评估氯化铁暴露大鼠心脏组织的变化:Chasmanthera dependens 甲醇叶提取物处理的影响

D. Calmday-Ombo, S.O. Innih
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引用次数: 0

摘要

背景和目的:铁是人体新陈代谢活动所必需的物质,但由于铁在氧化应激和组织损伤中的作用,过量的铁暴露会对心血管健康造成严重威胁。来自植物的天然铁螯合剂有望替代合成螯合剂,而且副作用可能更小。Chasmanthera dependens 作为植物性心脏保护剂螯合剂的功效尚未得到充分探索。本研究评估了暴露于氯化铁的大鼠的变化以及 MLECD 治疗的影响。方法:本研究使用了 25 只成年 Wistar 大鼠,平均体重在 185-225g 之间。每组五只,每天给药一次,治疗二十八天。A 组为对照组。B 组只给予每公斤体重 2 毫克的氯化亚铁溶液,C、D 和 E 组除每公斤体重 2 毫克的氯化亚铁溶液外,还分别给予每公斤体重 200、400 和 800 毫克的 MLECD。大鼠在氯仿下安乐死,摘取心脏并固定在中性缓冲福尔马林中进行苏木精和伊红组织染色,用光学显微镜检查组织切片。结果和结论:服用氯化铁后的组织病理学结果显示心肌变性、冠状血管溃疡、血管周围炎症和水肿,但 MLECD(尤其是最低剂量(200 毫克/千克 MLECD))对氯化铁诱导的铁毒性有保护作用,因此证明 MLECD 对过量铁暴露有心脏保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating Heart Tissue Changes in Iron Chloride-exposed Rats: Impact of Chasmanthera dependens Methanol Leaf Extract Treatment
BACKGROUND AND AIM: Iron is essential for body metabolic activities but excessive iron exposure poses a significant threat to cardiovascular health due to its role in oxidative stress and tissue damage. Natural iron-chelating agents from plants offer a promising alternative to synthetic chelators with potentially fewer side effects. The efficacy of Chasmanthera dependens as a plant-based cardioprotective agent chelating agent has not been fully explored. This study evaluates the changes in iron chloride-exposed rats and the impact of MLECD treatment. METHODOLOGY: Twenty-five adult Wistar rats averagely weighing between 185-225g were used for this study. They were divided into five rats per groups with daily administration for treatment for twenty-eight days. Group A served as the control group. Group B was given 2mg/kg body weight of FeCl2 only, groups C, D and E with 200, 400, and 800mg/kg body weights of MLECD in addition to 2mg/kg body weight of FeCl2 solution respectively. Rats were euthanized under chloroform and heart harvested and fixed in neutral buffered formalin for hematoxylin and eosin histological staining procedure, and histological slides were examined using light microscope. RESULTS AND CONCLUSION: Histopathological findings on FeCl2 administration showed myocardial degeneration, coronary vascular ulceration and perivascular inflammation and oedema but MLECD, especially at the lowest dose (200mg/kg MLECD), protected against FeCl2 induced iron-toxicity, consequently proving cardioprotective evidence of MLECD against excessive iron exposure.
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