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生长激素对脂肪组织的急性作用与抑制抗脂肪分解信号有关。

The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals.

机构信息

Medical Research Laboratory, Department of Clinical Medicine, Health, Aarhus University, Aarhus, Denmark.

Department of Endocrinology, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Physiol Rep. 2020 Feb;8(3):e14373. doi: 10.14814/phy2.14373.

Abstract

AIM

Since GH stimulates lipolysis in vivo after a 2-hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT).

METHODS

Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene array, and protein in AT biopsies after 30-120 min. Human data were corroborated in adipose-specific GH receptor knockout (FaGHRKO) mice versus wild-type mice. Expression of candidate genes identified in the array were investigated in 3T3-L1 adipocytes.

RESULTS

GH increased serum FFA and AT phosphorylation of STAT5b in human subjects. This was replicated in wild-type mice, but not in FaGHRKO mice. The array identified 53 GH-regulated genes, and Ingenuity Pathway analysis showed downregulation of PDE3b, an insulin-dependent antilipolytic signal, upregulation of PTEN that inhibits insulin-dependent antilipolysis, and downregulation of G0S2 and RASD1, both encoding antilipolytic proteins. This was confirmed in 3T3-L1 adipocytes, except for PDE3B, including reciprocal effects of GH and insulin on mRNA expression of PTEN, RASD1, and G0S2.

CONCLUSION

(a) GH directly stimulates AT lipolysis in a GHR-dependent manner, (b) this involves suppression of antilipolytic signals at the level of gene expression, (c) the underlying GH signaling pathways remain to be defined.

摘要

目的

由于 GH 在经历 2 小时的滞后阶段后会在体内刺激脂肪分解,我们研究了这是否涉及脂肪组织 (AT) 中的 GH 信号转导和基因表达。

方法

9 名受试者每人接受静脉内 GH 暴露与盐水暴露,在 30-120 分钟后测量血清 FFA 以及 AT 活检中的 GH 信号转导、基因阵列和蛋白质。人类数据在脂肪特异性 GH 受体敲除 (FaGHRKO) 小鼠与野生型小鼠中得到证实。在 3T3-L1 脂肪细胞中研究了阵列中鉴定出的候选基因的表达。

结果

GH 增加了人体血清 FFA 和 AT 中 STAT5b 的磷酸化。这在野生型小鼠中得到了复制,但在 FaGHRKO 小鼠中没有。该阵列鉴定出 53 个 GH 调节基因,Ingenuity 通路分析显示 PDE3b 的下调,PDE3b 是一种依赖胰岛素的抗脂肪分解信号,PTEN 的上调抑制依赖胰岛素的抗脂肪分解,以及 G0S2 和 RASD1 的下调,两者均编码抗脂肪分解蛋白。这在 3T3-L1 脂肪细胞中得到了证实,除了 PDE3B 之外,还包括 GH 和胰岛素对 PTEN、RASD1 和 G0S2 mRNA 表达的相互作用。

结论

(a) GH 以 GHR 依赖的方式直接刺激 AT 脂肪分解,(b) 这涉及基因表达水平上抗脂肪分解信号的抑制,(c) 潜在的 GH 信号通路仍有待确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b216/7029434/04c5b99d6660/PHY2-8-e14373-g001.jpg

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