Literature DB >> 60089

The pharmacology of butorphanol, a 3,14-dihydroxymorphinan narcotic antagonist analgesic.

A W Pircio, J A Gylys, R L Cavanagh, J P Buyniski, M E Bierwagen.   

Abstract

Butorphanol, a new, totally synthetic morphinan, which is chemically related to naloxone, has been demonstrated to have both analgesic and narcotic antagonist properties. In rodent antiwrithing analgesic tests, butorphanol was 4 to 30 times more potent than morphine and dl-pentazocine, respectively. As an antagonist, butorphanol was about equivalent to nalorphine and 30 times more potent than dl-pentazocine. On the basis of the naloxone-induced mouse jumping test and the lack of substitution in withdrawn morphine-dependent mice, it is estimated that the potential for physical dependence of butorphanol will be less than that of dl-pentazocine but greater than that of nalorphine and dl-cyclazocine. Animal data also show that agonistic actions of butorphanol, such as respiratory depression and miosis, reach ceiling effects which are lower than those seen with morphine with an increase in dosage. Thus, butorphanol differed from morphine which exhibited agonist effects in a dose-related manner. Butorphanol showed weak to moderate central depressant properties at doses which were considerably higher (greater than 100 X) than those producing analgesia. Minimal cardiovascular and respiratory effects were seen with butorphanol in conscious dogs.

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Year:  1976        PMID: 60089

Source DB:  PubMed          Journal:  Arch Int Pharmacodyn Ther        ISSN: 0003-9780


  14 in total

1.  Cross-tolerance and enhanced sensitivity to the response rate-decreasing effects of opioids with varying degrees of efficacy at the mu receptor.

Authors:  M J Picker; J Yarbrough
Journal:  Psychopharmacology (Berl)       Date:  1991       Impact factor: 4.530

2.  Update on butorphanol tartrate: use in small animals.

Authors:  D H Dyson
Journal:  Can Vet J       Date:  1990-02       Impact factor: 1.008

Review 3.  Butorphanol: a review of its pharmacological properties and therapeutic efficacy.

Authors:  R C Heel; R N Brogden; T M Speight; G S Avery
Journal:  Drugs       Date:  1978-12       Impact factor: 9.546

4.  Differential effects of opiate agonists-antagonists on morphine-induced hyperexcitability and analgesia in mice.

Authors:  U Filibeck; C Castellano; A Oliverio
Journal:  Psychopharmacology (Berl)       Date:  1981       Impact factor: 4.530

5.  Comparison of analgesia by intravenous butorphanol and meperidine in patients with post-operative pain.

Authors:  F M Galloway; J Hrdlicka; M Losada; R J Noveck; F S Caruso
Journal:  Can Anaesth Soc J       Date:  1977-01

6.  A double-blind comparison of butorphanol and meperidine in labour: maternal pain relief and effect on the newborn.

Authors:  A L Maduska; M Hajghassemali
Journal:  Can Anaesth Soc J       Date:  1978-09

7.  A double-blind study on the effects of butorphanol compared with morphine in balanced anaesthesia.

Authors:  A Del Pizzo
Journal:  Can Anaesth Soc J       Date:  1978-09

8.  Mu- and delta-opioid receptor antagonists precipitate similar withdrawal phenomena in butorphanol and morphine dependence.

Authors:  Y Z Feng; T Zhang; S Tokuyama; H Zhu; R W Rockhold; I K Ho
Journal:  Neurochem Res       Date:  1996-01       Impact factor: 3.996

9.  The absolute bioavailability of transnasal butorphanol in patients experiencing rhinitis.

Authors:  W C Shyu; K A Pittman; D S Robinson; R H Barbhaiya
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

10.  Abolished thermal and mechanical antinociception but retained visceral chemical antinociception induced by butorphanol in mu-opioid receptor knockout mice.

Authors:  Soichiro Ide; Masabumi Minami; Kumatoshi Ishihara; George R Uhl; Masamichi Satoh; Ichiro Sora; Kazutaka Ikeda
Journal:  Neuropharmacology       Date:  2008-03-27       Impact factor: 5.250

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