论文部分内容阅读
Objective: The purpose of this study was to investigate the effects and pharmacological mechanisms of Sodium hydrosulfide (NaHS , a H2S donor) on β-amyloid (Aβ) production and the major enzymes responsible for endogenous H2S generation in overexpressing human amyloid precursor protein (APP695swe) and presenilinl (PS1-dE9) transgenic mice model of AD.Methods: 9 months male APP/PS1 transgenic mice were randomly divided into two groups: APP/PS1 group and APP/PS1+NaHS (2.8mg/kg) group.Age-matched male wild-type (WT) littermates were randomly divided into two groups: WT group and WT+NaHS (2.8mg/kg) group.