TCDD誘導(dǎo)胎鼠腭裂的實(shí)驗(yàn)研究進(jìn)展
發(fā)布時(shí)間:2018-03-16 21:40
本文選題:-四氯二苯二英 切入點(diǎn):胎鼠 出處:《重慶醫(yī)科大學(xué)學(xué)報(bào)》2017年12期 論文類型:期刊論文
【摘要】:目的:總結(jié)歸納2,3,7,8-四氯二苯二英(2,3,7,8-tetrachlorodibenzo-p-dioxin,TCDD)誘導(dǎo)胎鼠腭裂的實(shí)驗(yàn)研究現(xiàn)狀,為深入探討TCDD致胎鼠腭裂的發(fā)生機(jī)制提供新的思路。方法:通過中國知網(wǎng)、NCBI等國內(nèi)外文獻(xiàn)庫檢索"TCDD""腭裂"等關(guān)鍵詞,搜集已有文獻(xiàn)資料。結(jié)果:目前的資料顯示,可以通過約20μg/kg劑量的TCDD給予孕第9~14天的小鼠單次灌胃建立穩(wěn)定的胎鼠腭裂模型。在此基礎(chǔ)上發(fā)現(xiàn),TCDD誘導(dǎo)不涉及腭突體積變化,主要通過抑制腭突接觸融合而發(fā)揮致腭裂效應(yīng)。對(duì)于發(fā)育中的腭組織細(xì)胞,TCDD能改變一系列調(diào)節(jié)細(xì)胞增殖、分化、凋亡的生長因子及其受體的表達(dá),主要包括表皮細(xì)胞生長因子(epidermal growth factor,EGF)、轉(zhuǎn)化生長因子(transforming growth factor,TGF)、芳香烴受體(aryl hydrocarbon receptor,AhR)。這些分子的表達(dá)變化尚存在爭議。腭融合過程中發(fā)揮關(guān)鍵作用的腭中縫上皮細(xì)胞(medial edge epithelium,MEE),其細(xì)胞命運(yùn)轉(zhuǎn)歸尚未闡明。結(jié)論:TCDD誘導(dǎo)胎鼠腭裂的體內(nèi)實(shí)驗(yàn)基礎(chǔ)相對(duì)完善。腭發(fā)育調(diào)控機(jī)制紛繁復(fù)雜,注重器官發(fā)育的時(shí)空動(dòng)態(tài)性對(duì)于進(jìn)一步研究至關(guān)重要。腭器官離體培養(yǎng)將是重要的體外實(shí)驗(yàn)環(huán)節(jié)。實(shí)驗(yàn)技術(shù)和條件的變革對(duì)于本領(lǐng)域的研究進(jìn)展顯得愈加迫切。
[Abstract]:Objective: to summarize the present situation of the experimental study on the cleft palate induced by TCDD in the fetal rats. In order to provide a new idea for exploring the mechanism of cleft palate induced by TCDD, methods: the key words of "TCDD" and "cleft palate" were searched by the domestic and foreign literature database of TCDD. Results: the present data showed that the cleft palate might be caused by cleft palate. A stable cleft palate model of fetal mice could be established by a single dose of 20 渭 g / kg TCDD on the 14th day of gestation, and it was found that the volume of palatine process was not involved in the induction of TCDD. TCDD can change the expression of a series of growth factors and its receptors that regulate cell proliferation, differentiation and apoptosis. It mainly includes epidermal growth factor (EGFN), transforming growth factor (TGFN) and aryl hydrocarbon receptor (AhRN). The expression of these molecules is still in dispute. The medial edge epithelium MEE, which plays a key role in palatal fusion, plays a key role in the process of palatal fusion. Conclusion the in vivo experimental basis of fetal cleft palate induced by TCDD is relatively perfect, and the mechanism of palatal development regulation is complicated. The emphasis on spatiotemporal dynamics of organ development is very important for further research. In vitro culture of palatal organs will be an important experimental link in vitro. The changes of experimental techniques and conditions are becoming more and more urgent for the research progress in this field.
【作者單位】: 重慶醫(yī)科大學(xué)附屬兒童醫(yī)院燒傷整形科兒童發(fā)育疾病研究教育部重點(diǎn)實(shí)驗(yàn)室重慶市兒科學(xué)重點(diǎn)實(shí)驗(yàn)室重慶市兒童發(fā)育重大疾病診治與預(yù)防國際科技合作基地;
【基金】:國家自然科學(xué)基金青年基金資助項(xiàng)目(編號(hào):81202167) 重慶市渝中區(qū)科技計(jì)劃資助項(xiàng)目(編號(hào):20130121、20150112) 國家臨床重點(diǎn)?平ㄔO(shè)資助項(xiàng)目(編號(hào):國衛(wèi)辦醫(yī)函[2013]544)
【分類號(hào)】:R782.22
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