PubMed:11932745
Annnotations
SMAFIRA_Feedback_Research_Goal
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1016-1018 | something | denotes | of |
T2 | 476-480 | something | denotes | soon |
T3 | 769-772 | something | denotes | LTP |
T4 | 156-166 | something | denotes | pathogenic |
T5 | 62-69 | something | denotes | inhibit |
UseCases_ArguminSci_Discourse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-113 | DRI_Background | denotes | Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo. |
T2 | 114-411 | DRI_Background | denotes | Although extensive data support a central pathogenic role for amyloid beta protein (Abeta) in Alzheimer's disease, the amyloid hypothesis remains controversial, in part because a specific neurotoxic species of Abeta and the nature of its effects on synaptic function have not been defined in vivo. |
T3 | 412-596 | DRI_Outcome | denotes | Here we report that natural oligomers of human Abeta are formed soon after generation of the peptide within specific intracellular vesicles and are subsequently secreted from the cell. |
T4 | 597-790 | DRI_Background | denotes | Cerebral microinjection of cell medium containing these oligomers and abundant Abeta monomers but no amyloid fibrils markedly inhibited hippocampal long-term potentiation (LTP) in rats in vivo. |
T5 | 791-877 | DRI_Approach | denotes | Immunodepletion from the medium of all Abeta species completely abrogated this effect. |
T6 | 878-1023 | DRI_Outcome | denotes | Pretreatment of the medium with insulin-degrading enzyme, which degrades Abeta monomers but not oligomers, did not prevent the inhibition of LTP. |
T7 | 1024-1201 | DRI_Challenge | denotes | Therefore, Abeta oligomers, in the absence of monomers and amyloid fibrils, disrupted synaptic plasticity in vivo at concentrations found in human brain and cerebrospinal fluid. |
T8 | 1202-1401 | DRI_Background | denotes | Finally, treatment of cells with gamma-secretase inhibitors prevented oligomer formation at doses that allowed appreciable monomer production, and such medium no longer disrupted LTP, indicating that |
T9 | 1402-1420 | Token_Label.OUTSIDE | denotes | synaptotoxic Abeta |
T10 | 1421-1463 | DRI_Background | denotes | oligomers can be targeted therapeutically. |
PubMed_ArguminSci
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 114-411 | DRI_Background | denotes | Although extensive data support a central pathogenic role for amyloid beta protein (Abeta) in Alzheimer's disease, the amyloid hypothesis remains controversial, in part because a specific neurotoxic species of Abeta and the nature of its effects on synaptic function have not been defined in vivo. |
T2 | 412-596 | DRI_Outcome | denotes | Here we report that natural oligomers of human Abeta are formed soon after generation of the peptide within specific intracellular vesicles and are subsequently secreted from the cell. |
T3 | 597-790 | DRI_Background | denotes | Cerebral microinjection of cell medium containing these oligomers and abundant Abeta monomers but no amyloid fibrils markedly inhibited hippocampal long-term potentiation (LTP) in rats in vivo. |
T4 | 791-877 | DRI_Approach | denotes | Immunodepletion from the medium of all Abeta species completely abrogated this effect. |
T5 | 878-1023 | DRI_Outcome | denotes | Pretreatment of the medium with insulin-degrading enzyme, which degrades Abeta monomers but not oligomers, did not prevent the inhibition of LTP. |
T6 | 1024-1201 | DRI_Challenge | denotes | Therefore, Abeta oligomers, in the absence of monomers and amyloid fibrils, disrupted synaptic plasticity in vivo at concentrations found in human brain and cerebrospinal fluid. |
T7 | 1202-1401 | DRI_Background | denotes | Finally, treatment of cells with gamma-secretase inhibitors prevented oligomer formation at doses that allowed appreciable monomer production, and such medium no longer disrupted LTP, indicating that |
T8 | 1421-1463 | DRI_Background | denotes | oligomers can be targeted therapeutically. |