TY - JOUR
T1 - The action of organic mercury compounds on the function of isolated mammalian heart muscle
AU - Halbach, Stefan
AU - Schönsteiner, Gerlinde
AU - Vierling, Wolfgang
PY - 1989/8/22
Y1 - 1989/8/22
N2 - The effects of four organic mercury compounds (methylmercuric chloride; bromomercurihydroypropane, BMHP; chlormerodrin; p-chloromercuribenzoic acid, PCMB) on mechanical and electrical functions of guinea-pig papillary muscles were investigated. An intial decline in contraction force was followed by a transient positive inotropic response. The first was accompanied by a shortening of the action-potential duration and by a reduction of the depolarization velocity and the duration of the Ca2+-dependent slow response. The latter was characterized by an indirect component (release of noradrenaline) and by a direct component, which was dependent on the stimulation rate and on the extracellular concentration of Na+ and K+. The direct positive effect, therefore, was likely to have resulted from inhibition of the sarcolemmal Na+ + K+-ATPase. This notion was confirmed by experiments with isolated membrane particles. The prevalence of the negative or positive inotropic action of these compounds could be ascribed to their lipophilic or hydrophilic properties, respectively.
AB - The effects of four organic mercury compounds (methylmercuric chloride; bromomercurihydroypropane, BMHP; chlormerodrin; p-chloromercuribenzoic acid, PCMB) on mechanical and electrical functions of guinea-pig papillary muscles were investigated. An intial decline in contraction force was followed by a transient positive inotropic response. The first was accompanied by a shortening of the action-potential duration and by a reduction of the depolarization velocity and the duration of the Ca2+-dependent slow response. The latter was characterized by an indirect component (release of noradrenaline) and by a direct component, which was dependent on the stimulation rate and on the extracellular concentration of Na+ and K+. The direct positive effect, therefore, was likely to have resulted from inhibition of the sarcolemmal Na+ + K+-ATPase. This notion was confirmed by experiments with isolated membrane particles. The prevalence of the negative or positive inotropic action of these compounds could be ascribed to their lipophilic or hydrophilic properties, respectively.
KW - Bromomercurihydroxypropane
KW - Ca action potential
KW - Chlormerodrin
KW - Contractility
KW - K-ATPase
KW - Methylmercury
KW - Myocardium (isolated)
KW - Na
KW - Transmembrane potential
KW - p-Chloromercuribenzoic acid
UR - http://www.scopus.com/inward/record.url?scp=0024378596&partnerID=8YFLogxK
U2 - 10.1016/0014-2999(89)90586-4
DO - 10.1016/0014-2999(89)90586-4
M3 - Article
C2 - 2531672
AN - SCOPUS:0024378596
SN - 0014-2999
VL - 167
SP - 255
EP - 264
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
IS - 2
ER -