Intestinal Permeability, Irritable Bowel Syndrome with Constipation, and the Role of Sodium-Hydrogen Exchanger Isoform 3 (NHE3)

被引:0
|
作者
Lacy, Brian E. [1 ]
Rosenbaum, David [2 ]
Edelstein, Susan [2 ]
Kozuka, Kenji [2 ]
Williams, Laura A. [2 ]
Kunkel, David C. [3 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Davis Bldg,4500 San Pablo Rd, Jacksonville, FL 32224 USA
[2] Ardelyx Inc, Waltham, MA USA
[3] Univ Calif San Diego, Div Gastroenterol, La Jolla, CA USA
关键词
tenapanor; abdominal pain; leaky gut; gut permeability; IBS-C; tight junction protein; transepithelial resistance; PREVALENCE; INFLAMMATION; MANAGEMENT; GUIDELINE; TENAPANOR; SYMPTOMS; HABIT; PAIN;
D O I
10.2147/CEG.S455101
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Increased intestinal permeability has been identified as one of the many pathophysiological factors associated with the development of irritable bowel syndrome (IBS), a common disorder of gut-brain interaction. The layer of epithelial cells that lines the intestine is permeable to a limited degree, and the amount of paracellular permeability is tightly controlled to enable the absorption of ions, nutrients, and water from the lumen. Increased intestinal permeability to macromolecules can be triggered by a variety of insults, including infections, toxins from food poisoning, or allergens, which in turn cause an inflammatory response and are associated with abdominal pain in patients with IBS. This review article discusses increased intestinal permeability in IBS, focusing on IBS with constipation (IBS-C) through the lens of a patient case with a reported prior diagnosis of "leaky gut syndrome" upon initial contact with a gastrointestinal specialist. We review advantages and disadvantages of several methods of measuring intestinal permeability in patients and discuss when measuring intestinal permeability is appropriate in the therapeutic journey of patients with IBS-C. Furthermore, we discuss a possible mechanism of restoring the intestinal barrier to its healthy state through altering intracellular pH by inhibiting sodium-hydrogen exchanger isoform 3 (NHE3). Tenapanor is a minimally absorbed, small-molecule inhibitor of NHE3 that has been approved by the US Food and Drug Administration for the treatment of IBS-C in adults. Preclinical studies showed that tenapanor may restore the intestinal barrier in IBS-C by affecting the conformation of tight junction proteins via NHE3 inhibition to block the paracellular transport of macromolecules from the intestinal lumen. Testing for increased permeability in patients with IBS-C who experience abdominal pain may help inform the choice of therapeutics and alter patients' misconceptions about "leaky gut syndrome".
引用
收藏
页码:173 / 183
页数:11
相关论文
共 50 条
  • [31] Solute carrier family 9, subfamily A, member 3 (SLC9A3)/sodium-hydrogen exchanger member 3 (NHE3) dysregulation and dilated intercellular spaces in patients with eosinophilic esophagitis
    Zeng, Chang
    Vanoni, Simone
    Wu, David
    Caldwell, Julie M.
    Wheeler, Justin C.
    Arora, Kavisha
    Noah, Taeko K.
    Waggoner, Lisa
    Besse, John A.
    Yamani, Amnah N.
    Uddin, Jazib
    Rochman, Mark
    Wen, Ting
    Chehade, Mirna
    Collins, Margaret H.
    Mukkada, Vincent A.
    Putnam, Philip E.
    Naren, Anjaparavanda P.
    Rothenberg, Marc E.
    Hogan, Simon P.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 142 (06) : 1843 - 1855
  • [32] Recovery from proton di/tripeptide transport-mediated intracellular acidification in the villous epithelium of sodium/hydrogen exchanger isoform 3 (NHE3) knockout mice
    Simpson, JE
    Walker, NM
    Clarke, LL
    GASTROENTEROLOGY, 2005, 128 (04) : A677 - A677
  • [33] Tethering, recycling and activation of the epithelial sodium-proton exchanger, NHE3
    Alexander, R. Todd
    Grinstein, Sergio
    JOURNAL OF EXPERIMENTAL BIOLOGY, 2009, 212 (11): : 1630 - 1637
  • [34] Ezrin Is Required for the Functional Regulation of the Epithelial Sodium Proton Exchanger, NHE3
    Hayashi, Hisayoshi
    Tamura, Atsushi
    Krishnan, Devishree
    Tsukita, Sachiko
    Suzuki, Yuichi
    Kocinsky, Hetal S.
    Aronson, Peter S.
    Orlowski, John
    Grinstein, Sergio
    Alexander, R. Todd
    PLOS ONE, 2013, 8 (02):
  • [35] NHE-1 is the sodium-hydrogen exchanger isoform present in erythroid cells (vol 1374, pg 56, 1998)
    Sarangarajan, R
    Dhabia, N
    Soleimani, M
    Baird, N
    Joiner, C
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2004, 1667 (01): : 101 - 101
  • [36] Identification of osmotic response elements from the rat sodium-hydrogen exchanger isoform 2 (NHE-2) gene
    Bai, LQ
    Collins, JF
    Muller, YL
    Xu, H
    Kiela, PR
    Ghishan, FK
    GASTROENTEROLOGY, 1999, 116 (04) : A857 - A857
  • [37] Rosiglitazone, RGZ, increases renal sodium/hydrogen exchanger 3, NHE3, protein and ammonium excretion to young rats.
    Ecelbarger, CA
    Welbourne, T
    FASEB JOURNAL, 2002, 16 (05): : A1169 - A1169
  • [38] NHE3 - A NA+/H+ EXCHANGER ISOFORM OF RENAL BRUSH-BORDER
    BIEMESDERFER, D
    PIZZONIA, J
    ABUALFA, A
    EXNER, M
    REILLY, R
    IGARASHI, P
    ARONSON, PS
    AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (05): : F736 - F742
  • [39] The apical Na+/H+ exchanger isoform NHE3 is regulated by the actin cytoskeleton
    Kurashima, K
    D'Souza, S
    Szászi, K
    Ramjeesingh, R
    Orlowski, J
    Grinstein, S
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (42) : 29843 - 29849
  • [40] Expression of the Na/H exchanger isoform NHE3 in epithelial cells of liver and pancreas.
    Negoianu, D
    Biemesderfer, D
    Mennone, A
    Boyer, IL
    Aronson, PS
    JOURNAL OF INVESTIGATIVE MEDICINE, 1998, 46 (03) : 210A - 210A