Ontology highlight
ABSTRACT: Background
Old age, the most important risk factor for Alzheimer's disease (AD), is associated with thermoregulatory deficits. Brown adipose tissue (BAT) is the main thermogenic driver in mammals and its stimulation, through β3 adrenergic receptor (β3AR) agonists or cold acclimation, counteracts metabolic deficits in rodents and humans. Studies in animal models show that AD neuropathology leads to thermoregulatory deficits, and cold-induced tau hyperphosphorylation is prevented by BAT stimulation through cold acclimation. Since metabolic disorders and AD share strong pathogenic links, we hypothesized that BAT stimulation through a β3AR agonist could exert benefits in AD as well.Methods
CL-316,243, a specific β3AR agonist, was administered to the triple transgenic mouse mode
SUBMITTER: Tournissac M
PROVIDER: S-EPMC8140479 | biostudies-literature | 2021 May
REPOSITORIES: biostudies-literature