Rat Liver Enzyme Release Depends on Blood Flow-Bearing Physical Forces Acting in Endothelium Glycocalyx rather than on Liver Damage


Por: Diaz-Juarez, Julieta A., Hernandez-Munoz, Rolando

Publicada: 1 ene 2017
Resumen:
We have found selective elevation of serum enzyme activities in rats subjected to partial hepatectomy (PH), apparently controlled by hemodynamic flow-bearing physical forces. Here, we assess the involvement of stretch-sensitive calcium channels and calcium mobilization in isolated livers, after chemical modifications of the endothelial glycocalyx and changing perfusion directionality. Inhibiting in vivo protein synthesis, we found that liver enzyme release is influenced by de novo synthesis of endothelial glycocalyx components, and released enzymes are confined into a liver "pool." Moreover, liver enzyme release depended on extracellular calcium entry possibly mediated by stretch-sensitive calcium channels, and this endothelial-mediated mechanotransduction in liver enzyme release was also evidenced by modifying the glycocalyx carbohydrate components, directionality of perfusing flow rate, and the participation of nitric oxide (NO) and malondialdehyde (MDA), leading to modifications in the intracellular distribution of these enzymes mainly as nuclear enrichment of "mitochondrial" enzymes. In conclusion, the flow-induced shear stress may provide fine-tuned control of released hepatic enzymes through mediation by the endothelium glycocalyx, which provides evidence of a biological role of the enzyme release rather to be merely a biomarker for evaluating hepatotoxicity and liver damage, actually positively influencing progression of liver regeneration in mammals. © 2017 Julieta A. Díaz-Juárez and Rolando Hernández-Muñoz.

Filiaciones:
Diaz-Juarez, Julieta A.:
 Univ Autonoma Metropolitana UAMXochimilco, Dept Atenc Salud, Div Ciencias Biol Salud, Mexico City 04960, DF, Mexico

Hernandez-Munoz, Rolando:
 Univ Nacl Autonoma Mexico, Inst Fisiol Celular, Dept Biol Celular Desarrollo, Mexico City 04510, DF, Mexico
ISSN: 19420900
Editorial
Hindawi Publishing Corporation, 410 PARK AVENUE, 15TH FLOOR, #287 PMB, NEW YORK, NY 10022 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 2017 Número:
Páginas:
WOS Id: 000397848700001
ID de PubMed: 28337244

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