Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10751615 | Biochemical and Biophysical Research Communications | 2015 | 7 Pages |
Abstract
Type 2 Diabetes is closely associated with our daily diets and has become a global health problem with an increasing number of patients. Recent observational and randomized studies on vitamin D3 suggested that higher plasma 25-hydroxyvitamin D3 [25(OH)D3] concentrations and more vitamin D3 intake are associated with lower risk of type 2 diabetes, which is characterized by postprandial hyperglycemia due to inappropriate glucose stimulated insulin secretion (GSIS) and its age-dependent increase of onset. However, rapid action of dietary vitamin D3 on the postprandial glucose profile has not been analyzed. When vitamin D3 is orally ingested in mice aged 12-14 weeks during an oral glucose tolerance test (OGTT), the serum glucose profile was not changed. In contrast, when OGTT was performed with old mice aged 30-34 weeks, the glucose profile was dramatically improved with increased insulin secretion, suggesting that orally ingested vitamin D3 potentiated GSIS in aged mice. Interestingly, there was also a significant increase in plasma GLP-1 in these aged mice. Our results suggest that orally ingested dietary vitamin D3 in aged mice improves glucose metabolism as a GLP-1 enhancer.
Keywords
RT-PCRGSISVDROGTTGIPGLP-11,25(OH)2D325(OH)D325-hydroxyvitamin D3[Ca2+]iOral glucose tolerance testInsulin secretionintracellular Ca2+ concentrationPostprandial hyperglycemiareverse transcription-polymerase chain reactionVitamin D3gastric inhibitory polypeptideglucagon like peptide-1Glucose stimulated insulin secretionvitamin D3 receptor
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Authors
Patricio L.M. Enciso, Lixiang Wang, Yuta Kawahara, Shohei Sakamoto, Shingo Shimada, Yukina Takeichi, Ryoichi Takayanagi, Masatoshi Nomura,