4.5 Article

Restricted daily consumption of a highly palatable food (chocolate Ensure (R)) alters striatal enkephalin gene expression

期刊

EUROPEAN JOURNAL OF NEUROSCIENCE
卷 18, 期 9, 页码 2592-2598

出版社

BLACKWELL PUBLISHING LTD
DOI: 10.1046/j.1460-9568.2003.02991.x

关键词

food motivation; nucleus accumbens; opioid peptide; rat

资金

  1. NIDA NIH HHS [DA09311, F32 DA14751] Funding Source: Medline
  2. NATIONAL INSTITUTE ON DRUG ABUSE [R01DA009311, F32DA014751] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Brain opioid peptide systems are known to play an important role in motivation, emotion, attachment behaviour, the response to stress and pain, and the control of food intake. Opioid peptides within the ventral striatum are thought to play a key role in the latter function, regulating the affective response to highly palatable, energy-dense foods such as those containing fat and sugar. It has been shown previously that stimulation of mu opiate receptors within the ventral striatum increases intake of palatable food. In the present study, we examined enkephalin peptide gene expression within the striatum in rats that had been given restricted daily access to an energy-dense, palatable liquid food, chocolate Ensure(R). Rats maintained on an ad libitum diet of rat chow and water were given 3-h access to Ensure(R) daily for two weeks. One day following the end of this period, preproenkephalin gene expression was measured with quantitative in situ hybridization. Compared with control animals, rats that had been exposed to Ensure(R) had significantly reduced enkephalin gene expression in several striatal regions including the ventral striatum (nucleus accumbens), a finding that was confirmed in a different group with Northern blot analysis. Rats fed this regimen of Ensure(R) did not differ in weight from controls. In contrast to chronic Ensure(R), acute ingestion of Ensure(R) did not appear to affect enkephalin peptide gene expression. These results suggest that repeated consumption of a highly rewarding, energy-dense food induces neuroadaptations in cognitive-motivational circuits.

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