Literature DB >> 19016076

Early effects of sodium valproate monotherapy on serum paraoxonase/arylesterase activities.

George A Karikas1, Kleopatra H Schulpis, Anastasia Bartzeliotou, Spyros Regoutas, Christina Thanopoulou, Vassiliki Papaevangelou, Aglaia Giannoulia-Karantana, Ioannis Papassotiriou, Athena Fytou-Pallikari.   

Abstract

OBJECTIVE: Valproic acid (VPA) treatment and paraoxonase1/arylesterase (PON1/Aryl) activities are related to the production of free radicals. Our aim was to study the PON1/Aryl activities in children on VPA therapy.
MATERIAL AND METHODS: Thirty-two children with seizures and 30 healthy child volunteers took part. Ill children underwent the common laboratory tests, as well as total antioxidant status (TAS), total oxidant status (TOS), lipid profile, liver enzymes and PON1/Aryl activities pre- and post-60 days on VPA therapy (30 mg/kg/24 h), whereas the healthy children were tested just once.
RESULTS: None of the studied biochemical parameters differed between volunteers and children with seizures pretreatment. Liver enzymes, lipids and TOS levels (124+/-30 versus 580+/-40 micromol/L; p<0.001) were significantly elevated, whereas the activities of PON1/Aryl (146+/-43 versus 118+/-40 U/mL/min 120+/-42 versus 98+/-38 KU/mL/min; p<0.01) and TAS levels (436+/-42 versus 288+/-39 micromol/L; p<0.001) were decreased in children after treatment. Additionally, strong negative correlations were found between PON1/Aryl activities, liver enzymes, TOS (r = -0.69) and VPA levels (r = -0.57), whereas PON1/Aryl activities correlated positively with TAS, HDL and Apo A-I in all groups.
CONCLUSIONS: Serum PON1/Aryl activities were decreased after 60 days on VPA treatment, probably due to liver dysfunction and free radicals production by VPA, without excluding the possibility of a direct action of the drug on the enzymes.

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Year:  2009        PMID: 19016076     DOI: 10.1080/00365510802248051

Source DB:  PubMed          Journal:  Scand J Clin Lab Invest        ISSN: 0036-5513            Impact factor:   1.713


  4 in total

1.  Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment.

Authors:  Nilüfer Dönmezdil; Mehmet Uğur Çevik; Hasan Hüseyin Özdemir; Muhterem Taşin
Journal:  Neuropsychiatr Dis Treat       Date:  2016-04-22       Impact factor: 2.570

2.  Carveol Attenuates Seizure Severity and Neuroinflammation in Pentylenetetrazole-Kindled Epileptic Rats by Regulating the Nrf2 Signaling Pathway.

Authors:  Arooj Mohsin Alvi; Lina Tariq Al Kury; Abdullah Alattar; Ikram Ullah; Asmaa Jan Muhammad; Reem Alshaman; Fawad Ali Shah; Arif Ullah Khan; Jinxing Feng; Shupeng Li
Journal:  Oxid Med Cell Longev       Date:  2021-08-11       Impact factor: 6.543

3.  1,3,4, Oxadiazole Compound A3 Provides Robust Protection Against PTZ-Induced Neuroinflammation and Oxidative Stress by Regulating Nrf2-Pathway.

Authors:  Arooj Mohsin Alvi; Fawad Ali Shah; Asmaa Jan Muhammad; Jinxing Feng; Shupeng Li
Journal:  J Inflamm Res       Date:  2021-12-29

4.  The role of reactive species in epileptogenesis and influence of antiepileptic drug therapy on oxidative stress.

Authors:  Boštjan Martinc; Iztok Grabnar; Tomaž Vovk
Journal:  Curr Neuropharmacol       Date:  2012-12       Impact factor: 7.363

  4 in total

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