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口服百里醌可改善顺铂对大鼠肾脏刷状缘膜酶、能量代谢和氧化还原状态的影响。

Oral thymoquinone administration ameliorates: the effect of cisplatin on brush border membrane enzymes, energy metabolism, and redox status in rat kidney.

机构信息

Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh, UP, 202002, India.

Department of Zoology, Faculty of Life Sciences, Aligarh Muslim University, Aligarh, UP, 202002, India.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2017 Dec;390(12):1271-1284. doi: 10.1007/s00210-017-1428-6. Epub 2017 Sep 24.

Abstract

Therapeutic use of cisplatin (CP), an effective anticancer drug, is limited by dose dependent nephrotoxicity. Thymoquinone (TQ), the major Nigella sativa seed oil constituent has been shown to prevent progression of various renal disorders. The present study investigates the protective effect of TQ on CP-induced nephrotoxicity. Rats were divided into six groups viz. control, CP, CPTQ, CPTQ, CPTQ, and TQ alone group. Animals in CP and TQ combination groups were administered TQ (0.5, 1.5, and 3 mg/kg bwt, orally) with single intraperitoneal dose of CP (6 mg/kg bwt). The effect of TQ administration was determined on CP-induced alterations in various serum/urine parameters and on the enzymes of brush border membrane enzyme (BBM), carbohydrate metabolism, and antioxidant defense system in renal cortex and medulla. Oral administration of TQ in all the three doses prior to and following a single dose CP treatment caused significant recovery of serum creatinine and blood urea nitrogen levels; however, maximum recovery was seen in CPTQ group. TQ administration averted CP-induced decline in BBM activities, both in the cortical and medullary homogenates and in isolated BBM vesicles. TQ administration also ameliorated CP-induced impairments in renal metabolic and antioxidant status. Histopathological studies supported these biochemical findings. TQ ameliorates CP-induced oxidative damage owing to its intrinsic antioxidant properties.

摘要

顺铂(CP)是一种有效的抗癌药物,但其治疗用途受到剂量依赖性肾毒性的限制。百里醌(TQ)是黑种草籽油的主要成分之一,已被证明可预防多种肾脏疾病的进展。本研究探讨了 TQ 对 CP 诱导的肾毒性的保护作用。将大鼠分为六组:对照组、CP 组、CPTQ 组、CPTQ 组、CPTQ 组和 TQ 组。CP 和 TQ 联合组的动物给予 TQ(0.5、1.5 和 3 mg/kg bwt,口服),同时单次腹腔内给予 CP(6 mg/kg bwt)。测定 TQ 给药对 CP 诱导的各种血清/尿液参数的影响,以及对肾皮质和髓质刷状缘膜酶(BBM)、糖代谢和抗氧化防御系统的酶的影响。在单次 CP 治疗前后,TQ 以所有三种剂量口服给药,导致血清肌酐和血尿素氮水平显著恢复;然而,CPTQ 组的恢复最大。TQ 给药可防止 CP 诱导的 BBM 活性下降,无论是在皮质和髓质匀浆中,还是在分离的 BBM 囊泡中。TQ 给药还改善了 CP 诱导的肾代谢和抗氧化状态的损伤。组织病理学研究支持了这些生化发现。TQ 可改善 CP 诱导的氧化损伤,这归因于其内在的抗氧化特性。

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