Dutschmann M, Paton J F R
Department of Physiology, School of Medical Sciences, University of Bristol, Bristol BS8 1TD, UK.
J Physiol. 2002 Sep 1;543(Pt 2):643-53. doi: 10.1113/jphysiol.2001.013466.
Eupnoeic breathing in mammals is dependent on the co-ordinated activity of cranial and spinal motor outputs to both ventilate the lungs and adjust respiratory airflow, which they do by regulating upper-airway resistance. We investigated the role of central glycinergic inhibition in the co-ordination of cranial and spinal respiratory motor outflows. We developed an arterially perfused neonatal rat preparation (postnatal age 0-4 days) to assess the effects of blocking glycine receptors with systemically administered strychnine (0.5-1 microM). We recorded respiratory neurones located within the ventrolateral medulla, inspiratory phrenic nerve activity (PNA) and recurrent laryngeal nerve activity (RLNA), as well as dynamic changes in laryngeal resistance. Central recordings of postinspiratory neurones revealed an earlier onset in firing relative to the onset of inspiratory PNA after exposure to strychnine (260 +/- 38.9 vs. 129 +/- 26.8 ms). After glycine receptor blockade, postinspiratory neurones discharged during the inspiratory phase. Strychnine also evoked a decrease in PNA frequency (from 38.6 +/- 4.7 to 30.7 +/- 2.8 bursts min(-1)), but amplitude was unaffected. In control conditions, RLNA comprised inspiratory and postinspiratory discharges; the amplitude of the latter exceeded that of the former. However, after administration of strychnine, the amplitude of inspiratory-related discharge increased (+65.2 +/- 15.2 %) and exceeded postinspiratory activity. Functionally this change in RLNA caused a paradoxical, inspiratory-related glottal constriction during PNA. We conclude that during the first days of life in the rat, glycine receptors are essential for the formation of the eupnoeic-like breathing pattern as defined by the co-ordinated activity of cranial and spinal motor inspiratory and postinspiratory activities.
哺乳动物的平静呼吸依赖于颅部和脊髓运动输出的协调活动,以实现肺部通气并通过调节上呼吸道阻力来调整呼吸气流。我们研究了中枢甘氨酸能抑制在颅部和脊髓呼吸运动输出协调中的作用。我们开发了一种动脉灌注新生大鼠制备方法(出生后0 - 4天),以评估全身给予士的宁(0.5 - 1微摩尔)阻断甘氨酸受体的效果。我们记录了位于延髓腹外侧的呼吸神经元、吸气膈神经活动(PNA)和喉返神经活动(RLNA),以及喉部阻力的动态变化。对吸气后神经元的中枢记录显示,暴露于士的宁后,相对于吸气PNA的起始,其放电起始更早(260±38.9毫秒对129±26.8毫秒)。甘氨酸受体阻断后,吸气后神经元在吸气期放电。士的宁还引起PNA频率降低(从38.6±4.7次/分钟降至30.7±2.8次/分钟),但幅度不受影响。在对照条件下,RLNA包括吸气和吸气后放电;后者的幅度超过前者。然而,给予士的宁后,吸气相关放电的幅度增加(+65.2±15.2%)并超过吸气后活动。从功能上讲,RLNA的这种变化在PNA期间导致了矛盾的、与吸气相关的声门收缩。我们得出结论,在大鼠出生后的头几天,甘氨酸受体对于由颅部和脊髓运动吸气和吸气后活动的协调活动所定义的类似平静呼吸模式的形成至关重要。