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本文引用的文献

1
3-Substituted pyrazole analogs of the cannabinoid type 1 (CB₁) receptor antagonist rimonabant: cannabinoid agonist-like effects in mice via non-CB₁, non-CB₂ mechanism.3-取代吡唑类大麻素 1 型受体(CB₁)拮抗剂利莫那班类似物:通过非 CB₁、非 CB₂机制在小鼠中产生类大麻素激动剂样作用。
J Pharmacol Exp Ther. 2012 Feb;340(2):433-44. doi: 10.1124/jpet.111.187815. Epub 2011 Nov 15.
2
Anti-obesity efficacy of LH-21, a cannabinoid CB(1) receptor antagonist with poor brain penetration, in diet-induced obese rats.LH-21,一种穿透血脑屏障能力差的大麻素 CB(1) 受体拮抗剂,在饮食诱导肥胖大鼠中的抗肥胖功效。
Br J Pharmacol. 2012 Apr;165(7):2274-91. doi: 10.1111/j.1476-5381.2011.01698.x.
3
Towards rational design of cannabinoid receptor 1 (CB1) antagonists for peripheral selectivity.朝向大麻素受体 1(CB1)拮抗剂外周选择性的合理设计。
Bioorg Med Chem Lett. 2011 Oct 1;21(19):5711-4. doi: 10.1016/j.bmcl.2011.08.032. Epub 2011 Aug 11.
4
CNS opioid signaling separates cannabinoid receptor 1-mediated effects on body weight and mood-related behavior in mice.CNS 阿片信号分离大麻素受体 1 介导的体重和与情绪相关的行为在小鼠中的作用。
Endocrinology. 2011 Oct;152(10):3661-7. doi: 10.1210/en.2011-1220. Epub 2011 Aug 2.
5
Structure-activity relationship studies of novel pyrazole and imidazole carboxamides as cannabinoid-1 (CB1) antagonists.新型吡唑和咪唑甲酰胺类化合物作为大麻素-1(CB1)拮抗剂的构效关系研究。
Bioorg Med Chem Lett. 2011 Aug 15;21(16):4913-8. doi: 10.1016/j.bmcl.2011.06.017. Epub 2011 Jul 7.
6
New drug targets for the treatment of obesity.治疗肥胖的新药物靶点。
Clin Pharmacol Ther. 2011 Jul;90(1):40-51. doi: 10.1038/clpt.2011.82. Epub 2011 Jun 8.
7
An overview of the metabolic effects of rimonabant in randomized controlled trials: potential for other cannabinoid 1 receptor blockers in obesity.利莫那班在随机对照试验中的代谢作用概述:其他大麻素 1 型受体阻滞剂在肥胖症中的应用潜力。
J Clin Pharm Ther. 2011 Feb;36(1):10-8. doi: 10.1111/j.1365-2710.2010.01164.x.
8
Structural and pharmacological analysis of O-2050, a putative neutral cannabinoid CB(1) receptor antagonist.O-2050 结构和药理学分析,一种假定的中性大麻素 CB(1)受体拮抗剂。
Eur J Pharmacol. 2011 Jan 25;651(1-3):96-105. doi: 10.1016/j.ejphar.2010.10.085. Epub 2010 Nov 27.
9
Synthesis and biological evaluation of bivalent ligands for the cannabinoid 1 receptor.合成和生物评价大麻素 1 受体的双价配体。
J Med Chem. 2010 Oct 14;53(19):7048-60. doi: 10.1021/jm1006676.
10
The peptide hemopressin acts through CB1 cannabinoid receptors to reduce food intake in rats and mice.这种肽类激素通过 CB1 型大麻素受体来减少老鼠的食物摄入量。
J Neurosci. 2010 May 26;30(21):7369-76. doi: 10.1523/JNEUROSCI.5455-09.2010.

吡唑和磺胺类大麻素的结构类似物:对小鼠急性食物摄入量的影响。

Structural analogs of pyrazole and sulfonamide cannabinoids: effects on acute food intake in mice.

机构信息

Research Triangle Institute, 3040 Cornwallis Drive, Research Triangle Park, NC 27709-2194, U.S.A.

出版信息

Eur J Pharmacol. 2012 Nov 15;695(1-3):62-70. doi: 10.1016/j.ejphar.2012.08.019. Epub 2012 Sep 6.

DOI:10.1016/j.ejphar.2012.08.019
PMID:22975289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3586205/
Abstract

Obesity contributes to a multitude of serious health problems. Given the demonstrated role of the endogenous cannabinoid system in appetite regulation, the purpose of the present study was to evaluate structural analogs of two cannabinoids, rimonabant (cannabinoid CB(1) receptor antagonist) and O-2050 (sulfonamide analog of Δ(8)-tetrahydrocannabinol), that showed appetite suppressant effects in previous studies. Structure-activity relationships of these two lead compounds were examined in several assays, including cannabinoid CB(1) and CB(2) receptor binding, food intake, and an in vivo test battery (locomotor activity, antinociception, ring immobility, and body temperature) in mice. Rimonabant and O-2050 reliably decreased feeding in mice; however, their analogs decreased feeding only at higher doses, even though some compounds had quite good cannabinoid CB(1) binding affinity. Results of the in vivo test battery were inconsistent, with some of the compounds producing effects characteristic of cannabinoid agonists while other compounds were inactive or were antagonists against an active dose of Δ(9)-tetrahydrocannabinol. These results demonstrate that reduction of food intake is not a characteristic effect of pyrazole and sulfonamide cannabinoid analogs with favorable cannabinoid CB(1) binding affinity, suggesting that development of these classes of cannabinoids for the treatment of obesity will require evaluation of their effects in a broad spectrum of pharmacological assays.

摘要

肥胖会导致许多严重的健康问题。鉴于内源性大麻素系统在食欲调节中的作用已得到证实,本研究旨在评估两种大麻素的结构类似物,利莫那班(大麻素 CB1 受体拮抗剂)和 O-2050(Δ8-四氢大麻酚的磺酰胺类似物),这两种物质在之前的研究中表现出了抑制食欲的效果。在几种测定方法中,包括大麻素 CB1 和 CB2 受体结合、摄食以及在活体测试中(运动活性、镇痛、环肢体不动和体温),对这两种先导化合物的结构-活性关系进行了检查。利莫那班和 O-2050 确实能减少小鼠的摄食;然而,它们的类似物仅在较高剂量下才会减少摄食,尽管有些化合物具有相当好的大麻素 CB1 结合亲和力。活体测试结果不一致,一些化合物产生了大麻素激动剂的特征效应,而其他化合物则不活跃或对活性剂量的 Δ9-四氢大麻酚呈拮抗作用。这些结果表明,降低食物摄入并不是具有良好大麻素 CB1 结合亲和力的吡唑和磺酰胺大麻素类似物的特征效应,这表明开发这些类别的大麻素用于治疗肥胖症将需要在广泛的药理学测定中评估它们的效果。