Effect of Enhydra fluctuans on Kidney Function in Alloxan-induced Diabetic Rats

Authors

  • Rina Delfita Department of Biology Education, Faculty of Tarbiyah and Teacher Training, IAIN Batusangkar, West Sumatera, Indonesia; Department of Biology, Faculty of Mathematics and Natural Science, Andalas University, West Sumatera, Indonesia
  • Dahelmi Dahelmi Department of Biology, Faculty of Mathematics and Natural Science, Andalas University, West Sumatera, Indonesia
  • Djong Tjong Department of Biology, Faculty of Mathematics and Natural Science, Andalas University, West Sumatera, Indonesia
  • Suhatri Suhatri Faculty of Pharmacy, Andalas University, West Sumatera, Indonesia

DOI:

https://doi.org/10.3889/oamjms.2021.7531

Keywords:

Alloxan, Creatinine, Diabetes mellitus, Enhydra fluctuans, Kidney

Abstract

AIM: The aim of this study was to explore the effect of n-hexane fraction of Enhydra fluctuans aerial on kidney function in alloxan induced diabetic rats.

METHODS: Five groups of diabetic Wistar rats were studied: Group 1 was given 0.5% Na-CMC (G0), group 2 was given glibenclamide 0.45 mg/kg (G1), groups 3, 4, and 5 were given a dose of n-hexane fraction 57.03, 114.06, and 171.09 mg/kg respectively. The experiment was completed in 21 days. Blood glucose was estimated on day 0 and day 21 of treatment. Histology of kidney, creatinine, and blood urea nitrogen (BUN) was examined. ANOVA was used to evaluate quantitative data, which was then followed by Duncan's new multiple range test (p < 0.05).

RESULTS: Our results demonstrate that n-hexane fraction dosages of 57.03 mg/kg and 114,06 mg/kg significantly improved blood glucose profile, BUN, and creatinine in diabetic rats. Moreover, the dosage of 57.03 mg/kg is effective to counteract necrosis and fibrosis of kidney cells.

 

CONCLUSION: Our findings revealed that the administration of the n-hexane fraction of E. fluctuans aerial improved the kidney function of diabetic rats, especially at the dosage of 57.03 mg/kg. Therefore, E. fluctuans can be relied upon to be a drug to prevent the development of diabetes mellitus and diabetic nephropathy.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Plum Analytics Artifact Widget Block

References

Uddandrao VV, Brahmanaidu P, Ravindarnaik R, Suresh P, Vadivukkarasi S, Saravanan G. Restorative potentiality of S-allyl cysteine against diabetic nephropathy through attenuation of oxidative stress and inflammation in streptozotocin-nicotinamideinduced diabetic rats. Eur J Nutr. 2019;58(6):2425-37. https://doi.org/10.1007/s00394-018-1795-x PMid:30062492 DOI: https://doi.org/10.1007/s00394-018-1795-x

Umanath K, Lewis JB. Update on diabetic nephropathy: Core curriculum 2018. Am J Kidney Dis. 2018;71(6):884-95. https://doi.org/10.1053/j.ajkd.2017.10.026 PMid:29398179 DOI: https://doi.org/10.1053/j.ajkd.2017.10.026

Bhatia K, Misra P, Singh A, Mukherjee B, Ambade VN. Study of blood urea nitrogen (BUN), serum creatinine in diabetic and nondiabetic patients in a Tertiary Care Hospital. Int J Med Biomed Stud. 2019;3(4):180-6. https://doi.org/10.32553/ijmbs.v3i4.216 DOI: https://doi.org/10.32553/ijmbs.v3i4.216

Fujita H, Fujishima H, Chida S, Takahashi K, Qi Z, Kanetsuna Y. Reduction of renal superoxide dismutase in progressive diabetic nephropathy. J Am Soc Nephrol. 2009;20(6):1303-13. https://doi.org/10.1681/asn.2008080844 PMid:19470681 DOI: https://doi.org/10.1681/ASN.2008080844

Gansevoort RT, Correa-Rotter R, Hemmelgarn BR, Jafar TH, Heerspink HJ, Mann JF. Chronic kidney disease and cardiovascular risk: Epidemiology, mechanisms, and prevention. Lancet. 2013;382(9889):339-52. https://doi.org/10.1016/S0140-6736(13)60595-4 PMid:23727170 DOI: https://doi.org/10.1016/S0140-6736(13)60595-4

Gross JL, Azevedo MJ, Silveiro SP, Canani LH, Caramori ML, Zelmanovitz T. Diabetic nephropathy: Diagnosis, prevention, and treatment. Diabetes Care. 2005;28(1):176-88. https://doi.org/10.2337/diacare.28.1.164 PMid:15616252 DOI: https://doi.org/10.2337/diacare.28.1.164

Yaribeygi H, Mohammadi MT, Rezaee R, Sahebkar A. Crocin improves renal function by declining Nox-4, IL-18, and p53 expression levels in an experimental model of diabetic nephropathy. J Cell Biochem. 2018;119(7):6080-93. https://doi.org/10.1002/jcb.26806 PMid:29575259 DOI: https://doi.org/10.1002/jcb.26806

Papachristoforou E, Lambadiari V, Maratou E, Makrilakis K. Association of glycemic indices (hyperglycemia, glucose variability, and hypoglycemia) with oxidative stress and diabetic complications. J Diabetes Res. 2020;2020:7489795. https://doi.org/10.1155/2020/7489795 PMid:33123598 DOI: https://doi.org/10.1155/2020/7489795

Travlos GS, Morris RW, Elwell MR, Duke A, Rosenblum S, Thompson MB. Frequency and relationships of clinical chemistry and liver and kidney histopathology findings in 13-week toxicity studies in rats. Toxicology. 1996;107(1):17-29. https://doi.org/10.1016/0300-483X(95)03197-N PMid:8597028 DOI: https://doi.org/10.1016/0300-483X(95)03197-N

Nwankpa P, Ekweogu C, Egwurugwu, JN, Chukwuemeka O, Etteh C, Ugwuezumba P, et al. Assessment of kidney function indices in male albino Wistar rats administered ethanol stem extract of Dennettia tripetala (Pepper fruit). Biochem Pharmacol Open Access. 2018;7(1):1-4. https://doi.org/10.4172/2167-0501.1000242 DOI: https://doi.org/10.4172/2167-0501.1000242

Herman ME, O’Keefe JH, Bell DS, Schwartz SS. Insulin therapy increases cardiovascular risk in Type 2 diabetes. Prog Cardiovasc Dis. 2017;60(3):422-34. https://doi.org/10.1016/j.pcad.2017.09.001 PMid:28958751 DOI: https://doi.org/10.1016/j.pcad.2017.09.001

Xu S, Wang B, Liu W, Wu C, Huang J. The effects of insulin therapy on mortality in diabetic patients undergoing percutaneous coronary intervention. Ann Transl Med. 2021;9(16):1294. https://doi.org/10.21037/atm-21-1911 PMid:34532431 DOI: https://doi.org/10.21037/atm-21-1911

Vasarri M, Barletta E, Vinci S, Ramazzotti M, Francesconi A, Manetti F. Annona cherimola miller fruit as a promising candidate against diabetic complications: An in vitro study and preliminary clinical results. Foods. 2020;9(10):1350. https://doi.org/10.3390/foods9101350 PMid:32987622 DOI: https://doi.org/10.3390/foods9101350

Ali R, Billah M, Hassan M, Rahman SM. Enhydra fluctuans Lour : A review. Res J Pharm Tech. 2013;6(9):927-9. https://doi.org/10.11114/ijsss.v4i5.1522

Stark A, Yahaya FH, Kurniawan Y. Tawa nan ampek: A traditional way of healing measles, keteguran and other disorders in West Sumatra. Int J Soc Sci Stud. 2016;4(5):90-4. https://doi.org/10.11114/ijsss.v4i5.1522 DOI: https://doi.org/10.11114/ijsss.v4i5.1522

Kumar SP, Jagannath PV, Chandra DS, Prasan ND. Hepatoprotective activity of Enhydra fluctuans Lour. Aerial parts against CCl4 induced hepatotoxicity in rats. Int J Res Ayurveda Pharm. 2012;3(6):893-6. https://doi.org/10.7897/2277-4343.03646 DOI: https://doi.org/10.7897/2277-4343.03646

Dua TK, Dewanjee S, Khanra R, Joardar S, Barma S. Cytoprotective and antioxidant Effects of an edible herb, Enhydra fluctuans Lour. (Asteraceae), against experimentally induced lead acetate intoxication. PLoS One. 2016;11(2):e0148757. https://doi.org/10.1371/journal.pone.0148757 PMid:26859407 DOI: https://doi.org/10.1371/journal.pone.0148757

Delfita R, Tjong DH, Dahelmi D, Suhatri S. Hypoglycemic effects of Enhydra fluctuans aerial extract on alloxan-induced diabetic rats. J Phys Conf Ser. 2021;1940(1):1-7. https://doi.org/10.1088/1742-6596/1940/1/012058 DOI: https://doi.org/10.1088/1742-6596/1940/1/012058

Hasan MN, Sabrin F, Rokeya B, Khan MS, Ahmed MU, Matondo A. Glucose and lipid-lowering effects of Enhydra fluctuans extract in cadmium treated normal and Type-2 diabetic model rats. BMC Complement Altern Med. 2019;19(1):278. https://doi.org/10.1186/s12906-019-2667-5 PMid:31640743 DOI: https://doi.org/10.1186/s12906-019-2667-5

Khalid U. Kidney ischaemia reperfusion injury in the rat: The EGTI scoring system as a valid and reliable tool for histological assessment. J Histol Histopathol. 2016;3(1):2-7. https://doi.org/10.7243/2055-091X-3-1 DOI: https://doi.org/10.7243/2055-091X-3-1

Zhao B, Wu F, Han X, Zhou W, Shi Q, Wang H. Protective effects of acarbose against insulitis in multiple low-dose streptozotocininduced diabetic mice. Life Sci. 2020;263:118490. https://doi.org/10.1016/j.lfs.2020.118490 PMid:32979357 DOI: https://doi.org/10.1016/j.lfs.2020.118490

Putra IB, Jusuf NK, Sumantri IB. The potency of Hibiscus rosa- sinensis Linn. leaves ethanol extract as hair growth. Open Access Maced J Med Sci. 2020;8(A):89-92. https://doi.org/10.3889/oamjms.2020.4211 DOI: https://doi.org/10.3889/oamjms.2020.4211

Saha M, Rohani S, Rayhana N, Toma IJ, Rana S, Rahmatullah M. An herbal formulation containing Zingiber officinale rhizomes and Allium sativum cloves can increase oral glucose tolerance in mice. Biol Eng Med. 2017;2(1):1-3. https://doi.org/10.15761/BEM.1000110 DOI: https://doi.org/10.15761/BEM.1000110

Giacco F, Brownlee M. Oxidative stress and diabetic complications. Circ Res. 2010;107(9):1058-70. https://doi.org/10.1161/circresaha.110.223545 PMid:21030723 DOI: https://doi.org/10.1161/CIRCRESAHA.110.223545

Lotfy M, Adeghate J, Kalasz H, Singh J, Adeghate E. Chronic complications of diabetes mellitus: A mini-review. Curr Diabetes Rev. 2016;13(1):3-10. https://doi.org/10.2174/1573399812666151016101622 PMid:26472574 DOI: https://doi.org/10.2174/1573399812666151016101622

Sedeek M, Callera G, Montezano A, Gutsol A, Heitz F, Szyndralewiez C. Critical role of Nox4-based NADPH oxidase in glucose-induced oxidative stress in the kidney: Implications in Type 2 diabetic nephropathy. Am J Physiol Renal Physiol. 2010;299(6):1348-59. https://doi.org/10.1152/ajprenal.00028.2010 PMid:20630933 DOI: https://doi.org/10.1152/ajprenal.00028.2010

Liang Y, Liu H, Fang Y, Lin P, Lu Z, Zhang P. Salvianolate ameliorates oxidative stress and podocyte injury through modulation of NOX4 activity in DB/DB mice. J Cell Mol Med. 2020;25(2):1012-23. https://doi.org/10.1111/jcmm.16165 PMid:33332718 DOI: https://doi.org/10.1111/jcmm.16165

Wang L, Zhang L, Yu Y, Wang Y, Niu N. The protective effects of taurine against early renal injury in STZ-induced diabetic rats, correlated with inhibition of renal LOX-1-mediated ICAM-1 expression. Ren Fail. 2008;30(8):763-71. https://doi.org/10.1080/08860220802272563 PMid:18791949 DOI: https://doi.org/10.1080/08860220802272563

Forbes JM, Coughlan MT, Cooper ME. Oxidative stress is a major culprit in kidney disease in diabetes. Diabetes. 2008;57(6):1446-54. https://doi.org/10.2337/db08-0057 PMid:18511445 DOI: https://doi.org/10.2337/db08-0057

Abdullah KM, Alam MM, Iqbal Z, Naseem I. Therapeutic effect of vitamin B3 on hyperglycemia, oxidative stress and DNA damage in the alloxan-induced diabetic rat model. Biomed Pharmacother. 2018;105(6):1223-31. https://doi.org/10.1016/j.biopha.2018.06.085 PMid:30021358 DOI: https://doi.org/10.1016/j.biopha.2018.06.085

Samra M, Abcar AC. False estimates of elevated creatinine. Perm J. 2012;16(2):51-2. https://doi.org/10.7812/tpp/11-121 PMid:22745616 DOI: https://doi.org/10.7812/tpp/11-121

Gonzalez-Burgos E, Gomez-Serranillos MP. Terpene compounds in nature: A review of their potential antioxidant activity. Curr Med Chem. 2012;19(31):5319-41. https://doi.org/10.2174/092986712803833335 PMid:22963623 DOI: https://doi.org/10.2174/092986712803833335

Abou El-Soud NH, El-Lithy NA, El-Saeed G, Wahby MS, Khalil MY, Morsy F, et al. Renoprotective effects of Caraway (Carum carvi L.) essential oil in streptozotocin-induced diabetic rats. J Appl Pharm Sci. 2014;4(2):27-33.

Mabhida SE, Dludla PV, Johnson R, Ndlovu M, Louw J, Opoku AR. Protective effect of triterpenes against diabetesinduced β-cell damage: An overview of in vitro and in vivo studies. Pharmacol Res. 2018;137:179-92. https://doi.org/10.1016/j.phrs.2018.10.004 PMid:30315968 DOI: https://doi.org/10.1016/j.phrs.2018.10.004

Sarkar P, Dalal A. Evaluation of antioxidant activity of Diplazium esculentum and Enhydra fluctuans of West Bengal. IOSR J Pharm Biol Sci. 2016;11(6):45-50.

Panigrahi R, Bhatnagar S. Cytotoxic, the phytochemical and antioxidant potential of marshy herb Enhydra fluctuans Lour. Int J Ethnobiol Ethnomed. 2015;1:1-5.

Downloads

Published

2021-11-29

How to Cite

1.
Delfita R, Dahelmi D, Tjong D, Suhatri S. Effect of Enhydra fluctuans on Kidney Function in Alloxan-induced Diabetic Rats. Open Access Maced J Med Sci [Internet]. 2021 Nov. 29 [cited 2024 Apr. 26];9(A):1187-94. Available from: https://oamjms.eu/index.php/mjms/article/view/7531