Detailed Information on Publication Record
2020
Natural Compounds Rosmarinic Acid and Carvacrol Counteract Aluminium-Induced Oxidative Stress
BARANAUSKAITE, J., I. SADAUSKIENE, A. LIEKIS, A. KASAUSKAS, R. LAZAUSKAS et. al.Basic information
Original name
Natural Compounds Rosmarinic Acid and Carvacrol Counteract Aluminium-Induced Oxidative Stress
Authors
BARANAUSKAITE, J., I. SADAUSKIENE, A. LIEKIS, A. KASAUSKAS, R. LAZAUSKAS, U. ZLABIENE (guarantor), Ruta MASTEIKOVÁ (203 Czech Republic, belonging to the institution), D. M. KOPUSTINSKIENE and J. BERNATONIENE
Edition
Molecules, Orlando, Florida, Academic Press, 2020, 1079-9796
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30104 Pharmacology and pharmacy
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.039
RIV identification code
RIV/00216224:14160/20:00118195
Organization unit
Faculty of Pharmacy
UT WoS
000534617300029
Keywords in English
aluminum toxicity; rosmarinic acid; carvacrol; oxidative stress; lipid peroxidation; brain; liver
Tags
International impact, Reviewed
Změněno: 24/2/2021 08:23, Mgr. Hana Hurtová
Abstract
V originále
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.