课题基金 / 基金详情

FEEDBACK REGULATIION OF PANCREATIC ENZYME SECRETION

FEEDBACK REGULATIION OF PANCREATIC ENZYME SECRETION
胰腺酶分泌的反馈调节
批准号:
6177113
负责人:
CHUNG OWYANG
金额:
$27.32万
依托单位国家:
美国
项目类别:
财政年份:
1983
资助国家:
美国
项目状态:
已结题
起止时间:
1983-08-01 至 2002-08-31

项目摘要

项目成果

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中文摘要
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英文摘要
DESCRIPTION: Cholecystokinin plays a major role in the mediation of pancreatic secretion and gallbladder contraction after a meal, however little is known about the mechanisms regulating its secretion. During previous cycles of this grant, the investigator explored mechanisms responsible for feedback modulation of CCK release by intraluminal proteases and identified a trypsin-sensitive CCK-releasing peptide factor which is secreted into the proximal bowel. This has now been purified and sequenced to demonstrate its identity with the diazepam-binding inhibitor. The aims of the current proposal revolve around the hypothesis that DBI is the CCK-releasing peptide responsible for feedback regulation of pancreatic secretion and post-prandial secretion of this hormone; that secretion of DBI is under neurohormonal control with release mediated by enteric neural circuitry involving serotonin enterochromaffin cells, substance P sensory neurons, and cholinergic secretomotor neurons; and that DBI acts directly on CCK-releasing cells. Component aims are focused to demonstrate that DBI is released into the lumen during diversion of bile-pancreatic juice and nutrient stimulation, and that its secretion parallels that of CCK. It is postulated that immunoneutralization of DBI in the duodenum should abolish CCK and pancreatic secretion under these conditions. Structure-function studies are planned utilizing both the in vivo rat model as well as STC-1 CCK-releasing cells to identify key regions for biological activity. Another aim is focused toward demonstrating that nutrient-stimulated release of DBI occurs via the neural circuitry previously suggested. Finally, the localization of CCK and DBI in the intestine and the benzodiazepine receptors that may mediate this activity will be performed using immunohistochemistry and receptor autoradiography. The benzodiazepine binding sites responsible for CCK release will be characterized by both biological and binding studies. Through these studies, the investigators hope to further their understanding of the mechanisms regulating CCK secretion.
期刊论文(12)
专著(0)
科研奖励(0)
会议论文
Inhibition of exocrine pancreatic secretion by opiates is mediated by suppression of cholinergic transmission: characterization of receptor subtypes.
阿片类药物对外分泌胰腺分泌的抑制是通过抑制胆碱能传递介导的:受体亚型的表征。
DOI: --
发表时间: 1988
期刊: The Journal of pharmacology and experimental therapeutics
影响因子: --
作者: [Louie,DS, Chen,HT, Owyang,C]
通讯作者: Owyang,C
Characterization of a new CCK antagonist, L364,718: in vitro and in vivo studies.
新型 CCK 拮抗剂 L364,718 的表征:体外和体内研究。
DOI: 10.1152/ajpgi.1988.255.3.g261
发表时间: 1988
期刊: The American journal of physiology
影响因子: --
作者: [Louie,DS, Liang,JP, Owyang,C]
通讯作者: Owyang,C
Cholinergic dependence of gallbladder response to cholecystokinin in the guinea pig in vivo.
豚鼠体内胆囊对胆囊收缩素反应的胆碱能依赖性。
DOI: 10.1152/ajpgi.1991.261.4.g565
发表时间: 1991
期刊: The American journal of physiology
影响因子: --
作者: [Takahashi,T, May,D, Owyang,C]
通讯作者: Owyang,C
A cholecystokinin releasing peptide mediates feedback regulation of pancreatic secretion.
胆囊收缩素释放肽介导胰腺分泌的反馈调节。
DOI: 10.1152/ajpgi.1989.256.2.g430
发表时间: 1989
期刊: The American journal of physiology
影响因子: --
作者: [Lu,L, Louie,D, Owyang,C]
通讯作者: Owyang,C
8
    In Vivo Animal and Human Studies Core
    Training in Basic and Translational Digestive Sciences
    Training in Basic and Translational Digestive Sciences
    Training in Basic and Translational Digestive Sciences
    海外基金