首页> 外文期刊>Brain research >Evidence for the involvement of G-proteins in the generation of the slow poststimulus afterdepolarisation (sADP) induced by muscarinic receptor activation in rat olfactory cortical neurones in vitro.
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Evidence for the involvement of G-proteins in the generation of the slow poststimulus afterdepolarisation (sADP) induced by muscarinic receptor activation in rat olfactory cortical neurones in vitro.

机译:有证据表明在体外大鼠嗅觉皮质神经元中毒蕈碱受体激活会诱导G蛋白参与缓慢的刺激后去极化(sADP)的产生。

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The involvement of G-proteins in generating the slow poststimulus afterdepolarising potential (sADP) induced by muscarinic receptor activation in immature (P10-20) rat olfactory cortical brain slice neurones was investigated under whole-cell patch clamp, using GTP-gamma-S (G-protein activator) or GDP-beta-S (G-protein blocker)-filled electrodes. In control experiments using K methylsulphate electrodes, cell resting potential (V(m)) and spike firing properties were unaffected over 10-15 min recording, although input resistance (R(N)) was slightly increased ( approximately 14%). Oxotremorine-M (OXO-M; 10 microM) produced a reversible slow depolarisation, an increase in R(N) ( approximately 90%) and induction of a slow poststimulus inward tail current (I(ADP)) (measured under voltage clamp at -60 mV) that was sustained during drug exposure (up to 15 min); the amplitude of slow inward rectifier (I(h)) currents activated from -50 mV were also apparently increased. By contrast, in GTP-gamma-S-loaded cells, R(N) was consistently decreased ( approximately 22%) and spike firing threshold (V(th)) was raised ( approximately 5 mV) after 10 min recording. In approximately 60% of loaded cells, a persistent muscarinic slow inward current and I(ADP) were induced by OXO-M; I(h) relaxation amplitude was also significantly decreased. The effects of GTP-gamma-S on R(N), V(th) and I(h) were partly counteracted by adding Ba(2+) (100 microM) to the bathing medium or mimicked by adding baclofen (GABA(B) receptor agonist; 100 microM) to normally-recorded cells. Intracellular GDP-beta-S (up to 30 min) had no effect on cell membrane properties or I(h), but irreversibly blocked the muscarinic slow inward current and I(ADP) induced by OXO-M. We conclude that both muscarinic responses require G-protein-linked transduction mechanisms for their generation.
机译:在全细胞膜片钳下,使用GTP-γ-S(GTP-γ-S( G蛋白激活剂)或GDP-β-S(G蛋白阻滞剂)填充电极。在使用K甲基硫酸盐电极的对照实验中,尽管输入电阻(R(N))略有增加(大约14%),但在10-15分钟的记录时间内,电池静息电位(V(m))和尖峰发射特性并未受到影响。 Oxotremorine-M(OXO-M; 10 microM)产生可逆的缓慢去极化,R(N)增加(约90%)并产生缓慢的刺激后向内尾电流(I(ADP))(在电压钳位下测量) -60 mV)在药物暴露期间持续(长达15分钟);从-50 mV激活的慢速向内整流器(I(h))电流的幅度也明显增加。相比之下,在GTP-γ-S加载的细胞中,记录10分钟后R(N)持续降低(约22%),尖峰发射阈值(V(th))升高(约5 mV)。在大约60%的负载细胞中,OXO-M诱导了持续的毒蕈碱缓慢内向电流和I(ADP)。 I(h)的弛豫幅度也显着降低。 GTP-γ-S对R(N),V(th)和I(h)的影响可通过向沐浴液中添加Ba(2+)(100 microM)或通过添加巴氯芬(GABA(B )受体激动剂; 100 microM)正常记录的细胞。细胞内GDP-β-S(长达30分钟)对细胞膜特性或I(h)没有影响,但不可逆地阻止了由OXO-M诱导的毒蕈碱型缓慢内向电流和I(ADP)。我们得出的结论是,两种毒蕈碱反应都需要G蛋白相关的转导机制才能产生。

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