4.7 Article

Glucose metabolism in vivo in four commonly used inbred mouse strains

Journal

DIABETES
Volume 57, Issue 7, Pages 1790-1799

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/db07-1615

Keywords

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Funding

  1. NIDDK NIH HHS [R21 DK066636, DK-59637, R01 DK054902, R01 DK050277, P60 DK020593, DK-50277, DK-68764, U24 DK059637, R37 DK050277, P30 DK020593, R21 DK063439, DK-20593, R01 DK068764, DK-69603, U01 DK089572, DK-54902, DK-63439, R01 DK069603, DK-66636, R56 DK054902, R33 DK066636] Funding Source: Medline
  2. BLRD VA [I01 BX000666] Funding Source: Medline

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OBJECTIVE-To characterize differences in whole-body glucose metabolism between commonly used inbred mouse strains. RESEARCH DESIGN AND METHODS-Hyperinsulinemic-euglycemic (similar to 8.5 mmol/l) and -hypoglycemic (similar to 3.0 mmol/l) clamps were done in catheterized, 5-h-fasted mice to assess insulin action and hypoglycemic counter-regulatory responsiveness. Hyperglycemic clamps (similar to 15 mmol/l) were done to assess insulin secretion and compared with results in perifused islets. RESULTS-Insulin action and hypoglycemic counter-regulatory and insulin secretory phenotypes varied considerably in four inbred mouse strains. In vivo insulin secretion was greatest in 129X1/Sv mice, but the counter-regulatory response to hypoglycemia was blunted. FVB/N mice in vivo showed no increase in glucose-stimulated insulin secretion, relative hepatic insulin resistance, and the highest counter-regulatory response to hypoglycemia. In DBA/2 mice, insulin action was lowest among the strains, and islets isolated had the greatest glucose-stimulated insulin secretion in vitro. In C57BL/6 mice, in vivo physiological responses to hyperinsulinemia at euglycemia, and hypoglycemia. were intermediate relative to other strains. Insulin secretion by C57BL/6 mice was similar to that in other strains in contrast to the blunted glucose-stimulated insulin secretion from isolated islets. CONCLUSIONS-Strain-dependent differences exist in four inbred mouse strains frequently used for genetic manipulation and study of glucose metabolism. These results are important for selecting inbred mice to study glucose metabolism and for interpreting and designing experiments.

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