Peripheral chemoreceptors determine the respiratory sensitivity of central chemoreceptors to CO2 : role of carotid body CO2.
Peripheral chemoreceptors determine the respiratory sensitivity of central chemoreceptors to CO2 : role of carotid body CO2.
复制标题
外周化学感受器决定中枢化学感受器对 CO2 的呼吸敏感性:颈动脉体 CO2 的作用。
DOI:
10.1113/jp270114
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发表时间:
2015
期刊:
影响因子:
--
通讯作者:
Dempsey,JeromeA
中科院分区:
文献类型:
--
作者:
Smith,CurtisA;Blain,GrégoryM;Henderson,KathleenS;Dempsey,JeromeA
Key PointsThe influence of specific carotid body (CB) normoxic hypocapnia, hypercapnia and normocapnia on the ventilatory sensitivity of central chemoreceptors to systemic hypercapnia was assessed in seven awake dogs with extracorporeal perfusion of the vascularly isolated CB.Chemosensitivity in this preparation was similar to that in the intact animal.Separation of CB circulation from that of the brain was confirmed.When the isolated CB was hypercapnicvs. hypocapnic and when the isolated CB was normocapnicvs. hypocapnic, the group mean central CO2response slopes of minute ventilation () (P≤ 0.01) and mean inspiratory flow rate (VT/TI) (P≤ 0.05) increased significantly. Tidal volume (VT), breathing frequency (fb)and rate of rise of diaphragm EMG were increased in 6 of 7 dogs but did not achieve statistical significance.We propose that hyperaddition is the dominant form of chemoreceptor interaction under conditions of quiet wakefulness in intact animals and over a wide range of CB and .AbstractWe asked if the type of carotid body (CB) chemoreceptor stimulus influenced the ventilatory gain of the central chemoreceptors to CO2. The effect of CB normoxic hypocapnia, normocapnia and hypercapnia (carotid body ≈ 22, 41 and 68 mmHg, respectively) on the ventilatory CO2sensitivity of central chemoreceptors was studied in seven awake dogs with vascularly‐isolated and extracorporeally‐perfused CBs. Chemosensitivity with one CB was similar to that in intact dogs. In four CB‐denervated dogs, absence of hyper‐/hypoventilatory responses to CB perfusion with of 19–75 mmHg confirmed separation of the perfused CB circulation from the brain. The group mean central CO2response slopes were increased 303% for minute ventilation ()(P≤ 0.01) and 251% for mean inspiratory flow rate (VT/TI) (P≤ 0.05) when the CB was hypercapnicvs. hypocapnic; central CO2response slopes for tidal volume (VT), breathing frequency (fb) and rate of rise of the diaphragm EMG increased in 6 of 7 animals but the group mean changes did not reach statistical significance. Group mean central CO2response slopes were also increased 237% for (P≤ 0.01) and 249% forVT/TI(P≤ 0.05) when the CB was normocapnicvs. hypocapnic, but no significant differences in any of the central ventilatory response indices were found between CB normocapnia and hypercapnia. These hyperadditive effects of CB hyper‐/hypocapnia agree with previous findings using CB hyper‐/hypoxia.We propose that hyperaddition is the dominant form of chemoreceptor interaction in quiet wakefulness when the chemosensory control system is intact, response gains physiological, and carotid body chemoreceptors are driven by a wide range of O2and/or CO2.