Abstract |
Hypoxemia is a common manifestation of various disorders and generates pressure overload to the heart. Here we analyzed the expression of lipocalin-type prostaglandin D synthase (L-PGDS) in the heart of C57BL/6 mice kept under normobaric hypoxia (10% O2) that generates hemodynamic stress. Northern and Western blot analyses revealed that the expression levels of L-PGDS mRNA and protein were significantly increased (> twofold) after 14 days of hypoxia, compared to the mice kept under normoxia. Immunohistochemical analysis indicated that L-PGDS was increased in the myocardium of auricles and ventricles and the pulmonary venous myocardium at 28 days of hypoxia. Moreover, using C57BL/6 mice lacking heme oxygenase-2 (HO-2(-/-)), a model of chronic hypoxemia, we showed that the expression level of L-PGDS protein was twofold higher in the heart than that of wild-type mouse. L-PGDS expression is induced in the myocardium under hypoxemia, which may reflect the adaptation to the hemodynamic stress.
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Authors | Feng Han, Kazuhisa Takeda, Kazunobu Ishikawa, Masao Ono, Fumiko Date, Satoru Yokoyama, Kazumichi Furuyama, Yotaro Shinozawa, Yoshihiro Urade, Shigeki Shibahara |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 385
Issue 3
Pg. 449-53
(Jul 31 2009)
ISSN: 1090-2104 [Electronic] United States |
PMID | 19470375
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Lipocalins
- Heme Oxygenase (Decyclizing)
- heme oxygenase-2
- Intramolecular Oxidoreductases
- prostaglandin R2 D-isomerase
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Topics |
- Animals
- Heme Oxygenase (Decyclizing)
(genetics)
- Hypoxia
(enzymology)
- Intramolecular Oxidoreductases
(biosynthesis)
- Lipocalins
(biosynthesis)
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Mutant Strains
- Myocardium
(enzymology)
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