摘要
目的观察大承气汤对心脏骤停后综合征(PCAS)兔血清肥大细胞类胰蛋白酶和单核细胞趋化蛋白-1(MCP-1)、白细胞介素8(IL-8)水平的影响。方法大耳白兔30只,随机分为假手术组、模型组、大承气汤组。采用窒息性心脏骤停制备兔PCAS模型。大承气汤组在自主循环恢复后15 min给予大承气汤每日15 g/kg灌胃(分2次使用)。分别在0、24、48、72 h观察反映器官功能的检测指标,采用ELISA测定兔血清类胰蛋白酶、MCP-1、IL-8的水平。结果大承气汤可明显减轻心、脑、肝、肾功能障碍。PCAS模型组血清类胰蛋白酶、MCP-1和IL-8含量均明显高于假手术组(P<0.01)。大承气汤组血清类胰蛋白酶含量(6 h)、MCP-1含量(6、24、48 h)和IL-8含量(6、24 h)均明显低于PCAS模型组(P<0.05或P<0.01)。结论大承气汤可降低PCAS兔血清类胰蛋白酶、MCP-1、IL-8的水平。
Objective To observe the effects of Dachengqi decoction on serum levels of mast cell tryptase, monocyte chemoattractant protein-1 (MCP-I) and interleukin-8 (IL-8) in rabbits with post-cardiac arrest syndrome (PCAS). Methods Thirty healthy male Japanese rabbits were randomly divided into three groups: sham-operation group, PCAS model group and Dachengqi decoction treatment group. The model of PCAS was established by asphyxia-induced cardiac arrest. Fifteen minutes after return of spontaneous circulation, Dachengqi decoction [15 g/(kg · d), bid] was given by intra-gastric adrrinistration in Dachengqi decoction treatment group. The indicators of organ function were evaluated 24, 48 and 72 hours after cardiac arrest. The serum levels of mast cell tryptase, MCP-1 and IL-8 were determined by ELISA. Results Dachengqi decoction alleviated the dysfunction significantly in heart, brain, liver and kidney. Compared with the sham group, the serum levels of mast cell tryptase, MCP-1 and IL-8 increased significantly in PCAS group (P 〈 0.01). Compared with the PCAS group, the serum levels of mast cell tryptase (at 6 hours), MCP-1 (at 6, 24 and 48 hours) and IL-8 (at 6 and 24 hours) decreased significantly in Dachengqi decoction treatment group ( P 〈 0.05 or P 〈 0.01 ). Conclusion Dachengqi decoction can reduce the serum levels of mast cell tryptase, MCP-1 and IL-8 in rabbits with post-cardiac arrest syndrome.
出处
《细胞与分子免疫学杂志》
CAS
CSCD
北大核心
2014年第10期1026-1029,共4页
Chinese Journal of Cellular and Molecular Immunology
基金
湖北省自然科学基金(2010CDBO9101)
关键词
心脏骤停综合征
大承气汤
类胰蛋白酶
炎性细胞因子
post-cardiac arrest syndrome
Dachengqi decoction
tryptase
inflammatory cytokines