NR APMW
AU Villa,S.; Cignarella,G.; Barlocco,D.; Gervasoni,M.; Carcassola,G.; Giannino,L.; Mantegazza,P.
TI Congo red analogues as potential anti-prion agents
QU Farmaco 2003 Sep; 58(9): 929-37
PT journal article
AB 'Transmissible Spongiform Encephalopathies' (TSE) are a group of degenerative, progressive and fatal disorders of CNS which affect both humans and animals, characterised by a long incubation time. The pathogenetic mechanism in TSE is the conversion of normal prion protein (PrP(sen)) to an altered protease resistant isoform (PrPres) that accumulates in amyloid deposits into the brain; therefore, PrPres is the primary target for therapeutic strategies. The discovery that the sulphonated azo dye Congo red (CR) is able to inhibit the replications of TSE agents and the accumulation of PrPres in animals and in scrapie infected mouse neuroblastoma cells induced us to designe molecules structurally related to CR (1a-f, 2f,g). The compounds were tested in vitro to evaluate their interaction with 263K PrPres. Six of the tested compounds were found to interact with PrPres molecules and to over-stabilise the PrPres aggregates, as CR does. However, none of them induced the reversion of PrPres to PrP(sen).
MH Animals; Cell-Free System; Comparative Study; Congo Red/*analogs & derivatives/*chemistry/pharmacology; Drug Design; Hamsters; Immunoblotting; In Vitro; Prions/*antagonists & inhibitors; Structure-Activity Relationship; Support, Non-U.S. Gov't
AD Istituto di Chimica Farmaceutica e Tossicologica, Universita degli Studi di Milano, Viale Abruzzi 42, I-20131 Milan, Italy. stefania.villa@unimi.it
SP englisch
PO Italien