Treatment of intracerebral hemorrhage in rats with 12 h, 3 days and 6 days of selective brain hypothermia

Exp Neurol. 2009 Sep;219(1):156-62. doi: 10.1016/j.expneurol.2009.05.007. Epub 2009 May 13.

Abstract

Intracerebral hemorrhage (ICH) is a devastating stroke with no proven treatment to reduce brain injury. In this study we modeled ICH by injecting 100 microL of autologous blood into the striatum of rats. We then tested whether hypothermia would reduce brain injury and improve recovery as has been repeatedly observed for ischemic and traumatic brain damage. Aside from reducing blood-brain barrier disruption, inflammation and edema, hypothermia has not consistently improved behavioral or histological outcome after ICH in animal studies. As this might relate to the choice of cooling method and the duration of hypothermia, we used a system that selectively cooled the injured hemisphere to approximately 32 degrees C (striatum) while the body remained normothermic. Cooling (vs. normothermia) started 1 h after ICH and lasted for 12 h, 3 days or 6 days followed by slow re-warming (approximately 1 degrees C/h). Functional impairment was evaluated from 2 to 3 weeks post-ICH at which time brain injury was determined. The ICH caused significant impairment on a neurological deficit scale and in tests of walking (horizontal ladder), skilled reaching (tray task) and spontaneous limb usage (cylinder test). Only the limb use asymmetry deficit was significantly mitigated by hypothermia, and then only by the longest treatment. Lesion volume, which averaged 16.9 mm3, was not affected. These results, in conjunction with earlier studies, suggest that prolonged mild hypothermia will not be a profound neuroprotectant for patients with striatal ICH, but it may nonetheless improve functional recovery in addition to its use for treating cerebral edema.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Temperature / physiology
  • Brain / metabolism
  • Brain / pathology
  • Brain / physiopathology*
  • Brain Edema / metabolism
  • Brain Edema / physiopathology
  • Brain Edema / therapy
  • Brain Infarction / etiology
  • Brain Infarction / pathology
  • Brain Infarction / physiopathology
  • Cerebral Hemorrhage / metabolism
  • Cerebral Hemorrhage / physiopathology*
  • Cerebral Hemorrhage / therapy*
  • Corpus Striatum / metabolism
  • Corpus Striatum / pathology
  • Corpus Striatum / physiopathology
  • Cytoprotection / physiology
  • Disease Models, Animal
  • Hypothermia, Induced / methods*
  • Male
  • Movement Disorders / diagnosis
  • Movement Disorders / etiology
  • Movement Disorders / physiopathology
  • Rats
  • Rats, Sprague-Dawley
  • Recovery of Function / physiology
  • Rewarming / methods
  • Time Factors
  • Treatment Outcome