Holson R R, Ali S F, Scallet A C, Slikker W, Paule M G
Division of Reproductive and Developmental Toxicology, National Center for Toxicological Research, Jefferson, Arkansas 72079.
Neurotoxicology. 1989 Fall;10(3):605-19.
Chronic exposure to cannabis extract or delta-9-tetrahydrocannabinol (THC) has been reported to produce hippocampal neuropathology in rats, as well as classical "hippocampal" behavioral deficits. In an attempt to replicate and extend these findings, male rats were exposed to THC for 13 consecutive weeks, beginning in early adolescence. Drugs were administered five consecutive days a week (Monday through Friday). There were five dose levels: vehicle control, 5, 10, or 20 mg/kg, p.o., and 20 mg/kg THC four days a week (Monday-Thursday), followed by 60 mg/kg on Friday. Following THC exposure, all animals were withdrawn from drugs for seven weeks prior to behavioral testing. Three behavioral tasks previously shown to be sensitive to hippocampal damage were assessed. These were habituation of open-field activity, 24-hr passive avoidance response retention, and complex maze performance. A fourth task, emergence latency, was also included because it has been determined to be sensitive to "anxiety" levels. To facilitate interpretation of the complex maze data, two additional experiments are also reported. One experiment tested rats exposed to trimethyltin (TMT, a potent hippocampal neurotoxicant) on the complex maze. The second assessed the affects of chronic/acute benzodiazepine (BZ) exposure upon maze performance. Test results did not suggest that chronic THC exposure produced behavioral deficits resembling those seen following hippocampal damage. Habituation rates in an activity monitor were identical for all exposure groups, and there was no passive avoidance retention deficit. Further, while TMT caused pronounced abnormalities in the complex maze, chronic THC exposure at the two highest dose levels significantly improved maze performance, similar to BZ effects on this task. Chronic THC also appeared to reduce freezing on the emergence task, another anxiolytic-like effect. These results support other reports of persistent long-term behavioral effects of chronic THC exposure. However, they suggest that some behavioral effects may more closely resemble the effects of minor tranquilizers rather than hippocampal damage.
据报道,长期接触大麻提取物或δ-9-四氢大麻酚(THC)会在大鼠中产生海马神经病理学变化,以及典型的“海马体”行为缺陷。为了重复并扩展这些研究结果,从青春期早期开始,雄性大鼠连续13周接触THC。每周连续五天(周一至周五)给药。有五个剂量水平:溶剂对照组、口服5、10或20 mg/kg,以及每周四天(周一至周四)给予20 mg/kg THC,周五给予60 mg/kg。THC暴露后,所有动物在行为测试前停药7周。评估了之前显示对海马损伤敏感的三项行为任务。这些任务包括旷场活动的习惯化、24小时被动回避反应保持以及复杂迷宫表现。还纳入了第四项任务——出现潜伏期,因为它已被确定对“焦虑”水平敏感。为便于解释复杂迷宫数据,还报告了另外两项实验。一项实验测试了接触三甲基锡(TMT,一种强效海马神经毒素)的大鼠在复杂迷宫中的表现。第二项实验评估了慢性/急性苯二氮䓬(BZ)暴露对迷宫表现的影响。测试结果并未表明长期接触THC会产生类似于海马损伤后出现的行为缺陷。所有暴露组在活动监测器中的习惯化率相同,且没有被动回避保持缺陷。此外,虽然TMT在复杂迷宫中导致了明显异常,但两个最高剂量水平的长期THC暴露显著改善了迷宫表现,类似于BZ对该任务的影响。长期接触THC似乎还能减少出现任务中的僵立反应,这是另一种类似抗焦虑的作用。这些结果支持了其他关于长期接触THC会产生持续行为影响的报道。然而,它们表明某些行为影响可能更类似于小剂量镇静剂的作用,而非海马损伤的影响。