Sporadic autonomic dysregulation and death associated with excessive serotonin autoinhibition

Science. 2008 Jul 4;321(5885):130-3. doi: 10.1126/science.1157871.

Abstract

Sudden infant death syndrome is the leading cause of death in the postneonatal period in developed countries. Postmortem studies show alterations in serotonin neurons in the brainstem of such infants. However, the mechanism by which altered serotonin homeostasis might cause sudden death is unknown. We investigated the consequences of altering the autoinhibitory capacity of serotonin neurons with the reversible overexpression of serotonin 1A autoreceptors in transgenic mice. Overexpressing mice exhibited sporadic bradycardia and hypothermia that occurred during a limited developmental period and frequently progressed to death. Moreover, overexpressing mice failed to activate autonomic target organs in response to environmental challenges. These findings show that excessive serotonin autoinhibition is a risk factor for catastrophic autonomic dysregulation and provide a mechanism for a role of altered serotonin homeostasis in sudden infant death syndrome.

Publication types

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

MeSH terms

  • Animals
  • Autonomic Nervous System / physiology*
  • Autoreceptors / metabolism
  • Body Temperature
  • Doxycycline / pharmacology
  • Electrocardiography
  • Feedback, Physiological
  • Heart Rate
  • Homeostasis
  • Humans
  • Infant
  • Mice
  • Mice, Transgenic
  • Motor Activity
  • Neural Inhibition*
  • Neurons / metabolism
  • Neurons / physiology*
  • Piperazines / administration & dosage
  • Piperazines / pharmacology
  • Pyridines / administration & dosage
  • Pyridines / pharmacology
  • Raphe Nuclei / cytology
  • Raphe Nuclei / metabolism
  • Receptor, Serotonin, 5-HT1A / genetics
  • Receptor, Serotonin, 5-HT1A / metabolism
  • Serotonin / metabolism*
  • Serotonin Antagonists / administration & dosage
  • Serotonin Antagonists / pharmacology
  • Sudden Infant Death / etiology*
  • Sympathetic Nervous System / physiology
  • Synaptic Transmission
  • Tryptophan / metabolism
  • Tryptophan / pharmacology

Substances

  • Autoreceptors
  • Piperazines
  • Pyridines
  • Serotonin Antagonists
  • Receptor, Serotonin, 5-HT1A
  • Serotonin
  • N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide
  • Tryptophan
  • Doxycycline