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Visceral hypersensitivity in inflammatory bowel diseases and irritable bowel syndrome: The role of proteases 被引量:7

Visceral hypersensitivity in inflammatory bowel diseases and irritable bowel syndrome: The role of proteases
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摘要 Proteases, enzymes catalyzing the hydrolysis of peptide bonds, are present at high concentrations in the gastrointestinal tract. Besides their well-known role in the digestive process, they also function as signaling molecules through the activation of protease-activated receptors(PARs). Based on their chemical mechanism for catalysis, proteases can be classified into several classes: serine, cysteine, aspartic, metallo- and threonine proteases represent the mammalian protease families. In particular, the class of serine proteases will play a significant role in this review. In the last decades, proteases have been suggested to play a key role in the pathogenesis of visceral hypersensitivity, which is a major factor contributing to abdominal pain in patients with inflammatory bowel diseases and/or irritable bowel syndrome. So far, only a few preclinical animal studies have investigated the effect of protease inhibitors specifically on visceral sensitivity while their effect on inflammation is described in more detail. In our accompanying review we describe their effect on gastrointestinal permeability. On account of their promising results in the field of visceral hypersensitivity, further research is warranted. The aim of this review is to give an overview on the concept of visceral hypersensitivity as well as on the physiological and pathophysiological functions of proteases herein. Proteases, enzymes catalyzing the hydrolysis of peptide bonds, are present at high concentrations in the gastrointestinal tract. Besides their well-known role in the digestive process, they also function as signaling molecules through the activation of protease-activated receptors(PARs). Based on their chemical mechanism for catalysis, proteases can be classified into several classes: serine, cysteine, aspartic, metallo- and threonine proteases represent the mammalian protease families. In particular, the class of serine proteases will play a significant role in this review. In the last decades, proteases have been suggested to play a key role in the pathogenesis of visceral hypersensitivity, which is a major factor contributing to abdominal pain in patients with inflammatory bowel diseases and/or irritable bowel syndrome. So far, only a few preclinical animal studies have investigated the effect of protease inhibitors specifically on visceral sensitivity while their effect on inflammation is described in more detail. In our accompanying review we describe their effect on gastrointestinal permeability. On account of their promising results in the field of visceral hypersensitivity, further research is warranted. The aim of this review is to give an overview on the concept of visceral hypersensitivity as well as on the physiological and pathophysiological functions of proteases herein.
出处 《World Journal of Gastroenterology》 SCIE CAS 2016年第47期10275-10286,共12页 世界胃肠病学杂志(英文版)
基金 Supported by University Research Fund Doctoral Projects(BOF-DOCPRO),No.DOCPRO4 2014/ID 2964 Research Foundation Flanders(FWO),No.G034113N
关键词 朊酶 激活朊酶的受体 朊酶禁止者 内脏的超敏性 内脏的疼痛 急躁的肠症候群 煽动性的肠疾病 Proteases Proteinase-activated receptors Protease inhibitors Visceral hypersensitivity Visceral pain Irritable bowel syndrome Inflammatory bowel diseases
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  • 1Benedicte Y De Winter,Joris G De,Man.Interplay between inflammation,immune system and neuronal pathways:Effect on gastrointestinal motility[J].World Journal of Gastroenterology,2010,16(44):5523-5535. 被引量:23
  • 2杨小军,官阳,钱伟,沈蕾,侯晓华.突触可塑性在急性束缚应激所致内脏高敏感中的作用[J].中华消化杂志,2007,27(10):670-674. 被引量:6
  • 3Roka R, wittmann T, bueno L. altered protease signalling in the gut: a novel pathophysiologieal factor in irritable bowel syndrome [J]. Neurogastroenterol Motility, 2008, 20: 853-6.
  • 4Cenac N, Andrews CN, Holzhausen M, et al. Role for protease activity in visceral pain in irritable bowel syndrome[J]. J Clin Invest, 2007, 117(3): 636-47.
  • 5Geese K, R6ka R, Ferrier L, et al. Increased faecal serine proteaseactivity in diarrhoeic IBS patients: a colonic lumenal factor impairing colonic permeability and sensitivity[J]. Gut, 2008, 57(5): 591-9.
  • 6Holzer P. Gastrointestinal afferents as targets of novel drugs for the treatment of functional bowel disorders and visceral pain[Jl. Eur J Pharmacol, 2001, 429(1/3): 177-93.
  • 7Crane JW, French KR, Buller KM. Patterns of neuronal activation in the rat brain and spinal cord in response to increasing durations of restraint stress[J]. Stress, 2005, 8(3): 199-211.
  • 8Gu6 M, Del Rio-Lacheze C, Eutamene H, et al. Stress-induced visceral hypersensitivity to rectal distension in rats: role of CRF and mast cells[J]. Neurogastroenterol Motil, 1997, 9(4): 271-9.
  • 9Kim DH, Cho YJ, Kim JH, et al. Stress-induced alterations in mast cell numbers and proteinase-activated receptor-2 expression of the colon: role of corticotrophin-releasing factor[J]. J Korean Med Sci, 2010, 25(9): 1330-5.
  • 10Tamura Y, Hirado M, Okamura K, et al. Synthetic inhibitors of trypsin, plasmin, kallikrein, thrombin, Clr-, and C1 esterase [J]. Biochim Biophys Acta, 1977, 484(2): 417-22.

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