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Islet Studies

Succinate Is a Preferential Metabolic Stimulus-Coupling Signal for Glucose-Induced Proinsulin Biosynthesis Translation

  1. Cristina Alarcon1,
  2. Barton Wicksteed1,
  3. Marc Prentki2,
  4. Barbara E. Corkey3 and
  5. Christopher J. Rhodes1
  1. 1Pacific Northwest Research Institute, Seattle, Washington
  2. 2Molecular Nutrition Unit, University of Montreal, Montreal, Canada
  3. 3Diabetes and Metabolism Unit, Boston University Medical School, Boston, Massachusetts
    Diabetes 2002 Aug; 51(8): 2496-2504. https://doi.org/10.2337/diabetes.51.8.2496
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    Abstract

    The secondary signals emanating from increased glucose metabolism, which lead to specific increases in proinsulin biosynthesis translation, remain elusive. It is known that signals for glucose-stimulated insulin secretion and proinsulin biosynthesis diverge downstream of glycolysis. Consequently, the mitochondrial products ATP, Krebs cycle intermediates, glutamate, and acetoacetate were investigated as candidate stimulus-coupling signals specific for glucose-induced proinsulin biosynthesis in rat islets. Decreasing ATP levels by oxidative phosphorylation inhibitors showed comparable effects on proinsulin biosynthesis and total protein synthesis. Although it is a cofactor, ATP is unlikely to be a metabolic stimulus-coupling signal specific for glucose-induced proinsulin biosynthesis. Neither glutamic acid methyl ester nor acetoacetic acid methyl ester showed a specific effect on glucose-stimulated proinsulin biosynthesis. Interestingly, among Krebs cycle intermediates, only succinic acid monomethyl ester specifically stimulated proinsulin biosynthesis. Malonic acid methyl ester, an inhibitor of succinate dehydrogenase, also specifically increased glucose-induced proinsulin biosynthesis without affecting islet ATP levels or insulin secretion. Glucose caused a 40% increase in islet intracellular succinate levels, but malonic acid methyl ester showed no further effect, probably due to efficient conversion of succinate to succinyl-CoA. In this regard, a GTP-dependent succinyl-CoA synthetase activity was found in cytosolic fractions of pancreatic islets. Thus, succinate and/or succinyl-CoA appear to be preferential metabolic stimulus-coupling factors for glucose-induced proinsulin biosynthesis translation.

    Footnotes

    • Address correspondence and reprint requests to Christopher J. Rhodes, Pacific Northwest Research Institute, 720 Broadway, Seattle, WA 98122. E-mail: cjr{at}pnri.org.

      Received for publication 3 August 2001 and accepted in revised form 24 April 2002.

      DNP, dinitrophenol; GDH, glutamate dehydrogenase; HPLC, high-performance liquid chromatography; IC50, half-maximal inhibitory concentration; KATP-channel, ATP-sensitive K+ channel; KRBH, Krebs-Ringer bicarbonate buffer with HEPES; LDH, lactate dehydrogenase; SCS, succinyl-CoA synthetase; TCA, trichloroacetic acid.

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    Succinate Is a Preferential Metabolic Stimulus-Coupling Signal for Glucose-Induced Proinsulin Biosynthesis Translation
    Cristina Alarcon, Barton Wicksteed, Marc Prentki, Barbara E. Corkey, Christopher J. Rhodes
    Diabetes Aug 2002, 51 (8) 2496-2504; DOI: 10.2337/diabetes.51.8.2496

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    Succinate Is a Preferential Metabolic Stimulus-Coupling Signal for Glucose-Induced Proinsulin Biosynthesis Translation
    Cristina Alarcon, Barton Wicksteed, Marc Prentki, Barbara E. Corkey, Christopher J. Rhodes
    Diabetes Aug 2002, 51 (8) 2496-2504; DOI: 10.2337/diabetes.51.8.2496
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    • Acyl-Ghrelin Influences Pancreatic β-Cell Function by Interference with KATP Channels
    • Pancreatic β-Cell–Specific Deletion of VPS41 Causes Diabetes Due to Defects in Insulin Secretion
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