Insulin Infusion Is Linked to Increased NPPC Expression in Muscle and Plasma C-type Natriuretic Peptide in Male Dogs

Author:

Gregory Justin M1ORCID,Kraft Guillaume2ORCID,Farmer Ben2,Smith Marta S2,LaNeve David C3,Williams Phillip E3,Tomasek Kelsey4,Su Yan Ru4,Wilson Christopher S1ORCID,Thompson Mark D5,Cherrington Alan D2ORCID,Coate Katie C6ORCID

Affiliation:

1. Ian M. Burr Division of Pediatric Endocrinology and Diabetes, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

2. Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

3. Section of Surgical Sciences, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

4. Division of Cardiovascular Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

5. MedGenome, Inc., Foster City, CA 94404, USA

6. Division of Diabetes, Endocrinology, & Metabolism, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

Abstract

Abstract The purpose of this study was to assess insulin-stimulated gene expression in canine skeletal muscle with a particular focus on NPPC, the gene that encodes C-type natriuretic peptide, a key hormonal regulator of cardiometabolic function. Four conscious canines underwent hyperinsulinemic, euglycemic clamp studies. Skeletal muscle biopsy and arterial plasma samples were collected under basal and insulin-stimulated conditions. Bulk RNA sequencing of muscle tissue was performed to identify differentially expressed genes between these 2 steady-state conditions. Our results showed that NPPC was the most highly expressed gene in skeletal muscle in response to insulin infusion, rising 4-fold between basal and insulin-stimulated conditions. In support of our RNA sequencing data, we found that raising the plasma insulin concentration 15-fold above basal elicited a 2-fold (P = 0.0001) increase in arterial plasma concentrations of N-terminal prohormone C-type natriuretic peptide. Our data suggest that insulin may play a role in stimulating secretion of C-type natriuretic peptide by skeletal muscle. In this context, C-type natriuretic peptide may act in a paracrine manner to facilitate muscle–vascular bed crosstalk and potentiate insulin-mediated vasodilation. This could serve to enhance insulin and glucose delivery, particularly in the postprandial absorptive state.

Funder

Ms. Rob Pierce and the Appleby Foundation

Vanderbilt University Faculty Research Scholars Program

National Institute of Diabetes and Digestive and Kidney Diseases

National Institutes of Health

JDRF Career Development Award

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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