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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Nephrotoxicity in rabbits after long-term nandrolone decanoate administration

Thumbnail
Συγγραφέας
Tsitsimpikou C., Vasilaki F., Tsarouhas K., Fragkiadaki P., Tzardi M., Goutzourelas N., Nepka C., Kalogeraki A., Heretis I., Epitropaki Z., Kouretas D., Tsatsakis A.M.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1016/j.toxlet.2016.06.1122
Λέξη-κλειδί
alanine aminotransferase
alkaline phosphatase
aspartate aminotransferase
biochemical marker
carbonyl derivative
catalase
creatinine
glutathione
nandrolone decanoate
telomerase
thiobarbituric acid reactive substance
urea
anabolic agent
biological marker
nandrolone
nandrolone decanoate
alanine aminotransferase blood level
alkaline phosphatase blood level
animal experiment
animal model
animal tissue
Article
aspartate aminotransferase blood level
controlled study
creatinine blood level
drug megadose
enzyme activity
histopathology
hyperemia
kidney fibrosis
kidney function
kidney parenchyma
lipid peroxidation
low drug dose
male
nephritis
nephrotoxicity
nonhuman
oxidative stress
priority journal
rabbit model
urea blood level
analogs and derivatives
animal
chemically induced
drug administration
drug effects
kidney disease
rabbit
Anabolic Agents
Animals
Biomarkers
Drug Administration Schedule
Kidney Diseases
Male
Nandrolone
Oxidative Stress
Rabbits
Elsevier Ireland Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Among the various side effects of supra-physiological dose of anabolic androgenic steroids that are described, renal toxicity remains the least evaluated. The present study provides evidence that long-term administration of nandrolone decanoate could lead to alterations of renal function and structure in the experimental rabbit model. A pronounced increase in serum urea, creatinine, SGOT and SGPT is observed in the treated animals, with intramuscular administration being more detrimental. Histopathological evaluation of kidneys indicated hyperaemia, fibrosis and focal inflammation. Furthermore, the significantly increased telomerase activity found in the kidneys of the intramuscularly treated animals could possibly represent a counteracting survival mechanism. Oxidative stress markers that were influenced the most were TBARS, indicating lipid peroxidation, and GSH. An interesting finding in our study though, was that while intramuscular administration showed the highest biochemical derangement, oxidative stress markers provided mixed results between intramuscularly and subcutaneously treated rabbits. In conclusion, nephrotoxicity of nandrolone decanoate remains a multi-factorial, partly irreversible effect that involves augmented tissue oxidative status. © 2016
URI
http://hdl.handle.net/11615/80059
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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