Fride Ester, Ponde Datta, Breuer Aviva, Hanus Lumir
Department of Behavioral Sciences, College of Judea and Samaria, Ariel 44837, Israel; Department of Molecular Biology, College of Judea and Samaria, Ariel 44837, Israel.
Neuropharmacology. 2005 Jun;48(8):1117-29. doi: 10.1016/j.neuropharm.2005.01.023. Epub 2005 Apr 26.
Delta-9 tetrahydrocannabinol (Delta(9)-THC) and (-)-cannabidiol ((-)-CBD) are major constituents of the Cannabis sativa plant with different pharmacological profiles: (Delta(9)-THC activates cannabinoid CB(1) and CB(2) receptors and induces psychoactive and peripheral effects. (-)-CBD possesses no, or very weak affinity for these receptors. We tested a series of (+)- and (-)-CBD derivatives for central and peripheral effects in mice. None of the (-)-CBD derivatives were centrally active, yet most inhibited intestinal motility. Of the five (+)-CBD derivatives, all with CB(1) receptor affinity, only (+)-7-OH-CBD-DMH (DMH=1,1-dimethylheptyl), acted centrally, while all five arrested defecation. The effects of (+)-CBD-DMH and (+)-7-OH-CBD-DMH were inhibited by the CB(1) receptor antagonist SR141716. The CB(2) receptor antagonist SR144528, and the vanilloid TRPV1 receptor antagonist capsazepine, had no influence. Further, the (-)-CBD derivatives (-)-7-COOH-CBD and (-)-7-COOH-CBD-DMH, displayed antiinflammatory activity. We suggest that (+)-CBD analogues have mixed agonist/antagonist activity in the brain. Second, (-)-CBD analogues which are devoid of cannabinoid receptor affinity but which inhibit intestinal motility, suggest the existence of a non-CB(1), non-CB(2) receptor. Therefore, such analogues should be further developed as antidiarrheal and/or antiinflammatory drugs. We propose to study the therapeutic potential of (-)- and (+)-CBD derivatives for complex conditions such as inflammatory bowel disease and cystic fibrosis.
Δ-9-四氢大麻酚(Δ9-THC)和(-)-大麻二酚((-)-CBD)是大麻植物的主要成分,具有不同的药理特性:Δ9-THC激活大麻素CB1和CB2受体,并产生精神活性和外周效应。(-)-CBD对这些受体没有或只有非常弱的亲和力。我们测试了一系列(+)-和(-)-CBD衍生物对小鼠的中枢和外周效应。所有(-)-CBD衍生物均无中枢活性,但大多数能抑制肠道蠕动。在五种具有CB1受体亲和力的(+)-CBD衍生物中,只有(+)-7-OH-CBD-DMH(DMH = 1,1-二甲基庚基)具有中枢作用,而所有五种都能抑制排便。(+)-CBD-DMH和(+)-7-OH-CBD-DMH的作用被CB1受体拮抗剂SR141716抑制。CB2受体拮抗剂SR144528和香草酸TRPV1受体拮抗剂辣椒素没有影响。此外,(-)-CBD衍生物(-)-7-COOH-CBD和(-)-7-COOH-CBD-DMH具有抗炎活性。我们认为(+)-CBD类似物在大脑中具有混合激动剂/拮抗剂活性。其次,缺乏大麻素受体亲和力但能抑制肠道蠕动的(-)-CBD类似物,提示存在一种非CB1、非CB2受体。因此,这类类似物应进一步开发为止泻和/或抗炎药物。我们建议研究(-)-和(+)-CBD衍生物对炎症性肠病和囊性纤维化等复杂病症的治疗潜力。