Literature DB >> 8856829

Naloxone effects on sucrose-motivated behavior.

J Cleary1, D T Weldon, E O'Hare, C Billington, A S Levine.   

Abstract

The opioid system plays an important role in feeding. In general, opioid agonists typically increase feeding and opioid antagonists decrease feeding in non-food restricted animals. In food restricted animals the effects of these drugs are substantially reduced. Opioid antagonists have shown a marked effectiveness at reducing consumption of sweet foods. Explanations for this robust effect have typically focused on drug induced changes in taste, taste perception, or palatability. The current study relates the effects of the opioid antagonist naloxone on motivation to obtain different sucrose concentrations to the drug's effects on unrestricted sucrose solution consumption. Changes in motivation to respond were assessed under a progressive ratio reinforcement schedule (PR) which required increased response cost for each successive unit of sucrose solution. Motivation, as measured by the PR, increased as sucrose concentration increased and naloxone produced a dose-dependent decrease in motivation to respond for a given sucrose concentration. Thus, the effectiveness of naloxone was indirectly related to strength of the sucrose concentration. Under unrestricted access to sucrose solutions, naloxone reduced consumption greatest under the higher concentrations. The data suggest at least part of naloxone's effects on sweet tasting food may be mediated through endogenous opioid reward systems that are reflected in measures of motivation.

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Year:  1996        PMID: 8856829     DOI: 10.1007/bf02246345

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


  24 in total

1.  Progressive ratio and fixed ratio schedules of cocaine-maintained responding in baboons.

Authors:  R R Griffiths; L D Bradford; J V Brady
Journal:  Psychopharmacology (Berl)       Date:  1979-10       Impact factor: 4.530

2.  Central opioid receptor subtype antagonists differentially alter sucrose and deprivation-induced water intake in rats.

Authors:  I W Beczkowska; W D Bowen; R J Bodnar
Journal:  Brain Res       Date:  1992-09-04       Impact factor: 3.252

3.  Effects of imipramine on responding reduced by methadone.

Authors:  J Cleary; M Nader; T Thompson
Journal:  Pharmacol Biochem Behav       Date:  1986-07       Impact factor: 3.533

4.  Centrally administered opioid peptides stimulate saccharin intake in nondeprived rats.

Authors:  B A Gosnell; M J Majchrzak
Journal:  Pharmacol Biochem Behav       Date:  1989-08       Impact factor: 3.533

5.  Effects of a selective mu opioid receptor agonist and naloxone on the intake of sodium chloride solutions.

Authors:  B A Gosnell; M J Majchrzak
Journal:  Psychopharmacology (Berl)       Date:  1990       Impact factor: 4.530

6.  Central opioid receptor subtype antagonists differentially reduce intake of saccharin and maltose dextrin solutions in rats.

Authors:  I W Beczkowska; J E Koch; M E Bostock; S F Leibowitz; R J Bodnar
Journal:  Brain Res       Date:  1993-08-06       Impact factor: 3.252

7.  Naltrexone suppresses hyperphagia induced in the rat by a highly palatable diet.

Authors:  M Apfelbaum; A Mandenoff
Journal:  Pharmacol Biochem Behav       Date:  1981-07       Impact factor: 3.533

8.  Naltrexone, an opioid blocker, alters taste perception and nutrient intake in humans.

Authors:  M Bertino; G K Beauchamp; K Engelman
Journal:  Am J Physiol       Date:  1991-07

9.  Naloxone blocks that portion of feeding driven by sweet taste in food-restricted rats.

Authors:  A S Levine; D T Weldon; M Grace; J P Cleary; C J Billington
Journal:  Am J Physiol       Date:  1995-01

10.  Taste responses and preferences for sweet high-fat foods: evidence for opioid involvement.

Authors:  A Drewnowski; D D Krahn; M A Demitrack; K Nairn; B A Gosnell
Journal:  Physiol Behav       Date:  1992-02
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  26 in total

1.  The cannabinoid receptor antagonist SR 141716 attenuates overfeeding induced by systemic or intracranial morphine.

Authors:  Aaron N A Verty; Malini E Singh; Iain S McGregor; Paul E Mallet
Journal:  Psychopharmacology (Berl)       Date:  2003-04-17       Impact factor: 4.530

2.  Selective reward deficit in mice lacking beta-endorphin and enkephalin.

Authors:  Michael D Hayward; John E Pintar; Malcolm J Low
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

3.  Differential involvement of endogenous opioids in sucrose consumption and food reinforcement.

Authors:  Michael D Hayward; Alexandra Schaich-Borg; John E Pintar; Malcolm J Low
Journal:  Pharmacol Biochem Behav       Date:  2006-12-12       Impact factor: 3.533

Review 4.  Opioids for hedonic experience and dopamine to get ready for it.

Authors:  M Flavia Barbano; Martine Cador
Journal:  Psychopharmacology (Berl)       Date:  2006-10-10       Impact factor: 4.530

Review 5.  Obesity: Current and potential pharmacotherapeutics and targets.

Authors:  Vidya Narayanaswami; Linda P Dwoskin
Journal:  Pharmacol Ther       Date:  2016-10-20       Impact factor: 12.310

6.  Prenatal ethanol increases sucrose reinforcement, an effect strengthened by postnatal association of ethanol and sucrose.

Authors:  Marcela Elena Culleré; Norman E Spear; Juan Carlos Molina
Journal:  Alcohol       Date:  2013-12-12       Impact factor: 2.405

7.  Naltrexone in primary hyperphagic obesity wity hypochondriacal disorder - a clinical study.

Authors:  R S Pandey; S C Arya; D K Subbakrishna
Journal:  Indian J Psychiatry       Date:  1999-04       Impact factor: 1.759

8.  Disruption of endogenous opioid activity during instrumental learning enhances habit acquisition.

Authors:  K M Wassum; I C Cely; N T Maidment; B W Balleine
Journal:  Neuroscience       Date:  2009-07-18       Impact factor: 3.590

9.  Operant responding for sucrose by rats bred for high or low saccharin consumption.

Authors:  Blake A Gosnell; Anaya Mitra; Ross A Avant; Justin J Anker; Marilyn E Carroll; Allen S Levine
Journal:  Physiol Behav       Date:  2010-01-22

10.  Insulin acts at different CNS sites to decrease acute sucrose intake and sucrose self-administration in rats.

Authors:  Dianne P Figlewicz; Jennifer L Bennett; Sepideh Aliakbari; Aryana Zavosh; Alfred J Sipols
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2008-06-04       Impact factor: 3.619

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