Literature DB >> 3026557

Increased food intake after opioid microinjections into nucleus accumbens and ventral tegmental area of rat.

R F Mucha, S D Iversen.   

Abstract

The nucleus accumbens (ACC) and ventral tegmental area (VTA), two areas believed to subserve reinforcement and increases in locomotor activity produced by opioid microinjections, were examined for their involvement in opioid-produced changes in ingestive behavior. Opioids were infused bilaterally, and food and water intakes were measured for 1 h thereafter. Different morphine doses were administered and, with placements in globus pallidus and lateral ventricles as controls for diffusion, it was found that only ACC and VTA microinjections (0.1-10 nmol) produced dose-related increases in food intake. In both the ACC and VTA low doses of morphine also produced increases in water intake while in ACC high doses produced a decrease. Administration of morphine and an enkephalin analogue (Tyr-D-Met-Gly-Phe(4-NO2)-Pro-NH2) at different depths in the ACC indicated that the increase in food intake occurred at a site separate from that of the decrease in water intake. Using levorphanol, dextrorphan and morphine mixed with naloxone, it was shown that the effects were due to activation of opioid receptors. Additional experiments demonstrated that food intake is increased by ACC morphine under different levels of deprivation, with different times of testing and with availabilities of various goal objects in addition to food. The effect also did not appear to undergo development of tolerance or sensitization. It was concluded that there are sites in the ACC and VTA where increased activity of endogenous opioid peptide systems reliably increase food intake and it was hypothesized that these sites may contribute to changes in ingestive behavior after systemic morphine administration. Also, together with other effects produced by opioid microinjections into the ACC and VTA, the present findings suggest that increased opioid activity in these areas produce a pattern of behaviors similar to that produced in normal animals by food conditioned stimuli.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3026557     DOI: 10.1016/0006-8993(86)90622-0

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  37 in total

1.  On lateral septum-like characteristics of outputs from the accumbal hedonic "hotspot" of Peciña and Berridge with commentary on the transitional nature of basal forebrain "boundaries".

Authors:  Daniel S Zahm; Kenneth P Parsley; Zachary M Schwartz; Anita Y Cheng
Journal:  J Comp Neurol       Date:  2013-01-01       Impact factor: 3.215

Review 2.  The ventral pallidum: Subregion-specific functional anatomy and roles in motivated behaviors.

Authors:  David H Root; Roberto I Melendez; Laszlo Zaborszky; T Celeste Napier
Journal:  Prog Neurobiol       Date:  2015-04-06       Impact factor: 11.685

3.  A systematic investigation of the differential roles for ventral tegmentum serotonin 1- and 2-type receptors on food intake in the rat.

Authors:  Wayne E Pratt; Kara A Clissold; Peagan Lin; Amanda E Cain; Alexa F Ciesinski; Thomas R Hopkins; Adeolu O Ilesanmi; Erin A Kelly; Zachary Pierce-Messick; Daniel S Powell; Ian A Rosner
Journal:  Brain Res       Date:  2016-07-16       Impact factor: 3.252

Review 4.  Discrete neurochemical coding of distinguishable motivational processes: insights from nucleus accumbens control of feeding.

Authors:  Brian A Baldo; Ann E Kelley
Journal:  Psychopharmacology (Berl)       Date:  2007-02-23       Impact factor: 4.530

Review 5.  The hormonal signature of energy deficit: Increasing the value of food reward.

Authors:  Sarah H Lockie; Zane B Andrews
Journal:  Mol Metab       Date:  2013-08-19       Impact factor: 7.422

6.  Mu-Opioids Suppress GABAergic Synaptic Transmission onto Orbitofrontal Cortex Pyramidal Neurons with Subregional Selectivity.

Authors:  Benjamin K Lau; Brittany P Ambrose; Catherine S Thomas; Min Qiao; Stephanie L Borgland
Journal:  J Neurosci       Date:  2020-06-29       Impact factor: 6.167

7.  Striatal regulation of morphine-induced hyperphagia: an anatomical mapping study.

Authors:  V P Bakshi; A E Kelley
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

8.  Morphine acts in the parabrachial nucleus, a pontine viscerosensory relay, to produce discriminative stimulus effects.

Authors:  T V Jaeger; D van der Kooy
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

9.  Dopamine or opioid stimulation of nucleus accumbens similarly amplify cue-triggered 'wanting' for reward: entire core and medial shell mapped as substrates for PIT enhancement.

Authors:  Susana Peciña; Kent C Berridge
Journal:  Eur J Neurosci       Date:  2013-03-17       Impact factor: 3.386

Review 10.  Metabolic hormones, dopamine circuits, and feeding.

Authors:  Nandakumar S Narayanan; Douglas J Guarnieri; Ralph J DiLeone
Journal:  Front Neuroendocrinol       Date:  2009-10-28       Impact factor: 8.606

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.