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10.1016/0014-2999(94)90477-4

http://scihub22266oqcxt.onion/10.1016/0014-2999(94)90477-4
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8088352!ä!8088352

suck abstract from ncbi


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pmid8088352      Eur+J+Pharmacol 1994 ; 258 (3): 167-72
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  • Influence of endothelium on Mg(2+)-induced relaxation in noradrenaline-contracted aorta from DOCA-salt hypertensive rat #MMPMID8088352
  • Laurant P; Berthelot A
  • Eur J Pharmacol 1994[Jun]; 258 (3): 167-72 PMID8088352show ga
  • The aim of this study was to examine the influence of vascular endothelium on the relaxation induced by increased extracellular Mg2+ concentrations on isolated and noradrenaline-precontracted aorta from deoxycorticosterone acetate-salt (DOCA-salt) hypertensive and normotensive rats. In Mg(2+)-free physiologic salt solution (PSS), addition of Mg2+ (0.1-6.0 nM) caused concentration-dependent relaxation of noradrenaline-precontracted aorta with intact or disrupted endothelium. Mg(2+)-induced relaxation in intact aorta, however, was less in DOCA-salt hypertensive rats than in normotensive rats. When endothelium was disrupted, Mg(2+)-induced relaxation was depressed in aorta from both DOCA-salt hypertensive and normotensive rats. The same observations were made in presence of N-nitro-L-arginine methyl ester (L-NAME), an inhibitor of endothelium-derived relaxing factor nitric oxide (EDRF/NO) biosynthesis. Mg(2+)-induced relaxation following contraction with noradrenaline was significantly less in intact aorta treated with L-NAME from DOCA-salt hypertensive rats than in intact aorta from normotensive rats. Indomethacin did not affect Mg(2+)-induced relaxation in intact aorta from normotensive rats whereas indomethacin significantly increased it in DOCA-salt hypertensive rats. It is concluded that (1) Mg(2+)-induced relaxation can be mediated by endothelium-dependent mechanisms implicating EDRF/NO; (2) the influence of EDRF/NO is more pronounced on the impaired Mg(2+)-induced relaxation of aorta from DOCA-salt hypertensive rats; (3) Mg(2+)-induced relaxation seems masked by vasoconstrictor prostaglandin release in DOCA-salt hypertensive rats; (4) these differences between normotensive and hypertensive rats could be related to the impaired endothelial function in aorta from DOCA-salt hypertensive rats.
  • |Animals[MESH]
  • |Arginine/analogs & derivatives/pharmacology[MESH]
  • |Desoxycorticosterone[MESH]
  • |Endothelium, Vascular/*physiology[MESH]
  • |Hypertension/chemically induced/*physiopathology[MESH]
  • |Magnesium/*pharmacology[MESH]
  • |Male[MESH]
  • |Muscle Contraction/drug effects[MESH]
  • |Muscle Relaxation/drug effects[MESH]
  • |Muscle, Smooth, Vascular/*drug effects[MESH]
  • |NG-Nitroarginine Methyl Ester[MESH]
  • |Nitric Oxide/antagonists & inhibitors[MESH]
  • |Norepinephrine/*pharmacology[MESH]
  • |Rats[MESH]


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