Nephroprotective and anti-inflammatory potential of aqueous extract from Persea americana seeds against cadmium-induced nephrotoxicity in Wistar rats

被引:17
|
作者
Osukoya, Olukemi Adetutu [1 ]
Oyinloye, Babatunji Emmanuel [1 ,2 ,3 ]
Ajiboye, Basiru Olaitan [1 ,3 ,4 ]
Olokode, Kehinde Ayooluwabomi [1 ]
Adeola, Henry A. [5 ]
机构
[1] Afe Babalola Univ, Coll Sci, Dept Biochem, Phytomed Biochem Toxicol & Biotechnol Res Labs, PMB 5454, Ado Ekiti 360001, Nigeria
[2] Univ Zululand, Dept Biochem & Microbiol, Biotechnol & Struct Biol BSB Grp, ZA-3886 Kwa Dlangezwa, South Africa
[3] Afe Babalola Univ, SE Bogoro Ctr, Inst Drug Res & Dev, PMB 5454, Ado Ekiti 360001, Nigeria
[4] Fed Univ Oye Ekiti, Dept Biochem, Phytomed & Mol Toxicol Res Lab, Oye, Ekiti, Nigeria
[5] Univ Cape Town, Groote Schuur Hosp, Fac Hlth Sci, Dept Me,Div Dermatol, Cape Town, South Africa
关键词
Cadmium toxicity; Renal failure; Livolin forte; Persea americana; Oxidative stress; INDUCED OXIDATIVE STRESS; INDUCED TOXICITY; PROTECTIVE ROLE; HEAVY-METALS; ACID; SELENIUM; DAMAGE; L; APOPTOSIS; KIDNEY;
D O I
10.1007/s10534-021-00333-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cadmium is a toxic metal and poses a high environmental risk to animals and humans, alike. It is thus pertinent to search for medicinal plants in protecting against cadmium toxicity. This study aims at investigating the ability of aqueous extract of Persea americana seeds (AEPA) in ameliorating the toxic effects of cadmium in the kidneys of cadmium-exposed Wistar rats. Male Wistar rats were grouped into five, of six animals each. Different groups of animals received normal saline (control group), 200 mg/kg body weight AEPA, 400 mg/kg AEPA, and standard drug, Livolin Forte, respectively. A last group of animals was left untreated. To induce toxicity, all animals, except the control group, were exposed to cadmium (200 mg/L, as CdCl2) in their main drinking water for 21 days. Biochemical analysis of serum kidney markers, oxidative stress and antioxidant status, as well as anti-inflammatory activities, was done using standard methods and kits. In silico analysis was performed on phytochemicals reported to be abundant in AEPA. Treatment with 400 mg/kg AEPA significantly reversed (P <= 0.05) the adverse effect of cadmium on serum creatinine, urea, uric acid and blood urea nitrogen, and restored (P <= 0.05) antioxidant status, evidenced by its significant effect on superoxide dismutase, catalase, glutathione-S-transferase, glutathione peroxidase, reduced glutathione, and lipid peroxidation activities. AEPA, at 400 mg/kg also exhibited significant anti-inflammatory effects, which was shown by reduced interleukin-2 and tumour necrosis factor alpha activities. Molecular docking of phytochemicals with the selected protein target also confirmed the therapeutic potential of AEPA. The study concluded that aqueous extract of AEPA protects against cadmium-induced kidney toxicity and inflammation.
引用
收藏
页码:1141 / 1153
页数:13
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