ACUTELY ISOLATED NEURONS OF THE RAT GLOBUS-PALLIDUS EXHIBIT 4 TYPES OF HIGH-VOLTAGE-ACTIVATED CA2+ CURRENT

被引:20
作者
SURMEIER, DJ [1 ]
SENO, N [1 ]
KITAI, ST [1 ]
机构
[1] SANDOZ PHARMACEUT,TSUKUBA RES INST,TSUKUBA,IBARAKI 30033,JAPAN
关键词
D O I
10.1152/jn.1994.71.3.1272
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. Large, projection-like neurons from the adult (>3 wk postnatal) rat globus pallidus (GP) were acutely isolated and subjected to whole-cell voltage-clamp (n = 37). Ca2+ currents were isolated pharmacologically in cells with whole-cell capacitances of 15-34 pF. 2. With 5 mM Ba2+ as a charge carrier, whole-cell currents began to activate near -40 mV and peaked near O mV. Based on activation threshold and inactivation kinetics, currents appeared to be of the high-voltage-activated type. 3. Cd2+ blocked whole-cell currents with an IC50 near 2 mu M. Currents activated at negative potentials were not relatively resistant to Cd2+, supporting the inference that low-voltage-activated currents were not prominent in these neurons. 4. The dihydropyridine, L-channel antagonist, nifedipine (5 mu M), reduced peak current by 21 +/- 4% (SD) (n = 10). The dihydropyridine agonist, BayK 8644 (1-2 mu M) enhanced peak current and slowed current deactivation (n = 4). 5. The N-channel antagonist, omega-conotoxin GVIA (omega-CgTx, 2 mu M) blocked 25 +/- 7% of the peak whole-cell current (n = 10). The blocks produced by omega-CgTx and nifedipine were additive, blocking an average of 46 +/- 8% of the current (n = 10). 6. The current resistant to the selective N- and L-channel antagonists was partially blocked by the P-channel antagonist omega-agatoxin IVA (omega-AgTx, 100 nM). omega-AgTx blocked about one-half of the current not attributable to N- and L-type channels (22 +/- 5% of the total current, n = 5). 7. Single cell aRNA amplification (n = 3) revealed the presence of rbC, rbB, and rbA alpha 1 subunit mRNA. 8. Our results suggest that GP projection neurons express four types of HVA current: L, N, P, and a current resistant to the available selective antagonists.
引用
收藏
页码:1272 / 1280
页数:9
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