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 GTP(35)gammaS 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 [GRAPHICS] 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.
机构:
Northeastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USANortheastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Mcglynn, Ryan P.
Cui, Meng
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Northeastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USANortheastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Cui, Meng
Brems, Brittany
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机构:
Northeastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USANortheastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Brems, Brittany
Holbrook, Otto
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Northeastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USANortheastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Holbrook, Otto
Booth, Raymond G.
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Northeastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USANortheastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
Booth, Raymond G.
ACS CHEMICAL NEUROSCIENCE,
2023,
15
(02):
: 357
-
370
机构:
Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Chengdu Med Coll, Dept Lab Med, Chengdu 610500, Sichuan, Peoples R ChinaChengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Pu, Zhong-Hui
Peng, Cheng
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机构:
Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Chengdu Univ Tradit Chinese Med, Inst Innovat Med Ingredients Southwest Specialty, Chengdu 611137, Sichuan, Peoples R ChinaChengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Peng, Cheng
Xie, Xiao-Fang
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机构:
Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R ChinaChengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Xie, Xiao-Fang
Luo, Min
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Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R ChinaChengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Luo, Min
Zhu, Huan
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Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Chengdu Univ Tradit Chinese Med, Inst Innovat Med Ingredients Southwest Specialty, Chengdu 611137, Sichuan, Peoples R ChinaChengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Zhu, Huan
Feng, Rui
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机构:
Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Chengdu Univ Tradit Chinese Med, Inst Innovat Med Ingredients Southwest Specialty, Chengdu 611137, Sichuan, Peoples R ChinaChengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Feng, Rui
Xiong, Liang
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机构:
Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
Chengdu Univ Tradit Chinese Med, Inst Innovat Med Ingredients Southwest Specialty, Chengdu 611137, Sichuan, Peoples R ChinaChengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
机构:
ERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDSERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDS
VILLALON, CM
BOM, AH
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ERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDSERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDS
BOM, AH
HEILIGERS, JPC
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ERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDSERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDS
HEILIGERS, JPC
DENBOER, MO
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ERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDSERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDS
DENBOER, MO
SAXENA, PR
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ERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDSERASMUS UNIV,FAC MED & HLTH SCI,DEPT PHARMACOL,POB 1738,3000 DR ROTTERDAM,NETHERLANDS
机构:
Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USAUniv Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
Kaiser, Eric A.
Kuburas, Adisa
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机构:
Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USAUniv Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
Kuburas, Adisa
Recober, Ana
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机构:
Univ Iowa, Dept Neurol, Iowa City, IA 52242 USAUniv Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
Recober, Ana
Russo, Andrew F.
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Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
Univ Iowa, Dept Neurol, Iowa City, IA 52242 USA
Vet Affairs Med Ctr, Iowa City, IA 52246 USAUniv Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
机构:
Erasmus MC, Div Vasc Med & Pharmacol, Dept Internal Med, NL-3015 GE Rotterdam, NetherlandsErasmus MC, Div Vasc Med & Pharmacol, Dept Internal Med, NL-3015 GE Rotterdam, Netherlands
Rosas, Martha B. Ramirez
Labruijere, Sieneke
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机构:
Erasmus MC, Div Vasc Med & Pharmacol, Dept Internal Med, NL-3015 GE Rotterdam, NetherlandsErasmus MC, Div Vasc Med & Pharmacol, Dept Internal Med, NL-3015 GE Rotterdam, Netherlands
Labruijere, Sieneke
Villalon, Carlos M.
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h-index: 0
机构:
Cinvestav Coapa, Dept Farmacobiol, Mexico City 14330, DF, MexicoErasmus MC, Div Vasc Med & Pharmacol, Dept Internal Med, NL-3015 GE Rotterdam, Netherlands
Villalon, Carlos M.
VanDenBrink, Antoinette Maassen
论文数: 0引用数: 0
h-index: 0
机构:
Erasmus MC, Div Vasc Med & Pharmacol, Dept Internal Med, NL-3015 GE Rotterdam, NetherlandsErasmus MC, Div Vasc Med & Pharmacol, Dept Internal Med, NL-3015 GE Rotterdam, Netherlands