Preliminary study on overproduction of reactive oxygen species by neutrophils in diabetes mellitus
AIM:To assess the amount and pattern of reactive oxygen species(ROS)production in diabetic patientderived neutrophils.METHODS:Blood samples from type 2 diabetes mellitus(DM)patients and volunteers(controls)were subjected to neutrophil isolation and the assessment of neutrophil oxidative burst using...
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Published in | 世界糖尿病杂志:英文版(电子版) no. 13; pp. 271 - 278 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
2016
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Subjects | |
Online Access | Get full text |
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Summary: | AIM:To assess the amount and pattern of reactive oxygen species(ROS)production in diabetic patientderived neutrophils.METHODS:Blood samples from type 2 diabetes mellitus(DM)patients and volunteers(controls)were subjected to neutrophil isolation and the assessment of neutrophil oxidative burst using chemiluminescence assay.Neutrophils were activated by using phorbol myristate acetate(PMA)and neutrophils without activation were kept as a negative control.The chemilu-minescence readings were obtained by transferring cell suspension into a 1.5 m L Eppendorf tube,with PMA and luminol.Reaction mixtures were gently vortexed and placed inside luminometer for a duration of 5 min.RESULTS:Our results showed that in the resting condition,the secretion of ROS in normal non-diabetic individuals was relatively low compared to diabetic patients.However,the time scale observation revealed that the secreted ROS declined accordingly with time in non-diabetic individuals,yet such a reduction was not detected in diabetic patients where at all the time points,the secretion of ROS was maintained at similar magnitudes.This preliminary study demonstrated that ROS production was significantly higher in patients with DM compared to non-diabetic subjects in both resting and activated conditions.CONCLUSION:The respiratory burst activity of neutrophils could be affected by DM and the elevation of ROS production might be an aggravating factor in diabetic-related complications. |
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Bibliography: | Noridzzaida Ridzuan;Cini Mathew John;Pratheep Sandrasaigaran;Maryam Maqbool;Lee Chuen Liew;Jonathan Lim;Rajesh Ramasamy;Immunology Laboratory, Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia;Stem Cell Research Laboratory, Genetic and Regenerative Medicine Research Center, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia;Department of Physiology and Phar-macology, Faculty of Medicine, University of Calgary;Department of Medicine, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia |
ISSN: | 1948-9358 1948-9358 |