Name | adenylyl cyclase |
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Synonyms | ADCY 7; ATP pyrophosphate lyase; Adenylyl cyclase; ADCY7; ADCY7 protein; ATP pyrophosphate lyase 7; Adenylate cyclase 7; Adenylate cyclase type 7… |
Name | strychnine |
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CAS | strychnidin-10-one |
PubMed | Abstract | RScore(About this table) | |
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7913402 | Puebla L, Arilla E: Somatostatin receptor-GTP binding regulatory protein-adenylyl cyclase system in hippocampal membranes of strychnine-treated rats. Brain Res. 1994 Apr 25;644(1):59-66. |
62(0,2,2,2) | Details |
8714523 | Puebla L, Arilla E: somatostatin receptors and somatostatin-mediated inhibition of the adenylate cyclase system in the rat hippocampus. J Neurosci Res. 1996 Feb 1;43(3):346-54. Since SS receptors are coupled via nucleotide-binding G proteins to the adenylyl cyclase (AC) system, we also examined the inhibitory effects of SS and the nucleotide Gpp (NH) p on AC activity in hippocampal membranes of control, - and strychnine plus -treated rats since the increase in SS receptors was observed only in this brain area. |
increases the number of 31(0,1,1,1) | Details |
8987801 | Bonci A, Williams JT: Increased probability of morphine. . J Neurosci. 1997 Jan 15;17(2):796-803. In addition, activation of adenylyl cyclase, with forskolin, and cAMP-dependent protein kinase, with Sp-cAMPS, caused a larger increase in IPSCs in slices from morphine-treated animals. |
release during withdrawal from 1(0,0,0,1) | Details |
11312281 | Hatton GI, Yang QZ: Ionotropic receptors and H2 receptors modulate supraoptic neuronal excitability and dye coupling. J Neurosci. 2001 May 1;21(9):2974-82. Because H (2) receptors are linked to activation of adenylyl cyclase, TM-stimulated reduction in coupling was blocked by GDP-betaS, pertussis toxin, and Rp-cAMPs and was mimicked by 8-bromo-cAMP, 3-isobutyl-1-methylxanthine, and Sp-cAMP. IPSPs were blocked by the Cl (-) channel blocker picrotoxin, but not by bicuculline or strychnine, and by H (2), but not by H (1) or H (3) receptor antagonists, suggesting the presence of an ionotropic receptor and the possible nonspecificity of currently used H (2) antagonists. |
1(0,0,0,1) | Details |