Literature DB >> 7195294

Physical dependence on nitrous oxide in mice: resemblance to alcohol but not to opiate withdrawal.

B Milne, F W Cervenko, K H Jhamandas.   

Abstract

Mice of two strains, Crl:CD-1(1CR)Br and C57BL6, were exposed to nitrous oxide at concentrations of 50, 65 and 80 per cent for 34 or 68 hours. Cessation of nitrous oxide resulted in characteristic convulsions similar to those seen in alcohol withdrawal in all mice. These peaked in severity within 2-3 minutes after removal from nitrous oxide and declined over 6 hours. The severity and duration of these convulsions were related to the nitrous oxide concentration and duration of exposure. Naloxone or naltrexone produced no significant increase in severity of convulsions. The narcotic antagonists did not precipitate acute weight loss or characteristic jumping behaviour seen in animals dependent on opiates. These results demonstrate that chronic exposure to nitrous oxide results in development of physical dependence which resembles alcohol and not opiate dependence. Analgesia and physical dependence produced by nitrous oxide appear to be mediated through separate mechanisms.

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Year:  1981        PMID: 7195294     DOI: 10.1007/bf03007289

Source DB:  PubMed          Journal:  Can Anaesth Soc J        ISSN: 0008-2856


  19 in total

Review 1.  On the specificity of naloxone as an opiate antagonist.

Authors:  J Sawynok; C Pinsky; F S LaBella
Journal:  Life Sci       Date:  1979-11-05       Impact factor: 5.037

2.  The effect of puromycin on the biological activity of Leu-enkephalin.

Authors:  Z Vogel; M Altstein
Journal:  FEBS Lett       Date:  1979-02-01       Impact factor: 4.124

3.  Nitrous oxide stimulation of locomotor activity: evidence for an opiate-like behavioral effect.

Authors:  M D Hynes; B A Berkowitz
Journal:  J Pharmacol Exp Ther       Date:  1979-05       Impact factor: 4.030

4.  Relationship of alcohol dose to intensity of withdrawal signs in mice.

Authors:  D B Goldstein
Journal:  J Pharmacol Exp Ther       Date:  1972-02       Impact factor: 4.030

5.  Simultaneous quantitative assessment of morphine tolerance and physical dependence.

Authors:  E L Way; H H Loh; F H Shen
Journal:  J Pharmacol Exp Ther       Date:  1969-05       Impact factor: 4.030

6.  The grocery store high.

Authors:  S H Block
Journal:  Am J Psychiatry       Date:  1978-01       Impact factor: 18.112

7.  Alcohol dependence and opiate dependence: lack of relationship in mice.

Authors:  A Goldstein; B A Judson
Journal:  Science       Date:  1971-04-16       Impact factor: 47.728

8.  Endogenous opioid peptides: multiple agonists and receptors.

Authors:  J A Lord; A A Waterfield; J Hughes; H W Kosterlitz
Journal:  Nature       Date:  1977-06-09       Impact factor: 49.962

9.  Nitrous oxide "analgesia": resemblance to opiate action.

Authors:  B A Berkowitz; S H Ngai; A D Finck
Journal:  Science       Date:  1976-11-26       Impact factor: 47.728

10.  Withdrawal convulsions in mice following nitrous oxide.

Authors:  M H Harper; P M Winter; B H Johnson; D D Koblin; E I Eger
Journal:  Anesth Analg       Date:  1980-01       Impact factor: 5.108

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  5 in total

1.  Propofol-related convulsions.

Authors:  J C Bevan
Journal:  Can J Anaesth       Date:  1993-09       Impact factor: 5.063

2.  Bibliography for the control of anxiety, fear and pain in dentistry.

Authors:  G L McAlister; C L Richardson
Journal:  Anesth Prog       Date:  1982 Nov-Dec

3.  The effect of naloxone and morphine on convulsions in mice following withdrawal from nitrous oxide.

Authors:  H J Manson; G Dyke; J Melling; M Gough
Journal:  Can Anaesth Soc J       Date:  1983-01

4.  Nitrous oxide and oral premedication.

Authors:  J A Giovannitti
Journal:  Anesth Prog       Date:  1984 Mar-Apr

5.  Similar 5F-APINACA Metabolism between CD-1 Mouse and Human Liver Microsomes Involves Different P450 Cytochromes.

Authors:  Samantha V Crosby; Izzeldin Y Ahmed; Laura R Osborn; Zeyuan Wang; Mary A Schleiff; William E Fantegrossi; Swati Nagar; Paul L Prather; Gunnar Boysen; Grover P Miller
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  5 in total

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