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Peripheral neuroplasticity of respiratory chemoreflexes, induced by prenatal nicotinic exposure: Implication for SIDS
Fadi Xu1, Lei Zhao1, Jianguo Zhuang1
1Pathophysiology Program, Lovelace Biomedical Research Institute, Albuquerque, NM 87108, USA.
Insights
Prenatal exposure to nicotine in rat pups impairs the hypoxic ventilatory response and prolongs apnea, suggesting peripheral chemoreflex dysfunction contributes to Sudden Infant Death Syndrome (SIDS) pathogenesis.
Area of Science:
- Neuroscience
- Respiratory Physiology
- Toxicology
Background:
- Sudden Infant Death Syndrome (SIDS) pathogenesis remains incompletely understood, with maternal smoking and hypoxemia implicated.
- Depressed hypoxic ventilatory response (dHVR) and apneas are observed in SIDS.
- Peripheral sensory afferents, including carotid bodies and C-fibers, play roles in respiratory control but their involvement in SIDS is under-explored.
Purpose of the Study:
- To investigate the role of peripheral sensory afferent-mediated respiratory chemoreflexes in a rat pup model of SIDS.
- To explore the effects of prenatal nicotinic exposure on hypoxic ventilatory response and apnea.
Main Methods:
- Utilized a rat pup model with prenatal exposure to nicotine.
- Assessed hypoxic ventilatory response (HVR) and apnea.
- Examined carotid body function, pulmonary C-fiber (PCF) and superior laryngeal C-fiber (SLCF) activity, and expression of related receptors (TRPV1, NK1R, IL1RI, 5-HT3R).
Main Results:
- Prenatal nicotinic exposure led to suppressed carotid body-mediated HVR due to reduced glomus cell number and sensitivity.
- PCF-mediated apnea was prolonged, associated with increased PCF density, pulmonary IL-1β and serotonin release, and enhanced receptor expression.
- SLCF-mediated apnea and neuronal currents were augmented by increased TRPV1 expression in superior laryngeal C-neurons.
Conclusions:
- Prenatal nicotinic exposure induces peripheral neuroplasticity, leading to dHVR and prolonged apnea in rat pups under hypoxia.
- Disorders in peripheral sensory afferent-mediated chemoreflexes, alongside potential central respiratory center disturbances, may contribute to SIDS.
- These findings offer insights into the mechanisms underlying SIDS, particularly concerning the impact of maternal smoking.
Abstract:
Sudden Infant Death Syndrome (SIDS) occurs during sleep in seemingly healthy infants. Maternal cigarette smoking and hypoxemia during sleep are assumed to be the major causal factors. Depressed hypoxic ventilatory response (dHVR) is observed in infants with high risk of SIDS, and apneas (lethal ventilatory arrest) appear during the fatal episode of SIDS. Disturbance of the respiratory center has been proposed to be involved, but the pathogenesis of SIDS is still not fully understood. Peripherally, the carotid body is critical to generate HVR, and bronchopulmonary and superior laryngeal C-fibers (PCFs and SLCFs) are important for triggering central apneas; however, their roles in the pathogenesis of SIDS have not been explored until recently. There are three lines of recently accumulated evidence to show the disorders of peripheral sensory afferent-mediated respiratory chemoreflexes in rat pups with prenatal nicotinic exposure (a SIDS model) in which acute severe hypoxia leads to dHVR followed by lethal apneas. (1) The carotid body-mediated HVR is suppressed with a reduction of the number and sensitivity of glomus cells. (2) PCF-mediated apneic response is largely prolonged via increased PCF density, pulmonary IL-1β and serotonin (5-hydroxytryptamine, 5-HT) release, along with the enhanced expression of TRPV1, NK1R, IL1RI and 5-HT3R in pulmonary C-neurons to strengthen these neural responses to capsaicin, a selective stimulant to C-fibers. (3) SLCF-mediated apnea and capsaicin-induced currents in superior laryngeal C-neurons are augmented by upregulation of TRPV1 expression in these neurons. These results, along with hypoxic sensitization/stimulation of PCFs, gain insight into the mechanisms of prenatal nicotinic exposure-induced peripheral neuroplasticity responsible for dHVR and long-lasting apnea during hypoxia in rat pups. Therefore, in addition to the disturbance in the respiratory center, the disorders of peripheral sensory afferent-mediated chemoreflexes may also be involved in respiratory failure and death denoted in SIDS victims.
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