Effects of Erdosteine on Experimental Acute Pancreatitis Model

被引:0
作者
Karapolat, Banu [1 ]
Karapolat, Sami [2 ]
Gurleyik, Emin [3 ]
Yasar, Mehmet [3 ]
机构
[1] Kanuni Training Hosp, Dept Gen Surg, Trabzon, Turkey
[2] Karadeniz Tech Univ, Dept Thorac Surg, Med Sch, Trabzon, Turkey
[3] Duzce Univ, Dept Gen Surg, Med Sch, Duzce, Turkey
来源
JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN | 2017年 / 27卷 / 10期
关键词
Cerulein; Inflammation; Acute pancreatitis; Erdosteine; Treatment;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To create acute pancreatitis condition experimentally in rats using cerulein, and to reveal histopathological effects in pancreatic tissue with erdosteine. Study Design: An experimental study. Place and Duration of Study: Department of General Surgery, Duzce University, Turkey, from June to October 2014. Methodology: Thirty male Wistar albino rats were divided into three groups. No procedures were applied to Group 1. The rats in Group 2 and Group 3 were injected cerulein, to establish an experimental pancreatitis model and the blood amylase and lipase values were examined. The rats in Group 3 were given 10 mg/kg erdosteine. This treatment was continued for another 2 days and the rats were sacrificed. The pancreatic tissues were examined histopathologically for edema, inflammation, acinar necrosis, fat necrosis, and vacuolization. Results: The lipase and amylase values and the histopathological examination of pancreatic tissues evidenced that the experimental acute pancreatitis model was established and edema, inflammation, acinar necrosis, fat necrosis, and vacuolization were observed in the pancreatic tissues. The statistical results suggest that erdosteine can decrease the edema, inflammation, acinar necrosis, fat necrosis and vacuolization scores in the tissues. Conclusion: The severity of acute pancreatitis, induced by cerulein in rats, is reduced with the use of erdosteine.
引用
收藏
页码:606 / 610
页数:5
相关论文
共 18 条
[1]   EFFECTS OF SOMATOSTATIN AND A LONG-ACTING SOMATOSTATIN ANALOG ON THE PREVENTION AND TREATMENT OF EXPERIMENTALLY INDUCED ACUTE-PANCREATITIS IN THE RAT [J].
BAXTER, JN ;
JENKINS, SA ;
DAY, DW ;
ROBERTS, NB ;
COWELL, DC ;
MACKIE, CR ;
SHIELDS, R .
BRITISH JOURNAL OF SURGERY, 1985, 72 (05) :382-385
[2]   Oxidative stress and NO generation in the rat pancreatitis induced by pancreatic duct ligation [J].
Buchwalow, Igor ;
Schnekenburger, Juergen ;
Atiakshin, Dmitri ;
Samoilova, Vera ;
Wolf, Eduard ;
Boecker, Werner ;
Tiemann, Katharina .
ACTA HISTOCHEMICA, 2017, 119 (03) :252-256
[3]   From Pathogenesis, Clinical Manifestation, and Diagnosis to Treatment: An Overview on Autoimmune Pancreatitis [J].
Cai, Ou ;
Tan, Shiyun .
GASTROENTEROLOGY RESEARCH AND PRACTICE, 2017, 2017
[4]   Effects of Clotrimazol on the Acute Necrotizing Pancreatitis in Rats [J].
Cekic, Arif Burak ;
Alhan, Etem ;
Usta, Arif ;
Turkyilmaz, Serdar ;
Kural, Birgul Vanizor ;
Ercin, Cengiz .
INFLAMMATION, 2013, 36 (06) :1576-1583
[5]   Erdosteine: Antitussive and anti-inflammatory effects [J].
Dal Negro, Roberto W. .
LUNG, 2008, 186 (Suppl 1) :S70-S73
[6]   Erdosteine [J].
Dechant, KL ;
Noble, S .
DRUGS, 1996, 52 (06) :875-881
[7]   The Effects of Erdosteine and N-Acetylcysteine on Apoptotic and Antiapoptotic Markers in Pulmonary Epithelial Cells in Sepsis [J].
Demiralay, Rezan ;
Gursan, Nesrin ;
Erdem, Havva .
EURASIAN JOURNAL OF MEDICINE, 2013, 45 (03) :167-175
[8]   FREE-RADICAL INHIBITION AND SERIAL CHEMILUMINESCENCE IN EVOLVING EXPERIMENTAL PANCREATITIS [J].
GOUGH, DB ;
BOYLE, B ;
JOYCE, WP ;
DELANEY, CP ;
MCGEENEY, KF ;
GOREY, TF ;
FITZPATRICK, JM .
BRITISH JOURNAL OF SURGERY, 1990, 77 (11) :1256-1259
[9]   NEUTROPHIL-DEPENDENT, OXYGEN-RADICAL MEDIATED LUNG INJURY ASSOCIATED WITH ACUTE-PANCREATITIS [J].
GUICE, KS ;
OLDHAM, KT ;
CATY, MG ;
JOHNSON, KJ ;
WARD, PA .
ANNALS OF SURGERY, 1989, 210 (06) :740-747
[10]   ACUTE INTERSTITIAL PANCREATITIS IN RAT INDUCED BY EXCESSIVE DOSES OF A PANCREATIC SECRETAGOGUE [J].
LAMPEL, M ;
KERN, HF .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1977, 373 (02) :97-117