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对呼吸前运动神经元和运动神经元的突触驱动的调节。

Modulation of the synaptic drive to respiratory premotor and motor neurons.

作者信息

McCrimmon D R, Zuperku E J, Hayashi F, Dogas Z, Hinrichsen C F, Stuth E A, Tonkovic-Capin M, Krolo M, Hopp F A

机构信息

Department of Physiology, Northwestern University Medical School, Chicago, IL 60611-3008, USA.

出版信息

Respir Physiol. 1997 Nov;110(2-3):161-76. doi: 10.1016/s0034-5687(97)00081-9.

Abstract

The characteristics of GABAergic inhibitory modulation of respiratory bulbospinal neuronal activity and short-term potentiation (STP) of phrenic motoneuronal activity were studied. Extracellular unit recording and picoejection techniques in anesthetized dogs showed that both the spontaneous rhythmic and reflexly induced discharge patterns of inspiratory (I) and expiratory (E) premotor neurons were proportionately amplified by the localized application of picomole amounts of bicuculline (Bic), a competitive GABAA antagonist. Intracellular recording and paired-pulse stimulation techniques in anesthetized rats demonstrated an STP of phrenic motor output that appears to be mediated by NMDA receptors and is associated with facilitation of EPSPs and prolonged depolarization of individual phrenic motoneurons. We speculate that both GABAergic gain modulation of premotor neuronal activity and NMDA-mediated STP of phrenic activity may be neural substrates which are involved with the optimization of respiratory and non-respiratory behaviors, via adaptive and/or differential control of breathing.

摘要

研究了呼吸球脊髓神经元活动的γ-氨基丁酸(GABA)能抑制调节特性以及膈运动神经元活动的短期增强(STP)。在麻醉犬中采用细胞外单位记录和微量注射技术表明,通过局部应用皮摩尔量的竞争性GABAA拮抗剂荷包牡丹碱(Bic),吸气(I)和呼气(E)前运动神经元的自发节律性和反射诱导放电模式均被成比例放大。在麻醉大鼠中采用细胞内记录和双脉冲刺激技术证明,膈运动输出的STP似乎由N-甲基-D-天冬氨酸(NMDA)受体介导,并与兴奋性突触后电位(EPSP)的易化和单个膈运动神经元的去极化延长有关。我们推测,前运动神经元活动的GABA能增益调节和膈活动的NMDA介导的STP可能都是神经基质,通过呼吸的适应性和/或差异性控制参与呼吸和非呼吸行为的优化。

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