Research Triangle Institute, 3040 Cornwallis Drive, Research Triangle Park, NC 27709-2194, U.S.A.
Eur J Pharmacol. 2012 Nov 15;695(1-3):62-70. doi: 10.1016/j.ejphar.2012.08.019. Epub 2012 Sep 6.
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.
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。