Now accepting submissions for the upcoming volume
Vol. 4 · Issue 1 · 2024 May 29, 2024 Research Articles

Therapeutic effect of the solvent fraction of hexane leaf extract of Tapinanthus bangwensis (Engl. & K. Krause) (Loranthaceae) in alloxan-induced pathology in diabetic rats

GI
Godwin Okwudiri Ihegboro Corresponding Nigeria Police Academy, Faculty of Science, Department of Biochemistry and Forensic Science, Wudil, Kano, Nigeria goihegboro@polac.edu.ng Nigeria
CO
Chimaobi James Ononamadu Nigeria Police Academy, Faculty of Science, Department of Biochemistry and Forensic Science, Wudil, Kano, Nigeria Nigeria
MF
Mujiburrahman Fadilu Nigeria Police Academy, Faculty of Science, Department of Biochemistry and Forensic Science, Wudil, Kano, Nigeria Nigeria
PO
Peter Prince Oghenekome Nigeria Police Academy, Faculty of Science, Department of Biochemistry and Forensic Science, Wudil, Kano, Nigeria Nigeria
BJ
Bello Jacob Nigeria Police Academy, Faculty of Science, Department of Biochemistry and Forensic Science, Wudil, Kano, Nigeria Nigeria
SE
Sunday Edwin Nigeria Police Academy, Faculty of Science, Department of Biochemistry and Forensic Science, Wudil, Kano, Nigeria Nigeria
Pages79-89 PublishedMay 29, 2024 LicenseOpen Access
Full Text
IJPBP 1 VOL 4 · 1
VOL 4 · NO 1 · 2024 View issue

Abstract

Plant-based products are gradually replacing pharmaceuticals in treating ailments, including diabetes, due to their safety, cost-effectiveness, potency, and availability. Therefore, the current study looked into the therapeutic effect of the solvent fraction of hexane leaf extract of Tapinanthus bangwensis (HEXETACF) (Loranthaceae) in alloxan-induced pathology in diabetic rats. The biochemical parameters were estimated using analytical grade kits via spectrophotometric method. The laboratory rats were distributed into group W (five rats on feed and water), group X (seven rats + 150 mg/kg alloxan solution only), group Y (seven rats + 150 mg/kg alloxan solution + 200 mg/kg BW silymarin for 21 days), and group Z (seven rats + 150 mg/kg alloxan solution + 250 mg/kg BW HEXETACF for 21 days). The results showed that HEXETACF and silymarin (SILY) reduced blood glucose concentration by 33.77% and 34.80%, respectively, after the 21 st day of treatment ( p < 0.05). Additionally, alkaline phosphatase (ALP) and alanine aminotransferase (ALT) activity in SILY and HEXETACF were significantly decreased compared to the diabetic group ( p < 0.05), but no significant decrease in aspartate aminotransferase (AST) activity was observed between the test samples and the diabetic group. Furthermore, the test samples lowered malondialdehyde (MDA) levels, by improving glutathione, superoxide dismutase (SOD), and catalase (CAT) activity. The HEXETACF and SILY significantly decreased triglyceride levels (TG) compared to the diabetic group at p < 0.05. They also reduced low-density lipoprotein (LDL) and cholesterol levels and increased the high-density lipoprotein levels compared to the diabetic group. Additionally, no significant decrease in serum electrolytes (Na + , K + , and Cl - ), urea, and creatinine (including albumin and total protein) values was observed in HEXETACF and SILY, while hematological indices increased compared to the diabetic group. Histology results revealed that the test samples had normalized glomeruli, β-islet cells, and hepatocytes. However, a trace of mild congestion was noticed in the STDG. But edemic blood congestion was observed in the diabetic group. In conclusion, the current result demonstrated that HEXETACF may be a promising antidiabetic agent that could replace mSILY.

Keywords

References

  1. Adaramoye, O. A., Akinwonmi, O., & Akanni, O. (2013). Effects of propofol, a sedative-hypnotic drug, on the lipid profile, antioxidant indices, and cardiovascular marker enzymes in wistar rats. International Scholarly Research Notices, 2013, 230261. https://doi.org/10.1155/2013/230261 DOI: https://doi.org/10.1155/2013/230261
  2. Adeyemi, O. S., & Orekoya, B. T. (2014). Lipid profile and oxidative stress markers in Wistar rats following oral and repeated exposure to fijk herbal mixture. Journal of Toxicology, 2014, 876035. https://doi.org/10.1155/2014/876035 DOI: https://doi.org/10.1155/2014/876035
  3. Alabi, K., & Oyeku, T. (2017). The chemical constituents extractable from teak tree (Tectona grandis Linn) obtained from Fountain University, Osogbo. Nigerian Journal of Basic and Applied Sciences, 25(1), 73-80. https://doi.org/10.4314/njbas.v25i1.10 DOI: https://doi.org/10.4314/njbas.v25i1.10
  4. Ananthan, R., Latha, M., Ramkumar, K., Pari, L., Baskar, C., & Bai, V. N. (2004). Modulatory effects of Gymnema montanum leaf extract on alloxan-induced oxidative stress in Wistar rats. Nutrition, 20(3), 280-285. https://doi.org/10.1016/j.nut.2003.11.016 DOI: https://doi.org/10.1016/j.nut.2003.11.016
  5. Asuk, A. A. (2018). Total serum protein and albumin levels of Wistar rats on administration of methanol-ethanol (1:1) leaf extracts of Anacardium occidentale and Jatropha tanjorensis. IDOSR Journal of Biology Chemistry and Pharmacy, 3(2), 20-26.
  6. Bachorik, P. S. (2000). Measurement of low-density-lipoprotein cholesterol. In N. Rifai, G. Warnick, & M. Dominiczak (Eds.), Handbook of Lipoprotein Testing (Vol. 2, pp. 245-264). AACC Press.
  7. Ben Salem, M., Ben Abdallah Kolsi, R., Dhouibi, R., Ksouda, K., Charfi, S., Yaich, M., Hammami, S., Sahnoun, Z., Zeghal, K. M., & Jamoussi, K. (2017). Protective effects of Cynara scolymus leaves extract on metabolic disorders and oxidative stress in alloxan-diabetic rats. BMC Complementary and Alternative Medicine, 17, 328. https://doi.org/10.1186/s12906-017-1835-8 DOI: https://doi.org/10.1186/s12906-017-1835-8
  8. Cho, N. H., Shaw, J., Karuranga, S., Huang, Y., da Rocha Fernandes, J., Ohlrogge, A., & Malanda, B. (2018). IDF Diabetes Atlas: Global estimates of diabetes prevalence for 2017 and projections for 2045. Diabetes Research and Clinical Practice, 138, 271-281. https://doi.org/10.1016/j.diabres.2018.02.023 DOI: https://doi.org/10.1016/j.diabres.2018.02.023
  9. Donald, V., & Judith, G. (1990). Biochemistry. First Edition: John Wiley and Sons Inc., United Sate of America, pp: 643-656.
  10. Egbung, G., Essien, N., Mgbang, J., & Egbung, J. (2020). Serum lipid and electrolyte profiles of Wistar rats fed with Vernonia amygdalina supplemented Vigna subterranea (Bambara groundnut) pudding. Calabar Journal of Health Sciences, 3(2), 40-45. DOI: https://doi.org/10.25259/CJHS_10_2019
  11. Elavarasi, S., Revathi, G., & Saravanan, K. (2020). Isolation, Identification, and Molecular Docking of Antidiabetic Compounds of Cyathea nilgiriensis (Holttum). In K. Saravanan, C. Egbuna, H. Averal, S. Kanna, S. Elavarasi, & B. Bahadur (Eds.), Drug Development for Cancer and Diabetes (pp. 293-303): Apple Academic Press. DOI: https://doi.org/10.1201/9780429330490-25
  12. Emordi, J. E., Agbaje, E. O., Oreagba, I. A., & Iribhogbe, O. I. (2018). Antidiabetic effects of the ethanolic root extract of Uvaria chamae P. Beauv (Annonaceae) in alloxan-induced diabetic rats: a potential alternative treatment for diabetes mellitus. Advances in Pharmacological and Pharmaceutical Sciences, 2018, 1314941. https://doi.org/10.1155/2018/1314941 DOI: https://doi.org/10.1155/2018/1314941
  13. Esievo, K. (2017). Veterinary Clinical Pathology. First Edition. 37. Spectrum Books, Ibadan, pages: 118-122.
  14. Ezeugwunne, I., Eriugo, R., Ogbodo, E., Oguaka, V., Analike, R., Madukwe, D., Okwara, E., Onyegbule, O., Ezego, A., & Okeke, K. (2017). Effect of Sida corymbosa leaf extract on serum uric acid, urea and creatinine levels of alloxan-induced diabetic albino wistar rats. International Journal of Basic, Applied and Innovative Research, 6(2), 51-57.
  15. Fatima, Z., Abderrahmane, B., Seddik, K., & Lekhmici, A. (2016). Antioxidant activity assessment of Tamus communis L. Roots. International Journal of Pharmacy and Pharmaceutical Sciences, 8(12), 64-71. http://dx.doi.org/10.22159/ijpps.2016v8i12.14327 DOI: https://doi.org/10.22159/ijpps.2016v8i12.14327
  16. Ferdosi, M. F., Khan, I. H., Javaid, A., Hafiz, M. S., Butt, I., & Munir, A. (2021). GC-MS analysis and bioactive components of flowers of Bergenia ciliata, a weed of rock crevices in Pakistan. Pakistan Journal of Weed Science Research, 27(4), 527-535. https://doi.org/10.28941/pjwsr.v27i4.1012 DOI: https://doi.org/10.28941/pjwsr.v27i4.1012
  17. Feyisayo, A. K., & Victor, A. C. (2019). Assessment of antioxidant and antidiabetic properties of Picralima nitida seed extracts. Journal of Medicinal Plants Research, 13(1), 9-17. https://doi.org/10.5897/JMPR2018.6680 DOI: https://doi.org/10.5897/JMPR2018.6680
  18. Hassan, M., Bala, S. Z., & Gadanya, A. M. (2022). Anticonvulsant effect of flavonoid-rich fraction of Ficus platyphylla stem bark on pentylenetetrazole induced seizure in mice. Nigerian Journal of Basic and Clinical Sciences, 19(1), 20-28. https://doi.org/10.4103/njbcs.njbcs_33_21 DOI: https://doi.org/10.4103/njbcs.njbcs_33_21
  19. Hoffman, R., Benz Jr, E. J., Silberstein, L. E., Heslop, H., Anastasi, J., & Weitz, J. (2013). Hematology: Basic Principles and Practice: Elsevier Health Sciences.
  20. Ighodaro, O., & Omole, J. (2012). Effects of Nigerian Piliostigma thonningii species leaf extract on lipid profile in Wistar rats. International Scholarly Research Notices, 2012, 387942. https://doi.org/10.5402/2012/387942 DOI: https://doi.org/10.5402/2012/387942
  21. Igwe, K., Ujowundu, C., Chukwudoruo, S., & Obasi, U. (2020). Assessment of hematological and serum electrolyte of albino rats administered with graded concentrations of ethanol extract of Ficus capensis. Asian Journal of Research in Botany, 4(3), 28-36.
  22. Ihegboro, G. O., Alhassan, A. J., Ononamadu, C. J., Owolarafe, T. A., & Sule, M. S. (2020a). Evaluation of the biosafety potentials of methanol extracts/fractions of Tapinanthus bangwensis and Moringa oleifera leaves using Allium cepa model. Toxicology Reports, 7, 671-679. https://doi.org/10.1016/j.toxrep.2020.05.001 DOI: https://doi.org/10.1016/j.toxrep.2020.05.001
  23. Ihegboro, G. O., Ononamadu, C. J., Owolarafe, T. A., Fadilu, M., & Joseph, O. E. (2022). Anti-reno-haematological tenacity of Calotropis procera aqueous-methanol root extract in alloxan-induced pancrotoxic Wistar rats. Comparative Clinical Pathology, 31, 211-219. https://doi.org/10.1007/s00580-022-03322-8 DOI: https://doi.org/10.1007/s00580-022-03322-8
  24. Ihegboro, G. O., Ononamadu, C. J., Owolarafe, T. A., Onifade, O., Udeh, J. J., Saliu, A. O., Abolaji, D. D., & Ibrahim, Y. M. (2024). In vitro Investigation and GC-MS Analysis of the Chemical Constituents in the Fraction of Hexane Leaf Extract of Tapinanthus bangwensis (Engl. and K. Krause) Loranthaceae. Tropical Journal of Phytochemistry and Pharmaceutical Sciences, 3(1), 143-152. http://www.doi.org/10.26538/tjpps/v3i1.5 DOI: https://doi.org/10.26538/tjpps/v3i1.5
  25. Ihegboro, G. O., Ononamadu, C. J., Owolarafe, T. A., & Shekwolo, I. (2020b). Screening for toxicological and anti-diabetic potential of n-hexane extract of Tapinanthus bangwensis leaves. Toxicology Research and Application, 4, 2397847320972042. https://doi.org/10.1177/2397847320972042 DOI: https://doi.org/10.1177/2397847320972042
  26. International Diabetes Federation. (2015). IDF Atlas. 7th edition. Brussels, Belgium. Diabetesatlas.org 12-week prospective trial.
  27. Jung, K. (2008). Tietz Fundamentals of Clinical Chemistry, 6th edition. Carl A. Burtis, Edward R. Ashwood, and David E. Bruns, editors. St Louis, MO: Saunders/Elsevier, 2008, 976 pp, $96.95. ISBN 978-0-7216-3865-2. Clinical Chemistry, 54(11), 1933-1933. https://doi.org/10.1373/clinchem.2007.101378 DOI: https://doi.org/10.1373/clinchem.2007.101378
  28. Katrenčíková, B., Vaváková, M., Paduchová, Z., Nagyová, Z., Garaiova, I., Muchová, J., Ďuračková, Z., & Trebatická, J. (2021). Oxidative stress markers and antioxidant enzymes in children and adolescents with depressive disorder and impact of omega-3 fatty acids in randomised clinical trial. Antioxidants, 10(8), 1256. https://doi.org/10.3390/antiox10081256 DOI: https://doi.org/10.3390/antiox10081256
  29. Kolagal, V., Karanam, S., Dharmavarapu, P., D'Souza, R., Upadhya, S., Kumar, V., Kedage, V., Muttigi, M., Shetty, J., & Prakash, M. (2009). Determination of oxidative stress markers and their importance in early diagnosis of uremia-related complications. Indian Journal of Nephrology, 19(1), 8-12. https://doi.org/10.4103/0971-4065.50673 DOI: https://doi.org/10.4103/0971-4065.50673
  30. Kolhe, S. S., & Rachh, P. R. (2018). Review on potent anti-diabetic plants or herbs from traditional medicine. Journal of Drug Delivery and Therapeutics, 8(5), 92-98. https://doi.org/10.22270/jddt.v8i5.1856 DOI: https://doi.org/10.22270/jddt.v8i5.1856
  31. Lozano-Grande, M. A., Gorinstein, S., Espitia-Rangel, E., Dávila-Ortiz, G., & Martínez-Ayala, A. L. (2018). Plant sources, extraction methods, and uses of squalene. International Journal of Agronomy, 1829160. https://doi.org/10.1155/2018/1829160 DOI: https://doi.org/10.1155/2018/1829160
  32. Macrelli, R., Ceccarelli M, M., & Fiorucci, L. (2013). Determination of serum albumin concentration in healthy and diseased Hermann's tortoises (Testudo hermanni): a comparison using electrophoresis and the bromocresol green dye-binding method. Journal of Herpetological Medicine and Surgery, 23(1-2), 20-24. https://doi.org/10.5818/1529-9651-23.1.20 DOI: https://doi.org/10.5818/1529-9651-23.1.20
  33. Mazani, M., Mahmoodzadeh, Y., Asl, M. M. C., Banaei, S., Rezagholizadeh, L., & Mohammadnia, A. (2018). Renoprotective effects of the methanolic extract of Tanacetum parthenium against carbon tetrachloride-induced renal injury in rats. Avicenna Journal of Phytomedicine, 8(4), 370-379. https://doi.org/10.22038/ajp.2018.10397
  34. Mirmiranpour, H., Rabizadeh, S., Mansournia, M., Salehi, S., Esteghamati, A., & Nakhjavani, M. (2018). Protective effect of palmitoleic, oleic, and vaccenic acid on structure-function of major antioxidant enzymes: catalase, superoxide dismutase and glutathione peroxidase in the hyperglycemic environment: an in vitro study. Austin Biochemistry, 3(1), 1017.
  35. Muhammad, N., Akolade, J., Usman, L., & Oloyede, O. (2012). Haematological parameters of alloxan-induced diabetic rats treated with leaf essential oil of Hoslundia opposita (Vahl). EXCLI Journal, 11, 670-676. http://dx.doi.org/10.17877/DE290R-10352
  36. Navya, G., Shirisha, Y., Girija, P., Venkateshwarlu, K., & Sirisha, K. (2018). Effect of Momordica charantia and Syzygium cumini extract on serum electrolytes in alloxan induced diabetic rats. International Journal of Pharmacy and Pharmaceutical Sciences, 10(11), 24-27. DOI: https://doi.org/10.22159/ijpps.2018v10i11.24963
  37. Num-Adom, S. M., Adamu, S., Aluwong, T., Ogbuagu, N. E., Umar, I. A., & Esievo, K. A. N. (2022). Ethanolic extract of Anogeissus leiocarpus ameliorates hyperglycaemia, hepato-renal damage, deranged electrolytes and acid-base balance in alloxan-induced diabetes in dogs. Scientific African, 16, e01183. https://doi.org/10.1016/j.sciaf.2022.e01183 DOI: https://doi.org/10.1016/j.sciaf.2022.e01183
  38. Ohlsson, A., & Aher, S. (2006). Early erythropoietin for preventing red blood cell transfusion in preterm and/or low birth weight infants. Cochrane Database System Reviews. https://doi.org/10.1002/14651858.CD004863.pub4 DOI: https://doi.org/10.1002/14651858.CD004863.pub2
  39. Ononamadu, C. J., Alhassan, A. J., Imam, A. A., Ibrahim, A., Ihegboro, G. O., Owolarafe, A. T., & Sule, M. S. (2019). In vitro and in vivo anti-diabetic and anti-oxidant activities of methanolic leaf extracts of Ocimum canum. Caspian Journal of Internal Medicine, 10(2), 162-175. http://dx.doi.org/10.22088/cjim.10.2.162
  40. Oyesola, O., Shallie, P., Osonuga, I., Soetan, O., & Owoeye, I. (2020). Momordica charantia improves biochemical indices in alloxan-induced diabetic rat model. National Journal of Physiology, Pharmacy and Pharmacology, 10(9), 788-794. https://doi.org/10.5455/njppp.2020.10.06169202016072020 DOI: https://doi.org/10.5455/njppp.2020.10.06169202016072020
  41. Queiroz, L. A., Assis, J. B., Guimarães, J., Sousa, E. S., Milhomem, A. C., Sunahara, K. K., Sá-Nunes, A., & Martins, J. O. (2021). Endangered lymphocytes: The effects of alloxan and streptozotocin on immune cells in type 1 induced diabetes. Mediators of Inflammation, 2021, 9940009. https://doi.org/10.1155/2021/9940009 DOI: https://doi.org/10.1155/2021/9940009
  42. Semwal, P., Painuli, S., Badoni, H., & Bacheti, R. K. (2018). Screening of phytoconstituents and antibacterial activity of leaves and bark of Quercus leucotrichophora A. Camus from Uttarakhand Himalaya. Clinical Phytoscience, 4, 30. https://doi.org/10.1186/s40816-018-0090-y DOI: https://doi.org/10.1186/s40816-018-0090-y
  43. Shah, N. A., & Khan, M. R. (2014). Antidiabetic effect of Sida cordata in alloxan induced diabetic rats. BioMed Research International, 2014, 671294. https://doi.org/10.1155/2014/671294 DOI: https://doi.org/10.1155/2014/671294
  44. Sun, H., Saeedi, P., Karuranga, S., Pinkepank, M., Ogurtsova, K., Duncan, B. B., Stein, C., Basit, A., Chan, J. C., & Mbanya, J. C. (2022). IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045. Diabetes Research and Clinical Practice, 183, 109119. https://doi.org/10.1016/j.diabres.2021.109119 DOI: https://doi.org/10.1016/j.diabres.2021.109119
  45. Thomas, D. R. (2008). Anemia in diabetic patients. Clinics in Geriatric Medicine, 24(3), 529-540. https://doi.org/10.1016/j.cger.2008.03.003 DOI: https://doi.org/10.1016/j.cger.2008.03.003
  46. Thomas, M. C., MacIsaac, R. J., Tsalamandris, C., Power, D., & Jerums, G. (2003). Unrecognized anemia in patients with diabetes: a cross-sectional survey. Diabetes Care, 26(4), 1164-1169. https://doi.org/10.2337/diacare.26.4.1164 DOI: https://doi.org/10.2337/diacare.26.4.1164
  47. Tietz, N. (2006). Clinical Guide to Chemistry Test, 4th Ed. Saunders Elsevier, pages: 78-83.
  48. Tuorkey, M. J., El-Desouki, N. I., & Kamel, R. A. (2015). Cytoprotective effect of silymarin against diabetes-induced cardiomyocyte apoptosis in diabetic rats. Biomedical and Environmental Sciences, 28(1), 36-43. https://doi.org/10.3967/bes2015.004
  49. Uhuo, E. N., Godwin, K. O., Alaebo, P. O., & Ezeh, H. C. (2022). Haematological and biochemical parameters assessment of alloxan-induced diabetic rats treated with ethanol leaf extract of Adansonia digitate (baobab) leaf. Animal Research International, 19(2), 4469–4477.
  50. Wang, L., Kong, D., Tian, J., Zhao, W., Chen, Y., An, Y., Liu, X., Wang, F., Cai, F., & Sun, X. (2022). Tapinanthus species: A review of botany and biology, secondary metabolites, ethnomedical uses, current pharmacology and toxicology. Journal of Ethnopharmacology, 296, 115462. https://doi.org/10.1016/j.jep.2022.115462 DOI: https://doi.org/10.1016/j.jep.2022.115462
  51. Wang, L., Song, R., Chen, Z., Wang, J., & Ling, F. (2015). Prevalence of depressive symptoms and factors associated with it in type 2 diabetic patients: a cross-sectional study in China. BMC Public Health, 15, 188. https://doi.org/10.1186/s12889-015-1567-y DOI: https://doi.org/10.1186/s12889-015-1567-y
  52. Wong, P. L., Zolkeflee, N. K. Z., Ramli, N. S., Tan, C. P., Azlan, A., Tham, C. L., Shaari, K., & Abas, F. (2024). Antidiabetic effect of Ardisia elliptica extract and its mechanisms of action in STZ-NA-induced diabetic rat model via 1H-NMR-based metabolomics. Journal of Ethnopharmacology, 318(Part B), 117015. https://doi.org/10.1016/j.jep.2023.117015 DOI: https://doi.org/10.1016/j.jep.2023.117015

License

CCBY 4.0
Creative Commons Attribution 4.0 International

This work is openly licensed — share and adapt freely with attribution to the authors and the journal. View license terms ↗

§ 06 — Related

Similar articles in this journal

Related peer-reviewed studies published in this journal.
View all issues

Evaluation of cytotoxic, antimicrobial, and antioxidant activities of Echium italicum L. in MCF-7 and HepG2 cell lines

Dilek Arslan Atessahin, Semih Dalkilic, Lütfiye Kadioglu Dalkilic, Dudu Bayindir, Elif Cetinkaya

The use of plants for medicinal purposes from past to present continues as traditional treatments. One of these plants, Echium species, is known for its high…

#Cytotoxic activity #Antimicrobial activity #Antioxidant activity #MCF-7 cell line
p. 25-32
10.62313/ijpbp.2025.259
DOI: https://doi.org/10.62313/ijpbp.2025.259

Biochemical and histological evaluation of kidney, liver, and hematological indices in normal Wistar rats administered dietary formulations of roasted Sphenotylis stenocarpa seeds (Af-rican yam bean)

Nene Hephzibah Chiaka-Onyemeze, Chinelo Chinenye Nkwocha, Affiong Asuquo Edeke, Emmanuel Chimeh Ezeako

Sphenotylis stenocarpa seeds (African yam bean) represent one of the under-exploited nutrient-rich legumes associated with African folklore and…

#Sphenostylis stenocarpa #Nephroprotective #Hepatoprotective #Antioxidant
p. 16-24
10.62313/ijpbp.2025.250
DOI: https://doi.org/10.62313/ijpbp.2025.250

Potentilla fulgens Wall ex Sims. exerts anti-diabetic effects by inhibiting α-amylase and α-glucosidase: deeper insights through molecular docking

Anita Kumari Rai, Careen Liza Pakyntein, Stability Nongrum, Daiahun Thabah, Shelareen Ediemi Sunn, Donkupar Syiem

Potentilla fulgens Wall ex Sims., a local medicinal plant used by the Khasi tribe of Meghalaya, India, has been reported to be rich in tannins, polyphenols,…

#α-Amylase #α-Glucosidase #Diabetes #Docking
p. 1-15
10.62313/ijpbp.2025.244
DOI: https://doi.org/10.62313/ijpbp.2025.244