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JoVE Journal
Bioengineering
Procedura per Decellularization di Rat Livers in un dispositivo di perfusione oscillante pressione
Procedura per Decellularization di Rat Livers in un dispositivo di perfusione oscillante pressione
JoVE Journal
Bioengineering
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JoVE Journal Bioengineering
Procedure for Decellularization of Rat Livers in an Oscillating-pressure Perfusion Device

Procedura per Decellularization di Rat Livers in un dispositivo di perfusione oscillante pressione

Full Text
10,839 Views
09:38 min
August 10, 2015

DOI: 10.3791/53029-v

Karl Hillebrandt1, Dietrich Polenz1, Antje Butter1, Peter Tang1, Anja Reutzel-Selke1, Andreas Andreou1, Hendrik Napierala1, Nathanael Raschzok1, Johann Pratschke1, Igor M. Sauer1, Benjamin Struecker1

1General, Visceral, and Transplantation Surgery,Charité – Universitätsmedizin Berlin

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This article presents techniques for liver harvesting, cannulation, and perfusion using a proprietary device to enhance decellularization and recellularization experiments in rat livers. The study focuses on optimizing the homogeneity of liver perfusion decellularization.

Key Study Components

Area of Science

  • Neuroscience
  • Biology
  • Regenerative Medicine

Background

  • Decellularization is crucial for organ transplantation and tissue engineering.
  • Current methods often lead to uneven decellularization results.
  • Arterial perfusion may improve outcomes compared to portal venous perfusion.
  • Oscillating pressure conditions can mimic physiological conditions during perfusion.

Purpose of Study

  • To evaluate the role of the perfusion root in liver decellularization.
  • To assess the effectiveness of arterial perfusion under oscillating pressure.
  • To improve the homogeneity of decellularization results in rat livers.

Methods Used

  • Cannulation of portal veins and hepatic arteries of rat livers.
  • Connection of livers to a perfusion device for selective perfusion.
  • Application of oscillating pressure changes during perfusion.
  • Assessment of decellularization through macroscopic observation and histological analysis.

Main Results

  • Arterial perfusion under oscillating pressure leads to more homogeneous decellularization.
  • Quicker decellularization observed compared to traditional methods.
  • Histological and biochemical analyses confirm improved outcomes.
  • Technique shows advantages over existing portal venous perfusion methods.

Conclusions

  • Optimizing liver perfusion techniques can enhance decellularization processes.
  • Arterial perfusion with oscillating pressure is a promising approach.
  • Further studies may expand on these findings for clinical applications.

Frequently Asked Questions

What is the main advantage of arterial perfusion?
Arterial perfusion under oscillating pressure conditions leads to more homogeneous decellularization results compared to portal venous perfusion.
How does oscillating pressure affect perfusion?
Oscillating pressure mimics intraabdominal pressure changes during respiration, optimizing liver micro perfusion.
What methods were used to assess decellularization?
Decellularization was assessed through macroscopic observation, histological analysis, and biochemical analysis.
What is the purpose of cannulating the liver?
Cannulation allows for selective perfusion of the portal veins and hepatic arteries, which is essential for the decellularization process.
Why is decellularization important?
Decellularization is crucial for organ transplantation and tissue engineering, allowing for the creation of scaffolds for cell repopulation.

Le tecniche presentate per il prelievo, l'incannulamento e la perfusione del fegato utilizzando il nostro dispositivo proprietario consentono sofisticate configurazioni di perfusione per migliorare gli esperimenti di decellularizzazione e ricellularizzazione nei fegati di ratto.

L'obiettivo generale del seguente esperimento è valutare il ruolo della radice di perfusione nell'ottimizzare l'omogeneità della decellularizzazione della perfusione epatica di ratto. Ciò si ottiene incannulando prima le vene portatrici e le arterie epatiche di fegati di ratto appena isolati. In una seconda fase, i fegati vengono collegati a un dispositivo di perfusione per la perfusione selettiva delle vene porta o delle arterie epatiche.

Successivamente, le variazioni di pressione oscillanti vengono applicate alla camera di perfusione per imitare le variazioni di pressione intraaddominale che si verificano durante la respirazione. Ottimizzando la microperfusione epatica, in ultima analisi, i fegati perfusi attraverso l'arteria epatica in condizioni di pressione oscillante mostrano una decellularizzazione più omogenea e più rapida come valutato dall'osservazione macroscopica e dall'analisi istologica e biochimica. Il vantaggio principale di questa tecnica rispetto ai metodi esistenti come la decellularizzazione della perfusione venosa portale è che la perfusione arteriosa utilizzando condizioni di pressione oscillante porta a un risultato di decellularizzazione più omogeneo.

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Bioingegneria Issue 102 Rat Liver decellularization Rat Liver perfusione periferica oscillanti Condizioni Pressione Rat Liver Ingegneria Arterial Rat Liver perfusione Portal venoso Rat Liver perfusione

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