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Pressor Responses to Ephedrine Are Mediated by a Direct Mechanism in the Rat
The mechanism of the pressor response to ephedrine is controversial. In the present study. i.v. injections of ephedrine increased systemic and pulmonary arterial pressure, and i.a. injections decreased hindlimb blood flow in a dose-related manner. Responses to ephedrine were inhibited by α-receptor...
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Published in: | The Journal of pharmacology and experimental therapeutics 2006-01, Vol.316 (1), p.95-105 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The mechanism of the pressor response to ephedrine is controversial. In the present study. i.v. injections of ephedrine increased
systemic and pulmonary arterial pressure, and i.a. injections decreased hindlimb blood flow in a dose-related manner. Responses
to ephedrine were inhibited by α-receptor blocking agents and were not attenuated by blockade of the norepinephrine reuptake
transporter (NET) or by catecholamine depletion using reserpine or a combination of reserpine and α-methyl-p-tyrosine, whereas
responses to tyramine and amphetamine were inhibited by these treatments. The magnitude of the pressor response to ephedrine
was similar in anesthetized and conscious rats. Tachyphylaxis developed to pressor responses to ephedrine and amphetamine
with sequential injections; however, ephedrine tachyphylaxis differed in that subsequent responses to α-receptor agonists
were attenuated. These results suggest that the systemic and pulmonary pressor and hindlimb vasoconstrictor responses to ephedrine
are mediated by direct action on α-adrenergic receptors and that the release of norepinephrine from adrenergic terminals plays
no significant role. These results provide support for the hypothesis that responses to ephedrine are directly mediated in
the intact rat, whereas responses to amphetamine are mediated in a large part by the release of norepinephrine from adrenergic
terminals. |
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ISSN: | 0022-3565 1521-0103 |
DOI: | 10.1124/jpet.105.090035 |