PUBLICATION

Anti-inflammatory potential of myristic acid and palmitic acid synergism against systemic candidiasis in Danio rerio (Zebrafish)

Authors
Prasath, K.G., Alexpandi, R., Parasuraman, R., Pavithra, M., Ravi, A.V., Pandian, S.K.
ID
ZDB-PUB-210101-14
Date
2021
Source
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie   133: 111043 (Journal)
Registered Authors
Keywords
Myristic acid, Palmitic acid, Synergism, Systemic candidiasis, Zebrafish
MeSH Terms
  • Animals
  • Anti-Inflammatory Agents/pharmacology*
  • Antifungal Agents/pharmacology*
  • Candida albicans/drug effects*
  • Candida albicans/growth & development
  • Candida albicans/pathogenicity
  • Candida tropicalis/drug effects*
  • Candida tropicalis/growth & development
  • Candida tropicalis/pathogenicity
  • Candidiasis/drug therapy*
  • Candidiasis/microbiology
  • Disease Models, Animal
  • Drug Synergism
  • Drug Therapy, Combination
  • Humans
  • Microbial Viability
  • Myristic Acid/pharmacology*
  • Palmitic Acid/pharmacology*
  • Virulence
  • Zebrafish
PubMed
33378951 Full text @ Biomed. Pharmacother.
Abstract
Nosocomial Candida colonization causes Systemic candidiasis in human with invasive infections in immunocompromised patients. Of all Candida spp., C. albicans is dominant in morbidity of all systemic candidiasis but C. tropicalis is phenomenal in mortality, virulence aspects and resistance development against antifungal drugs. The present study investigated the synergistic anti-virulent activity of myristic acid (MA) and palmitic acid (PA) against insidious dimorphic Candida spp. (C. albicans and C. tropicalis). In vitro and qPCR results revealed the mechanisms of MA-PA combination effectively inhibiting various virulence aspects such as biofilm, hyphal formation, secreted aspartyl proteases, lipases, ergosterol biosynthesis and drug effluxes. Further, in Danio rerio (Zebrafish), the MA-PA treatment increased the survival of animals and also the treated groups showed decreased level of fungal burden compared to the infected controls, after 3rd day of post infection. Histopathology of vital organs and SEM analysis of skin revealed a drastic recovery and reduced the inflammation of both Candida spp. infections in MA-PA treated animals. In addition, MA-PA treatment reduced the haemolysin and increased the susceptibility of Candida spp. in human blood model. Hence, this study suggested the therapeutic utilization of MA-PA as synergistic combination for their anti-inflammatory potency against systemic candidiasis and candidemia.
Genes / Markers
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Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
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Mapping