| Literature DB >> 34997711 |
Natalija Arsenijevic1, Dragica Selakovic2, Jelena S Katanic Stankovic3, Vladimir Mihailovic4, Slobodanka Mitrovic5, Jovana Milenkovic1, Pavle Milanovic1, Miroslav Vasovic1, Aleksandra Nikezic6, Olivera Milosevic-Djordjevic6,7, Marko Zivanovic3,8, Nenad Filipovic8,9, Vladimir Jakovljevic2,10, Nemanja Jovicic11, Gvozden Rosic2.
Abstract
We evaluated the influence of an antioxidant-rich extract of Filipendula ulmaria L. on anxiety levels induced by nano-sized particles of different calcium phosphates. Rats in experimental groups were administered with either nano-sized hydroxyapatite, tricalcium phosphate, or amorphous calcium phosphate in the presence of Filipendula ulmaria extract. Appropriate behavioral tests were performed to assess anxiety levels, while oxidative status and apoptosis parameters were determined in the hippocampus samples. The applied calcium phosphates increased oxidative stress markers in hippocampal tissue, accompanied by an enhanced pro-apoptotic mechanism. Moreover, the hippocampal immunoreactivity for brain-derived neurotrophic factor and GABAergic-A receptors was significantly lower following calcium phosphate nanoparticles intake. The observed functional and morphological alterations in the rat hippocampus occurred simultaneously with the anxiogenic response estimated in behavioral testing. The neuroprotective effect of Filipendula ulmaria was markedly manifested by the attenuation of oxidative damage induced by amorphous calcium phosphate and enhanced anti-apoptotic action in the rat hippocampus. The increased hippocampal immunoreactivity for brain-derived neurotrophic factor, GABAergic-A receptors and significant anxiolytic-like effects of Filipendula ulmaria may suggest a beneficial role of antioxidant supplementation in preventing anxiogenic response to nano-sized calcium phosphates.Entities:
Keywords: Anxiety; Apoptosis; Behavior; Calcium phosphates nanoparticles; Filipendula ulmaria; Oxidative stress
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Year: 2021 PMID: 34997711 DOI: 10.31083/j.jin2004089
Source DB: PubMed Journal: J Integr Neurosci ISSN: 0219-6352 Impact factor: 2.117