L-arginine-NO-cGMP signalling pathway in pancreatitis

被引:17
作者
Buchwalow, Igor [1 ]
Schnekenburger, Juergen [2 ]
Tiemann, Katharina [1 ]
Samoilova, Vera [1 ]
Bankfalvi, Agnes [3 ]
Poremba, Christopher [4 ]
Schleicher, Christine [5 ]
Neumann, Joachim [6 ]
Boecker, Werner [1 ]
机构
[1] Inst Hematopathol, D-22547 Hamburg, Germany
[2] Univ Munster, Ctr Bioproc Technol, D-48149 Munster, Germany
[3] Univ Hosp Essen, Inst Pathol & Neuropathol, D-45122 Essen, Germany
[4] CHCMD Trier, D-54296 Trier, Germany
[5] Univ Munster, Dept Surg, D-48149 Munster, Germany
[6] Univ Halle Wittenberg, Fac Med, Inst Pharmacol & Toxicol, D-06112 Halle, Saale, Germany
关键词
NITRIC-OXIDE SYNTHASE; CERULEIN-INDUCED PANCREATITIS; SMOOTH-MUSCLE; BETA-CELLS; EXPRESSION; SECRETION; ARGINASE; SOMATOSTATIN; MODEL;
D O I
10.1038/srep01899
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The role of nitric oxide (NO) in the human pancreas and in pancreatitis still remains controversial. Furthermore, conflicting conclusions have been reached by different laboratories about the localization of the NO-generating enzyme (NO synthase, NOS) in the pancreas. Here, we investigated the co-expression of NOS with enzymes involved in regulation of NO signalling in the normal human pancreas and in pancreatitis. We found that the whole NO signalling machinery was up-regulated in pancreatitis, especially within the exocrine compartment. Furthermore, the exocrine parenchymal cells revealed higher levels of oxidative stress markers, nitrotyrosine and 8-hydroxyguanosine, in pancreatitis, which reflects the exceptional susceptibility of the exocrine parenchyma to oxidative stress. This study provides a direct link between oxidative stress and the enzymatic control of the NO bioavailability at the cellular level and endows with further insight into fundamental mechanisms underlying pancreatic disorders associated with disruptions in the L-arginine-NO-cGMP signalling enzyme cascade.
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页数:5
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