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不同用于肝保护研究的实验模型的深入了解:综述。

An Insight into Different Experimental Models used for Hepatoprotective Studies: A Review.

机构信息

School of Pharmacy and Life Sciences, Centurion University of Technology and Management, Bhubaneswar, 751050, India.

School of Pharmaceutical Sciences, Siksha O Anusandhan Deemed to be University, Bhubaneswar, 751030, India.

出版信息

Curr Drug Discov Technol. 2024;21(4):e191223224660. doi: 10.2174/0115701638278844231214115102.

Abstract

Numerous factors, including exposure to harmful substances, drinking too much alcohol, contracting certain hepatitis serotypes, and using specific medicines, contribute to the development of liver illnesses. Lipid peroxidation and other forms of oxidative stress are the main mechanisms by which hepatotoxic substances harm liver cells. Pathological changes in the liver include a rise in the levels of blood serum, a decrease in antioxidant enzymes, as well as the formation of free radical radicals. It is necessary to find pharmaceutical alternatives to treat liver diseases to increase their efficacy and decrease their toxicity. For the development of new therapeutic medications, a greater knowledge of primary mechanisms is required. In order to mimic human liver diseases, animal models are developed. Animal models have been used for several decades to study the pathogenesis of liver disorders and related toxicities. For many years, animal models have been utilized to investigate the pathophysiology of liver illness and associated toxicity. The animal models are created to imitate human hepatic disorders. This review enlisted numerous hepatic damage and models using various toxicants, their probable biochemical pathways and numerous metabolic pathways via oxidative stressors, different serum biomarkers enzymes are discussed, which will help to identify the most accurate and suitable model to test any plant preparations to check and evaluate their hepatoprotective properties.

摘要

许多因素,包括接触有害物质、过量饮酒、感染某些肝炎血清型和使用某些药物,都会导致肝脏疾病的发生。脂质过氧化和其他形式的氧化应激是肝毒性物质损害肝细胞的主要机制。肝脏的病理变化包括血清水平升高、抗氧化酶减少以及自由基形成。为了提高治疗肝脏疾病的疗效并降低其毒性,有必要寻找药物替代物。为了开发新的治疗药物,需要更多地了解主要机制。为了模拟人类肝脏疾病,开发了动物模型。几十年来,动物模型一直被用于研究肝脏疾病的发病机制和相关毒性。多年来,动物模型一直被用于研究肝脏疾病的病理生理学及其相关毒性。动物模型被用来模拟人类的肝脏疾病。本文列出了使用各种毒物的多种肝损伤模型,讨论了其可能的生化途径和氧化应激源的多种代谢途径,不同的血清生物标志物酶,这将有助于确定最准确和合适的模型来测试任何植物制剂,以检查和评估其肝保护特性。

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