Dong C J, Picaud S A, Werblin F S
Department of Molecular and Cell Biology, University of California at Berkeley 94720.
J Neurosci. 1994 May;14(5 Pt 1):2648-58. doi: 10.1523/JNEUROSCI.14-05-02648.1994.
The effects of GABA and related agents were studied in solitary rod- and cone-driven horizontal cells, acutely isolated from the catfish retina using enzymatic and mechanical treatment. Both types of horizontal cells, which normally receive glutamatergic input from photoreceptors, responded to pressure ejection of the glutamate analog kainate (50 microM) with an inward current of 300-800 pA when voltage-clamped at -70 mV using the whole-cell patch-clamp technique. But pressure ejection of GABA (500 microM) elicited an inward current only in cone-driven horizontal cells. This current, ranging between 100 and 400 pA, consisted of two components: (1) a GABA receptor-gated chloride current that reversed near the chloride equilibrium potential and was blocked by bath application of picrotoxin (100-500 microM), and (2) a GABA transporter-mediated current that was picrotoxin resistant but was blocked by NO-711 (1 microM) and cis-4-hydroxynipecotic acid (250 microM), two potent GABA transporter blockers. The GABA transporter current could also be eliminated when sodium was replaced by either choline or lithium in the bathing medium. The picrotoxin-sensitive receptor-gated current could not be elicited by the GABAB receptor agonist baclofen, nor could it be blocked by the potent GABAB receptor antagonist 2-hydroxysaclofen. The picrotoxin-sensitive current could be divided into two components based on their sensitivity to the specific GABAA receptor antagonist bicuculline methiodide. The bicuculline-sensitive component was found only in some cells, whereas the bicuculline-resistant, picrotoxin-sensitive component was found in all cells tested. The bicuculline-resistant current was insensitive to pentobarbital, an allosteric modulator of GABAA receptor. To confirm the effectiveness of the specific batch of bicuculline methiodide and pentobarbital, we tested both drugs in ganglion cells in the salamander retinal slice preparation, where the GABA-elicited current is almost exclusively mediated by GABAA receptors. Bicuculline methiodide almost completely blocked, while pentobarbital significantly enhanced, the GABA current recorded in ganglion cells. Thus, in catfish cone horizontal cells the bicuculline-resistant GABA receptor current is most likely mediated by the GABAC receptor based on the above pharmacological profile. The relative effectiveness of GABA, muscimol, trans- and cis-4-aminocrotonic acid (TACA and CACA) was determined at this GABAC receptor site after cells were bathed in choline Ringer to eliminate the transporter current and in the presence of 100 microM bicuculline methiodide to block GABAA receptor current.(ABSTRACT TRUNCATED AT 400 WORDS)
利用酶解和机械处理从鲶鱼视网膜急性分离出单个视杆和视锥驱动的水平细胞,研究了γ-氨基丁酸(GABA)及相关药物的作用。这两种水平细胞通常接受来自光感受器的谷氨酸能输入,当使用全细胞膜片钳技术在-70 mV电压钳制时,对谷氨酸类似物海人酸(50 μM)的压力喷射产生300 - 800 pA的内向电流。但GABA(500 μM)的压力喷射仅在视锥驱动的水平细胞中引发内向电流。该电流在100至400 pA之间,由两个成分组成:(1)一种GABA受体门控氯离子电流,其反转电位接近氯离子平衡电位,可被浴槽中加入苦味毒(100 - 500 μM)阻断;(2)一种GABA转运体介导的电流,其对苦味毒有抗性,但可被两种有效的GABA转运体阻断剂NO - 711(1 μM)和顺式4 - 羟基烟酸(250 μM)阻断。当在浴槽液中用胆碱或锂替代钠时,GABA转运体电流也可被消除。苦味毒敏感的受体门控电流不能由GABAB受体激动剂巴氯芬引发,也不能被强效GABAB受体拮抗剂2 - 羟基 saclofen阻断。基于对特异性GABAA受体拮抗剂甲硫酸荷包牡丹碱的敏感性,苦味毒敏感电流可分为两个成分。仅在一些细胞中发现了对荷包牡丹碱敏感成分,而在所有测试细胞中均发现了对荷包牡丹碱耐药、对苦味毒敏感的成分。对荷包牡丹碱耐药的电流对戊巴比妥不敏感,戊巴比妥是GABAA受体的变构调节剂。为了证实特定批次甲硫酸荷包牡丹碱和戊巴比妥的有效性,我们在蝾螈视网膜切片标本中的神经节细胞中测试了这两种药物,在该标本中,GABA引发的电流几乎完全由GABAA受体介导。甲硫酸荷包牡丹碱几乎完全阻断了神经节细胞中记录到的GABA电流,而戊巴比妥则显著增强了该电流。因此,基于上述药理学特征,在鲶鱼视锥水平细胞中,对荷包牡丹碱耐药的GABA受体电流很可能由GABAC受体介导。在细胞用胆碱林格液浴用以消除转运体电流并在存在100 μM甲硫酸荷包牡丹碱以阻断GABAA受体电流的情况下,测定了GABA、蝇蕈醇、反式和顺式4 - 氨基巴豆酸(TACA和CACA)在该GABAC受体位点的相对效力。(摘要截短于400字)