Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, 53226, USA.
Neuroscience. 2010 Jan 13;165(1):61-78. doi: 10.1016/j.neuroscience.2009.09.078. Epub 2009 Oct 2.
A critical period in respiratory network development occurs in the rat around postnatal days (P) 12-13, when abrupt neurochemical, metabolic, and physiological changes were evident. As serotonin and its receptors are involved in respiratory modulation, and serotonergic abnormality is implicated in sudden infant death syndrome, we hypothesized that 5-HT receptors are significantly downregulated during the critical period. This was documented recently for 5-HT(2A)R in several respiratory nuclei. The present study represents a comprehensive analysis of postnatal development of 5-HT(1A)R and 5-HT(1B)R in 10 brain stem nuclei and 5-HT(2A)R in six nuclei not previously examined. Optical densitometric analysis of immunohistochemically-reacted neurons from P2 to P21 indicated four developmental patterns of expression: (1) Pattern I: a high level of expression at P2-P11, an abrupt and significant reduction at P12, followed by a plateau until P21 (5-HT(1A)R and 5-HT(1B)R in raphé magnus [RM], raphé obscurus [ROb], raphé pallidus [RP], pre-Bötzinger complex [PBC], nucleus ambiguus [Amb], and hypoglossal nucleus [XII; 5-HT(1A)R only]). (2) Pattern II: a high level at P2-P9, a gradual decline from P9 to P12, followed by a plateau until P21 (5-HT(1A)R and 5-HT(1B)R in the retrotrapezoid nucleus (RTN)/parafacial respiratory group (pFRG)). (3) Pattern III: a high level at P2-P11, followed by a gradual decline until P21 (5-HT(1A)R in the ventrolateral subnucleus of solitary tract nucleus [NTS(VL)] and the non-respiratory cuneate nucleus [CN]). (4) Pattern IV: a relatively constant level maintained from P2 to P21 (5-HT(1A)R in the commissural subnucleus of solitary tract nucleus (NTS(COM)); 5-HT(1B)R in XII, NTS(VL), NTS(COM), and CN; and 5-HT(2A)R in RM, ROb, RP, RTN/pFRG, NTS(VL), and NTS(COM)). Thus, a significant reduction in the expression of 5-HT(1A)R, 5-HT(1B)R, and 5-HT(2A)R in multiple respiratory-related nuclei at P12 is consistent with reduced serotonergic transmission during the critical period, thereby rendering the animals less able to respond adequately to ventilatory distress.
呼吸网络发育的关键时期发生在大鼠出生后第 12-13 天,此时明显出现神经化学、代谢和生理变化。由于血清素及其受体参与呼吸调节,而血清素能异常与婴儿猝死综合征有关,我们假设在关键时期 5-HT 受体显著下调。最近在几个呼吸核中已经证明了 5-HT(2A)R 的这种情况。本研究代表了对 10 个脑干核中 5-HT(1A)R 和 5-HT(1B)R 以及之前未检查的 6 个核中 5-HT(2A)R 的出生后发育的全面分析。从 P2 到 P21 的免疫组织化学反应神经元的光密度分析表明,表达有四种发育模式:(1)模式 I:P2-P11 时表达水平高,P12 时突然显著降低,然后直至 P21 时保持稳定(RM、ROb、RP、PBC、Amb 和 XII 中的 5-HT(1A)R 和 5-HT(1B)R;仅在 RM 中的 5-HT(1A)R)。(2)模式 II:P2-P9 时表达水平高,从 P9 到 P12 逐渐下降,然后直至 P21 时保持稳定(RTN/parafacial respiratory group [pFRG] 中的 5-HT(1A)R 和 5-HT(1B)R)。(3)模式 III:P2-P11 时表达水平高,然后逐渐下降直至 P21(NTS(VL)中的 5-HT(1A)R 和非呼吸性楔状核 [CN])。(4)模式 IV:从 P2 到 P21 保持相对稳定的水平(NTS(COM)中的 5-HT(1A)R;XII、NTS(VL)、NTS(COM)和 CN 中的 5-HT(1B)R;RM、ROb、RP、RTN/pFRG、NTS(VL)和 NTS(COM)中的 5-HT(2A)R)。因此,在 P12 时多个与呼吸相关的核中 5-HT(1A)R、5-HT(1B)R 和 5-HT(2A)R 的表达显著减少,与关键时期内血清素传递减少一致,从而使动物对通气窘迫的反应能力降低。