Affiliations 

  • 1 Department of Human Anatomy, Faculty of Medicine and Health Sciences Universiti Putra Malaysia, Serdang Selangor, Malaysia; Department of Human Anatomy, College of Medical Sciences University of Maiduguri, Borno state, Nigeria
  • 2 Department of Human Anatomy, Faculty of Medicine and Health Sciences Universiti Putra Malaysia, Serdang Selangor, Malaysia. Electronic address: [email protected]
  • 3 Department of Human Anatomy, Faculty of Medicine and Health Sciences Universiti Putra Malaysia, Serdang Selangor, Malaysia
  • 4 Faculty of Health Sciences UiTM Campus Puncak Alam, Puncak Alam Selangor, Malaysia
Biomed Pharmacother, 2018 Jul;103:1602-1608.
PMID: 29864948 DOI: 10.1016/j.biopha.2018.04.152

Abstract

Cognitive impairments and cholinergic dysfunctions have been well reported in old age disorders including Alzheimer's disease (AD). d-galactose (D-gal) has been reported as a senescence agent while aluminium act as a neurotoxic metal, but little is known about their combined effects at different doses. The aim of this study was to establish an animal model with cognitive impairments by comparing the effects of different doses of co-administrated D-gal and aluminium chloride (AlCl3). In this study male albino wistar rats were administered with D-gal 60 mg/kg.bwt intra peritoneally (I.P) injected and AlCl3 (100, 200, or 300 mg/kg.bwt.) was orally administered once daily for 10 consecutive weeks. Performance of the rats were evaluated through behavioural assessments; Morris water maze (MWM) and open field tests (OFT); histopathological examination was performed on the hippocampus; moreover biochemical measurements of acetylcholinesterase (AChE) and hyperphosphorylated tau protein (p-tau) were examined. The results of this experiment on rats treated with D-gal 60 + AlCl3 200 mg/kg.bwt showed near ideal cognitive impairments. The rats exhibited an obvious memory and learning deficits, marked neuronal loss in hippocampus, showed increase in AChE activities and high expression of p-tau within the tissues of the brain. This study concludes that D-gal 60 + AlCl3 200 mg/kg.bwt as the ideal dose for mimicking AD like cognitive impairments in albino wistar rats. It is also crucial to understand the pathogenesis of this neurodegenerative disease and for drug discovery.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.