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预先和后处理用超低剂量的 Δ9-四氢大麻酚 (THC) 可预防戊四氮 (PTZ) 诱导的认知损伤。

Pre- and post-conditioning treatment with an ultra-low dose of Δ9-tetrahydrocannabinol (THC) protects against pentylenetetrazole (PTZ)-induced cognitive damage.

机构信息

The Adelson Center for Biology of Addictive Diseases and The Mauerberger Chair in Neuropharmacology, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv 69978, Israel.

出版信息

Behav Brain Res. 2011 Jun 20;220(1):194-201. doi: 10.1016/j.bbr.2011.02.005. Epub 2011 Feb 18.

Abstract

Preconditioning, a phenomenon where a minor noxious stimulus protects from a subsequent more severe insult, and post-conditioning, where the protective intervention is applied following the insult, offer new insight into the neuronal mechanism(s) of neuroprotection and may provide new strategies for the prevention and treatment of brain damage. We have previously reported that a single administration of an extremely low dose of Δ(9)-tetrahydrocannabinol (THC; the psychoactive ingredient of marijuana) to mice induced minor long-lasting cognitive deficits. In the present study we examined the possibility that such a low dose of THC will protect the mice from more severe cognitive deficits induced by the epileptogenic drug pentylenetetrazole (PTZ). THC (0.002 mg/kg, a dose that is 3-4 orders of magnitude lower than the doses that induce the conventional effects of THC) was administered 1-7 days before, or 1-3 days after the injection of PTZ (60 mg/kg). The consequences of this treatment were studied 3-7 weeks later by various behavioral tests that evaluated different aspects of memory and learning. We found that a single administration of THC either before or after PTZ abolished the PTZ-induced long-lasting cognitive deficits. Biochemical studies indicated a concomitant reduction in phosphorylated-ERK (extracellular signal-regulated kinase) in the cerebella of mice 7 weeks following the injection of THC. Our results suggest that a pre- or post-conditioning treatment with extremely low doses of THC, several days before or after brain injury, may provide safe and effective long-term neuroprotection.

摘要

预处理是指轻微的有害刺激可以保护机体免受随后更严重的损伤,而后处理是指在损伤后应用保护干预措施。这些现象为神经元保护的机制提供了新的见解,并可能为预防和治疗脑损伤提供新的策略。我们之前的研究报道,单次给予极低剂量的 Δ(9)-四氢大麻酚(THC;大麻的精神活性成分)可导致小鼠出现轻微且持久的认知缺陷。在本研究中,我们研究了这种低剂量的 THC 是否可以保护小鼠免受戊四氮(PTZ;致痫药物)引起的更严重的认知缺陷。THC(0.002mg/kg,该剂量比诱导 THC 常规作用的剂量低 3-4 个数量级)在给予 PTZ(60mg/kg)之前 1-7 天或之后 1-3 天给药。3-7 周后,通过各种行为测试评估记忆和学习的不同方面,研究了这种治疗的后果。我们发现,在 PTZ 之前或之后给予单次 THC 给药可消除 PTZ 诱导的持久认知缺陷。生化研究表明,在给予 THC 7 周后,小鼠小脑内磷酸化-ERK(细胞外信号调节激酶)同时减少。我们的结果表明,在脑损伤前或后几天,给予极低剂量的 THC 进行预处理或后处理,可能提供安全有效的长期神经保护。

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