Abstract

Renal toxic injury can neither be predicted nor quantified exactly by the serum creatinine level. NGAL is a promising biomarker for early detection of AKI due to different causes. Our objective was to evaluate it�s value in the setting of nephrotoxic injury. We performed an experiment in which we administered gentamicin, atropine and fipronil at different doses to the laboratory mice to quantify the evolution of creatinine and NGAL. Compared to creatinine, NGAL increased faster and was detected at elevated levels from the first 4 h after administration of both low and high dose gentamicin. Fipronil, atropine and the combination caused a significant increase in NGAL serum values at 4 hours, an increase that lasted up to 24 and 72 h , respectively, compared to the control group, Its highest levels were recorded at 4 h. Compared to creatinine, NGAL increased faster and was detected at elevated levels from the first 4 h after administration of fipronil, atropine and the combination of them.

Highlights

  • Renal toxic injury can neither be predicted nor quantified exactly by the serum creatinine level

  • We can conclude that gentamicin administered at low dose resulted in a significant increase in serum creatinine from the second day of administration compared to the control group

  • We can conclude that the low dose of gentamicin determined a significant increase in NGAL starting at 4 hours after comparative administration with control group

Read more

Summary

Introduction

Renal toxic injury can neither be predicted nor quantified exactly by the serum creatinine level. We can conclude that gentamicin administered at low dose resulted in a significant increase in serum creatinine from the second day of administration compared to the control group.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call