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子宫内给予地塞米松可促进大鼠脑内新生胆碱能神经末梢的发育。

Dexamethasone treatment in utero enhances neonatal cholinergic nerve terminal development in rat brain.

作者信息

Zahalka E A, Seidler F J, Slotkin T A

机构信息

Department of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Res Commun Chem Pathol Pharmacol. 1993 Aug;81(2):191-8.

PMID:8210698
Abstract

Fetal glucocorticoid administration has been proposed to elicit both promotional and inhibitory effects on neuronal development. In the current study, pregnant rats were given 0.05, 0.2 or 0.8 mg/kg of dexamethasone on gestational days 17, 18 and 19, and the effects on development of central cholinergic projections was assessed on postnatal day 1 by measuring the specific binding of [3H]hemicholinium-3 to the high affinity choline transporter localized in cholinergic nerve terminal membranes. Dexamethasone produced a dose-dependent retardation of brain region growth, but enhanced [3H]hemicholinium-3 binding in both the forebrain and the midbrain + brainstem. At the highest dose, the promotional effect on [3H]hemicholinium-3 binding was lost in the forebrain, a region that is particularly sensitive during late gestation to inhibitory effects of glucocorticoids on neuronal development. These results indicate that, even in the face of growth retardation, glucocorticoids promote the development of central cholinergic projections; however, at high doses, inhibitory actions of the steroid can offset the promotional effects in some regions.

摘要

有人提出,给胎儿注射糖皮质激素会对神经元发育产生促进和抑制两种作用。在本研究中,于妊娠第17、18和19天给怀孕大鼠注射0.05、0.2或0.8毫克/千克的地塞米松,并在出生后第1天通过测量[3H]半胱氨酸-3与位于胆碱能神经末梢膜上的高亲和力胆碱转运体的特异性结合,评估对地中枢胆碱能投射发育的影响。地塞米松导致脑区生长出现剂量依赖性迟缓,但增强了前脑以及中脑+脑干中[3H]半胱氨酸-3的结合。在最高剂量时,前脑对[3H]半胱氨酸-3结合的促进作用消失,前脑是在妊娠后期对糖皮质激素抑制神经元发育作用特别敏感的区域。这些结果表明,即使面对生长迟缓,糖皮质激素仍能促进中枢胆碱能投射的发育;然而,在高剂量时,该类固醇的抑制作用会抵消某些区域的促进作用。

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