Abstract
Background: The process of liver regeneration is very complex and is dependent on the etiology and extent of liver
damage and the genetic background. Liver regeneration is still not fully understood. The liver is a unique organ, and
first in line, the hepatocytes encounter the potential to proliferate during cell mass loss. This phenomenon is tightly
controlled and resembles in some way the embryonic co-inhabitant cell lineage of the liver, the embryonic hematopoietic system. Methodology: The experimental research was conducted on white lab rats. The animals were divided in
two groups. First group consists of fetal rats (two weeks old), second group – 5 month age mature female rats. In both
of groups was done 25% resection of liver tissue. After 24, 48 and 72 hours was investigated time of maximal activity
of DNA, mitochondria synthesis and hepatocytes proliferation. Results: Laboratory investigations were shown, that
after 24 hours in 1-st group was significant increase of mitochondria synthesis. After 48 hours in 1-st group of experimental animals was not changes of hepatocyte size, while in 2-nd group were seen hepatocyte enlargement and temporary increase in numbers of lysosomes, autophagosomes, and micro bodies. There was the different commencement of
DNA synthesis and mitosis in the hepatocytes of 1-st with later extension in the hepatocytes of 2-nd group. Thus, the
time of maximal activity was indicated in 1-st group much more earlier than in 2-nd group of experimental animals.
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Copyright (c) 2016 Davit Tophuria, Inga Kakhniashvili, Levan Benashvili, Maia Matoshvili, Nino Adamia