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热休克蛋白70在瑞芬太尼后处理减轻大鼠肝脏缺血再灌注损伤中的作用
引用本文:李丽珍,钟炜昕,詹根明,林芩.热休克蛋白70在瑞芬太尼后处理减轻大鼠肝脏缺血再灌注损伤中的作用[J].福建医科大学学报,2021,55(5).
作者姓名:李丽珍  钟炜昕  詹根明  林芩
作者单位:福建中医药大学附属人民医院,福建医科大学孟超肝胆医院,福建中医药大学附属人民医院,福建中医药大学附属人民医院
基金项目:福建省卫生计生科研人才培养项目
摘    要:目的 探讨热休克蛋白70(HSP70)在瑞芬太尼后处理减轻大鼠肝脏缺血再灌注损伤(HIRI)中的作用。 方法 将24只SD大鼠随机分为4组(n=6):假手术组(S组)、HIRI组(I/R组)、瑞芬太尼组(R组)和槲皮素组(Q组)。制备大鼠HIRI模型。R组再灌注开始10 min内给予瑞芬太尼4 g/kg;Q组在给予瑞芬太尼前先给予槲皮素7 mg/kg。再灌注结束检测血清丙氨酸氨基转移酶(ALT)和天门氨酸氨基转移酶(AST)活性以及肝组织超氧化物歧化酶(SOD)活性、丙二醛(MDA)和HSP70含量。 结果 与S组比较,其余3组血清ALT、AST活性和肝组织MDA、HSP70含量均升高,而肝组织SOD活性I/R组和Q组降低,R组升高(P<0.05)。与I/R组比较,R组血清ALT、AST活性和MDA含量降低,而肝组织SOD活性和HSP70含量升高(P<0.05)。 结论 瑞芬太尼后处理可减轻大鼠HIRI的急性肝损伤,抑制肝脏脂质过氧化反应,其作用机制与增强肝组织HSP70表达有关。

关 键 词:瑞芬太尼  后处理    缺血再灌注损伤  脂质过氧化  热休克蛋白70
收稿时间:2021/7/11 0:00:00
修稿时间:2021/11/14 0:00:00

Role of heat shock protein 70 in remifentanil post-treatment-induced reduction of hepatic ischemia-reperfusion injury in rats
Li Lizhen,and Lin Qin.Role of heat shock protein 70 in remifentanil post-treatment-induced reduction of hepatic ischemia-reperfusion injury in rats[J].Journal of Fujian Medical University,2021,55(5).
Authors:Li Lizhen  and Lin Qin
Institution:People''s hospital affiliated to fujian university,,,
Abstract:Objective To explore the effect of heat shock protein 70(HSP70) on remifentanil-post-treatment-induced hepatic ischemia-reperfusion injury (HIRI) in rats. Methods Twenty-four Sprague-Dawley rats were randomly divided into four groups( n = 6 ): sham-operation group (group S), HIRI group ( group I/R) , remifentanil group(group R) and quercetin group (group Q).Rat HIRI model was prepared. In Group R, remifentanil 4 ug·kg-1 was given at the beginning of reperfusion within 10 minutes. In group Q, quercetin 7 mg·kg-1 was given before remifentanil treatment. The activities of serum alanine transaminase(ALT) and aspartate transaminase(AST) were measured after reperfusion, and the activity of superoxide dismutase(SOD) , the content of malondialdehyde (MDA ) and HSP70 in liver tissue were measured. Results Compared with group S,?serum ALT and AST activity , liver MDA and HSP70 content were increased in the other three groups, while SOD activity in group I/R and group Q were decreased and that in group R was increased ( P<0.05) .Compared with group I/R, serum ALT,AST activity and MDA content in group R were decreased, while liver SOD activity and HSP70 content were increased( P<0.05). Conclusion Remifentanil post-treatment can attenuate the acute liver injury induced by HIRI and inhibit the lipid peroxidation response, which is related to increasing the expression of HSP70 in liver.
Keywords:remifentanil  post-treatment  liver  ischemia/reperfusion injury  lipid peroxidation  heat shock protein 70
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