Wenger T, Fragkakis G, Giannikou P, Yiannikakis N
Department of Human Morphology and Developmental Biology, Semmelweis University Medical School, Budapest, Hungary.
Pharmacol Biochem Behav. 1997 Oct;58(2):537-44. doi: 10.1016/s0091-3057(97)00250-5.
We reported previously that the main psychoactive component of marihuana, delta9 tetrahydrocannabinol (THC), when injected prenatally, temporarily inhibited the developing hypothalamo-pituitary system in rat offspring. In the present study, we investigated the effects of the recently described endogenous ligand for the central cannabinoid receptor, arachidonyl-ethanolamide (anandamide, ANA), on the postnatal development of the hypothalamo-pituitary axis (HPA) when administered during the third week of gestation. Rat pups were killed every fifth day from delivery to the 20th postnatal day; gonads, pituitary, and rest of body were weighed, and samples were collected for analysis of gonadotropin releasing hormone in the hypothalamus and luteinizing hormone, follicle stimulating hormone, prolactin, and growth hormone in the pituitaries and sera. The effects of ANA and THC were compared. Both ANA and THC caused predominantly inhibitory effects on the measured parameters. The inhibition was most pronounced immediately following delivery, whereas at the end of the investigated period (20th postnatal day) no differences were observed. We conclude that endogenous and exogenous cannabinoids have similar but slightly different effects on the developing HPA and that the action is transitory. We postulate that ANA probably acts via central cannabinoid receptors and/or neuroendocrine receptors to function as a neuromodulator.
我们先前报道过,大麻的主要精神活性成分Δ9-四氢大麻酚(THC)在产前注射时,会暂时抑制大鼠后代发育中的下丘脑 - 垂体系统。在本研究中,我们研究了最近描述的中枢大麻素受体的内源性配体花生四烯酸乙醇酰胺(阿南达米德,ANA)在妊娠第三周给药时对下丘脑 - 垂体轴(HPA)产后发育的影响。从出生到出生后第20天,每隔五天处死一批幼鼠;称量性腺、垂体和身体其他部分的重量,并采集样本用于分析下丘脑中的促性腺激素释放激素以及垂体和血清中的黄体生成素、卵泡刺激素、催乳素和生长激素。比较了ANA和THC的作用。ANA和THC对所测参数主要都产生抑制作用。这种抑制在出生后立即最为明显,而在研究期结束时(出生后第20天)未观察到差异。我们得出结论,内源性和外源性大麻素对发育中的HPA有相似但略有不同的作用,且这种作用是暂时的。我们推测ANA可能通过中枢大麻素受体和/或神经内分泌受体起作用,作为一种神经调节剂。