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Inhibitory Effect of Relaxin-3 on Insulin Secretion in Isolated Pancreas and Insulinoma
被引:2
作者:
Yamamoto, Hiroyuki
[1
]
Arai, Takeo
[1
]
Tasaka, Ryota
[1
]
Mori, Yasunori
[1
]
Iguchi, Kazuaki
[1
]
Unno, Keiko
[1
]
Hoshino, Minoru
[1
]
机构:
[1] Univ Shizuoka, Sch Pharmaceut Sci, Bioorgan Chem Lab, Shizuoka 4228526, Japan
关键词:
relaxin-3;
G-protein-coupled receptor (GPCR)135;
insulin;
RECEPTORS;
IDENTIFICATION;
EXPRESSION;
LIGAND;
SOMATOSTATIN;
MECHANISM;
GENE;
LGR7;
D O I:
10.1248/jhs.55.132
中图分类号:
R99 [毒物学(毒理学)];
学科分类号:
100405 ;
摘要:
Relaxin-3 is a recently discovered member of the insulin superfamily and is a ligand for three orphan G-protein-coupled receptors: GPCR135, GPCR142 and LGR7 (leucine-rich repeat-containing G-protein-coupled receptor 7). GPCR135 mRNA is expressed in the pancreas, however, it is not known, whether the peptide affects pancreatic islet function. Reverse transcriptase (RT)-PCR and radioreceptor assay have shown that the relaxin-3 receptor (GPCR135) is expressed in pancreatic islets and rat insulinoma, but LGR7 is not expressed. Moreover, relaxin-3 has been revealed to inhibit the secretion of insulin from pancreatic islets. However, we can not detect relaxin-3 in small intestine and pancreas. These results suggest a novel role of relaxin-3 in the regulation of insulin release.
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页码:132 / 137
页数:6
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