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N-乙酰半胱氨酸早期干预可更好改善饮食诱导肥胖小鼠的胰岛素抵抗。

Early intervention of N-acetylcysteine better improves insulin resistance in diet-induced obesity mice.

机构信息

a Department of Internal Medicine , Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine , Kaohsiung , Taiwan.

b Mitochondrial Research Unit, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine , Kaohsiung , Taiwan.

出版信息

Free Radic Res. 2018 Dec;52(11-12):1296-1310. doi: 10.1080/10715762.2018.1447670.

Abstract

Reactive oxygen species (ROS) plays a crucial role in pathogenesis of insulin resistance (IR) and type 2 diabetes. In the United Kingdom, Prospective Diabetes Study and its 10-year post-trial monitoring, a beneficial effect of early optimisation of blood glucose control is clearly demonstrated. In this study, we investigated whether ROS scavenger N-acetylcysteine (NAC) and the time point of intervention can affect IR in a diet-induced obesity mouse model. Male C57B/L6 mice were fed chow diet (CD), high-fat high-sucrose diet (HFD), CD + NAC (NAC intervention 1st to 6th month), HFD + NAC, and HFD + NAC (NAC intervention 3rd to 6th month) for a 6-month treatment course. HFD group showed significantly increased body weight (BW) and body fat, decreased motor activity (MA), impaired intraperitoneal glucose tolerance test (IPGTT), and insulin tolerance test (IPITT) throughout the study. HFD + NAC, as compared with HFD group, had increased MA, improved IPGTT and IPITT since first month, followed by decreased BW and body fat. HFD + NAC group, although showed improved IPGTT and IPITT than HFD group, still had higher BW, decreased MA, and impaired IPGTT and IPITT as compared with HFD + NAC at the end of the study. NAC significantly increased MA, and ameliorated the HFD-induced mitochondrial and intracellular ROS expression, DNA and protein oxidative damage, and adipose tissue inflammation. We concluded that ROS scavenger can improve IR and chronic inflammation in diet-induced obesity mice. This action is likely better expressed through early intervention. The mechanism is probably through a virtuous circle of suppressed oxidative stress, and increased motor activity, which helps to reduce body fat.

摘要

活性氧(ROS)在胰岛素抵抗(IR)和 2 型糖尿病的发病机制中起着至关重要的作用。在英国,前瞻性糖尿病研究及其 10 年的试验后监测清楚地表明,早期优化血糖控制具有有益作用。在这项研究中,我们研究了 ROS 清除剂 N-乙酰半胱氨酸(NAC)及其干预时间点是否会影响饮食诱导肥胖小鼠模型中的 IR。雄性 C57B/L6 小鼠喂食标准饮食(CD)、高脂肪高蔗糖饮食(HFD)、CD+NAC(NAC 干预第 1 至 6 个月)、HFD+NAC 和 HFD+NAC(NAC 干预第 3 至 6 个月),治疗 6 个月。HFD 组在整个研究过程中表现出明显的体重(BW)和体脂肪增加、运动活动(MA)减少、腹腔内葡萄糖耐量试验(IPGTT)和胰岛素耐量试验(IPITT)受损。与 HFD 组相比,HFD+NAC 组 MA 增加,从第一个月开始,IPGTT 和 IPITT 改善,随后 BW 和体脂肪减少。尽管 HFD+NAC 组与 HFD 组相比,IPGTT 和 IPITT 有所改善,但与 HFD+NAC 组相比,BW 仍较高,MA 减少,IPGTT 和 IPITT 受损。NAC 显著增加 MA,并改善 HFD 诱导的线粒体和细胞内 ROS 表达、DNA 和蛋白质氧化损伤以及脂肪组织炎症。我们得出结论,ROS 清除剂可以改善饮食诱导肥胖小鼠的 IR 和慢性炎症。这种作用可能通过早期干预更好地表达。其机制可能是通过抑制氧化应激和增加运动活动的良性循环,有助于减少体脂肪。

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