Oku Yoshitaka, Masumiya Haruko, Okada Yasumasa
Department of Physiology, Hyogo College of Medicine, Nishinomiya, Hyogo 663-8501, Japan.
J Physiol. 2007 Nov 15;585(Pt 1):175-86. doi: 10.1113/jphysiol.2007.138180. Epub 2007 Sep 20.
Two putative respiratory rhythm generators (RRGs), the para-facial respiratory group (pFRG) and the pre-Bötzinger complex (preBötC), have been identified in the neonatal rodent brainstem. To elucidate their functional roles during the neonatal period, we evaluated developmental changes of these RRGs by optical imaging using a voltage-sensitive dye. Optical signals, recorded from the ventral medulla of brainstem-spinal cord preparations of neonatal (P0-P4) rats (n = 44), were analysed by a cross correlation method. With development during the first few postnatal days, the respiratory-related activity in the pFRG reduced and shifted from a preinspiratory (P0-P1) to an inspiratory (P2-P4) pattern, whereas preBötC activity remained unchanged. The mu-opioid agonist [D-Ala(2),N-Me-Phe(4),Gly(5)-ol]-enkephalin (DAMGO) augmented preinspiratory activity in the pFRG, while the mu-opioid antagonist naloxone induced changes in spatiotemporal activation profiles that closely mimicked the developmental changes. These results are consistent with the recently proposed hypothesis by Janczewski and Feldman that the pFRG is activated to compensate for the depression of the preBötC by perinatal opiate surge. We conclude that significant reorganization of the respiratory neuronal network, characterized by a reduction of preinspiratory activity in the pFRG, occurs at P1-P2 in rats. The changes in spatiotemporal activation profiles of the pFRG neurones may reflect changes in the mode of coupling of the two respiratory rhythm generators.
在新生啮齿动物脑干中已鉴定出两个假定的呼吸节律发生器(RRG),即面神经旁呼吸组(pFRG)和前包钦格复合体(preBötC)。为了阐明它们在新生儿期的功能作用,我们使用电压敏感染料通过光学成像评估了这些RRG的发育变化。通过互相关方法分析了从新生(P0 - P4)大鼠(n = 44)的脑干 - 脊髓制剂的延髓腹侧记录的光学信号。在出生后的头几天,随着发育,pFRG中与呼吸相关的活动减少,并从前吸气(P0 - P1)模式转变为吸气(P2 - P4)模式,而preBötC活动保持不变。μ-阿片受体激动剂[D - Ala(2),N - Me - Phe(4),Gly(5) - ol]-脑啡肽(DAMGO)增强了pFRG中的前吸气活动,而μ-阿片受体拮抗剂纳洛酮诱导的时空激活图谱变化与发育变化密切相似。这些结果与Janczewski和Feldman最近提出的假设一致,即pFRG被激活以补偿围产期阿片类药物激增对preBötC的抑制。我们得出结论,以pFRG中前吸气活动减少为特征的呼吸神经元网络的显著重组发生在大鼠的P1 - P2期。pFRG神经元时空激活图谱的变化可能反映了两个呼吸节律发生器耦合模式的变化。