Heat shock protein expression protects against death following exposure to heatstroke in rats

被引:46
作者
Yang, YL
Lu, KT
Tsay, HJ
Lin, CH
Lin, MT [1 ]
机构
[1] Natl Yang Ming Univ, Inst Physiol, Taipei 11221, Taiwan
[2] Natl Yang Ming Univ, Inst Neurosci, Taipei 11221, Taiwan
[3] Natl Cheng Kung Univ, Dept Physiol, Tainan 70101, Taiwan
[4] Natl Cheng Kung Univ, Dept Pharmacol, Tainan 70101, Taiwan
关键词
heatstroke; cerebral ischemia; cell death; survival;
D O I
10.1016/S0304-3940(98)00508-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rats 0, 16, or 48 h after heat shock (42 degrees C core temperature for 15 min) or chemical stress (5 mg/kg sodium arsenite, i.p.) were exposed to a high ambient temperature (43 degrees C) to induce heatstroke onset. The moment in which the mean arterial pressure and cerebral blood flow began to decrease from their peak values was taken as the onset of heatstroke. Prior heat shock or chemical stress conferred significant protection against heatstroke-induced arterial hypotension, cerebral ischemia, cerebral neuronal damage and death, and correlated with expression of HSP72 in brain, heart, liver and kidney at 16 h. However, at 48 h, when HSP72 expression returned to basal values, the above responses that occurred after the onset of heatstroke of two groups (0 h group VS 48 h group) were indistinguishable. The data suggest that HSP72 presence increases survival in rat heatstroke by attenuating arterial hypotension, cerebral ischemia and neuronal damage. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 12
页数:4
相关论文
共 16 条
[1]   INEFFECTIVENESS OF DANTROLENE SODIUM IN THE TREATMENT OF HEATSTROKE [J].
BOUCHAMA, A ;
CAFEGE, A ;
DEVOL, EB ;
LABDI, O ;
ELASSIL, K ;
SERAJ, M .
CRITICAL CARE MEDICINE, 1991, 19 (02) :176-180
[2]   Stress proteins and tolerance to focal cerebral ischemia [J].
Chen, J ;
Graham, SH ;
Zhu, RL ;
Simon, RP .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (04) :566-577
[3]   ROLE OF HSP70 IN CYTOKINE PRODUCTION [J].
HALL, TJ .
EXPERIENTIA, 1994, 50 (11-12) :1048-1053
[4]   HYPERTHERMIA PROTECTS MICE AGAINST THE LETHAL EFFECTS OF ENDOTOXIN [J].
HOTCHKISS, R ;
NUNNALLY, I ;
LINDQUIST, S ;
TAULIEN, J ;
PERDRIZET, G ;
KARL, I .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (06) :R1447-R1457
[5]   Brain serotonin depletion attenuates heatstroke-induced cerebral ischemia and cell death in rats [J].
Kao, TY ;
Lin, MT .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 80 (02) :680-684
[6]   Heatstroke-induced cerebral ischemia and neuronal damage - Involvement of cytokines and monoamines [J].
Lin, MT .
THERMOREGULATION: TENTH INTERNATIONAL SYMPOSIUM ON THE PHARMACOLOGY OF THERMOREGULATION, 1997, 813 :572-580
[7]   CEREBRAL-ISCHEMIA IS THE MAIN CAUSE FOR THE ONSET OF HEAT-STROKE SYNDROME IN RABBITS [J].
LIN, MT ;
LIN, SZ .
EXPERIENTIA, 1992, 48 (03) :225-227
[8]   Involvement of interleukin-1 receptor mechanisms in development of arterial hypotension in rat heatstroke [J].
Lin, MT ;
Liu, HH ;
Yang, YL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (04) :H2072-H2077
[9]   INTERLEUKIN-1-BETA PRODUCTION DURING THE ONSET OF HEAT-STROKE IN RABBITS [J].
LIN, MT ;
KAO, TY ;
SU, CF ;
HSU, SSF .
NEUROSCIENCE LETTERS, 1994, 174 (01) :17-20
[10]  
Paxinos G., 1997, RAT BRAIN STEROTAXIC, VThird