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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Age- and gender-related differences in GABAA receptor-mediated postsynaptic currents in GABAergic neurons of the substantia nigra reticulata in the rat.
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Age- and gender-related differences in GABAA receptor-mediated postsynaptic currents in GABAergic neurons of the substantia nigra reticulata in the rat.

机译:大鼠黑质网状GABA能神经元中GABA A受体介导的突触后电流的年龄和性别相关差异。

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摘要

The responsiveness of the rat anterior substantia nigra pars reticulata (SNR) GABAergic neurons to GABA(A)ergic drugs changes with age and gender, altering its role in seizure control. To determine whether maturational and gender-specific differences in the properties of spontaneous GABA(A)Rs-mediated inhibitory postsynaptic currents (sIPSCs) underlie these events, we studied sIPSCs at baseline and after application of the alpha1 GABA(A)Rs subunit selective agonist zolpidem, at postnatal days (PN) 5-9, PN12-15, and PN28-32. Results were correlated with the alpha1 and alpha 3 GABA(A)Rs subunit immunoreactivity (-ir) at PN5, PN15, and PN30, using immunochemistry. The mean frequency, amplitude and charge transfer increased whereas the 10-90% rise time and decay time accelerated with age in both genders. The faster sIPSC kinetics in older rats were paralleled by increased alpha1-ir and decreased alpha 3-ir. At PN5-9, males had more robust sIPSCs (frequency, amplitude, charge carried per event and charge transfer) than females. At PN28-32, males exhibited higher amplitudes and faster kinetics than females. The zolpidem-induced increase of decay times, amplitude and charge transfer and alpha1-ir expression were the lowest in PN5-9 males but increased with age, in both genders. Our findings demonstrate that alterations in GABA(A)Rs subunit expression partially underlie age- and gender-specific sIPSC changes in SNR neurons. However, the observation of gender differences in sIPSC kinetics that cannot be attributed to changes in perisomatic alpha1 expression suggests the existence of additional gender-specific factors that control the sIPSC kinetics in rat SNR.
机译:大鼠黑质前质网(SNR)GABA能神经元对GABA(A)能药物的反应性随年龄和性别而变化,从而改变其在癫痫发作控制中的作用。为了确定自发性GABA(A)Rs介导的抑制性突触后电流(sIPSCs)的特性是否成熟和性别差异,我们在基线和应用alpha1 GABA(A)Rs亚基选择性激动剂后研究了sIPSCs。唑吡坦,出生后(PN)5-9,PN12-15和PN28-32。使用免疫化学方法,结果与PN5,PN15和PN30处的alpha1和alpha 3 GABA(A)Rs亚基免疫反应性(-ir)相关。男女的平均频率,幅度和电荷转移均增加,而10-90%的上升时间和衰减时间随年龄增长而加快。老年大鼠更快的sIPSC动力学与增加的alpha1-ir和减少的alpha 3-ir并存。在PN5-9上,雄性比雌性具有更强健的sIPSC(频率,幅度,每次事件携带的电荷和电荷转移)。在PN28-32,雄性比雌性表现出更高的振幅和更快的动力学。唑吡坦诱导的衰变时间,幅度和电荷转移以及alpha1-ir表达的增加在PN5-9男性中最低,但随着年龄的增长而增加。我们的发现表明,GABA(A)Rs亚基表达的改变部分是SNR神经元中特定于年龄和性别的sIPSC变化的基础。但是,观察到不能归因于perisomatic alpha1表达变化的sIPSC动力学中的性别差异表明,存在控制大鼠SNR中sIPSC动力学的其他特定于性别的因素。

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