Affiliation:
1. Department of Chemical Sciences, Faculty of Science , Kings University , Ode-Omu , Osun State , Nigeria
2. Phytomedicine and Toxicology Laboratories , Department of Biochemistry, Faculty of Basic and Applied Sciences , Osun State University , Osogbo , Nigeria
Abstract
Abstract
Renal diseases have been documented as one of the massive health challenges, ranked as the 12th most common cause of death globally. This study was carried out to assess the chemopreventive effects of Vernonia amydalina on nitrobenzene mediated renal damage in rats. Rats were exposed to 100 mg/kg body weight of nitrobenzene via oral administration and treated with 200 mg/kg body weight (BW) and 400 mg/kg BW of methanol leaf extract of Vernonia amydalina (MLVA) and Vitamin E for 14 consecutive days. Nitrobenzene significantly induced a renal injury with a significant increase in the serum levels of urea and creatinine with the concomitant altered serum electrolyte profile. Also, nitrobenzene mediated the oxidative stress and lipid peroxidation with a significant increase in the renal level of malondialdehyde (MDA), hydrogen peroxide (H2O2), with a concomitant decrease in the level of reduced glutathione (GSH), Catalase (CAT) and Superoxide dismutase (SOD). Furthermore, an inflammation was observed in the nitrobenzene-treated rats with the elevated level of nitric oxide (NO) and myeloperoxidase (MPO). However, the treatment with methanol leaf extract of Vernonia amydalina reversed all the nitrobenzene-associated renal damage, electrolyte imbalance, oxidative stress, lipid peroxidation, inflammation and altered antioxidant defence system. Taken together, methanol leaf extract of Vernonia amydalina offers protection which may be beneficial for the treatment and management of kidney diseases or other related disorders via enhancing the serum electrolyte homeostasis, protecting the structural integrity of the kidney, antioxidant, anti-inflammatory mechanisms.
Reference38 articles.
1. 1. Wang H, Naghavi M, Allen C, et al. Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the global burden of disease study 2015. Lancet. 2016; 388: 1459–544.10.1016/S0140-6736(16)31012-1
2. 2. Joy J, Nair CK. Amelioration of cisplatin induced nephrotoxicity in Swiss albino mice by rubia cordifolia extract. J Can Res Ther. 2008; 4: 111–115.10.4103/0973-1482.43139
3. 3. Cattley RC, Everitt JI, Gross EA. Carcinogenicity and toxicity of inhaled nitrobenzene in B6C3F1 mice and F344 and CD rats. Toxicol. Sci. 1994; 22: 328–340.
4. 4. Howard PC, Beland FA, Cerniglia CE. Reduction of the carcinogen 1-nitropyrene to 1-aminopyrene by the rat intestinal bacteria. Carcinogenesis. 1983; 4: 985–990.10.1093/carcin/4.8.985
5. 5. International Programme on Chemical Safety (IPCS). Nitrobenzene environmental health. criteria 230. Geneva: WHO 2003.
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献