Experimental hepatotoxicity Inducing agents: A Review

Ashif Iqubal, M. K. Iqubal, S. Haque
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引用次数: 10

Abstract

Liver is the most important organ that performs vital function of the body. Hepatotoxicity is becoming a leading cause of death world-wide and prevalence is increasing exponentially. There are many traditional as well as allopathic medicines available which impart hepatoprotection but the treatment of chronic liver disease is still a challenge for health care professionals. For this purpose, rodents are routinely being used in the laboratory for induction of hepatotoxicity. Non-invasive methods that includes chemicals (CCL 4, thioacetamide, aflatoxin B1, Acrylamide etc), toxic metals (mercury, lead, arsenic and cadmium), drugs (NSAIDs, antibiotics, chemotherapeutic agents), radiation, high-fat diet and alcohol, are generally used to induce hepatic toxicity. Invasive methods used generally include bile duct ligation and portal vein ligation. This article provides an overview of different types of hepatic toxicants, their doses and time of induction. This review will help researchers in selecting the right model and studying and developing newer hepatoprotective drugs with minimum side effects.
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实验性肝毒性诱导剂的研究进展
肝脏是执行人体重要功能的最重要的器官。肝毒性正在成为世界范围内死亡的主要原因,患病率呈指数级增长。有许多传统的和对抗疗法的药物都可以保护肝脏,但是慢性肝病的治疗对卫生保健专业人员来说仍然是一个挑战。为此目的,啮齿类动物通常在实验室中用于肝毒性诱导。非侵入性方法通常用于诱导肝毒性,包括化学物质(ccl4、硫代乙酰胺、黄曲霉毒素B1、丙烯酰胺等)、有毒金属(汞、铅、砷和镉)、药物(非甾体抗炎药、抗生素、化疗药物)、辐射、高脂肪饮食和酒精。侵入性方法一般包括胆管结扎和门静脉结扎。本文概述了不同类型的肝毒物,它们的剂量和诱导时间。这一综述将有助于研究人员选择正确的模型,研究和开发副作用最小的新型肝保护药物。
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