Medium-chain and short-chain dehydrogenases/reductases in retinoid metabolism

X. Parés, J. Farrés, N. Kedishvili, G. Duester

Producción científica: Contribución a una revistaArtículo de revisiónInvestigaciónrevisión exhaustiva

145 Citas (Scopus)

Resumen

Retinoic acid (RA), the most active retinoid, is synthesized in two steps from retinol. The first step, oxidation of retinol to retinaldehyde, is catalyzed by cytosolic alcohol dehydrogenases (ADHs) of the medium-chain dehydrogenase/reductase (MDR) superfamily and microsomal retinol dehydrogenases (RDHs) of the short-chain dehydrogenase/reductase (SDR) superfamily. The second step, oxidation of retinaldehyde to RA, is catalyzed by several aldehyde dehydrogenases. ADH1 and ADH2 are the major MDR enzymes in liver retinol detoxification, while ADH3 (less active) and ADH4 (most active) participate in RA generation in tissues. Several NAD+- and NADP+- dependent SDRs are retinoid active. Their in vivo contribution has been demonstrated in the visual cycle (RDH5, RDH12), adult retinoid homeostasis (RDH1) and embryogenesis (RDH10). K m values for most retinoid-active ADHs and RDHs are close to 1 μM or lower, suggesting that they participate physiologically in retinol/retinaldehyde interconversion. Probably none of these enzymes uses retinoids bound to cellular retinol-binding protein, but only free retinoids. The large number of enzymes involved in the two directions of this step, also including aldo-keto reductases, suggests that retinaldehyde levels are strictly regulated. © 2008 Birkhäuser Verlag.
Idioma originalInglés
Páginas (desde-hasta)3936-3949
PublicaciónCellular and Molecular Life Sciences
Volumen65
N.º24
DOI
EstadoPublicada - 1 dic 2008

Huella

Profundice en los temas de investigación de 'Medium-chain and short-chain dehydrogenases/reductases in retinoid metabolism'. En conjunto forman una huella única.

Citar esto