Neuroprotective effects of sodium hydrosulfide against β-amyloid-induced neurotoxicity

作者：Li, Xiao-Hui; Deng, Yuan-Yuan; Li, Fei; Shi, Jing-Shan; Gong, Qi-Hai^*

来源：International Journal of Molecular Medicine, 2016, 38(4): 1152-1160.

DOI：10.3892/ijmm.2016.2701

• beta-amyloid
• phosphodiesterase type 5
• peroxisome proliferator-activated receptor
• neuroinflammation
• caspase-3

Alzheimer's disease (AD) is known to be caused by the accumulation of amyloid- peptide (A). The accumulation of A has been shown to cause learning and memory impairment in rats, and it has been shown that hydrogen sulfide donors, such as sodium hydrosulfide (NaHS) can attenuate these effects. However, the underlying mechanisms have not yet been fully eludicated. This study was designed to investigate whether NaHS attenuates the inflammation and apoptosis induced by A. We demonstrated that NaHS attenuated A(25-35)-induced neuronal reduction and apoptosis, and inhibited the activation of pro-caspase-3. It also decreased the protein expresion of phosphodiesterase 5 (PDE5) in the hippocampus of the rats. In addition, NaHS upregulated the expression of peroxisome proliferator-activated receptor (PPAR)- and PPAR-, but it did not affect the expression of PPAR-. Moreover, the A(25-35)-exposed rats exhibited a decrease in IB- degradation and an increase in nuclear factor-B (NF-B) p65 phosphorylation levels, whereas these effects were attenuated by NaHS. Our data suggest that NaHS prevents A-induced neurotoxicity via the upregulation of PPAR- and PPAR- and the inhibition of PDE5. Hence NaHS may prove to be beneficial in the treatment of AD.

• 出版日期2016-10
• 单位遵义医科大学