Key result
COMP-Ang-1 improved glucose metabolism in a tissue-specific manner by regulating HIF-1α transcriptional genes of GLUT-1 expression in db/db mice.
Why the study?
Although COMP-Ang-1 has shown therapeutic potential in hyperglycemia, the mechanisms underlying its antidiabetic effect were completely unknown.
Does COMP-Ang-1 improve glucose metabolism in a diabetic db/db mouse model?
Does COMP-Ang-1 improve glucose metabolism in a diabetic db/db mouse model?
COMP-Ang-1 improves glucose metabolism in a diabetic mouse model by regulating HIF-1α and GLUT-1 expression, highlighting its potential molecular mechanism for treating diabetes.
Supports further preclinical studies of COMP-Ang-1; leaves open clinical translation in diabetes.
Cartilage oligomeric matrix protein (COMP)-Angiopoietin-1 is a potent angiopoietin-1 (Ang-1) variant that possesses therapeutic potential in angiogenesis and vascular endothelial dysfunction. Noteworthy, we have shown that COMP-Ang-1 improves hyperglycemia and neuroregeneration in ob/ob mice. However, the mechanism of the antidiabetic effect of COMP-Ang-1 is completely unknown. Therefore, we elucidated the diabetes protective molecular mechanisms of COMP-Ang-1 in diabetic db/db mouse model. COMP-Ang-1 (0.5 ng/g body weight) or aqueous NaCl solution was injected intraperitoneally per day in 21 consecutive days into 3-month old, male db/db mice (n=10 per group). Blood glucose and HbA1c levels were determined at baseline and 21 days after COMP-Ang-1 or NaCl treatment. The effect of COMP-Ang-1 on glucose uptake was investigated by euglycemic-hyperinsulinemic clamp studies and key genes of glucose metabolism were studied by Western blot analysis. Our findings indicate that COMP-Ang-1 improves glucose metabolism in a tissue specific manner by regulating HIF-1α transcriptional genes of GLUT-1 expression.
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Baum et al. (2020) studied Type 2 Diabetes (n=20). COMP-Ang-1 vs. aqueous NaCl solution was evaluated on Glucose metabolism and uptake. COMP-Ang-1 improved glucose metabolism in a tissue-specific manner by regulating HIF-1α transcriptional genes of GLUT-1 expression in db/db mice.
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