摘要:目的:探討卡配因抑制劑3（MDL28170）對(duì)新生大鼠缺氧缺血性腦損傷(HIBD)神經(jīng)細(xì)胞凋亡的影響。方法:建立新生SD大鼠HIBD模型,治療組于缺養(yǎng)缺血后即刻、2 h、4 h腹腔內(nèi)注射MDL28170,對(duì)照組及手術(shù)組同時(shí)予生理鹽水。缺氧缺血后24 h用免疫組化方法觀察大腦皮質(zhì)及海馬CA1區(qū)Caspase3 蛋白表達(dá)、TUNEL法檢測(cè)細(xì)胞凋亡,觀察組織病理改變并計(jì)算海馬神經(jīng)元死亡數(shù),透射電鏡觀察細(xì)胞超微結(jié)構(gòu)。結(jié)果:缺氧缺血后24 h缺血側(cè)大腦皮質(zhì)及海馬CA1區(qū)Caspase3和TUNEL陽(yáng)性細(xì)胞數(shù)較對(duì)照組明顯增加,透射電鏡證實(shí)有凋亡細(xì)胞;MDL28170可減少陽(yáng)性細(xì)胞數(shù)量,抑制神經(jīng)元死亡,差異有顯著性(Plt;0.05)。結(jié)論:MDL28170可通過(guò)抑制神經(jīng)凋亡而對(duì)新生大鼠HIBD具有一定保護(hù)作用。Abstract: Objective: To investigate the effect of (Calpain inhibitor3) MDL28170 on neural apoptosis in a neonatal model of hypoxicischemic brain damage (HIBD). Methods: A neonatal model of HIBD was established, 7dayold SD rats were divided into three groups. The treatment group received MDL28170(ip) at 0 h,2 h,4 h after HI, whereas the other two groups were administered normal saline simultaneously. The expression of caspase3 (by immunohistochemistry), neural apoptosis (by TUNEL) in cortex and hippocampus ipsilateral to the insult were observed 24 h after HI; hippocampal CA1 neural loss and electromicroscopic changes were assessed at the same time. Results: Apoptotic body was observed by electromicroscopy. Caspase3 positive cells and apoptotic cells increased significantly in the ipsilateral cortex and hippocampal CA1 region compared to the control, and MDL28170 reduced the number of positive cells, attenuated CA1 neural loss with significance (Plt;0.05). Conclusion: It is suggested that MDL28170 may protect the brain of neonatal rats after HIBD by suppressing neural apoptosis.
目的 探討嬰兒急性白血?。↖AL）的臨床與實(shí)驗(yàn)室檢查特征。 方法 對(duì)1999年12月－2011年6月收治的15例嬰兒急性白血病的臨床資料進(jìn)行總結(jié)與分析。 結(jié)果 其中急性淋巴細(xì)胞白血?。ˋLL）6例，急性髓系白血?。ˋML）8例，分類不明1例，其中以M4（4例）、M5（3例）為主。臨床表現(xiàn)多樣，髓外浸潤(rùn)明顯。1例細(xì)胞形態(tài)學(xué)與免疫分型有差異，1例合并染色體異常。放棄治療者11例，死亡2例，正規(guī)治療的2例于誘導(dǎo)緩解后獲完全緩解。 結(jié)論 IAL預(yù)后差，需完善相關(guān)檢查并不斷總結(jié)臨床資料以提高IAL治愈率。