Korean J Physiol Pharmacol.
1998 Feb;2(1):49-54.
Effects of histamine H|2-receptor stimulation on Mg2+ efflux in perfused guinea pig heart
- Affiliations
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- 1College of Veterinary Medicine, Medical School, Chonbuk National University, Chonju, Chonbuk 561-756, Korea.
- 2Department of Pharmacology, Medical School, Chonbuk National University, Chonju, Chonbuk 561-756, Korea.
Abstract
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Mg2+ is an important regulator of many cardiac functions. However,
regulation of intracellular Mg2+ activity in the heart is not well
characterized. To assess the effect of histamine H2-receptor
stimulation on intracellular Mg2+ regulation, changes in extracellular
Mg2+ concentration were examined under a variety of conditions in
perfused guinea pig hearts. Mg2+ in the cardiac perfusate was measured
by atomic absorbance spectrophotometry. The histamine (10(-6) M induced a
marked Mg2+ efflux from the heart. The H2-receptor antagonists,
cimetidine (10(-5) M), ranitidine (10(-5) ND, but not a H1-receptor
antagonist, diphenhydramine (3 X 10(-6) M), completely blocked the
histamine-induced Mg2+ efflux. The Mg2+ efflux could also be induced by
forskolin (3 X 10(-6) M), 8-Cl-cAMP (2 X 10(-4) M), permeable cAMP
analogue, or dimaprit, (10(-5) M). However, the carbachol (10(-5) M)
considerably decreased the efflux of Mg2+. In the presence of
papaverine (10(-5) M), a phosphodiesterase inhibitor, dimaprit-induced
Mg2+ efflux was potentiated. These results suggest that a significant
Mg2+ efflux from perfused guinea pig heart by histamine can be induced
by the histamine H2-receptor stimulation and it is suggested that
cytosolic cAMP may be linked.