Anti‐ictogenic and antiepileptogenic properties of brivaracetam in mature and immature rats. (25th March 2015)
- Record Type:
- Journal Article
- Title:
- Anti‐ictogenic and antiepileptogenic properties of brivaracetam in mature and immature rats. (25th March 2015)
- Main Title:
- Anti‐ictogenic and antiepileptogenic properties of brivaracetam in mature and immature rats
- Authors:
- Dupuis, Nina
Matagne, Alain
Staelens, Ludovicus
Dournaud, Pascal
Desnous, Béatrice
Gressens, Pierre
Auvin, Stéphane - Abstract:
- <abstract abstract-type="main" id="epi12973-abs-0001"> <title>Summary</title> <sec id="epi12973-sec-0001" sec-type="section"> <title>Objective</title> <p>Brivaracetam (BRV) is a new antiepileptic drug candidate rationally designed for high affinity and selectivity for the synaptic vesicle protein 2A. This study explored anti‐ictogenic and antiepileptogenic effects of BRV in rats at different stages of development.</p> </sec> <sec id="epi12973-sec-0002" sec-type="section"> <title>Methods</title> <p>Using a rapid kindling model in P14, P21, P28, and P60 rats, we studied two doses of BRV: 10 and 100 mg/kg injected intraperitoneally 30 min before afterdischarge assessment. We also assessed blood and brain concentrations of BRV 30 min after the injection.</p> </sec> <sec id="epi12973-sec-0003" sec-type="section"> <title>Results</title> <p>BRV 100 mg/kg significantly increased the afterdischarge threshold (ADT) at all ages, whereas BRV at 10 mg/kg increased ADT in P60, P28, and P21 rats. BRV also shortens the afterdischarge duration (ADD), achieving statistical significance with 10 and 100 mg/kg at P60 and with 100 mg/kg at P21. At P60, BRV increases the number of stimulations required to achieve a stage 4–5 seizure in a dose‐dependent manner. At P28 and P21, BRV increased the number of stimulations required to develop a stage 4–5 seizure in a dose‐dependent manner with almost complete elimination of stage 4–5 seizures. In contrast, at P14, BRV had no effect on the number of stage<abstract abstract-type="main" id="epi12973-abs-0001"> <title>Summary</title> <sec id="epi12973-sec-0001" sec-type="section"> <title>Objective</title> <p>Brivaracetam (BRV) is a new antiepileptic drug candidate rationally designed for high affinity and selectivity for the synaptic vesicle protein 2A. This study explored anti‐ictogenic and antiepileptogenic effects of BRV in rats at different stages of development.</p> </sec> <sec id="epi12973-sec-0002" sec-type="section"> <title>Methods</title> <p>Using a rapid kindling model in P14, P21, P28, and P60 rats, we studied two doses of BRV: 10 and 100 mg/kg injected intraperitoneally 30 min before afterdischarge assessment. We also assessed blood and brain concentrations of BRV 30 min after the injection.</p> </sec> <sec id="epi12973-sec-0003" sec-type="section"> <title>Results</title> <p>BRV 100 mg/kg significantly increased the afterdischarge threshold (ADT) at all ages, whereas BRV at 10 mg/kg increased ADT in P60, P28, and P21 rats. BRV also shortens the afterdischarge duration (ADD), achieving statistical significance with 10 and 100 mg/kg at P60 and with 100 mg/kg at P21. At P60, BRV increases the number of stimulations required to achieve a stage 4–5 seizure in a dose‐dependent manner. At P28 and P21, BRV increased the number of stimulations required to develop a stage 4–5 seizure in a dose‐dependent manner with almost complete elimination of stage 4–5 seizures. In contrast, at P14, BRV had no effect on the number of stage 4–5 seizures. An age‐related decrease in blood and brain concentrations of BRV was observed 30 min after injection of BRV 10 mg/kg, whereas with 100 mg/kg there were no significant age‐correlated differences in brain and serum BRV concentrations.</p> </sec> <sec id="epi12973-sec-0004" sec-type="section"> <title>Significance</title> <p>BRV exerted dose‐dependent anti‐ictogenic effects from P60 to P14 independent of brain maturation. BRV also exhibited antiepileptogenic effects at P60, whereas this effect need to be further evaluated at P28 and P21. We did not observe any effect on epileptogenesis at P14 at either dose.</p> </sec> </abstract> … (more)
- Is Part Of:
- Epilepsia. Volume 56:issue 5(2015:May)
- Journal:
- Epilepsia
- Issue:
- Volume 56:issue 5(2015:May)
- Issue Display:
- Volume 56, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 56
- Issue:
- 5
- Issue Sort Value:
- 2015-0056-0005-0000
- Page Start:
- 800
- Page End:
- 805
- Publication Date:
- 2015-03-25
- Subjects:
- Epilepsy -- Periodicals
616.853 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=epi ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/epi.12973 ↗
- Languages:
- English
- ISSNs:
- 0013-9580
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3793.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3791.xml