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大鼠丘脑皮质神经元中不同类型GABAB受体对电压激活钙电流的调节作用

Modulation by different GABAB receptor types of voltage-activated calcium currents in rat thalamocortical neurones.

作者信息

Guyon A, Leresche N

机构信息

Laboratoire de Neurobiologie Cellulaire, Institut des Neurosciences, URA 1488 CNRS, Université Pierre et Marie Curie, Paris, France.

出版信息

J Physiol. 1995 May 15;485 ( Pt 1)(Pt 1):29-42. doi: 10.1113/jphysiol.1995.sp020710.

Abstract
  1. The effects of the GABAB receptor agonist baclofen on the voltage-dependent Ca2+ currents were studied in rat thalamocortical neurones with the use of whole cell voltage-clamp recordings in brain slices. 2. The contribution of N-, L- and P-types of Ca2+ channels to the total high voltage-activated Ca2+ (HVA Ca2+) current was assessed by the use of omega-conotoxin, nifedipine and omega-agatoxin IVA, respectively. No P-type current could be detected. Thus, the HVA Ca2+ current contained an N- and an L-type current (23 and 15% of the total current, respectively) and a residual current, which will be referred to as the 'R' component. 3. Baclofen (1-50 microM) had no effect on the low voltage-activated (LVA) Ca2+ current (IT). 4. At low concentrations (0.5-10 microM), baclofen decreased the HVA Ca2+ currents by about 10-20% without a marked modification on the kinetics, whereas 50 microM baclofen decreased the HVA Ca2+ currents by about 40% with a pronounced slowing down of the kinetics. 5. The 10-20% decrease of the total HVA Ca2+ currents produced by the low concentrations of baclofen occurred as the result of a 30% block of the 'R' component. The additional decrease observed with the dose of 50 microM was due to a full block of the N-type current. The L-type was unaffected by baclofen. 6. The effect of baclofen on the total HVA Ca2+ current was partially blocked by GABAB receptor antagonists indicating that it occurred through stimulation of GABAB receptors. 7. The effect of baclofen on the N-type current was abolished by CGP 35348 (100 microM) and CGP 55845A (100 nM). The effect on the 'R' component was also antagonized by CGP 55845A (100 nM) although with a lower potency, but was not blocked by CGP 35348 (100 microM). 8. We conclude that the effects of baclofen on the various components of the HVA Ca2+ currents occur through different types of GABAB receptors. One receptor has a high affinity for baclofen (i.e. saturated by concentrations as low as 0.5 microM), is insensitive to CGP 35348, is coupled to the 'R' component and is responsible for a maximum 20% decrease in the total HVA Ca2+ current. The other receptor has a lower affinity for baclofen (i.e. affected by a concentration of 50 microM), is sensitive to CGP 35348, is coupled to the N-type Ca2+ current and is responsible for the additional 20-30% decrease in the HVA Ca2+ current observed with 50 microM baclofen.
摘要
  1. 在脑片上运用全细胞电压钳记录技术,研究了γ-氨基丁酸B(GABAB)受体激动剂巴氯芬对大鼠丘脑皮质神经元电压依赖性Ca2+电流的影响。2. 分别使用ω-芋螺毒素、硝苯地平和ω-阿加毒素IVA评估N型、L型和P型Ca2+通道对总高电压激活Ca2+(HVA Ca2+)电流的贡献。未检测到P型电流。因此,HVA Ca2+电流包含N型和L型电流(分别占总电流的23%和15%)以及一个残余电流,将其称为“R”成分。3. 巴氯芬(1 - 50微摩尔)对低电压激活(LVA)Ca2+电流(IT)无影响。4. 在低浓度(0.5 - 10微摩尔)时,巴氯芬使HVA Ca2+电流降低约10 - 20%,动力学无明显改变,而50微摩尔巴氯芬使HVA Ca2+电流降低约40%,动力学明显减慢。5. 低浓度巴氯芬使总HVA Ca2+电流降低10 - 20%是由于“R”成分被阻断30%所致。50微摩尔剂量时观察到的额外降低是由于N型电流被完全阻断。L型电流不受巴氯芬影响。6. 巴氯芬对总HVA Ca2+电流的作用被GABAB受体拮抗剂部分阻断,表明其通过刺激GABAB受体发生作用。7. CGP 35348(100微摩尔)和CGP 55845A(100纳摩尔)消除了巴氯芬对N型电流的作用。CGP 55845A(100纳摩尔)也拮抗了对“R”成分的作用,尽管效力较低,但CGP 35348(100微摩尔)未阻断该作用。8. 我们得出结论,巴氯芬对HVA Ca2+电流各成分的作用通过不同类型的GABAB受体发生。一种受体对巴氯芬具有高亲和力(即低至0.5微摩尔的浓度即可饱和),对CGP 35348不敏感,与“R”成分偶联,导致总HVA Ca2+电流最大降低20%。另一种受体对巴氯芬亲和力较低(即受50微摩尔浓度影响),对CGP 35348敏感,与N型Ca2+电流偶联,导致用50微摩尔巴氯芬时观察到的HVA Ca2+电流额外降低20 - 30%。

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