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GABAA受体拮抗剂在控制呼吸神经元放电模式中的差异效应。

Differential effects of GABAA receptor antagonists in the control of respiratory neuronal discharge patterns.

作者信息

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

机构信息

Zablocki Veterans Affairs Medical Center, Medical College of Wisconsin, Milwaukee, Wisconsin 53295, USA.

出版信息

J Neurophysiol. 1998 Nov;80(5):2368-77. doi: 10.1152/jn.1998.80.5.2368.

Abstract

To ascertain the role of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) in shaping and controlling the phasic discharge patterns of medullary respiratory premotor neurons, localized pressure applications of the competitive GABAA receptor antagonist bicuculline (BIC) and the noncompetitive GABAA receptor antagonist picrotoxin (PIC) were studied. Multibarrel micropipettes were used in halothane anesthetized, paralyzed, ventilated, vagotomized dogs to record single unit activity from inspiratory and expiratory neurons in the caudal ventral respiratory group and to picoeject GABAA receptor antagonists. The moving time average of phrenic nerve activity was used to determine respiratory phase durations and to synchronize cycle-triggered histograms of discharge patterns. Picoejection of BIC and PIC had qualitatively different effects on the discharge patterns of respiratory neurons. BIC caused an increase in the discharge rate during the neuron's active phase without inducing activity during the neuron's normally silent phase. The resulting discharge patterns were amplified replicas (x2-3) of the underlying preejection phasic patterns. In contrast, picoejection of PIC did not increase the peak discharge rate during the neuron's active phase but induced a tonic level of activity during the neuron's normally silent phase. The maximum effective BIC dose (15 +/- 1.8 pmol/min) was considerably smaller than that for PIC (280 +/- 53 pmol/min). These findings suggest that GABAA receptors with differential pharmacology mediate distinct functions within the same neuron, 1) gain modulation that is BIC sensitive but PIC insensitive and 2) silent-phase inhibition blocked by PIC. These studies also suggest that the choice of an antagonist is an important consideration in the determination of GABA receptor function within the respiratory motor control system.

摘要

为了确定抑制性神经递质γ-氨基丁酸(GABA)在塑造和控制延髓呼吸前运动神经元的相位放电模式中的作用,研究了竞争性GABAA受体拮抗剂荷包牡丹碱(BIC)和非竞争性GABAA受体拮抗剂印防己毒素(PIC)的局部压力应用。在氟烷麻醉、麻痹、通气、迷走神经切断的犬中使用多管微吸管记录尾侧腹侧呼吸组吸气和呼气神经元的单单位活动,并微量注射GABAA受体拮抗剂。膈神经活动的移动时间平均值用于确定呼吸相持续时间,并同步放电模式的周期触发直方图。BIC和PIC的微量注射对呼吸神经元的放电模式有质的不同影响。BIC在神经元的活动期使放电率增加,而在神经元通常的静息期不诱导活动。由此产生的放电模式是基础注射前相位模式的放大复制品(x2 - 3)。相反,PIC的微量注射在神经元的活动期没有增加峰值放电率,但在神经元通常的静息期诱导了一个紧张性活动水平。最大有效BIC剂量(15±1.8 pmol/min)远小于PIC的剂量(280±53 pmol/min)。这些发现表明,具有不同药理学特性的GABAA受体在同一神经元内介导不同的功能,1)对BIC敏感但对PIC不敏感的增益调节,以及2)被PIC阻断的静息期抑制。这些研究还表明,在确定呼吸运动控制系统内GABA受体功能时,拮抗剂的选择是一个重要的考虑因素。

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