中华外科杂志
中華外科雜誌
중화외과잡지
CHINESE JOURNAL OF SURGERY
2010年
20期
1569-1572
,共4页
茅磊%王汉东%王笑亮%乔梁%印红霞
茅磊%王漢東%王笑亮%喬樑%印紅霞
모뢰%왕한동%왕소량%교량%인홍하
脊髓损伤%基因敲除%转录因子NF-E2相关因子2%基质金属蛋白酶-9
脊髓損傷%基因敲除%轉錄因子NF-E2相關因子2%基質金屬蛋白酶-9
척수손상%기인고제%전록인자NF-E2상관인자2%기질금속단백매-9
Spinal cord injury%Mice,knockout%Nuclear factor E2-related factor 2%Matrix metalloproteinase-9
目的 探讨转录因子NF-E2相关因子2(Nrf2)对小鼠脊髓损伤后脊髓内肿瘤坏死因子-α(TNF-α)及基质金属蛋白酶-9(MMP-9)表达的影响.方法 分别利用野生型Nrf2(+/+)小鼠及Nrf2(-/-)基因敲除小鼠制作脊髓钳夹损伤模型.在小鼠脊髓损伤后48 h用干湿比法测定脊髓水肿程度.在脊髓损伤后24 h,用逆转录聚合酶链式反应(RT-PCR)法测定脊髓组织MMP-9 mRNA含量的变化;酶联免疫吸附试验测定脊髓组织中TNF-α及MMP-9蛋白的含量;明胶酶谱法测定脊髓组织中MMP-9的酶活性.用SPSS 16.0软件进行统计学分析.结果 脊髓损伤后48 h,Nrf2(-/-)基因敲除小鼠及Nrf2(+/+)小鼠的脊髓均出现明显水肿,但Nrf2(-/-)基因敲除小鼠尤为严重(P<0.05).脊髓损伤后24 h,Nrf2(-/-)基因敲除小鼠及Nrf2(+/+)小鼠的脊髓内TNF-α与MMP-9的表达均增加,但Nrf2(-/-)基因敲除小鼠尤为显著(P<0.01).同时,Nrf2(-/-)基因敲除小鼠在脊髓损伤后24 h,脊髓内MMP-9明胶酶活性较Nrf2(+/+)小鼠的损伤组明显增强(P<0.01).结论 Nrf2在小鼠脊髓损伤后可能是通过减少炎性介质TNF-α及MMP-9的表达,降低MMP-9的明胶酶活性来减轻炎症反应,减轻脊髓水肿程度,起到神经保护的作用.
目的 探討轉錄因子NF-E2相關因子2(Nrf2)對小鼠脊髓損傷後脊髓內腫瘤壞死因子-α(TNF-α)及基質金屬蛋白酶-9(MMP-9)錶達的影響.方法 分彆利用野生型Nrf2(+/+)小鼠及Nrf2(-/-)基因敲除小鼠製作脊髓鉗夾損傷模型.在小鼠脊髓損傷後48 h用榦濕比法測定脊髓水腫程度.在脊髓損傷後24 h,用逆轉錄聚閤酶鏈式反應(RT-PCR)法測定脊髓組織MMP-9 mRNA含量的變化;酶聯免疫吸附試驗測定脊髓組織中TNF-α及MMP-9蛋白的含量;明膠酶譜法測定脊髓組織中MMP-9的酶活性.用SPSS 16.0軟件進行統計學分析.結果 脊髓損傷後48 h,Nrf2(-/-)基因敲除小鼠及Nrf2(+/+)小鼠的脊髓均齣現明顯水腫,但Nrf2(-/-)基因敲除小鼠尤為嚴重(P<0.05).脊髓損傷後24 h,Nrf2(-/-)基因敲除小鼠及Nrf2(+/+)小鼠的脊髓內TNF-α與MMP-9的錶達均增加,但Nrf2(-/-)基因敲除小鼠尤為顯著(P<0.01).同時,Nrf2(-/-)基因敲除小鼠在脊髓損傷後24 h,脊髓內MMP-9明膠酶活性較Nrf2(+/+)小鼠的損傷組明顯增彊(P<0.01).結論 Nrf2在小鼠脊髓損傷後可能是通過減少炎性介質TNF-α及MMP-9的錶達,降低MMP-9的明膠酶活性來減輕炎癥反應,減輕脊髓水腫程度,起到神經保護的作用.
목적 탐토전록인자NF-E2상관인자2(Nrf2)대소서척수손상후척수내종류배사인자-α(TNF-α)급기질금속단백매-9(MMP-9)표체적영향.방법 분별이용야생형Nrf2(+/+)소서급Nrf2(-/-)기인고제소서제작척수겸협손상모형.재소서척수손상후48 h용간습비법측정척수수종정도.재척수손상후24 h,용역전록취합매련식반응(RT-PCR)법측정척수조직MMP-9 mRNA함량적변화;매련면역흡부시험측정척수조직중TNF-α급MMP-9단백적함량;명효매보법측정척수조직중MMP-9적매활성.용SPSS 16.0연건진행통계학분석.결과 척수손상후48 h,Nrf2(-/-)기인고제소서급Nrf2(+/+)소서적척수균출현명현수종,단Nrf2(-/-)기인고제소서우위엄중(P<0.05).척수손상후24 h,Nrf2(-/-)기인고제소서급Nrf2(+/+)소서적척수내TNF-α여MMP-9적표체균증가,단Nrf2(-/-)기인고제소서우위현저(P<0.01).동시,Nrf2(-/-)기인고제소서재척수손상후24 h,척수내MMP-9명효매활성교Nrf2(+/+)소서적손상조명현증강(P<0.01).결론 Nrf2재소서척수손상후가능시통과감소염성개질TNF-α급MMP-9적표체,강저MMP-9적명효매활성래감경염증반응,감경척수수종정도,기도신경보호적작용.
Objective To investigate the role of nuclear factor erythroid 2-related factor 2 (Nrf2)as a key transcription factor of cytoprotection against inflammation in the spinal cord upregulation of matrix metalloproteinase-9 (MMP-9), tumor necrosis factor-α(TNF-α) after spinal cord injury (SCI). Methods Wild-type Nrf2 (+/+) and Nrf2 (-/-)-deficient mice were subjected to a murine SCI model induced by the application of vascular clips (force of 10 g) to the dura after a three-level T8-T10 laminectomy. The wet/dry weight ratio was used to reflect the percentage of water content of impaired spinal cord tissue at 48 h after SCI. The mRNA levels of MMP-9 were determined using reverse-transcriptase polymerase chain reaction (RT-PCR), and the protein levels of TNF-α and MMP-9 were detected by enzyme-linked immunosorbent assay at 24 h after SCI. Furthermore, gelatin zymography analysis was used to show MMP-9 activity of spinal cord tissue at 24 h after SCI. Software SPSS 16.0 was used for the statistical analysis.Results After SCI, spinal cord water content , the expression of TNF-α and MMP-9 all increased in both injured Nrf2 (+/+) and Nrf2 (-/-) mice compared with their respective sham-operated mice.However, Nrf2 (-/-) mice were shown to have more severe spinal cord edema, more TNF-α expression,more production and activity of MMP-9 compared with their wild-type Nrf2 (+/+) counterparts after SCI (P < 0. 05). Conclusions The results suggest that Nrf2 plays an important protective role in limiting the spinal cord upregulation of TNF-α and MMP-9 after SCI. It may be a new therapic target of SCI.