The neuroscience of pleasure. Focus on "Ventral pallidum firing codes hedonic reward: when a bad taste turns good".
The neuroscience of pleasure. Focus on "Ventral pallidum firing codes hedonic reward: when a bad taste turns good".
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快乐的神经科学。
DOI:
10.1152/jn.00727.2006
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发表时间:
2006
影响因子:
2.5
通讯作者:
Carelli,ReginaM
中科院分区:
文献类型:
--
作者:
Wheeler,RobertA;Carelli,ReginaM
For more than 2,000 years, philosophers have struggled to define, let alone explain, pleasure or hedonics. With contemporary animal models and techniques, scientists now have the ability to provide a comprehensive description of this affective state by examining its neural underpinnings. In this issue of the Journal of Neurophysiology (p. 2399–2409), Tindell and colleagues use an elegant, reductionist approach to take a profound step in defining these neural foundations (Tindell 2006). The authors control for various elements of reward that historically have confounded researchers ambitious enough to attempt to study such an intangible topic. Specifically, Tindell and colleagues establish a role for ventral pallidum (VP) neurons in encoding hedonics. The authors infused an unpalatable concentration of saline into the oral cavities of rats while recording the extracellular electrophysiological activity of single VP neurons. Aversive orofacial reactions to the unpalatable taste were simultaneously measured. Three days later, rats were made sodium deplete and retested. In a sodium-depleted state, these rats now exhibited a behavioral switch from aversive taste reactivity to appetitive taste reactivity coincident with increased VP activity to the infusion of saline (similar to responses for a palatable sucrose solution). The clever implicit controls indicate that the altered electrophysiological activity encodes a hedonic shift rather than alterations in motivated behavior or sensory coding. Despite the proposal over a century ago that affective state can be determined by behavioral expression (Darwin 1898), this notion remains controversial. Perhaps the most intriguing aspect of the current study is the use of taste reactivity reflecting hedonics, or in the author’s words,“liking.” Although it has been argued that this interpretation is not strong enough (Panksepp 2005), it certainly advances the conclusions of the original studies of taste reactivity as ingestion and rejection responses,(ie, a reflection of consummatory responses) that are sufficiently mediated by the caudal brain stem (Grill and Norgren 1978c). Recent pharamacological manipulations have shown that taste reactivity appears to be dissociable from consummatory behavior and is hierarchically modulated by rostral neural structures (Berridge 2000; Kelley and Berridge 2002). Taste reactivity also is distinct from motivated behavior. Rats increase appetitive taste reactivity for more palatable concentrations of intraorally infused solutions while increasing aversive taste reactivity to escalating concentrations of unpalatable tastants (Grill and Norgren 1978b). Likewise, taste reactivity is not a simple expression of reflexive sensation. When a rat learns that a sweet taste predicts illness, it doesn’t just avoid the tastant, it exhibits rejection responses as if the sweet taste is now unpalatable (Grill and Norgren 1978a).Similarly, if a palatable taste is paired with an intragastric glucose infusion, appetitive taste reactivity increases (Myers and Sclafani 2001). Thus taste reactivity appears to be reflective of the rat’s affective reaction to taste stimuli and therefore is a compelling measure of hedonics in non-humans (Berridge 2000).