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血清素的释放由十二指肠黏膜细胞上的毒蕈碱受体介导。

Serotonin release is mediated by muscarinic receptors on duodenal mucosal cells.

作者信息

Kuemmerle J F, Kraus H, Kellum J M

出版信息

J Surg Res. 1987 Aug;43(2):139-42. doi: 10.1016/0022-4804(87)90156-9.

DOI:10.1016/0022-4804(87)90156-9
PMID:3306152
Abstract

Serotonin (5-HT), found in abundance in intestinal enterochromaffin cells, has been shown to be released in response to neural, humoral, and intraluminal stimuli but the mechanisms controlling release are poorly understood. The purpose of this study was to determine whether 5-HT release induced by the muscarinic agonist, methacholine, is mediated by enteric nerves or is a direct action at the mucosal cell level. We mounted rabbit mucosal sheets containing intact submucosal neural elements, but stripped of muscularis propria and myenteric plexus, in modified Ussing chambers and measured the release of 5-HT in response to 5 X 10(-5) M methacholine added to both mucosal and serosal surface bathing solutions, in the presence and absence of selective neural blockade with 1 X 10(-6) M tetrodotoxin. 5-HT release in control tissues (no drugs) as measured by radioimmunoassay was 25.7 +/- 6 ng/cm2/30 min (mean +/- SEM). In the presence of mucosal and serosal methacholine, total 5-HT release increased significantly (P less than 0.05) to 66.7 +/- 9 ng/cm2/30 min. When tetrodotoxin alone was applied, 5-HT release significantly increased to 55.2 +/- 9 ng/cm2/30 min compared to matched control. In the presence of tetrodotoxin, methacholine increased 5-HT release to 79.3 +/- 9 ng/cm2/30 min, which was significantly greater than with tetrodotoxin alone. These results provide evidence of an inhibitory neural regulation of basal 5-HT release since release increased in the presence of neural blockade. They also suggest that a muscarinic receptor at or near the enterochromaffin cells mediates mucosal 5-HT release since 5-HT is further increased by methacholine even in the presence of neural blockade.

摘要

血清素(5-羟色胺,5-HT)在肠道肠嗜铬细胞中大量存在,已被证明可响应神经、体液和腔内刺激而释放,但控制其释放的机制尚不清楚。本研究的目的是确定毒蕈碱激动剂乙酰甲胆碱诱导的5-HT释放是由肠神经介导,还是在黏膜细胞水平的直接作用。我们将含有完整黏膜下神经成分但去除了固有肌层和肌间神经丛的兔黏膜片置于改良的Ussing室中,在存在和不存在用1×10⁻⁶ M河豚毒素进行选择性神经阻滞的情况下,测量添加到黏膜和浆膜表面浴液中的5×10⁻⁵ M乙酰甲胆碱引起的5-HT释放。通过放射免疫测定法测量,对照组织(无药物)中的5-HT释放为25.7±6 ng/cm²/30分钟(平均值±标准误)。在黏膜和浆膜存在乙酰甲胆碱的情况下,5-HT总释放量显著增加(P<0.05)至66.7±9 ng/cm²/30分钟。单独应用河豚毒素时,与匹配的对照相比,5-HT释放显著增加至55.2±9 ng/cm²/30分钟。在存在河豚毒素的情况下,乙酰甲胆碱使5-HT释放增加至79.3±9 ng/cm²/30分钟,这显著高于单独使用河豚毒素时。这些结果提供了基础5-HT释放存在抑制性神经调节的证据,因为在存在神经阻滞的情况下释放增加。它们还表明,即使在存在神经阻滞的情况下,乙酰甲胆碱仍可使5-HT进一步增加,这表明肠嗜铬细胞处或其附近的毒蕈碱受体介导了黏膜5-HT释放。

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