Abstract |
Butorphanol, a synthetic agonist/antagonist, has been shown to act on mu-, delta- and kappa-opioid receptors. However, the relative involvement of opioid receptor subtypes in mediating butorphanol dependence is not known. In the present study, naltrindole, a delta-selective non- peptide antagonist, was administered intracerebroventricularly (i.c.v.) to mask supraspinal delta-opioid receptors before and during the induction of butorphanol dependence. Treatment with naltrindole (0.1, 1, or 10 nmol/5 microliters per rat) significantly blocked naloxone-, a nonspecific antagonist, precipitated butorphanol withdrawal behaviors (escape behavior, teeth-chattering, wet shakes, forepaw tremors, ptosis, diarrhea, body weight loss, and hypothermia) at all doses tested, and decreased ejaculation at 0.1 nmol in butorphanol-infused rats. In contrast, naltrindole treatment had no effect on yawning, nor urination. These results indicate that central delta-opioid receptors are involved in mediating butorphanol dependence in rats.
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Authors | S P Jaw, B Hoskins, I K Ho |
Journal | European journal of pharmacology
(Eur J Pharmacol)
Vol. 240
Issue 1
Pg. 67-72
(Aug 10 1993)
ISSN: 0014-2999 [Print] Netherlands |
PMID | 8405123
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Enkephalins
- Receptors, Opioid, delta
- Naltrexone
- Enkephalin, D-Penicillamine (2,5)-
- naltrindole
- Butorphanol
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Topics |
- Animals
- Butorphanol
- Enkephalin, D-Penicillamine (2,5)-
- Enkephalins
(pharmacology)
- Male
- Naltrexone
(analogs & derivatives, pharmacology)
- Rats
- Rats, Sprague-Dawley
- Receptors, Opioid, delta
(physiology)
- Substance-Related Disorders
(etiology)
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