Nephroprotective Effect of Spermacoce hispida by reducing Oxidative and Nitrosative Stress in Experimental Model
Abstract
Present study was aimed to investigate the protective of Spermacoce hispida in Cisplatin induced nephrotoxicity using in vivo model. S. hispida was collected and extract of plant was prepared in different solvents and prepared extracts was used for phytochemical scrrening. Nephrotoxicity in rats was induced by a single intraperitoneal injection of Cisplatin at a dose of 5 mg/kg. S. hispida extract in different solvent at the dose 100 mg/kg used to find protective activity. Blood urea nitrogen (BUN), serum creatinine, oxidative stress, a proinflammatory cytokine, NO, and histological alteration was measured to estimate the therapeutic ability of S. hispida. BUN, creatinine, and inflammatory cytokine levels in rats were increased by Cisplatin but decreased by S. hispida treatment for 14 days. Besides, S. hispida treatment decreased oxidative stress and nitric oxide in Cisplatin-treated rats. Cisplatin treated rats shows altered structure of kidney tissue; meanwhile S. hispida normalizes the structure of kidney tissue. From this study, we conclude that S. hispida has nephroprotective activity by inhibiting the oxidative stress and NO production in rats from nephrotoxicity.
Keywords: Spermacoce hispida; Cisplatin; oxidative stress; Cytokine; Nitric oxide.
Keywords:
Spermacoce hispida, Cisplatin, oxidative stress, Cytokine, Nitric oxide, HEK-293 cell lineDOI
https://doi.org/10.22270/jddt.v12i1-S.5296References
Bednarek A., et al., Limitations of systemic oncological therapy in breast cancer patients with chronic kidney disease. J Oncol, 2020; 2020. https://doi.org/10.1155/2020/7267083
Shinde SD., et al., Abrogation of cisplatin-induced nephrotoxicity in rats and HEK-293 cell lines by formononetin: in vivo and in vitro study. Compa Clin Pathol, 2021; 1-9. https://doi.org/10.1007/s00580-021-03252-x
Do Amaral CL., et al., Resveratrol attenuates cisplatin-induced nephrotoxicity in rats. Arch Toxicol, 2008; 82(6):363-370. https://doi.org/10.1007/s00204-007-0262-x
Amin RP., et al., Identification of putative gene based markers of renal toxicity. Environm Health Perspec, 2004; 112(4):465-479. https://doi.org/10.1289/ehp.6683
Ekor M, Emerole GO, Farombi EO, Phenolic extract of soybean (Glycine max) attenuates cisplatin-induced nephrotoxicity in rats. Food Chem Toxicol, 2010; 48(4):1005-1012. https://doi.org/10.1016/j.fct.2009.12.027
Behling EB., et al., Comparative study of multiple dosage of quercetin against cisplatin-induced nephrotoxicity and oxidative stress in rat kidneys. Pharmacol Rep, 2006; 526-532.
Zhou H., et al., Urinary marker for oxidative stress in kidneys in cisplatin-induced acute renal failure in rats. Nephrol Dialy Transplan, 2006; 21(3):616-623. https://doi.org/10.1093/ndt/gfi314
Ozkok A, Edelstein CL, Pathophysiology of cisplatin-induced acute kidney injury. BioMed Res Interna, 2014; 2014. https://doi.org/10.1155/2014/967826
Rathi M., et al., Leaves of Spermacoce hispida as a Novel Cancer Therapeutic-An In Vitro Study. RJPT, 2011; 4(8):1288-1291.
Meti V, Mishra S, pharmacological activities of spermacoce hispida linn: a review. Interna J Res Ayur Pharm, 2013; 4(1). https://doi.org/10.7897/2277-4343.04115
Parthasarathy G., Evaluation of anti-inflammatory activity of methanolic extract of Spermacoce hispida Linn. J Pharma Res, 2010; 3(7).
Rajasudha V., Anburaj G, Manikandan R, Effect of various extracts of the leaves of Borreria hispida (Linn) on antibacterial activity. Meth, 2016; 25: 26.
Khairnar SI., et al., Disulfiram and its copper chelate attenuate cisplatin-induced acute nephrotoxicity in rats via reduction of oxidative stress and inflammation. Biologi trace ele Res, 2020; 193(1):174-184. https://doi.org/10.1007/s12011-019-01683-w
Atessahin A., et al., Effects of lycopene against cisplatin-induced nephrotoxicity and oxidative stress in rats. Toxicol, 2005; 212(2-3): 116-123. https://doi.org/10.1016/j.tox.2005.04.016
Antunes LMG, Darin JDAC, Bianchi MDLP, Protective effects of vitamin C against cisplatin-induced nephrotoxicity and lipid peroxidation in adult rats: a dose-dependent study. Pharmacol Res, 2000; 41(4):405-411. https://doi.org/10.1006/phrs.1999.0600
Jain PG., et al., Cardioprotective role of FA against isoproterenol induced cardiac toxicity. Mole Biol Rep, 2018; 45(5):1357-1365. https://doi.org/10.1007/s11033-018-4297-2
Jain PG., et al., The possible antioxidant capabilities of formononetin in guarding against streptozotocin-induced diabetic nephropathy in rats. Fut J Pharmaceu Sci, 2020; 6(1):1-9. https://doi.org/10.1186/s43094-020-00071-9
Shinde SD., et al., The Berberis aristata Ameliorates oxazolone induced contact dermatitis: in-vivo and in silico evidences. Adv Tradi Medi, 2020; 1-8. https://doi.org/10.1007/s13596-020-00476-0
Masule MV., et al., Evaluation of antioxidant and anti parkinsonism activity of betaine in experimental rats. JDDT, 2019; 9(2-s):417-421.
Sonawane VK., et al., A chemosensitizer drug: disulfiram prevents doxorubicin-induced cardiac dysfunction and oxidative stress in rats. Cardiovasc Toxicol, 2018; 18(5):459-470. https://doi.org/10.1007/s12012-018-9458-y
Barabas K., et al., Cisplatin: a review of toxicities and therapeutic applications. Veterina Compara Oncol, 2008; 6(1):1-18. https://doi.org/10.1111/j.1476-5829.2007.00142.x
Arunkumar P., et al., Science behind cisplatin-induced nephrotoxicity in humans: A clinical study. Asi Paci J Tropi Biomed, 2012; 2(8):640-644. https://doi.org/10.1016/S2221-1691(12)60112-9
Abdel Moneim AE, Othman MS, Aref AM, Azadirachta indica attenuates cisplatin-induced nephrotoxicity and oxidative stress. BioMed Res Interna, 2014: 2014. https://doi.org/10.1155/2014/647131
Zhang B., et al., Cisplatin-induced nephrotoxicity is mediated by tumor necrosis factor-α produced by renal parenchymal cells. Kid Interna, 2007; 72(1):37-44. https://doi.org/10.1038/sj.ki.5002242
Saad SY., et al., Inhibition of nitric oxide synthase aggravates cisplatin-induced nephrotoxicity: effect of 2-amino-4-methylpyridine. Chemother, 2002; 48(6):309-315. https://doi.org/10.1159/000069714
An Y., et al., Amelioration of cisplatin-induced nephrotoxicity by pravastatin in mice. Experi Toxicol Pathol, 2011; 63(3):215-219. https://doi.org/10.1016/j.etp.2009.12.002
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