Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Center for Integrated Brain Research, Seattle Children's Research Institute, Seattle, Washington.
J Appl Physiol (1985). 2021 Apr 1;130(4):1259-1273. doi: 10.1152/japplphysiol.00909.2020. Epub 2021 Feb 4.
Chronic hypercapnia (CH) is a hallmark of respiratory diseases such as chronic obstructive pulmonary disease. In such patients, mechanical ventilation is often used to restore normal blood-gas homeostasis. However, little is known regarding physiological changes and neuroplasticity within physiological control networks after termination of CH. Utilizing our goat model of increased inspired CO-induced CH, we determined whether termination of CH elicits time-dependent physiological and neurochemical changes within brain stem sites of physiological control. Thirty days of CH increased [Formula: see text] (+15 mmHg) and steady-state ventilation (SS V̇i; 283% of control). Within 24 h after terminating CH, SS V̇i, blood gases, arterial [H], and most physiological measurements returned to control. However, the acute ventilatory chemoreflex (ΔV̇i/Δ[H]) was greater than control, and measured SS V̇i exceeded ventilation predicted by arterial [H] and ΔV̇i/Δ[H]. Potentially contributing to these differences were increased excitatory neuromodulators serotonin and norepinephrine in the nucleus tractus solitarius, which contrasts with minimal changes observed at 24 h and 30 days of hypercapnia. Similarly, there were minimal changes found in markers of neuroinflammation and glutamate receptor-dependent neuroplasticity upon termination of CH, which were previously increased following 24 h of hypercapnia. Thus, following termination of CH: ) ventilatory, renal, and other physiological functions rapidly return to control; ) neuroplasticity within the ventilatory control network may contribute to the difference between measured vs. predicted ventilation and the elevation in the acute ventilatory [H] chemoreflex; and ) neuroplasticity is fundamentally distinct from acclimatization to CH. In healthy adult goats, steady-state ventilation and most physiological measures return to control within 24 h after termination of chronic hypercapnia (CH). However, the acute [H] chemoreflex is increased, and measured ventilation exceeds predicted ventilation. At 24 h of recovery, excitatory neuromodulators are above control, but other measured markers of neuroplasticity are unchanged from control. Our data suggest that CH elicits persistent physiological and neurochemical changes for up to 24 h after termination of CH.
慢性高碳酸血症(CH)是慢性阻塞性肺疾病等呼吸系统疾病的标志。在这些患者中,通常使用机械通气来恢复正常的血气平衡。然而,对于 CH 终止后生理控制网络内的生理变化和神经可塑性知之甚少。利用我们的山羊模型,我们确定了在 CH 诱导的增加的吸入 CO 后,CH 的终止是否会引起脑干内生理控制部位的时间依赖性生理和神经化学变化。30 天的 CH 增加了[公式:见正文](+15mmHg)和稳定的通气(SS V̇i;比对照高 283%)。在 CH 终止后 24 小时内,SS V̇i、血气、动脉[H]和大多数生理测量值均恢复到对照。然而,急性通气化学反射(ΔV̇i/Δ[H])大于对照,测量的 SS V̇i 超过了动脉[H]和ΔV̇i/Δ[H]预测的通气。可能导致这些差异的原因是孤束核中兴奋性神经调质 5-羟色胺和去甲肾上腺素增加,这与 CH 24 小时和 30 天时观察到的最小变化形成对比。同样,CH 终止时,神经炎症和谷氨酸受体依赖性神经可塑性的标志物也没有明显变化,而在 CH 24 小时后这些标志物增加。因此,CH 终止后:)呼吸、肾脏和其他生理功能迅速恢复到对照;)通气控制网络内的神经可塑性可能导致测量的通气与预测的通气之间的差异以及急性[H]化学反射的升高;)神经可塑性与 CH 的适应本质上不同。在健康成年山羊中,慢性高碳酸血症(CH)终止后 24 小时内,稳定通气和大多数生理测量值恢复到对照。然而,急性[H]化学反射增加,测量的通气超过预测的通气。在恢复的 24 小时时,兴奋性神经调质高于对照,但其他测量的神经可塑性标志物与对照相同。我们的数据表明,CH 终止后长达 24 小时会引起持续的生理和神经化学变化。