The effects of resveratrol on tissue injury, oxidative damage, and pro-inflammatory cytokines in an experimental model of acute pancreatitis View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-06

AUTHORS

Ahmet Gulcubuk, Damla Haktanir, Aris Cakiris, Duran Ustek, Ozlem Guzel, Muzaffer Erturk, Funda Yildirim, Ibrahim Akyazi, Hayriye Cicekci, Mehmet Hanifi Durak, Sema Sandikci-Altunatmaz, Kemal Altunatmaz

ABSTRACT

Acute pancreatitis (AP) is an acute inflammatory condition that results from the digestion of pancreatic tissue by its own enzymes released from the acinar cells. The objective of this study was to investigate the effects of resveratrol on oxidative damage, pro-inflammatory cytokines, and tissue injury involved with AP induced in a rat model using sodium taurocholate (n = 60). There were three treatment groups with 20 rats per group. Groups I and II received 3% sodium taurocholate solution, while group III underwent the same surgical procedure yet did not receive sodium taurocholate. In addition, group II received 30 mg/kg resveratrol solution. Rats were sacrificed at 2, 6, 12, and 24 h time points following the induction of AP. Blood and pancreatic tissue samples were collected and subjected to biochemical assays, Western blot assays, and histopathologic evaluations. Resveratrol did not reduce trypsin levels and prevent tissue damage. Resveratrol prevented IκB degradation (except for 6 h) and decreased nuclear factor-κB (NF-κB), activator protein-1 (AP-1) (except for 24 h), and levels of TNF-α, IL-6 (except for 24 h), and iNOS in the pancreatic tissue at all time points (P < 0.05). Serum nitric oxide (NO) levels were reduced as well (P < 0.05). Thus, we concluded that resveratrol did not reduce trypsin levels and did not prevent tissue injury despite the reduction in oxidative damage and pro-inflammatory cytokine levels detected in this model of AP. More... »

PAGES

397-406

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s13105-014-0317-4

DOI

http://dx.doi.org/10.1007/s13105-014-0317-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1006534225

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24549589


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