Endothelium-dependent influence of small changes in extracellular magnesium concentration on the tone of feline middle cerebral arteries

• Published in: Stroke (1970) Vol. 22; no. 6; pp. 785 - 789
• Main Authors: SZABO, C, FARAGO, M, DORA, E, HORVATH, I, KOVACH, A. G. B
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 01-06-1991
• Subjects: Amiloride - analogs & derivatives; Amiloride - pharmacology; Animals; Biological and medical sciences; Cats; Cerebral Arteries - drug effects; Cerebral Arteries - physiology; Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges; Endothelium, Vascular - physiology; Female; Fundamental and applied biological sciences. Psychology; In Vitro Techniques; Kinetics; Magnesium - pharmacology; Male; Methylene Blue - pharmacology; Muscle Relaxation - drug effects; Muscle Tonus - drug effects; Muscle, Smooth, Vascular - drug effects; Muscle, Smooth, Vascular - physiology; Nifedipine - pharmacology; Nitric Oxide - physiology; Norepinephrine - pharmacology; Oxyhemoglobins - pharmacology; Vasodilation - drug effects; Vertebrates: nervous system and sense organs; Fissipedia; Carnivora; Middle cerebral artery; Central nervous system; Concentration; Extracellular; Endothelium; Vertebrata; Vasomotricity; Mammalia; Animal; Cat; Endothelium derived relaxing factor; Magnesium; Brain (vertebrata)
• ISSN: 0039-2499; 1524-4628
• DOI: 10.1161/01.STR.22.6.785

The aim of this study was to investigate the effect of small alterations in the extracellular magnesium concentration on the tone of feline middle cerebral arteries and to examine the role of the endothelium in these responses. We measured the isometric tension of isolated arterial rings placed between two stainless steel wires in a tissue chamber containing Krebs-Henseleit solution aerated with a gas mixture containing 95% O2 and 5% CO2 at 37 degrees C. After precontraction with noradrenaline, a decrease of the extracellular magnesium concentration from 1.2 mM to 1.0 and 0.8 mM resulted in sustained relaxations, whereas elevation of the extracellular magnesium concentration from 0.8 mM to 1.2 mM caused an increase in vascular tone when the endothelium was intact. The magnesium deficiency-related dilations were absent in endothelium-denuded vessels and were inhibited by 5 x 10(-6) M oxyhemoglobin and 10(-5) M methylene blue, suggesting the involvement of an endothelium-derived relaxing factor in this vascular response. However, 5 x 10(-7) M nifedipine or 3 x 10(-5) M dichlorobenzamil did not affect the magnesium deficiency-related relaxations. Therefore, nifedipine-sensitive calcium channels or the sodium/calcium antiport system are not involved in this vascular action of magnesium. We conclude that small alterations in the extracellular magnesium concentration, possibly within the physiological range, are able to modify the basal formation and release of endothelium-derived relaxing factor and thus alter arterial smooth muscle tone in this vascular bed.