Betulinic acid attenuates cognitive dysfunction, oxidative stress, and inflammation in a model of T-2 toxin-induced brain damage

Environ Sci Pollut Res Int. 2022 Jul;29(34):52098-52110. doi: 10.1007/s11356-022-19498-z. Epub 2022 Mar 7.

Abstract

T-2 toxin is a mycotoxin that has harmful effects on the immune system and cognitive function. Betulinic acid (BA) is a plant-derived pentacyclic lupane-type triterpenoid which possesses a wide spectrum of bioactivities. The study was aimed to explore whether BA has a protective effect on cognitive impairment and oxidative stress caused by T-2 toxin. BA was suspended in 1% soluble starch by continuous intragastric administration for 14 days, then the brain damage in mice was induced by a single intraperitoneal injection of T-2 toxin (4 mg/kg). It was found that BA alleviated the reduction of discrimination index in T-2 toxin-treated mice, and enhanced dopamine (DA), 5-hydroxytryptamine (5-HT), and acetylcholine (ACH) levels of brain neurotransmitter. Meanwhile, BA pretreatment ameliorated oxidative stress through increase of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), and glutathione (GSH) levels, and inhibition of the generation of reactive oxygen species (ROS) and malondialdehyde (MDA) in the brain of mice exposed to T-2 toxin. Moreover, BA reduced brain hemorrhage and ecchymosis, improved the mitochondrial morphology, enriched the number of organelles, and inhibited cell apoptosis in brain challenged with T-2 toxin. Furthermore, BA inhibited mRNA expression of pro-inflammatory cytokines such as interleukin-1β (IL-1β), IL-6, and tumor necrosis factor-α (TNF-α) as well as enhanced mRNA expression of anti-inflammatory cytokine such as IL-10 in the brain of T-2 toxin-triggered mice. Therefore, BA could improve the cognitive function, enhance the antioxidant capacity, and inhibit the secretion of proinflammatory cytokines in brain, thereby playing a preventive and protective role against brain damage caused by T-2 toxin.

Keywords: Betulinic acid; Brain; Cognitive ability; Inflammatory cytokines; Oxidative damage; T-2 toxin.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Betulinic Acid
  • Brain
  • Cognitive Dysfunction* / chemically induced
  • Cytokines / metabolism
  • Glutathione / metabolism
  • Inflammation / chemically induced
  • Mice
  • Oxidative Stress
  • Pentacyclic Triterpenes / pharmacology
  • RNA, Messenger / metabolism
  • T-2 Toxin* / metabolism
  • T-2 Toxin* / toxicity

Substances

  • Antioxidants
  • Cytokines
  • Pentacyclic Triterpenes
  • RNA, Messenger
  • Glutathione
  • T-2 Toxin
  • Betulinic Acid