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Antioxidant agents and physiological responses in adult epileptic patients treated with lamotrigine
Authors:Elżbieta Płonka-Półtorak  Paweł Zagrodzki  Fergus Nicol  Jadwiga Kryczyk  Henryk Bartoń  Tuomas Westermarck  Pekka Kaipainen  Sakaewan Ounjaijean  Markus Kaski  Faik Atroshi
Affiliation:1. Antiepileptic Outpatient Clinic, Provincial Hospital No. 2, Lwowska 60, PL 35-301 Rzeszów, Poland;2. Department of Food Chemistry and Nutrition, Medical College, Jagiellonian University, Medyczna 9, PL 30-688 Kraków, Poland;3. Henryk Niewodniczański Institute of Nuclear Physics, Radzikowskiego 152, PL 31-342 Kraków, Poland;4. Vascular Health Division, Rowett Institute of Nutrition and Health, The University of Aberdeen, Bucksburn, Aberdeen AB21 9SB, UK;5. Rinnekoti Research Centre, FIN 02980 Espoo, Finland;6. Faculty of Pharmacy, Payap University, Chiang Mai 50000, Thailand;7. Department of Pharmacology and Toxicology, ELTDK, FIN 00014 University of Helsinki, Finland
Abstract:
BackgroundThe aim of our research was to evaluate some biochemical changes in blood during lamotrigine (LTG) monotherapy of adult patients with epilepsy, and to check possible associations between typical selenium status parameters and the frequency of seizures.MethodsThe study was performed by examining aspartate aminotransferase (AspAT), alanine aminotransferase (AlaAT), creatinine, ferric reducing ability of plasma (FRAP), serum uric acid (UA), uric-acid-independent FRAP (UAiFRAP), plasma glutathione peroxidase (GPX3), selenoprotein P (SelP), plasma superoxide dismutase (pSOD), 8-hydroxy-2’-deoxyguanosine (8-OHdG) in serum and urine, serum selenium (sSe) and zinc (sZn), in 22 adult patients with epilepsy and 22 healthy controls. Additionally, the levels of LTG were determined in patients.ResultspSOD activity was higher in the study group (5.32 ± 1.24 U/ml) compared with the controls (4.05 ± 0.92 U/ml, p = 0.008). No other statistical difference between patients and controls was found.ConclusionLack of difference in parameters other than SOD, particularly no difference in 8-OHdG concentrations between the patients treated with LTG compared to the control subjects suggests that these patients are at no particular risk of oxidative DNAdamage. In patients who are well or moderately well clinically controlled, selenium status parameters (sSe, GPX3, SelP) are not directly connected with the frequency of seizures.
Keywords:epilepsy  lamotrigine  oxidative stress  selenium  superoxide dismutase
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