Hyperbaric oxygen therapy attenuates pancreatic microcirculatory derangement and lung edema in an acute experimental pancreatitis model in rats

被引:31
作者
Chen, HM
Shyr, MH
Ueng, SWN
Chen, MF
机构
[1] Chang Gung Mem Hosp, Dept Surg, Taipei 10591, Taiwan
[2] Chang Gung Mem Hosp, Dept Anaesthesia, Taipei 10591, Taiwan
关键词
acute pancreatitis; hyperbaric oxygen; in vivo microscopy; microcirculation; multiple organ dysfunction;
D O I
10.1097/00006676-199807000-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
This study was designed to investigate hyperbaric oxygen (HBO) therapy as a treatment for managing animals with induced acute pancreatitis. Forty-five anesthetized male Sprague-Dawley rats were studied. A severe acute pancreatitis model was established by combining an intravenous infusion of cerulein (15 mu g/kg/h) and an intraductal injection of 0.1 ml of glycodeoxycholic acid (5 mM). Pathology, serum amylase level, pancreatic malondiadehyde levels and water content of the lungs and the pancreas were used to evaluate the severity of disease. Moreover, an in vivo microscopic technique was used to investigate microcirculatory derangement in the pancreas, i.e., flow velocity and leukocytes sticking in postcapillary venules. HBO was delivered in three regimens, i.e., 100% oxygen at 2.5 absolute atmospheric pressure (AAP), 40% oxy gen at 2.5 AAP, and 100% oxygen at 1 AAP, 6 h after the initiation of induction of acute pancreatitis. All animals survived until the end of the experiments. HBO significantly improved the pathologic conditions and pancreatic malondiadehyde levels. Concomitantly, it also significantly lessened the severity of lung edema and improved the microcirculatory environment in the pancreas. Our results support the findings that HBO therapy has a beneficial effect on pancreatic microcirculation and lung edema during acute pancreatitis in rats.
引用
收藏
页码:44 / 49
页数:6
相关论文
共 30 条
[21]  
SEALY R, 1989, CANCER, V64, P646, DOI 10.1002/1097-0142(19890801)64:3<646::AID-CNCR2820640314>3.0.CO
[22]  
2-J
[23]  
SHIBUYA K, 1993, MICROCIRC ANN, V9, P105
[24]   MEDICAL PROGRESS - ACUTE-PANCREATITIS [J].
STEINBERG, W ;
TENNER, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (17) :1198-1210
[25]   SPECIFIC INTERACTION OF PANCREATIC ELASTASE AND LEUKOCYTES TO PRODUCE OXYGEN RADICALS AND ITS IMPLICATION IN PANCREATITIS [J].
TSUJI, N ;
WATANABE, N ;
OKAMOTO, T ;
NIITSU, Y .
GUT, 1994, 35 (11) :1659-1664
[26]   INFLAMMATORY RESPONSE IN THE EARLY PREDICTION OF SEVERITY IN HUMAN ACUTE-PANCREATITIS [J].
VIEDMA, JA ;
PEREZMATEO, M ;
AGULLO, J ;
DOMINGUEZ, JE ;
CARBALLO, F .
GUT, 1994, 35 (06) :822-827
[27]  
WARD PA, 1991, J LAB CLIN MED, V118, P421
[28]   VASOACTIVE MEDIATORS AND THE PROGRESSION FROM EDEMATOUS TO NECROTIZING EXPERIMENTAL ACUTE-PANCREATITIS [J].
WEIDENBACH, H ;
LERCH, MM ;
GRESS, TM ;
PFAFF, D ;
TURI, S ;
ADLER, G .
GUT, 1995, 37 (03) :434-440
[29]   MORPHOLOGIC ANALYSIS OF THE MICROCIRCULATION DURING REPERFUSION OF ISCHEMIC SKELETAL-MUSCLE AND THE EFFECT OF HYPERBARIC-OXYGEN [J].
ZAMBONI, WA ;
ROTH, AC ;
RUSSELL, RC ;
GRAHAM, B ;
SUCHY, H ;
KUCAN, JO .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1993, 91 (06) :1110-1123
[30]   EFFECTS OF SC-41930 ON LEUKOCYTE ADHERENCE AND EMIGRATION IN RAT MESENTERIC VENULES [J].
ZIMMERMAN, BJ ;
GAGINELLA, TS ;
GRANGER, DN .
AGENTS AND ACTIONS, 1992, 37 (1-2) :80-84