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人空肠、回肠、近端结肠和胆囊对胆囊收缩素八肽的敏感性。

Sensitivities of human jejunum, ileum, proximal colon, and gallbladder to cholecystokinin octapeptide.

作者信息

Kellow J E, Miller L J, Phillips S F, Haddad A C, Zinsmeister A R, Charboneau J W

出版信息

Am J Physiol. 1987 Mar;252(3 Pt 1):G345-56. doi: 10.1152/ajpgi.1987.252.3.G345.

DOI:10.1152/ajpgi.1987.252.3.G345
PMID:3826375
Abstract

We compared in humans simultaneous motor responses of the jejunum, ileum, proximal colon, and gallbladder (GB) to intravenous cholecystokinin octapeptide (CCK-OP). To gauge the physiological relevance of the doses of CCK-OP, intestinal motility and GB contraction were also quantified after a fatty meal. Eight healthy volunteers participated in both experiments. Six graded, 30-min intravenous infusions had a mean range of 2.2 to 73.2 pmol X kg-1 X h-1 of CCK-OP; these spanned from subphysiological (negligible contraction of GB) to pharmacological (producing intestinal symptoms and a 70-99% contraction of GB) levels. CCK-OP inhibited interdigestive cycles of motility, though in some persons fasting patterns persisted with doses of CCK-OP, which produced up to 50% reduction in GB volume. Motility indices of the ileum and proximal colon responded to CCK-OP by decreasing initially but then increasing with larger doses; motility of the jejunum increased gradually at all doses. Judged by the gallbladder's response to food (reduction in volume down from 74 to 29% of original volume), the physiological range of infused CCK-OP was approximately 5-16 pmol X kg-1 X h-1. Within this range of doses of CCK-OP, motility of the jejunum increased, whereas motility of the proximal colon was reduced. These data are consistent with CCK being a "physiological" mediator of intestinal motility in humans; responses of the intestine to the peptide appear to vary regionally.

摘要

我们在人体中比较了空肠、回肠、近端结肠和胆囊对静脉注射八肽胆囊收缩素(CCK-OP)的同步运动反应。为了评估CCK-OP剂量的生理相关性,还在进食脂肪餐后对肠道运动和胆囊收缩进行了量化。八名健康志愿者参与了这两项实验。六次30分钟的静脉分级输注,CCK-OP的平均剂量范围为2.2至73.2 pmol×kg⁻¹×h⁻¹;这些剂量范围从低于生理水平(胆囊收缩可忽略不计)到药理水平(产生肠道症状和胆囊70-99%的收缩)。CCK-OP抑制了消化间期的运动周期,尽管在一些人身上,即使使用能使胆囊体积减少多达50%的CCK-OP剂量时禁食模式仍持续存在。回肠和近端结肠的运动指数对CCK-OP的反应最初是下降,但随着剂量增加随后上升;空肠的运动在所有剂量下都逐渐增加。根据胆囊对食物的反应(体积从原始体积的74%降至29%)判断,输注CCK-OP的生理剂量范围约为5-16 pmol×kg⁻¹×h⁻¹。在此CCK-OP剂量范围内,空肠运动增加,而近端结肠运动减少。这些数据与CCK作为人体肠道运动的“生理性”介质一致;肠道对该肽的反应似乎存在区域差异。

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