Literature DB >> 2536955

Modulation of calcium channels in cardiac and neuronal cells by an endogenous peptide.

G Callewaert1, I Hanbauer, M Morad.   

Abstract

Calcium channels mediate the generation of action potentials, pacemaking, excitation-contraction coupling, and secretion and signal integration in muscle, secretory, and neuronal cells. The physiological regulation of the L-type calcium channel is thought to be mediated primarily by guanine nucleotide-binding proteins (G proteins). A low molecular weight endogenous peptide has been isolated and purified from rat brain. This peptide regulates up and down the cardiac and neuronal calcium channels, respectively. In cardiac myocytes, the peptide-induced enhancement of the L-type calcium current had a slow onset (half-time approximately 75 seconds), occurred via a G protein-independent mechanism, and could not be inhibited by alpha 1-adrenergic, beta-adrenergic, or angiotensin II blockers. In neuronal cells, on the other hand, the negative effect had a rapid onset (half-time less than 500 milliseconds) and was observed on both T-type and L-type calcium channels.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2536955     DOI: 10.1126/science.2536955

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  12 in total

Review 1.  Psychopharmacological properties of calcium channel inhibitors.

Authors:  O Pucilowski
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

2.  Direct contact between sympathetic neurons and rat cardiac myocytes in vitro increases expression of functional calcium channels.

Authors:  S Ogawa; J V Barnett; L Sen; J B Galper; T W Smith; J D Marsh
Journal:  J Clin Invest       Date:  1992-04       Impact factor: 14.808

Review 3.  Do calcium antagonists have a place in the treatment of mood disorders?

Authors:  C Höschl
Journal:  Drugs       Date:  1991-11       Impact factor: 9.546

4.  Calciseptine, a peptide isolated from black mamba venom, is a specific blocker of the L-type calcium channel.

Authors:  J R de Weille; H Schweitz; P Maes; A Tartar; M Lazdunski
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-15       Impact factor: 11.205

5.  Three types of bovine chromaffin cell Ca2+ channels: facilitation increases the opening probability of a 27 pS channel.

Authors:  C R Artalejo; D J Mogul; R L Perlman; A P Fox
Journal:  J Physiol       Date:  1991-12       Impact factor: 5.182

6.  Internal and external effects of dihydropyridines in the calcium channel of skeletal muscle.

Authors:  H H Valdivia; R Coronado
Journal:  J Gen Physiol       Date:  1990-01       Impact factor: 4.086

7.  A peptide mimetic of calcium.

Authors:  J Dillon; W T Woods; V Guarcello; R D LeBoeuf; J E Blalock
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

8.  Selectivity of Ca2+ channel blockers in inhibiting muscular and nerve activities in isolated colon.

Authors:  S Lecchini; M Marcoli; F De Ponti; C A Castelletti; G M Frigo
Journal:  Br J Pharmacol       Date:  1991-03       Impact factor: 8.739

9.  In vivo labeling of L-type Ca2+ channels by fluorescent dihydropyridines: evidence for a functional, extracellular heparin-binding site.

Authors:  H G Knaus; T Moshammer; K Friedrich; H C Kang; R P Haugland; H Glossman
Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-15       Impact factor: 11.205

10.  Dual role of calmodulin in excitable cells.

Authors:  W R Vieth; K Nho; S Kale
Journal:  Ann Biomed Eng       Date:  1993 Nov-Dec       Impact factor: 3.934

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.