Literature DB >> 817294

Magnesium withdrawal and contraction of arterial smooth muscle: effects of EDTA, EGTA, and divalent cations.

B M Altura, B T Altura.   

Abstract

The divalent cation chelators, CaEDTA and EGTA, were demonstrated to exert opposite effects on contractions of rat aortic smooth muscle induced by withdrawal of external magnesium ([Mg2+]0). Addition of CaEDTA potentiated such contractions more than 100%, while EGTA promoted rapid relaxation. Rapid relaxation of contractions induced by withdrawal of [Mg2+]0 could also be induced by Mn, Ni, and Cd but not Sr. Using EC50's, a relative descending order of contractile inhibition was noted for the divalent cations: Mn greater than Cd greater than Mg greater than Ni. The ability of CaEDTA to potentiate contractions produced by withdrawal of [Mg2+]0, as well as the ability of divalent cations to relax contractions of aortic smooth muscle, appears to be related to actions on the transmembrane flux of Ca2+. These findings thus lend support to the view that Mg ions either play an important role in regulating membrane permeability to [Ca2+]0 or occupy membrane sites which are exchangeable with membrane-bound Ca in certain types of aterial smooth muscle.

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Year:  1976        PMID: 817294     DOI: 10.3181/00379727-151-39300

Source DB:  PubMed          Journal:  Proc Soc Exp Biol Med        ISSN: 0037-9727


  5 in total

Review 1.  Magnesium, electrolyte transport and coronary vascular tone.

Authors:  B M Altura; B T Altura
Journal:  Drugs       Date:  1984-10       Impact factor: 9.546

2.  Withdrawal of magnesium enhances coronary arterial spasms produced by vasoactive agents.

Authors:  B M Altura; P D Turlapaty
Journal:  Br J Pharmacol       Date:  1982-12       Impact factor: 8.739

3.  The effect of magnesium on the response of smooth muscle to 5-hydroxytryptamine.

Authors:  S Goldstein; T T Zsotér
Journal:  Br J Pharmacol       Date:  1978-04       Impact factor: 8.739

4.  Pregnancy-induced alterations of relaxation in response to magnesium in the rat aorta may be due to plasma-borne agents.

Authors:  M Ezimokhai; C P Aloamaka; J Morrison
Journal:  Heart Vessels       Date:  1995       Impact factor: 2.037

5.  Stimulation of inorganic-phosphate incorporation into phosphatidylinositol in rat thoracic aorta mediated through V1-vasopressin receptors.

Authors:  A P Takhar; C J Kirk
Journal:  Biochem J       Date:  1981-01-15       Impact factor: 3.857

  5 in total

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