Show simple item record

Inhibition of DNA synthesis by somatostatin in rat hepatocytes stimulated by hepatocyte growth factor or epidermal growth factor,

dc.contributor.authorKokudo, Norihiroen_US
dc.contributor.authorKothary, ]piyush C.en_US
dc.contributor.authorEckhauser, Frederic E.en_US
dc.contributor.authorNakamura, Toshikazuen_US
dc.contributor.authorRaper, Steven E.en_US
dc.date.accessioned2006-04-10T15:24:33Z
dc.date.available2006-04-10T15:24:33Z
dc.date.issued1992-01en_US
dc.identifier.citationKokudo, Norihiro, Kothary, ]Piyush C., Eckhauser, Frederic E., Nakamura, Toshikazu, Raper, Steven E. (1992/01)."Inhibition of DNA synthesis by somatostatin in rat hepatocytes stimulated by hepatocyte growth factor or epidermal growth factor,." The American Journal of Surgery 163(1): 169-173. <http://hdl.handle.net/2027.42/30314>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6VHS-4BX2FWP-VG/2/d2ba74ee7d7ea083bceb3a6c0eee7064en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30314
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1346360&dopt=citationen_US
dc.description.abstractThe antiproliferative effects of somatostatin on hepatocytes stimulated by hepatocyte growth factor (HGF) or epidermal growth factor (EGF) were investigated using primary cultures of adult rat hepatocytes. Somatostatin inhibits HGF-induced (at a dose of 10 ng/mL) or EGF-induced (at a dose of 100 ng/mL) 3H-thymidine incorporation into hepatocytes in a dose-dependent manner (10-10 to 10-8 M). This inhibition was confirmed by autoradiography. The effect of somatostatin was nontoxic as judged by preserved albumin synthesis, a marker for differentiated hepatocyte function. In the presence or absence of somatostatin, neither HGF nor EGF significantly altered intracellular cyclic adenosine monophosphate (cAMP). We conclude that somatostatin is a potent inhibitor of HGF-or EGF-induced deoxyribonucleic acid synthesis in adult rat hepatocytes. The mechanism of this inhibition appears to be independent of cAMP. The significance of somatostatin in liver regeneration has yet to been_US
dc.format.extent714707 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleInhibition of DNA synthesis by somatostatin in rat hepatocytes stimulated by hepatocyte growth factor or epidermal growth factor,en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelSurgery and Anesthesiologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumFrom the Department of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumFrom the Department of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumFrom the Department of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumFrom the Department of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherFrom the Department of Biology, Kyushu University, Fukuoka, Japanen_US
dc.identifier.pmid1346360en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30314/1/0000716.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9610(92)90271-Ren_US
dc.identifier.sourceThe American Journal of Surgeryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.