FEEDBACK REGULATIION OF PANCREATIC ENZYME SECRETION
FEEDBACK REGULATIION OF PANCREATIC ENZYME SECRETION
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
关键词:
autoradiography benzodiazepine receptor cholecystokinin chromaffin cells digestion endopeptidases enzyme feedback enzyme inhibitors enzyme mechanism hormone inhibitor hormone regulation /control mechanism immunocytochemistry laboratory rat neuroendocrine system nutrition related tag receptor binding secretion substance P
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.
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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
Mechanism of action of calcitonin gene-related peptide in inhibiting pancreatic enzyme secretion in rats.
降钙素基因相关肽抑制大鼠胰酶分泌的作用机制。
DOI:
10.1016/0016-5085(93)90026-9
发表时间:
1993
期刊:
Gastroenterology
影响因子:
29.4
作者:
[Li,Y, Kolligs,F, Owyang,C]
通讯作者:
Owyang,C
共 8 条
In Vivo Animal and Human Studies Core
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批准号:9978789
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项目类别:
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资助金额:$16.55万
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财政年份:2020
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负责人:CHUNG OWYANG
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依托单位:
Training in Basic and Translational Digestive Sciences
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批准号:8481546
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资助金额:$29.16万
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财政年份:2012
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Training in Basic and Translational Digestive Sciences
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资助金额:$25.15万
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财政年份:2012
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Training in Basic and Translational Digestive Sciences
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资助金额:$22.74万
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Training in Basic and Translational Digestive Sciences
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批准号:10207610
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资助金额:$27.9万
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Training in Basic and Translational Digestive Sciences
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批准号:8268221
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资助金额:$29.85万
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Role of clock genes in colonic motility
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资助金额:$6.95万
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Functioning of Nodose Ganglia in Diabetes
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财政年份:2010
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依托单位:
Functioning of Nodose Ganglia in Diabetes
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批准号:7887600
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资助金额:$38.63万
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财政年份:2010
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Functioning of Nodose Ganglia in Diabetes
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资助金额:$30.83万
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Functioning of Nodose Ganglia in Diabetes
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资助金额:$31.94万
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财政年份:2010
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Functioning of Nodose Ganglia in Diabetes
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负责人:CHUNG OWYANG
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Peptide Core
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财政年份:2008
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依托单位:
Role of clock genes in colonic motility
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Molecular Biology Core
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资助金额:$14.55万
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财政年份:2006
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负责人:CHUNG OWYANG
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Peptides and Proteomics Core
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批准号:7499790
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资助金额:$13.25万
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ACC Sensitization in Visceral Hypersensitive Rats
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负责人:CHUNG OWYANG
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Administrative Core
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资助金额:$45.16万
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财政年份:2006
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负责人:CHUNG OWYANG
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依托单位:
海外基金