Literature DB >> 6738790

Naltrexone effects on pituitary neurointermediate lobe and median eminence.

L C Saland, E Reyes, E Ortiz.   

Abstract

The long-acting opiate antagonist naltrexone hydrochloride was administered by intraperitoneal injection, in a dose response protocol, to adult rats. The drug was used to observe effects of opiate receptor blockade on cells of the pituitary gland and adjacent hypothalamus. At higher drug doses (5 mg/kg or 10 mg/kg), neurites directly innervating pars intermedia cells contained swollen vesicles and disrupted membranous elements. Fibers within the median eminence of the hypothalamus appeared swollen, and contained myelin figures. Despite the consistent degenerative changes appearing in neurites, measurements of levels of dopamine, norepinephrine, and epinephrine in striatum, and hypothalamus did not differ significantly between naltrexone-treated or control animals, although there was a significant elevation of norepinephrine in the pituitary after drug treatment. At all drug dose levels administered, supraependymal neuron-like cells appeared atop the ependyma of the third ventricle above the median eminence. These observations suggest that naltrexone produces specific "neurotoxic" effects on neurites of the tuberoinfundibular system, and may induce changes in the ventricular environment which stimulate the appearance of supraependymal neurons.

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Year:  1984        PMID: 6738790     DOI: 10.1007/BF00964168

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  25 in total

1.  Relation of endogenous opioid peptides and morphine to neuroendocrine functions.

Authors:  J Meites; J F Bruni; D A Van Vugt; A F Smith
Journal:  Life Sci       Date:  1979-04-09       Impact factor: 5.037

2.  Neurotoxic action of halogenated amphetamines.

Authors:  J A Harvey
Journal:  Ann N Y Acad Sci       Date:  1978-06-12       Impact factor: 5.691

3.  Evaluation of the neurotoxic effects of p-chloroamphetamine: a histological and biochemical study.

Authors:  V J Massari; Y Tizabi; E Sanders-Bush
Journal:  Neuropharmacology       Date:  1978-07       Impact factor: 5.250

4.  Reversal of induced ischemic neurologic deficit in gerbils by the opiate antagonist naloxone.

Authors:  Y Hosobuchi; D S Baskin; S K Woo
Journal:  Science       Date:  1982-01-01       Impact factor: 47.728

5.  Long-term effects of p-chloroamphetamine and related drugs on central serotonergic mechanisms.

Authors:  E Sanders-Bush; J A Bushing; F Sulser
Journal:  J Pharmacol Exp Ther       Date:  1975-01       Impact factor: 4.030

6.  Parallel stimulation of ACTH, beta-LPH + beta-endorphin and alpha-MSH release by alpha-adrenergic agents in rat anterior pituitary cells in culture.

Authors:  V Raymond; J Lépine; V Giguère; J C Lissitzky; J Côté; F Labrie
Journal:  Mol Cell Endocrinol       Date:  1981-06       Impact factor: 4.102

7.  Opiate receptor distribution in the cerebral cortex of the Rhesus monkey.

Authors:  S P Wise; M Herkenham
Journal:  Science       Date:  1982-10-22       Impact factor: 47.728

8.  Interaction of beta-endorphin, naloxone and dopamine: effects on melanocyte-stimulating hormone secretion of amphibian pituitaries in vitro.

Authors:  L C Saland; S P Mennin; R Selinfreund; P Rasmussen
Journal:  Regul Pept       Date:  1982-05

9.  Effects of p-chloroamphetamine, a serotonin-depleting drug, on the median eminence and pituitary pars intermedia.

Authors:  L C Saland; W G Dail; E Reyes
Journal:  J Neurobiol       Date:  1980-11

10.  Naloxone prevents dark-background adaptation in amphibians.

Authors:  S P Mennin; L C Saland
Journal:  Neuroendocrinology       Date:  1980-12       Impact factor: 4.914

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  1 in total

1.  Regulation of secretory granule formation in chronically hypersecretory melanotrophs in the rat pituitary.

Authors:  N Bäck; S Soinila
Journal:  Cell Tissue Res       Date:  1994-02       Impact factor: 5.249

  1 in total

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