Severe spontaneous bradycardia associated with respiratory disruptions in rat pups with fewer brain stem 5-HT neurons

Am J Physiol Regul Integr Comp Physiol. 2009 Jun;296(6):R1783-96. doi: 10.1152/ajpregu.00122.2009. Epub 2009 Apr 15.

Abstract

The medullary 5-HT system has potent effects on heart rate and breathing in adults. We asked whether this system mitigates the respiratory instability and bradycardias frequently occurring during the neonatal period. 5,7-Dihydroxytryptamine (5,7-DHT) or vehicle was administered to rat pups at postnatal day 2 (P2), and we then compared the magnitude of bradycardias occurring with disruptions to eupnea in treated and vehicle control littermates at P5-6 and P10-12. We then used a novel method that would allow accurate assessment of the ventilatory and heart rate responses to near square-wave challenges of hypoxia (10% O2), hypercapnia (5 and 8% CO2 in normoxia and hyperoxia), and asphyxia (8% CO2-10% O2), and to the induction of the Hering-Breuer inflation reflex (HBR), a potent, apnea-inducing reflex in newborns. The number of 5-HT-positive neurons was reduced approximately 80% by drug treatment. At both ages, lesioned animals had considerably larger bradycardias during brief apnea; at P5-6, average and severe events were approximately 50% and 70% greater, respectively, in lesioned animals (P = 0.002), whereas at P10-12, events were approximately 23% and 50% greater (P = 0.018). However, lesioning had no effect on the HR responses to sudden gas challenge or the HBR. At P5-6, lesioned animals had reduced breathing frequency and ventilation (Ve), but normal Ve relative to metabolic rate (Ve/Vo2). At P10-12, lesioned animals had a more unstable breathing pattern (P = 0.04) and an enhanced Ve response to moderate hypercapnia (P = 0.007). Within the first two postnatal weeks, the medullary 5-HT system plays an important role in cardiorespiratory control, mitigating spontaneous bradycardia, stabilizing the breathing pattern, and dampening the hypercapnic Ve response.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5,7-Dihydroxytryptamine / toxicity*
  • Adaptation, Physiological
  • Age Factors
  • Animals
  • Animals, Newborn
  • Apnea / metabolism
  • Apnea / physiopathology
  • Asphyxia / metabolism
  • Asphyxia / physiopathology
  • Body Weight / drug effects
  • Bradycardia / chemically induced*
  • Bradycardia / metabolism
  • Bradycardia / physiopathology
  • Brain Stem / drug effects*
  • Brain Stem / metabolism
  • Brain Stem / pathology
  • Brain Stem / physiopathology
  • Energy Metabolism / drug effects
  • Heart Rate / drug effects*
  • Humans
  • Hypercapnia / metabolism
  • Hypercapnia / physiopathology
  • Hypoxia / metabolism
  • Hypoxia / physiopathology
  • Infant
  • Infant, Newborn
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / pathology
  • Oxygen Consumption / drug effects
  • Pulmonary Ventilation / drug effects
  • Rats
  • Reflex / drug effects
  • Respiration Disorders / chemically induced*
  • Respiration Disorders / metabolism
  • Respiration Disorders / physiopathology
  • Respiratory Mechanics / drug effects*
  • Serotonin / metabolism*
  • Serotonin Agents / toxicity*
  • Sudden Infant Death

Substances

  • Serotonin Agents
  • 5,7-Dihydroxytryptamine
  • Serotonin