Journal
DIABETOLOGIA
Volume 55, Issue 6, Pages 1813-1823Publisher
SPRINGER
DOI: 10.1007/s00125-012-2509-1
Keywords
Ghrelin; Glucose metabolism; Rapamycin
Categories
Funding
- National Natural Science Foundation of China [81030012, 81170795, 30971434, 30871194, 30890043, 30971085]
- Major National Basic Research Program of the People's Republic of China [2010CB912504]
- National Institute of Health [RO1DK043225]
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Rapamycin impairs glucose tolerance and insulin sensitivity. Our previous study demonstrated that rapamycin significantly increases the production of gastric ghrelin, which is critical in the regulation of glucose metabolism. Here, we investigated whether ghrelin contributes to derangements of glucose metabolism induced by rapamycin. The effects of rapamycin on glucose metabolism were examined in mice receiving ghrelin receptor antagonist or with gene knockout. Changes in GLUT4, c-Jun N-terminal kinase (JNK) and phosphorylated ribosomal protein S6 (pS6) were investigated by immunofluorescent staining or western blotting. Related hormones were detected by radioimmunoassay kits. Rapamycin impaired glucose metabolism and insulin sensitivity not only in normal C57BL/6J mice but also in both obese mice induced by a high fat diet and mice. This was accompanied by elevation of plasma acylated ghrelin. Rapamycin significantly increased the levels of plasma acylated ghrelin in normal C57BL/6J mice, high-fat-diet-induced obese mice and mice. Elevation in plasma acylated ghrelin and derangements of glucose metabolism upon administration of rapamycin were significantly correlated. The deterioration in glucose homeostasis induced by rapamycin was blocked by -Lys3-GHRP-6, a ghrelin receptor antagonist, or by deletion of the gene. Ghrelin receptor antagonism and knockout blocked the upregulation of JNK activity and downregulation of GLUT4 levels and translocation in the gastrocnemius muscle induced by rapamycin. The current study demonstrates that ghrelin contributes to derangements of glucose metabolism induced by rapamycin via altering the content and translocation of GLUT4 in muscles.
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