Department of Physiology, Capital Medical University, Beijing, China.
Br J Pharmacol. 2010 Apr;159(8):1623-5. doi: 10.1111/j.1476-5381.2010.00653.x. Epub 2010 Mar 5.
5-Hydroxytryptamine (5-HT) is a key regulator of the gastrointestinal system and we have shown that submucosal neuronal 5-HT(3) receptors exerted a novel inhibitory effect on colonic ion transport. The aim of the present study was to investigate the precise mechanism(s) underlying this inhibitory effect.
Mucosa/submucosa or mucosa-only preparations from rat distal colon were mounted in Ussing chambers for measurement of short-circuit current (I(sc)) as an indicator of ion secretion. Somatostatin release was determined with radioimmunoassay. Intracellular cAMP content was measured with enzyme-linked immunoadsorbent assay (elisa). Immunohistochemical techniques were used to study the expression of 5-HT(3) receptors, somatostatin and somatostatin receptors in colonic tissue.
In rat distal colonic mucosa/submucosa preparations, pretreatment with 5-HT(3) receptor antagonists enhanced 5-HT-induced increases in I(sc). However, in mucosa-only preparations without retained neural elements, pretreatment with 5-HT(3) receptor antagonists inhibited 5-HT-induced DeltaI(sc). Pretreatment with a somatostatin-2 (sst(2)) receptor antagonist in mucosa/submucosa preparations augmented 5-HT-induced DeltaI(sc). Combination of sst(2) and 5-HT(3) receptor antagonists did not cause further enhancement of 5-HT-induced DeltaI(sc). Moreover, both sst(2) and 5-HT(3) receptor antagonists enhanced 5-HT-induced increase in intracellular cAMP concentration in the mucosa/submucosa preparations. 5-HT released somatostatin from rat colonic mucosa/submucosa preparations, an effect prevented by pretreatment with 5-HT(3) receptor antagonists. Immunohistochemical staining demonstrated the presence of 5-HT(3) receptors on submucosal somatostatin neurons and of sst(2) receptors on colonic mucosa.
Activation of neuronal 5-HT(3) receptors in the submucosal plexus of rat colon suppressed 5-HT-induced ion secretion by releasing somatostatin from submucosal neurons.
5-羟色胺(5-HT)是胃肠道的关键调节因子,我们已经表明,黏膜下神经元 5-HT(3)受体对结肠离子转运具有新的抑制作用。本研究的目的是探讨这种抑制作用的精确机制。
将大鼠远端结肠的黏膜/黏膜下层或仅黏膜制剂安装在 Ussing 室中,以测量短电路电流(I(sc))作为离子分泌的指标。采用放射免疫测定法测定生长抑素释放。用酶联免疫吸附试验(ELISA)测定细胞内 cAMP 含量。采用免疫组织化学技术研究结肠组织中 5-HT(3)受体、生长抑素和生长抑素受体的表达。
在大鼠远端结肠黏膜/黏膜下层制剂中,5-HT(3)受体拮抗剂预处理增强了 5-HT 诱导的 I(sc)增加。然而,在没有保留神经成分的仅黏膜制剂中,5-HT(3)受体拮抗剂预处理抑制了 5-HT 诱导的ΔI(sc)。在黏膜/黏膜下层制剂中,生长抑素-2(sst(2))受体拮抗剂预处理增强了 5-HT 诱导的ΔI(sc)。sst(2)和 5-HT(3)受体拮抗剂联合使用不会进一步增强 5-HT 诱导的ΔI(sc)。此外,sst(2)和 5-HT(3)受体拮抗剂均增强了黏膜/黏膜下层制剂中 5-HT 诱导的细胞内 cAMP 浓度增加。5-HT 从大鼠结肠黏膜/黏膜下层制剂中释放生长抑素,该作用可被 5-HT(3)受体拮抗剂预处理所阻止。免疫组织化学染色显示,黏膜下神经元存在 5-HT(3)受体,结肠黏膜存在 sst(2)受体。
激活大鼠结肠黏膜下神经丛中的神经元 5-HT(3)受体通过从黏膜下神经元释放生长抑素来抑制 5-HT 诱导的离子分泌。