Original Article
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World J Gastroenterol. Mar 7, 2013; 19(9): 1396-1404
Published online Mar 7, 2013. doi: 10.3748/wjg.v19.i9.1396
Influence of Kupffer cells and platelets on ischemia-reperfusion injury in mild steatotic liver
Koichi Ogawa, Tadashi Kondo, Takafumi Tamura, Hideki Matsumura, Kiyoshi Fukunaga, Tatsuya Oda, Nobuhiro Ohkohchi
Koichi Ogawa, Tadashi Kondo, Takafumi Tamura, Hideki Matsumura, Kiyoshi Fukunaga, Tatsuya Oda, Nobuhiro Ohkohchi, Department of Surgery, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8575, Japan
Author contributions: Ogawa K and Kondo T contributed equally to this work; Ogawa K, Kondo T, Tamura T and Matsumura H designed the study; Ogawa K and Tamura T performed the experiments; Fukunaga K, Oda T and Ohkohchi N contributed the analysis of the data; Ogawa K, Kondo T, Fukunaga K and Ohkohchi N wrote the manuscript.
Supported by The Ministry of Education, Culture, Sports, Science, and Technology of Japan, KAKENHI, No. 22591499
Correspondence to: Nobuhiro Ohkohchi, MD, PhD, Professor, Department of Surgery, Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8575, Japan. nokochi3@md.tsukuba.ac.jp
Telephone: +81-29-8533221  Fax: +81-29-8533222
Received: November 22, 2012
Revised: January 10, 2013
Accepted: January 18, 2013
Published online: March 7, 2013
Processing time: 110 Days and 14 Hours
Abstract

AIM: To investigate the effect of mild steatotic liver on ischemia-reperfusion injury by focusing on Kupffer cells (KCs) and platelets.

METHODS: Wistar rats were divided into a normal liver group (N group) and a mild steatotic liver group (S group) induced by feeding a choline-deficient diet for 2 wk. Both groups were subjected to 20 min of warm ischemia followed by 120 min of reperfusion. The number of labeled KCs and platelets in sinusoids and the blood perfusion in sinusoids were observed by intravital microscopy (IVM), which was performed at 30, 60 and 120 min after reperfusion. To evaluate serum alanine aminotransferase as a marker of liver deterioration, blood samples were taken at the same time as IVM.

RESULTS: In the S group, the number of platelets adhering to KCs decreased significantly compared with the N group (120 after reperfusion; 2.9 ± 1.1 cells/acinus vs 4.8 ± 1.2 cells/acinus, P < 0.01). The number of KCs in sinusoids was significantly less in the S group than in the N group throughout the observation periods (before ischemia, 19.6 ± 3.3 cells/acinus vs 28.2 ± 4.1 cells/acinus, P < 0.01 and 120 min after reperfusion, 29.0 ± 4.3 cells/acinus vs 40.2 ± 3.3 cells/acinus, P < 0.01). The blood perfusion of sinusoids 120 min after reperfusion was maintained in the S group more than in the N group. Furthermore, elevation of serum alanine aminotransferase was lower in the S group than in the N group 120 min after reperfusion (99.7 ± 19.8 IU/L vs 166.3 ± 61.1 IU/L, P = 0.041), and histological impairment of hepatocyte structure was prevented in the S group.

CONCLUSION: Ischemia-reperfusion injury in mild steatotic liver was attenuated compared with normal liver due to the decreased number of KCs and the reduction of the KC-platelet interaction.

Keywords: Steatotic liver; Mild steatotic liver; Kupffer cell; Platelet; Ischemia-reperfusion; Intravital microscopy