Neuroprotective Potential of Raloxifene via G-Protein-Coupled Estrogen Receptors in A beta-Oligomer-Induced Neuronal Injury

Amyloid-beta (A beta) is one of the causes of Alzheimer's disease (AD), damaging nerve membranes and inducing neurotoxicity. AD is more prevalent in female patients than in male patients, and women are more susceptible to developing AD due to the decline in estrogen levels around menopause. Raloxifene, a selective estrogen receptor modulator, exhibits protective effects by activating the transmembrane G-protein-coupled estrogen receptor (GPER). Additionally, raloxifene prevents mild cognitive impairment and restores cognition. However, the influence of raloxifene via GPER on highly toxic A beta-oligomers (A beta o)-induced neurotoxicity remains uncertain. In this study, we investigated the GPER-mediated neuroprotective effects of raloxifene against the neurotoxicity caused by A beta o-induced cytotoxicity. The impact of raloxifene on A beta o-induced cell damage was evaluated using measures such as cell viability, production of reactive oxygen species (ROS) and mitochondrial ROS, peroxidation of cell-membrane phospholipids, and changes in intracellular calcium ion concentration ([Ca2+]i) levels. Raloxifene hindered A fio-induced oxidative stress and reduced excessive [Ca2+]i, resulting in improved cell viability. Furthermore, these effects of raloxifene were inhibited with pretreatment with a GPER antagonist. Our findings suggest that raloxifene safeguards against A fio-induced neurotoxicity by modifying oxidative parameters and maintaining [Ca2+] i homeostasis. Raloxifene may prove effective in preventing and inhibiting the progression of AD.

Automated summary

Amyloid-beta (A beta) is linked to Alzheimer's disease (AD) and causes nerve damage and neurotoxicity. AD is more common in women, who are more susceptible due to declining estrogen levels. Raloxifene, a selective estrogen receptor modulator, activates the GPER and protects against cognitive impairment. However, the effect of raloxifene on A beta-induced neurotoxicity remains uncertain. This study investigates the neuroprotective effects of raloxifene mediated by GPER against A beta-induced cytotoxicity.