Jafaripour Leila, Naserzadeh Reza, Alizamani Ehsan, Javad Mashhadi Seyyed Mohammad, Moghadam Ebrahim Rahmani, Nouryazdan Negar, Ahmadvand Hassan
Department of Anatomy, School of Medicine, Dezful University of Medical Sciences, Dezful, Iran.
Student Research Committee, Dezful University of Medical Sciences, Dezful, Iran.
Indian J Nephrol. 2021 May-Jun;31(3):218-224. doi: 10.4103/ijn.IJN_14_20. Epub 2021 Jan 27.
Methotrexate (MTX), used in the treatment of cancerous patients, causes toxicity in the different organs of the body. This study of rosmarinic acid (RA) is as an antioxidant on nephrotoxicity and hepatotoxicity induced by MTX.
Rats (n = 32) were divided into four groups: sham; MTX; 100 mg\kg RA + MTX; 200 mg/kg RA + MTX. The amount of MTX was 20 mg/kg. 24 hours after injection of the last dose of MTX, the blood samples and kidneys and liver of rats were studied. The aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), urea, serum creatinine were assessed. Tissue antioxidant enzymes and malondialdehyde (MDA) levels were measured. The liver and kidney tissues were histopathologically examined.
MTX significantly increased the urea, creatinine, ALT, AST, ALP levels, and renal MDA and significantly decreased renal catalase (CAT), hepatic glutathione (GSH), and hepatic CAT activity. MTX induced necrosis, leukocyte infiltration, eosinophilic casts, glomerular damage in kidney tissue and necrosis, degeneration and cellular vacuolization in liver tissues. RA at 100 mg/kg caused a significant decrease in ALT and AST and at two doses significantly decreased urea, renal MDA, and liver MDA. RA at 200 mg/kg significantly increased the renal CAT and liver GSH. RA in two doses significantly decreased necrosis and Leukocyte infiltration. RA caused a significant decrease in degeneration and cellular vacuolization in liver tissues.
RA with its antioxidant and anti-inflammatory characteristics decreased the MTX induced nephrotoxicity and hepatotoxicity.
甲氨蝶呤(MTX)用于治疗癌症患者时,会对身体的不同器官产生毒性。本研究旨在探讨迷迭香酸(RA)作为抗氧化剂对MTX诱导的肾毒性和肝毒性的影响。
将32只大鼠分为四组:假手术组;MTX组;100mg/kg RA + MTX组;200mg/kg RA + MTX组。MTX的剂量为20mg/kg。在注射最后一剂MTX 24小时后,对大鼠的血液样本以及肾脏和肝脏进行研究。评估了氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、碱性磷酸酶(ALP)、尿素、血清肌酐。测量了组织抗氧化酶和丙二醛(MDA)水平。对肝脏和肾脏组织进行了组织病理学检查。
MTX显著提高了尿素、肌酐、ALT、AST、ALP水平以及肾脏MDA水平,并显著降低了肾脏过氧化氢酶(CAT)、肝脏谷胱甘肽(GSH)和肝脏CAT活性。MTX诱导了肾组织坏死、白细胞浸润、嗜酸性管型、肾小球损伤以及肝组织坏死、变性和细胞空泡化。100mg/kg的RA显著降低了ALT和AST水平,两种剂量的RA均显著降低了尿素、肾脏MDA和肝脏MDA水平。200mg/kg的RA显著提高了肾脏CAT和肝脏GSH水平。两种剂量的RA均显著降低了坏死和白细胞浸润。RA显著降低了肝组织的变性和细胞空泡化。
RA凭借其抗氧化和抗炎特性降低了MTX诱导的肾毒性和肝毒性。