Independent Regulation of In Vivo Insulin Action on Glucose Versus K+ Uptake by Dietary Fat and K+ Content

  1. Cheol S. Choi,
  2. Felix N. Lee,
  3. Alicia A. McDonough and
  4. Jang H. Youn
  1. From the Department of Physiology and Biophysics, University of Southern California Keck School of Medicine, Los Angeles, California

    Abstract

    Insulin stimulates both glucose and K+ uptake, and high-fat feeding is known to decrease insulin-stimulated glucose uptake. The purpose of this study was to examine whether insulin’s actions on glucose and K+ uptake are similarly decreased by a high-fat diet. Wistar rats were fed a standard control (12.2% fat; n = 6) or high-fat (66.5% fat; n = 13) diet for 15 days. Because K+ content was 1% in the control and 0.5% in the high-fat diet and because the rats ate less of the high-fat diet, we also compared the high-fat diet with 0.5% K+ (HFD; n = 7) to a high-fat diet supplemented with 1.5% K+ (HFD+K; n = 6). K+ intake was matched between the control and HFD+K groups (246 ± 8 vs. 224 ± 2 mg/day), but was lower in the HFD group (78 ± 10 mg/day; P < 0.05). Insulin-stimulated glucose and K+ uptake were determined by hyperinsulinemic (5 mU · kg−1 · min−1) glucose and K+ clamps. The HFD depressed both insulin-stimulated glucose uptake compared to the control (133 ± 5 vs. 166 ± 7 μmol · kg−1 · min−1; P < 0.05) and K+ uptake (5.5 ± 0.9 vs. 8.9 ± 1.0 μmol · kg−1 · min−1; P < 0.05) compared to the control. However, insulin-stimulated K+ uptake was unchanged in the HFD+K versus in the control group (10.0 ± 0.6 vs. 8.9 ± 1.0 μmol · kg−1 · min−1; P > 0.05), whereas insulin-stimulated glucose uptake in the HFD+K group was decreased to a rate (137 ± 9 μmol · kg−1 · min−1), similar to that of the HFD group. We concluded that the decrease in insulin-stimulated K+ uptake during high-fat feeding was a result of decreased K+ intake, and that insulin’s actions on glucose uptake and K+ uptake are independently regulated by dietary fat and K+ content, respectively.

    Footnotes

    • Address correspondence and reprint requests to Jang H. Youn, Ph.D., Diabetes Research Center, Department of Physiology and Biophysics, USC Keck School of Medicine, 1333 San Pablo St., MMR 626, Los Angeles, CA 90089-9142. E-mail: youn{at}usc.edu.

      Received for publication 11 October 2001 and accepted in revised form 8 January 2002.

      C.S.C. is currently affiliated with the Endocrinology Department, Hallym University Medical School, Anyang City, Kyonggi-do, Korea.

      FFA, free fatty acid; GINF, glucose infusion rate; KINF, K+ infusion rate; PI, phosphatidylinositol.

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