Fletcher P J
Psychopharmacology (Berl). 1987;92(2):192-5. doi: 10.1007/BF00177914.
The behavioural specificity of the eating elicited by the serotonergic agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) was investigated. In non-deprived rats 8-OH-DPAT (60-240 micrograms/kg) increased the consumption of solid food pellets. The consumption of an 18% glucose solution was unaffected by 60 micrograms/kg 8-OH-DPAT, and markedly reduced by 120 micrograms/kg 8-OH-DPAT. When rats were pre-fed glucose, to reduce glucose intake under control conditions, 60 micrograms/kg 8-OH-DPAT significantly decreased subsequent glucose consumption. The failure of 8-OH-DPAT to induce a hyperphagic response to glucose suggests that this compound does not elicit eating by an action upon feeding motivation. Observational analyses showed that 8-OH-DPAT-treated rats exhibited several oro-facial motor responses, including gnawing, which were attenuated by pretreatment with haloperidol. It is likely, therefore, that the increase in solid food intake elicited by 8-OH-DPAT is incidental to drug-induced gnawing. Possible mechanisms of this action are discussed.
研究了血清素能激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)引发的进食行为特异性。在未禁食的大鼠中,8-OH-DPAT(60 - 240微克/千克)增加了固体食物颗粒的摄入量。60微克/千克的8-OH-DPAT对18%葡萄糖溶液的摄入量没有影响,而120微克/千克的8-OH-DPAT则使其显著减少。当大鼠预先喂食葡萄糖以在对照条件下减少葡萄糖摄入量时,60微克/千克的8-OH-DPAT显著降低了随后的葡萄糖消耗量。8-OH-DPAT未能诱导对葡萄糖的贪食反应,这表明该化合物并非通过作用于进食动机来引发进食。观察分析表明,经8-OH-DPAT处理的大鼠表现出几种口面部运动反应,包括啃咬,这些反应在预先用氟哌啶醇处理后减弱。因此,8-OH-DPAT引起的固体食物摄入量增加可能是药物诱导的啃咬行为的附带结果。本文讨论了这种作用的可能机制。