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The direct effect of halothane on myocardial contraction in rat myocytes with poorly developed gap junctional intercellular communication
Author(s) -
Kanaya N.,
Kimura H.,
Nakayama M.,
Tsuchida H.,
Ohshika H.,
Namiki A.
Publication year - 1999
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1034/j.1399-6576.1999.430119.x
Subject(s) - halothane , myocyte , gap junction , medicine , heptanol , contraction (grammar) , intracellular , contractility , endocrinology , biophysics , anesthesia , microbiology and biotechnology , biology
Background: The gap junction channel plays an important role in synchronous beating in the heart, and the reduction in the amount of gap junctional intercellular communication (GJIC) is thought to be the main arrhythmogenic factor in diseased heart. However, the effect of halothane on myocardial contraction in heart tissue with less GJIC is not well known. The purpose of the present study is to examine the direct effect of halothane on myocardium with poorly expressed GJIC. Methods: Ventricular myocytes were obtained from neonatal rats by enzymatic digestion with collagenase and then cultured for 3 or 7 d. We have previously reported that the number of gap junctions at 3 d is approximately 10% of that at 7 d (1). The myocytes were stabilized in serum‐free medium, and the spontaneous beating rate and amplitude were measured by a fiberoptic sensor. Results: Heptanol (2 mM), an inhibitor of GJIC, abolished synchronized beating in myocytes cultured for 7 d. Halothane decreased the beating rate and amplitude in both groups of myocytes in a concentration‐dependent manner ( P <0.05). Halothane at 1 and 2 MAC (adult rat MAC) decreased the beating rate more in myocytes cultured for 3 d than in myocytes cultured for 7 d ( P <0.05). Halothane reduced beating amplitude equally in both groups. Asynchronous contraction developed more frequently among myocytes cultured for 3 d than for those at 7 d. Conclusion: Halothane may block the GJIC channels, and when the number of these channels is reduced, exposure to halothane may cause asynchronous beating and decrease the beating rate. However, the halothane‐induced decrease in amplitude is probably not due to blockade of GJIC because reducing the number of GJIC channels did not alter halothane’s depressant effect.