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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >The effects of prenatally administered endogenous cannabinoid on rat offspring.
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The effects of prenatally administered endogenous cannabinoid on rat offspring.

机译:产前施用内源性大麻素对大鼠后代的影响。

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摘要

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.
机译:我们以前曾报道过,大麻的主要精神活性成分,delta9四氢大麻酚(THC),在产前注射时,会暂时抑制大鼠后代下丘脑-垂体系统的发育。在本研究中,我们调查了最近描述的中枢大麻素受体内源性配体花生四烯酸乙醇酰胺(anandamide,ANA)对在下丘脑-垂体轴(HPA)产后发育的影响。妊娠。从分娩到产后第20天,每五天杀死一次幼崽。称量性腺,垂体和身体的其余部分,并收集样品以分析下丘脑中的促性腺激素释放激素和垂体和血清中的促黄体生成激素,促卵泡激素,催乳激素和生长激素。比较了ANA和THC的作用。 ANA和THC均对测量参数产生主要抑制作用。分娩后立即抑制最明显,而在研究期末(产后第20天)未观察到差异。我们得出的结论是,内源性和外源性大麻素对正在发育的HPA具有相似但略有不同的作用,且作用是暂时的。我们假设ANA可能通过中枢大麻素受体和/或神经内分泌受体发挥作用,充当神经调节剂。

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