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Cytochromes P450 in synthesis of cholesterol and bile acids: from mouse models to human diseases
Lorbek, Gregor (Avtor), Lewinska, Monika (Avtor), Rozman, Damjana (Avtor)

URLURL - Predstavitvena datoteka, za dostop obiščite http://onlinelibrary.wiley.com/doi/10.1111/j.1742-4658.2011.08432.x/abstract Povezava se odpre v novem oknu

Izvleček
This review describes the transgenic mouse models designed to evaluate the functions of cytochromes P450 involved in cholesterol and bile acid synthesis,and their link to disease. The knockout of cholesterogenic Cyp51 is embrionally lethal with symptoms of Antley-Bixler syndrome in mice, while the evidence for this association is conflicting in humans. Disruption of Cyp7a1 from classic bile acid (BA) synthesis in mice leads to either increased postnatal death or to a milder phenotype with elevated serum cholesterol. The latter is similar to humans, where CYP7A1 mutations associate with high plasmaLDL and hepatic cholesterol content, and a deficient BA excretion. Disruption of Cyp8b1 from alternative BA pathway results in absence of cholic acid and a reduced absorption of dietary lipids, however, the human CYP8B1 polymorphism fails to explain differences in BA composition. Surprisingly, theapparently normal Cyp27a1(-/-) mice still synthesize BAs that originate from the compensatory pathway. In humans CYP27A1 mutations cause cerebrotendinous xanthomatosis, suggesting that only mice can compensate for the loss of alternative BA synthesis. In line with this, Cyp7b1 knockouts are also apparently normal while human CYP7B1 mutations cause congenital bile acidsynthesis defect in children or spastic paraplegia in adults. Mouse knockouts of the brain-specific Cyp46a1 have reduced brain cholesterol excretion, while in humans CYP46A1 polymorphisms associate with cognitive impairment. CYP39 is at present poorly characterized. Despite important physiological differences between humans and mice, mouse models prove to be aninvaluable tool for understanding the multifactorial facets of cholesterol and BA related disorders.

Jezik:Angleški jezik
Vrsta gradiva:Delo ni kategorizirano (r6)
Tipologija:1.08 - Objavljeni znanstveni prispevek na konferenci
Organizacija:MF - Medicinska fakulteta
Leto izida:2012
Št. strani:str. 1516-1533
Številčenje:Vol. 279, iss. 9, spec. iss.
UDK:577
ISSN pri članku:1742-464X
DOI:10.1111/j.1742-4658.2011.08432.x Povezava se odpre v novem oknu
COBISS.SI-ID:29158105 Povezava se odpre v novem oknu
Število ogledov:489
Število prenosov:104
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