Antioxidant, anti-inflammatory, and anti-DNA damage effects of carnosic acid against aflatoxin B1-induced hepatic, renal, and cardiac toxicities in rats.

IF 2.2 4区 医学 Q3 TOXICOLOGY Toxicology Research Pub Date : 2024-05-31 eCollection Date: 2024-06-01 DOI:10.1093/toxres/tfae083
Ghadeer M Albadrani, Ahmed E Altyar, Osama A Kensara, Mohie A M Haridy, Mohamed Sayed Zaazouee, Alaa Ahmed Elshanbary, Amany A Sayed, Mohamed M Abdel-Daim
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Abstract

Background: Aflatoxin B1 (AFB1) food contamination is a global health hazard that has detrimental effects on both human and animal health. The objective of the current study is to assess the protective impact of carnosic acid against AFB1-induced toxicities in the liver, kidneys, and heart.

Methods: Forty male Wistar Albino rats (weighting 180 ~ 200 g) were allocated into 5 groups (8 rats each); the 1st group received saline as served as a control, the 2nd group received carnosic acid (CA100) at a dose of 100 mg/kg bw/day by gavage for 14 days, the 3rd group received AFB1 at a dose of 2.5 mg/kg bw, orally twice on days 12 and 14, the 4th group (AFB1-CA50) received AFB1 as in the 3rd group and CA at a dose of 50 mg/kg bw/day, and the 5th group (AFB1-CA100) received AFB1 as in the 3rd group and CA as in the 2nd group.

Results: CA significantly decreased the liver enzymes (ALT, AST. ALP), renal function products (LDH, BUN, creatinine), and cardiac enzymes (CK and CK-MB) to control levels after the high increment by AFB1 exposure. Moreover, CA significantly decreased the oxidative stress (MDA, NO, 8-OHdG) and increased the antioxidant enzyme activities (CAT, GSH, GSH-Px, and SOD) after severe disruption of oxidant/antioxidant balance by AFB1 exposure. Interestingly, CA significantly decreased the proinflammatory mediators (IL-6, IL-1β, and TNF-α) to the control levels after severe inflammation induced by AFB1 exposure.

Conclusions: Conclusively, CA had antioxidant, anti-inflammatory, and anti-DNA damage effects against hepatic, renal, and cardiac AFB1-induced toxicities.

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肉毒碱对黄曲霉毒素 B1 诱导的大鼠肝、肾和心脏毒性的抗氧化、抗炎和抗 DNA 损伤作用。
背景:黄曲霉毒素 B1(AFB1)食品污染是一种全球性的健康危害,对人类和动物的健康都有不利影响。本研究的目的是评估左旋肉碱对 AFB1 引起的肝脏、肾脏和心脏毒性的保护作用:将 40 只雄性 Wistar Albino 大鼠(体重 180 ~ 200 克)分为 5 组(每组 8 只):第一组接受生理盐水作为对照,第二组接受肌肽酸(CA100),剂量为 100 毫克/千克体重/天,灌胃 14 天,第三组接受 AFB1,剂量为 2.第 4 组(AFB1-CA50)的 AFB1 剂量与第 3 组相同,CA 剂量为 50 毫克/千克体重/天;第 5 组(AFB1-CA100)的 AFB1 剂量与第 3 组相同,CA 剂量与第 2 组相同:结果:CA能明显降低肝酶(ALT、AST、ALP)、肾功能产物(LDH、BUN、肌酐)和心肌酶(CK和CK-MB),使其在接触AFB1高浓度后达到控制水平。此外,在 AFB1 暴露严重破坏氧化剂/抗氧化剂平衡后,CA 能明显降低氧化应激(MDA、NO、8-OHdG),提高抗氧化酶活性(CAT、GSH、GSH-Px 和 SOD)。有趣的是,AFB1暴露诱发严重炎症后,CA能明显降低促炎介质(IL-6、IL-1β和TNF-α)至对照组水平:结论:CA对AFB1诱导的肝、肾和心脏毒性具有抗氧化、抗炎和抗DNA损伤作用。
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来源期刊
Toxicology Research
Toxicology Research TOXICOLOGY-
CiteScore
3.60
自引率
0.00%
发文量
82
期刊介绍: A multi-disciplinary journal covering the best research in both fundamental and applied aspects of toxicology
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