Hepatoprotective effects of Nigella sativa seed extract against acetaminophen-induced oxidative stress

被引:42
作者
Adam, Gareeballa Osman [1 ,2 ]
Rahman, Md. Mahbubur [2 ]
Lee, Sei-Jin [3 ]
Kim, Gi-Beum [2 ]
Kang, Hyung-Sub [2 ]
Kim, Jin-Shang [2 ]
Kim, Shang-Jin [2 ]
机构
[1] Sudan Univ Sci & Technol, Coll Vet Med, Dept Vet Med & Surg, POB 204, Khartoum, Sudan
[2] Chonbuk Natl Univ, Coll Vet Med, Dept Vet Pharmacol & Toxicol, Iksan Campus,79 Gobong Ro, Iksan 570752, Jeollabuk Do, South Korea
[3] Korea Basic Sci Inst Jeonju Ctr, 567 Baekje Daero, Jeonju 561756, Jeollabuk Do, South Korea
基金
新加坡国家研究基金会;
关键词
Nigella sativa; Acetaminophen; Antioxidants; Oxidative stress; TIB-73; cells; Rat; MITOCHONDRIAL PERMEABILITY TRANSITION; INDUCED HEPATOTOXICITY; RATS; INJURY; MICE; OIL;
D O I
10.1016/j.apjtm.2016.01.039
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: To investigate the protective effects of Nigella saliva seed extract (NSSE) against acetaminophen (APAP)-induced hepatotoxicity in TIB-73 cells and rats. Methods: Toxicity in TIB-73 cells was induced with 10 mu mol/L APAP and the protective effects of NSSE were evaluated at 25. 50. 75, 100 mu g/mL. For in vivo examination, a total of 30 rats were equally divided into five experimental groups; normal control (vehicle), APAP (800 mg/kg body weight single IP injection) as a hepatotoxic control, and three APAP and NS pretreated (2 weeks) groups (APAP+NSSE 100 me; APAP+NSSE 300 mg and APAP+NSSE 900 mg/kg). Results: TIB-73 cell viability was drastically decreased by (49.0 +/- 11.9)% after the 10 union. APAP treatment, which also increased reactive oxygen species production. Co-treatment with NSSE at 25. 50, 75, and 100 mu g/mL significantly improved cell viability and suppressed reactive oxygen species generation. In vivo, the APAP induced alterations in blood lactate levels, pH, anionic gap. and ion levels (HCO3-, Mg2+ and K+), which tended to normalize with the NSSE pretreatment. The NSSE also significantly decreased elevated serum levels of alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase, and alkaline phosphatase induced by APAP, which correlated with decreased levels of hepatic lipid peroxidation (malondialdehyde), increased superoxide dismutase levels, and reduced glutathione concentrations. Improved hepatic histology was also found in the treatment groups other than APAP group. Conclusions: The in vitro and in vivo findings of this study demonstrated that the NSSE has protective effects against APAP-induced hepatotoxicity and metabolic disturbances by improving antioxidant activities and suppressing both lipid peroxidation and ROS generation.
引用
收藏
页码:217 / 222
页数:6
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