Woodland P, Batista-Lima F, Lee C, Preston S L, Dettmar P, Sifrim D
Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK;
Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK; Universidade Federal do Ceará, Fortaleza, Brazil; and.
Am J Physiol Gastrointest Liver Physiol. 2015 Jun 15;308(12):G975-80. doi: 10.1152/ajpgi.00424.2014. Epub 2015 Apr 23.
Patients with nonerosive reflux disease exhibit impaired esophageal mucosal integrity, which may underlie enhanced reflux perception. In vitro topical application of an alginate solution can protect mucosal biopsies against acid-induced changes in transepithelial electrical resistance (TER). We aimed to confirm this finding in a second model using 3D cell cultures and to assess prolonged protection in a biopsy model. We assessed the protective effect of a topically applied alginate solution 1 h after application. 3D cell cultures were grown by using an air-liquid interface and were studied in Ussing chambers. The apical surface was "protected" with 200 μl of either alginate or viscous control or was unprotected. The tissue was exposed to pH 3 + bile acid solution for 30 min and TER change was calculated. Distal esophageal mucosal biopsies were taken from 12 patients and studied in Ussing chambers. The biopsies were coated with either alginate or viscous control solution. The biopsies were then bathed in pH 7.4 solution for 1 h. The luminal chamber solution was replaced with pH 2 solution for 30 min. Percentage changes in TER were recorded. In five biopsies fluorescein-labeled alginate solution was used to allow immunohistological localization of the alginate after 1 h. In the cell culture model, alginate solution protected tissue against acid-induced change in TER. In biopsies, 60 min after protection with alginate solution, the acidic exposure caused a -8.3 ± 2.2% change in TER compared with -25.1 ± 4.5% change after protection with the viscous control (P < 0.05). Labeled alginate could be seen coating the luminal surface in all cases. In vitro, alginate solutions can adhere to the esophageal mucosa for up to 1 h and exert a topical protectant effect. Durable topical protectants can be further explored as first-line/add-on therapies for gastroesophageal reflux disease.
非糜烂性反流病患者存在食管黏膜完整性受损的情况,这可能是反流感知增强的基础。在体外,局部应用藻酸盐溶液可保护黏膜活检组织免受酸诱导的跨上皮电阻(TER)变化的影响。我们旨在使用三维细胞培养在第二个模型中证实这一发现,并在活检模型中评估其延长的保护作用。我们在应用藻酸盐溶液1小时后评估其局部应用的保护效果。三维细胞培养通过气液界面生长,并在尤斯灌流小室中进行研究。顶表面用200微升藻酸盐或粘性对照溶液“保护”,或不进行保护。组织暴露于pH 3 +胆汁酸溶液中30分钟,并计算TER变化。从12名患者获取远端食管黏膜活检组织,并在尤斯灌流小室中进行研究。活检组织用藻酸盐或粘性对照溶液包被。然后将活检组织在pH 7.4溶液中孵育1小时。将腔室溶液替换为pH 2溶液30分钟。记录TER的百分比变化。在五份活检组织中,使用荧光素标记的藻酸盐溶液,以便在1小时后进行藻酸盐的免疫组织学定位。在细胞培养模型中,藻酸盐溶液可保护组织免受酸诱导的TER变化的影响。在活检组织中,用藻酸盐溶液保护60分钟后,酸性暴露导致TER变化为-8.3±2.2%,而用粘性对照溶液保护后为-25.1±4.5%(P<0.05)。在所有情况下均可见标记的藻酸盐覆盖在腔表面。在体外,藻酸盐溶液可附着于食管黏膜长达1小时,并发挥局部保护作用。持久的局部保护剂可作为胃食管反流病的一线/附加治疗方法进一步探索。