The binding of [3H]nitrendipine to receptors for calcium channel antagonists in the heart, cerebral cortex, and ileum of rats.
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A new mode of mineralocorticoid receptor antagonism by a potent and selective nonsteroidal molecule.L-type cardiac calcium channels in doxorubicin cardiomyopathy in rats morphological, biochemical, and functional correlationsPhotoaffinity labelling of the cardiac calcium channel. (-)-[3H]azidopine labels a 165 kDa polypeptide, and evidence against a [3H]-1,4-dihydropyridine-isothiocyanate being a calcium-channel-specific affinity ligandNitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated statePreclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis.Neurochemical profile of eltoprazine.High and concentration-proportional accumulation of [3H]-nitrendipine by intact cardiac tissue.[3H]-verapamil binding to rat cardiac sarcolemmal membrane fragments; an effect of ischaemia.Tissue response selectivity of calcium antagonists is not due to heterogeneity of [3H]-nitrendipine binding sites.Chronic caffeine alters the density of adenosine, adrenergic, cholinergic, GABA, and serotonin receptors and calcium channels in mouse brain.Antischizophrenic drugs of the diphenylbutylpiperidine type act as calcium channel antagonists.A unitary mechanism of calcium antagonist drug action.Conformationally restricted analogs of somatostatin with high mu-opiate receptor specificity.Calcium antagonist receptors. Clinical and physiological relevance.Calcium, the control of smooth muscle function and bronchial hyperreactivity.Calcium-independent inhibition of glucose transport in PC-12 and L6 cells by calcium channel antagonists.Dual calcium-channel blocker therapy in the treatment of hypertension.[3H]Nitrendipine binding to calcium channels in bovine and rat pituitary.Interference of sodium with [3H]-nitrendipine binding to cardiac membranes.Comparative potencies of calcium channel antagonists and antischizophrenic drugs on central and peripheral calcium channel binding sites.Direct inhibitory effects of some 'calcium-antagonists' and trifluoperazine on the contractile proteins in smooth muscle.Voltage-sensitive calcium channels in differentiated neuroblastoma X glioma hybrid (NG108-15) cells: characterization by quin 2 fluorescence.A calmodulin-like ca receptor in the ca channel.Reversible dihydropyridine isothiocyanate binding to brain calcium channels.The receptor occupation and plasma concentration of NKY-722, a water-soluble dihydropyridine-type calcium antagonist, in spontaneously hypertensive rats.Discovery of BAY 94-8862: a nonsteroidal antagonist of the mineralocorticoid receptor for the treatment of cardiorenal diseases.Photoalteration of calcium channel blockade in the cardiac Purkinje fiber.Receptor binding profiles of amiloride analogues provide no evidence for a link between receptors and the Na+/H+ exchanger, but indicate a common structure on receptor proteins.Manganese ions induce tonic contraction after relaxation in a high-K+ medium in ileal longitudinal smooth muscle of guinea-pig.BAY K 8644, a 1,4-dihydropyridine Ca2+ channel activator: dissociation of binding and functional effects in brain synaptosomes.Calcium antagonism by cobalt ions on contraction of guinea-pig taenia coli.Effects of temperature and allosteric modulators on [3H] nitrendipine binding: methods for detecting potential Ca2+ channel blockers.Interaction of the calcium channel activating 3H-BAY K 8644 and inhibiting 3H-verapamil with specific receptor sites on cultured beating myocardial cells.Comparison of voltage-dependent 45Ca2+ uptake rates by synaptosomes isolated from rat brain regions.Ontogenic appearance of Ca2+ channels characterized as binding sites for nitrendipine during development of nervous, skeletal and cardiac muscle systems in the rat.45Ca2+ uptake into rat whole brain synaptosomes unaltered by dihydropyridine calcium antagonists.POSTER COMMUNICATIONS
P2860
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P2860
The binding of [3H]nitrendipine to receptors for calcium channel antagonists in the heart, cerebral cortex, and ileum of rats.
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年学术文章
@wuu
1982年学术文章
@zh
1982年学术文章
@zh-cn
1982年学术文章
@zh-hans
1982年学术文章
@zh-my
1982年学术文章
@zh-sg
1982年學術文章
@yue
1982年學術文章
@zh-hant
name
The binding of [3H]nitrendipin ...... ral cortex, and ileum of rats.
@en
The binding of [3H]nitrendipin ...... ral cortex, and ileum of rats.
@nl
type
label
The binding of [3H]nitrendipin ...... ral cortex, and ileum of rats.
@en
The binding of [3H]nitrendipin ...... ral cortex, and ileum of rats.
@nl
prefLabel
The binding of [3H]nitrendipin ...... ral cortex, and ileum of rats.
@en
The binding of [3H]nitrendipin ...... ral cortex, and ileum of rats.
@nl
P2093
P1433
P1476
The binding of [3H]nitrendipin ...... ral cortex, and ileum of rats.
@en
P2093
P304
P356
10.1016/0024-3205(82)90293-4
P407
P577
1982-06-01T00:00:00Z