Literature DB >> 18827713

Increased serum resistin concentration in patients with chronic pancreatitis: possible cause of pancreatic fibrosis.

Krystian Adrych1, Marian Smoczynski, Tomasz Sledzinski, Agnieszka Dettlaff-Pokora, Elzbieta Goyke, Julian Swierczynski.   

Abstract

BACKGROUND: Resistin is an adipokine, which displays proinflammatory properties. Thus, it is likely that resistin can influence the course of chronic pancreatitis, and/or that chronic pancreatitis may affect the serum resistin concentration. GOALS: The aim of the present study was to determine the serum resistin concentration in patients with chronic pancreatitis and to analyze the relationship between serum resistin concentration and serum concentrations of leptin (proinflammatory adipokine) and adiponectin (anti-inflammatory adipokine). STUDY: A total of 23 male, nondiabetic patients with chronic pancreatitis of alcoholic origin and 16 healthy subjects were examined. Fasting blood samples were collected from patients in both groups. Serum resistin concentration was assayed by enzyme-linked immunosorbent assay. Serum adiponectin, leptin, and insulin concentrations were determined by radioimmunoassay.
RESULTS: Serum resistin concentration was significantly higher in patients with chronic pancreatitis as compared with control subjects. In contrast, patients with chronic pancreatitis had lower serum leptin and insulin concentrations than healthy subjects. There were no statistically significant differences in serum adiponectin concentration between patients with pancreatitis and healthy subjects.
CONCLUSIONS: The results presented in this paper indicate that chronic pancreatitis in human is associated with the increase in serum resistin concentration and with the decrease in serum leptin and insulin concentrations. It can be supposed that resistin, by stimulation of tumor necrosis factor-alpha synthesis in blood mononuclear cells and in macrophages, increases the concentration of tumor necrosis factor-alpha, which in turn activates stellate cells. Activated stellate cells can produce collagen, eventually resulting in the development of pancreatic fibrosis.

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Year:  2009        PMID: 18827713     DOI: 10.1097/MCG.0b013e31815cda0a

Source DB:  PubMed          Journal:  J Clin Gastroenterol        ISSN: 0192-0790            Impact factor:   3.062


  6 in total

1.  Human pancreatic polypeptide in a phospholipid-based micellar formulation.

Authors:  Amrita Banerjee; Hayat Onyuksel
Journal:  Pharm Res       Date:  2012-03-08       Impact factor: 4.200

2.  Resistin is not an appropriate biochemical marker to predict severity of acute pancreatitis: a case-controlled study.

Authors:  Hamdi Al-Maramhy; Abdelrahman I Abdelrahman; Samer Sawalhi
Journal:  World J Gastroenterol       Date:  2014-11-07       Impact factor: 5.742

3.  Decreased serum essential and aromatic amino acids in patients with chronic pancreatitis.

Authors:  Krystian Adrych; Marian Smoczynski; Magdalena Stojek; Tomasz Sledzinski; Ewa Slominska; Elzbieta Goyke; Ryszard-Tomasz Smolenski; Julian Swierczynski
Journal:  World J Gastroenterol       Date:  2010-09-21       Impact factor: 5.742

Review 4.  Local and Systemic Expression of Immunomodulatory Factors in Chronic Pancreatitis.

Authors:  Hannah M Komar; Phil A Hart; Zobeida Cruz-Monserrate; Darwin L Conwell; Gregory B Lesinski
Journal:  Pancreas       Date:  2017-09       Impact factor: 3.327

Review 5.  Sarcopenia in Chronic Pancreatitis - Prevalence, Diagnosis, Mechanisms and Potential Therapies.

Authors:  Matthew Fasullo; Endashaw Omer; Matthew Kaspar
Journal:  Curr Gastroenterol Rep       Date:  2022-04

6.  Fibrosis reduces severity of acute-on-chronic pancreatitis in humans.

Authors:  Chathur Acharya; Rachel A Cline; Deepthi Jaligama; Pawan Noel; James P Delany; Kyongtae Bae; Alessandro Furlan; Catherine J Baty; Jenny M Karlsson; Bedda L Rosario; Krutika Patel; Vivek Mishra; Chandra Dugampudi; Dhiraj Yadav; Sarah Navina; Vijay P Singh
Journal:  Gastroenterology       Date:  2013-05-15       Impact factor: 22.682

  6 in total

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