| dc.creator | Hazell | |
| dc.creator | Alan S.; Afadlal | |
| dc.creator | Szeifoul; Cheresh | |
| dc.creator | David A.; Azar | |
| dc.creator | Ashraf | |
| dc.date | 2017 | |
| dc.date | mar | |
| dc.date | 2017-11-13T13:56:25Z | |
| dc.date | 2017-11-13T13:56:25Z | |
| dc.date.accessioned | 2018-03-29T06:09:45Z | |
| dc.date.available | 2018-03-29T06:09:45Z | |
| dc.identifier | Neuroscience Letters. Elsevier Ireland Ltd, v. 642, p. 163 - 167, 2017. | |
| dc.identifier | 0304-3940 | |
| dc.identifier | 1872-7972 | |
| dc.identifier | WOS:000397356300028 | |
| dc.identifier | 10.1016/j.neulet.2017.01.041 | |
| dc.identifier | http://www-sciencedirect-com.ez88.periodicos.capes.gov.br/science/article/pii/S0304394017300617?via%3Dihub | |
| dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/329849 | |
| dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1366874 | |
| dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description | Recent clinical trials suggest that patients with myelofibrosis can develop Wernicke's encephalopathy (WE) when treated with fedratinib, a specific Janus kinase-2 (JAK-2) inhibitor. To investigate this issue, we have examined (1) if fedratinib can produce or alter the course of this disorder, (2) its effects on thiamine dependent enzyme activity and thiamine status, and (3) its influence on the uptake of thiamine. Animals administered fedratinib for 28 days at a comparable dose used to treat human cases of myelofibrosis showed no evidence of clinical signs of thiamine deficiency (TD). Rats treated with a combination of fedratinib and TD exhibited no neurological differences in their progress to the symptomatic stage when compared to thiamine-deficient animals only. Treatment with the JAK-2 inhibitor did not compromise erythrocyte transketolase activity, and thiamine status was not affected in a major way unlike animals with TD. In addition, treatment of cultured astrocytes with fedratinib did not diminish the uptake of thiamine into these cells. Our findings suggest that treatment with fedratinib does not lead to or alter the progress of TD, and do not support the notion that administration of this JAK-2 inhibitor directly results in the development of WE due to inhibition of thiamine transport. Known adverse effects of fedratinib involving compromised gastrointestinal function may be an important indirect contributing factor to previously reported cases of WE in patients with myelofibrosis. (C) 2017 Elsevier B.V. All rights reserved. | |
| dc.description | 642 | |
| dc.description | 163 | |
| dc.description | 167 | |
| dc.description | Fundacao de Amparo a Pesquisa do Estado de Sao Paulo | |
| dc.description | Canadian Institutes of Health Research | |
| dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.language | English | |
| dc.publisher | Elsevier Ireland LTD | |
| dc.publisher | Clare | |
| dc.relation | Neuroscience Letters | |
| dc.rights | fechado | |
| dc.source | WOS | |
| dc.subject | Vitamin B1 | |
| dc.subject | Thiamine Deficiency | |
| dc.subject | Myelofibrosis | |
| dc.subject | Astrocyte | |
| dc.subject | Neurodegeneration | |
| dc.subject | Excitotoxicity | |
| dc.title | Treatment Of Rats With The Jak-2 Inhibitor Fedratinib Does Not Lead To Experimental Wernicke's Encephalopathy | |
| dc.type | Artículos de revistas | |
