Recordings from brain stem neurons responding to chemical stimulation of the subarachnoid space

J Neurophysiol. 1997 Jun;77(6):3122-33. doi: 10.1152/jn.1997.77.6.3122.

Abstract

The subarachnoid space at the base of the skull was perfused continuously with artificial cerebrospinal fluid in anesthetized rats. A combination of inflammatory mediators consisting of histamine, bradykinin, serotonin, and prostaglandin E2 (10(-5) M) at pH of 6.1 was introduced into the flow for defined periods to stimulate meningeal primary afferents. Secondary neurons in the caudal nucleus of the trigeminal brain stem were searched by electrical stimulation of the cornea. Of the units receiving oligosynaptic input from the cornea, 44% were excited by stimulation of the meninges with inflammatory mediators. Most of these units had small receptive fields including cornea and the periorbital region, and their responsiveness was restricted to stimuli of noxious intensity. Three types of responses to stimulation of the meninges with algogenic agents were encountered: responses that did not outlast the stimulus period, responses outlasting the stimulus period for several minutes, and oscillating response patterns containing periods of enhanced and suppressed activity. The response pattern of a unit was reproducible, however, upon repetitive stimulation at 20-min intervals; the response magnitude showed tachyphylaxis upon stimulus repetition. The preparation presented mimics pathophysiolocial states normally accompanied by headache, e.g., subarachnoidal bleeding. Responsiveness of neurons in the caudal nucleus of the trigeminal brain stem to inflammatory mediators may play a role in the generation and maintenance of headache, e.g., migraine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Afferent Pathways / physiology
  • Animals
  • Brain Mapping
  • Brain Stem / physiology*
  • Chemoreceptor Cells / physiology*
  • Cornea / innervation
  • Evoked Potentials / physiology
  • Headache / physiopathology
  • Inflammation Mediators / physiology*
  • Male
  • Meninges / physiology*
  • Migraine Disorders / physiopathology
  • Models, Neurological
  • Neurons / physiology
  • Nociceptors / physiology
  • Orbit / innervation
  • Pain Threshold / physiology
  • Rats
  • Rats, Wistar
  • Subarachnoid Hemorrhage / physiopathology
  • Subarachnoid Space / physiology*
  • Trigeminal Nuclei / physiology

Substances

  • Inflammation Mediators