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神经抑素通过直接作用于胰腺α细胞来抑制葡萄糖刺激的胰岛素分泌。

Neuronostatin inhibits glucose-stimulated insulin secretion via direct action on the pancreatic α-cell.

作者信息

Salvatori Alison S, Elrick Mollisa M, Samson Willis K, Corbett John A, Yosten Gina L C

机构信息

Department of Pharmacological and Physiological Science, Saint Louis University School of Medicine, St. Louis, Missouri; and.

Department of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

Am J Physiol Endocrinol Metab. 2014 Jun 1;306(11):E1257-63. doi: 10.1152/ajpendo.00599.2013. Epub 2014 Apr 15.

Abstract

Neuronostatin is a recently described peptide hormone encoded by the somatostatin gene. We previously showed that intraperitoneal injection of neuronostatin into mice resulted in c-Jun accumulation in pancreatic islets in a pattern consistent with the activation of glucagon-producing α-cells. We therefore hypothesized that neuronostatin could influence glucose homeostasis via a direct effect on the α-cell. Neuronostatin enhanced low-glucose-induced glucagon release in isolated rat islets and in the immortalized α-cell line αTC1-9. Furthermore, incubation with neuronostatin led to an increase in transcription of glucagon mRNA, as determined by RT-PCR. Neuronostatin also inhibited glucose-stimulated insulin secretion from isolated islets. However, neuronostatin did not alter insulin release from the β-cell line INS 832/13, indicating that the effect of neuronostatin on insulin secretion may be secondary to a direct action on the α-cell. In agreement with our in vitro data, intra-arterial infusion of neuronostatin in male rats delayed glucose disposal and inhibited insulin release during a glucose challenge. These studies suggest that neuronostatin participates in maintaining glucose homeostasis through cell-cell interactions between α-cells and β-cells in the endocrine pancreas, leading to attenuation in insulin secretion.

摘要

神经抑素是一种最近发现的由生长抑素基因编码的肽类激素。我们之前的研究表明,向小鼠腹腔注射神经抑素会导致胰岛中c-Jun的积累,其模式与产生胰高血糖素的α细胞的激活一致。因此,我们推测神经抑素可能通过对α细胞的直接作用来影响葡萄糖稳态。神经抑素增强了分离的大鼠胰岛和永生化α细胞系αTC1-9中低葡萄糖诱导的胰高血糖素释放。此外,通过逆转录聚合酶链反应(RT-PCR)测定,与神经抑素孵育导致胰高血糖素mRNA转录增加。神经抑素还抑制了分离胰岛中葡萄糖刺激的胰岛素分泌。然而,神经抑素并未改变β细胞系INS 832/13的胰岛素释放,这表明神经抑素对胰岛素分泌的影响可能继发于对α细胞的直接作用。与我们的体外数据一致,在雄性大鼠中动脉内输注神经抑素会延迟葡萄糖的清除,并在葡萄糖激发试验期间抑制胰岛素释放。这些研究表明,神经抑素通过内分泌胰腺中α细胞和β细胞之间的细胞间相互作用参与维持葡萄糖稳态,从而导致胰岛素分泌减少。

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