(Hypertension. 1995;25:507-510.)
© 1995 American Heart Association, Inc.
Articles |
From the Institute of Pharmacology and Toxicology, Faculty of Medicine and Surgery, II University of Naples (Italy).
Correspondence to Dr Liberato Berrino, Institute of Pharmacology and Toxicology, Faculty of Medicine and Surgery, II University of Naples, Via Costantinopoli 16, 80138 Naples, Italy.
Abstract We investigated the possible relationship between
endothelin-1 injection into the dorsolateral periaqueductal gray area
and the glutamatergic system in the control of cardiovascular function.
Endothelin-1 was injected into the dorsolateral periaqueductal gray
area of freely moving rats at doses ranging from 0.1 to 10 pmol.
Endothelin-1 increased arterial blood pressure (from 7.0±1.6 to
55.0±4.1 mm Hg, mean±SEM) in a dose-dependent manner and induced
characteristic behavioral changes such as longitudinal rolling of the
body (barrel-rolling). DL-2-Amino-5-phosphonovaleric acid
and
(5R,10S)-(+)-5-methyl-10,11-dihydro-5H-dibenzo[D-
]cyclohepten-5,10-imine
hydrogen maleate, both selective
N-methyl-D-aspartate excitatory amino acid
receptor antagonists, but not 6-cyano-7-nitroquinoxaline-2,3-dione, a
nonN-methyl-D-aspartate excitatory amino
acid receptor antagonist, significantly decreased endothelin-1induced
cardiovascular and behavioral changes (P<.01). Prazosin and
propranolol, adrenergic blocking agents, and reserpine, a depletor of
catecholamine stores, also prevented these effects. We propose that the
glutamatergic system may exert, via
N-methyl-D-aspartate receptors, a significant
influence on endothelin-1induced cardiovascular and behavioral
effects after its injection into the periaqueductal area.
Key Words: receptors, N-methyl-D-aspartate rats endothelins periaqueductal gray hypertension, experimental
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