Natural Compounds Rosmarinic Acid and Carvacrol Counteract Aluminium-Induced Oxidative Stress
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
PubMed
32326410
PubMed Central
PMC7221925
DOI
10.3390/molecules25081807
PII: molecules25081807
Knihovny.cz E-zdroje
- Klíčová slova
- aluminum toxicity, brain, carvacrol, lipid peroxidation, liver, oxidative stress, rosmarinic acid,
- MeSH
- antioxidancia farmakologie MeSH
- biologické přípravky chemie farmakologie MeSH
- cinnamáty chemie farmakologie MeSH
- cymeny chemie farmakologie MeSH
- depsidy chemie farmakologie MeSH
- erytrocyty účinky léků metabolismus MeSH
- hliník škodlivé účinky chemie MeSH
- játra účinky léků metabolismus MeSH
- kyselina rozmarýnová MeSH
- malondialdehyd metabolismus MeSH
- mozek účinky léků metabolismus MeSH
- myši MeSH
- oxidační stres účinky léků MeSH
- peroxidace lipidů účinky léků MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antioxidancia MeSH
- biologické přípravky MeSH
- carvacrol MeSH Prohlížeč
- cinnamáty MeSH
- cymeny MeSH
- depsidy MeSH
- hliník MeSH
- malondialdehyd MeSH
Aluminum accumulation, glutathione (GSH) and malondialdehyde (MDA) concentrations as well as catalase (CAT) and superoxide dismutase (SOD) activities were determined in erythrocytes and brain and liver homogenates of BALB/c mice treated with Al3+ (7.5 mg/kg/day (0.15 LD50) as AlCl3 (37.08 mg/kg/day), whereas HCl (30.41 mg/kg/day) was used as Cl- control, the treatments were performed for 21 days, i.p., in the presence and absence of rosmarinic acid (0.2805 mg/kg/day (0.05 LD50), 21 days, i.g.) or carvacrol (0.0405 mg/kg/day (0.05 LD50), 21 days, i.g.). The treatment with AlCl3 increased GSH concentration in erythrocytes only slightly and had no effect on brain and liver homogenates. Rosmarinic acid and carvacrol strongly increased GSH concentration in erythrocytes but decreased it in brain and liver homogenates. However, AlCl3 treatment led to Al accumulation in mice blood, brain, and liver and induced oxidative stress, assessed based on MDA concentration in the brain and liver. Both rosmarinic acid and carvacrol were able to counteract the negative Al effect by decreasing its accumulation and protecting tissues from lipid peroxidation. AlCl3 treatment increased CAT activity in mice brain and liver homogenates, whereas the administration of either rosmarinic acid or carvacrol alone or in combination with AlCl3 had no significant effect on CAT activity. SOD activity remained unchanged after all the treatments in our study. We propose that natural herbal phenolic compounds rosmarinic acid and carvacrol could be used to protect brain and liver against aluminum induced oxidative stress leading to lipid peroxidation.
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