Cargando…

Constructing a continuous hemodiafiltration‐type circulatory model of acute kidney injury in pigs

INTRODUCTION: Animal‐model experimental systems capable of reflecting the effects of devices for continuous renal replacement therapy (CRRT) on living organisms are limited; thus, aimed to construct an animal model of AKI‐CRRT using pigs. METHODS: Pigs were subjected to renal artery ischemia–reperfu...

Descripción completa

Detalles Bibliográficos
Autores principales: Horikawa, Takumi, Maehata, Junichi, Hashimoto, Fumihiro, Ikuhara, Toshihiko, Araki, Hitomi, Umeno, Hiroshi, Sano, Yusuke, Ishikawa, Chika, Takagi, Hisayoshi, Watanabe, Atsushi, Koizumi, Toshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310588/
https://www.ncbi.nlm.nih.gov/pubmed/35247221
http://dx.doi.org/10.1111/1744-9987.13826
Descripción
Sumario:INTRODUCTION: Animal‐model experimental systems capable of reflecting the effects of devices for continuous renal replacement therapy (CRRT) on living organisms are limited; thus, aimed to construct an animal model of AKI‐CRRT using pigs. METHODS: Pigs were subjected to renal artery ischemia–reperfusion injury (IRI) and then to a maximum of 24 h of continuous hemodiafiltration (CHDF)‐type CRRT. RESULTS: Post‐IRI, pigs' creatinine levels rose threefold, and they exhibited 24 h of anuria and clear aggravation of oxidative stress, demonstrating successful induction of AKI for CRRT. Post‐CRRT, no significant changes in their vital signs or hematological parameters were observed. Creatinine and blood urea nitrogen clearance, as well as suppression of increases in oxidative stress, were also confirmed. CONCLUSION: We believe that the use of our model can enable the preclinical evaluation of the effects of under‐development CRRT devices on living organisms under conditions similar to those encountered in an actual clinical setting.