Luteolin ameliorates colistin-induced nephrotoxicity in the rat models

38Citations
Citations of this article
31Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Introduction and aim: To study the protective, preventive effect of luteolin from colistin-induced nephrotoxicity. Material and method: Four different treatment options were tested on rats: colistin, luteolin, and a combination of colistin and luteolin, intraperitoneally as two doses a day, for seven days. Another group of rats were used as the control and treated with sterile saline. Serum creatinine levels were measured before and after treatment. Histological changes and colistin-induced apoptosis (Insitu BrdU-red DNA Fragmentation Assay Kit) of the renal tissues were examined after the scarification procedure. Results: In the Colistin Group, post-treatment creatinine levels were statistically higher than the pretreatment levels (p =.001). In the remaining groups, no significant changes were observed. Cells that undergo apoptosis were counted and it was shown that all groups except the colistin-treated group had a similar number of apoptotic cells, whereas the colistin-treated group had statistically higher number of apoptotic cells compared to other groups (p=.0001). Renal histological damage was also measured and the score of the colistin treated group was higher as compared to other groups. Conclusion: The results obtained from this study demonstrated us that luteolin was capable of preventing colistin-induced nephrotoxicity and that this effect was significant at histopathological level.

Author supplied keywords

Cite

CITATION STYLE

APA

Arslan, B. Y., Arslan, F., Erkalp, K., Alagöl, A., Sevdi, M. S., Yıldız, G., … Altınay, S. (2016). Luteolin ameliorates colistin-induced nephrotoxicity in the rat models. Renal Failure, 38(10), 1735–1740. https://doi.org/10.1080/0886022X.2016.1229995

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free