PROTECTION AGAINST HIPPOCAMPAL CA1 CELL LOSS BY POSTISCHEMIC HYPOTHERMIA IS DEPENDENT ON DELAY OF INITIATION AND DURATION

被引:132
|
作者
CARROLL, M
BEEK, O
机构
[1] Department of Pharmacology, Burroughs Wellcome Co., Research Triangle Park, 27709, North Carolina
关键词
HYPERTHERMIA; DELAYED NEURONAL DEATH; REPERFUSION;
D O I
10.1007/BF01000440
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The temporal constraints of protection of neuronal damage by post-ischemic hypothermia was investigated in the gerbil model of global ischemia. Three experimental paradigms were used: 1) Hypothermia was initiated prior to ischemia followed by warming to normothermia immediately post ischemia; 2) Hypothermia of different durations was initiated immediately after reflow and 3) Six hours of hypothermia was initiated at various times following reperfusion. Hypothermia during 5 minutes of ischemia followed by warming to normal body temperature immediately post ischemia resulted in near complete protection of the hippocampus from CA1 cell loss. Hypothermic durations of 1/2, 1, 2, 4, and 6 hours beginning immediately following reperfusion resulted in progressively increased protection from ischemic damage (6 +/- 6%, 21 +/- 10%, 34 +/- 15%, 75 +/- 16% and 77 +/- 12%, respectively). Six hours of hypothermia delayed for 1 hour after reperfusion resulted in 49 +/- 9% protection. No reduction of ischemic damage was observed if 6 hours of hypothermia was delayed for 3 hour after reflow. These data suggest that: 1) Hypothermia during ischemia protects the brain from damage; 2) Hypothermia initiated immediately following reperfusion must have a duration of 2 hours or more to be effective and 3) Six hours of hypothermia is effective if initiated within 1 hour of reperfusion.
引用
收藏
页码:45 / 50
页数:6
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