Affiliations 

  • 1 Faculty of Medicine and Health Sciences, School of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, United Kingdom; School of Biosciences, University of Nottingham, Loughborough LE12 5RD, United Kingdom; Rivers State University, Nkpolu - Oroworukwo P.M.B 5080, Port Harcourt, Rivers, Nigeria
  • 2 Department of Biomedical Science, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Bertam Campus, Kepala Batas, Pulau Pinang 13200, Malaysia
  • 3 Academic Ophthalmology, School of Medicine, University of Nottingham, Nottingham NG7 2RD, United Kingdom
  • 4 Academic Ophthalmology, School of Medicine, University of Nottingham, Nottingham NG7 2RD, United Kingdom; Department of Ophthalmology, Queen's Medical Centre, Nottingham NG7 2UH, United Kingdom
  • 5 School of Science and Technology, Nottingham Trent University, Nottingham NG11 8NS, United Kingdom
  • 6 Laboratory of Parasitic Diseases, College of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi 030801, China
  • 7 School of Biosciences, University of Nottingham, Loughborough LE12 5RD, United Kingdom
  • 8 Faculty of Medicine and Health Sciences, School of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, United Kingdom. Electronic address: [email protected]
Acta Trop, 2023 Jan;237:106729.
PMID: 36280206 DOI: 10.1016/j.actatropica.2022.106729

Abstract

We examined the anti-acanthamoebic efficacy of green tea Camellia sinensis solvent extract (SE) or its chemical constituents against Acanthamoeba castellanii by using anti-trophozoite, anti-encystation, and anti-excystation assays. C. sinensis SE (625-5000 µg/mL) inhibited trophozoite replication within 24-72 h. C. sinensis SE exhibited a dose-dependent inhibition of encystation, with a marked cysticidal activity at 2500-5000 µg/mL. Two constituents of C. sinensis, namely epigallocatechin-3-gallate and caffeine, at 100 μM and 200 μM respectively, significantly inhibited both trophozoite replication and encystation. Cytotoxicity analysis showed that 156.25-2500 µg/mL of SE was not toxic to human corneal epithelial cells, while up to 625 µg/mL was not toxic to Madin-Darby canine kidney cells. This study shows the anti-acanthamoebic potential of C. sinensis SE against A. castellanii trophozoites and cysts. Pre-clinical studies are required to elucidate the in vivo efficacy and safety of C. sinensis SE.

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