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Adenosine (1 microM) activation of the Na+/Ca2+-exchanger and the Ca(2+)-channel was studied on isolated smooth muscle cells of the rat aorta. The Na+/Ca2+-exchanger was activated by adenosine. It was shown that activation of the Na+/Ca2+-exchanger by adenosine is realized through phosphorylation of a protein binding adenosine, activation of the Na+/Ca2+-exchanger by adenosine is realized through phosphorylation of a protein binding adenosine. Na+/Ca2+-exchanger requires the participation of phosphorylation of a protein bound by adenosine in order to restore the fluxes of Na+ and Ca2+ through the cell membrane. Adenosine activation of the Ca2+-channel produces an increase in the intracellular concentration of Ca2+. This effect can be achieved by both the efflux and influx of Ca2+ through the Ca2+-channels opened by adenosine. The observation of the kinetics of Ca2+ transients showed that Na+/Ca2+-exchanger activation by adenosine provides a fast but transitory inactivation of the Ca(2+)-channels and the Na+/Ca2+-exchanger activation by adenosine provides a fast but transitory inactivation of the Ca(2+)-channels and Ca(2+)-channels are resistant to the effect of Na+/Ca2+-exchanger activation by adenosine.Biology, chemistry, and biochemistry of high-pressure mercury vapor.
Mercury has many uses in medical and industrial applications, but the increasing demand for these applications has led to an increase in the environmental loads of mercury.
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