Insulin regulates its own delivery to skeletal muscle by feed-forward actions on the vasculature

被引:142
作者
Barrett, Eugene J. [1 ]
Wang, Hong [1 ]
Upchurch, Charles T. [1 ]
Liu, Zhenqi [1 ]
机构
[1] Univ Virginia, Dept Med, Sch Med, Charlottesville, VA 22908 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2011年 / 301卷 / 02期
基金
美国国家卫生研究院;
关键词
caveolae; endothelium; microvasculature; insulin transport; POSITRON-EMISSION-TOMOGRAPHY; ENDOTHELIUM-DEPENDENT VASODILATION; HUMAN FOREARM MUSCLE; I IGF-I; BLOOD-FLOW; NITRIC-OXIDE; CAPILLARY RECRUITMENT; GLUCOSE-UPTAKE; MICROVASCULAR RECRUITMENT; MIXED MEAL;
D O I
10.1152/ajpendo.00186.2011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Barrett EJ, Wang H, Upchurch CT, Liu Z. Insulin regulates its own delivery to skeletal muscle by feed-forward actions on the vasculature. Am J Physiol Endocrinol Metab 301: E252-E263, 2011. First published May 31, 2011; doi:10.1152/ajpendo.00186.2011.-Insulin, at physiological concentrations, regulates the volume of microvasculature perfused within skeletal and cardiac muscle. It can also, by relaxing the larger resistance vessels, increase total muscle blood flow. Both of these effects require endothelial cell nitric oxide generation and smooth muscle cell relaxation, and each could increase delivery of insulin and nutrients to muscle. The capillary microvasculature possesses the greatest endothelial surface area of the body. Yet, whether insulin acts on the capillary endothelial cell is not known. Here, we review insulin's actions at each of three levels of the arterial vasculature as well as recent data suggesting that insulin can regulate a vesicular transport system within the endothelial cell. This latter action, if it occurs at the capillary level, could enhance insulin delivery to muscle interstitium and thereby complement insulin's actions on arteriolar endothelium to increase insulin delivery. We also review work that suggests that this action of insulin on vesicle transport depends on endothelial cell nitric oxide generation and that insulin's ability to regulate this vesicular transport system is impaired by inflammatory cytokines that provoke insulin resistance.
引用
收藏
页码:E252 / E263
页数:12
相关论文
共 123 条
[31]   Hyperinsulinemia rapidly increases human muscle microvascular perfusion but fails to increase muscle insulin clearance - Evidence that a saturable process mediates muscle insulin uptake [J].
Eggleston, Emma M. ;
Jahn, Linda A. ;
Barrett, Eugene J. .
DIABETES, 2007, 56 (12) :2958-2963
[32]   Regulation of vascular function and insulin sensitivity by adipose tissue: Focus on perivascular adipose tissue [J].
Eringa, Etto C. ;
Bakker, Wineke ;
Smulders, Yvo M. ;
Serne, Erik H. ;
Yudkin, John S. ;
Stehouwer, Coen D. A. .
MICROCIRCULATION, 2007, 14 (4-5) :389-402
[33]   The neck of caveolae is a distinct plasma membrane subdomain that concentrates insulin receptors in 3T3-L1 adipocytes [J].
Foti, Michelangelo ;
Porcheron, Genevieve ;
Fournier, Margot ;
Maeder, Christine ;
Carpentier, Jean-Louis .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (04) :1242-1247
[34]   DELAYED-ONSET OF INSULIN ACTIVATION OF THE INSULIN-RECEPTOR KINASE IN-VIVO IN HUMAN SKELETAL-MUSCLE [J].
FREIDENBERG, GR ;
SUTER, S ;
HENRY, RR ;
NOLAN, J ;
REICHART, D ;
OLEFSKY, JM .
DIABETES, 1994, 43 (01) :118-126
[35]   INSULIN-LIKE GROWTH-FACTOR-I EXERTS GROWTH HORMONE-LIKE AND INSULIN-LIKE ACTIONS ON HUMAN MUSCLE PROTEIN-METABOLISM [J].
FRYBURG, DA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (02) :E331-E336
[36]   GROWTH-HORMONE STIMULATES SKELETAL-MUSCLE PROTEIN-SYNTHESIS AND ANTAGONIZES INSULINS ANTIPROTEOLYTIC ACTION IN HUMANS [J].
FRYBURG, DA ;
LOUARD, RJ ;
GEROW, KE ;
GELFAND, RA ;
BARRETT, EJ .
DIABETES, 1992, 41 (04) :424-429
[37]   INSULIN AND INSULIN-LIKE GROWTH-FACTOR-I ENHANCE HUMAN SKELETAL-MUSCLE PROTEIN ANABOLISM DURING HYPERAMINOACIDEMIA BY DIFFERENT MECHANISMS [J].
FRYBURG, DA ;
JAHN, LA ;
HILL, SA ;
OLIVERAS, DM ;
BARRETT, EJ .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (04) :1722-1729
[38]   Blood flow is an important determinant of forearm glucose uptake following a mixed meal [J].
Fugmann, A ;
Sarabi, M ;
Karlström, B ;
Berne, C ;
Lithell, H ;
Lind, L .
ACTA DIABETOLOGICA, 2003, 40 (03) :113-117
[39]   Direct measurements of the permeability surface area for insulin and glucose in human skeletal muscle [J].
Gudbjörnsdóttir, S ;
Sjöstrand, M ;
Strindberg, L ;
Wahren, J ;
Lönnroth, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (10) :4559-4564
[40]   Specific impairment of endothelium-dependent vasodilation in subjects with type 2 diabetes independent of obesity [J].
Hogikyan, RV ;
Galecki, AT ;
Pitt, B ;
Halter, JB ;
Greene, DA ;
Supiano, MA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (06) :1946-1952