Donitriptan, a Unique High-Efficacy 5-HT1B/1D Agonist: Key Features and Acute Antimigraine Potential

G. John, Michel Perez, P. Pauwels, B. Grand, Y. Verscheure, F. Colpaert
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引用次数: 6

Abstract

We hypothesized that the limited acute therapeutic effectiveness of tryptamine derivatives in alleviating migraine headache could be explained by the relatively low intrinsic activity of these agents at 5-HT1B/1D receptors. Donitriptan is a novel arylpiperazide 5-hydroxytryptamine (5-HT) derivative which was designed to exploit the higher potency and efficacy properties of 5-HT compared to tryptamine at 5-HT1B/1D receptors. In vitro, donitriptan has subnanomolar affinity for nonhuman and human 5-HT1B/1D receptors and micromolar affinity for the 5-HTip subtype. Donitritpan potently inhibited forskolin-induced cAMP formation and enhanced specific GTP35γS specific binding to a greater extent than tryptamine derivatives and equivalent to 5-HT in C6 cells expressing human 5-HT1B or 5-HT1D receptors. Donitriptan produced more potent and larger amplitude increases in hyperpolarizing Ca2+-dependent K+ current than sumatriptan in guinea pig isolated trigeminal ganglion neurons, and was more potent than tryptamine derivatives in eliciting contractile responses in rabbit isolated saphenous vein rings. In vivo, donitriptan evoked more potent, longer-lasting and greater amplitude carotid vasoconstrictor responses than tryptamine derivatives in anesthetized pigs; and in contrast to sumatriptan, naratriptan or zolmitriptan, produced long-lasting, dose-dependent decreases in unilateral carotid blood flow in conscious dogs at doses from 0.63 mg/kg p.o. without affecting heart rate or behavior. Oral donitriptan also evoked hypothermic responses in guinea pigs suggesting that the compound gains access to the brain. Donitriptan is thus a selective, potent 5-HT1B/1D receptor agonist which can be distinguished from tryptamine derivatives in consistently exerting high intrinsic activity at these receptors in a series of vascular and neuronal models relevant to migraine. Advantages in terms of therapeutic effectiveness in the acute relief of migraine headache over currently available triptans can be expected to include greater response rates and consistency of pain relief, a lower incidence of migraine recurrence and better tolerability. The acute anti-migraine potential of the first high efficacy 5-HT1B/1D agonist of its kind, donitriptan, is currently being investigated in man.
多尼曲坦,一种独特的高效5-HT1B/1D激动剂:主要特征和急性抗偏头痛潜力
我们假设,色胺衍生物在缓解偏头痛方面有限的急性治疗效果可以通过这些药物在5-HT1B/1D受体上相对较低的内在活性来解释。Donitriptan是一种新的芳基哌嗪类5-羟色胺(5-HT)衍生物,其设计目的是利用5-HT在5-HT1B/1D受体上比5-羟色胺更高的效力和功效。在体外,多尼曲坦对非人和人5-HT1B/1D受体具有亚纳摩尔亲和力,对5-HT1B/1D亚型具有微摩尔亲和力。在表达人5-HT1B或5-HT1D受体的C6细胞中,多硝立泮能有效抑制福斯克林诱导的cAMP形成,并增强GTP35γS特异性结合,其程度大于色胺衍生物,相当于5-HT。在豚鼠离体三叉神经节神经元中,多尼曲坦比苏马曲坦产生更强、更大幅度的Ca2+依赖性K+超极化电流增加,在兔离体隐静脉环中,多尼曲坦比色胺衍生物更能引起收缩反应。在体内,与色胺衍生物相比,多尼曲坦在麻醉猪体内引起的颈动脉血管收缩反应更有效、持续时间更长、幅度更大;与舒马曲坦相比,纳曲普利坦或唑米曲坦在0.63 mg/kg的剂量下,对有意识的狗的单侧颈动脉血流量产生持久的剂量依赖性减少,而不影响心率或行为。口服多尼曲坦也能引起豚鼠的低温反应,这表明这种化合物可以进入大脑。因此,多尼曲坦是一种选择性的、有效的5-HT1B/1D受体激动剂,在与偏头痛相关的一系列血管和神经元模型中,多尼曲坦与色胺衍生物在这些受体上持续发挥高的内在活性。与目前可用的曲坦类药物相比,该药在急性偏头痛缓解方面的治疗效果优势包括更高的缓解率和疼痛缓解的一致性,更低的偏头痛复发发生率和更好的耐受性。首个高效5-HT1B/1D激动剂多尼曲坦的急性抗偏头痛潜力目前正在研究中。
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