Channelpedia

PubMed 26417684


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Kv1.5 , Slo1



Title: Cecal inoculum peritonitis: An alternative model for sepsis vascular dysfunction study.

Authors: Shinichi Asano, Nandini D P K Manne, Geeta Nandyala, Bing Ma, Vellaisamy Selvaraj, Ravikumar Arvapalli, Kevin M Rice, Eric R Blough

Journal, date & volume: Life Sci., 2015 Nov 15 , 141, 108-18

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26417684


Abstract
Sepsis is a life threatening condition that is characterized by the loss of vascular reactivity. The factor(s) responsible for the diminished vascular function seen in sepsis are not well understood. The purpose of this study was to characterize the vascular dysfunction from the rat cecal inoculum (CI) sepsis model using cecal ligation and puncture (CLP), and lipopolysaccharide (LPS) sepsis as reference models.Experiments were performed on isolated aorta from CI, CLP and LPS treated rats using a combination of pharmacological approaches.Phenylephrine (PE)-induced aortic contraction was significantly decreased in each model (p<0.05) and not normalized by L-NAME or indomethacin. The vascular response elicited in the CI model for acetylcholine (Ach) was more similar to that seen in the CLP than the LPS model. The removal of the endothelial layer increased sensitivity to L-NAME (p<0.05) in aortae from CI group. Inhibition of the large conductance Ca(2+)/voltage sensitive K(+) (BKCa) channel did not normalize PE hyporesponsiveness but did abolish sepsis-induced contractile oscillation. Inhibition of the voltage dependent Kv1.5 channel was not able to reverse the vascular hyporesponsiveness, however, inhibition of the ATP dependent (KATP) channel inhibition partially restored the contractile response (p<0.05). Elevation of VCAM expression and aortic structural alternation were observed in each model.These results suggest that the CI model may be an additional tool that could be used to investigate the mechanisms of vascular hyporesponsiveness in sepsis.