Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine

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Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine. / Haanes, Kristian Agmund; Edvinsson, Lars.

I: PloS one, Bind 9, Nr. 9, e108782, 2014, s. 1-8.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Haanes, KA & Edvinsson, L 2014, 'Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine', PloS one, bind 9, nr. 9, e108782, s. 1-8. https://doi.org/10.1371/journal.pone.0108782

APA

Haanes, K. A., & Edvinsson, L. (2014). Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine. PloS one, 9(9), 1-8. [e108782]. https://doi.org/10.1371/journal.pone.0108782

Vancouver

Haanes KA, Edvinsson L. Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine. PloS one. 2014;9(9):1-8. e108782. https://doi.org/10.1371/journal.pone.0108782

Author

Haanes, Kristian Agmund ; Edvinsson, Lars. / Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine. I: PloS one. 2014 ; Bind 9, Nr. 9. s. 1-8.

Bibtex

@article{5eb34ef04d9d4a7da2bca5bf9d943790,
title = "Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine",
abstract = "The dura mater and its vasculature have for decades been central in the hypothesis of migraine and headache pathophysiology. Although recent studies have questioned the role of the vasculature as the primary cause, dural vessel physiology is still relevant in understanding the complex pathophysiology of migraine. The aim of the present study was to isolate the middle meningeal artery (MMA) from rodents and characterize their purinergic receptors using a sensitive wire myograph method and RT-PCR. The data presented herein suggest that blood flow through the MMA is, at least in part, regulated by purinergic receptors. P2X1 and P2Y6 receptors are the strongest contractile receptors and, surprisingly, ADPβS caused contraction most likely via P2Y1 or P2Y13 receptors, which is not observed in other arteries. Adenosine addition, however, caused relaxation of the MMA. The adenosine relaxation could be inhibited by SCH58261 (A2A receptor antagonist) and caffeine (adenosine receptor antagonist). This gives one putative molecular mechanism for the effect of caffeine, often used as an adjuvant remedy of cranial pain. Semi-quantitative RT-PCR expression data for the receptors correlate well with the functional findings. Together these observations could be used as targets for future understanding of the in vivo role of purinergic receptors in the MMA.",
author = "Haanes, {Kristian Agmund} and Lars Edvinsson",
year = "2014",
doi = "10.1371/journal.pone.0108782",
language = "English",
volume = "9",
pages = "1--8",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "9",

}

RIS

TY - JOUR

T1 - Expression and Characterization of Purinergic Receptors in Rat Middle Meningeal Artery–Potential Role in Migraine

AU - Haanes, Kristian Agmund

AU - Edvinsson, Lars

PY - 2014

Y1 - 2014

N2 - The dura mater and its vasculature have for decades been central in the hypothesis of migraine and headache pathophysiology. Although recent studies have questioned the role of the vasculature as the primary cause, dural vessel physiology is still relevant in understanding the complex pathophysiology of migraine. The aim of the present study was to isolate the middle meningeal artery (MMA) from rodents and characterize their purinergic receptors using a sensitive wire myograph method and RT-PCR. The data presented herein suggest that blood flow through the MMA is, at least in part, regulated by purinergic receptors. P2X1 and P2Y6 receptors are the strongest contractile receptors and, surprisingly, ADPβS caused contraction most likely via P2Y1 or P2Y13 receptors, which is not observed in other arteries. Adenosine addition, however, caused relaxation of the MMA. The adenosine relaxation could be inhibited by SCH58261 (A2A receptor antagonist) and caffeine (adenosine receptor antagonist). This gives one putative molecular mechanism for the effect of caffeine, often used as an adjuvant remedy of cranial pain. Semi-quantitative RT-PCR expression data for the receptors correlate well with the functional findings. Together these observations could be used as targets for future understanding of the in vivo role of purinergic receptors in the MMA.

AB - The dura mater and its vasculature have for decades been central in the hypothesis of migraine and headache pathophysiology. Although recent studies have questioned the role of the vasculature as the primary cause, dural vessel physiology is still relevant in understanding the complex pathophysiology of migraine. The aim of the present study was to isolate the middle meningeal artery (MMA) from rodents and characterize their purinergic receptors using a sensitive wire myograph method and RT-PCR. The data presented herein suggest that blood flow through the MMA is, at least in part, regulated by purinergic receptors. P2X1 and P2Y6 receptors are the strongest contractile receptors and, surprisingly, ADPβS caused contraction most likely via P2Y1 or P2Y13 receptors, which is not observed in other arteries. Adenosine addition, however, caused relaxation of the MMA. The adenosine relaxation could be inhibited by SCH58261 (A2A receptor antagonist) and caffeine (adenosine receptor antagonist). This gives one putative molecular mechanism for the effect of caffeine, often used as an adjuvant remedy of cranial pain. Semi-quantitative RT-PCR expression data for the receptors correlate well with the functional findings. Together these observations could be used as targets for future understanding of the in vivo role of purinergic receptors in the MMA.

U2 - 10.1371/journal.pone.0108782

DO - 10.1371/journal.pone.0108782

M3 - Journal article

C2 - 25265286

VL - 9

SP - 1

EP - 8

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 9

M1 - e108782

ER -

ID: 135499265