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

Authors :
Williams IM
McClatchey PM
Bracy DP
Bonner JS
Valenzuela FA
Wasserman DH
Source :
Obesity (Silver Spring, Md.) [Obesity (Silver Spring)] 2020 Feb; Vol. 28 (2), pp. 303-314. Date of Electronic Publication: 2020 Jan 05.
Publication Year :
2020

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.<br />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.<br />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.<br />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.<br /> (© 2020 The Authors. Obesity published by Wiley Periodicals, Inc. on behalf of The Obesity Society (TOS).)

Details

Language :
English
ISSN :
1930-739X
Volume :
28
Issue :
2
Database :
MEDLINE
Journal :
Obesity (Silver Spring, Md.)
Publication Type :
Academic Journal
Accession number :
31903723
Full Text :
https://doi.org/10.1002/oby.22683