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Article type: Research Article
Authors: Zaky, Amiraa; * | Bassiouny, Ahmada | Farghaly, Mahitabb | El-Sabaa, Bassma M.c
Affiliations: [a] Department of Biochemistry, Faculty of Science, Alexandria University, Alexandria, Egypt | [b] Department of Environmental Research at National Center for Social & Criminological Research, Giza, Egypt | [c] Department of Pathology, Faculty of Medicine, Alexandria University, Alexandria, Egypt
Correspondence: [*] Correspondence to: Amira Zaky, Department of Biochemistry, Faculty of Science, Alexandria University, Alexandria, Moharram Bake, P.O Box 21511, Egypt. Tel.: +20 1223584529; Fax: +20 203 3911794; E-mail: amzakyha@alexu.edu.eg.
Abstract: Background:Experimental studies have demonstrated that aluminum is an environmental toxin that induces neuroinflammation and the development of Alzheimer’s disease. Objective:In this report, we investigated the beneficial effect of a combination of resveratrol and curcumin to reduce aluminum-induced neuroinflammation. Method:We employed both an in vivo model of aluminum-induced neuroinflammation and an in vitro aluminum stimulated cultured PC-12 cells. Neuroinflammation in rats was assessed by measuring the expression of β-secretase, amyloid-β protein precursor, and γ-subunits (PS-1 and PS-2), along with the inflammatory COX-2, Il-1β, Il-1α, and TNF-α. Furthermore, we measured the expression profiles of neuro-protective Apurinic/apyrimidinic endonuclease 1 (APE1) protein and let-7c microRNA. In parallel, PC-12 cells were treated with 0.5 mM aluminum to induce a neuroinflammation-like state. In addition, curcumin effect, as a selective COX-2 expression inhibitor, was detected in a time course manner. Results:An overall significant attenuation of the inflammatory markers, as well as a decrease in the amyloidogenic mediators, was observed in resveratrol-curcumin treated rats. The therapeutic effect was also confirmed by transmission electron microscopic analysis of the brain cortexes. APE1 was significantly induced by resveratrol-curcumin combination. Both in vivo and in vitro studies indicated that Let-7c expression is significantly reduced after aluminum stimulation, an effect that was partially suppressed by co-addition of either resveratrol or curcumin and totally restored to the normal level by their combination. Conclusions:The present study clearly indicates the synergistic and therapeutic effect of a resveratrol-curcumin combination. We also show that both compounds exert beneficial effect either cooperatively or through differential molecular mechanisms in counteracting aluminum-induced neuroinflammation.
Keywords: Aluminum, apurinic/apyrimidinic endonuclease 1, curcumin, cyclooxygenase-2, microRNA Let-7c, resveratrol
DOI: 10.3233/JAD-161115
Journal: Journal of Alzheimer's Disease, vol. 60, no. s1, pp. S221-S235, 2017
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