Role of Kir2.2 in hypercapnic ventilatory response during postnatal development of mouse

Respir Physiol Neurobiol. 2005 Feb 15;145(2-3):143-51. doi: 10.1016/j.resp.2004.11.003.

Abstract

In order to determine the role of Kir2.2 in the hypercapnic ventilatory response (HCVR) during postnatal development, we measured the response of the Kir2.2-knockout (Kir2.2-/-) mouse in an unanesthetized unrestrained state by means of pressure plethysmography on postnatal days 9-10, 14-15 and 18, and compared the response with that in its wild counterpart, the FVB mouse. We also examined developmental changes in m-RNA expression of Kir2.2 in the brainstem of the FVB mouse using quantitative real-time PCR assay. Kir2.2-/- exhibited a smaller increase in tidal volume and minute ventilation volume than the FVB mouse in response to hypercapnic challenge on days 14-15. Meanwhile, the FVB mouse showed a transient increase in m-RNA expression of Kir2.2 in the brainstem on days 14-15. These findings suggest that Kir2.2 in the brainstem plays a transient role in HCVR, possibly through central ventilatory chemosensitivity, during postnatal development.

Publication types

  • Comparative Study

MeSH terms

  • Age Factors
  • Analysis of Variance
  • Animals
  • Animals, Newborn / growth & development*
  • Blotting, Southern / methods
  • Brain Stem / growth & development
  • Brain Stem / metabolism
  • Gene Expression Regulation, Developmental / physiology
  • Genotype
  • Hypercapnia / genetics
  • Hypercapnia / physiopathology*
  • Mice
  • Mice, Knockout
  • Phenotype
  • Plethysmography / methods
  • Potassium Channels, Inwardly Rectifying / deficiency
  • Potassium Channels, Inwardly Rectifying / physiology*
  • RNA, Messenger / metabolism
  • Respiration*
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Tidal Volume / genetics
  • Wakefulness / physiology

Substances

  • Kir2.2 channel
  • Potassium Channels, Inwardly Rectifying
  • RNA, Messenger