Literature DB >> 15504953

Physiological hyperinsulinemia in dogs augments access of macromolecules to insulin-sensitive tissues.

Martin Ellmerer1, Stella P Kim, Marianthe Hamilton-Wessler, Katrin Hücking, Erlinda Kirkman, Richard N Bergman.   

Abstract

Pharmacological doses of insulin increase limb blood flow and enhance tissue recruitment for small solutes such as glucose. We investigated whether elevating insulin within the physiological range (68 +/- 6 vs. 425 +/- 27 pmol/l) can influence tissue recruitment of [(14)C]inulin, an inert diffusionary marker of molecular weight similar to that of insulin itself. During hyperinsulinemic-euglycemic clamps, transport parameters and distribution volumes of [(14)C]inulin were determined in conscious dogs by applying a three-compartment model to the plasma clearance data of intravenously injected [(14)C]inulin (0.8 microCi/kg). In a second set of experiments in anesthetized dogs with direct cannulation of the hindlimb skeletal muscle lymphatics, we measured a possible effect of physiological hyperinsulinemia on the response of the interstitial fluid of skeletal muscle to intravenously injected [(14)C]inulin and compared this response with the model prediction from plasma data. Physiological hyperinsulinemia caused a 48 +/- 10% (P < 0.005) and a 35 +/- 15% (P < 0.05) increase of peripheral and splanchnic interstitial distribution volumes for [(14)C]inulin. Hindlimb lymph measurements directly confirmed the ability of insulin to enhance the access of macromolecules to the peripheral interstitial fluid compartment. The present results show that physiological hyperinsulinemia will enhance the delivery of a substance of similar molecular size to insulin to previously less intensively perfused regions of insulin-sensitive tissues. Our data suggest that the delivery of insulin itself to insulin-sensitive tissues could be a mechanism of insulin action on cellular glucose uptake independent of and possibly synergistic with either enhanced blood flow distribution or GLUT4 transporter recruitment to enhance glucose utilization. Because of the differences between inulin and insulin itself, whether delivery of the bioactive hormone is increased remains speculative.

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Year:  2004        PMID: 15504953     DOI: 10.2337/diabetes.53.11.2741

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  6 in total

Review 1.  The barrier within: endothelial transport of hormones.

Authors:  Cathryn M Kolka; Richard N Bergman
Journal:  Physiology (Bethesda)       Date:  2012-08

2.  Modest hyperglycemia prevents interstitial dispersion of insulin in skeletal muscle.

Authors:  Cathryn M Kolka; Ana Valeria B Castro; Erlinda L Kirkman; Richard N Bergman
Journal:  Metabolism       Date:  2014-11-04       Impact factor: 8.694

Review 3.  Impaired microvascular perfusion: a consequence of vascular dysfunction and a potential cause of insulin resistance in muscle.

Authors:  Michael G Clark
Journal:  Am J Physiol Endocrinol Metab       Date:  2008-07-08       Impact factor: 4.310

Review 4.  The endothelium in diabetes: its role in insulin access and diabetic complications.

Authors:  Cathryn M Kolka; Richard N Bergman
Journal:  Rev Endocr Metab Disord       Date:  2013-03       Impact factor: 6.514

5.  Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion.

Authors:  Alexander H Turaihi; Erik M van Poelgeest; Victor W M van Hinsbergh; Erik H Serné; Yvo M Smulders; Etto C Eringa
Journal:  J Vis Exp       Date:  2017-03-20       Impact factor: 1.355

6.  Diet-induced obesity prevents interstitial dispersion of insulin in skeletal muscle.

Authors:  Cathryn M Kolka; L Nicole Harrison; Maya Lottati; Jenny D Chiu; Erlinda L Kirkman; Richard N Bergman
Journal:  Diabetes       Date:  2009-12-03       Impact factor: 9.461

  6 in total

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