Boroushaki Mohammad Taher, Fanoudi Sahar, Rajabian Arezoo, Boroumand Samaneh, Aghaee Azita, Hosseini Azar
Department of Pharmacology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran.
Drug Res (Stuttg). 2019 Aug;69(8):434-438. doi: 10.1055/a-0821-5653. Epub 2019 Mar 1.
Hexachlorobutadien is nephrotoxic agent in rodents. The mechanism of toxicity includes generation of free radicals, depletion of thiol groups and production of toxic metabolites. Antioxidant compounds may reduce HCBD-nephrotoxicity. In this research we investigated the effect of Rheum turkeatanicum extract against HCBD-toxicity. The animals were divided to 4 groups which were including control (saline, 1 mL/kg), HCBD (100 mg/kg) and treatment groups which received extract at doses 100 and 200 mg/kg. The extract were administered as intraperitoneally (i.p.) 1 h before HCBD injection (i.p.). The animals were anesthetized by ether, 24 h after HCBD administration. The results showed elevation of serum creatinine, serum urea, urinary protein, urinary glucose, malondialdehyde levels in kidney and reduction of thiol in kidney by HCBD. The histopathological studies showed that there was apoptosis and necrosis in HCBD treated groups. Administration of R.turkestanicum reduced HCBD toxicity. The extract reduced hitopathological changes in kidney. It may be concluded that the nephroprotective effect of extract may be due to different mechanisms such as antioxidant activity or by decreasing the toxic metabolites of HCBD or inhibition of enzymes which are involved in the bioactivation of HCBD such as glutathione-S-transferase (GST) or cysteine-S-conjugate β-lyase.
六氯丁二烯是啮齿动物的肾毒性剂。其毒性机制包括自由基的产生、硫醇基团的消耗以及有毒代谢产物的生成。抗氧化化合物可能会降低六氯丁二烯的肾毒性。在本研究中,我们研究了土耳其大黄提取物对六氯丁二烯毒性的影响。将动物分为4组,包括对照组(生理盐水,1毫升/千克)、六氯丁二烯组(100毫克/千克)和治疗组,治疗组分别接受100和200毫克/千克剂量的提取物。提取物在腹腔注射六氯丁二烯前1小时腹腔内给药。在腹腔注射六氯丁二烯24小时后,用乙醚麻醉动物。结果显示,六氯丁二烯使血清肌酐、血清尿素、尿蛋白、尿葡萄糖、肾脏丙二醛水平升高,肾脏硫醇减少。组织病理学研究表明,六氯丁二烯处理组存在细胞凋亡和坏死。给予土耳其大黄提取物可降低六氯丁二烯的毒性。该提取物减轻了肾脏的组织病理学变化。可以得出结论,提取物的肾保护作用可能归因于不同的机制,如抗氧化活性、减少六氯丁二烯的有毒代谢产物或抑制参与六氯丁二烯生物活化的酶,如谷胱甘肽-S-转移酶(GST)或半胱氨酸-S-共轭β-裂解酶。