Palliative effect of Moringa olifera-mediated zinc oxide nanoparticles against acrylamide-induced neurotoxicity in rats

Food Chem Toxicol. 2023 Jan:171:113537. doi: 10.1016/j.fct.2022.113537. Epub 2022 Nov 26.

Abstract

Repeated acrylamide (ACR) exposure in experimental animals and humans causes variable degrees of neuronal damage. Because of its unique features, several green synthesized nanomaterials are explored for neuromodulatory activity. Hence, this study investigated the effect of green synthesized zinc oxide nanoparticles using Moriga olifera leaves extract (MO-ZnONP) against acrylamide (ACR)-induced neurobehavioral and neurotoxic impacts in rat. Forty male Sprague Dawley rats were distributed into four groups orally given distilled water, MO-ZnONP (10 mg/kg b.wt), ACR (20 mg/kg b.wt), or MO-ZnONP + ACR for 60 days. Gait quality and muscular, motor, and sensory function were assessed. Acetylcholinesterase (AChE), dopamine, catalase, malondialdehyde (MDA), and Zn brain contents were determined. Brain histopathology and immunohistochemical localization of the amyloid-β protein and abnormal Tau were performed. The results revealed that MO-ZnONP significantly reduced ACR-induced sensory dysfunctions, hind limb abnormality, and motor deficits. Additionally, the ACR-induced increase in dopamine and AChE were significantly supressed by MO-ZnONP. Besides, MO-ZnONP significantly restored catalase and Zn content but reduced increased MDA brain content resulting from ACR. Furthermore, the ACR-induced neurodegenerative changes and increased amyloid-β and phosphorylated Tau immunoexpression was significantly abolished by MO-ZnONP. Conclusively, MO-ZnONP could be used as a biologically effective compound for mitigating ACR's neurotoxic and neurobehavioral effects.

Keywords: Acrylamide; Amyloid-β; Green synthesis; Moringa olifera; Sensorimotor functions; Zinc oxide nanoparticles.

MeSH terms

  • Acetylcholinesterase / metabolism
  • Acrylamide / toxicity
  • Animals
  • Catalase / metabolism
  • Dopamine
  • Humans
  • Male
  • Nanoparticles*
  • Neurotoxicity Syndromes* / etiology
  • Oxidative Stress
  • Rats
  • Rats, Sprague-Dawley
  • Zinc Oxide* / pharmacology

Substances

  • Catalase
  • Zinc Oxide
  • Acrylamide
  • Acetylcholinesterase
  • Dopamine