Activation of somatostatin receptor subtype 2 inhibits insulin secretion in the isolated perfused human pancreas

被引:18
作者
Brunicardi, FC
Atiya, A
Moldovan, S
Lee, TC
Fagan, SP
Kleinman, RM
Adrian, TE
Coy, DH
Walsh, JH
Fisher, WE
机构
[1] Baylor Coll Med, Dept Surg, Houston, TX 77030 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Surg & Med, Los Angeles, CA USA
[3] Creighton Univ, Sch Med, Dept Biomed Sci, Omaha, NE 68178 USA
[4] Tulane Univ, Sch Med, Peptide Res Labs, New Orleans, LA 70112 USA
关键词
somatostatin; somatostatin receptor; islet physiology;
D O I
10.1097/00006676-200311000-00019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Five distinct somatostatin receptors (SSTRs) have been cloned, characterized, and designated SSTRs 1 - 5. The role of these receptors in B-cell signaling has not been well characterized. Methods: In the current study, the isolated perfused human pancreas model was used to determine the specific effect of 4 different somatostatin receptor agonists on insulin secretion. Conclusion: We demonstrated that the SSTR 2 agonist and octreotide significantly suppressed insulin secretion. Furthermore, even during the immunoneutralization of endogenous intrapancreatic somatostatin, the SSTR 2 agonist was able to reverse the effect of somatostatin immunoneutralization by suppressing insulin secretion. These results demonstrate that activation of SSTR 2 suppresses insulin secretion in the isolated perfused human pancreas.
引用
收藏
页码:E84 / E89
页数:6
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