Senn Roey, Keren Ora, Hefetz Aya, Sarne Yosef
The Mauerberger Chair in Neuropharmacology, Department of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv 69978, Israel.
Pharmacol Biochem Behav. 2008 Jan;88(3):230-7. doi: 10.1016/j.pbb.2007.08.005. Epub 2007 Aug 23.
We have previously reported that an injection of a single, extremely low dose (0.001 mg/kg) of delta 9-tetrahydrocannabinal (THC, the major psychoactive ingredient of marijuana) to mice deteriorated their performance in the Morris water maze test 3 weeks later. In the present study we verify our original findings and show that the long-term cognitive deficits that are induced in mice by a low dose of THC are even more pronounced in another behavioral test-the water T-maze. This effect was abolished by the CB1 receptor antagonist SR141716A, indicating the involvement of CB1 receptors. In an attempt to find a biochemical correlate to these deleterious consequences of such a low dose of THC, we investigated its effect on the activation of extracellular signal-regulated kinase (ERK1/2) in the cerebellum and hippocampus of the mice, two brain regions that were shown to participate in spatial learning. A significant increase in ERK1/2 phosphorylation was found in the cerebellum of mice 24 h following the injection of 0.001 mg/kg THC. These findings lead to further studies into the neuronal mechanisms underlying the long-term deleterious effects of THC and should be taken into consideration when evaluating the therapeutic benefits of cannabinoid drugs.
我们之前报道过,给小鼠注射单次极低剂量(0.001毫克/千克)的δ9-四氢大麻酚(THC,大麻的主要精神活性成分),3周后其在莫里斯水迷宫试验中的表现变差。在本研究中,我们验证了最初的发现,并表明低剂量THC在小鼠中诱导的长期认知缺陷在另一行为测试——水T迷宫中更为明显。CB1受体拮抗剂SR141716A消除了这种效应,表明CB1受体参与其中。为了找到与这种低剂量THC的这些有害后果相关的生化关联,我们研究了其对小鼠小脑和海马体中细胞外信号调节激酶(ERK1/2)激活的影响,这两个脑区已被证明参与空间学习。注射0.001毫克/千克THC后24小时,小鼠小脑中ERK1/2磷酸化显著增加。这些发现促使人们进一步研究THC长期有害作用的神经元机制,并且在评估大麻素药物的治疗益处时应予以考虑。