Cargando…

Does dexmedetomidine prevent colistin nephrotoxicity?

BACKGROUND: In this study, we aimed to investigate the effect of dexmedetomidine on colistin nephrotoxicity in rats. METHODS: Thirty-two Wistar albino rats were allocated into four groups. Intraperitoneal (ip) saline at 1 mL.kg(−1) was administered to the control group and 10 mg.kg(−1) ip colistin w...

Descripción completa

Detalles Bibliográficos
Autores principales: Talih, Gamze, Esmaoğlu, Aliye, Bayram, Adnan, Yazici, Cevat, Deniz, Kemal, Talih, Tutkun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391814/
https://www.ncbi.nlm.nih.gov/pubmed/29885938
http://dx.doi.org/10.1016/j.bjane.2018.01.021
_version_ 1784770934236774400
author Talih, Gamze
Esmaoğlu, Aliye
Bayram, Adnan
Yazici, Cevat
Deniz, Kemal
Talih, Tutkun
author_facet Talih, Gamze
Esmaoğlu, Aliye
Bayram, Adnan
Yazici, Cevat
Deniz, Kemal
Talih, Tutkun
author_sort Talih, Gamze
collection PubMed
description BACKGROUND: In this study, we aimed to investigate the effect of dexmedetomidine on colistin nephrotoxicity in rats. METHODS: Thirty-two Wistar albino rats were allocated into four groups. Intraperitoneal (ip) saline at 1 mL.kg(−1) was administered to the control group and 10 mg.kg(−1) ip colistin was given to the colistin group. In the DEX10 group 10 mcg.kg(−1) dexmedetomidine ip was given 20 min before the injection of 10 mg.kg(−1) ip colistin. In the DEX20 group ip 20 mcg.kg(−1) dexmedetomidine was injected 20 min before the administration of 10 mg.kg(−1) ip colistin. These treatments were continued twice a day for seven days. Samples were taken on the eighth day. BUN, Cr, KIM-1, TAS, and TOS were examined in blood samples and caspase-3 was examined in kidney tissue samples. RESULTS: The values for BUN, Cr and TOS were significantly higher in the colistin group than in the control group. BUN, Cr and TOS changes in the DEX10 and DEX20 groups were not significant compared with the control group but they were significantly lower compared with the colistin group. TAS values in the DEX10 group were significantly lower than in the control group. Apoptotic activity was significantly higher in the colistin group compared with the control group, but there was no significant difference in terms of caspase-3 staining activity when DEX10 and DEX20 groups were compared with the control group. CONCLUSION: Oxidative damage and apoptosis played roles in colistin nephrotoxicity, and colistin nephrotoxicity could be prevented by treatment with dexmedetomidine.
format Online
Article
Text
id pubmed-9391814
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-93918142022-08-21 Does dexmedetomidine prevent colistin nephrotoxicity? Talih, Gamze Esmaoğlu, Aliye Bayram, Adnan Yazici, Cevat Deniz, Kemal Talih, Tutkun Braz J Anesthesiol Scientific Article BACKGROUND: In this study, we aimed to investigate the effect of dexmedetomidine on colistin nephrotoxicity in rats. METHODS: Thirty-two Wistar albino rats were allocated into four groups. Intraperitoneal (ip) saline at 1 mL.kg(−1) was administered to the control group and 10 mg.kg(−1) ip colistin was given to the colistin group. In the DEX10 group 10 mcg.kg(−1) dexmedetomidine ip was given 20 min before the injection of 10 mg.kg(−1) ip colistin. In the DEX20 group ip 20 mcg.kg(−1) dexmedetomidine was injected 20 min before the administration of 10 mg.kg(−1) ip colistin. These treatments were continued twice a day for seven days. Samples were taken on the eighth day. BUN, Cr, KIM-1, TAS, and TOS were examined in blood samples and caspase-3 was examined in kidney tissue samples. RESULTS: The values for BUN, Cr and TOS were significantly higher in the colistin group than in the control group. BUN, Cr and TOS changes in the DEX10 and DEX20 groups were not significant compared with the control group but they were significantly lower compared with the colistin group. TAS values in the DEX10 group were significantly lower than in the control group. Apoptotic activity was significantly higher in the colistin group compared with the control group, but there was no significant difference in terms of caspase-3 staining activity when DEX10 and DEX20 groups were compared with the control group. CONCLUSION: Oxidative damage and apoptosis played roles in colistin nephrotoxicity, and colistin nephrotoxicity could be prevented by treatment with dexmedetomidine. Elsevier 2018-02-21 /pmc/articles/PMC9391814/ /pubmed/29885938 http://dx.doi.org/10.1016/j.bjane.2018.01.021 Text en © 2018 Sociedade Brasileira de Anestesiologia. Published by Elsevier Editora Ltda. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Scientific Article
Talih, Gamze
Esmaoğlu, Aliye
Bayram, Adnan
Yazici, Cevat
Deniz, Kemal
Talih, Tutkun
Does dexmedetomidine prevent colistin nephrotoxicity?
title Does dexmedetomidine prevent colistin nephrotoxicity?
title_full Does dexmedetomidine prevent colistin nephrotoxicity?
title_fullStr Does dexmedetomidine prevent colistin nephrotoxicity?
title_full_unstemmed Does dexmedetomidine prevent colistin nephrotoxicity?
title_short Does dexmedetomidine prevent colistin nephrotoxicity?
title_sort does dexmedetomidine prevent colistin nephrotoxicity?
topic Scientific Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391814/
https://www.ncbi.nlm.nih.gov/pubmed/29885938
http://dx.doi.org/10.1016/j.bjane.2018.01.021
work_keys_str_mv AT talihgamze doesdexmedetomidinepreventcolistinnephrotoxicity
AT esmaoglualiye doesdexmedetomidinepreventcolistinnephrotoxicity
AT bayramadnan doesdexmedetomidinepreventcolistinnephrotoxicity
AT yazicicevat doesdexmedetomidinepreventcolistinnephrotoxicity
AT denizkemal doesdexmedetomidinepreventcolistinnephrotoxicity
AT talihtutkun doesdexmedetomidinepreventcolistinnephrotoxicity