Hypothesis about mechanisms through which nicotine might exert its effect on the interdependence of inflammation and gut barrier function in ulcerative colitis
Corresponding Author
Victoria E. McGilligan
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, UK BT52 1SASearch for more papers by this authorJulie M. W. Wallace
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorPatricia M. Heavey
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorDiana L. Ridley
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorIan R. Rowland
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorCorresponding Author
Victoria E. McGilligan
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, UK BT52 1SASearch for more papers by this authorJulie M. W. Wallace
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorPatricia M. Heavey
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorDiana L. Ridley
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorIan R. Rowland
From Northern Ireland Centre for Food and Health (NICHE), Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, United Kingdom
Search for more papers by this authorAbstract
Ulcerative colitis (UC) is characterized by impairment of the epithelial barrier and the formation of ulcer-type lesions, which result in local leaks and generalized alterations of mucosal tight junctions. Ultimately, this results in increased basal permeability. Although disruption of the epithelial barrier in the gut is a hallmark of inflammatory bowel disease and intestinal infections, it remains unclear whether barrier breakdown is an initiating event of UC or rather a consequence of an underlying inflammation, evidenced by increased production of proinflammatory cytokines. UC is less common in smokers, suggesting that the nicotine in cigarettes may ameliorate disease severity. The mechanism behind this therapeutic effect is still not fully understood, and indeed it remains unclear if nicotine is the true protective agent in cigarettes. Nicotine is metabolized in the body into a variety of metabolites and can also be degraded to form various breakdown products. It is possible these metabolites or degradation products may be the true protective or curative agents. A greater understanding of the pharmacodynamics and kinetics of nicotine in relation to the immune system and enhanced knowledge of gut permeability defects in UC are required to establish the exact protective nature of nicotine and its metabolites in UC. This review suggests possible hypotheses for the protective mechanism of nicotine in UC, highlighting the relationship between gut permeability and inflammation, and indicates where in the pathogenesis of the disease nicotine may mediate its effect.
(Inflamm Bowel Dis 2007;13:108–115)
REFERENCES
- 1 Brant SR, Panhuysen CL, Nicolae, D, et al. MDR1 Ala893 Polymorphism is associated with inflammatory Bowel Disease. Am J Hum Genet. 2003; 73: 1282–1292.
- 2 Ogura Y, Bonen DK, Inohara N, et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature. 2001; 411: 603–606.
- 3 Hugot JP, Chamaillard M, Zouali H, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature. 2001; 411: 599–603.
- 4 Bonapace CR, Mays DS. The effect of mesalamine and nicotine in the treatment of inflammatory bowel disease Ann Pharmacother. 1997; 31: 907–913.
- 5 Targan SR, Karp LC. Defects in mucosal immunity leading to ulcerative colitis. Immunol Rev. 2005; 206: 296–305.
- 6 Stedman RL, Chamberlain WJ, Miller RC. High molecular weight pigment in cigarette smoke. Chem Ind. 1966; 10: 1560–1562.
- 7 Becker CG, Dubin T, Wiedemann HP. Hypersensitivity to tobacco antigen. Proc Natl Acad Sci U S A. 1973; 73: 1712–1716.
- 8 Francus T, Romano PM, Manzo G, et al. IL-1, IL-6, and PDGF mRNA expression in alveolar cells following stimulation with tobacco-derived antigen. Cell Immunol. 1992; 145: 156–174.
- 9 Sopori ML, Kozak W. Immunomodulatory effects of cigarette smoke. J Neuroimmunol. 1998; 83: 148–156.
- 10 Tyndale RF, Pianezza ML, Sellers EM. A Common genetic defect in nicotine metabolism decreases risk for dependence and lowers cigarette consumption. Nicotine Tob Res. 1999; 1: supp2: : S63–S67.
- 11 Harries AD, Briad A, Rhodes J. Non-smoking: a feature of ulcerative colitis. Br Med J. 1982; 284: 706.
- 12 Calkins BM. A meta analysis of the role of smoking in inflammatory bowel disease. Dig Dis Sci. 1988; 29: 352–357.
- 13 Motley RJ, Rhodes J, Ford GA. Time relationships between cessation of smoking and onset of ulcerative colitis. Digestion. 1987; 37: 1257.
- 14 Beaugeries L, Massot N, Carbonnel F, et al. Impact of cessation of smoking on the course of Ulcerative Colitis. Am J Gastroenterol. 2001; 96: 2113.
- 15 Rudra Y, Motley R, Rhodes J. Does smoking improve colitis? Scand J Gastroenterol 1989; 24( suppl. 170): 61.
- 16 Nejdfors P, Wang Q, Ekelund M, et al. Increased colonic permeability in patients with ulcerative colitis: an in vitro study. Scand J Gastroenterol. 1998; 33: 749–753.
- 17 Katz KD, Hollander D, Vadheim CM, et al. Intestinal permeability in patients with Crohn's disease and their healthy relatives. Gastroenterology. 1989; 97: 927–931.
- 18 Teahon K, Smethurst P, Levi AJ, et al. Intestinal permeability in patients with Crohn's disease and their first degree relatives. Gut. 1992; 33: 320–323.
- 19 Parkes M, Jewell D. Ulcerative colitis and Crohn's disease: molecular genetics and clinical implications. Expert Rev Mol Med. 2001; 2001: 1–18. Available at: http://www.expertreviews.org/0100391Xh.htm. Accessed: August 15, 2006.
- 20 Schmitz H, Barueyer C, Fromm M, et al. Altered tight junction structure contributes to the impaired epithelial barrier function in UC. Gastroenterology. 1999; 116: 301–309.
- 21 Gitter AH, Wullstein F, Fromm M, et al. Epithelial barrier defects in ulcerative colitis characterisation and quantification by electrophysiological imaging. Gastroenterology. 2001; 121: 1320–1325.
- 22 Burgel N, Bojarski C, Manhertz J, et al. Mechanisms of diarrhea in collagenous colitis. Gastroenterology. 2002; 123: 433–443.
- 23 Ginochetti P, Campieri M, Belluzzi A, et al. Interleukin 1 beta release from fresh and cultured colonic mucosa in patients with ulcerative colitis. Agents Actions. 1992; Spec No: C50–C52.
- 24 Reinecker HC, Steffen M, Witthoeft T, et al. Enhanced secretion of tumour necrosis factor-alpha, IL-6, and IL-1 beta by isolated lamina propria mononuclear cells from patients with ulcerative colitis and Crohn's disease. Clin Exp Immunol. 1993; 94(1): 171–181.
- 25 Murata Y, Ishiguro Y, Itoh J, et al. The role of proinflammatory and immunoregulatory cytokines in the pathogenesis of ulcerative colitis. J Gastroenterol. 1995; 30: 56–60.
- 26 Daig R, Andus Y, Aschenbrenner E, et al. Increased interleukin-8 expression in the colon mucosa of patients with inflammatory bowel disease. Gut. 1996; 38: 216.
- 27 Fuss IJ, Neurath M, Boirvant M, et al. Disparate CD4+ lamina propria (LP) lymphokine secretion profiles in inflammatory bowel disease. Crohn's disease LP cells manifest increased secretion of IFN-gamma, whereas ulcerative colitis LP cells manifest increased secretion of IL-5. J Immunol. 1996; 157: 1261–1270.
- 28 Mitsuyama K, Sasalli E, Toyonaya A, et al. Colonic mucosal interleukin-6 in inflammatory bowel disease. Digestion. 1991; 50: 104–111.
- 29 Seegert D, Rosentiel P, Pfahler H, et al. Increased expression of IL-16 in inflammatory bowel disease. Gut. 2001; 48: 326–332.
- 30 Fujino S, Andoh A, Bamba S, et al. Increased expression of interleukin 17 in inflammatory bowel disease. Gut. 2003; 52: 65–70.
- 31 Melgar S, Yeung MMW, Bas A, et al. Over-expression of interleukin 10 in mucosal T cells of patients with active ulcerative colitis. Clin Exp Immunol. 2003; 134: 127–137.
- 32 Fuss IJ, Heller F, Boirivant M, et al. Non-classical CD1d-restricted NK T cells that produce IL–13 characterize an atypical Th2 response in ulcerative colitis. J Clin Invest. 2004; 113: 1490–1497.
- 33 Heller F, Florian P, Bojarski C, et al. Interleukin-13 is the key effector Th2 cytokine in ulcerative colitis that affects epithelial tight junctions, apoptosis, and cell restitution. Gastroenterology. 2005; 129: 550–564.
- 34 Nishiwaki T, Ina K, Goto H, et al. Possible involvement of the interleukin-15 and interleukin-15 receptor system in a heightened state of lamina propria B cell activation and differentiation in patients with inflammatory bowel disease. Gastroenterology. 2005; 40: 128–136.
- 35 Colgan SP, Resnick MB, Parkos CA, et al. IL-4 directly modulates function of a model human intestinal epithelium. J Immunol. 1994; 153: 2122–2129.
- 36 Youakim A, Ahdieh M. Interferon gamma decreases barrier function in T84 cells by reducing ZO-1 levels and disrupting apical actin. Am J Physiol. 1999; G1279–G1288.
- 37 Schmitz H, Fromm M, Bentzel CJ, et al. Tumour necrosis factor alpha regulates the epithelial barrier in the human intestinal cell line Ht-29/B6. J Cell Sci. 1999; 112: 137–146.
- 38 Bruewer M, Leugering A, Kucharzik T, et al. Pro-inflammatory cytokines disrupt epithelial barrier function by apoptosis independent mechanisms. J Immunol. 2003; 171: 6164–6172.
- 39 Tazuke Y, Drongowski RA, Teitelbaum DH, et al. Interleukin-6 changes tight junction permeability and intracellular phospholipid content in a human enterocyte cell culture model. Pediatr Surg Int. 2003; 19: 321–325.
- 40 Ma TY, Iwamolo GK, Hoa NT, et al. TNFα induced increase in intestinal epithelial tight junction permeability requires NF-kappa B activation. Am J Physiol Gastrointest Liver Physiol. 2004; 286: G367–G376.
- 41 Kinugasa T, Sakaguchi T, Gu X. Reinecher, HC. Claudins regulate the intestinal barrier in response to immune mediators. Gastroenterology. 2000; 118: 1001–1011.
- 42 Madsen KL, Lewis SA, Taernini MM, et al. Interleukin-10 prevents cytokine-induced disruption of T84 monolayer barrier integrity and limits chloride secretion. Gastroenterology. 2000; 113: 151–159.
- 43 Nishiyama R, Sakayuchi T, Kinugasa T, et al. Interleukin-2 receptor beta subunit-dependent and independent regulation of intestinal epithelial tight junctions. J Biol Chem. 2001; 276: 35571–35580.
- 44 Barmeyer C, Harren M, Schmitz H, et al. Mechanics of diarrhoea in the interleukin-2 deficient mouse model of colonic inflammation. Am J Physiol Gastrointest Liver Physiol. 2004; 286: G244–G252.
- 45 Clayburgh DR, Shen L, Turner JR. A porous defense: the leaky epithelial barrier in intestinal disease. Lab Invest. 2004; 84: 282–291.
- 46 Jung HC, Eckmann L, Yang SK, et al. A distinct array of pro-inflammatory cytokines is expressed in human colon epithelial cells in response to bacterial invasion. J Clin Invest. 1995; 95(1): 55–65.
- 47 Shanahan F. Inflammatory bowel disease: Immunodiagnostics, immunotherapeutics and ecotherapeutics. Gastroenterology. 2001; 120: 622–635.
- 48 Guaner F and Malagelada JR. Gut flora in health and disease. Lancet. 2003; 361: 512–519.
- 49 Guarner F, Bourdet-Sicard R, Brandtzaeg P, et al. Mechanisms of disease: the hygiene hypothesis revisited. Nat Clin Pract Gastroenterol Hepatol. 2006; 3: 275–284.
- 50 Gaya DR, Russell RK, Nimmo ER, et al. New genes in inflammatory bowel disease: lessons for complex diseases? Lancet. 2006; 367: 1271–1284.
- 51 Cuthbert AP, Fisher SA, Mirza MM, et al. The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. Gastroenterology. 2002; 122: 867–874.
- 52 Buhner S, Buning C, Genschel K, et al. Genetic basis for increased intestinal permeability in families with Crohn's disease: role of CARD15 3020insC mutation? Gut. 2006; 55: 342–347.
- 53 Parkes M, Michael Barmada, Jack Satsangi, et al. The IBD2 locus shows linkage heterogeneity between ulcerative colitis and Crohn's disease. Am J Hum Genet. 2000; 67: 1605–1610.
- 54 Danese S, Miquel S, Fiocchi C. Inflammatory bowel disease: the role of environmental factors. Autoimmun Revs. 2004; 3: 394–400.
- 55 Prytz H, Benoni C, Tahesson C. Does smoking tighten the gut? Scand J Gastroenterol. 1989; 24: 1084–1088.
- 56 Suenaert P, Bulteel V, Den Hond E, et al. The effects of smoking and indometacin on small intestinal permeability. Aliment Pharmacol Ther. 2000; 14: 819–822.
- 57 Madretsma GS, Donze GJ, Van Dijk, et al. Nicotine inhibits the in vitro production of IL-2 and TNFα by human mononuclear cells. Immunopharmacology. 1996; 35: 47–51.
- 58 Van Djik JPM, Madretsma GS, Keuskamp ZJ, et al. Nicotine inhibits cytokine synthesis by mouse colonic mucosa. Eur J Pharmacol. 1995; 278: R11–R12.
- 59 Eliakim R, Karmeli F. Divergent effects of nicotine administration on cytokine levels in small bowel mucosa, colonic mucosa and blood. Isr Med Assoc J. 2000; 5(3): 178–180.
- 60 Bhatti MA, Hodgson HJF. Peripheral blood pro-inflammatory cytokine profile in active inflammatory bowel disease (IBD) differs between smokers and non-smokers. Gut. 1997; 40( suppl 1): A24.
- 61 Sykes AP, Brampton C, Klee S, et al. An investigation into the effect and mechanisms of action of nicotine in inflammatory bowel disease. Inflammation. 2000; 49: 311–319.
- 62 Louvet B, Buissine MP, Desreumaux P, et al. Transdermal nicotine decreases mucosal IL-8 expression but has no effect on mucin getne expression in ulcerative colitis. Inflamm Bowel Dis. 1999; 5: 174–181.
- 63 Thomas GAO, Rhodes J, Ingram JR. Mechanisms of disease: nicotine—a review of its actions in the context of gastrointestinal disease. Nat Clin Pract Gastroenterol Hepatol. 2005; 2: 536–544.
- 64 Roberts CJ, Diggle R. Non-smoking: a feature of ulcerative colitis. Br Med J. 1982; 285: 440.
- 65 Perera DR, Janeway CM. Smoking and ulcerative colitis. Br Med J (Clin Res Ed). 1984; 288: 1533.
- 66 Lashner BA, Hanauer SB, Silverstein MD. Testing nicotine gum for ulcerative colitis patients. Experience with single patient trials. Dig Dis Sci. 1990; 35: 827–832.
- 67 Watson JP, Lewis RA. UC Responsive to smoking and to nicotine chewing gum in a patient with alpha 1 anti-trypsin deficiency. Respir Med. 1995; 89: 635–636.
- 68 Ingram JR, Rhodes J, Evans BK, et al. Preliminary observations of oral nicotine therapy for inflammatory bowel disease: an open-label phase I-II study of tolerance. Inflamm Bow Dis. 2005; 11: 1092–1096.
- 69 Srivastava ED, Russell MAH, Feyerabend C, et al. Sensitivity and tolerance to nicotine in smokers and non-smokers. Psychopharmacol. 1991; 105: 63–68.
- 70 Gulandi M, Tittobello A. Steroid-sparing effect of transdermal nicotine in ulcerative colitis. J Clin Gastroenterol. 1994; 18: 347–350.
- 71 Pullan RD, Rhodes J, Ganesh S, et al. Transdermal nicotine for active ulcerative colitis. N Engl J Med. 1994; 330: 811–815.
- 72 Thomas GAO, Rhodes J, Mani V, et al. Transdermal nicotine as maintenance therapy for ulcerative colitis. N Engl J Med. 1995; 332: 988–992.
- 73 Guslandi M, Titobello A. Pilot trial of nicotine patches as an alternative to corticosteroids in ulcerative colitis. J Gastroenterol. 1996; 31: 627–629.
- 74 Thomas GAO, Rhodes J, Ragunath K, et al. Transdermal nicotine compared with oral prednisolone therapy for active ulcerative colitis. Eur J Gastroenterol Hepatol. 1996; 8: 769–776.
- 75 Sandborn WJ, Tremaine WJ, Offord KP, et al. Transdermal nicotine for mildly to moderately active ulcerative colitis. A randomised, double-blind, placebo-controlled trial. Ann Intern Med. 1997; 126: 364–371.
- 76 Guslandi M, Tittobello A. Outcome of ulcerative colitis after treatment with transdermal nicotine. Eur J Gastroenterol Hepatol. 1998; 10: 513–515.
- 77 Sandborn WJ, Tremaine WJ, Leighton JA. Nicotine tartrate liquid enemas for mildly to moderately active left-sided ulcerative colitis unresponsive to first-line therapy: a pilot study. Aliment Pharmacol Ther. 1997; 11: 663–671.
- 78 Green JT, Thomas GA, Rhodes J, et al. Nicotine enemas for active ulcerative colitis—a pilot study. Aliment Pharmacol Ther. 1997; 11: 859–863.
- 79 Ingram JR, Thomas GA, Rhodes J, et al. A randomised trial of nicotine enemas for active ulcerative colitis. Clin Gastroenterol Hepatol. 2005; 3: 1107–1114.
- 80
N.L. Benowitz,, Eds.
Nicotine safety and toxicity.
New York,
Oxford University Press,
1998.
10.1093/oso/9780195114966.001.0001 Google Scholar
- 81
Gorrod JW,
Jacob P III.
Analytical Determination of Nicotine and Related Compounds and Their Metabolites.
Amsterdam, The Netherlands:
Elsevier;
1999.
10.1016/B978-044450095-3/50004-8 Google Scholar
- 82 Zhang S, Petro TM. The effect of nicotine on murine CD4 T cell responses. Int J Immunopharmacol. 1996; 18: 467–478.
- 83 Geng Y, Savage SM, Razani-Boroujerdi S, et al. Effects of nicotine on the immune response -(ii) chronic nicotine treatment induces T cell anergy. J Immunol. 1996; 156: 2384–2390.
- 84 Hegazi RAF, Rao KN, Mayle A, et al. Carbon monoxide ameliorates chronic murine colitis through a heme oxygenase 1-dependent pathway. J Environ Monit. 2005; 202: 1703–1713.
- 85 Pae HO, Oh GS, Choi BM, et al. Carbon monoxide produced by Heme oxygenase-1 suppresses T cell proliferation via inhibition of IL-2 production. J Immunol. 2004; 172: 4744–4751.
- 86 Otterbein LE, Bach FH, Alam J, et al. Carbon monoxide has anti-inflammatory effects involving the mitogen-activated protein kinase pathway. Nat Med. 2000; 6: 422–428.
- 87 Benoni C, Prytz H. Effects of smoking on the urine excretion of oral 51Cr-EDTA in UC. Gut. 1998; 42: 656–658.
- 88 Suenaert P, Bulteel V, Den Hond E, et al. In vivo influence of nicotine on human basal and NSAID induced gut barrier function. Scand J Gastroenterol. 2003; 38: 399–408.
- 89 Summers AE, Whelan CJ, Parsons ME. Nicotinic acetylcholine receptor subunits and receptor activity in the epithelial cell line HT29. Life Sci. 2003; 72: 2091–2094.
- 90 Morgan D, Parsons ME, Whelan CJ. Investigation of nicotine binding to THP-1 cells: evidence for a non-cholinergic binding site. Biochem Pharmacol. 2001; 61: 733–740.
- 91
Lindstrom J.
Acetylcholine receptors and myasthenia.
Muscle Nerve.
2000;
23:
453–471.
10.1002/(SICI)1097-4598(200004)23:4<453::AID-MUS3>3.0.CO;2-O CAS PubMed Web of Science® Google Scholar
- 92 Lustig LR, Peng H, Hiel H, et al. Molecular cloning and mapping of the human nicotinic acetylcholine receptor alpha 10 (CHRNA 10). Genomics. 2001; 73: 272–283.
- 93 Unwin N. Nicotinic acetylcholine receptor at 9A resolution. J Mol Biol. 1993; 229: 1101–1124.
- 94 Unwin N. Acetylcholine receptor channel imaged in the open state. Nature. 1995; 373: 37–43.
- 95 Wang F, Gerzanich V, Wills GB, et al. Assembly of human neuronal nicotinic receptor alpha 5 subunits with alpha 3, beta 2 and beta 4 subunits. J Biol Chem. 1996; 271: 17656–17665.
- 96 Richardson CE, Morgan JM, Jasani N, et al. Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is associated with absence of the alpha 3 nicotinic acetylcholine receptor subunit. Gastroenterology. 2001; 121: 350–357.
- 97 Grando SA, Horton RM, Pereira EF, et al. Albuquerque EX, Conti-Fine BM. A nicotinic acetylcholine receptor. Invest regulating cell adhesion and motility is expressed in human keratinocytes. J Dermatol. 1995; 105: 774–781.
- 98 Zia S, Nadoye A, Nguyen VT, et al. Nicotine enhances expression of the alpha 3 alpha 4, alpha 5 and alpha 7 nicotinic receptors modulating calcium metabolism and regulating adhesion and motility of respiratory epithelial cells. Res Commun Mol Pathol Pharmacol. 1997; 97: 243–262.
- 99 Richardson CE, Morgan JM, Jasani B, et al. Effect of smoking and transdermal nicotine on colonic nicotinic acetylcholine receptors in ulcerative colitis. Q J Med. 2003; 96: 57–65.
- 100 Kwashima K, Fujii Y. Expression of non-neuronal acetylcholine in lymphocytes and its contribution to the regulation of immune function. Front Biosci. 2004; 9: 2063–2085.
- 101 Morgan D, Parsons ME, Whelan CJ. Investigation of nicotine binding to THP-1 cells: evidence for a non-cholinergic binding site. Biochem Pharmacol. 2001; 61: 733–740.
- 102 Fukada A, Jideyuki S, Inui KI. Transport mechanisms of nicotine across the human intestinal epithelial cell line caco-2. J Pharmacol Exp Ther. 2002; 302: 532–538.
- 103 Hannigan B. Biomedical Sciences Explained: Immunology. London: Hodder Arnold Press; 2000.
- 104 Mawdsley JE, Rampton DS. Psychological stress in IBD: new insights into pathogenic and therapeutic implications. Gut. 2005; 54: 1481–1491.
- 105 Salas R, Pieri F, Fung B, et al. Altered anxiety-related responses in mutant mice lacking the β4 subunit of the nicotinc receptor. J Neurosci. 2002; 23: 6255–6263.
- 106 Piciotto MR, Brunzell DH, Caldarone BJ. Effect of nicotine and nicotinic receptors on anxiety and depression. Neuroreport. 2002; 13: 1097–1106.
- 107 Wang H, Liao H, Ochani M, et al. Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis. Nat Med. 2004; 10: 1216–1221.
- 108 Ma TY, Iwanoto GK, Hoa NT, et al. TNF-alpha-induced increase in intestinal epithelial tight junction permeability requires NF-kappa B activation. Am J Physiol Gastrointest Liver Physiol. 2004; 286: G367–G376.
- 109 Hollenbach, E, Neumann M, Vieth M, et al. Inhibition of p38 MAP kinase and RICK/NF-κB-signaling suppresses inflammatory bowel disease. FASEB J. 2004; 18: 1550–1552.
- 110 Waetzig GH, Seegert D, Rosenstiel P, et al. P38 mitogen activated protein kinase is activated and linked to TNF-alpha signalling in inflammatory bowel disease. J Immunol. 2002; 168: 5342–5351.l