Article ; Online: S
2017 Volume 85, Issue 9
Abstract: Artesunate remains the mainstay of treatment for cerebral malaria, but it is less effective in later stages of disease when the host inflammatory response and blood-brain barrier integrity dictate clinical outcomes. Nitric oxide (NO) is an important ... ...
Abstract | Artesunate remains the mainstay of treatment for cerebral malaria, but it is less effective in later stages of disease when the host inflammatory response and blood-brain barrier integrity dictate clinical outcomes. Nitric oxide (NO) is an important regulator of inflammation and microvascular integrity, and impaired NO bioactivity is associated with fatal outcomes in malaria. Endogenous NO bioactivity in mammals is largely mediated by |
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MeSH term(s) | Alcohol Dehydrogenase/deficiency ; Animals ; Antimalarials/administration & dosage ; Artemisinins/administration & dosage ; Disease Models, Animal ; Female ; Malaria, Cerebral/drug therapy ; Malaria, Cerebral/pathology ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; Nitric Oxide/metabolism ; Plasmodium berghei/pathogenicity ; Survival Analysis ; T-Lymphocytes/immunology ; Treatment Outcome |
Chemical Substances | Antimalarials ; Artemisinins ; Nitric Oxide (31C4KY9ESH) ; artesunate (60W3249T9M) ; Adh5 protein, mouse (EC 1.1.1.1) ; Alcohol Dehydrogenase (EC 1.1.1.1) |
Language | English |
Publishing date | 2017-09 |
Publishing country | United States |
Document type | Journal Article |
ZDB-ID | 218698-6 |
ISSN | 1098-5522 ; 0019-9567 |
ISSN (online) | 1098-5522 |
ISSN | 0019-9567 |
DOI | 10.1128/IAI.00371-17 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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