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Intermittent treatment with Apremilast, a phosphodiesterase-4 inhibitor, ameliorates Alzheimer’s-like pathology and symptoms through multiple targeting actions in aged T2D rats

مؤلف البحث
Adel A. Gomaa a,*, Hanan S.M. Farghaly a, Asmaa M. Ahmed b, Fahmy K. Hemida
تاريخ البحث
مجلة البحث
International Immunopharmacology
المشارك في البحث
الناشر
Elsevier
تصنيف البحث
5.72
عدد البحث
117
موقع البحث
https://doi.org/10.1016/j.intimp.2023.109927
سنة البحث
2023
صفحات البحث
109927
ملخص البحث

Background: Apremilast (Apre), a novel phosphodiesterase-4 (PDE4) inhibitor, has been shown to have antiinflammatory, immunomodulator, neuroprotective and senolytic properties, therefore, Apre like other PDE4 inhibitors may be a promising candidate for treatment of Alzheimer’s disease (AD).
Objective: To evaluate the effectiveness of Apre on Alzheimer’s like pathology and symptoms in an animal model.
Methods: The effects of Apre and cilostazol, a reference drug, on the behavioral, biochemical, and pathological features of Alzheimer’s disease induced by a high-fat/high-fructose diet combined with low-dose streptozotocin
(HF/HFr/L-STZ) were investigated.
Result: Apre 5 mg/kg IP/day for 3 consecutive days per week for 8 weeks attenuated memory and learning deficits tested by novel object recognition, Morris water maze and passive avoidance tests. Apre treatment significantly decreased the number of degenerating cells, and abnormal suppression of gene expression of AMPA
and NMDA receptor subunits in the cortex and hippocampus of the AD rat model compared to rats that received vehicle. A significant decrease in elevated levels of hippocampal amyloid beta, tau-positive cell count, cholinesterase activity, and hippocampal caspase-3, a biomarker of neurodegeneration, was also observed after
treatment with Apre in AD rats compared to rats that received placebo. Furthermore, a significant decrease in pro-inflammatory cytokines, oxidative stress, insulin resistance and GSK-3 was demonstrated in AD aged rats treated by Apre.
Conclusion: Our findings demonstrate that intermittent treatment with Apre can enhance cognitive function in HF/HFr/L-STZ rats which may be related to decreased pro-inflammatory cytokines, oxidative stress, insulin resistance and GSK-3β.