Corchero Javier, Fuentes José A, Manzanares Jorge
Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain.
J Psychopharmacol. 2002 Dec;16(4):283-9. doi: 10.1177/026988110201600401.
Chronic exposure to delta9-tetrahydrocannabinol (delta9-THC) produces an activation of preproenkephalin (PENK) gene expression in the rat hypothalamus. The levels of circulating gonadal steroids concurrently modulate this neuropeptide in male and female rats. However, whether gonadal steroids regulate delta9-THC effects on PENK gene expression in the hypothalamus of male and female rats remains unknown. To test this hypothesis, experiments were carried out on intact, 2-week-gonadectomized, 1-week-gonadectomized, 1-week-dihydrotestosterone (DHT) replaced male rats, and 2-week-gonadectomized, 1-week-gonadectomized, 1-week-oestradiol replaced female rats. One week after hormonal replacement, animals were treated with vehicle or delta9-THC (5 mg/kg/day, i.p. 7 days). In males, delta9-THC administration to intact animals induced PENK mRNA in the paraventricular nucleus (PVN) and ventromedial nucleus (VMN) of the hypothalamus. Orchidectomy did not affect basal PENK mRNA levels in the PVN, but reduced PENK mRNA levels in the VMN. However, delta9-THC treatment induced PENK gene expression to the same extent in both hypothalamic nuclei of intact, castrated and DHT-replaced males. In females, ovariectomy decreased PENK gene expression in PVN and VMN. delta9-THC administration increased PENK gene expression in castrated females, but had no effect in the oestradiol-replaced group. Taken together, these results suggest gender differences in the response of chronic exposure to cannabinoids on PENK gene expression in the hypothalamus. Furthermore, it appears that alterations in opioid gene expression induced by cannabinoids in female rats depend upon the presence or absence of circulating oestradiol.
长期暴露于9-四氢大麻酚(delta9-THC)会使大鼠下丘脑前脑啡肽原(PENK)基因表达激活。循环中的性腺类固醇水平同时调节雄性和雌性大鼠的这种神经肽。然而,性腺类固醇是否调节delta9-THC对雄性和雌性大鼠下丘脑PENK基因表达的影响仍不清楚。为了验证这一假设,对完整的、切除性腺2周的、切除性腺1周的、用二氢睾酮(DHT)替代1周的雄性大鼠,以及切除性腺2周的、切除性腺1周的、用雌二醇替代1周的雌性大鼠进行了实验。激素替代1周后,动物接受溶剂或delta9-THC(5毫克/千克/天,腹腔注射,共7天)处理。在雄性大鼠中,给完整动物注射delta9-THC可诱导下丘脑室旁核(PVN)和腹内侧核(VMN)中的PENK mRNA表达。去势对PVN中的基础PENK mRNA水平没有影响,但降低了VMN中的PENK mRNA水平。然而,delta9-THC处理在完整、去势和DHT替代的雄性大鼠的两个下丘脑核中诱导PENK基因表达的程度相同。在雌性大鼠中,卵巢切除降低了PVN和VMN中的PENK基因表达。给去势雌性大鼠注射delta9-THC可增加PENK基因表达,但对雌二醇替代组没有影响。综上所述,这些结果表明,长期接触大麻素对下丘脑PENK基因表达的反应存在性别差异。此外,大麻素在雌性大鼠中诱导的阿片类基因表达变化似乎取决于循环雌二醇的存在与否。