نتایج جستجو برای: tacrine

تعداد نتایج: 1379  

2007

The general nature of the carcinogenic process induced by chemicals and radiat ion can be conceived of as a release of the cell from normal intrinsic and extrinsic growth controls through (a) an act ivat ion of a latent virus or the formation of a virus, or (b) a heritable change resulting from reactions between the carcinogen and critical physiological entries. Such concepts may correspond to ...

2015
Jan Misik Jan Korabecny Eugenie Nepovimova Pavla Cabelova Jiri Kassa

Aims. The number of approved drugs for the clinical treatment of Alzheimer disease remains limited. For this reason, there is extensive search for novel therapies. Of these, cholinesterase inhibitors have some proven benefit in slowing the disease progression and still remain the first-line therapeutic approach. In this study, the pro-cognitive effect of four novel tacrine-related inhibitors wa...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2016
Nicoletta Schintu Xiaoqun Zhang Alexandra Alvarsson Roberta Marongiu Michael G Kaplitt Paul Greengard Per Svenningsson

The reduced movement repertoire of Parkinson's disease (PD) is mainly due to degeneration of nigrostriatal dopamine neurons. Restoration of dopamine transmission by levodopa (L-DOPA) relieves motor symptoms of PD but often causes disabling dyskinesias. Subchronic L-DOPA increases levels of adaptor protein p11 (S100A10) in dopaminoceptive neurons of the striatum. Using experimental mouse models ...

Journal: :Molecular pharmacology 1999
H M Dodds L P Rivory

Irinotecan (CPT-11) is an anticancer drug that occasionally produces acute cholinergic side effects. Preliminary findings suggest that these are mediated through the inhibition of acetylcholinesterase (AChE). In this study, the inhibition of various AChEs by CPT-11 was studied. The lactone form of CPT-11 resulted in apparent noncompetitive inhibition of electric eel and both human recombinant a...

2005
Rui WANG Han YAN Xi-can TANG

Huperzine A (HupA), a novel alkaloid isolated from the Chinese herb Huperzia serrata, is a potent, highly specific and reversible inhibitor of acetylcholinesterase (AChE). Compared with tacrine, donepezil, and rivastigmine, HupA has better penetration through the blood-brain barrier, higher oral bioavailability, and longer duration of AChE inhibitory action. HupA has been found to improve cogni...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1989

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