Stimulation of Central α2 Receptors Attenuates Experimental Necrotizing Pancreatitis. Issue 2 (February 2016)

• Record Type: Journal Article
• Authors: Schneider, Lutz; Jabrailova, Bahar; Salem, Mohammed; Kilk, Karl; Hofer, Stefan; Brenner, Thorsten; Strobel, Oliver; Hackert, Thilo; Werner, Jens
• Is Part Of: Pancreas. Volume 45:Issue 2(2016)
• Publication Date: 2016-02
• Subjects: acute pancreatitis -- clonidine -- dexmedetomidine -- inflammation -- cholinergic anti-inflammatory pathway; Pancreas -- Diseases -- Periodicals; Pancreas -- Periodicals; Neuroendocrine tumors -- Periodicals; 616.37005
• DOI: 10.1097/MPA.0000000000000474
• Languages: English
• ISSNs: 0885-3177

Abstract

Abstract : Objectives: Severe necrotizing pancreatitis (SNP) is a disease with relevant morbidity and mortality until today. No specific therapy is in sight. Central α2 agonists such as clonidine and dexmedetomidine are known to have anti-inflammatory effects though the cholinergic anti-inflammatory pathway and are implemented in the clinical routine as adjunct sedative drugs. Their potential effect on SNP has not yet been tested. Methods: Severe necrotizing pancreatitis was induced in male Wistar rats. Four treatment groups received either clonidine or dexmedetomidine before (prophylactic) or after induction of SNP (therapeutic). After 12 hours, pancreatic morphologic injury, systemic proinflammatory high-mobility group box 1 protein, and pancreatic and pulmonary myeloperoxidase levels were evaluated. Results: Severe necrotizing pancreatitis was fully established 12 hours after induction. "Prophylactic" and "therapeutic" administration of clonidine and dexmedetomidine reduced pancreatic morphologic injury ( P < 0.05 vs SNP), serum proinflammatory high-mobility group box 1 protein ( P < 0.0001 vs SNP), as well as pancreatic and pulmonary myeloperoxidase levels ( P < 0.01 vs SNP). Conclusions: Prophylactic and therapeutic applications of the central α2 agonists clonidine and dexmedetomidine are effective to attenuate local and systemic injury in experimental SNP and should be evaluated in the clinical setting.