Bright Fiona M, Vink Robert, Byard Roger W, Duncan Jhodie R, Krous Henry F, Paterson David S
Discipline of Anatomy and Pathology, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.
Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA, United States of America.
PLoS One. 2017 Sep 20;12(9):e0184958. doi: 10.1371/journal.pone.0184958. eCollection 2017.
Sudden infant death syndrome (SIDS) involves failure of arousal to potentially life threatening events, including hypoxia, during sleep. While neuronal dysfunction and abnormalities in neurotransmitter systems within the medulla oblongata have been implicated, the specific pathways associated with autonomic and cardiorespiratory failure are unknown. The neuropeptide substance P (SP) and its tachykinin neurokinin-1 receptor (NK1R) have been shown to play an integral role in the modulation of homeostatic function in the medulla, including regulation of respiratory rhythm generation, integration of cardiovascular control, and modulation of the baroreceptor reflex and mediation of the chemoreceptor reflex in response to hypoxia. Abnormalities in SP neurotransmission may therefore result in autonomic dysfunction during sleep and contribute to SIDS deaths. [125I] Bolton Hunter SP autoradiography was used to map the distribution and density of the SP, NK1R to 13 specific nuclei intimately related to cardiorespiratory function and autonomic control in the human infant medulla of 55 SIDS and 21 control (non-SIDS) infants. Compared to controls, SIDS cases exhibited a differential, abnormal developmental profile of the SP/NK1R system in the medulla. Furthermore the study revealed significantly decreased NK1R binding within key medullary nuclei in SIDS cases, principally in the nucleus tractus solitarii (NTS) and all three subdivisions of the inferior portion of the olivo-cerebellar complex; the principal inferior olivary complex (PIO), medial accessory olive (MAO) and dorsal accessory olive (DAO). Altered NK1R binding was significantly influenced by prematurity and male sex, which may explain the increased risk of SIDS in premature and male infants. Abnormal NK1R binding in these medullary nuclei may contribute to the defective interaction of critical medullary mechanisms with cerebellar sites, resulting in an inability of a SIDS infant to illicit appropriate respiratory and motor responses to life threatening challenges during sleep. These observations support the concept that abnormalities in a multi-neurotransmitter network within key nuclei of the medullary homeostatic system may underlie the pathogenesis of a subset of SIDS cases.
婴儿猝死综合征(SIDS)涉及在睡眠期间对包括缺氧在内的潜在危及生命事件的觉醒失败。虽然延髓内的神经元功能障碍和神经递质系统异常已被牵连,但与自主神经和心肺功能衰竭相关的具体途径尚不清楚。神经肽P物质(SP)及其速激肽神经激肽-1受体(NK1R)已被证明在延髓稳态功能的调节中起不可或缺的作用,包括呼吸节律产生的调节、心血管控制的整合、压力感受器反射的调节以及对缺氧的化学感受器反射的介导。因此,SP神经传递异常可能导致睡眠期间自主神经功能障碍,并导致SIDS死亡。[125I]博尔顿·亨特SP放射自显影术被用于绘制55例SIDS婴儿和21例对照(非SIDS)婴儿的人类婴儿延髓中与心肺功能和自主神经控制密切相关的13个特定核团中SP、NK1R的分布和密度。与对照组相比,SIDS病例在延髓中表现出SP/NK1R系统的不同异常发育特征。此外,该研究还显示,SIDS病例关键延髓核内的NK1R结合显著减少,主要在孤束核(NTS)以及橄榄小脑复合体下部的所有三个亚区;主要下橄榄复合体(PIO)、内侧副橄榄核(MAO)和背侧副橄榄核(DAO)。NK1R结合的改变受早产和男性性别的显著影响,这可能解释了早产和男性婴儿中SIDS风险增加的原因。这些延髓核内异常的NK1R结合可能导致关键延髓机制与小脑部位的相互作用缺陷,导致SIDS婴儿在睡眠期间无法对危及生命的挑战做出适当的呼吸和运动反应。这些观察结果支持这样一种概念,即延髓稳态系统关键核内多神经递质网络的异常可能是一部分SIDS病例发病机制的基础。