Calcium antagonist receptors.
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Summary
The mechanism by which calcium enters excitable cells following electrical stimulation, and, more specifically, the ways in which drugs modify this process are focused on.
- Type
- article
- Published
- 1988-01-01
- Cited by
- 26
- References
- 220
- OpenAlex
- https://openalex.org/W2856492
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:27185605
Keywords
Political science, Humanities, Art
References
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- Dopamine receptors, neuroleptics, and schizophrenia.
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- Separation of cardiac plasmalemma into cell surface and T-tubular components. Distribution of saxitoxin- and nitrendipine-binding sites.
- [3H]nitrendipine receptors in skeletal muscle.
- Subcellular distribution of [3H]nitrendipine binding in smooth muscle.
- Tumor promoter phorbol myristate acetate inhibits Ca2+ influx through voltage-gated Ca2+ channels in two secretory cell lines, PC12 and RINm5F.
- Characterization of verapamil binding sites in cardiac membrane vesicles.
- Calcium antagonists High-affinity binding and inhibition of calcium transport in a clonal cell line.
- Selective inhibition of Na+-induced Ca2+ release from heart mitochondria by diltiazem and certain other Ca2+ antagonist drugs.
- The sodium channel from rat brain. Role of the beta 1 and beta 2 subunits in saxitoxin binding.
- Molecular properties of the slow inward calcium channel. Molecular weight determinations by radiation inactivation and covalent affinity labeling.
- The sodium channel from rat brain. Reconstitution of neurotoxin-activated ion flux and scorpion toxin binding from purified components.
- Target size analysis of skeletal muscle Ca2+ channels
- Voltage-sensitive nitrendipine binding in an isolated cardiac sarcolemma preparation.
- Characterization and photoaffinity labeling of receptor sites for the Ca2+ channel inhibitors d-cis-diltiazem, (+/-)-bepridil, desmethoxyverapamil, and (+)-PN 200-110 in skeletal muscle transverse tubule membranes.
Cited by
- Neamine and 2‐deoxystreptamine neomycin derivatives exhibit antinociceptive activity in rat models of phasic, incision and neuropathic pain
- Effects of intrathecally administered aminoglycoside antibiotics, calcium-channel blockers, nickel and calcium on acetic acid-induced writhing test in mice.
- Differential effects of L-type calcium channel blockers and stimulants on naloxone-precipitated withdrawal in mice acutely dependent on morphine
- Omega-conotoxin- and nifedipine-insensitive voltage-operated calcium channels mediate K(+)-induced release of pro-thyrotropin-releasing hormone-connecting peptides Ps4 and Ps5 from perifused rat hypothalamic slices.
- Inhibition of Ca-channels by diazepam compared with that by nicardipine in pheochromocytoma PC12 cells.
- Alterations in Calcium Antagonist Receptors and Sodium-Calcium Exchange in Cardiomyopathic Hamster Tissues
- Antinociception induced by intracerebroventricular or intrathecal administration of gentamicin in rats.
- Ca2+ channel actions of the non-dihydropyridine Ca2+ channel antagonist Ro 40-5967 in vascular muscle cells cultured from dog coronary and saphenous arteries
- Effects of diltiazem, a Ca2+ channel blocker, on naloxone-precipitated changes in dopamine and its metabolites in the brains of opioid-dependent rats
- Substituent Effects on the Electrochemistry and Photostability of Model Compounds of Calcium Channel Antagonist Drugs
- Blockade by calmodulin inhibitors of Ca2+ channels in smooth muscle from rat vas deferens
- Involvement of plasma membrane calcium influx in bacterial induction of the k/h and hypersensitive responses in tobacco.
- Pimozide is effective in delirium secondary to hypercalcemia when other neuroleptics fail.
- Calcium channel blocking activity of thioridazine, clomipramine and fluoxetine in isolated rat vas deferens: a relative potency measurement study.
- Nimodipine protects cultured spinal cord neurones from depolarization-induced inhibition of neurite outgrowth.
- Analgesic effects of centrally administered aminoglycoside antibiotics in mice.
- Calcium channels at the adrenergic neuroeffector junction in the rabbit ear artery
- The relative dependence of calcium antagonists and neuroleptics binding to brain and heart receptors on drug lipophilicity
- Effect of TaiCatoxin (TCX) on the electrophysiological, mechanical and biochemical characteristics of spontaneously beating ventricular cardiomyocytes
- Properties of cyclic nucleotide-gated channels mediating olfactory transduction. Activation, selectivity, and blockage
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