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刘光艺,朱继芳,李洋.谷氨酰胺对肝移植大鼠肠黏膜NF-κB、ICAM-1、TNF-α表达的影响[J].陆军军医大学学报(原第三军医大学学报),2013,35(12):1205-1209.
Liu Guangyi,Zhu Jifang,Li Yang.Effect of glutamine on expression of NF-κB,ICAM-1 and TNF-α in intestinal mucosa after liver transplantation in rats[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(12):1205-1209.
刘光艺,朱继芳,李洋.谷氨酰胺对肝移植大鼠肠黏膜NF-κB、ICAM-1、TNF-α表达的影响[J].陆军军医大学学报(原第三军医大学学报),2013,35(12):1205-1209. DOI:
Liu Guangyi,Zhu Jifang,Li Yang.Effect of glutamine on expression of NF-κB,ICAM-1 and TNF-α in intestinal mucosa after liver transplantation in rats[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(12):1205-1209. DOI:
目的 研究谷氨酰胺(Glutamine
Gln)对原位肝移植(orthotopic liver transplantation
OLT)大鼠肠黏膜内核转录因子-κB(NF-κB)、细胞间黏附分子-1(ICAM-1)、肿瘤坏死因子-α(TNF-α)表达的影响。 方法 选择健康雄性Wistar大鼠70只,按随机数字表法分为对照组(n=10)、原位肝移植组(OLT组,n=30)和原位肝移植+Gln组(EEN组,n=30);对照组只分离肝十二指肠韧带,OLT组和EEN组按改良的两袖套法进行原位肝移植。EEN组受体在术前3 d、术后3 h开始给予肠内营养混悬液能全力+谷氨酰胺灌胃,OLT组及对照组受体仅给予肠内营养混悬液。对照组分离肝十二指肠韧带12 h后,OLT组和EEN组肝移植后12、24、72 h分别取回肠肠壁组织免疫组化测定肠组织NF-κB与ICAM-1的表达,荧光定量PCR(fluorescence quantitive- polymerase chain reaction
FQ-PCR)测定肠黏膜TNF-α mRNA表达、HE染色观察回肠组织的病理改变,测定微绒毛长度。 结果 与对照组比较OLT组和EEN组肝移植后12、24、72 h,NF-κB、ICAM-1、TNF-α mRNA表达明显升高,肠黏膜损害明显加重,差异有统计学意义(
P
0.01);而肝移植后12、24、72 h EEN组与OLT组比较,NF-κB、ICAM-1、TNF-α mRNA表达明显下降,肠黏膜损害明显减轻,差异有统计学意义(
P
0.01)。 结论 大鼠原位肝移植可引起肠组织中NF-κB活化,ICAM-1、TNF-α表达上调导致肠黏膜屏障损伤,Gln能抑制肝移植大鼠肠黏膜NF-κB活性,减少ICAM-1、TNF-α的表达而起到肠黏膜保护作用。
Objective To investigate the effect of glutamine (Gln) on the expression of nuclear factor kappa B (NF-κB)
intercellular adhesion molecule-1 (ICAM-1) and tumor necrosis factor α (TNF-α) in intestinal mucosa after orthotopic liver transplan
tation (OLT) in rats. Methods Seventy healthy male Wistar rats were divided randomly into three groups including a normal control group (control group
n=10)
an orthotopic liver transplantation group (OLT group
n=30) and an early enteral nutrition group (EEN group
n=30). Only hepatoduodenal ligament dissection was performed in the control group
and OLT was performed by modified two-cuff method in the OLT group and EEN group. For the EEN group
the recipients were supplied with Nutrison Fiber 125 mL/(kg·d) plus Gln 0.3 g/(kg·d) for 3 d by gastric perfusion before surgery
and Nutrison Fiber plus Gln was administered again until the animal was killed at 3 h after OLT. For the OLT group and control group
the same volume of the Nutrison Fiber was supplied by gastric perfusion at the same time. The expression of NF-κB and ICAM-1 in the ileal mucosa were determined by immunohisto chemistry
the mRNA level of TNF-α in the ileal mucosa was detected with fluorescence quantitative-polymerase chain reaction (FQ-PCR)
and the ultrastructural changes of the ileal mucosa were observed with transmission electron microscopy (TEM) at 12 h after hepatoduodenal ligament dissection in the control group and at 12
24 and 72 h after OLT in the OLT group and EEN group. Results Compared with the control group
the levels of NF-κB
ICAM-1 and TNF-α mRNA significantly increased and the mucosal lesion significantly aggravated in the OLT group and EEN group at 12
24 and 72 h after OLT (P0.01). Compared with the OLT group
the levels of NF-κB
ICAM-1 and TNF-α mRNA were significantly decreased and the mucosal lesion was significantly relieved in the EEN group at 12
24 and 72 h after OLT (
P
0.01). Conclusion OLT can activate NF-κB in intestinal mucosa
and up-regulate the expression of ICAM-1 and TNF-α to induce the injury of intestinal mucosal barrier. Gln can protect the intestinal mucosal barrier through suppressing the activation of NF-κB and reducing the expression of ICAM-1 and TNF-α after
OLT.
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