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Ximenia americana heteropolysaccharides ameliorate inflammation and visceral hypernociception in murine caerulein-induced acute pancreatitis: Involvement of CB2 receptors

Authors :
Maria Gonçalves Pereira
Alana de Freitas Pires
Arcelina Pacheco Cunha
Deysen Kerlla Fernandes Bezerra Girão
Kaira Emanuella Sales da Silva-Leite
Nágila M.P.S. Ricardo
Pedro Almir Feitosa de Moraes
David N. Criddle
Marcellus H.L.P. Souza
Pedro Marcos Gomes Soares
Ana Maria Sampaio Assreuy
Source :
BIOMEDICINE & PHARMACOTHERAPY
Publication Year :
2018

Abstract

Background This study aimed to investigate and characterize the anti-inflammatory and anti-hypernociceptive effects of the total polysaccharides of X. americana (TPL-Xa) bark in a mouse model of acute pancreatitis-induced by caerulein and the potential involvement of cannabinoid receptors. Methods TPL-Xa was characterized by1H and 13C NMR spectroscopy. Animals received TPL-Xa (10 mg/kg, i.v.) 30 min before and after caerulein (50 μg/kg, 10×, i.p.) administration. To evaluate the involvement of cannabinoid receptors, AM281 (3 mg/kg, s.c.) and AM630 (1 mg/kg, s.c.) were administered 30 min before TPL-Xa. Plasma levels of amylase and lipase, pancreatic myeloperoxidase (MPO), histology, visceral hypernociception and motor coordination were evaluated 11 and 24 h after acute pancreatitis (AP) induction. Results TPL-Xa, containing a heteropolysaccharide composed of glucose, galactose, arabinose, rhamnose, fucose and galacturonic acid, reduced amylase and lipase levels, MPO activity, acinar cell necrosis, edema and neutrophil infiltration. TPL-Xa increased the threshold of visceral hypernociception, an effect reversed by AM630, an antagonist of cannabinoid receptor type 2 (CB2). In addition, TPL-Xa did not alter the animals’ motor coordination. Conclusions TPL-Xa contains heteropolysaccharides that inhibit inflammation and hypernociception in the experimental model of caerulein-induced AP, by a mechanism involving type CB2 receptors.

Details

Language :
English
Database :
OpenAIRE
Journal :
BIOMEDICINE & PHARMACOTHERAPY
Accession number :
edsair.doi.dedup.....1b3e9c5911d2cd2d27b405ccc38acbc3