这项工作是由来自墨西哥议会科学与技术（国家科学技术委员会，207268和233395迈克尔·施诺尔）资助。 KFCO是国家科学技术委员会津贴（396260）的获得者，获得硕士学位。

所有的动物实验已通过CINVESTAV的机构动物护理和使用委员会。 1. DSS饮用水的制备及结肠炎的诱导<ol><li>制备3.5％w / v的葡聚糖硫酸钠（DSS）在高压灭菌的饮用水溶液。 DSS容易溶解并且不要求过滤最终的解决方案。 注:7天DSS处理诱发严重的结肠炎。如果诱导轻度结肠炎，3 - 推荐治疗4天。只要DSS的饮用水保持清晰，这是没有必要改变水。然而，如果它变成浑浊，它必须被更换。 </li><li>记录雄性小鼠的基线重量。确保他们8 - 年龄和范围21 12周内 - 25克体重。 注:适当浓度DSS必须在每个实验室进行优化。结果可以变化很大，这取决于外壳的条件。在2.5的浓度 - 5％通常被报道诱导精通Colitis在C57BL / 6J WT小鼠10。 DSS来自不同公司和不同批应测试，作为结果还可以与决策支持系统的不同来源的不同而不同。 </li><li>提供水自由采食 ，必要时用新鲜的3.5％DSS水代替它。 </li></ol>灌胃营养补剂2.应用<ol><li>准备在适当的溶剂中的"给送"所需的营养补充品的溶液。在这项研究中，我们使用含有200毫克/千克L-精氨酸，83毫克/公斤维生素C，46毫克/公斤维生素E，77毫克/公斤的二十碳五烯酸（EPA），和115毫克/千克二十二碳六烯酸（混合物的DHA ）以1:水和红花油1溶液。 </li><li>填充1毫升注射器连接到灌胃针（15克×50毫米）与营养补充剂混合物。擦拭灌胃针的外面以除去任何化合物的针之外，并确保适当的剂量应用时。 </li><li>通过抓住尾部与基座抑制鼠标一方面通过在颈部的用另一只手的拇指和食指背面牢固地把持皮肤褶皱。放置第三手指和保持该颈部同一只手的拇指的基部之间的尾巴。 </li><li>同时保持在直立位置的鼠标，针头插入动物的嘴的左侧，认真遵循口定位食道的屋顶。如果遇到没有抵抗力，对促进胃针。 注:验证动物继续之前正常呼吸。 </li><li>辖混合物慢慢地，慢慢拔出注射器取出试管，然后松开鼠标。结肠炎实验的过程中，每天一次申请的营养补充剂通过管饲法。 </li></ol> 3.疾病活动指数的测定注:本病活动指数是分数减肥，肛周出血，大便的一致性，这是肥胖的组合tained每天13。 <ol><li>每日测量体重并根据重量损失百分数得分的0分配到4（0:0％，1:1 - 5％，2:5 - 10％，3:10 - 20％，4:&gt; 20 ％）。 注:体重损失是由DSS结肠炎的诱导和实际重量之前计算的基底重量％之间的差来确定。 </li><li>要确定肛周出血的水平，收集新鲜粪便样品，并使用所提供的喷头就从零陵香大便隐血检测试剂盒的幻灯片薄薄涂抹。使用新鲜涂抹器对每个样品。 <ol><li>关闭的前盖并打开滑盖背面的窗口。施加显影剂溶液的两滴在样品位置的背面。 </li><li> 30 s后读取结果。蓝色的痕迹是潜血阳性。分配比分0比4（0:无，0.5 - 2.5:积极的愈创木大便潜血试验（取决于信号强度），和3 - 4:常务顾问小组还将SS出血）。 注意:如果便血是可见的，愈创木脂的粪便潜隐血测试没有被执行，和3的得分，3.5，或4分配，这取决于可见血液量。 </li></ol></li><li>通过观察一个新鲜粪便样品确定大便的一致性。得分为0分配给4（0:正常/固，0.5 - 2.5:糊状大便，3 - 4:腹泻）。 </li></ol> 4.确定肠上皮通透性在体内被伊文思蓝含量<ol><li>通过在盐水溶液（0.9％NaCl）中稀释氯胺酮（100mg / kg的体重）的混合物和甲苯噻嗪（13毫克/公斤体重）腹膜内注射它们麻醉动物，并通过监控夹送评估麻醉深度撤回反射。 </li><li>放置麻醉动物处于仰卧位置和进行剖腹，露出肠道。 </li><li>找到盲肠和作一小切口在结肠近段scendens（理想情况下，紧邻盲肠）。 </li><li>插入喂食针（G22）中，用使用公共丝线一个结扎固定。小心地冲洗管PBS丰富来冲从结肠粪便全部。灌输伊文思蓝溶液（1.5％w / v的在PBS中）进入结肠，直到它到达肛门。 </li><li>孵育Evans蓝15分钟。冲洗丰富PBS管，直到肛周冲洗明确洗出的染料。 </li><li>通过颈脱位安乐死动物。 </li><li>切除结肠和丰富PBS再冲洗。用1mL 6毫Ñ-acetylcysteine在PBS中冲洗一次，以消除任何染料粘到结肠粘液。 </li><li>纵向切开结肠，用PBS和1mL 6毫米ñ-acetylcysteine的一次冲洗。 </li><li>记录重量和长度。以提取伊文思蓝染料，过夜放置结肠在2mL的N，N-二甲基甲酰胺在室温下轻轻agitatioñ。分光光度计测量染料浓度在610纳米。 </li></ol> 5.组织收集<ol><li>通过在盐水溶液（0.9％NaCl）中稀释氯胺酮（100mg / kg的体重）的混合物和甲苯噻嗪（13毫克/公斤体重）腹膜内注射它们麻醉动物，并通过监控夹送评估麻醉深度撤回反射。 </li><li>通过颈脱位安乐死动物。 </li><li>放置动物处于仰卧位置和进行剖腹，露出腹腔。 </li><li>使用剪刀，解剖整个结肠和记录它的长度。 </li><li>用冷的PBS冲洗结肠仔细几次以除去粪便。记录组织重量和用于下面的实验中制备，如在步骤5.6中所述 - 5.8。 </li><li>对于RNA分离和髓过氧化物酶（MPO）测定法，切断一个大小合适的组织样品（100毫克通常是足够的），将其放置一管内，和SNA在液氮中对 - 冻结它。在-80℃，以备将来使用存储的组织。 </li><li>对于免疫荧光染色和氧化应力测定（见下文），切一个小结肠样品（0.5 - 1厘米），并在填充有最佳切割温度（OCT）化合物小的铝杯浸没它。放置在干冰上的杯，并让他们慢慢冻结，以避免形成气泡。冷冻组织样品可以储存在-80℃以供将来使用。 </li><li>瑞士卷14，纵向打开结肠，小心使用镊子取出粪便。把它卷起来，与粘膜向内，用细尖镊子或薄，圆木棍。小心地将其放在包埋盒里面，然后继续步骤6.1。 注:DSS诱导的结肠损害。然而，损伤分布从近端到远端结肠而变化，与通常在远端结肠和直肠看出大多数损害。因此，我们建议在分析组织学无论是在山坳远端上或在整个结肠的瑞士角色。 </li></ol> 6.苏木伊红染色分析结肠组织学<ol><li> 组织准备 <ol><li>对于组织学分析，淹没或瑞士卷或从控制的某些结肠区域的小组织片段和处理的小鼠在5毫升10％的甲醛，在室温下（RT）下48小时，以实现适当的固定。 注:在第6步中所有其他的步骤都在室温下进行，除非另有说明。 </li><li>用自来水洗18小时。 </li><li>用15mL 70％的乙醇的脱水它们1小时，1小时96％，和1小时的无水乙醇。在进行下一浓度之前重复用新鲜的醇每一个步骤。 </li><li>继续脱水在7.5毫升无水乙醇和7.5毫升无水二甲苯中1小时的混合。传递样本以15毫升无水二甲苯中1小时，然后重复一次。用新鲜的二甲苯重复此步骤一次。 </li></OL&gt; </li><li> 在石蜡包埋结肠组织样本 <ol><li>沉浸在50mL液体石蜡的样品17小时。重复此步骤一次，但只有3小时。 </li><li>在810毫升液体石蜡:浸入立方体样品（22×22×22 mm塑料，模具方形，大小）。 </li><li>允许与结肠组织样本的石蜡固化在室温24小时。 </li></ol></li><li> 切割用切片组织的横截面 <ol><li>切使用切片机结肠样品，按制造商的说明，在其厚度为5微米。 </li><li>收集在水浴（1L）含有0.3％明胶的削减。这可以防止组织的横截面的折叠。恢复组织切片和它们安装在载玻片上。 </li></ol></li><li> 组织横截面的苏木精和曙红染色 <ol><li>在培养箱Deparaffinize 18小时的样品在60℃。为了这个目的，使用玻璃小号立德架带把手。 </li><li>脱石蜡后，浸泡在70毫升绝对二甲苯的载玻片5分钟。用新鲜的二甲苯重复此步骤一次。 </li><li>转移样品到70毫升无水乙醇的1分钟。用新鲜的酒精重复此步骤一次。 </li><li>孵育在70毫升乙醇中96％的结肠组织样品1分钟。用新鲜的酒精重复此步骤一次。 </li><li>在洗净的自来水样本进行两次2秒。 </li><li>孵育在哈里斯苏木组织7分钟。 </li><li>在洗净的自来水样本进行两次2秒。 </li><li>孵育在酸性醇的样品（70毫升乙醇的70％和700微升的1M盐酸）为7秒。 </li><li>在洗净的自来水样本进行两次2秒。 </li><li>孵育在70毫升碳酸锂（1克碳酸锂在100毫升的蒸馏水）为7秒的组织样本。 </li><li>在洗净的自来水样本进行两次2秒。 </li><li>孵育样品在70毫升乙醇80％1分钟。 </li><li>转移到样品70毫升曙红-Y为15秒。 </li><li>孵育它们在70毫升96％乙醇中1分钟。用新鲜的酒精重复此步骤一次。 </li><li>孵育在70毫升的无水乙醇（乙醇绝对无水的）组织样品1分钟。用新鲜的酒精重复此步骤一次。 </li><li>孵育在70毫升35毫升无水乙醇的35毫升无水二甲苯中1分钟的混合物的样品。 </li><li>转移样品到70毫升无水二甲苯中1分钟。在70毫升新鲜绝对二甲苯重复此步骤5分钟。 </li><li>添加80μL的合成树脂的结肠组织样品，用盖玻片覆盖它们，让它们干燥在室温24小时。最后，分析使用明场显微镜8样本。 </li></ol></li></ol>通过免疫荧光分析7结组成<ol><li>如步骤5.7所述，准备组织切成8微米厚截面使用低温恒温器。 </li><li>固定，并在-20℃下透化用96％的乙醇结肠横截面为20分钟。 注意:所有后续孵育应于RT下进行，除非另有说明，在潮湿的暗箱，防止干燥和荧光染料褪色。 </li><li>风干样品，然后冲洗一下5分钟3次，每次用1×PBS </li><li>用封闭溶液（含有的PBS 0.01％吐温和2％BSA）中2小时孵育样品。 </li><li>除去封闭溶液，并用PBS-0.01％吐温冲洗10分钟。 </li><li>在此期间，稀释的初级抗体，以在PBS-0.01％吐温所需浓度。 </li><li>除去洗涤液，应用来自前面步骤的抗体溶液中，并在加湿箱在4℃孵育过夜。 </li><li>除去抗体溶液并用PBS-0.01％吐温用去离子水洗涤3次，每次5分钟，一次10分钟，用非常温和搅拌。 </li><li>虽然洗涤，离心氟ochromeconjugated，种特异性在4℃在14,000rpm xg离心20分钟，二次抗体。 </li><li>稀释而不沉淀的二级抗体通过在PBS-0.01％吐温的提供者所指示的，应用它们，并在室温下孵育1小时。 </li><li>重复步骤7.8和完全去除清洗液成为可能。 </li><li>吸管4μL的防褪色剂在幻灯片上每个样品。 </li><li>盖上盖玻片样品。 </li><li>空气干燥1小时。 </li><li>用指甲油密封幻灯片。玻片可以储存在-20℃直至进一步分析。 </li><li>共聚焦激光显微镜分析8。 </li></ol> 8.测定氧化应激乙锭氧化<ol><li>经过7天DSS结肠炎，在厚度为5微米的低温恒温器在步骤5.7所描述和切结肠段准备组织。安装的横截面到玻片上用聚-L-赖氨酸溶液处理并孵育样品机智H 5在水中二氢乙（DHE），在37℃下在黑暗中30分钟的微米。 </li><li>用PBS（pH为7.6），用于与在RT轻轻搅动每15分钟三次洗样品。空气干燥该样品，并添加封固剂，以保护荧光的下降。观察激光扫描共聚焦显微镜氧化乙啶（放大40倍，568波长）的荧光。 </li></ol> 9. MPO含量分析白细胞募集<ol><li>经过7天DSS结肠炎，收集结肠组织和使样品均质化 - 用在冰上均化器（200 400毫克）用1mL十六烷基的（HTAB）缓冲液（在50mM 0.5％HTAB磷酸盐缓冲液，pH 6.0）。 </li><li>用1 HTAB毫升缓冲漂洗均化的尖端两次以包括溶解物所有组织和超声处理它在40％振幅五次，每次10秒。冻融在液氮中三次。 </li><li>离心在14,000rpm xg离心15分钟，回收上清。通过混合柠檬酸钠（在水中的1M），0.1毫升过氧化氢的ABTS，5毫升制备2,2&#39;-连氮基 - 双（3​​-乙基苯并噻唑-6-磺酸）（ABTS）溶液，和45毫升双向的-蒸馏水。 </li><li>混合0.1mL的含0.1 ABTS毫升溶液每种上清液在96孔平底板上。 10分钟后，测量在使用分光光度计460nm处的吸光度。 </li></ol> 10.评估促炎性细胞因子的通过PCR表达<ol><li> 组织均质 <ol><li>使用功率匀浆均质结肠组织样本50到100mg的1ml的酸性硫氰酸胍 - 苯酚 - 氯仿混合物。 </li><li>孵育，在室温下15分钟。 </li></ol></li><li> 相分离 <ol><li>加入0.2毫升氯仿，剧烈摇晃30秒。 </li><li>孵育在4℃下30分钟。 </li><li>离心机以12,000 xg离心在4℃下60分钟。 </li><li>转移的UPPER水相到一个新的管（〜500μL）。 </li></ol></li><li> RNA沉淀和再悬浮 <ol><li>加入0.5毫升异丙醇中并在4℃孵育样品60分钟。 </li><li>离心机以12,000 xg离心在4℃下30分钟。 </li><li>彻底去除上清。 </li><li>加入1毫升乙醇的75％和旋涡。 </li><li>离心机以12,000 xg离心在4℃下30分钟。 </li><li>去除上清。 </li><li>使剩余的乙醇风干3-5分钟。 注意:不要让RNA沉淀完全干燥，因为这将极大地降低其溶解度是很重要的。 </li><li>重新溶解在0.3毫升酸二乙酯的（DEPC）处理的水的颗粒。立即转录RNA样品为cDNA（更稳定，见步骤10.5），或储存在-80℃。 </li></ol></li><li> RNA定量 <ol><li>稀释的RNA 1微升99微升DEPC处理过的水。 </li><li>阅读日在260nm和使用UV / VIS分光光度计来确定样品浓度和纯度280纳米ë外径。 </li></ol></li><li> cDNA合成 <ol><li>与寡的1微升（dT）的12-18（0.5微克/微升）和DEPC处理的水（12微升的总体积）在无RNase无菌试管混合的RNA样品（1-5微克）。 </li><li>孵育在70℃下10分钟。 </li><li>加入2微升10X PCR缓冲液，50毫1微升的MgCl 2，10毫dNTP混合物1μL的，和0.1M二硫苏糖醇的2微升（DTT）。 </li><li>孵育在4℃下5分钟。 </li><li>加逆转录酶的1微升并在42℃下孵育5分钟。 </li><li>孵育在70℃下15分钟。 </li><li>孵育在4℃下15分钟。 cDNA可被储存在-20℃直至进一步使用。 </li></ol></li><li> PCR <ol><li>拌2.5微升10X PCR缓冲液中，有25毫1.5微升MgCl 2的，10毫的dNTP 0.5μL混合，0.25μ大号Taq DNA聚合酶，引物各0.25微升（10μM）和cDNA（100毫微克），以及无菌水至25微升的总体积。 </li><li>上的96孔热循环仪上运行样本。为了防止基因组DNA的扩增，正向和反向引应位于不同的外显子:IL1β-FW:GCAACTGTTCCTGAACTCAACT和IL1β-RE:TCTTTTGGGGTCCGTCAACT; IL6-FW:CCTTCCTACCCCAATTTCCAA和IL6-RE:AGATGAATTGGATGGTCTTGGTC; KC-FW:TGTCAGTGCCTGCAGACCAT和KC-RE:CCTGAGGGCAACACCTTCA;和肌动蛋白FW:TATCCACCTTCCAGCAGATGT和肌动蛋白-RE:AGCTCAGTAACAGTCCGCCTA。使用以下PCR条件:95℃5分钟，随后30个循环的95℃15秒，58℃30秒，72℃30秒，再加上在72℃最后延伸10分钟。 </li></ol></li></ol>

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N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Does+everyone+with+inflammatory+bowel+disease+need+to+be+treated+with+combination+therapy.">Does everyone with inflammatory bowel disease need to be treated with combination therapy.</a> Curr Opin Gastroenterol. , (2016).</li><li>Nanau, R. M., Neuman, M. 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A., Schnoor, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Antioxidative+diet+supplementation+reverses+high-fat+diet-induced+increases+of+cardiovascular+risk+factors+in+mice.">Antioxidative diet supplementation reverses high-fat diet-induced increases of cardiovascular risk factors in mice.</a> Ox Med Cell Longev. 2015, 467471 (2015).</li><li>Perse, M., Cerar, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dextran+sodium+sulphate+colitis+mouse+model:+traps+and+tricks.">Dextran sodium sulphate colitis mouse model: traps and tricks.</a> J Biomed Biotechnol. 2012, 718617 (2012).</li><li>Chassaing, B., Aitken, J. D., Malleshappa, M., Vijay-Kumar, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dextran+sulfate+sodium+(DSS)-induced+colitis+in+mice.">Dextran sulfate sodium (DSS)-induced colitis in mice.</a> Curr. Protoc. Immunol. 104, 25 (2014).</li><li>Laroui, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dextran+sodium+sulfate+(DSS)+induces+colitis+in+mice+by+forming+nano-lipocomplexes+with+medium-chain-length+fatty+acids+in+the+colon.">Dextran sodium sulfate (DSS) induces colitis in mice by forming nano-lipocomplexes with medium-chain-length fatty acids in the colon.</a> PLoS One. 7, 32084 (2009).</li><li>Mennigen, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Probiotic+mixture+VSL#3+protects+the+epithelial+barrier+by+maintaining+tight+junction+protein+expression+and+preventing+apoptosis+in+a+murine+model+of+colitis.">Probiotic mixture VSL#3 protects the epithelial barrier by maintaining tight junction protein expression and preventing apoptosis in a murine model of colitis.</a> Am J Physiol Gastrointest Liver Physiol. 296, 1140-1149 (2009).</li><li>Park, C. 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作者什么都没有透露。

为了使用在临床研究中的营养补充品，所述的这类补充剂的安全必须小心地在动物研究中体内评价。在结肠炎的情况下，类似于IBD的临床征兆若干适当的动物模型已经建立，包括使用的DSS，TNBS，或乙酸化学模型;敲除（KO）等车型IL10-KO;和使用过继T细胞转移19-21免疫细胞介导的结肠炎。结肠炎的DSS模型是诱导结肠炎类似于人类IBD的许多疾病的症状和在研究调查结肠炎22?...

结肠炎是能引起腹泻和腹痛结肠的炎性病症。结肠炎可以是急性，响应于感染或压力，或者它可以发展为慢性疾病，如溃疡性结肠炎（UC），其属于下组的炎性肠疾病（IBD）的。尽管UC的临床症状得到了很好的描述，发病机制仍然知之甚少1。据专家们承认，UC是多因素疾病，与遗传突变和异常的免疫反应扮演一个重要的角色2。然而，环境因素，如生活和营养的样式，也有助于疾病的发生和发展3。 不幸的是，IBD是不可治愈的，但也有旨在缓解临床症状很多的治疗方案。目前的治疗包括抗炎药，如柳氮磺吡啶和皮质类固醇;免疫抑制剂，如azathioPRINE;单克隆抗体是捕获促炎细胞因子，如肿瘤坏死因子α（TNF-α），或嵌段粘附分子，如整，以降低白细胞募集过度;并针对触发促炎症途径，如Janus激酶（JAK）4激酶抑制剂。并非所有的患者对所有治疗，这样的治疗策略必须个体化5。此外，大多数的这些治疗药物干扰了代谢和免疫反应，常常引起严重的副作用。出于这个原因，替代治疗方案进行了研究。 替代治疗包括益生菌和营养补充剂，已在动物模型和临床试验中成功6,7-不同程度的应用。我们最近发现，不同的单营养补充剂，作为抗氧化维生素或ω3-多不饱和脂肪酸，例如应用（PUFAS），不如这种补充剂的组合在减轻结肠炎和心血管疾病的症状8,9中的应用。这些研究在小鼠中进行，因此，临床研究必须在人类中进行，以确定这些结果是否也将是适用于人类。临床研究开始之前，新的治疗方案的有效性和安全性，必须在动物模型中进行评估。 对于IBD的葡聚糖硫酸钠（DSS）的模式已被广泛用于研究疾病发展的机制以及药物和营养补充剂6,10的有益效果。在大多数研究中，只有一种急性疾病超过七天被诱导的时间段;然而，在这些动物中观察到的临床症状密切类似于那些在IBD患者中观察到（ 即，血性腹泻，体重减轻，上皮功能障碍，和免疫细胞浸润）10。 DSS诱导糜烂在粘膜，导致屏障功能障碍和增加肠道上皮通透性11。确切机制尚不清楚。然而，研究表明，DSS与中链长度的脂肪酸的相互作用形成的纳米lipocomplexes是能够进入上皮细胞和诱导炎症信号传导途径12。在本文中，我们详细描述如何结肠炎是引起并在小鼠中，补充剂如何营养通过管饲法应用到确保在每个动物的恒定剂量分析，以及如何进行检查各种结肠炎症状例如补充剂的效果。

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			<td height="21" style="height:21px;width:439px;">0.3% of gelatin&#160;</td>
			<td style="width:184px;">Bioxon</td>
			<td style="width:139px;">158</td>
			<td style="width:191px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">10% formaldehyde</td>
			<td style="width:184px;">J.T. Baker</td>
			<td style="width:139px;">2106-03</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">96-well plate with flat bottom</td>
			<td style="width:184px;">Corning</td>
			<td style="width:139px;">3368</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Absolute ethanol&#160;</td>
			<td style="width:184px;">J.T. Baker</td>
			<td style="width:139px;">9000-03</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Absolute xylene</td>
			<td style="width:184px;">J.T. Baker</td>
			<td style="width:139px;">9490-03</td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">ABTS</td>
			<td style="width:184px;">Sigma Aldrich</td>
			<td style="width:139px;">H5882</td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Bovine Serum Albumin</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">9048-46-8</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">ColoScreen</td>
			<td style="width:184px;">Helena Laboratories</td>
			<td style="width:139px;">5072</td>
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			<td height="21" style="height:21px;width:439px;">Corabion (Kindly provided by Merck, Naucalpan, Mexico)</td>
			<td style="width:184px;">Merck</td>
			<td style="width:139px;"></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Dextran Sulfate Sodium Salt</td>
			<td style="width:184px;">Affymetrix</td>
			<td style="width:139px;">9011-18-1</td>
			<td style="width:191px;">(M.W. 40,000-50,000)</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Dihydroethidium</td>
			<td style="width:184px;">Life Technology</td>
			<td style="width:139px;">D11347</td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Eosin-Y&#160;</td>
			<td style="width:184px;">J.T. Baker</td>
			<td style="width:139px;">L087-03</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Evans blue</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">314-13-6</td>
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		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Feeding&#160; needle</td>
			<td style="width:184px;">Cadence Science Inc.</td>
			<td style="width:139px;">9921</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Glass slide rack with handle</td>
			<td style="width:184px;">Electron Microscopy</td>
			<td style="width:139px;">70312-16</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Glass Slides</td>
			<td style="width:184px;">Corning</td>
			<td style="width:139px;">2947</td>
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		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Harris hematoxylin&#160;</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">H3136</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Hexadecyltrimethyammonium (HTAB)</td>
			<td style="width:184px;">Sigma Aldrich</td>
			<td style="width:139px;">H6269</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Histosette (Embedding cassette)</td>
			<td style="width:184px;">Simport</td>
			<td style="width:139px;">M498.2</td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Hydrochloric acid 1 M</td>
			<td style="width:184px;">J.T. Baker</td>
			<td style="width:139px;">9535-62</td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Hydrogen peroxide</td>
			<td style="width:184px;">Sigma Aldrich</td>
			<td style="width:139px;">H3410</td>
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			<td height="21" style="height:21px;width:439px;">Ketamine</td>
			<td style="width:184px;">PiSA Agropecuaria</td>
			<td style="width:139px;">Q-7833-028</td>
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			<td height="21" style="height:21px;width:439px;">Liquid paraffin&#160;</td>
			<td style="width:184px;">Paraplast</td>
			<td style="width:139px;">39501-006</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Lithium carbonate&#160;</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">2362</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">N,N-dimethylformamide</td>
			<td style="width:184px;">J.T. Baker</td>
			<td style="width:139px;">68-12-2</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">N-acetylcysteine</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">A9165</td>
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		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Plastic cubes</td>
			<td style="width:184px;">Electron Microscopy</td>
			<td style="width:139px;">70181</td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Poly-L-Lysine Solution</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">25988-63-0</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Prism 5 statistical software</td>
			<td style="width:184px;">GraphPad Software</td>
			<td style="width:139px;">Prism 5</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Saline Solution 0.9% NaCl</td>
			<td style="width:184px;">CS PiSA</td>
			<td style="width:139px;">Q-7833-009</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Sodium citrate</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">W302600</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Synthetic resin&#160;</td>
			<td style="width:184px;">Poly Mont</td>
			<td style="width:139px;">7987</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Taq DNA polymerase</td>
			<td style="width:184px;">Invitrogen</td>
			<td style="width:139px;">11615-010</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Tissue-tek. O.C.T Compound</td>
			<td style="width:184px;">Sakura Finetek</td>
			<td style="width:139px;">4583</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Tuberculine Syringe</td>
			<td style="width:184px;">BD Plastipak</td>
			<td style="width:139px;">305945</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Tween 20</td>
			<td style="width:184px;">Sigma-Aldrich</td>
			<td style="width:139px;">9005-64-5</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">VECTASHIELD Antifade Mounting Medium with DAPI</td>
			<td style="width:184px;">Vector Laboratories</td>
			<td style="width:139px;">H-1200</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:439px;">Xylazine</td>
			<td style="width:184px;">PiSA Agropecuaria</td>
			<td style="width:139px;">Q-7833-099</td>
			<td></td>
		</tr>
	</tbody>
</table>

analyzing beneficial effects of nutritional supplements on intestinal epithelial barrier functions during experimental colitis

炎症性肠疾病（IBD），包括克罗恩病和溃疡性结肠炎，是肠内的慢性复发病症。他们造成严重的问题，如腹部绞痛，血性腹泻，体重减轻，在受影响的个人。不幸的是，目前还没有治愈的是，和治疗仅旨在减轻症状。目前的治疗包括抗炎和免疫抑制药物，可能导致严重的副作用。这是值得的替代治疗方案，如营养补充剂，不引起副作用的搜索。他们在临床研究中的应用之前，这种化合物必须进行严格测试在动物模型的有效性和安全性。一个可靠的实验模型是在小鼠葡聚糖硫酸钠（DSS）结肠炎模型，其再现许多的溃疡性结肠炎在人体中的临床症状。我们最近应用该模型以测试含营养补充剂的有益效果维生素C和E，L-精氨酸，和ω3多不饱和脂肪酸（PUFA）。我们分析了各种疾病参数，发现这补充能够改善水肿形成，组织损伤，白细胞浸润，氧化应激和促炎性细胞因子，导致在疾病活动指数的整体改善。在这篇文章中，我们详细使用C57BL / 6小鼠的DSS结肠炎模型的营养补充品的正确使用，以及如何疾病参数，如组织学，氧化应激和炎症进行评估解释。分析不同饮食补充剂的有益效果可接着最终打开的替代治疗策略，减轻IBD的症状和/或延长缓解期的相位，而不会引起严重的副作用的发展新的途径。

饮食补充剂可以从DSS结肠炎保护抗炎和抗氧化的饮食补充剂，例如维生素C，维生素E，所述一氧化氮（NO）-source L-精氨酸，和ω3多不饱和脂肪酸（ω3多不饱和脂肪酸），已被用于在动物不同的成功模型以减轻炎性疾病3,6,15的迹象。营养不良，氧化应激和促炎细胞因子的可触发的急性和慢性结肠炎3。在先前的研究?...

Watch this Scientific Journal Video about Analyzing Beneficial Effects of Nutritional Supplements on Intestinal Epithelial Barrier Functions During Experimental Colitis at JoVE.com

Analyzing Beneficial Effects of Nutritional Supplements on Intestinal Epithelial Barrier Functions During Experimental Colitis

炎症性肠病（IBD）的当前治疗的目的是减轻疾病的症状，但可能会导致严重的副作用。因此，替代战略被动物结肠炎模型研究。在这里，我们介绍如何补充营养的临床体征IBD的有利影响在这样的肠炎模型进行了分析。

分析营养补充剂的有益作用于肠上皮屏障功能在实验性结肠炎

Inflammatory bowel diseases (IBD), including Crohn&#39;s disease and ulcerative colitis, are chronic relapsing disorders of the intestines. They cause ...

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Unit 1

Drugs for Chronic Bowel Disorders

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12.2K 次观看.  Center for Research and Advanced Studies of the National Polytechnic Institute. 炎症性肠病（IBD）的当前治疗的目的是减轻疾病的症状，但可能会导致严重的副作用。因此，替代战略被动物结肠炎模型研究。在这里，我们介绍如何补充营养的临床体征IBD的有利影响在这样的肠炎模型进行了分析。 

视频: Analyzing Beneficial Effects of Nutritional Supplements on Intestinal Epithelial Barrier Functions During Experimental Colitis

Isolation of Mouse Respiratory Epithelial Cells and Exposure to Experimental Cigarette Smoke at Air Liquid Interface

Pulmonary epithelial cells can be isolated from the respiratory tract of mice and cultured at air-liquid interface (ALI) as a model of differentiated respiratory epithelium. A protocol is described for isolating and exposing these cells to mainstream cigarette smoke (CS), in order to study epithelial cell responses to CS exposure. The protocol consists of three parts: the isolation of airway epithelial cells from mouse trachea, the culturing of these cells at air-liquid interface (ALI) as fully differentiated epithelial cells, and the delivery of calibrated mainstream CS to these cells in culture. The ALI culture system allows the culture of respiratory epithelia under conditions that more closely resemble their physiological setting than ordinary liquid culture systems. The study of molecular and lung cellular responses to CS exposure is a critical component of understanding the impact of environmental air pollution on human health. Research findings in this area may ultimately contribute towards understanding the etiology of chronic obstructive pulmonary disease (COPD), and other tobacco-related diseases, which represent major global health problems.

Pulmonary epithelial cells can be isolated from the respiratory tract of mice and cultured at air-liquid interface as a model of differentiated respiratory epithelium. A protocol is described for isolating, culturing and exposing these cells to mainstream cigarette smoke, in order to study molecular responses to this environmental toxin.

小鼠呼吸道上皮细胞和实验香烟烟雾暴露在空气分离液界面

Pulmonary epithelial cells can be isolated from the respiratory tract of mice and cultured at air-liquid interface (ALI) as a model of differentiated ...

科研

医学

DNBS/TNBS Colitis Models: Providing Insights Into Inflammatory Bowel Disease and Effects of Dietary Fat

Inflammatory Bowel Diseases (IBD), including Crohn&#39;s Disease and Ulcerative Colitis, have long been associated with a genetic basis, and more recently host immune responses to microbial and environmental agents. Dinitrobenzene sulfonic acid (DNBS)-induced colitis allows one to study the pathogenesis of IBD associated environmental triggers such as stress and diet, the effects of potential therapies, and the mechanisms underlying intestinal inflammation and mucosal injury. In this paper, we investigated the effects of dietary n-3 and n-6 fatty acids on the colonic mucosal inflammatory response to DNBS-induced colitis in rats. All rats were fed identical diets with the exception of different types of fatty acids [safflower oil (SO), canola oil (CO), or fish oil (FO)] for three&#160;weeks prior to exposure to intrarectal DNBS. Control rats given intrarectal ethanol continued gaining weight over the 5 day study, whereas, DNBS-treated rats fed lipid diets all lost weight with FO and CO fed rats demonstrating significant weight loss by 48&#160;hr and rats fed SO by 72&#160;hr. Weight gain resumed after 72&#160;hr post DNBS, and by 5 days post DNBS, the FO group had a higher body weight than SO or CO groups. Colonic sections collected 5&#160;days post DNBS-treatment showed focal ulceration, crypt destruction, goblet cell depletion, and mucosal infiltration of both acute and chronic inflammatory cells that differed in severity among diet groups. The SO fed group showed the most severe damage followed by the CO, and FO fed groups that showed the mildest degree of tissue injury. Similarly, colonic myeloperoxidase (MPO) activity, a marker of neutrophil activity was significantly higher in SO followed by CO fed rats, with FO fed rats having significantly lower MPO activity. These results demonstrate the use of DNBS-induced colitis, as outlined in this protocol, to determine the impact of diet in the pathogenesis of IBD.

DNBS/TNBS induced colitis offers an alternative and inexpensive method to study the pathobiology of inflammatory bowel disease. The protocol discussed in this paper outlines the successful application of DNBS to induce colitis in mice and rats and allows one to thoroughly study host-mediated intestinal responses.

二硝基苯磺酸/ TNBS结肠炎模型:提供洞察炎症性肠病和膳食脂肪的影响

Inflammatory Bowel Diseases (IBD), including Crohn&#39;s Disease and Ulcerative Colitis, have long been associated with a genetic basis, and more recently ...

Long-Term Catheterization of the Intestinal Lymph Trunk and Collection of Lymph in Neonatal Pigs

Catheterization of the intestinal lymph trunk in neonatal pigs is a technique allowing for the long-term collection of large quantities of intestinal (central) efferent lymph. Importantly, the collection of central lymph from the intestine enables researchers to study both the mechanisms and lipid constitutes associated with lipid metabolism, intestinal inflammation and cancer metastasis, as well as cells involved in immune function and immunosurveillance. A ventral mid-line surgical approach permits excellent surgical exposure to the cranial abdomen and relatively easy access to the intestinal lymph trunk vessel that lies near the pancreas and the right ventral segment of the portal vein underneath the visceral aspect of the right liver lobe. The vessel is meticulously dissected and released from the surrounding fascia and then dilated with sutures allowing for insertion and subsequent securing of the catheter into the vessel. The catheter is exteriorized and approximately 1 L/24 hr of lymph is collected over a 7 day period. While this technique enables the collection of large quantities of central lymph over an extended period of time, the success depends on careful surgical dissection, tissue handling and close attention to proper surgical technique. This is particularly important with surgeries in young animals as the lymph vessels can easily tear, potentially leading to surgical and experimental failure. The video demonstrates an excellent surgical technique for the collection of intestinal lymph.

We present a surgical procedure to catheterize the intestinal lymph trunk in neonatal pigs to collect large quantities of lipid metabolism components from efferent lymph.

在新生儿猪淋巴的肠淋巴躯干和收集的长期导尿

Catheterization of the intestinal lymph trunk in neonatal pigs is a technique allowing for the long-term collection of large quantities of intestinal ...

A Step by Step Protocol for Subretinal Surgery in Rabbits

Age related macular degeneration (AMD), retinitis pigmentosa, and other RPE related diseases are the most common causes for irreversible loss of vision in adults in industrially developed countries. RPE transplantation appears to be a promising therapy, as it may replace dysfunctional RPE, restore its function, and thereby vision.
Here we describe a method for transplanting a cultured RPE monolayer on a scaffold into the subretinal space (SRS) of rabbits. After vitrectomy xenotransplants were delivered into the SRS using a custom made shooter consisting of a 20-gauge metallic nozzle with a polytetrafluoroethylene (PTFE) coated plunger. The current technique evolved in over 150 rabbit surgeries over 6 years. Post-operative follow-up can be obtained using non-invasive and repetitive in vivo imaging such as spectral domain optical coherence tomography (SD-OCT) followed by perfusion-fixed histology.
The method has well-defined steps for easy learning and high success rate. Rabbits are considered a large eye animal model useful in preclinical studies for clinical translation. In this context rabbits are a cost-efficient and perhaps convenient alternative to other large eye animal models.

Retinal pigment epithelium (RPE) replacement strategies and gene-based therapy are considered for several retinal degenerative conditions. For clinical translation, large eye animal models are required to study surgical techniques applicable in patients. Here we present a rabbit model for subretinal surgery geared towards RPE transplantation, which is versatile and cost-efficient.

一种用于兔视网膜下手术分步协议

Age related macular degeneration (AMD), retinitis pigmentosa, and other RPE related diseases are the most common causes for irreversible loss of vision in ...

Multimodal Quantitative Phase Imaging with Digital Holographic Microscopy Accurately Assesses Intestinal Inflammation and Epithelial Wound Healing

The incidence of inflammatory bowel disease, i.e., Crohn&#39;s disease and Ulcerative colitis, has significantly increased over the last decade. The etiology of IBD remains unknown and current therapeutic strategies are based on the unspecific suppression of the immune system. The development of treatments that specifically target intestinal inflammation and epithelial wound healing could significantly improve management of IBD, however this requires accurate detection of inflammatory changes. Currently, potential drug candidates are usually evaluated using animal models in vivo or with cell culture based techniques in vitro. Histological examination usually requires the cells or tissues of interest to be stained, which may alter the sample characteristics and furthermore, the interpretation of findings can vary by investigator expertise. Digital holographic microscopy (DHM), based on the detection of optical path length delay, allows stain-free quantitative phase contrast imaging. This allows the results to be directly correlated with absolute biophysical parameters. We demonstrate how measurement of changes in tissue density with DHM, based on refractive index measurement, can quantify inflammatory alterations, without staining, in different layers of colonic tissue specimens from mice and humans with colitis. Additionally, we demonstrate continuous multimodal label-free monitoring of epithelial wound healing in vitro, possible using DHM through the simple automated determination of the wounded area and simultaneous determination of morphological parameters such as dry mass and layer thickness of migrating cells. In conclusion, DHM represents a valuable, novel and quantitative tool for the assessment of intestinal inflammation with absolute values for parameters possible, simplified quantification of epithelial wound healing in vitro and therefore has high potential for translational diagnostic use.

Accurate assessment of anti-inflammatory effects is of utmost importance for the evaluation of potential new drugs for the treatment of inflammatory bowel disease. Digital holographic microscopy provides assessment of inflammation in murine and human colonic tissue samples as well as automated multimodal evaluation of epithelial wound healing in vitro.

多式联运定量相成像数字全息显微准确评估肠道炎症和上皮伤口愈合

The incidence of inflammatory bowel disease, i.e., Crohn&#39;s disease and Ulcerative colitis, has significantly increased over the last decade. The ...

Effects of Allogeneic Platelet-Rich Plasma (PRP) on the Healing Process of Sectioned Achilles Tendons of Rats: A Methodological Description

This article describes the experimental procedures used to observe if PRP can positively affect tendon healing. There are 4 main steps to follow: induce a lesion in the Achilles tendon; prepare PRP and inject it (or the saline solution); remove the tendon; and perform biomechanical, molecular, and histological evaluations. At each step, all the procedures and methods are described in detail, so they can be reproduced easily.
Achilles tendons have been surgically sectioned (removal of a 5-mm long section). Afterwards, PRP or saline solution was injected to study whether PRP has a positive effect on the healing of the tendon. Three groups of 40 animals (a total of 120 rats were used in this study) were subdivided into 2 subgroups: PRP injection group and a saline injection control group. Rats were sacrificed at increasing time points (Group A: 5 days; Group B: 15 days; Group C: 30 days) and tendons were removed. 90 tendons underwent biomechanical testing before performing transcriptomic analysis and the 30 remaining tendons were submitted to histological analysis.

Effects of Allogeneic Platelet-Rich Plasma PRP on the Healing Process of Sectioned Achilles Tendons of Rats: A Methodological Description

This protocol describes the evaluation process of healing tendons in rats that have been injected with allogeneic platelet rich plasma (PRP) or saline solution after removing part of the Achilles tendon. The progress of tendon healing is evaluated at several time points using different types of analyses.

同种异体富血小板血浆 (PRP) 对大鼠分段腱愈合过程的影响: 方法学描述

This article describes the experimental procedures used to observe if PRP can positively affect tendon healing. There are 4 main steps to follow: induce a ...

Ultrasonography in Experimental Reproductive Investigations on Rats

With the development of assisted reproductive technology and the ethical limitations of research on humans, rat animal models have been widely used in reproductive medicine. In the past, the study of reproductive system development in rodents has been based on one-time histological examination of excised tissues. Recently, with the development of high-resolution transabdominal ultrasound, high-quality sonography can now be performed to evaluate the reproductive organs of rats, allowing a new method for studying the reproductive system. Images were obtained using a high-resolution ultrasonographic system. Gynecological ultrasonography was performed on 28 eight-week-old non-pregnant rats and 5 pregnant Sprague-Dawley rats. We describe how to recognize organs of the reproductive system and associated structures in typical views during different phases of the estrus cycle. Color flow Doppler was used to measure uterine artery blood flow and evaluate uterine blood flow pattern changes during different stages of pregnancy. We have demonstrated that ultrasound exploration is a useful method for evaluating changes in internal reproductive organs. Its use raises the possibility of conducting additional experiments, including medical or surgical procedures, and provides the ability to monitor sonographic changes to internal organs without sacrificing animals.

This manuscript describes the utility of ultrasound performed on female rats to design experimental models for reproductive and gynecological investigation. A step-by-step explanation of how to perform ultrasonographic evaluation is shown.

大鼠实验性生殖研究中的超声检查

With the development of assisted reproductive technology and the ethical limitations of research on humans, rat animal models have been widely used in ...

Improved Method for the Establishment of an In Vitro Blood-Brain Barrier Model Based on Porcine Brain Endothelial Cells

The aim of this protocol presents an optimized procedure for the purification and cultivation of pBECs and to establish in vitro blood-brain barrier (BBB) models based on pBECs in mono-culture (MC), MC with astrocyte-conditioned medium (ACM), and non-contact co-culture (NCC) with astrocytes of porcine or rat origin. pBECs were isolated and cultured from fragments of capillaries from the brain cortices of domestic pigs 5-6 months old. These fragments were purified by careful removal of meninges, isolation and homogenization of grey matter, filtration, enzymatic digestion, and centrifugation. To further eliminate contaminating cells, the capillary fragments were cultured with puromycin-containing medium. When 60-95% confluent, pBECs growing from the capillary fragments were passaged to permeable membrane filter inserts and established in the models. To increase barrier tightness and BBB characteristic phenotype of pBECs, the cells were treated with the following differentiation factors: membrane permeant 8-CPT-cAMP (here abbreviated cAMP), hydrocortisone, and a phosphodiesterase inhibitor, RO-20-1724 (RO). The procedure was carried out over a period of 9-11 days, and when establishing the NCC model, the astrocytes were cultured 2-8 weeks in advance. Adherence to the described procedures in the protocol has allowed the establishment of endothelial layers with highly restricted paracellular permeability, with the NCC model showing an average transendothelial electrical resistance (TEER) of 1249 &#177; 80 &#937; cm2, and paracellular permeability (Papp) for Lucifer Yellow of 0.90 10-6 &#177; 0.13 10-6 cm sec-1 (mean &#177; SEM, n=55). Further evaluation of this pBEC phenotype showed good expression of the tight junctional proteins claudin 5, ZO-1, occludin and adherens junction protein p120 catenin. The model presented can be used for a range of studies of the BBB in health and disease and, with the highly restrictive paracellular permeability, this model is suitable for studies of transport and intracellular trafficking.

Improved Method for the Establishment of an In Vitro Blood-Brain Barrier Model Based on Porcine Brain Endothelial Cells

The aim of the protocol is to present an optimized procedure for the establishment of an in vitro blood-brain barrier (BBB) model based on primary porcine brain endothelial cells (pBECs). The model shows high reproducibility, high tightness, and is suitable for studies of transport and intracellular trafficking in drug discovery.

一种基于猪脑内皮细胞的体外血脑屏障模型的改进方法

The aim of this protocol presents an optimized procedure for the purification and cultivation of pBECs and to establish in vitro blood-brain barrier (BBB) ...

Microscopy Based Methods for the Assessment of Epithelial Cell Migration During In Vitro Wound Healing

Cell migration is a mandatory aspect for wound healing. Creating artificial wounds on research animal models often results in costly and complicated experimental procedures, while potentially lacking in precision. In vitro culture of epithelial cell lines provides a suitable platform for researching the cell migratory behavior in wound healing and the impact of treatments on these cells. The physiology of epithelial cells is often studied in non-confluent conditions; however, this approach may not resemble natural wound healing conditions. Disrupting the epithelium integrity by mechanical means generates a realistic model, but may impede the application of molecular techniques. Consequently, microscopy based techniques are optimal for studying epithelial cell migration in vitro. Here we detail two specific methods, the artificial wound scratch assay and the artificial migration front assay, that can obtain quantitative and qualitative data, respectively, on the migratory performance of epithelial cells.

Microscopy Based Methods for the Assessment of Epithelial Cell Migration During  In Vitro Wound Healing

This manuscript describes how incision-like lesions made on cultured epithelial cell monolayers conveniently model wound healing in vitro, allowing for imaging by confocal or laser scanning microscopy, and which can provide high-quality quantitative and qualitative data for studying both cell behavior and the mechanisms involved in migration.

以显微镜为基础的方法评估上皮细胞迁移过程中的体外创面愈合

Cell migration is a mandatory aspect for wound healing. Creating artificial wounds on research animal models often results in costly and complicated ...

Measuring the Effects of Bacteria and Chemicals on the Intestinal Permeability of Caenorhabditis elegans

In living organisms, intestinal hyperpermeability is a serious symptom that leads to many inflammatory bowel diseases (IBDs). Caenorhabditis elegans is a nonmammalian animal model that is widely used as an assay system due to its short lifespan, transparency, cost-effectiveness, and lack of animal ethics issues. In this study, a method was developed to investigate the effects of different bacteria and 3,3'-diindolylmethane (DIM) on the intestinal permeability of C. elegans with a high-throughput image analysis system. The worms were infected with different gut bacteria or cotreated with DIM for 48 h and fed with fluorescein isothiocyanate (FITC)-dextran overnight. Then, the intestinal permeability was examined by comparing the fluorescence images and the fluorescence intensity inside the worm bodies. This method may also have the potential to identify probiotic and pathogenic intestinal bacteria that affect intestinal permeability in the animal model and is effective for examining the effects of harmful or health-promoting chemicals on intestinal permeability and intestinal health. However, this protocol also has some considerable limitations at the genetic level, especially for determining which genes are altered to control illness, because this method is mostly used for phenotypic determination. In addition, this method is limited to determining exactly which pathogenic substrates cause inflammation or increase the permeability of the worms' intestines during infection. Therefore, further in-depth studies, including investigation of the molecular genetic mechanism using mutant bacteria and nematodes as well as chemical component analysis of bacteria, are required to fully evaluate the function of bacteria and chemicals in determining intestinal permeability.