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豚鼠海马体中GABAB受体介导的突触前抑制是由突触前Ca2+内流减少引起的。

GABAB receptor-mediated presynaptic inhibition in guinea-pig hippocampus is caused by reduction of presynaptic Ca2+ influx.

作者信息

Wu L G, Saggau P

机构信息

Division of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

J Physiol. 1995 Jun 15;485 ( Pt 3)(Pt 3):649-57. doi: 10.1113/jphysiol.1995.sp020759.

Abstract
  1. The hypothesis that activation of GABAB receptors inhibits evoked synaptic transmission by reducing the presynaptic Ca2+ influx was tested using a recently developed technique for simultaneously recording the presynaptic Ca2+ transient ([Ca2+]t) and the field excitatory postsynaptic potential (fEPSP) evoked by a single electrical stimulus at CA3 to CA1 synapses of guinea-pig hippocampus. 2. The GABAB receptor agonist baclofen reversibly blocked, in a dose-dependant manner, both the fEPSP and the presynaptic [Ca2+]t with similar time courses. During application of baclofen, the fEPSP was proportional to about the fourth power of the presynaptic [Ca2+]t, and the presynaptic fibre volley and the resting Ca2+ level did not change. These results are similar to those we previously observed following application of several voltage-dependent Ca2+ channel blockers, suggesting that baclofen inhibits the fEPSP by blocking the presynaptic Ca2+ influx. 3. The inhibition by baclofen of both the fEPSP and the presynaptic [Ca2+]t was blocked by the GABAB receptor antagonist CGP 35348, consistent with the causal relationship between the GABAB receptor-mediated presynaptic inhibition of the [Ca2+]t and the fEPSP. 4. The inhibition by baclofen of the [Ca2+]t was partially occluded by application of the voltage-dependent Ca2+ channel blocker omega-conotoxin-GVIA (omega-CgTX-GVIA), but not omega-agatoxin-IVA (omega-AgaTX-IVA), suggesting that baclofen reduces the presynaptic [Ca2+]t by blocking Ca2+ channels including the omega-CgTX-GVIA-sensitive type. 5. We conclude that baclofen inhibits evoked transmitter release by reducing presynaptic Ca2+ influx.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 采用一种最近开发的技术来测试γ-氨基丁酸B(GABAB)受体激活是否通过减少突触前钙离子内流来抑制诱发的突触传递,该技术可同时记录豚鼠海马体CA3至CA1突触处单个电刺激诱发的突触前钙离子瞬变([Ca2+]t)和场兴奋性突触后电位(fEPSP)。2. GABAB受体激动剂巴氯芬以剂量依赖方式可逆地阻断fEPSP和突触前[Ca2+]t,且时间进程相似。在应用巴氯芬期间,fEPSP与突触前[Ca2+]t的约四次方成正比,突触前纤维群峰电位和静息钙离子水平未改变。这些结果与我们之前应用几种电压依赖性钙离子通道阻滞剂后观察到的结果相似,表明巴氯芬通过阻断突触前钙离子内流来抑制fEPSP。3. GABAB受体拮抗剂CGP 35348可阻断巴氯芬对fEPSP和突触前[Ca2+]t的抑制作用,这与GABAB受体介导的突触前对[Ca2+]t的抑制与fEPSP之间的因果关系一致。4. 应用电压依赖性钙离子通道阻滞剂ω-芋螺毒素-GVIA(ω-CgTX-GVIA)可部分阻断巴氯芬对[Ca2+]t的抑制作用,但ω-蜘蛛毒素-IVA(ω-AgaTX-IVA)则不能,这表明巴氯芬通过阻断包括ω-CgTX-GVIA敏感型在内的钙离子通道来降低突触前[Ca2+]t。5. 我们得出结论,巴氯芬通过减少突触前钙离子内流来抑制诱发的神经递质释放。(摘要截选至250字)

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