Organ microcirculatory disturbances in experimental acute pancreatitis. A role of nitric oxide

被引:22
|
作者
Dobosz, M
Hac, S
Mionskowska, L
Dymecki, D
Dobrowolski, S
Wajda, Z
机构
[1] St Vincent Paulo Hosp, Dept Gen & Gastroenterol Surg, Gdynia, Poland
[2] Med Univ Gdansk, Dept Gen Endocrine & Transplant Surg, Gdansk, Poland
关键词
acute pancreatitis; microcirculation; nitric oxide;
D O I
10.33549/physiolres.930637
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Microcirculatory disturbances are important early pathophysiological events in various organs during acute pancreatitis (AP). The aim of the study was to investigate an influence of L-arginine (nitric oxide substrate) and N-G-nitro-L-arginine (L-NNA, nitric oxide synthase inhibitor) on organ microcirculation in experimental acute pancreatitis induced by four consecutive intraperitoneal cerulein injections (15 mu g/kg/h). The microcirculation of pancreas, liver, kidney, stomach, colon and skeletal muscle was measured by laser Doppler flowmeter. Serum interleukin 6 and hematocrit levels were analyzed. AP resulted in a significant drop of microperfusion in all examined organ. L-arginine administration (2x100 mg/kg) improved the microcirculation in the pancreas, liver, kidney, colon and skeletal muscle, and lowered hematocrit levels. L-NNA treatment (2x25 mg/kg) caused aggravation of edematous AP to the necrotizing situation, and increased IL-6 and hematocrit levels. A further reduction of blood perfusion was noted in the stomach only. It is concluded that L-arginine administration has a positive influence on organ microcirculatory disturbances accompanying experimental cerulein-induced AP. NO inhibition aggravates the course of pancreatitis.
引用
收藏
页码:363 / 368
页数:6
相关论文
共 50 条
  • [31] Hydrogen sulfide and nitric oxide synthases in experimental acute necrotizing pancreatitis
    Chooklin, S.
    Chuklin, S.
    Pidhirnyy, Ya.
    Usach, O.
    EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2016, 46 : 49 - 49
  • [32] Persistent SIRS precedes the development of early organ dysfunction in acute pancreatitis.
    Buter, A
    Robertson, SA
    Evans, S
    Carter, RR
    Imrie, CW
    McKay, CJ
    GASTROENTEROLOGY, 2000, 118 (04) : A1143 - A1143
  • [33] The role of intestinal juice in experimental reproduction of hemorrhagic pancreatitis.
    Binet, L
    Brocq, P
    COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES, 1920, 83 : 340 - 341
  • [34] Role of early ERCP and sphincterotomy in the management of acute pancreatitis.
    Sheikh, AM
    Warshafsky, S
    Wolf, DC
    Lebovics, E
    GASTROINTESTINAL ENDOSCOPY, 2000, 51 (04) : AB79 - AB79
  • [35] The role of nitric oxide in caerulein-induced acute pancreatitis in mice
    Adhikari, S.
    Ang, A. D.
    Moore, P. K.
    Bhatia, M.
    PANCREAS, 2006, 33 (04) : 442 - 442
  • [36] Changes in time of constitutive and inducible nitric oxide synthase activities in L-arginine-induced acute pancreatitis.
    Czako, L
    Takacs, T
    Morschl, E
    Laszlo, F
    Hegyi, P
    Rakonczay, Z
    Lonovics, J
    GASTROENTEROLOGY, 2000, 118 (04) : A425 - A425
  • [37] Expression of pancreatic enzymes in the initial phase of experimental acute pancreatitis.
    Uhl, W
    Haggblom, JU
    Friess, H
    Riesle, E
    Nevalainen, TJ
    Buchler, MW
    GASTROENTEROLOGY, 1996, 110 (04) : A439 - A439
  • [39] A crucial role of nitric oxide in acute lung injury secondary to the acute necrotizing pancreatitis
    Cheng, Shi
    Yan, Wen-Mao
    Yang, Bin
    Shi, Jing-dong
    Song, Mao-min
    Zhao, Yuqian
    HUMAN & EXPERIMENTAL TOXICOLOGY, 2010, 29 (04) : 329 - 337
  • [40] Dietary antioxidant treatment and nitric oxide inhibition in a rat model of chronic pancreatitis.
    Fredstrom, S
    Gallaher, DD
    FASEB JOURNAL, 2001, 15 (05): : A1089 - A1089