1976Experimental Biology and MedicineRequires access

Magnesium Withdrawal and Contraction of Arterial Smooth Muscle: Effects of EDTA, EGTA, and Divalent Cations

B. M. Altura, B. T. Altura

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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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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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Available 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.

Key concepts: EGTA, Divalent, Chemistry, Biophysics, Magnesium, Calcium, Contraction (grammar), Chelation

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