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姜黄素对阿贝西利给药大鼠肝组织脂质谱、纤维化和细胞凋亡的影响。

Effect of curcumin on lipid profile, fibrosis, and apoptosis in liver tissue in abemaciclib-administered rats.

机构信息

Department of Biochemistry, Faculty of Medicine, Van Yuzuncu Yil University, Van, Turkey.

Department of Histology and Embryology, Faculty of Medicine, Van Yuzuncu Yil University, Van, Turkey.

出版信息

Drug Chem Toxicol. 2023 Nov;46(6):1138-1146. doi: 10.1080/01480545.2022.2135007. Epub 2022 Oct 19.

Abstract

Abemaciclib (ABEM) is an important antitumor agent for breast cancer treatment. However, the side-effects of ABEM are unclear in the liver. This study investigated the protective effect of curcumin (CURC) on liver damage caused by ABEM. The rats were divided into five groups with eight animals in each group; Control, DMSO (150 µL for per rats), CURC, 30 mg/kg/day), ABE (26 mg/kg/day), and ABE + CURC (26 mg/kg/day ABE, 30 mg/kg/day) groups. Injections were administered daily for 28 days. The levels of AST, LDH, HDL, LDL, triglyceride, and total cholesterol in serum, and hepatic tissue fibrosis, caspase-3, Bax, and TNF-α expression were higher in the ABE group compared to the control group ( < 0.05). Also, these parameters in the ABEM + CURC group were lower than in the ABE group ( < 0.05). The results showed that ABE administration could cause liver damage and increase fibrosis in the liver. In addition, it was shown that co-administration of CURC with ABE could suppress the levels of AST, LDH, HDL, LDL, triglyceride, and total cholesterol in serum, and fibrosis, caspase-3, Bax, and TNF-α expressions in the liver. These data are the first in the literature. Therefore, the administration of CURC following ABE may be a therapeutic agent in preventing liver damage.

摘要

阿贝西利(ABEM)是一种重要的乳腺癌治疗抗肿瘤药物。然而,ABEM 在肝脏中的副作用尚不清楚。本研究探讨了姜黄素(CURC)对 ABEM 引起的肝损伤的保护作用。将大鼠分为五组,每组 8 只;对照组、DMSO(150μL/只)、CURC(30mg/kg/天)、ABE(26mg/kg/天)和 ABE+CURC(26mg/kg/天 ABE,30mg/kg/天)组。每天注射一次,持续 28 天。与对照组相比,ABE 组大鼠血清中天冬氨酸转氨酶(AST)、乳酸脱氢酶(LDH)、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、甘油三酯和总胆固醇水平以及肝组织纤维化、caspase-3、Bax 和 TNF-α 表达均升高(<0.05)。此外,ABE+CURC 组的这些参数低于 ABE 组(<0.05)。结果表明,ABE 给药可导致肝脏损伤并增加肝脏纤维化。此外,还表明 CURC 与 ABE 联合给药可抑制血清中 AST、LDH、HDL、LDL、甘油三酯和总胆固醇水平以及肝脏纤维化、caspase-3、Bax 和 TNF-α 表达。这些数据是文献中的首次报道。因此,在 ABE 给药后给予 CURC 可能是预防肝脏损伤的治疗剂。

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