Attenuating brain inflammation, ischemia, and oxidative damage by Xuebijing in heat stroke rats

被引:0
作者
Pan, Zhi-Guo [1 ]
Tang, Shao-Hui [2 ]
Shao, Yu [3 ]
Dong, Wen-Peng [4 ]
Liu, Chen-Xi [5 ]
Chen, Yi [1 ]
Jin, Hui [1 ]
Tang, Li-Qun [1 ]
Su, Lei [1 ]
机构
[1] Guangzhou Mil Command, Guangzhou Gen Hosp, Dept ICU, Guangzhou 510010, Guangdong, Peoples R China
[2] Guangzhou Mil Command, Guangzhou Gen Hosp, Dept Emergency, Guangzhou 510010, Guangdong, Peoples R China
[3] Guangzhou Mil Command, Guangzhou Gen Hosp, Dept Internal Med 7, Cadre Ward, Guangzhou 510010, Guangdong, Peoples R China
[4] Guangzhou Mil Command, Guangzhou Gen Hosp, Dept Cardiovasc Surg, Guangzhou 510010, Guangdong, Peoples R China
[5] Guangzhou Mil Command, Guangzhou Gen Hosp, Informat Ctr, Guangzhou 510010, Guangdong, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | 2016年 / 9卷 / 04期
关键词
Xuebijing; heat stroke; inflammation; ischemia; oxidative damage; TUMOR-NECROSIS-FACTOR; ACTIVATED PROTEIN-C; CORD BLOOD-CELLS; EXPERIMENTAL HEATSTROKE; LIVER-INJURY; MICE; RESUSCITATION; LETHALITY; CYTOKINE;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Xuebijing (XBJ) is a Chinese medicine compound preparation. The aim of the present study was to ascertain whether the brain inflammation, ischemia, apoptosis and oxidative damage in heat stroke (HS) rats can be attenuated by pre-treatment with XBJ. Anesthetized rats were divided into a normothermic group, a vehicle-treated HS group (4 mL phosphate-buffered saline per kg body weight twice daily for 3 days) and an XBJ-treated HS group (4 mL XBJ per kg body weight twice daily for 3 days). HS and XBJ-treated groups were exposed to an ambient temperature of 42.4 degrees C for 1 hour to induce HS. Negative control (NCs) was exposed to room temperature (26 degrees C). Their survival time, core temperatures, mean arterial pressures, inflammatory molecules, number of apoptotic cells in the hypothalamus and neuronal damage scores were determined. Hypothalamic neurons were treated with LPS (lipopolysaccharide) with or without XBJ and cell apoptosis was determined. The survival time for the XBJ-treated HS rats increased from the control values of 74-89 minutes to new values of 109-156 minutes. XBJ therapy caused a reduction of HS-induced cellular ischemia, hypoxia, inflammation, cell apoptosis and oxidative damage in the hypothalamus. XBJ significantly inhibited LPS-induced apoptosis of hypothalamic neurons. Our results suggest that XBJ treatment can reduce HS-induced inflammatory, ischemic, apoptotic and oxidative damage to the hypothalamus and can inhibit the apoptosis of hypothalamic neurons induced by LPS.
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收藏
页码:7524 / 7533
页数:10
相关论文
共 25 条
  • [1] INEFFECTIVENESS OF DANTROLENE SODIUM IN THE TREATMENT OF HEATSTROKE
    BOUCHAMA, A
    CAFEGE, A
    DEVOL, EB
    LABDI, O
    ELASSIL, K
    SERAJ, M
    [J]. CRITICAL CARE MEDICINE, 1991, 19 (02) : 176 - 180
  • [2] Experimental heatstroke in baboon: Analysis of the systemic inflammatory response
    Bouchama, A
    Al Mohanna, F
    El-Sayed, R
    Eldali, A
    Saussereau, E
    Collet-Martin, S
    Ollivier, V
    de Prost, D
    Roberts, G
    [J]. SHOCK, 2005, 24 (04): : 332 - 335
  • [3] Medical progress - Heat stroke
    Bouchama, A
    Knochel, JP
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (25) : 1978 - 1988
  • [4] Oxidative stress and ischemic injuries in heat stroke
    Chang, Chen-Kuei
    Chang, Ching-Ping
    Liu, Shyun-Yeu
    Lin, Mao-Tsun
    [J]. NEUROBIOLOGY OF HYPERTHERMIA, 2007, 162 : 525 - 546
  • [5] Prevention and repair of circulatory shock and cerebral ischemia/injury by various agents in experimental heatstroke
    Chang, Cheng-Kuei
    Chang, Ching-Ping
    Chiu, Wen-Ta
    Lin, Mao-Tsun
    [J]. CURRENT MEDICINAL CHEMISTRY, 2006, 13 (26) : 3145 - 3154
  • [6] Therapeutic treatment with L-arginine rescues mice from heat stroke-induced death: Physiological and molecular mechanisms
    Chatterjee, S
    Premachandran, S
    Sharma, D
    Bagewadikar, RS
    Poduval, TB
    [J]. SHOCK, 2005, 24 (04): : 341 - 347
  • [7] Arginine metabolic pathways determine its therapeutic benefit in experimental heatstroke:: Role of Th1/Th2 cytokine balance
    Chatterjee, Saurabh
    Premachandran, Sudha
    Bagewadikar, Raghavendra S.
    Bhattacharya, Sayanti
    Chattopadhyay, Subrata
    Poduval, T. B.
    [J]. NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2006, 15 (04): : 408 - 416
  • [8] Activated Protein C Improves Heatstroke Outcomes Through Restoration of Normal Hypothalamic and Thermoregulatory Function
    Chen, Chien-Chang
    Chen, Zhih-Cherng
    Lin, Mao-Tsun
    Hsu, Chuan-Chih
    [J]. AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2009, 338 (05) : 382 - 387
  • [9] Resuscitation from experimental heatstroke by transplantation of human umbilical cord blood cells
    Chen, SH
    Chang, FM
    Tsai, YC
    Huang, KF
    Lin, MT
    [J]. CRITICAL CARE MEDICINE, 2005, 33 (06) : 1377 - 1383
  • [10] Xuebijing injection alleviates liver injury by inhibiting secretory function of Kupffer cells in heat stroke rats
    Chen, Yi
    Tong, Huasheng
    Zhang, Xingqin
    Tang, Liqun
    Pan, Zhiguo
    Liu, Zhifeng
    Duan, Pengkai
    Su, Lei
    [J]. JOURNAL OF TRADITIONAL CHINESE MEDICINE, 2013, 33 (02) : 243 - 249