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        west china medical publishers
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        find Keyword "mTOR 通路" 2 results
        • Effects of metformin on airway remodeling in rat asthma model

          ObjectiveTo observe the effect of metformin on airway remodeling in asthma and its possible mechanism.MethodsTwenty-eight B/N rats were randomly divided into control group, asthma group, metformin intervention group and rapamycin intervention group. After that, the asthma model was established and intervened with metformin and rapamycin. The airway resistance and airway reactivity were measured 48 hours after the last challenge, and then the lung tissue samples were collected. Histopathological examination was used to observe airway inflammatory cell infiltration, goblet cell proliferation, airway wall fibrosis and remodeling, as well as airway smooth muscle proliferation. The expression of AMPK/mTOR pathway related proteins was detected by Western blot.ResultsCompared with the asthma group, metformin and rapamycin significantly reduced the airway responsiveness induced by high concentration of acetylcholine (P<0.05), reduced the infiltration of inflammatory cells in lung tissue and the changes of airway wall structure (P<0.05), reduced goblet cell proliferation in airway epithelium, collagen fiber deposition in lung tissue and bronchial smooth muscle hyperplasia (P<0.05). Further studies showed that the effects of metformin and rapamycin were related to AMPK/mTOR pathway. Compared with the asthma group, metformin and rapamycin could significantly reduce the expression of p-mTOR, p-p70s6k1 and SKP2, while p21 protein expression was significantly increased (P<0.05). In addition, metformin and rapamycin had similar effects (P>0.05).ConclusionMetformin can alleviate airway hyperresponsiveness and airway remodeling by activating AMPK and then inhibiting mTOR pathway, which may be a potential drug for treating asthma and preventing airway remodeling.

          Release date:2021-03-25 10:46 Export PDF Favorites Scan
        • DEPDC5 基因突變與癲癇

          mTOR 通路對于神經元活性和大腦發育有重要作用,其活性異常與癲癇發生有很大的相關性。DEPDC5 是 mTOR 通路的重要組成之一,其最早發現是家族性可變灶局灶性癲癇的主要病因,隨著基因測序技術的發展,常染色體顯性夜間額葉癲癇和家族性顳葉癲癇等家族性局灶性癲癇、Rolandic 癲癇以及散發性局灶性癲癇也被發現與 DEPDC5 突變相關。近期發現 DEPDC5 也可能與全面性癲癇相關。文獻報道 DEPDC5 相關癲癇較為難治,部分患者伴有局灶性皮質發育不良、半側巨腦畸形,但具體機制尚不明確。DEPDC5 突變可能增加癲癇意外猝死的發生率。體內實驗發現 DEPDC5 的功能對于胚胎生長和大腦的發育具有重要的作用。體內外研究表明 DEPDC5 突變是通過增加 mTOR 通路的活性影響神經元形態及活性導致癲癇發生的。mTOR 通路抑制劑西羅莫司和依維莫司以及 DEPDC5 結構類似物或 DEPDC5 功能增效劑可能會改善 DEPDC5 相關癲癇的預后。此外,生酮飲食能降低 mTORC1 活性,可能對于 DEPDC5 相關癲癇的治療有較好的效果。文章將總結 DEPDC5 相關癲癇的表型,分析其致病機制并探討可能的有效治療。

          Release date:2020-01-09 08:49 Export PDF Favorites Scan
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