Literature DB >> 1970267

Changes in preganglionic sympathetic nerve function following chronic morphine treatment in rats.

C M Leung1, S Dai, C W Ogle.   

Abstract

1. The effects of acute or chronic morphine treatment on the changes in blood pressure and pulse rate in response to ganglionic stimulation or blockade and to vagal stimulation, and of isolated atria to field stimulation or noradrenaline, were studied. 2. In pithed rats, intravenously injected hexamethonium significantly depressed the blood pressure responses to sympathetic nerve stimulation. The ganglionic blocking effects of hexamethonium were significantly greater in chronically morphine-treated rats, but were not significantly affected by acute morphine administration in naive animals. 3. Intravenous administration of nicotine dose-dependently increased blood pressure and pulse rate. The magnitudes of these changes were not significantly affected by acute or chronic morphine pretreatment. 4. Studies with rat isolated atrial preparations revealed that the changes in atrial contractile rate and force in response to noradrenaline or field stimulation were not influenced by either acute or chronic morphine treatment. 5. Cervical vagal stimulation produced voltage- or frequency-dependent decreases in pulse rate and blood pressure. The responses were not significantly affected by chronic morphine treatment. 6. These findings suggest that the site of the changes in sympathetic function following prolonged exposure to the opiate appears to be on the preganglionic nerve fibres.

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Year:  1990        PMID: 1970267      PMCID: PMC1917369          DOI: 10.1111/j.1476-5381.1990.tb14689.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  20 in total

1.  Noradrenaline supersensitivity of the mouse vas deferns after long-term treatment with morphine.

Authors:  G A Rae; J P Neto; S De Moraes
Journal:  J Pharm Pharmacol       Date:  1977-05       Impact factor: 3.765

2.  The actions of nicotine on central nervous system functions.

Authors:  H SILVETTE; E C HOFF; P S LARSON; H B HAAG
Journal:  Pharmacol Rev       Date:  1962-03       Impact factor: 25.468

3.  Cellular site of opiate dependence.

Authors:  H O Collier
Journal:  Nature       Date:  1980-02-14       Impact factor: 49.962

4.  Hypersensitivity to noradrenaline in cortex after chronic morphine: relevance to tolerance and dependence.

Authors:  C Llorens; M P Martres; M Baudry; J C Schwartz
Journal:  Nature       Date:  1978-08-10       Impact factor: 49.962

5.  Evidence for the presence of enkephalins in the heart.

Authors:  R E Lang; K Hermann; R Dietz; W Gaida; D Ganten; K Kraft; T Unger
Journal:  Life Sci       Date:  1983-01-24       Impact factor: 5.037

6.  Field stimulation as a means of effecting the graded release of autonomic transmitters in isolated heart muscle.

Authors:  J R Blinks
Journal:  J Pharmacol Exp Ther       Date:  1966-02       Impact factor: 4.030

7.  Morphine preference in rats previously morphine dependent.

Authors:  S Dai; S C Hui; C W Ogle
Journal:  Pharmacol Res Commun       Date:  1984-05

8.  Cellular mechanisms of opiate receptor stimulation in cat middle cerebral artery.

Authors:  D R Harder; J A Madden
Journal:  Eur J Pharmacol       Date:  1984-07-20       Impact factor: 4.432

9.  Supersensitivity to noradrenaline in vas deferens from morphine-dependent mice is confirmed.

Authors:  G A Rae; S De Moraes
Journal:  Eur J Pharmacol       Date:  1983-01-21       Impact factor: 4.432

10.  Opiate tolerance/dependence in the isolated guinea pig ileum is associated with an increased sensitivity to acetylcholine.

Authors:  W Kromer; N Steigemann
Journal:  Pharmacology       Date:  1982       Impact factor: 2.547

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