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Purinergic signaling in cognitive impairment and neuropsychiatric symptoms of Alzheimer's disease.
Ribeiro, Deidiane Elisa; Petiz, Lyvia Lintzmaier; Glaser, Talita; Oliveira-Giacomelli, Ágatha; Andrejew, Roberta; Saab, Fernando de Azevedo Ribeiro; Milanis, Milena da Silva; Campos, Henrique Correia; Sampaio, Vanessa Fernandes Arnaud; La Banca, Sophia; Longo, Beatriz Monteiro; Lameu, Claudiana; Tang, Yong; Resende, Rodrigo Ribeiro; Ferreira, Sergio T; Ulrich, Henning.
Afiliação
  • Ribeiro DE; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil. Electronic address: deidiane@hotmail.com.
  • Petiz LL; Department of Biochemistry and Molecular Biology, Universidade Federal do Paraná, Curitiba, Brazil.
  • Glaser T; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • Oliveira-Giacomelli Á; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • Andrejew R; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • Saab FAR; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • Milanis MDS; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • Campos HC; Laboratory of Neurophysiology, Department of Physiology, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
  • Sampaio VFA; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • La Banca S; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • Longo BM; Laboratory of Neurophysiology, Department of Physiology, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
  • Lameu C; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil.
  • Tang Y; International Collaborative Centre on Big Science Plan for Purinergic Signalling, Chengdu University of Traditional Chinese Medicine, Chengdu, 610075, China; Acupuncture and Chronobiology Key Laboratory of Sichuan Province, Chengdu, 610075, China.
  • Resende RR; Department of Biochemistry and Immunology, Federal University of Minas Gerais Belo Horizonte, MG, Brazil.
  • Ferreira ST; Institute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil; Institute of Medical Biochemistry Leopoldo de Meis, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Ulrich H; Department of Biochemistry, Chemistry Institute, University of São Paulo (USP), São Paulo, Brazil; International Collaborative Centre on Big Science Plan for Purinergic Signalling, Chengdu University of Traditional Chinese Medicine, Chengdu, 610075, China. Electronic address: henning@iq.usp.br.
Neuropharmacology ; 226: 109371, 2023 03 15.
Article em En | MEDLINE | ID: mdl-36502867
ABSTRACT
About 10 million new cases of dementia develop worldwide each year, of which up to 70% are attributable to Alzheimer's disease (AD). In addition to the widely known symptoms of memory loss and cognitive impairment, AD patients frequently develop non-cognitive symptoms, referred to as behavioral and psychological symptoms of dementia (BPSDs). Sleep disorders are often associated with AD, but mood alterations, notably depression and apathy, comprise the most frequent class of BPSDs. BPSDs negatively affect the lives of AD patients and their caregivers, and have a significant impact on public health systems and the economy. Because treatments currently available for AD are not disease-modifying and mainly aim to ameliorate some of the cognitive symptoms, elucidating the mechanisms underlying mood alterations and other BPSDs in AD may reveal novel avenues for progress in AD therapy. Purinergic signaling is implicated in the pathophysiology of several central nervous system (CNS) disorders, such as AD, depression and sleep disorders. Here, we review recent findings indicating that purinergic receptors, mainly the A1, A2A, and P2X7 subtypes, are associated with the development/progression of AD. Current evidence suggests that targeting purinergic signaling may represent a promising therapeutic approach in AD and related conditions. This article is part of the Special Issue on "Purinergic Signaling 50 years".
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Sono-Vigília / Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Neuropharmacology Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Sono-Vigília / Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Neuropharmacology Ano de publicação: 2023 Tipo de documento: Article