Popoola Daniel O, Cameron Nicole M
Department of Psychology, Center for Developmental and Behavioral Neuroscience, Binghamton University, Binghamton, New York.
Developmental Exposure Alcohol Research Center, Binghamton University, Binghamton, New York.
Dev Psychobiol. 2018 May;60(4):380-394. doi: 10.1002/dev.21607. Epub 2018 Feb 14.
This study investigated the effect of maternal care on adolescent ethanol consumption, sensitivity to ethanol-induced hypnosis, as well as gonadal hormones and γ-aminobutyric acid type-A (GABA ) systems. Long Evans rat dams were categorized by maternal licking/grooming (LG) frequency into High- and Low-LG mothers. Both female and male offspring from Low-LG rats demonstrated a greater sensitivity to ethanol-induced hypnosis in the loss-of-righting-reflex test at ethanol doses of 3.0 and 3.5 g/kg during late-adolescence (postnatal Day 50) but not at mid-adolescence (postnatal Day 42). However, we found no effect of maternal care on consumption of a 5% ethanol solution in a two-bottle choice test. We further investigated the association between the observed variations in sensitivity to ethanol-induced hypnosis and baseline hormonal levels in males. In male offspring from Low-LG mothers compared to High-LG mothers, baseline plasma corticosterone and progesterone levels were higher. GABA α1 and δ subunit expressions were also higher in the cerebral cortex of Low-LG males but lower in the cerebellar synaptosomal fraction. Early environmental influences on adolescent sensitivity to ethanol-induced hypnosis, consumption, and preference may be mediated by gonadal hormones and possibly through GABAergic functions.
本研究调查了母性关怀对青少年乙醇消费、乙醇诱导催眠的敏感性以及性腺激素和γ-氨基丁酸A型(GABA)系统的影响。将Long Evans大鼠母鼠按舔舐/梳理(LG)频率分为高LG和低LG母鼠。低LG大鼠的雌性和雄性后代在青春期后期(出生后第50天)乙醇剂量为3.0和3.5 g/kg的翻正反射消失试验中对乙醇诱导的催眠表现出更高的敏感性,但在青春期中期(出生后第42天)则没有。然而,我们发现在双瓶选择试验中母性关怀对5%乙醇溶液的消费没有影响。我们进一步研究了观察到的对乙醇诱导催眠的敏感性变化与雄性基线激素水平之间的关联。与高LG母亲的雄性后代相比,低LG母亲的雄性后代基线血浆皮质酮和孕酮水平更高。低LG雄性大鼠大脑皮质中GABAα1和δ亚基的表达也更高,但在小脑突触体部分则更低。早期环境对青少年对乙醇诱导催眠的敏感性、消费和偏好的影响可能由性腺激素介导,也可能通过GABA能功能介导。