D'Agostino Dominic, Mazza Emilio, Neubauer Judith A
Div. of Pulmonary & Critical Care Medicine, Dept. of Medicine, UMDNJ-Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.
Am J Physiol Regul Integr Comp Physiol. 2009 Jan;296(1):R102-18. doi: 10.1152/ajpregu.90325.2008. Epub 2008 Oct 29.
Heme oxygenase has been linked to the oxygen-sensing function of the carotid body, pulmonary vasculature, cerebral vasculature, and airway smooth muscle. We have shown previously that the cardiorespiratory regions of the rostral ventrolateral medulla are excited by local hypoxia and that heme oxygenase-2 (HO-2) is expressed in the hypoxia-chemosensitive regions of the rostral ventrolateral medulla (RVLM), the respiratory pre-Bötzinger complex, and C1 sympathoexcitatory region. To determine whether heme oxygenase is necessary for the hypoxic-excitation of dissociated RVLM neurons (P1) cultured on confluent medullary astrocytes (P5), we examined their electrophysiological responses to hypoxia (NaCN and low Po(2)) using the whole-cell perforated patch clamp technique before and after blocking heme oxygenase with tin protoporphyrin-IX (SnPP-IX). Following the electrophysiological recording, immunocytochemistry was performed on the recorded neuron to correlate the electrophysiological response to hypoxia with the expression of HO-2. We found that the responses to NaCN and hypoxia were similar. RVLM neurons responded to NaCN and low Po(2) with either depolarization or hyperpolarization and SnPP-IX blocked the depolarization response of hypoxia-excited neurons to both NaCN and low Po(2) but had no effect on the hyperpolarization response of hypoxia-depressed neurons. Consistent with this observation, HO-2 expression was present only in the hypoxia-excited neurons. We conclude that RVLM neurons are excited by hypoxia via a heme oxygenase-dependent mechanism.
血红素加氧酶与颈动脉体、肺血管系统、脑血管系统及气道平滑肌的氧传感功能有关。我们之前已经表明,延髓头端腹外侧的心肺区域可被局部缺氧所兴奋,并且血红素加氧酶-2(HO-2)在延髓头端腹外侧(RVLM)的缺氧化学感受区域、呼吸前包钦格复合体及C1交感兴奋区域表达。为了确定血红素加氧酶对于在融合的延髓星形胶质细胞(P5)上培养的解离的RVLM神经元(P1)的缺氧兴奋是否必要,我们在使用锡原卟啉-IX(SnPP-IX)阻断血红素加氧酶之前和之后,采用全细胞穿孔膜片钳技术检测了它们对缺氧(氰化钠和低氧分压)的电生理反应。在电生理记录之后,对记录的神经元进行免疫细胞化学检测,以将对缺氧的电生理反应与HO-2的表达相关联。我们发现对氰化钠和缺氧的反应相似。RVLM神经元对氰化钠和低氧分压的反应既有去极化也有超极化,并且SnPP-IX阻断了缺氧兴奋神经元对氰化钠和低氧分压的去极化反应,但对缺氧抑制神经元的超极化反应没有影响。与这一观察结果一致,HO-2表达仅存在于缺氧兴奋的神经元中。我们得出结论,RVLM神经元通过血红素加氧酶依赖性机制被缺氧所兴奋。