Ueno S, Zempel J M, Steinbach J H
Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Brain Res. 1996 Apr 1;714(1-2):49-56. doi: 10.1016/0006-8993(95)01457-8.
We had earlier found that granule neurons in cultures of small explants of neonatal rat cerebellar cortex could be placed in two groups: cells in one group showed spontaneous synaptic activity and also had a large response to applications of 1 microM gamma-aminobutyric acid (GABA) while cells in the other lacked spontaneous activity and also showed much lower sensitivity to GABA [25]. For convenience, the more responsive cells will be termed A-type neurons, while the less responsive cells will be termed B-type. We have undertaken a comparison of the responses mediated by activation of GABA A receptors for the two types of neurons. A-type neurons have a larger maximal response to GABA (about 10 times that for B-type neurons), suggesting that they express more functional GABA(A) receptors. The concentration of GABA producing half-maximal activation of A-type neurons is somewhat less (12 mu M) than that for B-type neurons (41 microM), while the Hill coefficients are similar. Responses of both types of cell desensitize to prolonged applications of GABA. At a given concentration of GABA the responses of A-type neurons desensitize more rapidly than the responses of B-type neurons, indicating that the physiological properties of the receptors differ. Responses of A-type neurons are also potentiated to a significantly lesser extent by either chlordiazepoxide or alphaxalone than are the responses of B-type neurons, indicating that the pharmacological properties of the receptors differ. These data indicate that A-type and B-type granule neurons in our cultures express GABA(A) receptors which differ in number, physiological properties and pharmacological responsiveness. We have also confirmed the observation that almost all A-type neurons also show spontaneous synaptic currents, while almost no B-type neurons do.
我们之前发现,新生大鼠小脑皮质小块外植体培养物中的颗粒神经元可分为两组:一组细胞表现出自发性突触活动,并且对施加1微摩尔γ-氨基丁酸(GABA)有较大反应,而另一组细胞缺乏自发性活动,并且对GABA的敏感性也低得多[25]。为方便起见,反应性较高的细胞将被称为A型神经元,而反应性较低的细胞将被称为B型神经元。我们对这两种类型神经元由GABA A受体激活介导的反应进行了比较。A型神经元对GABA的最大反应更大(约为B型神经元的10倍),这表明它们表达了更多功能性GABA(A)受体。使A型神经元产生半数最大激活的GABA浓度(12微摩尔)略低于B型神经元(41微摩尔),而希尔系数相似。两种类型细胞的反应在长时间施加GABA时都会脱敏。在给定的GABA浓度下,A型神经元的反应比B型神经元的反应脱敏更快,这表明受体的生理特性不同。与B型神经元的反应相比,A型神经元的反应被氯氮卓或alphaxalone增强的程度也明显较小,这表明受体的药理特性不同。这些数据表明,我们培养物中的A型和B型颗粒神经元表达的GABA(A)受体在数量、生理特性和药理反应性方面存在差异。我们还证实了以下观察结果:几乎所有A型神经元也表现出自发性突触电流,而几乎没有B型神经元表现出这种电流。