Literature DB >> 9888659

The effect of sennosides on bacterial translocation and survival in a model of acute hemorrhagic pancreatitis.

X Chen1, J F Valente, J W Alexander.   

Abstract

Bacterial translocation leading to subsequent infectious complications is a significant determinant of outcome in acute hemorrhagic pancreatitis (AHP). The colonic ileus and impaired intestinal barrier function that often accompany AHP may predispose to translocation. Sennoside is a naturally occurring cathartic and choleretic agent that stimulates intestinal mucous secretion and has potent promotility effects. The impact of sennoside-induced intestinal motility and secretory function on bacterial translocation and survival was studied in a rat model of AHP. Severe acute pancreatitis was induced in rats by the intraductal infusion of 2% sodium deoxycholate (DCA, 0.4 ml/kg). A group of sham-operated rats (group A) received intraductal saline, whereas experimental animals were subsequently administered distilled water (group B) or sennoside solution (group C) by gavage every 8 h. After 48 h, intestinal transit of fluorescein isothiocyanate-labeled dextran, serum endotoxin, and amylase levels, and bacterial translocation to mesenteric lymph nodes (MLNs) and pancreatic tissue were determined. The pancreas and intestine were sampled for histologic study. All group A animals survived and did not develop pancreatitis or endotoxemia, whereas groups B and C all demonstrated severe hemorrhagic pancreatitis with evidence of necrosis. Mortality at 48 h was 55% in group B versus 12.5% in group C. Inhibition of intestinal motility was noted in 40% versus 20%, and endotoxin levels were 61.36+/-28.26 pg/L versus 5.41+/-3.58 pg/L in group B versus group C rats, respectively (p<0.001). Pancreatic tissue and MLN cultures were positive in 100% of group B survivors versus 14% of group C survivors (p<0.05). Histologic examination of the intestine in group C animals showed increased mucous secretion, proliferation of goblet cells, and evidence of rapid turnover/renewal of enterocytes. Treatment with the cathartic agent, sennoside, reduced translocation of endotoxin and bacteria, restored intestinal motility, increased mucous secretion, and reduced mortality in a model of acute hemorrhagic pancreatitis in the rat. Other cathartics may have similar properties and may be useful in preventing infectious complications in acute pancreatitis.

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Year:  1999        PMID: 9888659     DOI: 10.1097/00006676-199901000-00006

Source DB:  PubMed          Journal:  Pancreas        ISSN: 0885-3177            Impact factor:   3.327


  6 in total

1.  Lipopolysaccharide directly affects pancreatic acinar cells: implications on acute pancreatitis pathophysiology.

Authors:  M I Vaccaro; E L Calvo; A M Suburo; D O Sordelli; G Lanosa; J L Iovanna
Journal:  Dig Dis Sci       Date:  2000-05       Impact factor: 3.199

2.  The Effects of Total Colectomy on Bacterial Translocation in a Model of Acute Pancreatitis.

Authors:  Rahman Şenocak; Taner Yigit; Zafer Kılbaş; Ali Kağan Coşkun; Ali Harlak; Mustafa Öner Menteş; Abdullah Kılıç; Armağan Günal; Orhan Kozak
Journal:  Indian J Surg       Date:  2013-01-31       Impact factor: 0.656

3.  Involvement of interstitial cells of Cajal in experimental severe acute pancreatitis in rats.

Authors:  Liang-Liang Shi; Ming-Dong Liu; Min Chen; Xiao-Ping Zou
Journal:  World J Gastroenterol       Date:  2013       Impact factor: 5.742

4.  The role of the intestine in the pathophysiology and management of severe acute pancreatitis.

Authors:  R S Flint; J A Windsor
Journal:  HPB (Oxford)       Date:  2003       Impact factor: 3.647

5.  Saikosaponin a attenuates hyperlipidemic pancreatitis in rats via the PPAR-γ/NF-κB signaling pathway.

Authors:  Pingping Feng; Yanfang Xu; Baoyan Tong; Xiaoqun Tong; Yinyan Bian; Shufen Zhao; Hongbo Shen
Journal:  Exp Ther Med       Date:  2019-12-13       Impact factor: 2.447

6.  Combinatory antibiotic treatment protects against experimental acute pancreatitis by suppressing gut bacterial translocation to pancreas and inhibiting NLRP3 inflammasome pathway.

Authors:  Lingling Jia; Hao Chen; Jun Yang; Xin Fang; Wenying Niu; Ming Zhang; Jiahong Li; Xiaohua Pan; Zhengnan Ren; Jia Sun; Li-Long Pan
Journal:  Innate Immun       Date:  2019-10-15       Impact factor: 2.680

  6 in total

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