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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Downgrading the systemic condition of rabbits after long term exposure to cypermethrin and piperonyl butoxide

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Autor
Vardavas A.I., Fragkiadaki P., Alegakis A.K., Dimitrios K., Goutzourelas N., Tsiaoussis J., Tsitsimpikou C., Stivaktakis P.D., Carvalho F., Tsatsakis A.M.
Datum
2016
Language
en
DOI
10.1016/j.lfs.2015.12.026
Schlagwort
carbonyl derivative
catalase
cypermethrin
glutathione
hemoglobin
piperonyl butoxide
telomerase
thiobarbituric acid reactive substance
cypermethrin
pesticide
piperonyl butoxide
pyrethroid
telomerase
animal cell
animal experiment
Article
concentration (parameters)
controlled study
defense mechanism
enzyme activity
enzyme blood level
experimental rabbit
hemoglobin blood level
inflammation
long term exposure
male
mononuclear cell
nonhuman
oxidative stress
peripheral blood mononuclear cell
protein blood level
animal
chemically induced
drug effects
inflammation
metabolism
oxidative stress
rabbit
Animals
Inflammation
Male
Oxidative Stress
Pesticides
Piperonyl Butoxide
Pyrethrins
Rabbits
Telomerase
Elsevier Inc.
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Zusammenfassung
Aim The aim of this study is to clarify the effect of cypermethrin (CY) on the oxidative stress (OS) and inflammation status of animals exposed to it and the synergistic role of piperonyl butoxide (PB0). Main methods Markers of oxidative stress, such as total antioxidant activity (TAC), protein carbonyls, hemoglobin (Hb), reduced glutathione (GSH), thiobarbituric-acid reactive substances (TBARS), along with the telomerase activity in PBMCs (peripheral blood mononuclear cells) were analyzed. Key findings Oxidative stress markers showed statistically significant differences between groups in TAC (p < 0.001), GSH (p = 0.018) and CAT activity (p = 0.029), which depended on dose and combined effect of both compounds. Telomerase activity also showed a statistically significant difference between all groups (F = 43.48, df = 6, 14, p < 0.001) with cypermethrin, piperonyl butoxide and the co-exposed groups being significantly different from the control group (p < 0.05). Significance: The observed results for TBARS, GSH, Hb, TAC, Crbnls and CAT from our exposed groups showed altered levels compared to control groups that could be linked to doses and combined effects of each chemical substance (cypermethrin and piperonyl butoxide). Oxidative stress markers suggest that cypermethrin, piperonyl butoxide and the co-exposed groups, induce oxidative stress as well as induction of telomerase activity. © 2015 Elsevier Inc. All rights reserved.
URI
http://hdl.handle.net/11615/80400
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