Literature DB >> 826938

Effects of morphine alone and in combination with naloxone or d-amphetamine on shock-maintained behavior in the squirrel monkey.

L D Byrd.   

Abstract

Key-pressing behavior in the squirrel monkey was maintained under an 8-min fixed-interval (FI) schedule of electric-shock delivery. The acute i.m. administration of morphine prior to a daily session decreased response rates at doses of 1.0--3.0 mg/kg but had little systematic effect on rate at doses of 0.03-0.3 mg/kg. When naloxone was administered concomitantly with morphine prior to a session, 0.01 mg/kg naloxone required a three-fold increase in the dose of morphine necessary to obtain decreased response rates, 0.1 mg/kg naloxone required a 30-fold increase in morphine, and 1.0 mg/kg required more than a 30-fold increase in morphine. Moreover, the administration of naloxone with morphine resulted in increased rates of responding at certain combinations of doses of the two drugs. The administration of d-amphetamine (0.03 or 0.1 mg/kg) alone increased mean response rates under the FI schedule; when combined with 0.03-0.3 mg/kg morphine the increases in responding were greater than obtained with d-amphetamine alone. The negative slope of the linear regression lines relating the effects of morphine to control rates of responding engendered under the FI schedule was decreased when morphine was combined with naloxone, but not with d-amphetamine. These results show that naloxone, but not d-amphetamine, can antagonize the response-rate decreasing effect of morphine when responding in the squirrel monkey is maintained by response-produced electric shock.

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Year:  1976        PMID: 826938     DOI: 10.1007/BF00426821

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  32 in total

Review 1.  Rate-dependent effects of drugs: a review of the literature.

Authors:  D J Sanger; D E Blackman
Journal:  Pharmacol Biochem Behav       Date:  1976-01       Impact factor: 3.533

2.  EFFECTS OF DRUGS ON AVOIDANCE AND ESCAPE BEHAVIOR.

Authors:  L COOK; A C CATANIA
Journal:  Fed Proc       Date:  1964 Jul-Aug

3.  The effect of morphine sulfate on avoidance and escape behavior.

Authors:  T VERHAVE; J E OWEN; E B ROBBINS
Journal:  J Pharmacol Exp Ther       Date:  1959-03       Impact factor: 4.030

4.  Responding in the squirrel monkey under second-order schedules of shock delivery.

Authors:  L D Byrd
Journal:  J Exp Anal Behav       Date:  1972-07       Impact factor: 2.468

5.  Fixed-interval schedules of electric shock presentation: extinction and recovery of performance under different shock intensities and fixed-interval durations.

Authors:  J W McKearney
Journal:  J Exp Anal Behav       Date:  1969-03       Impact factor: 2.468

6.  Behavioral effects of separate and combined administration of naloxone and d-amphetamine.

Authors:  S G Holtzman
Journal:  J Pharmacol Exp Ther       Date:  1974-04       Impact factor: 4.030

7.  Maintenance of responding under a fixed-interval schedule of electric shock-presentation.

Authors:  J W McKearney
Journal:  Science       Date:  1968-06-14       Impact factor: 47.728

8.  Effects of morphine on behavior maintained by four simple food-reinforcement schedules.

Authors:  T Thompson; J Trombley; D Luke; D Lott
Journal:  Psychopharmacologia       Date:  1970

9.  Antagonism of the behavioral effects of morphine and methadone by narcotic antagonists in the pigeon.

Authors:  D E McMillan; P S Wolf; R A Carchman
Journal:  J Pharmacol Exp Ther       Date:  1970-11       Impact factor: 4.030

10.  Some effects of morphine and morphine antagonists on schedule-controlled behavior.

Authors:  D E McMillan; W H Morse
Journal:  J Pharmacol Exp Ther       Date:  1967-07       Impact factor: 4.030

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  1 in total

1.  Effects of clonidine and some alpha-adrenergic antagonists alone and in combination on schedule-controlled behavior in pigeons and mice.

Authors:  J L Katz
Journal:  Psychopharmacology (Berl)       Date:  1984       Impact factor: 4.530

  1 in total

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