Daily isoflurane exposure increases barbiturate insensitivity in medullary respiratory and cortical neurons via expression of ε-subunit containing GABA ARs

PLoS One. 2015 Mar 6;10(3):e0119351. doi: 10.1371/journal.pone.0119351. eCollection 2015.

Abstract

The parameters governing GABAA receptor subtype expression patterns are not well understood, although significant shifts in subunit expression may support key physiological events. For example, the respiratory control network in pregnant rats becomes relatively insensitive to barbiturates due to increased expression of ε-subunit-containing GABAARs in the ventral respiratory column. We hypothesized that this plasticity may be a compensatory response to a chronic increase in inhibitory tone caused by increased central neurosteroid levels. Thus, we tested whether increased inhibitory tone was sufficient to induce ε-subunit upregulation on respiratory and cortical neurons in adult rats. Chronic intermittent increases in inhibitory tone in male and female rats was induced via daily 5-min exposures to 3% isoflurane. After 7d of treatment, phrenic burst frequency was less sensitive to barbiturate in isoflurane-treated male and female rats in vivo. Neurons in the ventral respiratory group and cortex were less sensitive to pentobarbital in vitro following 7d and 30d of intermittent isoflurane-exposure in both male and female rats. The pentobarbital insensitivity in 7d isoflurane-treated rats was reversible after another 7d. We hypothesize that increased inhibitory tone in the respiratory control network and cortex causes a compensatory increase in ε-subunit-containing GABAARs.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Barbiturates / pharmacology*
  • Cerebral Cortex / metabolism*
  • Female
  • Gene Expression Regulation / drug effects
  • Isoflurane / pharmacology*
  • Male
  • Neurons / metabolism*
  • Pregnancy
  • Rats
  • Receptors, GABA-A / biosynthesis*
  • Respiratory Center / metabolism*
  • Sex Characteristics

Substances

  • Barbiturates
  • Receptors, GABA-A
  • Isoflurane
  • barbituric acid