Esophageal Mucosal Integrity in Nonerosive Reflux Disease

被引:51
作者
Woodland, Philip [1 ]
Sifrim, Daniel [1 ]
机构
[1] Queen Mary Univ London, Neurogastroenterol Grp, Barts & London Sch Med & Dent, London, England
关键词
GERD; nonerosive reflux disease; mucosal integrity; dilated intercellular spaces; impedance; transepithelial electrical resistance; DILATED INTERCELLULAR SPACES; PROTON PUMP INHIBITORS; ACID REFLUX; PARACELLULAR CONDUCTANCE; POTENTIAL DIFFERENCE; TIGHT JUNCTIONS; HIATUS-HERNIA; E-CADHERIN; HEARTBURN; INJURY;
D O I
10.1097/MCG.0b013e318299f181
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Gastroesophageal reflux disease, especially when refractory to standard therapy, remains a significant clinical problem. Although symptom pathogenesis in erosive reflux disease is relatively easy to understand, it is less clear how exposure of the macroscopically normal mucosa in nonerosive reflux disease (NERD) is able to cause heartburn. Over recent years it has become apparent that there may be microscopic and functional defects in the esophageal epithelial barrier in NERD, a so-called impairment of esophageal mucosal integrity. This can be expressed in morphologic or in functional terms. Morphologically the epithelium in NERD displays dilated intercellular spaces, which may represent a failed epithelial barrier, probably due to disruption of cell apical junctional complexes. Functionally, the mucosa in NERD displays more permeability to ions and small molecules than that of control subjects. Both morphologic and functional changes can be induced by exposure to refluxate-like solutions in vitro and in vivo. This article summarizes the evidence for impairment of esophageal mucosal integrity, and discusses its possible role in disease pathogenesis.
引用
收藏
页码:6 / 12
页数:7
相关论文
共 55 条
[1]
Claudins and paracellular transport: an update [J].
Angelow, Susanne ;
Yu, Alan S. L. .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2007, 16 (05) :459-464
[2]
Altered localization and expression of tight-junction proteins in a rat model with chronic acid reflux esophagitis [J].
Asaoka, D ;
Miwa, H ;
Hirai, S ;
Ohkawa, A ;
Kurosawa, A ;
Kawabe, M ;
Hojo, M ;
Nagahara, A ;
Minoo, T ;
Ohkura, R ;
Ohkusa, T ;
Sato, N .
JOURNAL OF GASTROENTEROLOGY, 2005, 40 (08) :781-790
[3]
ASL YU, 2003, J BIOL CHEM, V278, P17350
[4]
The pathogenesis of heartburn in nonerosive reflux disease: A unifying hypothesis [J].
Barlow, WJ ;
Orlando, RC .
GASTROENTEROLOGY, 2005, 128 (03) :771-778
[5]
TRANSMURAL POTENTIAL DIFFERENCE IN PATIENTS WITH HIATUS HERNIA AND OESOPHAGEAL ULCER [J].
BECK, IT ;
HERNANDEZ, NA .
GUT, 1969, 10 (06) :469-+
[6]
Determinants of perception of heartburn and regurgitation [J].
Bredenoord, AJ ;
Weusten, BLAM ;
Curvers, WL ;
Timmer, R ;
Smout, AJPM .
GUT, 2006, 55 (03) :313-318
[7]
Reversibility of GERD ultrastructural alterations and relief of symptoms after omeprazole treatment [J].
Calabrese, C ;
Bortolotti, M ;
Fabbri, A ;
Areni, A ;
Cenacchi, G ;
Scialpi, C ;
Miglioli, M ;
Di Febo, G .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (03) :537-542
[8]
Depletion of E-cadherin disrupts establishment but not maintenance of cell junctions in Madin-Darby canine kidney epithelial cells [J].
Capaldo, Christopher T. ;
Macara, Ian G. .
MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (01) :189-200
[9]
Gastro-oesophageal reflux disease in primary care: an international study of different treatment strategies with omeprazole [J].
Carlsson, R ;
Dent, J ;
Watts, R ;
Riley, S ;
Sheikh, R ;
Hatlebakk, J ;
Haug, K ;
de Groot, G ;
van Oudvorst, A ;
Dalvag, A ;
Junghard, O ;
Wiklund, I .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1998, 10 (02) :119-124
[10]
CARNEY CN, 1981, LAB INVEST, V45, P198