Project Details
Abstract
Portal vein embolization (PVE) and portal vein ligation (PVL) have been increasingly
applied prior to major hepatic resection with aims of increasing resectability rates and
minimizing postoperative liver failure. The amount of liver regeneration concerning
future liver remnant (FLR) varies enormously, with an increased volume of 7% to
79%, depending on quality of the liver parenchyma. Along with growing number of
metabolic syndrome patients, the incidence of non-alcohol fatty liver disease
(NAFLD) are expected to increase dramatically. Meanwhile, steatohepatitis induced
by chemotherapeutic drugs, is drawing great attention because staged hepatectomy
with or without PVE/PVL is desirable.
EPO has currently been discovered to have a potential tissue protector in various
organs such as the brain for stroke, cardiomyocytes for coronary artery disease, and
kidney for reperfusion disease. Currently, Epo has also been shown to have a positive
effect on liver regeneration after reperfusion injury and/or hepatectomy. The aims of
this study are to audit whether and how Epo can be employed to enhance liver
regeneration of steatotic liver after PVL to a maximum extent, as well its molecular
mechanism.
Project IDs
Project ID:PC10007-0375
External Project ID:NSC100-2314-B182-012
External Project ID:NSC100-2314-B182-012
Status | Finished |
---|---|
Effective start/end date | 01/08/11 → 31/07/12 |
Keywords
- portal vein ligation
- liver regeneration
- steatosis
- Kuppfer cell
- cytokine
- 99mTc-DISIDA scintigraphy
- adiponectin
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