Affiliations 

  • 1 Centre for Drug Research, Universiti Sains Malaysia, Penang, Malaysia
  • 2 School of Chemical Sciences, Universiti Sains Malaysia, Penang, Malaysia
  • 3 Department of Neurosciences, School of Medical Sciences, USM Health Campus Kota Bharu, Kelantan, Malaysia
  • 4 Centre for Drug Research, Universiti Sains Malaysia, Penang, Malaysia; Discipline of Pharmacology, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Penang, Malaysia
  • 5 Centre for Drug Research, Universiti Sains Malaysia, Penang, Malaysia. Electronic address: zurina_hassan@usm.my
Ageing Res Rev, 2023 Aug;89:101990.
PMID: 37343678 DOI: 10.1016/j.arr.2023.101990

Abstract

Research employing a bio-enhanced fraction of Clitoria ternatea (CT) to treat cognitive decline in the animal model has not yet been found. This study aimed to determine the neuroprotective effect of CT root bioactive fraction (CTRF) in chronic cerebral hypoperfusion (CCH) rat model. CTRF and its major compound, clitorienolactones A (CLA), were obtained using column chromatography. A validated HPLC-UV method was employed for the standardization of CTRF. CCH rats were given orally either vehicle or fraction (10, 20 and 40 mg/kg). Behavioural and hippocampal neuroplasticity studies were conducted following 4 weeks post-surgery. The brain hippocampus was extracted for proteins and neurotransmitters analyses. HPLC analysis showed that CTRF contained 25% (w/w) of CLA. All tested doses of CTRF and CLA (10 mg/kg) significantly restored cognitive deficits and reversed the inhibition of neuroplasticity by CCH. However, only CTRF (40 mg/kg) and CLA (10 mg/kg) significantly reversed the elevation of amyloid-beta plaque. Subsequently, treatment with CTRF (40 mg/kg) and CLA (10 mg/kg) alleviated the downregulation of molecular synaptic signalling proteins levels caused by CCH. The neurotransmitters level was restored following treatment of CTRF and CLA. Our finding suggested that CTRF improves memory and neuroplasticity in CCH rats which was mainly contributed by CLA.

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