A rat model of dual-flow liver machine perfusion system.

Masayuki Ohara, Jun Ishikawa, Syuhei Yoshimoto, Yoji Hakamata, Eiji Kobayashi
Author Information
  1. Masayuki Ohara: Nippon Veterinary and Life Science University - School of Veterinary Nursing and Technology - Tokyo, Japan. ORCID
  2. Jun Ishikawa: Nippon Veterinary and Life Science University - School of Veterinary Nursing and Technology - Tokyo, Japan. ORCID
  3. Syuhei Yoshimoto: Screen Holdings Co., Ltd. - Innovation Development Department - Tokyo, Japan. ORCID
  4. Yoji Hakamata: Nippon Veterinary and Life Science University - School of Veterinary Nursing and Technology - Tokyo, Japan. ORCID
  5. Eiji Kobayashi: Nippon Veterinary and Life Science University - School of Veterinary Nursing and Technology - Tokyo, Japan. ORCID

Abstract

PURPOSE: As clinical liver perfusion systems use portal vein and artery flow, dual perfusion techniques are required even in small animal models in order to reproduce clinical setting. The aim of this study was to construct a new dual-flow perfusion system in rat model and optimized the oxygen supply to ensure the aerobic metabolization.
METHODS: The dual-flow circuit was fabricated using rat liver and whole blood samples as perfusates. The oxygen supply was controlled according to the amount of dissolved oxygen in the perfusate. Perfusate parameters and adenosine triphosphate (ATP) levels were analyzed to evaluate organ function and metabolic energy state. Stored whole blood also tested the suitability as perfusate.
RESULTS: Stored blood showed decrease oxygen delivery and liver function compared to fresh blood. Using fresh blood as perfusate with air only, the dissolved oxygen levels remained low and anaerobic metabolism increased. In contrast, with oxygen control at living body level, anaerobic metabolism was well suppressed, and tissue ATP content was increased.
CONCLUSIONS: We developed a new dual-flow system that enable to reproduce the clinical settings. The perfusion system showed the possibility to improve the energy metabolic state of the perfused organ under appropriate partial pressure of oxygen.

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MeSH Term

Rats
Animals
Liver
Adenosine Triphosphate
Perfusion
Oxygen

Chemicals

Adenosine Triphosphate
Oxygen

Word Cloud

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