{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,23]],"date-time":"2025-09-23T13:40:51Z","timestamp":1758634851444},"reference-count":25,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2005,2,7]],"date-time":"2005-02-07T00:00:00Z","timestamp":1107734400000},"content-version":"vor","delay-in-days":6,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Liver International"],"published-print":{"date-parts":[[2005,2]]},"abstract":"<jats:p><jats:bold>Abstract: Background: <\/jats:bold> In this study, we investigated the influence of brain death on inflammatory response and the effects of brain death on liver function both directly after explantation and after reoxygenation.<\/jats:p><jats:p><jats:bold>Methods: <\/jats:bold> The influence of brain death on liver function was studied in rats using a brain death model and the liver slice model to mimic reoxygenation. Liver function was assessed by measuring the ATP content and the ATP\u2010driven urea synthesis. The activation of non\u2010parenchymal cells was studied by measuring mRNA levels of IL\u201010, cytokine production (IL\u201010 and IL\u20101\u03b2) and inducible nitric oxide synthases (iNOS) upregulation (mRNA) and protein level.<\/jats:p><jats:p><jats:bold>Results: <\/jats:bold> Brain death had no direct influence on the ATP content of the liver. However, it led to induction of several cytokines because of activation of non\u2010parenchymal cells, which led to upregulation of iNOS and to nitric oxide metabolites production. It is known that cytokine production may influence the drug metabolism capacity; however, no influence of brain death on drug metabolism was observed. An explanation may be the relatively short experimental period.<\/jats:p><jats:p><jats:bold>Conclusions: <\/jats:bold> Kupffer cells seem to be activated during the onset of brain death induction; however, they become quiescent when liver slices of brain dead rats were reoxygenated during incubation. Other non\u2010parenchymal cells, possibly the endothelial cells, remain activated during incubation and reoxygenation in slices from brain death donors but not in slices from control livers. Future experiments in our rat liver transplantation model need to elucidate the implications of these findings.<\/jats:p>","DOI":"10.1111\/j.1478-3231.2005.01035.x","type":"journal-article","created":{"date-parts":[[2005,2,7]],"date-time":"2005-02-07T13:34:12Z","timestamp":1107783252000},"page":"109-116","source":"Crossref","is-referenced-by-count":26,"title":["The influence of brain death on liver function"],"prefix":"10.1111","volume":"25","author":[{"given":"Peter","family":"Olinga","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joost A. B.","family":"Van Der Hoeven","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marjolijn T.","family":"Merema","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rennie L.","family":"Freund","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rutger J.","family":"Ploeg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Geny M. M.","family":"Groothuis","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,2,7]]},"reference":[{"key":"e_1_2_7_2_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM199508103330601"},{"key":"e_1_2_7_3_2","unstructured":"Annual Report of the U.S. Scientific Registry of Transplant Recipients and the Organ Procurement and Transplantation Network.Transplantation Data from 1989\u20131998. 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