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[人Bcl-2基因转染对大鼠肝移植缺血/再灌注损伤的肝脏保护作用]

[Transfection of hBcl-2 gene protects the liver against ischemia/reperfusion injury in rats during liver transplantation].

作者信息

Liu Ji-tong, Liu Jing-shi, Jiang Jin-yu, Zhou Li-xue, Liang Gang, Li Yan-chun

机构信息

Department of Anesthesiology, People's Hospital of Hunan Province, Changsha, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2010 Dec;30(12):2679-82.

Abstract

OBJECTIVE

To study the effect of hBcl-2 gene transfer on rat liver against ischemia-reperfusion injury, and explore the feasibility of this approach to reduce ischemia-reperfusion injury in liver transplantation.

METHODS

We constructed the replication-deficient recombinant adenoviruses Adv-EGFP and Adv-Bcl-2 and transfected them into 293 cells and packaged into adenovirus particles for amplification and purification. The empty plasmid vector virus was constructed similarly. Male SD rats were randomized into Adv-Bcl-2-transfected group, Adv-EGFP-transfected group, ischemia-reperfusion group, and sham-operated group, and liver allograft transplantation model was established by sleeve method. In the transfected groups, the recombinant viruses were administered by perfusion through the portal vein, and the ischemia-reperfusion and sham-operated groups received no treatment. Real-time quantitative PCR and Western blotting were used to detect the mRNA and protein expressions of bcl-2 in the liver tissue of each group, and at 0, 60 and 180 min after reperfusion, serum AST, LDH, and MDA levels were measured. Histological changes of the liver cells were evaluated by HE staining.

RESULTS

Bcl-2 mRNA and protein expressions in Adv-Bcl-2-transfected group, as compared with those in Adv-EGFP-transfected group and control group, were significantly increased (P<0.01); the serum levels of AST, LDH and MDA in Adv-Bcl-2-transfected group were significantly lower than those of Adv-EGFP-transfected group and ischemia-reperfusion group (P<0.05 or 0.01). Compared with the sham-operated group, Adv-Bcl-2 treatment group showed lessened edema and vacuolar degeneration of the liver cells without patches or spots of necrosis. In ischemia-reperfusion and Adv-EGFP group, HE staining revealed hepatic lobular destruction and extensive liver cell swelling, enlargement, vacuolar degeneration, edema and occasional focal necrosis.

CONCLUSION

Adv-Bcl-2 transfection can induce the expression of bcl-2 gene to reduce ischemia-reperfusion injury of the liver graft in rats.

摘要

目的

研究hBcl-2基因转导对大鼠肝脏缺血再灌注损伤的影响,探讨该方法减轻肝移植中缺血再灌注损伤的可行性。

方法

构建复制缺陷型重组腺病毒Adv-EGFP和Adv-Bcl-2,转染293细胞并包装成腺病毒颗粒进行扩增和纯化。以同样方法构建空质粒载体病毒。将雄性SD大鼠随机分为Adv-Bcl-2转染组、Adv-EGFP转染组、缺血再灌注组和假手术组,采用套管法建立肝移植模型。在转染组中,通过门静脉灌注给予重组病毒,缺血再灌注组和假手术组不做处理。采用实时定量PCR和蛋白质印迹法检测各组肝组织中bcl-2的mRNA和蛋白质表达,并在再灌注后0、60和180分钟测定血清AST、LDH和MDA水平。通过HE染色评估肝细胞的组织学变化。

结果

Adv-Bcl-2转染组的Bcl-2 mRNA和蛋白质表达与Adv-EGFP转染组和对照组相比显著增加(P<0.01);Adv-Bcl-2转染组的血清AST、LDH和MDA水平显著低于Adv-EGFP转染组和缺血再灌注组(P<0.05或0.01)。与假手术组相比,Adv-Bcl-2治疗组肝细胞水肿和空泡变性减轻,无片状或点状坏死。在缺血再灌注组和Adv-EGFP组中,HE染色显示肝小叶破坏,肝细胞广泛肿胀、增大、空泡变性、水肿,偶见局灶性坏死。

结论

Adv-Bcl-2转染可诱导bcl-2基因表达,减轻大鼠移植肝的缺血再灌注损伤。

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