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    A novel approach in the treatment of osteoarthritis: In vitro and in vivo evaluation of Allium sativum microemulsion
    (Wiley, 2022) Okur, Mehmet Evren; Kolbaşı, Bircan; Şahin, Mustafa; Karadağ, Ayşe Esra; Reis, Rengin; Çağlar, Emre Şefik; Kaplan, Arife Ahsen; Sipahi, Hande; Keskin, İlknur; Demiralp, Bahtiyar; Üstündağ Okur, Neslihan
    Osteoarthritis (OA) is the most prevalent kind of joint disease, affecting millions of individuals worldwide. Allium sativum L. was used as a therapeutic agent in the microemulsion system against osteoarthritis due to allicin's high antioxidant and anti-inflammatory effects. HPLC was used to evaluate the chemical components of the Allium sativum methanol extract. Water-in-oil (w/o) type of microemulsions loaded with Allium sativum extract was produced. To create the microemulsions, a titration approach was employed. The microemulsions were prepared using isopropyl myristate (IPM) as oil, Polysorbate 60, Sorbitan monolaurate 80 as surfactants, and Polyethylene glycol 400, ethanol as cosurfactants. The pH, droplet size, viscosity, polydispersity index values were measured to characterize of microemulsions. In addition, L929 healthy mouse fibroblasts and CHON-001 healthy human cartilage fibroblast cells were tested for cytocompatibility in vitro. The therapeutic potential of Allium sativum microemulsion was investigated in rats that had osteoarthritis surgically simulated. HPLC analysis revealed a significant concentration of allicin in the extract. The titration approach was used to create an A. sativum microemulsion (AS) with a narrow droplet size and PDI range. In L929 and CHON-001 cells, cytocompatibility experiments revealed that the maximum dosages of AS microemulsion 5% (v/v) exerted 93.41 +/- 3.11% and 75.59 +/- 2.69% cell viabilities, respectively. Different concentrations of AS (1.25%, 2.5%, and 5% v/v) demonstrated cytoprotective efficacy against H2O2-induced oxidative damage. When compared to the control group, in vivo investigations revealed fewer irregularities on the articular surface and typically arranged chondrocytes in the positive control and treated groups.
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    Energy drink induced lipid peroxidation and oxidative damage in rat liver and brain when used alone or combined with alcohol
    (Wiley, 2017) Reis, Rengin; Charehsaz, Mohammad; Sipahi, Hande; Doğan Ekici, Asiye Işın; Macit, Çağlar; Akkaya, Hatice; Aydın, Ahmet
    Energy drinks (ED) are containing large doses of metabolic stimulants and its use with ethanol has increased dramatically among young adults. In this study, we examined the effects of ED exposure either alone or in combination with ethanol on oxidative stress parameters including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), and lipid peroxidation parameter malondialdehyde (MDA) in rat. Some histopathological findings were also evaluated. ED exposure led to a dose-dependent increase in liver MDA compared to the control indicating oxidative damage. Histopathological findings also revealed that ED alone may generate liver damage. Ethanol exposure increased MDA level and SOD, CAT, and GSH-Px activity in both the brain and the liver. The combination of ethanol and ED produced greater damage which is considered by further increases in SOD and GSH-Px activity in the brain. Similar results for MDA were observed in both the liver and brain as well. Our findings suggest that ED consumption alone or combination with ethanol may represent a significant public health concern.
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    Phytochemical and in vitro pharmacological evaluation of Phlomis Pungens
    (Ankara University, 2022) Okur, Mehmet Evren; Karadağ, Ayşe Esra; Reis, Rengin; Sipahi, Hande; Arslan, Rana; Demirci, Betül; Demirci, Fatih
    Objective: This study aimed to investigate the in vitro wound healing, anti-inflammatory, antimicrobial and antioxidant activity of Phlomis pungens Willd. extract derived from the aerial parts. Material and Method: The phytochemical analysis was performed using GC-MS in order to identify the volatile components of the bioactive Hex extract. The wound healing activity of P. pungens extract was evaluated based on in vitro antimicrobial, antioxidant, anti-inflammatory, and, scratch activity was studied. In addition, the in vitro cytotoxicity of the extract was also evaluated. Result and Discussion: P. pungens methanol extract depicted a 5-LOX inhibitory activity at 78.2µg/mL (IC50), while the antioxidant activity by DPPH radical provided an IC50=2.41mg/mL, and the ABTS radical showed IC50=3.32mg/mL, respectively. The extract showed dose-dependently anti-inflammatory activity while L-NAME and P. pungens methanol extract significantly decreased LPS stimulated PGE2 production. According to the scratch assay results, all treatments led to an increase in cell migration rate with a dose-dependent effect. Our findings suggested that P. pungens methanol extract may have a role in wound healing according to the scratch test, and it is thought that its antioxidant and anti-inflammatory activity also contributed. Further evaluations are ongoing to confirm the in vitro activity under in vivo conditions.