Author:
Mitašíková M,Lin H,Soukup T,Imanaga I,Tribulová N
Abstract
We have examined the changes of intercellular electrical coupling
protein connexin-43 (Cx43) and of PKC-ε in heart atria of diabetic
rats and/or after the treatment with triiodothyronine (T3).
Diabetes was induced in Wistar-Kyoto rats by streptozotocin
(50 mg/kg, i.v.) and atria were examined after 5 (acute stage)
and 10 (chronic stage) weeks. T3 (10 μg/100 g/day) was applied
via a gastric tube for the last 10 days prior to the end of the
experiments to non-diabetic and to the half of diabetic rats.
Expression and phosphorylated status of Cx43, as well as
expression of PKC-ε, were analyzed by Western blots using
mouse monoclonal anti-Cx43 and rabbit polyclonal anti-PKC-ε
antibodies. We found that the Cx43 expression was significantly
increased after the treatment with T3 and in the acute diabetes.
Both in diabetes and after T3 treatment the phosphorylation of
Cx43 isoforms was markedly suppressed compared to the nondiabetic and T3-untreated controls. Such a down-regulation was
less pronounced in diabetic rats after the T3-treatment. The
expression of atrial PKC-ε was increased in diabetic rats. This
increase was suppressed after T3 administration and the
expression was decreased in T3-treated non-diabetic rats. We
suggest that the reduced Cx43 phosphorylation in diabetic and
hyperthyroid rats can deteriorate a cell-to-cell coupling and
consequently facilitate a development of atrial tachyarrhythmia in
diabetic or hyperthyroid animals.
Publisher
Institute of Physiology of the Czech Academy of Sciences
Subject
General Medicine,Physiology
Cited by
40 articles.
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