Matrix metalloproteinase 2 gene knockout has no effect on acute brain injury after focal ischemia

Neuroreport. 2001 Sep 17;12(13):3003-7. doi: 10.1097/00001756-200109170-00050.

Abstract

Matrix metalloproteinases (MMPs) may contribute to tissue damage after cerebral ischemia. In this study, wildtype and MMP-2 knockout mice were subjected to permanent and transient (2 h) occlusions of the middle cerebral artery. Gelatin zymography showed that MMP-9 levels were increased in all brains after ischemia. MMP-2 levels did not show a significant increase in wildtype mice, and were not detectable in knockout mice. Laser doppler flowmetry demonstrated equivalent ischemic reductions in perfusion in wildtype and knockout mice. In both permanent and transient occlusion paradigms, there were no statistically significant differences between wildtype and knockout mice in terms of 24 h ischemic lesion volumes. These data suggest that MMP-2 does not contribute to acute tissue damage in this model of focal ischemia.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain / blood supply
  • Brain / enzymology
  • Brain / pathology
  • Brain Ischemia / enzymology*
  • Brain Ischemia / pathology
  • Brain Ischemia / physiopathology
  • Cerebral Infarction / enzymology*
  • Cerebral Infarction / pathology
  • Cerebral Infarction / physiopathology
  • Cerebrovascular Circulation / physiology
  • Male
  • Matrix Metalloproteinase 2 / deficiency*
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • Mice
  • Mice, Knockout
  • Nerve Degeneration / enzymology*
  • Nerve Degeneration / pathology
  • Nerve Degeneration / physiopathology

Substances

  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9