نتایج جستجو برای: cck antagonists

تعداد نتایج: 54329  

Journal: :Endocrinology 2007
Paolo Giacobini Susan Wray

Pulsatile secretion of GnRH-1 regulates gonadotropin release from anterior pituitary and thus is essential for reproduction. The present study focused on the role of cholecystokinin (CCK) in the GnRH-1 system. CCK is a neuropeptide abundantly expressed in the brain, which is implicated in activation of female reproductive behaviors and release of anterior pituitary hormones. Using dual-label im...

Journal: :The Yale Journal of Biology and Medicine 1992
J. H. Grendell

A variety of receptors on pancreatic acinar and duct cells regulate both pancreatic exocrine secretion and intracellular processes. These receptors are potential sites of action for therapeutic agents in the treatment of pancreatitis. Cholecystokinin (CCK) receptor antagonists, which may reduce the level of metabolic "stress" on acinar cells, have been shown to mitigate the severity of acute pa...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1992
J R Ghilardi C J Allen S R Vigna D C McVey P W Mantyh

125I-Bolton-Hunter sulfated cholecystokinin-8 was used to localize and characterize cholecystokinin (CCK) receptor binding sites in trigeminal and dorsal root ganglia, and in the spinal cord of the rat, rabbit, and monkey. In the rabbit and monkey, a substantial number, 90 +/- 21% and 24 +/- 8%, respectively, of trigeminal and dorsal root ganglion neurons express CCK binding sites. In the spina...

Journal: :American journal of physiology. Regulatory, integrative and comparative physiology 2006
Daniela M Sartor Arthur Shulkes Anthony J M Verberne

Ingestion of a meal results in gastrointestinal (GI) hyperemia and is associated with systemic and paracrine release of a number of peptide hormones, including cholecystokinin (CCK) and 5-hydroxytryptamine (5-HT). Systemic administration of CCK octapeptide inhibits a subset of presympathetic neurons of the rostroventrolateral medulla (RVLM) that may be responsible for driving the sympathetic va...

Journal: :Frontiers in bioscience : a journal and virtual library 2004
Zoltán Szelényi Miklós Székely Zoltán Hummel Márta Balaskó Andrej A Romanovsky Erika Pétervári

Thermoregulatory effects of cholecystokinin (CCK) peptides are reviewed with special emphasis on two types of responses, that is hyperthermia (fever) and hypothermia. Central microinjection of CCK in rats induces a thermogenic response that can be attenuated by CCK-B receptor antagonists, but some authors observed a hypothermia. By contrast to its central fever-inducing effect, in rodents expos...

Journal: :Journal of the National Cancer Institute 1996
I Camby I Salmon A Danguy J L Pasteels J Brotchi J Martinez R Kiss

BACKGROUND Gastrin and cholecystokinin (CCK) mediate their effects through at least two types of receptors (CCK receptors A and B). While it has been hypothesized that gastrin, a stimulator of gastric acid secretion, is also a neurotransmitter and a stimulator of cell proliferation in various normal and neoplastic tissues, its effect on astrocytic brain tumors has not been actively investigated...

Journal: :Gut 1989
S J Konturek J Tasler J W Konturek M Cieszkowski K Szewczyk M Hładij P S Anderson

Postprandial pancreatic secretion results from the interaction of neural and hormonal factors but their contribution to the net postprandial secretion is unknown. Recent description of highly specific and potent cholecystokinin (CCK) receptor antagonists allows the determination of the physiological role of CCK in the postprandial pancreatic secretion. In six dogs with chronic pancreatic fistul...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 1998
Yana Zavros William R Fleming Kenneth J Hardy Arthur Shulkes

CCK and gastrin stimulate somatostatin (SOM) secretion and thus modulate their direct effects on the parietal cell. Although SOM is stored in D cells of the fundus and antrum, the nature of the cell type differs, and it is not known whether both regions respond to the stimulatory effects of CCK and gastrin. The objectives of the present study were to determine the separate effects of CCK and ga...

Journal: :Journal of medicinal chemistry 2000
A Ursini A M Capelli R A Carr P Cassarà M Corsi O Curcuruto G Curotto M Dal Cin S Davalli D Donati A Feriani H Finch G Finizia G Gaviraghi M Marien G Pentassuglia S Polinelli E Ratti A M Reggiani G Tarzia G Tedesco M E Tranquillini D G Trist F T Van Amsterdam

A series of 5-phenyl-3-ureidobenzodiazepine-2,4-diones was synthesized and evaluated as cholecystokinin-B (CCK-B) receptor antagonists. Structure-activity relationship (SAR) studies revealed the importance of the N-1 substituent for potent and selective CCK-B affinity. Addition of substituents at the urea side chain provided in some cases more potent compounds. Moreover the introduction of bulk...

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