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Effects of the Novel Acetylcholinesterase InhibitorN-Octyl-1,2,3,4-tetrahydro-9-aminoacridine on Locomotor Activity and Avoidance Learning in Mice
Authors:Francesca Capone   Alberto Oliverio   Massimo Pomponi   Maurizio Marta   Franco Gatta  Flaminia Pavone
Affiliation:a Dipartimento di Genetica e Biologia Molecolare, Università “La Sapienza,” Rome, Italy;c Facoltà di Medicina “A. Gemelli” Istituto di Chimica e Chimica Clinica, U.C.S.C. Rome, Italy;d Laboratorio Chimica del Farmaco, Istituto Superiore di Sanità, Rome, Italy;b Istituto di Psicobiologia e Psicofarmacologia, CNR, Rome, Italy
Abstract:The acetylcholinesterase reversible inhibitorN-octyl-1,2,3,4-tetrahydro-9-aminoacridine (THA-C8) is a new synthesized derivative of tacrine (THA) characterized by an alkyl chain in the molecular structure which ameliorates the penetrability of the compound into the central nervous system. THA-C8 (0.1–5 mg/kg) significantly reduced spontaneous locomotor activity in CD1 mice at a dose of 3 mg/kg. Moreover, THA-C8 (0.2–2 mg/kg) significantly improved shuttle-box avoidance acquisition at doses (0.25, 0.3, 1 mg/kg) not affecting locomotion and that are much lower than the doses reported to be effective for THA in animal models. From the data reported it seems that the new compound could be interesting for therapeutic purposes.
Keywords:acetylcholinesterase inhibitor   tacrine   THA-C8   active avoidance   locomotor activity   mice
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