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Dietary L-arginine supplementation reduces Methotrexate-induced intestinal mucosal injury in rat

dc.contributor.authorKoppelmann, Tal
dc.contributor.authorPollak, Yulia
dc.contributor.authorMogilner, Jorge
dc.contributor.authorBejar, Jacob
dc.contributor.authorCoran, Arnold G
dc.contributor.authorSukhotnik, Igor
dc.date.accessioned2015-08-07T17:49:49Z
dc.date.available2015-08-07T17:49:49Z
dc.date.issued2012-04-30
dc.identifier.citationBMC Gastroenterology. 2012 Apr 30;12(1):41
dc.identifier.urihttps://hdl.handle.net/2027.42/112921en_US
dc.description.abstractAbstract Background Arginine (ARG) and nitric oxide maintain the mucosal integrity of the intestine in various intestinal disorders. In the present study, we evaluated the effects of oral ARG supplementation on intestinal structural changes, enterocyte proliferation and apoptosis following methotrexate (MTX)-induced intestinal damage in a rat. Methods Male rats were divided into four experimental groups: Control rats, CONTR-ARG rats, were treated with oral ARG given in drinking water 72 hours before and 72 hours following vehicle injection, MTX rats were treated with a single dose of methotrexate, and MTX-ARG rats were treated with oral ARG following injection of MTX. Intestinal mucosal damage, mucosal structural changes, enterocyte proliferation and enterocyte apoptosis were determined 72 hours following MTX injection. RT-PCR was used to determine bax and bcl-2 mRNA expression. Results MTX-ARG rats demonstrated greater jejunal and ileal bowel weight, greater ileal mucosal weight, greater ileal mucosal DNA and protein levels, greater villus height in jejunum and ileum and crypt depth in ileum, compared to MTX animals. A significant decrease in enterocyte apoptosis in the ileum of MTX-ARG rats (vs MTX) was accompanied by decreased bax mRNA and protein expression and increased bcl-2 protein levels. Conclusions Treatment with oral ARG prevents mucosal injury and improves intestinal recovery following MTX- injury in the rat.
dc.titleDietary L-arginine supplementation reduces Methotrexate-induced intestinal mucosal injury in rat
dc.typeArticleen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/112921/1/12876_2011_Article_712.pdf
dc.identifier.doi10.1186/1471-230X-12-41en_US
dc.language.rfc3066en
dc.rights.holderKoppelmann et al; licensee BioMed Central Ltd.
dc.date.updated2015-08-07T17:49:49Z
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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