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肾周和附睾脂肪影响大鼠的肝脏代谢。

Perinephric and epididymal fat affect hepatic metabolism in rats.

机构信息

The Research Center for Digestive Tract and Liver Diseases, Tel-Aviv Sourasky Medical Center and the Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

出版信息

Obesity (Silver Spring). 2012 Jan;20(1):151-6. doi: 10.1038/oby.2011.261. Epub 2011 Aug 4.

Abstract

The present study examined whether the perinephric and epididymal visceral fat (PEVF) depot under short-term excess nutrient protected the liver by trapping nutrient-derived nonesterified free fatty acids (NEFAs) or had deleterious effects on hepatic triglycerides (TGs) accumulation and insulin resistance due to adipokine secretion. Young rats pre-emptively underwent surgical PEVF removal or sham operations and were fed with either high-fat diet (HFD) (PEVF-HFD) or regular chow (RC) (PEVF-RC) for 3 days. Insulin sensitivity was measured by hyperinsulinemic-euglycemic clamp. Liver TG, serum NEFA, and fat-derived adipokines were assessed. Insulin and lipogenesis signaling were assessed by western blots. Pre-emptive PEVF removal significantly decreases insulin-induced suppression of hepatic glucose production (HGP) both in RC and in HFD-fed rats. In accordance with the clamp results, hepatic TG accumulation is also significantly reduced by PEVF excision both in RC and HFD-fed rats. These results are further validated by insulin signaling results, which show that pre-emptive PEVF removal increases phosphorylation of hepatic Akt, irrespective of diet. Notably, high levels of serum leptin induced by HFD are significantly reduced by pre-emptive PEVF excision. Additionally, expression of lipogenic enzyme p-acetyl-CoA-carboxylase, denoting reduced lipogenesis, is increased in the PEVF-HFD rats. In conclusion, PEVF has a deleterious effect on the liver as a source of insulin resistance-inducing adipokines irrespective of diet, and does not serve as a buffer for excess nutrients.

摘要

本研究旨在探讨短期过量营养物质是否通过捕获营养衍生的非酯化游离脂肪酸(NEFA),或者通过脂联素分泌对肝甘油三酯(TGs)积累和胰岛素抵抗产生有害影响,从而保护肾脏周围和附睾内脏脂肪(PEVF)库。年轻大鼠预先接受手术 PEVF 切除或假手术,并分别用高脂肪饮食(HFD)(PEVF-HFD)或常规饮食(RC)(PEVF-RC)喂养 3 天。通过高胰岛素-正常血糖钳夹法测量胰岛素敏感性。评估肝 TG、血清 NEFA 和脂肪衍生的脂联素。通过 Western blot 评估胰岛素和脂肪生成信号。预先切除 PEVF 可显著降低 RC 和 HFD 喂养大鼠胰岛素诱导的肝葡萄糖生成(HGP)抑制。与钳夹结果一致,预先切除 PEVF 还可显著减少 RC 和 HFD 喂养大鼠的肝 TG 积累。这些结果通过胰岛素信号结果进一步得到验证,结果显示,无论饮食如何,预先切除 PEVF 均可增加肝 Akt 的磷酸化。值得注意的是,HFD 诱导的血清瘦素水平显著降低。此外,PEVF-HFD 大鼠中表示脂肪生成减少的脂解酶 p-乙酰辅酶 A-羧化酶的表达增加。总之,PEVF 作为诱导胰岛素抵抗的脂联素的来源,对肝脏具有有害影响,而不是作为多余营养物质的缓冲器。

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