The Pivotal Role of TRP Channels in Homeostasis and Diseases throughout the Gastrointestinal Tract

被引:29
作者
Alaimo, Alessandro [1 ]
Rubert, Josep [1 ]
机构
[1] Univ Trento, Dept Cellular Computat & Integrat Biol CIBIO, Via Sommar 9, I-38123 Povo, Tn, Italy
关键词
transient receptor potential ion channels; gastrointestinal tract; sensory transduction; visceral hypersensitivity; inflammatory bowel disease; colorectal cancer; microbioma; RECEPTOR POTENTIAL CHANNELS; IRRITABLE-BOWEL-SYNDROME; ION-CHANNEL; VISCERAL HYPERSENSITIVITY; EXPERIMENTAL COLITIS; VANILLOID RECEPTOR; PEPPERMINT OIL; INTESTINAL FIBROSIS; INFLAMMATORY PAIN; AFFERENT NEURONS;
D O I
10.3390/ijms20215277
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transient receptor potential (TRP) channels superfamily are a large group of proteins that play crucial roles in cellular processes. For example, these cation channels act as sensors in the detection and transduction of stimuli of temperature, small molecules, voltage, pH, and mechanical constrains. Over the past decades, different members of the TRP channels have been identified in the human gastrointestinal (GI) tract playing multiple modulatory roles. Noteworthy, TRPs support critical functions related to the taste perception, mechanosensation, and pain. They also participate in the modulation of motility and secretions of the human gut. Last but not least, altered expression or activity and mutations in the TRP genes are often related to a wide range of disorders of the gut epithelium, including inflammatory bowel disease, fibrosis, visceral hyperalgesia, irritable bowel syndrome, and colorectal cancer. TRP channels could therefore be promising drug targets for the treatment of GI malignancies. This review aims at providing a comprehensive picture of the most recent advances highlighting the expression and function of TRP channels in the GI tract, and secondly, the description of the potential roles of TRPs in relevant disorders is discussed reporting our standpoint on GI tract-TRP channels interactions.
引用
收藏
页数:17
相关论文
共 153 条
[1]   A combination of peppermint oil and caraway oil attenuates the post-inflammatory visceral hyperalgesia in a rat model [J].
Adam, B ;
Liebregts, T ;
Best, J ;
Bechmann, L ;
Lackner, C ;
Neumann, J ;
Koehler, S ;
Holtmann, G .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2006, 41 (02) :155-160
[2]   Increased capsaicin receptor TRPV1-expressing sensory fibres in irritable bowel syndrome and their correlation with abdominal pain [J].
Akbar, A. ;
Yiangou, Y. ;
Facer, P. ;
Walters, J. R. F. ;
Anand, P. ;
Ghosh, S. .
GUT, 2008, 57 (07) :923-929
[3]   Expression of the TRPV1 receptor differs in quiescent inflammatory bowel disease with or without abdominal pain [J].
Akbar, Ayesha ;
Yiangou, Yiangos ;
Facer, Paul ;
Brydon, W. G. ;
Walters, Julian R. F. ;
Anand, Praveen ;
Ghosh, Subrata .
GUT, 2010, 59 (06) :767-774
[4]  
Almaraz L, 2014, HANDB EXP PHARMACOL, V222, P547, DOI 10.1007/978-3-642-54215-2_22
[5]  
[Anonymous], NEUROGASTROENTEROL M
[6]  
[Anonymous], TRP CHANNELS THERAPE, DOI [10.1016/B978-0-12-420024-1.00022-9, DOI 10.1016/B978-0-12-420024-1.00022-9]
[7]   Global patterns and trends in colorectal cancer incidence and mortality [J].
Arnold, Melina ;
Sierra, Monica S. ;
Laversanne, Mathieu ;
Soerjomataram, Isabelle ;
Jemal, Ahmedin ;
Bray, Freddie .
GUT, 2017, 66 (04) :683-691
[8]   Expression of transforming growth factors alpha and beta in colonic mucosa in inflammatory bowel disease [J].
Babyatsky, MW ;
Rossiter, G ;
Podolsky, DK .
GASTROENTEROLOGY, 1996, 110 (04) :975-984
[9]   Transient receptor potential ion channel function in sensory transduction and cellular signaling cascades underlying visceral hypersensitivity [J].
Balemans, Dafne ;
Boeckxstaens, Guy E. ;
Talavera, Karel ;
Wouters, Mira M. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2017, 312 (06) :G635-G648
[10]   Resolvin D1 attenuates activation of sensory transient receptor potential channels leading to multiple anti-nociception [J].
Bang, S. ;
Yoo, S. ;
Yang, T. J. ;
Cho, H. ;
Kim, Y. G. ;
Hwang, S. W. .
BRITISH JOURNAL OF PHARMACOLOGY, 2010, 161 (03) :707-720