Amla (Emblica officinalis) alleviates doxorubicin-induced cardiotoxicity and nephrotoxicity in rats

Mandeep Kumar Arora , Mary Singh , Ritu Tomar , Lakhveer Singh , Ashok Jangra
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Abstract

Introduction

Doxorubicin (DOX) is a widely used anticancer drug known for its significant cardiotoxic and nephrotoxic effects. Seeking remedies to mitigate these adverse effects is crucial. This study investigates the potential of Emblica officinalis (Amla) extract, a prominent component in Chinese and Indian traditional medicine systems, in alleviating DOX-induced cardiotoxicity and nephrotoxicity.

Methods

DOX (20 mg/kg i.p., once) was given to rats to cause acute cardiotoxicity and nephrotoxicity. Rats received 16 similar and cumulative doses of DOX (1.25 mg/kg, i.p.) on alternate days for chronic cardiotoxicity and nephrotoxicity. Biochemical and histological evaluations were done to confirm the onset of cardiotoxicity and nephrotoxicity.

Results

The cardioprotective and nephroprotective effects of Amla extract (AE) (150 mg/kg p.o. and 300 mg/kg p.o) were evaluated in comparison to Vitamin E (25 mg/kg p.o.). The treatment with AE (300 mg/kg/day, p.o.) considerably prevented DOX-induced cardiotoxicity, nephrotoxicity, and oxidative stress by positively altering the integrity of glomeruli, restoring the tissue GSH and decreasing serum TBARS. AE (300 mg/kg) was found to be more cardioprotective and nephroprotective than Vitamin E (25 mg/kg p.o.).

Discussion

It may be concluded that the induction of cardiotoxicity and nephrotoxicity in rats may be due to DOX-induced oxidative stress, and chronic treatment with AE (300 mg/kg) is an effective way to alleviate the cardiotoxic and nephrotoxic adverse effects of DOX in rats. Moreover, given Amla's historical and contemporary significance in Chinese and Indian traditional medicine systems, its potential therapeutic role merits further exploration in clinical settings.

Abstract Image

阿木拉(Emblica officinalis)可减轻多柔比星引起的大鼠心脏毒性和肾毒性
导言多柔比星(Doxorubicin,DOX)是一种广泛使用的抗癌药物,具有明显的心脏毒性和肾毒性作用。寻找减轻这些不良反应的疗法至关重要。本研究调查了中国和印度传统医学体系中的一种重要成分--恩巴拉(Amla)提取物在减轻 DOX 引起的心脏毒性和肾毒性方面的潜力。隔天给大鼠注射 16 次类似的累积剂量 DOX(1.25 毫克/千克,静脉注射),以产生慢性心脏毒性和肾毒性。结果与维生素 E(25 毫克/千克/只)相比,评估了阿木拉提取物(AE)(150 毫克/千克/只和 300 毫克/千克/只)对心脏和肾脏的保护作用。AE(300 毫克/千克/天,口服)通过积极改变肾小球的完整性、恢复组织 GSH 和降低血清 TBARS,大大预防了 DOX 引起的心脏毒性、肾毒性和氧化应激。AE(300 毫克/千克)比维生素 E(25 毫克/千克 p.o.)更具有心脏保护和肾脏保护作用。讨论可以得出结论,大鼠心脏毒性和肾毒性的诱导可能是由于 DOX 诱导的氧化应激所致,而 AE(300 毫克/千克)的慢性治疗是缓解 DOX 对大鼠心脏毒性和肾毒性不良影响的有效方法。此外,鉴于阿木拉在中国和印度传统医学体系中的历史和现代意义,其潜在的治疗作用值得在临床环境中进一步探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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