Benzophenone-2 Concentration and Its Effect on Oxidative Stress and Apoptosis Markers in Rat Brain
Autor: | Weronika Krzyżanowska, Maria Walczak, Bartosz Pomierny, Beata Bystrowska, Beata Starek-Świechowicz, Żaneta Broniowska, Bogusława Budziszewska |
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Rok vydání: | 2019 |
Předmět: |
Male
0301 basic medicine medicine.medical_specialty Brain concentration Hippocampus Adipose tissue Apoptosis Toxicology medicine.disease_cause Benzophenones 03 medical and health sciences 0302 clinical medicine Benzophenone-2 UV filters Internal medicine medicine Animals Rats Wistar Chemistry General Neuroscience Sex hormone receptor Rat brain In vitro Frontal Lobe Oxidative Stress 030104 developmental biology Endocrinology Original Article 030217 neurology & neurosurgery Oxidative stress |
Zdroj: | Neurotoxicity Research |
ISSN: | 1476-3524 1029-8428 |
DOI: | 10.1007/s12640-019-0011-y |
Popis: | Benzophenones, frequently used as UV chemical filters, are absorbed through the skin and can exert systemic adverse effects. So far, most of the data are related to their action on sex hormone receptors whereas potential neurotoxic effect is expected mainly on the basis of in vitro studies. The aim of the present study was to determine concentrations of BP-2, oxidative stress and apoptosis markers in the rat brain after topical administration of this compound. Male Wistar rats were treated dermally with BP-2 (100 mg/kg, 4 weeks), and next, blood and tissue BP-2 concentrations and oxidative stress and apoptotic markers in the frontal cortex and hippocampus were determined. After dermal BP-2 administration, blood level of this compound was about 300 ng/ml while in the liver and adipose tissue 1354 and 823 ng/g wt tissue, respectively. In the studied brain structures, the levels of the test compound were from 5 to 19 ng/g tissue. In the hippocampus, where BP-2 level was about 3.5-fold lower than in the frontal cortex, no significant changes in either oxidative stress and apoptosis markers were observed. There was also no change in apoptosis markers in the frontal cortex but unexpectedly the oxidative stress markers were reduced. The research showed that BP-2 passes through the blood-brain barrier but its concentration in the brain structures are much lower than in the blood. This compound did not exacerbate oxidative stress and apoptosis markers in the hippocampus and frontal cortex, and even lowered oxidative stress in the frontal cortex. |
Databáze: | OpenAIRE |
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