The protective effects of dexmedetomidine on the liver and kidney injury in heat stroke rats

被引:0
作者
Yang, Xiaoming [1 ,2 ,3 ]
Liu, Jun [4 ]
Wang, Shanshan [1 ,2 ,3 ]
Wang, Tao [1 ]
机构
[1] Chinese PLA Air Force Gen Hosp, Dept Anesthesiol, 30 Fucheng Rd, Beijing 100142, Peoples R China
[2] Xuzhou Med Coll, Jiangsu Prov Key Lab Anesthesiol, Xuzhou 221002, Peoples R China
[3] Jiangsu Prov Key Lab Anesthesiol & Analgesia Appl, Xuzhou 221002, Peoples R China
[4] Chinese PLA Air Force Gen Hosp, Dept Informat, Beijing 100142, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | 2016年 / 9卷 / 02期
关键词
Dexmedetomidine; heat stroke; inflammation; cytokine; INFLAMMATORY RESPONSES; CYTOKINES; CARE;
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
The current study aimed to explore whether dexmedetomidine could attenuate heat-induced liver and kidney injury in rats and the possible mechanism. Forty eight male anesthetized SD rats were randomly divided into following three groups (n=16): blank control group (group C), heat stroke model group (group HS) and dexmedetomidine group (group Dex). The model and dexmedetomidine groups were subjected to heat stress (40 +/- 0.5 degrees C) to induce heat stroke. A bolus injection of normal saline or dexmedetomidine (25 mu g/kg) was administrated intraperitoneally immediately after the onset of heat stroke. Blood samples were gained at 1 h (T1) and 6 h (T6) after injection, the serum concentrations of ALT, AST, Cr, BUN, IL-1 beta, IL-6 and TNF-alpha were measured. The serum concentrations of liver and kidney injury markers (ALT, AST, BUN, Cr) and inflammatory cytokines (IL-1 beta, IL-6, TNF-alpha) in group HS were significantly higher than in group C in T1 and T6 (P<0.05). In addition, the concentrations of ALT, AST, BUN, Cr, IL-1 beta, IL-6 and TNF-alpha in group Dex were lower than in group HS in two time points (P<0.05). Systemic delivery of dexmedetomidine at the time point of onset of heat stroke may ameliorate the liver and kidney injury by regulating inflammation and decreasing the inflammatory cytokines.
引用
收藏
页码:3775 / 3779
页数:5
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