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肥胖雄性小鼠骨骼肌毛细血管内皮胰岛素转运受损。

Transendothelial Insulin Transport is Impaired in Skeletal Muscle Capillaries of Obese Male Mice.

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, USA.

Mouse Metabolic Phenotyping Center, Vanderbilt University, Nashville, Tennessee, USA.

出版信息

Obesity (Silver Spring). 2020 Feb;28(2):303-314. doi: 10.1002/oby.22683. Epub 2020 Jan 5.

Abstract

OBJECTIVE

The continuous endothelium of skeletal muscle (SkM) capillaries regulates insulin's access to skeletal myocytes. Whether impaired transendothelial insulin transport (EIT) contributes to SkM insulin resistance (IR), however, is unknown.

METHODS

Male and female C57/Bl6 mice were fed either chow or a high-fat diet for 16 weeks. Intravital microscopy was used to measure EIT in SkM capillaries, electron microscopy to assess endothelial ultrastructure, and glucose tracers to measure indices of glucose metabolism.

RESULTS

Diet-induced obesity (DIO) male mice were found to have a ~15% reduction in EIT compared with lean mice. Impaired EIT was associated with a 45% reduction in endothelial vesicles. Despite impaired EIT, hyperinsulinemia sustained delivery of insulin to the interstitial space in DIO male mice. Even with sustained interstitial insulin delivery, DIO male mice still showed SkM IR indicating severe myocellular IR in this model. Interestingly, there was no difference in EIT, endothelial ultrastructure, or SkM insulin sensitivity between lean female mice and female mice fed a high-fat diet.

CONCLUSIONS

These results suggest that, in male mice, obesity results in ultrastructural alterations to the capillary endothelium that delay EIT. Nonetheless, the myocyte appears to exceed the endothelium as a contributor to SkM IR in DIO male mice.

摘要

目的

骨骼肌(SkM)毛细血管的连续内皮调节胰岛素进入骨骼肌细胞的途径。然而,内皮细胞间胰岛素转运(EIT)受损是否导致 SkM 胰岛素抵抗(IR)尚不清楚。

方法

雄性和雌性 C57/Bl6 小鼠分别用普通饲料或高脂肪饮食喂养 16 周。使用活体显微镜测量 SkM 毛细血管中的 EIT,电子显微镜评估内皮超微结构,葡萄糖示踪剂测量葡萄糖代谢指标。

结果

与瘦鼠相比,饮食诱导肥胖(DIO)雄性小鼠的 EIT 降低了约 15%。受损的 EIT 与内皮小泡减少 45%有关。尽管 EIT 受损,高胰岛素血症仍能将胰岛素持续输送到 DIO 雄性小鼠的细胞间隙。即使在持续的细胞间胰岛素输送的情况下,DIO 雄性小鼠仍然表现出 SkM IR,表明该模型中存在严重的肌细胞 IR。有趣的是,瘦鼠和高脂肪饮食喂养的雌性小鼠之间的 EIT、内皮超微结构或 SkM 胰岛素敏感性没有差异。

结论

这些结果表明,在雄性小鼠中,肥胖导致毛细血管内皮的超微结构改变,从而延迟 EIT。尽管如此,在 DIO 雄性小鼠中,肌细胞似乎超过了内皮细胞,成为 SkM IR 的主要贡献者。

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