DuBois Dustin W, Parrish Alan R, Trzeciakowski Jerome P, Frye Gerald D
Department of Medical Pharmacology and Toxicology, Texas A&M University System Health Science Center, College Station, TX 77843-1114, United States.
Brain Res Dev Brain Res. 2004 Sep 17;152(2):199-212. doi: 10.1016/j.devbrainres.2004.06.017.
Whole cell GABA(A)R currents of septal neurons isolated from rat pups increase rapidly during the first weeks of life when inhibitory synapses are forming. Early postnatal binge ethanol intubation on days 4-9 delays this maturational up-regulation in septal neurons isolated several days later suggesting inhibitory synapse formation could be disrupted [S.-H. Hsiao, J.L. Acevedo, D.W. DuBois, K.R. Smith, J.R. West, G.D. Frye, Early postnatal ethanol intubation blunts GABA(A) receptor upregulation and modifies 3alpha-hydroxy-5alpha-pregnan-20-one sensitivity in rat MS/DB neurons, Brain Res. Dev. Brain Res. 130 (2001) 25-40]. Surprisingly, whole cell GABA(A)R function does not increase rapidly when septal neurons are grown for the same period in vitro and is not blunted by comparable ethanol exposure of the cultures [S.-H. Hsiao, D.W. DuBois, R.C. Miranda, G.D. Frye, Critically timed ethanol exposure reduces GABA(A)R function on septal neurons developing in vivo but not in vitro, Brain Res Dev. Brain Res. 1008 (2004) 69-80]. Because GABAergic miniature postsynaptic currents (mPSCs) show parallel patterns of maturation whether cortical neurons are growing in vivo or in vitro [D.D. Dunning, C.L. Hoover, I. Soltesz, M.A. Smith, D.K. ODowd, GABA(A) receptor-mediated miniature postsynaptic currents and alpha-subunit expression in developing cortical neurons, J. Neurophysiol. 82 (1999) 3286-3297], we examined the impact of binge ethanol exposure on synaptic receptors activated by these currents in septal cultures. Binge ethanol treatment of embryonic septal neurons over 6-11 days in vitro (DIV) slightly reduced GABA(A)R-mediated mPSC amplitude and frequency, but also substantially slowed decay kinetics when mPSCs were recorded later on DIV 13-18. Decreased frequency and slowed mPSC decay kinetics after ethanol were consistent with parameters measured in immature neurons. Untreated septal neurons exhibited decreased mPSC amplitude and frequency with acute 30-100 mM ethanol, without changing decay kinetics suggesting a direct inhibition of postsynaptic receptors. Sustained inhibition of GABA(A)Rs with 100 microM picrotoxin on DIV 6-11 decreased mPSC amplitude and frequency and slowed decay kinetics similar to binge ethanol exposure. These results suggest that binge ethanol exposure delays mPSC maturation by interfering with trophic postsynaptic GABA(A)R signaling during the early development of septal neurons.
从新生大鼠中分离出的隔区神经元的全细胞GABA(A)R电流,在出生后的头几周内,随着抑制性突触的形成而迅速增加。在出生后第4至9天进行早期产后暴饮乙醇插管,会延迟几天后分离出的隔区神经元的这种成熟上调,这表明抑制性突触的形成可能会受到干扰[S.-H.萧,J.L.阿塞韦多,D.W.杜波依斯,K.R.史密斯,J.R.韦斯特,G.D.弗莱,产后早期乙醇插管减弱大鼠内侧隔核/斜角带核神经元中GABA(A)受体上调并改变3α-羟基-5α-孕烷-20-酮敏感性,《脑研究.发育脑研究》130 (2001) 25 - 40]。令人惊讶的是,当隔区神经元在体外培养相同时间时,全细胞GABA(A)R功能并不会迅速增加,并且在培养物中进行类似的乙醇暴露时也不会减弱[S.-H.萧,D.W.杜波依斯,R.C.米兰达,G.D.弗莱,关键时期的乙醇暴露降低体内而非体外发育的隔区神经元上的GABA(A)R功能,《脑研究.发育脑研究》1008 (2004) 69 - 80]。因为无论皮质神经元是在体内还是体外生长,GABA能微小突触后电流(mPSCs)都呈现出平行的成熟模式[D.D.邓宁,C.L.胡佛,I.索尔泰斯,M.A.史密斯,D.K.奥多德,发育中的皮质神经元中GABA(A)受体介导的微小突触后电流和α亚基表达,《神经生理学杂志》82 (1999) 3286 - 3297],我们研究了暴饮乙醇暴露对隔区培养物中由这些电流激活的突触受体的影响。在体外培养6 - 11天(DIV)期间对胚胎隔区神经元进行暴饮乙醇处理,会轻微降低GABA(A)R介导的mPSC幅度和频率,但当在DIV 13 - 18后期记录mPSCs时,也会显著减慢其衰减动力学。乙醇处理后频率降低和mPSC衰减动力学减慢与在未成熟神经元中测量的参数一致。未处理的隔区神经元在急性给予30 - 100 mM乙醇时,mPSC幅度和频率降低,但衰减动力学没有改变,这表明对突触后受体有直接抑制作用。在DIV 6 - 11期间用100 μM荷包牡丹碱持续抑制GABA(A)Rs,会降低mPSC幅度和频率,并减慢衰减动力学,类似于暴饮乙醇暴露。这些结果表明,暴饮乙醇暴露通过在隔区神经元早期发育过程中干扰营养性突触后GABA(A)R信号传导,延迟了mPSC的成熟。