Z Gastroenterol 2015; 53(03): 199-204
DOI: 10.1055/s-0034-1385705
Originalarbeit
© Georg Thieme Verlag KG Stuttgart · New York

The imbalance between matrix metalloproteinase 9 and tissue inhibitor of metalloproteinase 1 in acute pancreatitis

Das Ungleichgewicht zwischen Matrix-Metalloproteinase 9 und „tissue inhibitors of matrix metalloproteinases“ bei akuter Pankreatitis
U. Wereszczynska-Siemiatkowska
1   Department of Gastroenterology and Internal Medicine, Medical University of Bialystok, Poland
,
A. Siemiatkowski
2   Department of Anaesthesiology and Intensive Care, Medical University of Bialystok, Poland
,
A. Swidnicka-Siergiejko
1   Department of Gastroenterology and Internal Medicine, Medical University of Bialystok, Poland
,
B. Mroczko
3   Department of Neurodegeneration Diagnostics, Medical University of Bialystok, Poland
,
A. Dabrowski
1   Department of Gastroenterology and Internal Medicine, Medical University of Bialystok, Poland
› Author Affiliations
Further Information

Publication History

13 June 2014

10 November 2014

Publication Date:
16 March 2015 (online)

Abstract

Background: The balanced activity of matrix metalloproteinases and their tissue inhibitors is an important, albeit still not completely understood, determinant of extracellular matrix homeostasis, a factor involved in the pathogenesis of acute pancreatitis (AP).

Aims: The aim of this study was to compare serum concentrations of matrix metalloproteinase 9 (MMP-9) and its tissue inhibitor (TIMP-1) in patients with AP of various severity and to investigate their relationship with prognostic indicators of AP severity, e. g., polymorphonuclear leukocyte elastase (PMN-E).

Patients and Methods: The study included 37 patients with mild (n = 18) or severe AP (n = 19) and 15 healthy controls. Serum concentrations of MMP-9 and TIMP-1 were determined on admission (day 1) and on days 2, 3, 5 and 10.

Results: Throughout the study period, the serum MMP-9 concentration in patients with severe AP was significantly higher than those in individuals with mild AP and in healthy controls. In turn, the serum MMP-9 concentrations in persons with mild AP did not differ significantly from those of the controls. The serum TIMP-1 concentrations in both groups were significantly higher than in the controls. Beginning from the 2nd day of hospital stay, the serum TIMP-1 concentration in patients with severe AP was significantly higher than in individuals with mild AP. There were significant correlations between: MMP-9 and PMN-E, TIMP-1 and PMN-E, and MMP-9 and TIMP-1.

Conclusion: A disturbed balance between MMP-9 and TIMP-1 observed during the early stages of severe AP suggests that endogenous TIMP-1 is unable to prevent excessive activation and release of MMP-9. MMP-9 may represent a new marker of AP severity.

Zusammenfassung

Hintergrund: Eine ausgewogene Aktivität von Matrix Metalloproteinasen (MMPs) und ihrer Inhibitoren (tissue inhibitors of matrix metalloproteinases, TIMPs) ist ein wichtiger determinierender Faktor der extrazellulären Matrixhomöostase, der auch an einem Krankheitsverlauf von akuter Pankreatitis (AP) beteiligt ist.

Ziele: Vergleich der Serumkonzentration von Matrix-Metalloproteinase 9 (MMP-9) und TIMP-1 bei Patienten mit AP unterschiedlichen Schweregrads, die Untersuchung ihres Verhältnisses mit den Belastungsanzeigen, z. B. Granulozyt Elastase (polymorphonuclear leukocyte elastase, PMN-E).

Material und Methodik: Die Untersuchung umfasst 37 Patienten mit leichter AP (N = 18), mit schwerer AP (N = 19) und 15 gesunde Kontrollpersonen. Die Serumkonzentrationen von MMP-9 und TIMP-1 wurden am Anfang, am 2., 3., 5. und 10. Tag der Untersuchung festgestellt.

Ergebnisse: Während der ganzen Untersuchungszeit war die Serumkonzentration von MMP-9 bei Patienten mit schwerer AP erheblich höher als bei Patienten mit leichter AP und bei den gesunden Kontrollpersonen. Im Rahmen der gesamten Untersuchungszeit war der Unterschied zwischen der Serumkonzentration von MMPs bei Patienten mit leichter AP und den gesunden Kontrollpersonen nicht signifikant. Die Serumkonzentrationen von TIMP-1 bei beiden Gruppen von Patienten mit AP waren erheblich höher als bei den gesunden Kontrollpersonen. Ab dem 2. Tag des Krankenhausaufenthalts war die Serumkonzentration von TIMP-1 bei den Patienten mit schwerer AP erheblich höher als bei den Patienten mit leichter AP. Es wurden statistisch wesentliche Korrelationen zwischen MMP-9 und PMN-E; TIMP-1 und PMN-E; und TIMP-1 und MMP-9 festgestellt.

Schlussfolgerung: Das gestörte Gleichgewicht zwischen MMP-9 und TIMP-1, das während des Anfangsstadiums von schwerer AP observiert wurde, suggeriert, dass das endogene TIMP-1 nicht imstande ist, übermäßige Aktivierung und Freistellung von MMP-9 zu verhindern. MMP-9 kann einen neuen Schweregradmarker der AP begründen.

 
  • References

  • 1 Swaroop VS, Chari ST, Clain JE. Severe acute pancreatitis. JAMA 2004; 291: 2865-2868
  • 2 Lankisch PG, Pflichthofer D, Lehnick D. Acute pancreatitis: which patient is most at risk?. Pancreas 1999; 19: 321-324
  • 3 Wereszczynska-Siemiatkowska U, Dabrowski A, Siemiatkowski A et al. Serum profiles of E-selectin, interleukin-10, and interleukin-6 and oxidative stress parameters in patients with acute pancreatitis and nonpancreatic acute abdominal pain. Pancreas 2003; 26: 144-152
  • 4 Wereszczynska-Siemiatkowska U, Mroczko B, Siemiatkowski A. Serum profiles of interleukin-18 in different severity forms of human acute pancreatitis. Scand J Gastroenterol 2002; 37: 1097-1102
  • 5 Wereszczynska-Siemiatkowska U, Mroczko B, Siemiatkowski A et al. The importance of interleukin 18, glutathione peroxidase, and selenium concentration changes in acute pancreatitis. Dig Dis Sci 2004; 49: 642-650
  • 6 Bhatia M, Brady M, Shokuhi S et al. Inflammatory mediators in acute pancreatitis. J Pathol 2000; 190: 117-125
  • 7 Dabrowski A, Tribillo I, Dabrowska MI et al. Activation of mitogen-activated protein kinases in different models of pancreatic acinar cell damage. Z Gastroenterlog 2008; 38: 469-481
  • 8 Wereszczynska S, Dabrowski A, Jedynak M et al. Oxidative stress as an early prognostic factor in acute pancreatitis (AP): its correlation with serum phospholipase A2 (PLA2) and plasma polymorphonuclear elastase (PMN-E) in different-severity forms of human AP. Pancreas 1998; 17: 163-168
  • 9 Dabrowski A, Gabryelewicz A. Oxidative stress. An early phenomenon characteristic of acute experimental pancreatitis. Int J Pancreatol 1992; 12: 193-199
  • 10 Wereszczynska-Siemiatkowska U, Dlugosz JW, Siemiatkowski A et al. Lysosomal activity of pulmonary alveolar macrophages in acute experimental pancreatitis in rats with reference to positive PAF-antagonist (BN 52021) effect. Exp Toxicol Pathol 2000; 52: 119-125
  • 11 Osada J, Wereszczyńska-Siemiatkowska U, Daborwski A et al. Platelet activation in acute pancreatitis. Pancreas 2012; 41: 1219-1324
  • 12 Cohnheim J. Lectures of general pathology. In a Handbook for practitioners and students. London: The New Sydenham Society 1889
  • 13 Goetzl EJ, Banda MJ, Leppert D. Matrix metalloproteinases in immunity. J Immunol 1996; 156: 1-4
  • 14 Keck T, Balcom JH, Fernandez-del Castillo C et al. Matrix metalloproteinase-9 promotes neutrophil migration and alveolar capillary leakage in pancreatitis-associated lung injury in the rat. Gastroenterology 2002; 122: 188-201
  • 15 Yong VW, Krekoski CA, Forsyth PA et al. Matrix metalloproteinases and diseases of the CNS. Trends Neurosci 1998; 21: 75-80
  • 16 Nagase H. Activation mechanisms of matrix metalloproteinases. Biol Chem 1997; 378: 151-160
  • 17 Gomez DE, Alonso DF, Yoshiji H et al. Tissue inhibitors of metalloproteinases: structure, regulation and biological functions. Eur J Cell Biol 1997; 74: 111-122
  • 18 Muhs BE, Patel S, Yee H et al. Inhibition of matrix metalloproteinases reduces local and distant organ injury following experimental acute pancreatitis. J Surg Res 2003; 109: 110-117
  • 19 Kihara Y, Tashiro M, Nakamura H et al. Role of TGF-beta1, extracellular matrix, and matrix metalloproteinase in the healing process of the pancreas after induction of acute necrotizing pancreatitis using arginine in rats. Pancreas 2001; 23: 288-295
  • 20 Nakae H, Endo S, Inoue Y et al. Matrix metalloproteinase-1 and cytokines in patients with acute pancreatitis. Pancreas 2003; 26: 134-138
  • 21 Abraham M, Shapiro S, Lahat N et al. The role of IL-18 and IL-12 in the modulation of matrix metalloproteinases and their tissue inhibitors in monocytic cells. Int Immunol 2002; 14: 1449-1457
  • 22 Gerdes N, Sukhova GK, Libby P et al. Expression of interleukin (IL)-18 and functional IL-18 receptor on human vascular endothelial cells, smooth muscle cells, and macrophages: implications for atherogenesis. J Exp Med 2002; 195: 245-257
  • 23 Zhang Y, McCluskey K, Fujii K et al. Differential regulation of monocyte matrix metalloproteinase and TIMP-1 production by TNF-alpha, granulocyte-macrophage CSF, and IL-1 beta through prostaglandin-dependent and -independent mechanisms. J Immunol 1998; 161: 3071-3076
  • 24 Ranson JH, Rifkind KM, Roses DF et al. Prognostic signs and the role of operative management in acute pancreatitis. Surg Gynecol Obstet 1974; 139: 69-81
  • 25 Balthazar EJ. CT diagnosis and staging of acute pancreatitis. Radiol Clin North Am 1989; 27: 19-37
  • 26 Bradley EL. A clinically based classification system for acute pancreatitis. Summary of the International Symposium on Acute Pancreatitis, Atlanta, Ga, September 11 through 13, 1992. Arch Surg 1993; 128: 586-590
  • 27 Wilson C, Heath DI, Imrie CW. Prediction of outcome in acute pancreatitis: a comparative study of APACHE II, clinical assessment and multiple factor scoring systems. Br J Surg 1990; 77: 1260-1264
  • 28 Robert JH, Frossard JL, Mermillod B et al. Early prediction of acute pancreatitis: prospective study comparing computed tomography scans, Ranson, Glascow, Acute Physiology and Chronic Health Evaluation II scores, and various serum markers. World J Surg 2002; 26: 612-619
  • 29 Marshall JC, Cook DJ, Christou NV et al. Multiple organ dysfunction score: a reliable descriptor of a complex clinical outcome. Crit Care Med 1995; 23: 1638-1652
  • 30 Vincent JL, de Mendonca A, Cantraine F et al. Use of the SOFA score to assess the incidence of organ dysfunction/failure in intensive care units: results of a multicenter, prospective study. Working group on "sepsis-related problems" of the European Society of Intensive Care Medicine. Crit Care Med 1998; 26: 1793-1800
  • 31 Muhs BE, Patel S, Yee H et al. Increased matrix metalloproteinase expression and activation following experimental acute pancreatitis. J Surg Res 2001; 101: 21-28
  • 32 Werner J, Muller C, Hartwig W et al. Early prediction of severity and pulmonary complications in acute pancreatitis by matrix metalloproteinase-9 (MMP-9). Pancreatology 2003; 3: 45
  • 33 Guo J, Xue P, Yang XN et al. Serum matrix metalloproteinase-9 is an early marker of pancreatic necrosis in patients with severe acute pancreatitis. Hepatogastroenterology 2012; 59: 1594-1598
  • 34 Quiding-Jarbrink M, Smith DA, Bancroft GJ. Production of matrix metalloproteinases in response to mycobacterial infection. Infect Immun 2001; 69: 5661-5670
  • 35 Mikami Y, Dobschutz EV, Sommer O et al. Matrix metalloproteinase-9 derived from polymorphonuclear neutrophils increases gut barrier dysfunction and bacterial translocation in rat severe acute pancreatitis. Surgery 2009; 145: 147-156
  • 36 Sochor M, Richter S, Schmidt A et al. Inhibition of matrix metalloproteinase-9 with doxycycline reduces pancreatitis-associated lung injury. Digestion 2009; 80: 65-73
  • 37 Awla D, Abdulla A, Syk I et al. Neutrophil-derived matrix metalloproteinase-9 is a potent activator of trypsinogen in acinar cells in acute pancreatitis. J Leukoc Biol 2012; 91: 711-719