Proanaphylactic action of morphine is mediated through a central cholinergic mechanism.

Abstract:

:Intracerebroventricular (i.c.v.) or intravenous (i.v.) administration of morphine (10 micrograms or 25 mg/kg, respectively) increased the mortality rate in experimental anaphylaxis in mice. This effect was blocked by the opiate antagonist naltrexone administered systemically (5 mg/kg) or i.c.v. (10 micrograms). Moreover, the effect of morphine was blocked by i.c.v. administration of the muscarine antagonist methyl atropine (10 micrograms). The systemic administration of 5 mg/kg methyl atropine was ineffective in blocking the action of morphine. The results suggest that the proanaphylactic effect of morphine involves activation of cholinergic mechanisms in the central nervous system.

journal_name

Eur J Pharmacol

authors

Amir S

doi

10.1016/0014-2999(83)90274-1

subject

Has Abstract

pub_date

1983-11-11 00:00:00

pages

117-9

issue

1-2

eissn

0014-2999

issn

1879-0712

pii

0014-2999(83)90274-1

journal_volume

95

pub_type

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