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Glucagon-Iike peptide I receptor plays a critical role in geniposide-regulated insulin secretion in INS-1 cells
by
Li-xia GUO Zhi-ning XlA Xue GAO Fei YIN Jian-hui LIU
in
RNA干扰
/ 受体
/ 栀子苷
/ 细胞调节
/ 肽
/ 胰岛素分泌
/ 胰高血糖素
/ 酶联免疫吸附试验
2012
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Glucagon-Iike peptide I receptor plays a critical role in geniposide-regulated insulin secretion in INS-1 cells
by
Li-xia GUO Zhi-ning XlA Xue GAO Fei YIN Jian-hui LIU
in
RNA干扰
/ 受体
/ 栀子苷
/ 细胞调节
/ 肽
/ 胰岛素分泌
/ 胰高血糖素
/ 酶联免疫吸附试验
2012
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Glucagon-Iike peptide I receptor plays a critical role in geniposide-regulated insulin secretion in INS-1 cells
Journal Article
Glucagon-Iike peptide I receptor plays a critical role in geniposide-regulated insulin secretion in INS-1 cells
2012
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Overview
Aim: To explore the role of the glucagon-like peptide 1 receptor (GLP-1R) in geniposide regulated insulin secretion in rat INS-1 insulinoma cells.
Methods: Rat INS-1 insulinoma cells were cultured. The content of insulin in the culture medium was measured with ELISA assay. GLP-1R gene in INS-1 cells was knocked down with shRNA interference. The level of GLP-1R protein in INS-1 cells was measured with Western blotting.
Results: Geniposide (0.01-100 pmol/L) increased insulin secretion from INS-1 cells in a concentration-dependent manner. Geniposide (10 pmol/L) enhanced acute insulin secretion in response to both the low (5.5 mmol/L) and moderately high levels (11 mmol/L) of glucose. Blockade of GLP-1R with the GLP-1R antagonist exendin (9-39) (200 nmol/L) or knook-down of GLP-1R with shRNA interfer- ence in INS-1 cells decreased the effect of geniposide (10 IJmol/L) on insulin secretion stimulated by glucose (5.5 mmol/L).
Conclusion: Geniposide increases insulin secretion through glucagon-like peptide 1 receptors in rat INS-1 insulinoma cells.
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