Asiatic acid nullified aluminium toxicity in in vitro model of Alzheimer’s disease

Mashoque Ahmad Rather, Arokiasamy Justin Thenmozhi, Thamilarasan Manivasagam, Jegadeesan Nataraj, Mohamed Musthafa Essa, Saravana Babu Chidambaram

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Aluminium (Al) is a ubiquitously distributed environmental toxicant that lacks biological functions; however, its accumulation in the brain has been demonstrated to be linked to several neuropathological conditions particularly Alzheimer’s disease (AD). Asiatic acid (AA), a triterpene extracted from Centella asiatica, has been reported to cross the blood brain barrier and also displayed antioxidant and neuroprotective activities. The present study was aimed to explore the neuroprotective effect of AA against aluminium maltolate (Al(mal)3) induced neurotoxicity by assessing cell viability, mitochondrial membrane potential, levels of reactive oxygen species (ROS), DNA damage and apoptosis (Hoechst and dual staining, comet assay; expressions of pro-apoptotic, anti-apoptotic and signaling indices) via AKT/GSK-3β signaling pathway in SH-SY 5Y neuroblastoma cells. Pre-treatment with AA significantly enhanced cell viability, attenuated rotenone-induced ROS, mitochondrial membrane dysfunction and apoptosis regulating AKT/GSK-3β signaling pathway. Downregulation of Al induced neurodegeneration may be one of the approaches to control the impairment of metal ion homeostasis leading to neuronal injury in early development of AD. However, more extensive work in animal model is desirable to confirm its neuroprotective action.

Original languageEnglish
Pages (from-to)287-299
Number of pages13
JournalFrontiers in Bioscience - Elite
Volume10
Issue number2
Publication statusPublished - Jan 1 2018

Fingerprint

Aluminum
Glycogen Synthase Kinase 3
Toxicity
Alzheimer Disease
Reactive Oxygen Species
Cell Survival
Centella
Cells
Apoptosis
Membranes
Rotenone
Triterpenes
Comet Assay
Mitochondrial Membrane Potential
Mitochondrial Membranes
Neuroprotective Agents
Blood-Brain Barrier
Neuroblastoma
DNA Damage
Metal ions

Keywords

  • Acid
  • AKT/GSK-3β signaling pathway
  • Aluminium Maltolate
  • Apoptosis
  • Mitochondrial dysfunction
  • Oxidative stress

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)

Cite this

Rather, M. A., Thenmozhi, A. J., Manivasagam, T., Nataraj, J., Essa, M. M., & Chidambaram, S. B. (2018). Asiatic acid nullified aluminium toxicity in in vitro model of Alzheimer’s disease. Frontiers in Bioscience - Elite, 10(2), 287-299.

Asiatic acid nullified aluminium toxicity in in vitro model of Alzheimer’s disease. / Rather, Mashoque Ahmad; Thenmozhi, Arokiasamy Justin; Manivasagam, Thamilarasan; Nataraj, Jegadeesan; Essa, Mohamed Musthafa; Chidambaram, Saravana Babu.

In: Frontiers in Bioscience - Elite, Vol. 10, No. 2, 01.01.2018, p. 287-299.

Research output: Contribution to journalArticle

Rather, MA, Thenmozhi, AJ, Manivasagam, T, Nataraj, J, Essa, MM & Chidambaram, SB 2018, 'Asiatic acid nullified aluminium toxicity in in vitro model of Alzheimer’s disease', Frontiers in Bioscience - Elite, vol. 10, no. 2, pp. 287-299.
Rather MA, Thenmozhi AJ, Manivasagam T, Nataraj J, Essa MM, Chidambaram SB. Asiatic acid nullified aluminium toxicity in in vitro model of Alzheimer’s disease. Frontiers in Bioscience - Elite. 2018 Jan 1;10(2):287-299.
Rather, Mashoque Ahmad ; Thenmozhi, Arokiasamy Justin ; Manivasagam, Thamilarasan ; Nataraj, Jegadeesan ; Essa, Mohamed Musthafa ; Chidambaram, Saravana Babu. / Asiatic acid nullified aluminium toxicity in in vitro model of Alzheimer’s disease. In: Frontiers in Bioscience - Elite. 2018 ; Vol. 10, No. 2. pp. 287-299.
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