Zobrazeno 1 - 10 of 10 pro vyhledávání: '"B. R. Bianchi"'
1
Persistent activation of the dopamine D1 receptor contributes to prolonged receptor desensitization: studies with A-77636
Autor: C W, Lin, B R, Bianchi, T R, Miller, M A, Stashko, S S, Wang, P, Curzon, L, Bednarz, K E, Asin, D R, Britton
Publikováno v: The Journal of pharmacology and experimental therapeutics. 276(3)
A-77636 is a dopamine (DA) D1 receptor-selective agonist that was previously shown to elicit beneficial responses in animal models of Parkinson's disease (PD) (Kebabian et al.: Eur. J. Pharmacol. 229: 203, 1992). However, A-77636 is of limited potent
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ab561fabbb24dc8d89a53e6066319237
https://pubmed.ncbi.nlm.nih.gov/8786531
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2
Characterization of cloned human dopamine D1 receptor-mediated calcium release in 293 cells
Autor: C W, Lin, T R, Miller, D G, Witte, B R, Bianchi, M, Stashko, A M, Manelli, D E, Frail
Publikováno v: Molecular pharmacology. 47(1)
Dopamine (DA) D1 receptors are generally known to couple only to Gs and cAMP production. Recently, D1 receptors expressed in mouse Ltk- cells have been shown to induce cAMP production, phosphoinositide (PI) hydrolysis, and calcium mobilization [Mol.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::199be5031cb20c2947d9181b672d2565
https://pubmed.ncbi.nlm.nih.gov/7838121
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3
Novel CCK analogues and bombesin: a detailed analysis between phosphoinositide breakdown and high-dose inhibition of pancreatic enzyme secretion in three rodent species
Autor: B R, Bianchi, T R, Miller, D G, Witte, C W, Lin
Publikováno v: The Journal of pharmacology and experimental therapeutics. 268(2)
Cholecystokinin octapeptide (26-33) (CCK-8) stimulates pancreatic amylase secretion in a biphasic manner. Amylase secretion is stimulated in a dose-dependent manner up to a maximal level, but reduced secretion is observed at supramaximal concentratio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cf497dd1c2aac208b40f38a2d3301d6a
https://pubmed.ncbi.nlm.nih.gov/7509394
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7
Characterization of two novel cholecystokinin tetrapeptide (30-33) analogues, A-71623 and A-70874, that exhibit high potency and selectivity for cholecystokinin-A receptors
Autor: C W, Lin, K, Shiosaki, T R, Miller, D G, Witte, B R, Bianchi, C A, Wolfram, H, Kopecka, R, Craig, F, Wagenaar, A M, Nadzan
Publikováno v: Molecular pharmacology. 39(3)
Based on their relative affinities for cholecystokinin octapeptide (26-33) (CCK-8), cholecystokinin tetrapeptide (30-33) (CCK-4), desulfated CCK-8, and gastrin, cholecystokinin (CCK) receptors have been classified as CCK-A (alimentary) and CCK-B (bra
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::55f979d07ffdbdc7f94e091dd270c1c9
https://pubmed.ncbi.nlm.nih.gov/1706470
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8
Cholecystokinin receptors: relationships among phosphoinositide breakdown, amylase release and receptor affinity in pancreas
Autor: C W, Lin, B R, Bianchi, D, Grant, T, Miller, E A, Danaher, M D, Tufano, H, Kopecka, A M, Nadzan
Publikováno v: The Journal of pharmacology and experimental therapeutics. 236(3)
The gut hormone cholecystokinin (CCK) octapeptide stimulates the release of amylase from exocrine pancreas, a process believed to be the result of the breakdown of phosphatidylinositol lipids. To examine further the relationship between phosphoinosit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::642417e785761b52a0f26f3ac80bfe00
https://pubmed.ncbi.nlm.nih.gov/2419543
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