Corchero J, Romero J, Berrendero F, Fernandez-Ruiz J, Ramos J A, Fuentes J A, Manzanares J
Departamento de Farmacología, Facultad de Farmacia and Unidad de Cartografía Cerebral, Instituto Pluridisciplinar, Paseo Juan XXIII, 1, Universidad Complutense de Madrid, 28040, Madrid, Spain.
Brain Res Mol Brain Res. 1999 Apr 6;67(1):148-57. doi: 10.1016/s0169-328x(99)00053-4.
The purpose of the present study was to examine the time-related effects of repeated administration of Delta9-tetrahydrocannabinol during 1, 3, 7 and 14 days on cannabinoid and mu-opioid receptor agonist-stimulated [35S]GTPgammaS binding, and CB1 cannabinoid receptor and proenkephalin gene expression in the caudate-putamen. Repeated administration with Delta9-tetrahydrocannabinol produced a time-related reduction in cannabinoid receptor synthesis and activation of signal transduction mechanisms in the caudate-putamen. Indeed, WIN-55,212-2-stimulated [35S]GTPgammaS binding decreased 24% on day 1 and then progressively decreased finding a 42% decrease on day 14. Similarly, CB1 cannabinoid receptor mRNA levels decreased (22%) on day 3, reaching 50% reduction on day 7. In contrast, a pronounced increase is detected in DAMGO-stimulated [35S]GTPgammaS binding and proenkephalin mRNA levels in the caudate-putamen. The highest degree of increase was reached on day 7 of the treatment (35% of proenkephalin mRNA levels and 62% of DAMGO-stimulated [35S]GTPgammaS binding) and then values slightly decreased on day 14. Taken together, the results of the present study indicate that, in the caudate-putamen, repeated administration with Delta9-tetrahydrocannabinol produces a time-related increase in proenkephalin gene expression and mu-opioid receptor activation of G-proteins, and a time-related decrease in CB1 cannabinoid receptor gene expression and reduction in CB1 cannabinoid receptor activation of G-proteins. These results also suggest a possible interaction between the cannabinoid and opioid systems in the caudate-putamen which may be potentially relevant in the understanding of the alterations of motor behavior that occur after prolonged exposure to cannabinoids.
本研究的目的是检测连续1、3、7和14天重复给予Δ9-四氢大麻酚对大麻素和μ-阿片受体激动剂刺激的[35S]GTPγS结合,以及尾状核-壳核中CB1大麻素受体和前脑啡肽基因表达的时间相关影响。重复给予Δ9-四氢大麻酚导致尾状核-壳核中大麻素受体合成及信号转导机制激活呈时间相关的减少。实际上,WIN-55,212-2刺激的[35S]GTPγS结合在第1天下降了24%,随后逐渐下降,在第14天下降了42%。同样,CB1大麻素受体mRNA水平在第3天下降了(22%),在第7天下降了50%。相反,在尾状核-壳核中,DAMGO刺激的[35S]GTPγS结合和前脑啡肽mRNA水平检测到明显增加。在治疗第7天达到最高增加程度(前脑啡肽mRNA水平增加35%,DAMGO刺激的[35S]GTPγS结合增加62%),然后在第14天数值略有下降。综上所述,本研究结果表明,在尾状核-壳核中,重复给予Δ9-四氢大麻酚导致前脑啡肽基因表达和G蛋白的μ-阿片受体激活呈时间相关增加,以及CB1大麻素受体基因表达和G蛋白的CB1大麻素受体激活呈时间相关减少。这些结果还提示了尾状核-壳核中大麻素和阿片系统之间可能存在相互作用,这可能与理解长期接触大麻素后发生的运动行为改变潜在相关。