芝司明对循环胺诱导的肝毒性,分子机制和组织病理学特征的治疗作用
Abdulmajeed M Jali1, Mohammad Firoz Alam1, Ali Hanbashi1,2
1Department of Pharmacology and Toxicology, College of Pharmacy, Jazan University, Jazan 45142, Saudi Arabia.
Biomedicines
|December 23, 2023
概括
芝胺是一种天然抗氧化剂,有效地保护了老鼠肝脏免受循环胺化疗造成的损伤. 这项研究表明,素可能有助于减少化疗.
科学领域:
- 药理学和毒理学 药理学和毒理学
- 肝脏保护剂 肝脏保护剂
- 自然产品化学 自然产品化学
背景情况:
- 环胺 (化疗) 会导致肝损伤 (肝毒性).
- 胺是一种植物性抗氧化剂,具有潜在的治疗益处.
- 需要制定减轻化疗引起的肝损伤的策略.
研究的目的:
- 评价芝对大鼠肝脏的肝脏保护作用,以防止循环胺诱导的肝脏毒性.
- 调查胺的保护作用背后的机制.
主要方法:
- 鼠被分为对照组,循环胺,芝麻胺和芝麻胺预处理组.
- 循环胺是通过腹膜内注射的;芝麻胺是通过口服给予的.
- 进行了生化 (肝酶,细胞因子,氧化应激标志物) 和本病理学分析.
主要成果:
- 环胺显著增加了肝酶 (AST,ALT,ALP,BIL),炎症类细胞因子 (TNFα,IL-1β),-3和MDA.
- 环胺降低了抗氧化剂水平 (GSH) 和酶 (CAT,SOD).
- 胺治疗逆转了这些变化,减少了肝损伤标志物,改善了抗氧化剂状况.
结论:
- 在大鼠模型中,胺有效地减轻了环胺诱导的肝毒性.
- 芝的保护作用包括细胞因子网络的调节,亡和氧化应激.
- 芝麻素作为一种辅助疗法,有望减少化疗相关的肝损伤.
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