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血管紧张素 1-7 可刺激棕色脂肪组织并减少饮食诱导的肥胖。

Angiotensin 1-7 stimulates brown adipose tissue and reduces diet-induced obesity.

机构信息

Department of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science , Kyoto , Japan.

Department of Orthopaedics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science , Kyoto , Japan.

出版信息

Am J Physiol Endocrinol Metab. 2018 Feb 1;314(2):E131-E138. doi: 10.1152/ajpendo.00192.2017. Epub 2017 Oct 24.

Abstract

The renin-angiotensin system is a key regulator of metabolism with beneficial effects of the angiotensin 1-7 (Ang 1-7) peptide. We hypothesized that the antiobesity effect of Ang 1-7 was related to the stimulation of brown adipose tissue (BAT). We administered Ang 1-7 (0.54 mg kg day) for 28 days via implanted micro-osmotic pumps to mice with high-fat diet (HFD)-induced obesity. Ang 1-7 treatment reduced body weight, upregulated thermogenesis, and ameliorated impaired glucose homeostasis without affecting food consumption. Furthermore, Ang 1-7 treatment enlarged BAT and the increased expression of UCP1, PRDM16, and prohibitin. Alterations in PRDM16 expression correlated with increased AMPK and phosphorylation of mTOR. Ang 1-7 treatment elevated thermogenesis in subcutaneous white adipose tissue without altering UCP1 expression. These changes occurred in the context of decreased lipid accumulation in BAT from HFD-fed mice, preserved insulin signaling concomitant with phosphorylation of hormone-sensitive lipase and decreased expression of perilipin. These data suggest that Ang 1-7 induces brown adipocyte differentiation leading to upregulation of thermogenesis and improved metabolic profile in diet-induced obesity. Enhancing Ang 1-7 action represents a promising therapy to increase BAT and to reduce the metabolic complications associated with diet-induced obesity.

摘要

肾素-血管紧张素系统是代谢的关键调节剂,血管紧张素 1-7(Ang 1-7)肽具有有益作用。我们假设 Ang 1-7 的抗肥胖作用与其对棕色脂肪组织(BAT)的刺激有关。我们通过植入的微渗透泵给高脂肪饮食(HFD)诱导肥胖的小鼠施用 Ang 1-7(0.54 mg kg day)28 天。Ang 1-7 治疗可减轻体重,上调产热,并改善葡萄糖稳态受损,而不影响食物消耗。此外,Ang 1-7 治疗可增大 BAT 并增加 UCP1、PRDM16 和 prohibitin 的表达。PRDM16 表达的改变与 AMPK 的增加和 mTOR 的磷酸化相关。Ang 1-7 治疗可增加皮下白色脂肪组织的产热,而不改变 UCP1 的表达。这些变化发生在从 HFD 喂养的小鼠的 BAT 中脂质积累减少的背景下,同时保持胰岛素信号传导,伴随着激素敏感性脂肪酶的磷酸化和 perilipin 的表达降低。这些数据表明,Ang 1-7 诱导棕色脂肪细胞分化,导致产热增加和改善饮食诱导肥胖的代谢特征。增强 Ang 1-7 的作用代表了一种有前途的治疗方法,可以增加 BAT 并减少与饮食诱导肥胖相关的代谢并发症。

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