Key result
Donitriptan dose-dependently decreased total carotid blood flow and vascular conductance (maximum response: -25 +/- 3%) by selectively reducing the cephalic arteriovenous anastomotic fraction.
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Donitriptan selectively constricts arteriovenous anastomoses via 5-HT1B receptor activation without compromising blood flow to vital organs, supporting its potential safety and efficacy for aborting migraine headaches.
We investigated the effects of donitriptan, which possesses a uniquely high affinity and efficacy at 5-HT1B/1D receptors, on carotid and systemic haemodynamics in anaes thetized pigs. Donitriptan (0.16-100 microg kg(-1), i.v.) dose-dependently decreased total carotid blood flow and vascular conductance (maximum response: -25 +/- 3%). This effect was entirely due to a selective reduction in the cephalic arteriovenous anastomotic fraction (maximum response: - 63 +/- 3%; ED50%: 92 +/- 31 nmol/kg); the nutrient vascular conductance increased. Donitriptan did not decrease vascular conductances in or blood flow to a number of organs, including the heart and kidneys; in fact, vascular conductances in the skin, brain and skeletal muscles increased. Cardiac output was slightly decreased by donitriptan, but this effect was confined to peripheral arteriovenous anastomoses. The haemodynamic effects of donitriptan were substantially reduced by the 5-HT1B/1D receptor antagonist GR127935. These results show that donitriptan selectively constricts arteriovenous anastomoses via 5-HT1B receptor activation. The drug should be able to abort migraine headaches and it is unlikely to compromize blood flow to vital organs.
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Tom et al. (2002) studied Migraine (animal model). Donitriptan was evaluated on Total carotid blood flow and vascular conductance. Donitriptan dose-dependently decreased total carotid blood flow and vascular conductance (maximum response: -25 +/- 3%) by selectively reducing the cephalic arteriovenous anastomotic fraction.
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