骨髓间充质干细胞可缓解甲氨蝶呤诱导的白血病大鼠肾毒性

Hanan abdellatief
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摘要

背景:化疗药物甲氨蝶呤(MTX)用于治疗多种癌症。目的:确定骨髓间充质干细胞(BM-MSCs)是否能保护大鼠免受 MTX 对肾脏的损害。材料与方法 :将大鼠分为五组:(i) 对照组接受 2.5 毫升生理盐水。(ii)MTX组:单次IP注射20毫克/千克体重的MTX。(iii) LEUK 组:苯诱导白血病组每 2 天静脉注射 0.2 毫升苯,连续 3 周。(iv) LEUK/MTX 组:每 2 天静脉注射 0.2 毫升苯,连续 3 周,然后腹腔注射 2.5 毫克/千克体重/周 MTX,连续 4 周。(v) (LEUK/MTX/MSCs)组连续 3 周每 2 天静脉注射 0.2 毫升苯,并连续 4 周腹腔注射 2.5 毫克/千克体重/周 MTX。该组还留置 8 天进行肾损伤诱导,然后静脉注射单剂量 3x10 6 MSCs。间充质干细胞移植 4 周后。对肾脏组织病理学、过氧化氢酶和超氧化物歧化酶活性以及Capase-3表达水平进行检测。结果甲氨蝶呤诱导了明显的病理损伤,其特征为局灶性坏死、细胞浸润和TGF-β1的高免疫表达。此外,间充质干细胞治疗成功改善了 MTX 对肾脏的严重影响,恢复了组织学结构,氧化酶和细胞凋亡标志物证实了这一点。
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Bone Marrow Mesenchymal Stem Cells Alleviate Methotrexate-Induced Renal Toxicity in leukemia Rats
Background: The chemotherapeutic drug methotrexate (MTX) is administered for managing multiple kinds of cancer. Aim: To determine if bone marrow mesenchymal stem cells (BM-MSCs) might protect rats against renal damage brought on by MTX. Materials and Methods : Rats were divided into five groups : (i) Control group received 2.5 ml saline. (ii) group received MTX as a single IP of 20 mg/Kg body weight. (iii) LEUK group: Benzene-induced leukemia group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene. (iv) LEUK/MTX group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene and treated by intraperitoneal injection of 2.5 mg/kg.bw/week MTX for 4 consecutive weeks. (v) (LEUK/ MTX/MSCs) group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene and treated by intraperitoneal injection of 2.5 mg/kg.bw/week MTX for 4 consecutive weeks. This group was also left for 8 days for kidney injury induction then injected intravenously with a single dose of 3x10 6 MSCs. After 4 weeks of MSCs transplantation. Kidney histopathology, Catalase and Superoxide dismutase activities as well as Capase-3 expression levels were examined. Results: Methotrexate induced marked pathological lesion which characterized by focal necrosis, cell infiltration and high immuno-expression ofTGF-β1 . Besides, treatment with MSCs successfully improved the severe effects of MTX on the kidney and restored histological architecture which confirmed by oxidative enzymes and apoptosis marker
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