首页> 外文期刊>American Journal of Physiology >Differential 5-HT3 mediation of human gastrocolonic response and colonic peristaltic reflex.
【24h】

Differential 5-HT3 mediation of human gastrocolonic response and colonic peristaltic reflex.

机译:5-HT3差异介导人类胃结肠反应和结肠蠕动反射。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Colonic motor function is modulated by extended and local neural reflexes involving unknown mediators. To test the role of serotonin (5-HT3) pathways, increases in colonic tone during antral distension and duodenal lipid perfusion (gastrocolonic responses) and changes in orad and caudad colonic tone in response to local colonic distension (peristaltic reflex) were measured after double-blind granisetron (10 microg/kg) or placebo infusion in healthy human volunteers. Antral distension evoked increases in colonic tone, which were blunted by granisetron (P < 0.05) without effects on antral compliance. Intraduodenal lipid perfusion also evoked increased colonic tone, which was reduced by granisetron (P < 0.05). In contrast, orad colonic contractions and caudad relaxations and contractions during colonic distension were unaffected by granisetron. In conclusion, 5-HT3 receptor antagonism blunts both the mechano- and chemoreceptor components of the human gastrocolonic response without altering antral compliance. In contrast, 5-HT3 pathways play no role in the ascending or descending components of the colonic peristaltic reflex. These findings demonstrate different roles for 5-HT3 receptors in the control of colonic motor function by the proximal gastrointestinal tract and by local neural reflexes.
机译:结肠运动功能受到涉及未知介体的扩展和局部神经反射的调节。为了测试5-羟色胺(5-HT3)途径的作用,在两次重复测量后,测量了肛门扩张和十二指肠脂质灌注(结肠结肠反应)过程中结肠张力的增加以及响应局部结肠扩张(蠕动反射)而导致的Orad和caudad结肠张力的变化。在健康的人类志愿者中进行盲式Granisetron(10微克/千克)或安慰剂输注。肛门扩张引起结肠张力增加,这被格拉司琼减弱(P <0.05),而对肛门顺应性没有影响。十二指肠内脂质灌注也引起结肠张力增加,而格拉司琼降低了结肠张力(P <0.05)。相比之下,Granisetron不影响orad结肠收缩和结肠扩张期间的松弛和收缩。总之,5-HT 3受体拮抗作用减弱了人胃结肠反应的机械感受器和化学感受器成分,而不会改变肛门顺应性。相反,5-HT3途径在结肠蠕动反射的上升或下降成分中不起作用。这些发现表明5-HT 3受体在通过近端胃肠道和局部神经反射来控制结肠运动功能中的不同作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号