Effect of fermentation on ameliorative properties of tamarind seed (Tamarindus indica) in sucrose-induced diabetic-like biochemical alterations in Drosophila melanogaster
Corresponding Author
Esther E. Nwanna
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Correspondence
Esther E. Nwanna, Biochemistry Department, Federal University of Technology, P.M.B. 704 Akure, Gaga, Nigeria.
Email: [email protected]
Search for more papers by this authorOlayemi Philemon Aro
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Drosophila Research Lab, Functional Foods and Nutraceuticals Unit, Biochemistry Department, Federal University of Technology, Akure, Ondo, Nigeria
Search for more papers by this authorOpeyemi Babatunde Ogunsuyi
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Drosophila Research Lab, Functional Foods and Nutraceuticals Unit, Biochemistry Department, Federal University of Technology, Akure, Ondo, Nigeria
Department of Biomedical Science, Federal University of Technology, Akure, Nigeria
Search for more papers by this authorGaniyu Oboh
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Drosophila Research Lab, Functional Foods and Nutraceuticals Unit, Biochemistry Department, Federal University of Technology, Akure, Ondo, Nigeria
Search for more papers by this authorCorresponding Author
Esther E. Nwanna
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Correspondence
Esther E. Nwanna, Biochemistry Department, Federal University of Technology, P.M.B. 704 Akure, Gaga, Nigeria.
Email: [email protected]
Search for more papers by this authorOlayemi Philemon Aro
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Drosophila Research Lab, Functional Foods and Nutraceuticals Unit, Biochemistry Department, Federal University of Technology, Akure, Ondo, Nigeria
Search for more papers by this authorOpeyemi Babatunde Ogunsuyi
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Drosophila Research Lab, Functional Foods and Nutraceuticals Unit, Biochemistry Department, Federal University of Technology, Akure, Ondo, Nigeria
Department of Biomedical Science, Federal University of Technology, Akure, Nigeria
Search for more papers by this authorGaniyu Oboh
Biochemistry Department, Federal University of Technology, Akure, Nigeria
Drosophila Research Lab, Functional Foods and Nutraceuticals Unit, Biochemistry Department, Federal University of Technology, Akure, Ondo, Nigeria
Search for more papers by this authorAbstract
Earlier studies have reported that tamarind seed, which is an underused part of the tamarind fruit tree, may be able to help treat diabetes. The seed has rich nutrient content, but its consumption is limited due to its hard structure and the presence of anti-nutrients. To get over this constraint, the seed is usually pre-treated to minimize anti-nutrients and improve palatability. This study was carried out to determine the effect of fermentation on the ameliorative properties of tamarind seeds in sucrose-induced diabetic-like biochemical alterations in Drosophila melanogaster. Flies were divided into six (6) groups of 40 flies each; group I (control) was fed a basal diet, group II was fed 30% sucrose only, and groups III–VI were fed 30% sucrose each and treated with varying concentrations of the sample (raw and fermented) for 14 days. The survival rate and behavioral studies were assessed after treatment. Furthermore, the homogenates were assayed for inhibitory activities of carbohydrate metabolizing enzymes (α-amylase and α-glucosidase). Total thiol content and antioxidant enzyme activities like catalase, superoxide dismutase, and glutathione-S-transferase were also carried out. The results showed a reduction in survival rate and locomotor performance in the flies fed with high-sucrose diet (HSD). Elevated levels of α-amylase, α-glucosidase, ROS, and significantly reduced antioxidant enzyme activities were also observed in flies fed with HSD. These alterations were ameliorated in flies treated with dietary inclusions of both raw and fermented seeds; while no significant difference was observed between the ameliorative effects of raw and fermented samples against elevated α-amylase and α-glucosidase activities. However, fermented samples exhibited significantly higher antioxidant properties. Conclusively, this study revealed that the antidiabetic properties of tamarind seeds were conserved by fermentation with improved antioxidant properties in the Drosophila model of diabetes-like biochemical alteratios.
Practical applications
The fermentation processing method is one of the earliest in food processing and preservation. This approach has a variety of consequences for the bioactive elements in functional foods, hence, it is important to consider. Tamarind seeds have been reported in several studies for their anti-hyperglycemic properties, but with a dearth of information on how different processing methods could affect this therapeutic effect. Therefore, this study was carried out to determine the effect of fermentation, a food processing, and preservation method, on some behavioral and biochemical indices in the Drosophila model of diabetes-like biochemical alterations.
CONFLICT OF INTEREST
The authors have declared no conflicts of interest for this article.
Open Research
DATA AVAILABILITY STATEMENT
The data that support the findings of this study are available from the corresponding author upon reasonable request.
REFERENCES
- Adachi, Y., Ota, K., Minami, I., Yamada, T., & Watanabe, T. (2021). Lower insulin secretion is associated with hippocampal and parahippocampal gyrus atrophy in elderly patients with type 2 diabetes mellitus. Journal of Diabetes Investigation, 12, 1908–1913. https://doi.org/10.1111/jdi.13554
- Adedara, I. A., Abolaji, A. O., Rocha, J. B. T., & Farombi, E. O. (2016). Diphenyl diselenide protects against mortality, locomotor deficits and oxidative stress in Drosophila melanogaster model of manganese-induced neurotoxicity. Neurochemical Research, 41, 1430–1438. https://doi.org/10.1007/s11064-016-1852-x
- Adedayo, B. C., Ogunsuyi, O. B., Akinniyi, S. T., & Oboh, G. (2020). Effect of Andrographis paniculata and Phyllanthus amarus leaf extracts on selected biochemical indices in Drosophila melanogaster model of neurotoxicity. Drug and Chemical Toxicology, 45, 407–416. https://doi.org/10.1080/01480545.2019.1708377
- Adefegha, S. A., Oyeleye, S. I., & Oboh, G. (2015). Distribution of phenolic contents, antidiabetic potentials, antihypertensive properties, and antioxidative effects of soursop (Annona muricata L.) fruit parts in vitro. Biochemistry Research International, 2015, 1–8. https://doi.org/10.1155/2015/347673
- Ademiluyi, A. O., & Oboh, G. (2012). Attenuation of oxidative stress and hepatic damage by some fermented tropical legume condiment diets in streptozotocin-induced diabetes in rats. Asian Pacific Journal of Tropical Medicine, 5(9), 692–697. https://doi.org/10.1016/S1995-7645(12)60108-4
- Ademiluyi, A. O., Oboh, G., Boligon, A. A., & Athayde, M. L. (2014). Effect of fermented soybean condiment supplemented diet on α-amylase and α-glucosidase activities in Streptozotocin-induced diabetic rats. Journal of Functional Foods, 9, 1–9. https://doi.org/10.1016/j.jff.2014.04.003
- Ademiluyi, A. O., Oboh, G., Boligon, A. A., & Athayde, M. L. (2015). Dietary supplementation with fermented legumes modulate hyperglycemia and acetylcholinesterase activities in Streptozotocin-induced diabetes. Pathophysiology, 22, 195–201. https://doi.org/10.1016/j.pathophys.2015.08.003
- Agu, K. C., Okolie, N. P., Falodun, A., Erharuyi, O., Igbe, I., Elekofehinti, O. O., Edosa, R. O., & Oghagbon, S. E. (2017). Isolation and elucidation of 15-acetylguanacone from soursop (Annona muricata Linn) fruit and molecular docking experiments. Journal of Applied Sciences and Environmental Management, 21, 236–243. https://doi.org/10.4314/jasem.v21i2.3
- Aloulou, A., Hamden, K., Elloumi, D., Ali, M. B., Hargafi, K., Jaouadi, B., Ayadi, F., Elfeki, A., & Ammar, E. (2012). Hypoglycemic and antilipidemic properties of kombucha tea in alloxan-induced diabetic rats. BMC Complementary and Alternative Medicine, 12, 1–9. https://doi.org/10.1186/1472-6882-12-63
- Altun, E., Yazici, H., Arslan, E., Tulaci, K. G., & Erken, H. A. (2019). The impact of type II diabetes on tongue dysplasia and p16-related aging process: An experimental study. Analytical Cellular Pathology, 2019, 1–6. https://doi.org/10.1155/2019/3563215
- American Society for Testing and Materials (ASTM). (1999). ASTM D5712-99e1, standard test method for analysis of aqueous extractable protein in natural rubber and its products using the modified lowry method. ASTM International. August 10, 1999. 83.040.10. http://www.astm.org/Standards/D5719-99e1.html.
- Ayala, A., Muñoz, M. F., & Argüelles, S. (2014). Lipid peroxidation: Production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxidative Medicine and Cellular Longevity, 2014, 1–31. https://doi.org/10.1155/2014/360438
- Bagul, M., Sonawane, S. K., & Arya, S. S. (2015). TARs. 34(June). TARs.
- Bagul, M. B., Sonawane, S. K., & Arya, S. S. (2018). Bioactive characteristics and optimization of tamarind seed protein hydrolysate for antioxidant-rich food formulations. 3 Biotech, 8, 1–8. https://doi.org/10.1007/s13205-018-1240-0
- Bai, Y., Li, K., Shao, J., Luo, Q., & Jin, L. H. (2018). Flos Chrysanthemi Indici extract improves a high-sucrose diet-induced metabolic disorder in Drosophila. Experimental and Therapeutic Medicine, 16, 2564–2572. https://doi.org/10.3892/etm.2018.6470
- Balaji, R., Duraisamy, R., & Kumar, M. P. S. (2019). Complications of diabetes mellitus: A review. Drug Invention Today, 12, 98–103.
- Benderitter, M., Maupoil, V., Vergely, C., Dalloz, F., Briot, F., & Rochette, L. (1998). Studies by electron paramagnetic resonance of the importance of iron in the hydroxyl scavenging properties of ascorbic acid in plasma: Effects of iron chelators. Fundamental and Clinical Pharmacology, 12, 510–516. https://doi.org/10.1111/j.1472-8206.1998.tb00979.x
- Bhadoriya, S. S., Mishra, V., Raut, S., Ganeshpurkar, A., & Jain, S. K. (2012). Anti-inflammatory and antinociceptive activities of a hydroethanolic extract of Tamarindus indica leaves. Scientia Pharmaceutica, 80, 685–700. https://doi.org/10.3797/scipharm.1110-09
- Bier, E., & Bodmer, R. (2004). Drosophila, an emerging model for cardiac disease. Gene, 342, 1–11. https://doi.org/10.1016/j.gene.2004.07.018
- Bormann, H., & Melzig, M. F. (2000). Inhibition of metallopeptidases by flavonoids and related compounds. Die Pharmazie, 55, 129–132.
- Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72, 248–254. https://doi.org/10.1016/0003-2697(76)90527-3
- Brennan, L., Shine, A., Hewage, C., Malthouse, J. P. G., Brindle, K. M., McClenaghan, N., Flatt, P. R., & Newsholme, P. (2002). A nuclear magnetic resonance-based demonstration of substantial oxidative L-alanine metabolism and L-alanine-enhanced glucose metabolism in a clonal pancreatic β-cell line: Metabolism of L-alanine is important to the regulation of insulin secretion. Diabetes, 51, 1714–1721. https://doi.org/10.2337/diabetes.51.6.1714
- Brunner, J. H. (1984). Direct spectrophometer dertermination of saponin. Animal Chemistry, 34, 1314–1326.
- Charles, S., & Henquin, J. C. (1983). Distinct effects of various amino acids on 45Ca2+ fluxes in rat pancreatic islets. Biochemical Journal, 214, 899–907. https://doi.org/10.1042/bj2140899
- Chu, Y. F., Sun, J., Wu, X., & Liu, R. H. (2002). Antioxidant and antiproliferative activities of common vegetables. Journal of Agricultural and Food Chemistry, 50, 6910–6916. https://doi.org/10.1021/jf020665f
- Das, L., Bhaumik, E., Raychaudhuri, U., & Chakraborty, R. (2012). Role of nutraceuticals in human health. Journal of Food Science and Technology, 49, 173–183. https://doi.org/10.1007/s13197-011-0269-4
- Day, R. A., & Underwood, A. L. (1999). Quantitative analysis ( 6th ed., pp. 701) In Analytical Chemistry. Hall publication.
- DeFronzo, R. A., Ferrannini, E., Groop, L., Henry, R. R., Herman, W. H., Holst, J. J., Hu, F. B., Kahn, C. R., Raz, I., Shulman, G. I., Simonson, D. C., Testa, M. A., & Weiss, R. (2015). Type 2 diabetes mellitus. Nature Reviews Disease Primers, 1, 1–22. https://doi.org/10.1038/nrdp.2015.19
- Dixon, G., Nolan, J., McClenaghan, N., Flatt, P. R., & Newsholme, P. (2003). A comparative study of amino acid consumption by rat islet cells and the clonal beta-cell line BRIN-BD11 - The functional significance of L-alanine. Journal of Endocrinology, 179, 447–454. https://doi.org/10.1677/joe.0.1790447
- Ecker, A., Gonzaga, T. K. S. d. N., Seeger, R. L., dos Santos, M. M., Loreto, J. S., Boligon, A. A., Meinerz, D. F., Lugokenski, T. H., da Rocha, J. B. T., & Barbosa, N. V. (2017). High-sucrose diet induces diabetic-like phenotypes and oxidative stress in Drosophila melanogaster: Protective role of Syzygium cumini and Bauhinia forficata. Biomedicine and Pharmacotherapy, 89, 605–616. https://doi.org/10.1016/j.biopha.2017.02.076
- Ellman, G. L. (1959). Tissue sulfhydryl groups. Archives of Biochemistry and Biophysics, 82, 70–77. https://doi.org/10.1016/0003-9861(59)90090-6
- Gerber, P. A., & Rutter, G. A. (2017). The role of oxidative stress and hypoxia in pancreatic beta-cell dysfunction in diabetes mellitus. Antioxidants and Redox Signaling, 26, 501–518. https://doi.org/10.1089/ars.2016.6755
- Glew, R. S., Vanderjagt, D. J., Chuang, L. T., Huang, Y. S., Millson, M., & Glew, R. H. (2005). Nutrient content of four edible wild plants from West Africa. Plant Foods for Human Nutrition, 60, 187–193. https://doi.org/10.1007/s11130-005-8616-0
- Graham, P., & Pick, L. (2017). Drosophila as a model for diabetes and diseases of insulin resistance. Current Topics in Developmental Biology, 121, 397–419. https://doi.org/10.1016/bs.ctdb.2016.07.011
- Habig, W. H., & Jakoby, W. B. (1981). Assays for differentiation of glutathione S-transferases. In Methods in enzymology (Vol. 77, pp. 398–405). Academic Press. https://doi.org/10.1016/S0076-6879(81)77053-8
- Hewlings, S. J., & Kalman, D. S. (2017). Curcumin: A review of its effects on human health. Foods, 6, 92. https://doi.org/10.3390/foods6100092
- Iyer, S. R., & Iyer, R. R. (1995). Anti leishmanial therapy--The changing scene. The Journal of the Association of Physicians of India, 43(3), 234.
- Joya-Galeana, J., Fernandez, M., Cervera, A., Reyna, S., Ghosh, S., Triplitt, C., Musi, N., Defronzo, R. A., & Cersosimo, E. (2011). Effects of insulin and oral anti-diabetic agents on glucose metabolism, vascular dysfunction and skeletal muscle inflammation in type 2 diabetic subjects. Diabetes/Metabolism Research and Reviews, 27, 373–382. https://doi.org/10.1002/dmrr.1185
- Kelly, F. J. (1998). Use of antioxidants in the prevention and treatment of disease. Journal of the International Federation of Clinical Chemistry/IFCC, 10, 21–23.
- Kunnumakkara, A. B., Banik, K., Bordoloi, D., Harsha, C., Sailo, B. L., Padmavathi, G., Roy, N. K., Gupta, S. C., & Aggarwal, B. B. (2018). Googling the guggul (Commiphora and Boswellia) for prevention of chronic diseases. Frontiers in Pharmacology, 9, 686. https://doi.org/10.3389/fphar.2018.00686
- Kuru, P. (2014). Tamarindus indica and its health related effects. Asian Pacific Journal of Tropical Biomedicine, 4, 676–681. https://doi.org/10.12980/APJTB.4.2014APJTB-2014-0173
10.12980/APJTB.4.2014APJTB-2014-0173 Google Scholar
- Leung, P. S. (2016). The potential protective action of vitamin D in hepatic insulin resistance and pancreatic islet dysfunction in type 2 diabetes mellitus. Nutrients, 8, 147. https://doi.org/10.3390/nu8030147
- Long, A. N., & Dagogo-Jack, S. (2011). Comorbidities of diabetes and hypertension: Mechanisms and approach to target organ protection. Journal of Clinical Hypertension, 13, 244–251. https://doi.org/10.1111/j.1751-7176.2011.00434.x
- Maiti, R., Jana, D., Das, U. K., & Ghosh, D. (2004). Antidiabetic effect of aqueous extract of seed of Tamarindus indica in streptozotocin-induced diabetic rats. Journal of Ethnopharmacology, 92, 85–91. https://doi.org/10.1016/j.jep.2004.02.002
- Makkar, H. P. S. (2003). Quantification of tannins in tree and shrub foliage: A laboratory manual. Springer Science & Business Media. https://doi.org/10.1007/978-94-017-0273-7
10.1007/978-94-017-0273-7 Google Scholar
- Marín, A., Ferreres, F., Tomás-Barberán, F. A., & Gil, M. I. (2004). Characterization and quantitation of antioxidant constituents of sweet pepper (Capsicum annuum L.). Journal of Agricultural and Food Chemistry, 52, 3861–3869. https://doi.org/10.1021/jf0497915
- Marklund, S., & Marklund, G. (1974). Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. European Journal of Biochemistry, 47, 469–474. https://doi.org/10.1111/j.1432-1033.1974.tb03714.x
- Materska, M., & Perucka, I. (2005). Antioxidant activity of the main phenolic compounds isolated from hot pepper fruit (Capsicum annuum L.). Journal of Agricultural and Food Chemistry, 53, 1750–1756. https://doi.org/10.1021/jf035331k
- Meas, T., & Guillausseau, P. J. (2011). Abnormalities in insulin secretion in type 2 diabetes mellitus. In M. Wang (Ed.), Metabolic syndrome: Underlying mechanisms and drug therapies. Wiley Online Library. https://doi.org/10.1002/9780470910016.ch3
10.1002/9780470910016.ch3 Google Scholar
- Mohammad Alizadeh, A. H., & Mohammad Khah, M. T. (2016). Metabolic syndrome in patients with gallstone. Journal of Liver, 2(5), 2–4. https://doi.org/10.4172/2167-0889.1000138
10.4172/2167-0889.1000138 Google Scholar
- Mohsenpour, B., Alizadeh, N., Alizadeh, N., Arasteh, M., & Karimian, F. (2013). Comparison of sexual dysfunction between diabetic and non-diabetic women. Journal of Mid-Life Health, 4, 167–171. https://doi.org/10.4103/0976-7800.119001
- Musselman, L. P., Fink, J. L., Narzinski, K., Ramachandran, P. V., Hathiramani, S. S., Cagan, R. L., & Baranski, T. J. (2011). A high-sugar diet produces obesity and insulin resistance in wild-type Drosophila. DMM Disease Models and Mechanisms, 4, 842–849. https://doi.org/10.1242/dmm.007948
- Ndisang, J. F. (2010). Role of heme oxygenase in inflammation, insulin-signalling, diabetes and obesity. Mediators of Inflammation, 2010, 18. https://doi.org/10.1155/2010/359732
- Oboh, G., Puntel, R. L., & Rocha, J. B. T. (2007). Hot pepper (Capsicum annuum, Tepin and Capsicum chinese, Habanero) prevents Fe2+−induced lipid peroxidation in brain - in vitro. Food Chemistry, 102, 178–185. https://doi.org/10.1016/j.foodchem.2006.05.048
- Oboh, G., Ogunsuyi, O. B., Adegbola, D. O., Ademiluyi, A. O., & Oladun, F. L. (2019). Influence of gallic and tannic acid on therapeutic properties of acarbose in vitro and in vivo in Drosophila melanogaster. Biomedical Journal, 42, 317–327. https://doi.org/10.1016/j.bj.2019.01.005
- Oboh, G., Ogunsuyi, O. B., Ojelade, M. T., & Akomolafe, S. F. (2018). Effect of dietary inclusions of bitter kola seed on geotactic behavior and oxidative stress markers in Drosophila melanogaster. Food Science and Nutrition, 6, 2177–2187. https://doi.org/10.1002/fsn3.782
- Ogunsuyi, O. B., Ademiluyi, A. O., & Oboh, G. (2020). Solanum leaves extracts exhibit antioxidant properties and inhibit monoamine oxidase and acetylcholinesterase activities (in vitro) in Drosophila melanogaster. Journal of Basic and Clinical Physiology and Pharmacology, 31(3), 20190256. https://doi.org/10.1515/jbcpp-2019-0256
- Ogunsuyi, O. B., Olagoke, O. C., Afolabi, B. A., Oboh, G., Ijomone, O. M., Barbosa, N. V., & da Rocha, J. B. T. (2021). Dietary inclusions of Solanum vegetables mitigate aluminum-induced redox and inflammation-related neurotoxicity in Drosophila melanogaster model. Nutritional Neuroscience, 25(10), 2077–2091. https://doi.org/10.1080/1028415X.2021.1933331
- Ohkawa, H., Ohishi, N., & Yagi, K. (1979). Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95, 351–358. https://doi.org/10.1016/0003-2697(79)90738-3
- Okwu, D. E., & Josiah, C. (2006). Evaluation of the chemical composition of two Nigerian medicinal plants. African Journal of Biotechnology, 5, 357–361.
- Owusu-Ansah, E., & Perrimon, N. (2014). Modeling metabolic homeostasis and nutrient sensing in Drosophila: Implications for aging and metabolic diseases. DMM Disease Models and Mechanisms, 7, 343–350. https://doi.org/10.1242/dmm.012989
- Parada, J., & Aguilera, J. M. (2007). Food microstructure affects the bioavailability of several nutrients. Journal of Food Science, 72, R21–R32. https://doi.org/10.1111/j.1750-3841.2007.00274.x
- Patil, A., Nirmal, S., Pattan, S., Tambe, V., & Tare, M. (2012). Antidiabetic effect of polyherbal combinations in STZ induced diabetes involve inhibition of α-amylase and α-glucosidase with amelioration of lipid profile. Phytopharmacology, 2, 46–57.
- Paula, F. S., Kabeya, L. M., Kanashiro, A., de Figueiredo, A. S. G., Azzolini, A. E. C. S., Uyemura, S. A., & Lucisano-Valim, Y. M. (2009). Modulation of human neutrophil oxidative metabolism and degranulation by extract of Tamarindus indica L. fruit pulp. Food and Chemical Toxicology, 47, 163–170. https://doi.org/10.1016/j.fct.2008.10.023
- Pearson, D. (1976). Chemical analysis of foods ( 7th ed.). Churchill Livingstons.
- Podsedek, A. (2007). Natural antioxidants and antioxidant capacity of Brassica vegetables: A review. LWT - Food Science and Technology, 40, 1–11. https://doi.org/10.1016/j.lwt.2005.07.023
- Rajendiran, D., Packirisamy, S., & Gunasekaran, K. (2018). A review on role of antioxidants in diabetes. Asian Journal of Pharmaceutical and Clinical Research, 11, 48–53. https://doi.org/10.22159/ajpcr.2018.v11i2.23241
10.22159/ajpcr.2018.v11i2.23241 Google Scholar
- Santini, A., Tenore, G. C., & Novellino, E. (2017). Nutraceuticals: A paradigm of proactive medicine. European Journal of Pharmaceutical Sciences, 96, 53–61. https://doi.org/10.1016/j.ejps.2016.09.003
- Sener, A., & Malaisse, W. J. (1980). L-leucine and a nonmetabolized analogue activate pancreatic islet glutamate dehydrogenase. Nature, 288, 187–189. https://doi.org/10.1038/288187a0
- Shahraki, M. R., Harati, M., & Shahraki, A. R. (2011). Prevention of high fructose-induced metabolic syndrome in male wistar rats by aqueous extract of Tamarindus indica seed. Acta Medica Iranica, 49, 277–283.
- Siddhuraju, P. (2007). Antioxidant activity of polyphenolic compounds extracted from defatted raw and dry heated Tamarindus indica seed coat. LWT - Food Science and Technology, 40, 982–990. https://doi.org/10.1016/j.lwt.2006.07.010
- Sinha, A. K. (1972). Colorimetric assay of catalase. Analytical Biochemistry, 47, 389–394. https://doi.org/10.1016/0003-2697(72)90132-7
- Smith, P. A., Sakura, H., Coles, B., Gummerson, N., Proks, P., & Ashcroft, F. M. (1997). Coupling in mouse pancreatic Fl-cells. Physiology, 499, 625–635.
- Snyder, R. W., & Berns, J. S. (2004). Use of insulin and oral hypoglycemic medications in patients with diabetes mellitus and advanced kidney disease. Seminars in Dialysis, 17, 365–370. https://doi.org/10.1111/j.0894-0959.2004.17346.x
- Sofowara, L. A. (1993). Medicinal plants and traditional medicine in Africa. Spectrum Books Ltd.
- Sofowora, A. (1996). Research on medicinal plants and traditional medicine in Africa. Journal of Alternative and Complementary Medicine, 2, 365–372. https://doi.org/10.1089/acm.1996.2.365
- Sole, S. S., Srinivasan, B. P., & Akarte, A. S. (2013). Anti-inflammatory action of Tamarind seeds reduces hyperglycemic excursion by repressing pancreatic β-cell damage and normalizing SREBP-1c concentration. Pharmaceutical Biology, 51, 350–360. https://doi.org/10.3109/13880209.2012.729067
- Sole, S. S., & Srinivasan, B. P. (2012). Aqueous extract of tamarind seeds selectively increases glucose transporter-2, glucose transporter-4, and islets' intracellular calcium levels and stimulates β-cell proliferation resulting in improved glucose homeostasis in rats with streptozotocin-induce. Nutrition Research, 32, 626–636. https://doi.org/10.1016/j.nutres.2012.06.015
- Sun, L., Warren, F. J., & Gidley, M. J. (2019). Natural products for glycaemic control: Polyphenols as inhibitors of alpha-amylase. Trends in Food Science and Technology, 91, 262–273. https://doi.org/10.1016/j.tifs.2019.07.009
- Wheeler, E., & Ferrel, R. E. (1971). A method for phytic acid determination in wheat and wheat fractions. Cereal Chemistry, 48, 312–320.
- Zhou, Y., Liu, Z., Chen, Y., & Jin, L. H. (2016). Identification of the protective effects of traditional medicinal plants against SDS-induced Drosophila gut damage. Experimental and Therapeutic Medicine, 12, 2671–2680. https://doi.org/10.3892/etm.2016.3641