Significance of apoptotic cell death in systemic complications with severe acute pancreatitis

被引:136
作者
Takeyama, Y [1 ]
机构
[1] Kinki Univ, Sch Med, Dept Surg, Osakasayama 5898511, Japan
关键词
severe acute pancreatitis; apoptosis; multiple organ failure; immunosuppression; bacterial translocation;
D O I
10.1007/s00535-004-1505-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In severe acute pancreatitis, multiple organ failure in the early stage after onset, and sepsis in the late stage, due to infection of pancreatic or peripancreatic devitalized tissue, contribute to its high mortality. In analogy with sepsis, evidence has accumulated of the significance of apoptotic cell death in the systemic manifestations associated with acute pancreatitis. Since we identified apoptosis-inducing activity in pancreatitis-associated ascitic fluid in 1995, a number of investigators, including our group, have reported, through animal experiments, that apoptosis occurred in the parenchymal cells constituting organs, such as alveolar epithelial cells in the lung, renal tubular cells in the kidney, and hepatocytes in the liver, and this apoptosis was involved in organ dysfunction with severe acute pancreatitis. Moreover, through clinical and experimental investigations, apoptosis has been revealed to be involved in the mechanism of infectious complications in acute pancreatitis. Namely, apoptosis in lymphatic tissues and peripherally circulating lymphocytes is involved in the impairment of cellular immunity, and apoptosis in gut epithelial cells is implicated in bacterial translocation. These results suggest that apoptotic cell death may play a considerable role in affecting mortality and morbidity in severe acute pancreatitis. Control of apoptosis could be a potent strategy for improvement of the clinical outcome in severe acute pancreatitis.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 67 条
[1]   INTERLEUKIN-1 BETA-INDUCED NITRIC-OXIDE PRODUCTION ACTIVATES APOPTOSIS IN PANCREATIC RINM5F CELLS [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BRUNE, B ;
NICOTERA, P .
EXPERIMENTAL CELL RESEARCH, 1994, 213 (01) :172-177
[2]  
ANTAL L, 1978, ACTA MED HUNG, V35, P81
[3]   Initial evidence of endothelial cell apoptosis as a mechanism of systemic capillary leak syndrome [J].
Assaly, R ;
Olson, D ;
Hammersley, J ;
Fan, PS ;
Liu, J ;
Shapiro, JI ;
Kahaleh, MB .
CHEST, 2001, 120 (04) :1301-1308
[4]   Use of some pre-, pro- and synbiotics in critically ill patients [J].
Bengmark, S .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2003, 17 (05) :833-848
[5]   Apoptosis versus necrosis in acute pancreatitis [J].
Bhatia, M .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2004, 286 (02) :G189-G196
[6]   Apoptosis of pancreatic acinar cells in acute pancreatitis: is it good or bad? [J].
Bhatia, M .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :402-409
[7]  
Bohlinger I, 1996, AM J PATHOL, V149, P1381
[8]   CONTROLLED DEATH (APOPTOSIS) OF NORMAL AND PUTATIVE PRENEOPLASTIC CELLS IN RAT-LIVER FOLLOWING WITHDRAWAL OF TUMOR PROMOTERS [J].
BURSCH, W ;
LAUER, B ;
TIMMERMANNTROSIENER, I ;
BARTHEL, G ;
SCHUPPLER, J ;
SCHULTEHERMANN, R .
CARCINOGENESIS, 1984, 5 (04) :453-458
[9]   Diminished lung injury with vascular adhesion molecule-1 blockade in choline-deficient ethionine diet-induced pancreatitis [J].
Callicutt, CS ;
Sabek, O ;
Fukatsu, K ;
Lundberg, AH ;
Gaber, L ;
Wilcox, H ;
Kotb, M ;
Gaber, AO .
SURGERY, 2003, 133 (02) :186-196
[10]   C-REACTIVE PROTEIN AND LACTATE-DEHYDROGENASE ISOENZYMES IN THE ASSESSMENT OF THE PROGNOSIS OF ACUTE-PANCREATITIS [J].
CHEN, CC ;
WANG, SS ;
CHAO, Y ;
LU, CW ;
LEE, SD ;
TSAL, YT ;
LO, KJ .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1992, 7 (04) :363-366