alpha-eudesmol, a P/Q-type Ca(2+) channel blocker, inhibits neurogenic vasodilation and extravasation following electrical stimulation of trigeminal ganglion (Q30890357)

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English	alpha-eudesmol, a P/Q-type Ca(2+) channel blocker, inhibits neurogenic vasodilation and extravasation following electrical stimulation of trigeminal ganglion	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

alpha-eudesmol, a P/Q-type Ca(2+) channel blocker, inhibits neurogenic vasodilation and extravasation following electrical stimulation of trigeminal ganglion (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

author name string

Asakura K

1

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

Kanemasa T

2

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

Minagawa K

3

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

Kagawa K

4

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

Yagami T

5

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

Nakajima M

6

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

Ninomiya M

7

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

language of work or name

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publication date

1 August 2000

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Europe PubMed Central

PubMed publication ID

27 June 2017

number of pages

8

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based on heuristic

inferred from page(s)

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Europe PubMed Central

PubMed publication ID

27 June 2017

873

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Europe PubMed Central

PubMed publication ID

27 June 2017

1

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Europe PubMed Central

PubMed publication ID

27 June 2017

94-101

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Europe PubMed Central

PubMed publication ID

27 June 2017

Sumatriptan inhibits the release of CGRP and substance P from the rat spinal cord

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The nonpeptide alpha-eudexp6l from Juniperus virginiana Linn. (Cupressaceae) inhibits omega-agatoxin IVA-sensitive Ca2+ currents and synaptosomal 45Ca2+ uptake

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P/Q-type Ca2+ channel blocker omega-agatoxin IVA protects against brain injury after focal ischemia in rats

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Splicing of alpha 1A subunit gene generates phenotypic variants of P- and Q-type calcium channels

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Rizatriptan has central antinociceptive effects against durally evoked responses

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Blockade of spinal N- and P-type, but not L-type, calcium channels inhibits the excitability of rat dorsal horn neurones produced by subcutaneous formalin inflammation.

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Release of substance P, calcitonin gene-related peptide and prostaglandin E2 from rat dura mater encephali following electrical and chemical stimulation in vitro

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The modulation of the increase in rat facial skin blood flow observed after trigeminal ganglion stimulation

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Trigeminal ganglion stimulation increases facial skin blood flow in the rat: a major role for calcitonin gene-related peptide

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Multiphasic effect of morphine on the release of substance P from rat trigeminal nucleus slices

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Effect of omega-conotoxin GVIA and omega-agatoxin IVA on the capsaicin-sensitive calcitonin gene-related peptide release and autoregulatory vasodilation in rat pial arteries

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Time-dependent blockade of neurogenic plasma extravasation in dura mater by 5-HT1B/D agonists and endopeptidase 24.11.

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Mode of action of the anti-migraine drug sumatriptan

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kappa-opioid agonist U50488 inhibits P-type Ca2+ channels by two mechanisms

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Increase of meningeal blood flow after electrical stimulation of rat dura mater encephali: mediation by calcitonin gene‐related peptide

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Distribution and functional significance of the P-type, voltage-dependent Ca2+ channels in the mammalian central nervous system

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P-type calcium channels are blocked by the alkaloid daurisoline

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Multiple calcium channel types control glutamatergic synaptic transmission in the hippocampus

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Voltage-sensitive calcium channels in spinal nociceptive processing: blockade of N- and P-type channels inhibits formalin-induced nociception.

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Receptor specificity and trigemino-vascular inhibitory actions of a novel 5-HT1B/1D receptor partial agonist, 311C90 (zolmitriptan).

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Release of immunoreactive substance P in the brain stem upon stimulation of the cranial dura mater with low pH - inhibition by the serotonin (5-HT1) receptor agonist CP 93,129.

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P-type calcium channels blocked by the spider toxin ω-Aga-IVA

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Action potentials must admit calcium to evoke transmitter release

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Omega-agatoxin IVA, a P-type calcium channel antagonist, reduces nociceptive processing in spinal cord neurons with input from the inflamed but not from the normal knee joint--an electrophysiological study in the rat in vivo

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The non-peptide NK-1 receptor antagonist LY303870 inhibits neurogenic dural inflammation in guinea pigs

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Pharmacological dissection of multiple types of Ca2+ channel currents in rat cerebellar granule neurons

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L-733,060, a novel tachykinin NK1 receptor antagonist; effects in [Ca2+]i mobilisation, cardiovascular and dural extravasation assays

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Differential Effects of 5-HT 1B/1D Receptor Agonists on Neurogenic Dural Plasma Extravasation and Vasodilation in Anaesthetized Rats

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The non‐peptide neurokinin1 receptor antagonist, RP 67580, blocks neurogenic plasma extravasation in the dura mater of rats

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Blockade of calcium channels can prevent the onset of secondary hyperalgesia and allodynia induced by intradermal injection of capsaicin in rats

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Identifiers

10.1016/S0006-8993(00)02527-0

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 June 2017

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