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首页> 外文期刊>American Journal of Physiology >Regulation of fundic and antral somatostatin secretion by CCK and gastrin.
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Regulation of fundic and antral somatostatin secretion by CCK and gastrin.

机译:CCK和胃泌素调节胃底和肛门生长抑素的分泌。

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摘要

CCK and gastrin stimulate somatostatin (SOM) secretion and thus modulate their direct effects on the parietal cell. Although SOM is stored in D cells of the fundus and antrum, the nature of the cell type differs, and it is not known whether both regions respond to the stimulatory effects of CCK and gastrin. The objectives of the present study were to determine the separate effects of CCK and gastrin on fundic and antral SOM secretion and to assess the type of receptor involved, using CCK-A (L-364,718) and CCK-B/gastrin (L-365,260) receptor antagonists. Changes in SOM were measured in plasma collected from cannulas draining blood from the fundus (gastric vein) and antrum (gastroepiploic vein) in anesthetized sheep. Both CCK and gastrin significantly stimulated SOM from the fundus and antrum. Sulfated CCK-8 (CCK-8S) increased SOM secretion from the fundus and antrum through interaction with both type A and B receptors. In contrast to CCK-8S, sulfated gastrin-17 (G-17S) stimulated SOM from the fundus via the type B receptor alone, whereas in the antrum G-17S stimulated SOM secretion independent of the A and B receptors. Histamine mediated, at least in part, the SOM-stimulatory effects; an H2-receptor antagonist blocked CCK-stimulated SOM secretion in both the fundus and antrum and reduced gastrin-stimulated SOM secretion in the fundus. The present study demonstrates regionally distinct regulatory mechanisms for gastric SOM secretion by CCK and gastrin.
机译:CCK和胃泌素刺激生长抑素(SOM)分泌,从而调节它们对顶细胞的直接作用。尽管SOM存储在眼底和胃窦的D细胞中,但细胞类型的性质不同,尚不清楚两个区域是否都对CCK和胃泌素的刺激作用作出反应。本研究的目的是使用CCK-A(L-364,718)和CCK-B /胃泌素(L-365,260)确定CCK和胃泌素对胃底和胃窦SOM分泌的单独作用并评估所涉及的受体的类型)受体拮抗剂。测量从麻醉绵羊的眼底(胃静脉)和胃窦(胃上静脉)引流的插管中收集的血浆中SOM的变化。 CCK和胃泌素均显着刺激眼底和胃窦的SOM。硫酸化的CCK-8(CCK-8S)通过与A型和B型受体的相互作用而增加了眼底和胃窦的SOM分泌。与CCK-8S相反,硫酸化胃泌素17(G-17S)仅通过B型受体刺激了眼底的SOM,而在胃窦中,G-17S刺激了独立于A和B受体的SOM分泌。组胺至少部分介导了SOM的刺激作用; H2受体拮抗剂可阻断CCK刺激的眼底和胃窦SOM分泌,并降低胃泌素刺激的眼底SOM分泌。本研究表明CCK和胃泌素胃SOM分泌的区域不同的调节机制。

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