Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2009-6-15
pubmed:abstractText
Patients with cystic fibrosis (CF) and Cftr-knockout mice (CF mice) display an imbalance in fatty acids, with high arachidonic acid (AA) and low docosahexaenoic acid (DHA) concentrations. Our recent studies demonstrated defects in another class of lipids, ceramides, in patients with CF and in CF mice. This study investigates the relationship between ceramide, AA, DHA, and the correction of lipid imbalances in CF mice after treatment with fenretinide. Concentrations of AA, DHA, and ceramide were assessed in plasma from 58 adult patients with CF and 72 healthy control subjects. After 28 days of treatment with fenretinide, the same analysis was performed in wild-type and CF mice from plasma and organs (lung, ileum, pancreas, and liver). Low ceramide levels were associated with high AA and low DHA concentrations in patients with CF. No correlation was observed in healthy control subjects. Greater deficiencies were seen in patients with CF who were diagnosed before the age of 18, specifically with statistically significant higher levels of AA. Treatment with fenretinide (N-(4-hydroxyphenyl)retinamide; 4-HPR) normalized high levels of AA and low levels of ceramide, and increased the levels of DHA in CF mice. As in patients with CF, low ceramide levels correlated with higher AA and lower DHA levels in plasma of CF mice. Lipid abnormalities correlated with ceramide deficiencies in patients with CF and CF mice. We found that fenretinide treatment normalizes the fatty acid imbalance in CF mice with reducing AA to WT levels and increasing DHA. We propose that fenretinide treatment might improve this pathological phenotype in patients with CF.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1535-4989
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
100-6
pubmed:meshHeading
pubmed-meshheading:19059886-Adolescent, pubmed-meshheading:19059886-Adult, pubmed-meshheading:19059886-Aged, pubmed-meshheading:19059886-Animals, pubmed-meshheading:19059886-Arachidonic Acid, pubmed-meshheading:19059886-Case-Control Studies, pubmed-meshheading:19059886-Ceramides, pubmed-meshheading:19059886-Cystic Fibrosis, pubmed-meshheading:19059886-Disease Models, Animal, pubmed-meshheading:19059886-Docosahexaenoic Acids, pubmed-meshheading:19059886-Female, pubmed-meshheading:19059886-Fenretinide, pubmed-meshheading:19059886-Forced Expiratory Volume, pubmed-meshheading:19059886-Humans, pubmed-meshheading:19059886-Ileum, pubmed-meshheading:19059886-Liver, pubmed-meshheading:19059886-Lung, pubmed-meshheading:19059886-Male, pubmed-meshheading:19059886-Mice, pubmed-meshheading:19059886-Mice, Inbred CFTR, pubmed-meshheading:19059886-Middle Aged, pubmed-meshheading:19059886-Pancreas, pubmed-meshheading:19059886-Pseudomonas Infections, pubmed-meshheading:19059886-Pseudomonas aeruginosa, pubmed-meshheading:19059886-Severity of Illness Index, pubmed-meshheading:19059886-Young Adult
pubmed:year
2009
pubmed:articleTitle
Cystic fibrosis fatty acid imbalance is linked to ceramide deficiency and corrected by fenretinide.
pubmed:affiliation
Department of Medicine, McGill University, Montreal, Quebec, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't