TY - JOUR
T1 - A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus
AU - Inomata, Kenta
AU - Tajima, Kazuki
AU - Yagi, Hiroshi
AU - Higashi, Hisanobu
AU - Shimoda, Hirofumi
AU - Matsubara, Kentaro
AU - Hibi, Taizo
AU - Abe, Yuta
AU - Tsujikawa, Hanako
AU - Kitago, Minoru
AU - Shinoda, Masahiro
AU - Obara, Hideaki
AU - Itano, Osamu
AU - Soto-Gutierrez, Alejandro
AU - Kitagawa, Yuko
N1 - Funding Information:
This work was supported by Japan Agency for Medical Research and Development (AMED), Research Center Network for Realization of Regenerative Medicine Projects to H. Yagi and Y. Kitagawa. The authors wish to acknowledge Dr. Shingo Akimoto, Specially-Appointed Associate Professor, Keio University School of Medicine, for his technical help in performing the Western blotting for this study.
Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - A feasible large animal model to evaluate regenerative medicine techniques is vital for developing clinical applications. One such appropriate model could be to use retrorsine (RS) together with partial hepatectomy (PH). Here, we have developed the first porcine model using RS and PH. RS or saline control was administered intraperitoneally to Göttingen miniature pigs twice, two weeks apart. Four weeks after the second dose, animals underwent PH. Initially, we tested different doses of RS and resection of different amounts of liver, and selected 50 mg/kg RS with 60% hepatectomy as our model for further testing. Treated animals were sacrificed 3, 10, 17 or 28 days after PH. Blood samples and resected liver were collected. Serum and liver RS content was determined by Liquid Chromatograph-tandem Mass Spectrometer. Blood analyses demonstrated liver dysfunction after PH. Liver regeneration was significantly inhibited 10 and 17 days after PH in RS-treated animals, to the extent of 20%. Histological examination indicated hepatic injury and regenerative responses after PH. Immunohistochemical staining demonstrated accumulation of Cyclin D1 and suppression of Ki-67 and PCNA in RS-treated animals. We report the development of the first large animal model of sustained liver injury with suppression of hepatic regeneration.
AB - A feasible large animal model to evaluate regenerative medicine techniques is vital for developing clinical applications. One such appropriate model could be to use retrorsine (RS) together with partial hepatectomy (PH). Here, we have developed the first porcine model using RS and PH. RS or saline control was administered intraperitoneally to Göttingen miniature pigs twice, two weeks apart. Four weeks after the second dose, animals underwent PH. Initially, we tested different doses of RS and resection of different amounts of liver, and selected 50 mg/kg RS with 60% hepatectomy as our model for further testing. Treated animals were sacrificed 3, 10, 17 or 28 days after PH. Blood samples and resected liver were collected. Serum and liver RS content was determined by Liquid Chromatograph-tandem Mass Spectrometer. Blood analyses demonstrated liver dysfunction after PH. Liver regeneration was significantly inhibited 10 and 17 days after PH in RS-treated animals, to the extent of 20%. Histological examination indicated hepatic injury and regenerative responses after PH. Immunohistochemical staining demonstrated accumulation of Cyclin D1 and suppression of Ki-67 and PCNA in RS-treated animals. We report the development of the first large animal model of sustained liver injury with suppression of hepatic regeneration.
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U2 - 10.1038/s41598-018-32889-y
DO - 10.1038/s41598-018-32889-y
M3 - Article
C2 - 30301901
AN - SCOPUS:85054778548
SN - 2045-2322
VL - 8
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 14987
ER -