The potential role of substance P in brainstem homeostatic control in the pathogenesis of sudden infant death syndrome (SIDS). (August 2018)

• Record Type: Journal Article
• Authors: Bright, Fiona M.; Vink, Robert; Byard, Roger W.
• Is Part Of: Neuropeptides. Volume 70(2018)
• Page Start: 1
• Page End: 8
• Publication Date: 2018-08
• Subjects: Sudden infant death syndrome -- Substance P -- NK1 receptor -- Serotonin -- Medulla oblongata -- Brainstem -- Neurotransmitter; Neuropeptides -- Periodicals; Neuropeptides; Neuropeptides -- Périodiques; Neuropeptides; Electronic journals; Periodicals; 572.65
• DOI: 10.1016/j.npep.2018.02.006
• Languages: English
• ISSNs: 0143-4179

Abstract

Abstract: Victims of sudden infant death syndrome (SIDS) are believed to have an underlying dysfunction in medullary homeostatic control that impairs critical responses to life threatening challenges such as hypoxia, hypercarbia and asphyxia, often during a sleep period. This failure is thought to result from abnormalities in a network of neural pathways in the medulla oblongata that control respiration, chemosensitivity, autonomic function and arousal. Studies have mainly focused on the role of serotonin, 5-hydroxytyptamine (5HT), although the neuropeptide substance P (SP) has also been shown to play an integral role in the modulation of medullary homeostatic function, often in conjunction with 5-HT. Actions of SP include regulation of respiratory rhythm generation, integration of cardiovascular control, modulation of the baroreceptor reflex and mediation of the chemoreceptor reflex in response to hypoxia. Abnormalities in SP neurotransmission may, therefore, also play a significant role in homeostatic dysfunction of the neurotransmitter network in SIDS. This review focuses on the pathways within the medulla involving SP and its tachykinin NK1 receptor, their potential relationship with the medullary 5-HT system, and possible involvement in the pathogenesis of SIDS. Highlights: Neuropathological investigations identified significant abnormalities in homeostatic networks in the brainstems of SIDS infants. Investigators must broaden the scope of SIDS neuropathology research to determine the interaction of multiple neurotransmitter networks. Extensive role of SP neurotransmission in brainstem homeostatic control and its intimate relationship with medullary 5-HT pathways Abnormalities in SP and its NK1R may be significant contributors to the lethal mechanisms underpinning SIDS cases