Department of Respiration Physiology, Mossakowski Medical Research Centre, Polish Academy of Sciences, Pawińskiego 5, 02-106, Warsaw, Poland.
Department of Experimental and Clinical Pharmacology, Centre for Preclinical Research (CePT), Medical University of Warsaw, Warsaw, Poland.
J Physiol Sci. 2020 Mar 11;70(1):16. doi: 10.1186/s12576-020-00743-4.
Respiratory disturbances present in Parkinson's disease (PD) are not well understood. Thus, studies in animal models aimed to link brain dopamine (DA) deficits with respiratory impairment are needed. Adult Wistar rats were lesioned with injection of 6-hydroxydopamine (6-OHDA) into the third cerebral ventricle. Two weeks after hypoxic test was performed in whole-body plethysmography chamber, phrenic (PHR) and hypoglossal (HG) nerve activities were recorded in normoxic and hypoxic conditions in anesthetized, vagotomized, paralyzed and mechanically ventilated rats. The effects of activation and blockade of dopaminergic carotid body receptors were investigated during normoxia in anesthetized spontaneously breathing rats. 6-OHDA injection affected resting respiratory pattern in awake animals: an increase in tidal volume and a decrease in respiratory rate had no effect on minute ventilation. Hypoxia magnified the amplitude and minute activity of the PHR and HG nerve of 6-OHDA rats. The ratio of pre-inspiratory to inspiratory HG burst amplitude was reduced in normoxic breathing. Yet, the ratio of pre-inspiratory time to total time of the respiratory cycle was increased during normoxia. 6-OHDA lesion had no impact on DA and domperidone effects on the respiratory pattern, which indicate that peripheral DA receptors are not affected in this model. Analysis of monoamines confirmed substantial striatal depletion of dopamine, serotonin and noradrenaline (NA) and reduction of NA content in the brainstem. In bilateral 6-OHDA model changes in activity of both nerves: HG (linked with increased apnea episodes) and PHR are present. Demonstrated respiratory effects could be related to specific depletion of DA and NA.
帕金森病(PD)中存在的呼吸紊乱尚不清楚。因此,需要在动物模型中进行研究,以将大脑多巴胺(DA)缺乏与呼吸障碍联系起来。成年 Wistar 大鼠通过将 6-羟多巴胺(6-OHDA)注射到第三脑室中来进行损伤。缺氧测试后两周,在全身 plethysmography 室中进行了缺氧测试,在麻醉、迷走神经切断、麻痹和机械通气的大鼠中,在正常和缺氧条件下记录膈神经(PHR)和舌下神经(HG)的神经活动。在麻醉、自主呼吸的大鼠中,在正常氧合条件下,研究了激活和阻断多巴胺能颈动脉体受体对呼吸的影响。6-OHDA 注射影响清醒动物的静息呼吸模式:潮气量增加和呼吸频率降低对分钟通气量没有影响。缺氧放大了 6-OHDA 大鼠的 PHR 和 HG 神经的振幅和分钟活动。在正常呼吸时,预吸气期与吸气期 HG 爆发幅度的比值降低,但在正常氧合时,吸气期与呼吸周期总时间的比值增加。6-OHDA 损伤对 DA 没有影响,也没有影响多潘立酮对呼吸模式的影响,这表明外周 DA 受体在该模型中不受影响。单胺分析证实纹状体多巴胺、血清素和去甲肾上腺素(NA)明显耗竭,脑干 NA 含量减少。在双侧 6-OHDA 模型中,两条神经(与呼吸暂停发作增加相关的 HG 和 PHR)的活性均发生变化。所证明的呼吸作用可能与 DA 和 NA 的特异性耗竭有关。