A Combination of Resveratrol and Curcumin is Effective Against Aluminum Chloride-Induced Neuroinflammation in Rats

J Alzheimers Dis. 2017;60(s1):S221-S235. doi: 10.3233/JAD-161115.

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.

MeSH terms

  • Acetylcholinesterase / metabolism
  • Aluminum Chloride
  • Aluminum Compounds / toxicity*
  • Animals
  • Brain / metabolism
  • Brain / pathology
  • Brain / ultrastructure
  • Catalase / metabolism
  • Chlorides / toxicity*
  • Curcumin / therapeutic use*
  • Cyclooxygenase 2 / metabolism
  • Disease Models, Animal
  • Drug Combinations
  • Encephalitis / chemically induced*
  • Encephalitis / drug therapy*
  • Encephalitis / pathology
  • Glutathione Transferase / metabolism
  • Lipid Peroxidation / drug effects
  • Male
  • Neuroprotective Agents / therapeutic use*
  • Oxidative Stress / drug effects
  • PC12 Cells
  • Rats
  • Rats, Wistar
  • Resveratrol
  • Stilbenes / toxicity*
  • Superoxide Dismutase / metabolism

Substances

  • Aluminum Compounds
  • Chlorides
  • Drug Combinations
  • Neuroprotective Agents
  • Stilbenes
  • Aluminum Chloride
  • Catalase
  • Cyclooxygenase 2
  • Ptgs2 protein, rat
  • Superoxide Dismutase
  • Glutathione Transferase
  • Acetylcholinesterase
  • Curcumin
  • Resveratrol