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Anti-Migraine Compounds Fail to Modulate the Propagation of Cortical Spreading Depression in the Cat

1994; Karger Publishers; Volume: 34; Issue: 1 Linguagem: Inglês

10.1159/000117004

1421-9913

Holger Kaube, Peter J. Goadsby,

Neuroendocrine regulation and behavior

Leao's cortical spreading depression (SD) is often cited as the pathophysiological substrate for the neurological symptoms of migraine with aura. If this is the case it might be expected that drugs useful as anti-migraine agents, particularly those useful in prohylaxis, may alter or prevent SD. Indeep it has been suggested that the anti-migraine compound dihydroergotamine (DHE) blocks or reduces the speed of propagation of SD in the rabbit. In this study we attempted to further investigate the effects of DHE and other anti-migraine drugs on SD by measuring cortical blood flow with laser Doppler flowmetry (CBFLDF) and cortical single unit activity in the a-chloralose-anaesthetised cat. The following substances were tested: DHE, acetylsalicylic acid, lignocaine, metoprolol, clonazepam and valproate. The NMDA-receptor blocker MK-801 and halothane (1.5%) were used as reference substances that reliably block SD. The outcome measures were speed of propagation of the wave of SD across the cortex and the CBFLDFincrease during the hyperaemic phase of SD. Data were taken from three control episodes (60 min apart) and after drug administration. The rate of propagation was significantly reduced from the first control period (3.0 ± 0.3 mm/min) to the subsequent 2 control observations (2.3 ± 0.1 mm/min) even without any drug treatment. Following the control observations the test drug was administered and a further SD elicited. This fourth SD was reliably blocked by MK-801 and halothane. None of the other test drugs inhibited SD, reduced the rate of propagation or changed the amplitude of the CBFLDF increase. It is therefore possible that anti-migraine drugs that are active in prophylaxis do not have their effect through a modulation of SD. Indeed if SD is the explanation for the aura phase of migraine it may be an epiphenomenon driven by some further central process rather than the causal initiator of the migraine attack.