Jarrett Maegan M, Scantlebury Jordan, Parker Linda A
Department of Psychology Wilfrid Laurier University Waterloo, Ontario, Canada N2L 3C5.
Physiol Behav. 2007 Feb 28;90(2-3):425-30. doi: 10.1016/j.physbeh.2006.10.003. Epub 2006 Nov 21.
Here we provide evidence that the cannabinoid agonist, Delta9-tetrahydrocannabinol (Delta9-THC) enhances quinine palatability and the CB1 antagonist/inverse agonist, AM251, reduces sucrose and quinine palatability using the taste reactivity test, which provides a direct measure of palatability independently of appetitive behavior. In Experiment 1, rats were treated with a low dose of Delta9-THC (0.5 mg/kg) or Vehicle 30 min, 60 min, 120 min or 240 min prior to a 5-min intraoral infusion of a highly unpalatable 0.05% quinine solution. Regardless of the post-injection interval, Delta9-THC reduced rejection of quinine. The Delta9-THC-induced palatability shift was reversed by AM251. In Experiment 2, rats were injected with either AM251 (1 mg/kg) or Vehicle prior to receiving a 5-min intraoral infusion of either 32% sucrose or 0.05% quinine solution. AM251 significantly decreased sucrose-elicited hedonic reactions across both time intervals; however, AM251 did not significantly modify the rejection of 0.05% quinine solution. When the concentration of the quinine solution was reduced to 0.01% in Experiment 3, AM251 enhanced quinine aversion. Although the range of concentrations of the solutions tested in the present data is limited, our results suggest that the cannabinoid system may modulate the palatability of ingested substances regardless of the palatability of the ingested substance.
在此,我们提供证据表明,使用味觉反应测试,大麻素激动剂Δ9-四氢大麻酚(Δ9-THC)可提高奎宁的适口性,而CB1拮抗剂/反向激动剂AM251则会降低蔗糖和奎宁的适口性,该测试可独立于食欲行为直接测量适口性。在实验1中,在给大鼠口腔内输注5分钟高不可口的0.05%奎宁溶液前30分钟、60分钟、120分钟或240分钟,用低剂量的Δ9-THC(0.5毫克/千克)或赋形剂对其进行处理。无论注射后的间隔时间如何,Δ9-THC均减少了对奎宁的排斥。AM251逆转了Δ9-THC诱导的适口性变化。在实验2中,在给大鼠口腔内输注5分钟32%蔗糖或0.05%奎宁溶液前,给大鼠注射AM251(1毫克/千克)或赋形剂。在两个时间间隔内,AM251均显著降低了蔗糖引发的享乐反应;然而,AM251并未显著改变对0.05%奎宁溶液的排斥。在实验3中,当奎宁溶液的浓度降至0.01%时,AM251增强了对奎宁的厌恶。尽管本数据中测试的溶液浓度范围有限,但我们的结果表明,大麻素系统可能会调节摄入物质的适口性,而与摄入物质的适口性无关。