inhibitors, such as sitagliptin and alogliptin, have been investigated and used as antidiabetics. Recently, several peptides derived from food materials have also been reported to exhibit DPP-IV inhibitory activity (Cermeño et al. 2019; Ji et al. 2017a; Jin et al. 2020; Ketnawa et al. 2019; Nongonierma et al. 2018). Therefore, we investigated the development of a functional food material with DPP-IV inhibitory activity using chum salmon milt, which is an unused resource that is discarded in large quantities during fishery processing.
Initially, to hydrolyse the salmon milt, food-grade enzymes were selected based on their DPP-IV inhibitory activities and yields. Among these, Protease P “Amano” 3SD showed the strongest DPP-IV inhibitory activity (Table 1). Additionally, given that this enzyme also exhibited a good yield, it was used to prepare SMPs, which exhibited DPP-IV inhibitory activity with an IC50 value of 529 μg/mL, which is stronger than that of whey protein hydrolysate (1.33 mg/mL) (Nongonierma and FitzGerald 2013), peptides derived from Antarctic krill protein (1.6272 mg/mL; Ji et al. 2017a) and hydrolysates derived from gelatin extracted from salmon skin (1.54 mg/mL; Jin et al. 2020) and muscle (4.8 mg/mL; Ketnawa et al. 2019), which are food materials with DPP-IV inhibitory activity. Subsequently, an oral starch tolerance test involving SD rats was realised, and the active ingredients were identified. As shown in Table 2, in the 300 mg/kg SMPs group, the blood glucose level at 60 min after SMPs administration as well as the AUC were significantly lower than those corresponding to the control group. These findings show that SMPs exhibit a suppressive effect on postprandial hyperglycaemia.
We then investigated the SMPs components that were active against DPP-IV. Using the level of DPP-IV inhibitory activity as an index, the bioassay-guided separation was repeated using various chromatographic techniques, and LC–MS/MS analysis was carried out on the active fraction to determine the peptide sequences. Thereafter, the deduced peptides were prepared using a peptide synthesiser and their sequences were confirmed by comparison with the peptides present in SMPs. As shown in Table 3, 12 active di-, tri- and tetrapeptides, including Phe-Pro-Val-Gly, Leu-Pro-Val-Leu, Val-Pro-Phe-Pro and Ile-Pro-Leu as four new DPP-IV inhibitory peptides, were identified. We also observed that all of the these peptides contain Pro at the second position from the N-terminus. As already noted, DPP-IV is a serine protease that recognises and cleaves to the second Pro or Ala residue from the N-terminus of peptides, showing a strong activity against peptides possessing Pro and Ala at this position (Davy et al. 2000). Indeed, it has also been demonstrated that most peptides with DPP-IV inhibitory activity have Pro at the second position. Therefore, among the 12 peptides identified from SMPs, the DPP-IV inhibitory activity of eight peptides has already been reported. Specifically, Ile-Pro-Ile, Val-Pro-Leu and Val-Pro-Ile have been reported as Diprotins A, B and C, respectively (Umezawa et al. 1984; Wiedeman and Trevillyan 2003), whereas Leu-Pro-Leu has been reported as the DPP-IV inhibitory peptide present in milk protein-derived peptides (Nongonierma and FitzGerald 2014). Leu-Pro-Phe was first reported to have angiotensin-converting enzyme inhibitory activity (Wu et al. 2006). Furthermore, a patent application has been filed for Leu-Pro-Phe, which is present in zein hydrolysates, owing to its DPP-IV inhibitory activity (Hara et al. 2011). The dipeptides Ile-Pro, Leu-Pro and Phe-Pro, which are known to be present in many food materials, have been reported to exhibit DPP-IV inhibitory activity (Endröczi et al.1990; Hatanaka et al. 2012). Moreover, to the best of our knowledge, the tetrapeptides Phe-Pro-Val-Gly, Leu-Pro-Val-Leu and Val-Pro-Phe-Pro, as well as the tripeptide Ile-Pro-Leu, all of which were identified in our SMPs sample, are novel. Overall, our results suggest that these components are involved in the DPP-IV inhibitory activity of SMPs.
The IC50 values and contents of these identified peptides were investigated to calculate their respective contribution ratios to DPP-IV inhibitory activity as previously described (Seki et al. 1996). Among the identified peptides, Ile-Pro was found to make the highest contribution to DPP-IV inhibitory activity (1.3%), followed by Val-Pro-Phe-Pro (0.9%). Overall, SMPs were found to be a mixture of several active DPP-IV inhibitory peptides that showed combined DPP-IV inhibitory activity, with Ile-Pro being the most active fraction (i.e. fraction 3-2), implying that it is the core peptide responsible for the DPP-IV inhibitory activity of SMPs. More proline-containing active peptides were obtained from salmon milt in comparison to muscle, probably because the proline content of salmon milt was 6.9 mol% versus 4.2 mol% in muscle (data not shown). These results suggest that SMPs have a relatively stronger DPP-IV inhibitory activity than peptides from other food ingredients.
Overall, this study revealed that SMPs, which is produced from unused resources discarded in large quantities following fishery processing, at an oral dose of 300 mg/kg exhibited a strong inhibitory activity against DPP-IV and suppressed the increase in blood glucose levels compared with the control, based on the oral starch tolerance test in SD rats. We also confirmed that SMPs exert a suppressive effect on postprandial hyperglycaemia and is, consequently, a promising potential functional food material. Clinical trials using SMPs have been conducted, and the results will be reported in the near future.
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Takahashi, Y., Kamata, A. & Konishi, T. Dipeptidyl peptidase-IV inhibitory peptides derived from salmon milt and their effects on postprandial blood glucose level. Fish Sci 87, 619–626 (2021). https://doi.org/10.1007/s12562-021-01530-9
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DOI: https://doi.org/10.1007/s12562-021-01530-9