EFFECTS OF ANTIEPILEPTIC DRUGS ON SPREADING DEPRESSION IN THE CHICK RETINA: IMPLICATIONS FOR MIGRAINE PROPHYLAXIS

Author(s):  
João Baptista Mascarenhas de Moraes Neto ◽  
Hiss Martins- Ferreira ◽  
Jean Cristopher Houzel ◽  
Lenny Abreu Cavalcante ◽  
Gilmar da Silva Aleixo ◽  
...  
Cephalalgia ◽  
2009 ◽  
Vol 29 (10) ◽  
pp. 1095-1114 ◽  
Author(s):  
C Ayata

Despite the relatively well-characterized headache mechanisms in migraine, upstream events triggering individual attacks are poorly understood. This lack of mechanistic insight has hampered a rational approach to prophylactic drug discovery. Unlike targeted abortive and analgesic interventions, mainstream migraine prophylaxis has been largely based on serendipitous observations (e.g. propranolol) and presumed class effects (e.g. anticonvulsants). Recent studies suggest that spreading depression is the final common pathophysiological target for several established or investigational migraine prophylactic drugs. Building on these observations, spreading depression can now be explored for its predictive utility as a preclinical drug screening paradigm in migraine prophylaxis.


Cephalalgia ◽  
2010 ◽  
Vol 31 (5) ◽  
pp. 537-542 ◽  
Author(s):  
Ulrike Hoffmann ◽  
Ergin Dileköz ◽  
Chiho Kudo ◽  
Cenk Ayata

Background: Cortical spreading depression is the electrophysiological substrate of migraine aura, and may trigger headache. Recently, chronic treatment with five migraine prophylactic drugs was shown to suppress cortical spreading depression, implicating spreading depression as a common therapeutic target in migraine prophylaxis. Materials and methods: In order to assess the negative predictive value of spreading depression susceptibility as a preclinical drug screening tool, we tested oxcarbazepine, an anti-epileptic ineffective in migraine prophylaxis. Valproate served as the positive control. Cortical spreading depression susceptibility was measured in rats using topical KCl or electrical stimulation. Results: Oxcarbazepine did not suppress spreading depression either after a single dose or after daily treatment for 5 weeks. As previously shown, valproate suppressed spreading depression susceptibility after chronic dosing, while a single dose was ineffective. Conclusions: These data provide further support for spreading depression as a relevant target in migraine prophylaxis, and demonstrate the predictive utility of employed spreading depression models.


1971 ◽  
Vol 11 ◽  
pp. 171-IN26 ◽  
Author(s):  
H. Martins-Ferreira ◽  
G. De Oliveira Castro

2004 ◽  
Vol 5 (S2) ◽  
pp. s67-s70 ◽  
Author(s):  
Giovanni Mazzotta ◽  
Francesca Floridi ◽  
Andrea Alberti ◽  
Paola Sarchielli

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