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雷公藤甲素對大鼠坐骨神經(jīng)冷保存后細(xì)胞活性及異體移植后神經(jīng)再生的影響

發(fā)布時間:2022-02-04 18:37
  目的探討雷公藤甲素(T10)對冷保存大鼠坐骨神經(jīng)生物活性和異體移植后神經(jīng)再生的影響。方法取對數(shù)生長期施萬細(xì)胞(SCs),CCK-8檢測10-66 mol/L、10-77 mol/L、10-88 mol/L、10-99 mol/L T10溶液對SCs增殖的影響。取Sprague-Dawley雌性大鼠雙側(cè)坐骨神經(jīng)15 mm,分別在含0 mol/L、10-66 mol/L、10-7mol/L、10-88 mol/L、10-99 mol/L T10的DMEM液中,4℃或37℃培養(yǎng)24 h(n=6),Western blotting檢測神經(jīng)生長因子(NGF)、神經(jīng)膠質(zhì)細(xì)胞源性神經(jīng)營養(yǎng)因子(GDNF)、腦源性神經(jīng)營養(yǎng)因子(BDNF)表達(dá)。另取大鼠坐骨神經(jīng)15 mm,隨機分成新鮮神經(jīng)組(A組,n=30)、DMEM保存組(B組,n=30)、T10保存組(C組,n=30)、T10預(yù)處理后DMEM保存組(D組,n=30)、T10預(yù)處... 

【文章來源】:重慶醫(yī)科大學(xué)重慶市

【文章頁數(shù)】:52 頁

【學(xué)位級別】:碩士

【部分圖文】:

雷公藤甲素對大鼠坐骨神經(jīng)冷保存后細(xì)胞活性及異體移植后神經(jīng)再生的影響


雷公藤甲素(T10)對雪旺細(xì)胞的細(xì)胞毒性Fig1.CytotoxicityofT10onSCs.Comparisonbetweenthe10-6MT10-treatedand

坐骨神經(jīng),雷公藤甲素,誘導(dǎo)培養(yǎng),預(yù)處理


圖 2: 雷公藤甲素預(yù)處理誘導(dǎo)培養(yǎng)坐骨神經(jīng) NGF、BDNF、GDNF 蛋白表達(dá)Fig 2. Levels of NGF, BDNF, and GDNF in cultured sciatic nerves pretreated withT10. Note :1) Significantly increased levels of NGF, BDNF, and GDNF were detectedfor all of the 37°C pretreatment groups compared with those for all of the 4°Cpretreatment groups (P<0.001, P<0.001, and P<0.001, respectively, Fig. 2A-C). 2) Forthe 4°C pretreatment groups, the 10-8M T10-treated group had significantly increasedNGF levels and increased levels of BDNFcompared with the groups receiving otherconcentrations of T10 (*P<0.001and *P=0.03, Fig. 2A and 2C).But no obviousdifferences were observed for GDNF expression levels among the groups (*P=0.147,Fig. 2B). 3) For the 37°C pretreatment groups, the 10-8M T10-treated groups hadsignificantly increased levels of NGF、GDNF and BDNF expression compared withthe other T10-treated groups ( **P<0.001, P<0.001, and P<0.001, respectively, Fig.2A-C).

激光共聚焦顯微鏡,神經(jīng)細(xì)胞,組圖


D 組 E 組圖 3:激光共聚焦顯微鏡觀察冷保存神經(jīng)細(xì)胞活性Fig 3. Observation of cryopreserved nerve cell activity using laser confocalmicroscopy.

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