Animal models of migraine-like pain enabling ongoing study of behaviour typically involve the systemic administration of chemical vasodilators or dural administration of inflammatory algogens. However, neither method mediates prolonged effects on behavior indicative of enduring pathophysiological changes occurring within dural or trigeminal pain circuits. We generated successive generations of a unique inbred rat strain, spontaneous trigeminal allodynia (STA) rats, previously reported to exhibit an episodic migraine-like behavioural phenotype. We show that both male and female STA rats display robust and sustained reductions in periorbital thresholds to cutaneous mechanical stimulation. Otherwise, the general behavior (e.g. locomotor, grooming) of these rats appeared normal. In female STA rats, the mechanical hypersensitivity was confined to the cephalic region, manifested after puberty through adolescence, and was sustained into adulthood recapitulating the clinical manifestation of migraine. We exploited this hitherto unidentified chronic phenotype to show that the migraine-specific drugs sumatriptan (5-HT 1B/1D receptor agonist) and olcegepant (CGRP receptor antagonist) could completely reverse cephalic hypersensitivity using a within subject cross-over paradigm. Our findings indicate that STA rats actually possess a phenotype indicative of migraine chronicity which is exquisitely sensitive to migraine therapeutics. This unique strain could prove to be an invaluable resource in preclinical migraine drug discovery.Animal models of migraine-like pain enabling evaluation of disease-relevant behaviours, typically in mice or rats, are frequently induced by chemical provocation using systemic administration of vasodilating agents such as nitric oxide (NO) donors or dural application of inflammatory mediators 1-6 . These models have variously proven to be of some value in the preclinical setting but have their limitations 7 . Crucially, even with repeated dosing, the systemic administration of NO donors (e.g. glyceryl trinitrate; GTN or isosorbide dinitrate) in rodents has never been reported to produce sustainable cephalic or extracephalic hypersensitivity lasting longer than 1-2 weeks 2,8-10 , thereby limiting their utility in long term behavioural studies.The use of genetic models of migraine-like pain in animals might be expected to partially mitigate such issues. Familial Hemiplegic Migraine is a rare monogenic migraine subtype associated with aura, characterized by weakness on one side of the body during the aura phase 11 . To date, the involvement of three genes has been confirmed in this migraine subtype of which the humanized knock in CACNA1A-related R192Q mouse is probably the best studied 12 . These mice display increased unilateral head grooming and are photosensitive in accordance with a migraine-like phenotype. An advantage of using such models is that the animals possess a pre-defined phenotype, circumventing the need for complicated dosing protocols using NO donors or surgical procedures (e.g. dural ...