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The Role of CD38 in the Pathogenesis of Cardiorenal Metabolic Disease and Aging, an Approach from Basic Research.
Kitada, Munehiro; Araki, Shin-Ichi; Koya, Daisuke.
Afiliação
  • Kitada M; Department of Internal Medicine, Hamada Neurosurgery and Internal Medicine Clinic, Wakayama 641-8509, Japan.
  • Araki SI; Department of Nephrology, Wakayama Medical University, Wakayama 641-8509, Japan.
  • Koya D; Department of Nephrology, Wakayama Medical University, Wakayama 641-8509, Japan.
Cells ; 12(4)2023 02 12.
Article em En | MEDLINE | ID: mdl-36831262
ABSTRACT
Aging is a major risk factor for the leading causes of mortality, and the incidence of age-related diseases including cardiovascular disease, kidney disease and metabolic disease increases with age. NAD+ is a classic coenzyme that exists in all species, and that plays a crucial role in oxidation-reduction reactions. It is also involved in the regulation of many cellular functions including inflammation, oxidative stress and differentiation. NAD+ declines with aging in various organs, and the reduction in NAD+ is possibly involved in the development of age-related cellular dysfunction in cardiorenal metabolic organs through the accumulation of inflammation and oxidative stress. Levels of NAD+ are regulated by the balance between its synthesis and degradation. CD38 is the main NAD+-degrading enzyme, and CD38 is activated in response to inflammation with aging, which is associated with the reduction in NAD+ levels. In this review, focusing on CD38, we discuss the role of CD38 in aging and the pathogenesis of age-related diseases, including cardiorenal metabolic disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Envelhecimento / ADP-Ribosil Ciclase 1 / Doenças Metabólicas Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Envelhecimento / ADP-Ribosil Ciclase 1 / Doenças Metabólicas Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article