High-fat diet-induced β-cell proliferation occurs prior to insulin resistance in C57Bl/6J male mice

Author:

Mosser Rockann E.12,Maulis Matthew F.12,Moullé Valentine S.3,Dunn Jennifer C.12,Carboneau Bethany A.4,Arasi Kavin2,Pappan Kirk5,Poitout Vincent36,Gannon Maureen1274

Affiliation:

1. Department of Veterans Affairs Tennessee Valley, Nashville, Tennessee;

2. Departments of 2Medicine,

3. Montreal Diabetes Research Center, Research Center of the University of Montreal Hospital Cente, and

4. Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee;

5. Metabolon, Inc., Durham, North Carolina

6. Department of Medicine, University of Montreal, Montreal, Quebec, Canada; and

7. Cell and Developmental Biology, and

Abstract

Both short- (1 wk) and long-term (2–12 mo) high-fat diet (HFD) studies reveal enhanced β-cell mass due to increased β-cell proliferation. β-Cell proliferation following HFD has been postulated to occur in response to insulin resistance; however, whether HFD can induce β-cell proliferation independent of insulin resistance has been controversial. To examine the kinetics of HFD-induced β-cell proliferation and its correlation with insulin resistance, we placed 8-wk-old male C57Bl/6J mice on HFD for different lengths of time and assayed the following: glucose tolerance, insulin secretion in response to glucose, insulin tolerance, β-cell mass, and β-cell proliferation. We found that β-cell proliferation was significantly increased after only 3 days of HFD feeding, weeks before an increase in β-cell mass or peripheral insulin resistance was detected. These results were confirmed by hyperinsulinemic euglycemic clamps and measurements of α-hydroxybutyrate, a plasma biomarker of insulin resistance in humans. An increase in expression of key islet-proliferative genes was found in isolated islets from 1-wk HFD-fed mice compared with chow diet (CD)-fed mice. These data indicate that short-term HFD feeding enhances β-cell proliferation before insulin resistance becomes apparent.

Funder

U.S. Department of Veterans Affairs (VA)

Juvenile Diabetes Research Foundation International (JDRF)

ADA/Takeda Mentor based postdoctoral fellowship

HHS | National Institutes of Health (NIH)

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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