Author/Authors :
Liszewska, Agata Department of Dermatology and Venereology - Medical University of Lodz, Poland , Robak, Ewa Department of Dermatology and Venereology - Medical University of Lodz, Poland , Bernacka, Małgorzata Department of Dermatology and Venereology - Medical University of Lodz, Poland , Bogaczewicz, Jarosław Department of Dermatology and Venereology - Medical University of Lodz, Poland , Woźniacka, Anna Department of Dermatology and Venereology - Medical University of Lodz, Poland
Abstract :
Methotrexate inhibits tetrahydrofolic acid production and influences mitochondrial oxygen uptake and activity of several enzymes in the respiratory chain reactions, which utilize nicotinamide adenine dinucleotide-linked (NAD-linked) substrates. Hyperproliferation of keratinocytes in psoriasis requires oxidative phosphorylation, in which the reduced form of nicotinamide adenine dinucleotide (NADH) is an electron donor. One hypothesis links increased cellular metabolism to the increased NADH/NAD+ ratio; as expected, the topical application of NAD+ (oxidized form of nicotinamide-adenine dinucleotide) resulted in a clinical improvement of psoriatic lesions in one study. Nevertheless, another report revealed reduced fluorescence of NADH in psoriatic plaques. The biological activity of NADH is not limited only to serving as the electron donor. It was also found to regulate gene transcription.
Keywords :
methotrexate , psoriasis , nicotinamide-adenine dinucleotide , spectrophotometry , mitochondria
