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角鲨烯可减轻氧化应激,并激活AKT/mTOR信号通路,以对抗顺铂诱导的小鼠肾损伤。

Squalene attenuates the oxidative stress and activates AKT/mTOR pathway against cisplatin-induced kidney damage in mice.

作者信息

Sakul Arzu, Ozansoy Mehmet, Elibol Birsen, Ayla Şule, Günal Mehmet Yalçın, Yozgat Yasemin, Başağa Hüveyda, Şahin Kazım, Kazancioğlu Rümeyza, Kiliç Ülkan

机构信息

Department of Medical Pharmacology, School of Medicine, İstanbul Medipol University, İstanbul, Turkey.

Department of Physiology, School of Medicine, İstanbul Medipol University, İstanbul, Turkey.

出版信息

Turk J Biol. 2019 Jun 13;43(3):179-188. doi: 10.3906/biy-1902-77. eCollection 2019.

Abstract

The clinical use of cisplatin, which is a first-line anticancer agent, is highly restricted due to its adverse effects on kidneys that lead to nephrotoxicity. Therefore, some potential reno-protective substances have been used in combination with cisplatin to cope with nephrotoxicity. Due to its high antitumor activity and oxygen-carrying capacity, we investigated the molecular effects of squalene against cisplatin-induced oxidative stress and kidney damage in mice. Single dose of cisplatin (7 mg/kg) was given to male Balb/c mice. Squalene (100 mg/kg/day) was administered orogastrically to mice for 10 days. Following sacrification, molecular alterations were investigated as analysis of the levels of oxidative stress index (OSI), inflammatory cytokines and cell survival-related proteins in addition to histopathological examinations in mice kidney tissue. The level OSI and Interferon-gamma (IFN-γ) decreased in the cisplatin and squalene cotreated mice compared to cisplatin-treated mice. Squalene treatment also increased the activation of protein kinase B (AKT). Furthermore, cisplatin-induced inactivation of mammalian target of rapamycin (mTOR) and histopathological damages were reversed by squalene. It may be suggested that squalene ameliorated the cisplatin-induced histopathological damages in the kidney through activation of AKT/mTOR signaling pathway by regulating the balance of the redox system due to its antioxidative effect.

摘要

顺铂作为一线抗癌药物,因其对肾脏的不良反应会导致肾毒性,其临床应用受到高度限制。因此,一些潜在的肾脏保护物质已与顺铂联合使用以应对肾毒性。由于角鲨烯具有高抗肿瘤活性和携氧能力,我们研究了角鲨烯对顺铂诱导的小鼠氧化应激和肾脏损伤的分子作用。给雄性Balb/c小鼠单次注射顺铂(7mg/kg)。将角鲨烯(100mg/kg/天)经口灌胃给予小鼠,持续10天。处死后,除了对小鼠肾脏组织进行组织病理学检查外,还通过分析氧化应激指数(OSI)、炎性细胞因子和细胞存活相关蛋白的水平来研究分子变化。与顺铂处理的小鼠相比,顺铂和角鲨烯联合处理的小鼠中OSI水平和干扰素-γ(IFN-γ)降低。角鲨烯处理还增加了蛋白激酶B(AKT)的激活。此外,角鲨烯逆转了顺铂诱导的哺乳动物雷帕霉素靶蛋白(mTOR)失活和组织病理学损伤。可以认为,角鲨烯通过其抗氧化作用调节氧化还原系统的平衡,激活AKT/mTOR信号通路,从而减轻了顺铂诱导的肾脏组织病理学损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadd/6620038/9413c8b6b347/turkjbio-43-179-g001.jpg

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