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Original Research Article | OPEN ACCESS

Colchicine protects against acute pancreatitis via down-regulation of cytokine levels

Nan Zhang1, Meng Liang2, Kuo Wang1, Tao Sun1, Xiaoxu Ding1, Yan Zhou1, Zhanbiao Yu1

1Department of Critical Care Medicine; 2Department of Hepatobiliary Surgery, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, China.

For correspondence:-    

Accepted: 20 November 2019        Published: 31 December 2019

Citation: Zhang N, Liang M, Wang K, Sun T, Ding X, Zhou Y, et al. Colchicine protects against acute pancreatitis via down-regulation of cytokine levels. Trop J Pharm Res 2019; 18(12):2551-2556 doi: 10.4314/tjpr.v18i12.13

© 2019 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the effect of colchicine on acute pancreatitis (AP) in a rat model, and the molecular mechanism involved.
Methods: Acute pancreatitis (AP) was induced in rats by injection with 5 % sodium taurocholate.  Changes in histology of pancreatic tissues were determined following treatment with colchicine. Serum amylase activity was measured using Automated Biochemistry Analyser.
Results: Hematoxylin and eosin (H & E) staining showed that colchicine prevented histopathological changes such as infiltration of interstitial leukocytes and erythrocytes, cell necrosis, oedema formation and vacuolization in the rat pancreas. Treatment of AP rats with colchicine significantly and dose-dependently decreased ascite volume in the abdominal cavity. Serum amylase activity was significantly suppressed in AP rats on treatment with 100 mg/kg colchicine. Furthermore, treatment of the AP rats with colchicine caused marked decrease in the expressions of interleukin 6 and tumor necrosis factor α, and upregulated expressions of IL 10 in serum. Colchicine treatment of AP rats also caused significant increase in CGRP level in the plasma.
Conclusion: Colchicine prevents pancreatic tissue damage induced by AP by down-regulating pro-inflammatory cytokines, upregulation of anti-inflammatory cytokines, and enhancing CGRP release. Therefore, colchicine may be useful for the treatment of acute pancreatitis.

Keywords: Colchicine, Acute pancreatitis, Anti-inflammation, Calcitonin, Interleukin

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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