Centre for Clinical Pharmacology and Therapeutics, Division of Medicine, University College London, London, UK.
Center for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative, and Pain Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Clin Pharmacol Ther. 2018 Oct;104(4):675-686. doi: 10.1002/cpt.980. Epub 2018 Jan 30.
Anabasum is a synthetic analog of Δ -tetrahydrocannabinol (THC)-11-oic acid that in preclinical models of experimental inflammation exerts potent anti-inflammatory actions with minimal central nervous system (CNS) cannabimimetic activity. Here we used a novel model of acute inflammation driven by i.d. UV-killed E. coli in healthy humans and found that anabasum (5 mg) exerted a potent anti-inflammatory effect equivalent to that of prednisolone in terms of inhibiting neutrophil infiltration, the hallmark of acute inflammation. These effects arose from the inhibition of the neutrophil chemoattractant LTB , while the inhibition of antiphagocytic prostanoids (PGE , TxB , and PGF α) resulted in enhanced clearance of inflammatory stimulus from the injected site. Anabasum at the higher dose of 20 mg possessed the additional properties of triggering the biosynthesis of specialized pro-resolving lipid mediators including LXA , LXB , RvD1, and RvD3. Collectively, we demonstrate for the first time a striking anti-inflammatory and pro-resolution effects of a synthetic analog of THC in healthy humans.
Anabasum 是一种合成的 Δ -四氢大麻酚(THC)-11-羧酸类似物,在实验性炎症的临床前模型中,它具有强大的抗炎作用,而对中枢神经系统(CNS)的大麻样活性最小。在这里,我们使用了一种新的急性炎症模型,该模型由健康人体中经皮紫外线杀死的大肠杆菌驱动,发现 anabasum(5mg)在抑制中性粒细胞浸润方面具有与强的松龙相当的强大抗炎作用,这是急性炎症的标志。这些作用来自于对中性粒细胞趋化因子 LTB 的抑制,而对抗吞噬性前列腺素(PGE、TxB 和 PGFα)的抑制导致炎症刺激物从注射部位的清除增强。Anabasum 的高剂量 20mg 还具有触发包括 LXA、LXB、RvD1 和 RvD3 在内的专门的促解决脂质介质的生物合成的额外特性。总的来说,我们首次在健康人群中证明了 THC 合成类似物具有显著的抗炎和促解决作用。