首页> 外文期刊>Psychopharmacology >Cannabinoid CB1 antagonists and dopamine antagonists produce different effects on a task involving response allocation and effort-related choice in food-seeking behavior.
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Cannabinoid CB1 antagonists and dopamine antagonists produce different effects on a task involving response allocation and effort-related choice in food-seeking behavior.

机译:大麻素CB1拮抗剂和多巴胺拮抗剂对涉及食物分配行为的分配和努力相关选择的任务产生不同的影响。

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RATIONALE: Cannabinoid CB1 antagonists/inverse agonists suppress food-motivated behaviors and are being evaluated as potential appetite suppressants. It has been suggested that the effects of CB1 antagonism on food motivation could be related to actions on mesolimbic dopamine (DA). If this were true, then the effects of interference with cannabinoid CB1 transmission should closely resemble the effects of interference with DA transmission. OBJECTIVE: To directly compare the effects of DA antagonists with those of CB1 antagonists/inverse agonists, the present studies employed a concurrent lever-pressing/chow-intake procedure. With this task, interference with DA transmission shifts choice behavior such that lever pressing for a preferred food is decreased but chow intake is increased. RESULTS: Rats treated with IP injections of the DA D1 antagonist SCH39166 (ecopipam; 0.05-0.2 mg/kg) or the D2 antagonist eticlopride (0.025-0.1 mg/kg) showed substantial decreases in lever pressing and concomitant increases in chow consumption. In contrast, IP administration of the CB1 neutral antagonist AM4113 (4.0-16.0 mg/kg) or the CB1 antagonist/inverse agonist AM251 (2.0-8.0 mg/kg) decreased operant responding for pellets, but there was no corresponding increase in chow intake. CONCLUSIONS: These effects of CB1 antagonists/inverse agonists were similar to those produced by the appetite suppressant fenfluramine and by prefeeding. In contrast, low doses of DA antagonists leave primary food motivation intact, but shift behaviors toward food reinforcers that can be obtained with lower response costs. These results suggest that the effects of interference with CB1 transmission are readily distinguishable from those of reduced DA transmission.
机译:理由:大麻素CB1拮抗剂/反向激动剂可抑制食物刺激行为,并被评估为潜在的食欲抑制剂。有人提出,CB1拮抗作用对食物动机的影响可能与中脑边缘多巴胺(DA)的作用有关。如果属实,那么对大麻素CB1传播的干扰效应应与对DA传播的干扰效应极为相似。目的:为了直接比较DA拮抗剂与CB1拮抗剂/反向激动剂的作用,本研究采用了同时进行的杠杆压入/摄入过程。通过此任务,对DA传输的干扰会改变选择行为,从而减少了对首选食物的操纵杆压力,但增加了食物摄入量。结果:IP注射DA D1拮抗剂SCH39166(依库帕坦; 0.05-0.2 mg / kg)或D2拮抗剂依替普利(0.025-0.1 mg / kg)进行IP注射治疗的大鼠,杠杆压迫力显着降低,同时食物消耗增加。相比之下,IP施用CB1中性拮抗剂AM4113(4.0-16.0 mg / kg)或CB1拮抗剂/反向激动剂AM251(2.0-8.0 mg / kg)降低了对药丸的反应性,但食物摄入量却没有相应增加。结论:CB1拮抗剂/反向激动剂的这些作用与食欲抑制剂芬氟拉明和预喂养产生的作用相似。相比之下,低剂量的DA拮抗剂可以使主要的食物动机保持原样,但是可以将行为转向可以以较低的响应成本获得的食物强化剂。这些结果表明,干扰CB1传输的影响很容易与降低DA传输的影响区分开。

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