Liver regeneration is promoted by increasing serotonin content in rat liver with secondary biliary cirrhosis

Aim:  Liver cirrhosis clinically shows thrombocytopenia and hypersplenism. Although splenectomy is performed to achieve higher platelet count and better hemostasis, the effect of splenectomy for liver cirrhosis remains unclear. The aim of the present study that was focused on serotonin was to invest...

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Veröffentlicht in:Hepatology research 2011-08, Vol.41 (8), p.784-794
Hauptverfasser: Nagao, Yoshihiro, Akahoshi, Tomohiko, Kamori, Masahiro, Uehara, Hideo, Hashimoto, Naotaka, Kinjo, Nao, Shirabe, Ken, Taketomi, Akinobu, Tomikawa, Morimasa, Hashizume, Makoto, Maehara, Yoshihiko
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container_end_page 794
container_issue 8
container_start_page 784
container_title Hepatology research
container_volume 41
creator Nagao, Yoshihiro
Akahoshi, Tomohiko
Kamori, Masahiro
Uehara, Hideo
Hashimoto, Naotaka
Kinjo, Nao
Shirabe, Ken
Taketomi, Akinobu
Tomikawa, Morimasa
Hashizume, Makoto
Maehara, Yoshihiko
description Aim:  Liver cirrhosis clinically shows thrombocytopenia and hypersplenism. Although splenectomy is performed to achieve higher platelet count and better hemostasis, the effect of splenectomy for liver cirrhosis remains unclear. The aim of the present study that was focused on serotonin was to investigate the relationship between splenectomy and liver regeneration in rats with secondary biliary cirrhosis. Methods:  Liver cirrhosis was induced in Sprague–Dawley rats by bile duct ligation (BDL). In addition, splenectomy and administration of ketanserin, which selectively antagonizes 5‐HT2A and 2B serotonin receptors, were performed. Three weeks after the interventions, whole blood, plasma, serum, and liver specimens were obtained for the following studies: peripheral platelet counts, hemodynamics of serotonin, histopathological examination, immunostaining, and quantification of mRNA expression. Results:  Splenectomy induced thrombocytosis, and increased serotonin content in cirrhotic liver. Stimulation of liver regeneration was indicated by the following parameters: hepatocyte ratio to the entire liver area, Ki67‐positive hepatocyte count, and expression of phosphorylated extracellular signal‐regulated kinases. This enhancement of liver regeneration was negated by ketanserin. Conclusion:  Our results showed that splenectomy promoted liver regeneration by increasing serotonin content in liver even under cirrhotic conditions.
doi_str_mv 10.1111/j.1872-034X.2011.00828.x
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Although splenectomy is performed to achieve higher platelet count and better hemostasis, the effect of splenectomy for liver cirrhosis remains unclear. The aim of the present study that was focused on serotonin was to investigate the relationship between splenectomy and liver regeneration in rats with secondary biliary cirrhosis. Methods:  Liver cirrhosis was induced in Sprague–Dawley rats by bile duct ligation (BDL). In addition, splenectomy and administration of ketanserin, which selectively antagonizes 5‐HT2A and 2B serotonin receptors, were performed. Three weeks after the interventions, whole blood, plasma, serum, and liver specimens were obtained for the following studies: peripheral platelet counts, hemodynamics of serotonin, histopathological examination, immunostaining, and quantification of mRNA expression. Results:  Splenectomy induced thrombocytosis, and increased serotonin content in cirrhotic liver. Stimulation of liver regeneration was indicated by the following parameters: hepatocyte ratio to the entire liver area, Ki67‐positive hepatocyte count, and expression of phosphorylated extracellular signal‐regulated kinases. This enhancement of liver regeneration was negated by ketanserin. Conclusion:  Our results showed that splenectomy promoted liver regeneration by increasing serotonin content in liver even under cirrhotic conditions.</description><identifier>ISSN: 1386-6346</identifier><identifier>EISSN: 1872-034X</identifier><identifier>DOI: 10.1111/j.1872-034X.2011.00828.x</identifier><identifier>PMID: 21699634</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>ketanserin ; liver regeneration ; secondary biliary cirrhosis ; serotonin ; splenectomy</subject><ispartof>Hepatology research, 2011-08, Vol.41 (8), p.784-794</ispartof><rights>2011 The Japan Society of Hepatology</rights><rights>2011 The Japan Society of Hepatology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4598-ef6420829c51abfcf0e598c0f6a98b5bfda06e47e13aa199d4155a7e3137ed773</citedby><cites>FETCH-LOGICAL-c4598-ef6420829c51abfcf0e598c0f6a98b5bfda06e47e13aa199d4155a7e3137ed773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1872-034X.2011.00828.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1872-034X.2011.00828.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21699634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagao, Yoshihiro</creatorcontrib><creatorcontrib>Akahoshi, Tomohiko</creatorcontrib><creatorcontrib>Kamori, Masahiro</creatorcontrib><creatorcontrib>Uehara, Hideo</creatorcontrib><creatorcontrib>Hashimoto, Naotaka</creatorcontrib><creatorcontrib>Kinjo, Nao</creatorcontrib><creatorcontrib>Shirabe, Ken</creatorcontrib><creatorcontrib>Taketomi, Akinobu</creatorcontrib><creatorcontrib>Tomikawa, Morimasa</creatorcontrib><creatorcontrib>Hashizume, Makoto</creatorcontrib><creatorcontrib>Maehara, Yoshihiko</creatorcontrib><title>Liver regeneration is promoted by increasing serotonin content in rat liver with secondary biliary cirrhosis</title><title>Hepatology research</title><addtitle>Hepatol Res</addtitle><description>Aim:  Liver cirrhosis clinically shows thrombocytopenia and hypersplenism. Although splenectomy is performed to achieve higher platelet count and better hemostasis, the effect of splenectomy for liver cirrhosis remains unclear. The aim of the present study that was focused on serotonin was to investigate the relationship between splenectomy and liver regeneration in rats with secondary biliary cirrhosis. Methods:  Liver cirrhosis was induced in Sprague–Dawley rats by bile duct ligation (BDL). In addition, splenectomy and administration of ketanserin, which selectively antagonizes 5‐HT2A and 2B serotonin receptors, were performed. Three weeks after the interventions, whole blood, plasma, serum, and liver specimens were obtained for the following studies: peripheral platelet counts, hemodynamics of serotonin, histopathological examination, immunostaining, and quantification of mRNA expression. Results:  Splenectomy induced thrombocytosis, and increased serotonin content in cirrhotic liver. Stimulation of liver regeneration was indicated by the following parameters: hepatocyte ratio to the entire liver area, Ki67‐positive hepatocyte count, and expression of phosphorylated extracellular signal‐regulated kinases. This enhancement of liver regeneration was negated by ketanserin. 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Stimulation of liver regeneration was indicated by the following parameters: hepatocyte ratio to the entire liver area, Ki67‐positive hepatocyte count, and expression of phosphorylated extracellular signal‐regulated kinases. This enhancement of liver regeneration was negated by ketanserin. Conclusion:  Our results showed that splenectomy promoted liver regeneration by increasing serotonin content in liver even under cirrhotic conditions.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>21699634</pmid><doi>10.1111/j.1872-034X.2011.00828.x</doi><tpages>11</tpages></addata></record>
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subjects ketanserin
liver regeneration
secondary biliary cirrhosis
serotonin
splenectomy
title Liver regeneration is promoted by increasing serotonin content in rat liver with secondary biliary cirrhosis
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