Ameliorative effect of costus ethanolic extract against Oxaliplatin-induced hepatotoxicity in adult rats

被引:2
作者
Elshater, Abd Elraheem [1 ]
Ashry, Mahmoud [2 ,5 ]
Ahmed, Hend [1 ]
Abdel-Wahhab, Khaled [3 ]
Morsy, Fatma Adly [4 ]
Abd-Elstar, Rana [1 ]
机构
[1] South Valley Univ, Fac Sci, Dept Zool, Qena, Egypt
[2] Al Azhar Univ, Fac Sci, Dept Zool, Assiut, Egypt
[3] Natl Res Ctr, Med Physiol Dept, Med Div, Giza, Egypt
[4] Natl Res Ctr, Pathol Dept, Med Div, Giza, Egypt
[5] Al Azhar Univ, Fac Sci, Dept Zool, Assiut, Egypt
关键词
costus; hepatotoxicity; immunomodulation; Oxaliplatin; rat; OXIDATIVE STRESS; DEHYDROCOSTUS LACTONE; LIVER-INJURY; IN-VITRO; CHEMOTHERAPY; ACTIVATION; CELLS; SESQUITERPENE; NEUROTOXICITY; COSTUNOLIDE;
D O I
10.4103/epj.epj_44_21
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and objective Cancer is a disease associated with an abnormal proliferation and growth of living cells; treatment with the anticancer therapy, Oxaliplatin (OXP) results in hepatotoxicity. The objective of this study was to evaluate the protective effect of costus ethanolic extract (CEE) against OXP-induced hepatotoxicity in a trail to improve its clinical use. Materials and methods Adult male Wistar rats (150-180 g body weight) were randomly divided into four groups (10 rats each): (a) healthy control group, (b) healthy rats treated orally with CEE (50 mg/kg/day), (c) rats injected intraperitoneally with OXP (10 mg/kg once/week), and (d) rats treated with CEE in combination with OXP. Results and conclusion After 6 weeks of treatment, the results revealed that CEE succeeded to decline OXP-induced hepatotoxicity; this was evidenced by the significant reduction in serum alanine aminotransferase (ALAT), aspartate aminotransferases (ASAT), GGT, alkaline phosphatase (ALP), total cholesterol, triglycerides, low dense lipoprotein-cholesterol (LDL-c), tumor necrosis factor-alpha (TNF-alpha), Interleukin -1 Beta (IL-1 beta), and alpha-fetoprotein values as well as hepatic malondialdehyde, nitric oxide, and DNA fragmentation coupled with a marked rise in serum CD4, albumin and high dense lipoprotein-cholesterol (HDL-c) levels, and hepatic glutathione, superoxide dismutase, and catalase values. These effects agonized the structural restoration of the histological picture of liver. It could be concluded that CEE succeeded to a great extent to counteract the oxidative stress of OXP and protect the liver against its toxic effects; CEE may be considered as a promising supplement-candidate for the protection of liver against the side effects of that anticancer drugs.
引用
收藏
页码:30 / 39
页数:10
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