[PDF][PDF] Biochemistry and biophysics of excitation-contraction coupling

S Fleischer, M Inui - Annual review of biophysics and biophysical …, 1989 - researchgate.net
Muscle contraction and relaxation are regulated by the myoplasmic free calcium
concentration, which in turn is regulated by membranes. Sarco plasmic reticulum (SR) has a …

Calbindin D-28k and parvalbumin in the rat nervous system

MR Celio - Neuroscience, 1990 - Elsevier
This paper describes the distribution of structures stained with mono-and polyclonal
antibodies to the calcium-binding proteins calbindin D-28k and parvalbumin in the nervous …

Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state.

BP Bean - Proceedings of the National Academy of …, 1984 - National Acad Sciences
Block of Ca2+ currents by the dihydropyridine drug nitrendipine was studied in single canine
ventricular cells by using the whole-cell variant of the patch clamp technique. When cells …

Discovery of BAY 94‐8862: a nonsteroidal antagonist of the mineralocorticoid receptor for the treatment of cardiorenal diseases

L Bärfacker, A Kuhl, A Hillisch, R Grosser… - …, 2012 - Wiley Online Library
Aldosterone is a hormone that exerts manifold deleterious effects on the kidneys, blood
vessels, and heart which can lead to pathophysiological consequences. Inhibition of the …

Selective activation of Ca2+-dependent K+ channels by novel benzimidazolone

SP Olesen, E Munch, P Moldt, J Drejer - European journal of pharmacology, 1994 - Elsevier
Activators and blockers of specific ion channels are important pharmacological tools for
characterizing ion channels and their influence on cell function. The large-conductance Ca …

A new mode of mineralocorticoid receptor antagonism by a potent and selective nonsteroidal molecule

J Fagart, A Hillisch, J Huyet, L Bärfacker, M Fay… - Journal of Biological …, 2010 - ASBMB
Limitations of current steroidal mineralocorticoid receptor (MR) antagonists have stimulated
the search for a new generation of molecules. We screened for novel nonsteroidal …

KV11.1, NaV1.5, and CaV1.2 Transporter Proteins as Antitarget for Drug Cardiotoxicity

M Kowalska, J Nowaczyk, A Nowaczyk - International Journal of …, 2020 - mdpi.com
Safety assessment of pharmaceuticals is a rapidly develo** area of pharmacy and
medicine. The new advanced guidelines for testing the toxicity of compounds require …

Drug and neurotransmitter receptors in the brain

SH Snyder - Science, 1984 - science.org
Biochemical investigation of receptors for neurotransmitters and drugs in the brain has been
one of the most active areas of molecular neuroscience during the past decade. This work …

Chronic caffeine alters the density of adenosine, adrenergic, cholinergic, GABA, and serotonin receptors and calcium channels in mouse brain

D Shi, O Nikodijević, KA Jacobson, JW Daly - Cellular and molecular …, 1993 - Springer
Chronic ingestion of caffeine by male NIH strain mice alters the density of a variety of central
receptors. 2. The density of cortical A 1 adenosine receptors is increased by 20%, while the …

[3H] nitrendipine receptors in skeletal muscle.

M Fosset, E Jaimovich, E Delpont… - Journal of Biological …, 1983 - Elsevier
The richest source of receptors for the organic calcium channel blocker [3H] nitrendipine in
muscle is the transverse tubule membrane. The tubular membrane preparation binds [3H] …