Opioids as agents of reward-related feeding: a consideration of the evidence

被引:96
作者
Levine, AS
Billington, CJ
机构
[1] Dept VAMC, Minnesota Obes Ctr, Minneapolis, MN 55417 USA
[2] Univ Minnesota, Dept Psychiat, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
关键词
food intake; reward; palatability; peptides; NPY; CCK; opioids; ingestive behavior;
D O I
10.1016/j.physbeh.2004.04.032
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Gerard Smith was one of the pioneers in the field of neuropeptidergic control of food intake. He established methodology and criteria used to determine whether a neuropeptide acts as an endogenous satiety factor. More recently, he theorized that there are direct and indirect controls of meal size. Direct controls include those that depend upon contact of food with preabsorptive receptors from the tip of the tongue to the end of the small intestine, and indirect controls include those that do not depend upon direct contact of mucosal receptors, such as learning and metabolism. In this review, we consider the evidence that opioids are mediators of reward-related feeding. We address these issues adopting Smith's approach to problem solving, including an evaluation of the opioids as controllers of the meal. We also present a novel concept of "hedonic restriction," resulting in a change in opioid gene expression. Overall, we believe the evidence supporting opioid participation in reward-driven and other types of ingestion is very strong, but much work remains before we understand how opioids contribute to the widely distributed neural network that controls ingestive behavior. Published by Elsevier Inc.
引用
收藏
页码:57 / 61
页数:5
相关论文
共 56 条
  • [1] The effect of naltrexone on taste detection and recognition threshold
    Arbisi, PA
    Billington, CJ
    Levine, AS
    [J]. APPETITE, 1999, 32 (02) : 241 - 249
  • [2] Naltrexone fails to block the acquisition or expression of a flavor preference conditioned by intragastric carbohydrate infusions
    Azzara, AV
    Bodnar, RJ
    Delamater, AR
    Sclafani, A
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2000, 67 (03) : 545 - 557
  • [3] CENTRAL OPIOID RECEPTOR SUBTYPE ANTAGONISTS DIFFERENTIALLY ALTER SUCROSE AND DEPRIVATION-INDUCED WATER-INTAKE IN RATS
    BECZKOWSKA, IW
    BOWEN, WD
    BODNAR, RJ
    [J]. BRAIN RESEARCH, 1992, 589 (02) : 291 - 301
  • [4] CENTRAL OPIOID RECEPTOR SUBTYPE ANTAGONISTS DIFFERENTIALLY REDUCE INTAKE OF SACCHARIN AND MALTOSE DEXTRIN SOLUTIONS IN RATS
    BECZKOWSKA, IW
    KOCH, JE
    BOSTOCK, ME
    LEIBOWITZ, SF
    BODNAR, RJ
    [J]. BRAIN RESEARCH, 1993, 618 (02) : 261 - 270
  • [5] NALTREXONE, AN OPIOID BLOCKER, ALTERS TASTE PERCEPTION AND NUTRIENT INTAKE IN HUMANS
    BERTINO, M
    BEAUCHAMP, GK
    ENGELMAN, K
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (01): : R59 - R63
  • [6] OPIATE ANTAGONISTS ENHANCE THE WORKING MEMORY OF RATS IN THE RADIAL MAZE
    CANLI, T
    COOK, RG
    MICZEK, KA
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 36 (03) : 521 - 525
  • [7] Evidence that intermittent, excessive sugar intake causes endogenous opioid dependence
    Colantuoni, C
    Rada, P
    McCarthy, J
    Patten, C
    Avena, NM
    Chadeayne, A
    Hoebel, BG
    [J]. OBESITY RESEARCH, 2002, 10 (06): : 478 - 488
  • [8] Excessive sugar intake alters binding to dopamine and mu-opioid receptors in the brain
    Colantuoni, C
    Schwenker, J
    McCarthy, J
    Rada, P
    Ladenheim, B
    Cadet, JL
    Schwartz, GJ
    Moran, TH
    Hoebel, BG
    [J]. NEUROREPORT, 2001, 12 (16) : 3549 - 3552
  • [9] Pharmacology of sucrose-reinforced place-preference conditioning: Effects of naltrexone
    Delamater, AR
    Sclafani, A
    Bodnar, RJ
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2000, 65 (04) : 697 - 704
  • [10] AN OPIOID ANTAGONIST, NALTREXONE, REDUCES PREFERENCE FOR SUCROSE IN HUMANS
    FANTINO, M
    HOSOTTE, J
    APFELBAUM, M
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (01): : R91 - R96