The reactivity of copper complexes with neuronal peptides promoted by catecholamines and its impact on neurodegeneration (Record no. 54241)

MARC details
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fixed length control field 02451nam a2200313Ia 4500
003 - CONTROL NUMBER IDENTIFIER
control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625162443.0
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Transcribing agency CICY
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-20138
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245 10 - TITLE STATEMENT
Title The reactivity of copper complexes with neuronal peptides promoted by catecholamines and its impact on neurodegeneration
490 0# - SERIES STATEMENT
Volume/sequential designation Coordination Chemistry Reviews, 471, p.214756, 2022
520 3# - SUMMARY, ETC.
Summary, etc. In this review we give an updated outlook of the reactivity of catecholamines, particularly dopamine, and the redox effects produced by their interaction with copper(II)and dioxygen, with emphasis to the extensive studies carried out by our group. The interaction between copper(II)ions and neuronal proteins and peptides can contribute to neurodegeneration because in many cases the peptide fragments contain high affinity binding sites and the resulting complexes exhibit increased redox reactivity. It has become apparent in recent years that the redox reactivity of Cu-peptide complexes can be substantially improved by catecholamines, which are redox reactive molecules by themselves but also relatively good ligands for copper ions. Therefore, the toxic effects of copper dyshomeostasis will be particularly harmful in the brain areas producing and releasing catecholamines, i.e. the axon terminals of the substantia nigra and locus coeruleus. These are the brain regions which become affected in the early stages of Parkinson and Alzheimer's disease, indicating that copper neurotoxicity may contribute to the outset of the diseases. Copper-?-amyloid and copper-prion complexes exhibit the highest redox activity induced by catecholamines; their reactivity is modulated by interaction with membranes, which tend to depress the reactivity unless the peptides interact with each other strengthening the binding of copper(II).
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element COPPER-PEPTIDE COMPLEXES
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element DOPAMINE
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element OXIDATIVE STRESS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element ?-AMYLOID
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PRION PROTEIN
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element A-SYNUCLEIN
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element TAU PROTEIN
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element QUINONE-PROTEIN MODIFICATION
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Bacchella, C.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Dell'Acqua, S.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Nicolis, S.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Monzani, E.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Casella, L.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/12NS11ndFtbT_1flqyW5xEAraQNC3IBVO/view?usp=drivesdk">https://drive.google.com/file/d/12NS11ndFtbT_1flqyW5xEAraQNC3IBVO/view?usp=drivesdk</a>
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Source of classification or shelving scheme Clasificación local
Koha item type Documentos solicitados
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  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-20138 25.06.2025 25.06.2025 Documentos solicitados