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本文引用的文献

1
A novel peripherally restricted cannabinoid receptor antagonist, AM6545, reduces food intake and body weight, but does not cause malaise, in rodents.一种新型的外周受限型大麻素受体拮抗剂 AM6545,可减少啮齿动物的食物摄入和体重,但不会引起不适。
Br J Pharmacol. 2010 Oct;161(3):629-42. doi: 10.1111/j.1476-5381.2010.00908.x.
2
The CB1 inverse agonist AM251, but not the CB1 antagonist AM4113, enhances retention of contextual fear conditioning in rats.大麻素 CB1 反向激动剂 AM251,但不是 CB1 拮抗剂 AM4113,可增强大鼠情境恐惧条件反射的保持。
Pharmacol Biochem Behav. 2010 Jun;95(4):479-84. doi: 10.1016/j.pbb.2010.03.011. Epub 2010 Mar 27.
3
Potential anxiogenic effects of cannabinoid CB1 receptor antagonists/inverse agonists in rats: comparisons between AM4113, AM251, and the benzodiazepine inverse agonist FG-7142.大麻素 CB1 受体拮抗剂/反向激动剂在大鼠中的潜在焦虑作用:AM4113、AM251 和苯二氮䓬类反向激动剂 FG-7142 的比较。
Eur Neuropsychopharmacol. 2010 Feb;20(2):112-22. doi: 10.1016/j.euroneuro.2009.11.002. Epub 2009 Dec 16.
4
Intracerebroventricular administration of cannabinoid CB1 receptor antagonists AM251 and AM4113 fails to alter food-reinforced behavior in rats.向大鼠脑室内注射大麻素CB1受体拮抗剂AM251和AM4113不会改变大鼠的食物强化行为。
Psychopharmacology (Berl). 2009 Oct;206(2):223-32. doi: 10.1007/s00213-009-1602-8. Epub 2009 Jul 10.
5
The future of endocannabinoid-oriented clinical research after CB1 antagonists.CB1拮抗剂之后以内源性大麻素为导向的临床研究的未来。
Psychopharmacology (Berl). 2009 Jul;205(1):171-4. doi: 10.1007/s00213-009-1506-7. Epub 2009 Mar 20.
6
Oral bioavailability of the novel cannabinoid CB1 antagonist AM6527: effects on food-reinforced behavior and comparisons with AM4113.新型大麻素CB1拮抗剂AM6527的口服生物利用度:对食物强化行为的影响及与AM4113的比较。
Pharmacol Biochem Behav. 2009 Jan;91(3):303-6. doi: 10.1016/j.pbb.2008.07.013. Epub 2008 Jul 24.
7
The cannabinoid CB1 receptor inverse agonist AM 251 and antagonist AM 4113 produce similar effects on the behavioral satiety sequence in rats.大麻素CB1受体反向激动剂AM 251和拮抗剂AM 4113对大鼠行为饱腹感序列产生相似的影响。
Behav Brain Res. 2008 Nov 21;193(2):298-305. doi: 10.1016/j.bbr.2008.06.010. Epub 2008 Jun 17.
8
Multiple-dose pharmacokinetics, pharmacodynamics, and safety of taranabant, a novel selective cannabinoid-1 receptor inverse agonist, in healthy male volunteers.新型选择性大麻素-1受体反向激动剂tarabant在健康男性志愿者中的多剂量药代动力学、药效学及安全性研究
J Clin Pharmacol. 2008 Jun;48(6):734-44. doi: 10.1177/0091270008317591.
9
Cannabinoid CB1 antagonists and dopamine antagonists produce different effects on a task involving response allocation and effort-related choice in food-seeking behavior.大麻素CB1拮抗剂和多巴胺拮抗剂对一项涉及觅食行为中反应分配和努力相关选择的任务产生不同影响。
Psychopharmacology (Berl). 2008 Mar;196(4):565-74. doi: 10.1007/s00213-007-0988-4. Epub 2007 Nov 15.
10
A neutral CB1 receptor antagonist reduces weight gain in rat.一种中性CB1受体拮抗剂可减轻大鼠体重增加。
Am J Physiol Regul Integr Comp Physiol. 2007 Dec;293(6):R2185-93. doi: 10.1152/ajpregu.00663.2007. Epub 2007 Oct 24.

新型大麻素 CB1 拮抗剂 AM6545 抑制摄食和食物强化行为。

The novel cannabinoid CB1 antagonist AM6545 suppresses food intake and food-reinforced behavior.

机构信息

Department of Psychology, University of Connecticut, Storrs, CT 06269-1020, USA.

出版信息

Pharmacol Biochem Behav. 2010 Nov;97(1):179-84. doi: 10.1016/j.pbb.2010.07.021. Epub 2010 Aug 14.

DOI:10.1016/j.pbb.2010.07.021
PMID:20713079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3522179/
Abstract

Drugs that interfere with cannabinoid CB1 transmission suppress food-motivated behaviors, and may be useful clinically as appetite suppressants. However, there may also be undesirable side effects (e.g., nausea, malaise, anxiety, and depression) that are produced by the current generation of CB1 inverse agonists such as rimonabant and taranabant. For that reason, it is important to continue research on novel cannabinoid antagonists. The present studies examined the effects of the novel compound AM6545, which is a neutral antagonist of CB1 receptors that is thought to have relatively poor penetrability into the central nervous system. Intraperitoneal administration of AM6545 significantly reduced food-reinforced operant responding at doses of 4.0, 8.0 and 16.0 mg/kg. AM6545 also produced a strong suppression of the intake of high-carbohydrate and high-fat diets in the same dose range, but only produced a mild suppression of lab chow intake at the highest dose (16.0 mg/kg). Although AM6545 did not affect food handling, it did reduce time spent feeding and feeding rate. Taken together, these results suggest that AM6545 is a compound that warrants further study as a potential appetite suppressant drug.

摘要

干扰大麻素 CB1 传递的药物会抑制与食物相关的行为,并且可能作为食欲抑制剂在临床上有用。然而,当前一代的 CB1 反向激动剂(例如利莫那班和塔兰班坦)可能会产生不良的副作用(例如恶心、不适、焦虑和抑郁)。因此,继续研究新型大麻素拮抗剂非常重要。本研究检查了新型化合物 AM6545 的作用,该化合物是 CB1 受体的中性拮抗剂,据认为其对中枢神经系统的穿透力相对较差。腹腔内给予 AM6545 可显著减少 4.0、8.0 和 16.0 mg/kg 剂量的食物强化操作性反应。AM6545 还在相同剂量范围内强烈抑制高碳水化合物和高脂肪饮食的摄入,但在最高剂量(16.0 mg/kg)时仅轻度抑制实验室饲料的摄入。尽管 AM6545不影响食物处理,但它确实减少了进食时间和进食速度。总的来说,这些结果表明 AM6545 是一种值得进一步研究作为潜在食欲抑制剂药物的化合物。