Animal models of pain and migraine in drug discovery

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Animal models of pain and migraine in drug discovery. / Munro, Gordon; Jansen-Olesen, Inger; Olesen, Jes.

I: Drug Discovery Today, Bind 22, Nr. 7, 2017, s. 1103-1111.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Munro, G, Jansen-Olesen, I & Olesen, J 2017, 'Animal models of pain and migraine in drug discovery', Drug Discovery Today, bind 22, nr. 7, s. 1103-1111. https://doi.org/10.1016/j.drudis.2017.04.016

APA

Munro, G., Jansen-Olesen, I., & Olesen, J. (2017). Animal models of pain and migraine in drug discovery. Drug Discovery Today, 22(7), 1103-1111. https://doi.org/10.1016/j.drudis.2017.04.016

Vancouver

Munro G, Jansen-Olesen I, Olesen J. Animal models of pain and migraine in drug discovery. Drug Discovery Today. 2017;22(7):1103-1111. https://doi.org/10.1016/j.drudis.2017.04.016

Author

Munro, Gordon ; Jansen-Olesen, Inger ; Olesen, Jes. / Animal models of pain and migraine in drug discovery. I: Drug Discovery Today. 2017 ; Bind 22, Nr. 7. s. 1103-1111.

Bibtex

@article{7719dce6bc43411d8bd74401f403c7e6,
title = "Animal models of pain and migraine in drug discovery",
abstract = "Preclinical research activities in relation to pain typically involve the 'holy trinity' of nociceptive, inflammatory and neuropathic pain for purposes of target validation and defining target product profiles of novel analgesic compounds. For some reason it seems that headache or migraine are rarely considered as additional entities to explore. Frontline medications used in the treatment of, for example, inflammatory pain, neuropathic pain and migraine (NSAIDs versus pregabalin/duloxetine versus triptans) reveal distinct differences in pathophysiology that partially explain this approach. Nevertheless, for many patients enduring chronic pain, regardless of aetiology, high unmet needs remain. By focusing more on commonalities shared between neuropathic pain and headache disorders such as migraine, drug discovery efforts could be spread more efficiently across a larger indication area. Here, some of the most commonly used models and methods employed within 'pain and migraine' drug development will be presented. Recent advances within these disciplines suggest that, with the addition of a few extra carefully chosen ancillary models and/or endpoints, the relative value in terms of resources used, reciprocal flow of information and net worth of a 'typical' package could be increased substantially for the pain and migraine fields.",
keywords = "Animals, Chronic Pain, Disease Models, Animal, Drug Discovery, Humans, Migraine Disorders",
author = "Gordon Munro and Inger Jansen-Olesen and Jes Olesen",
note = "Copyright {\textcopyright} 2017 Elsevier Ltd. All rights reserved.",
year = "2017",
doi = "10.1016/j.drudis.2017.04.016",
language = "English",
volume = "22",
pages = "1103--1111",
journal = "Drug Discovery Today: BIOSILICO",
issn = "1359-6446",
publisher = "Elsevier Ltd. * Trends Journals",
number = "7",

}

RIS

TY - JOUR

T1 - Animal models of pain and migraine in drug discovery

AU - Munro, Gordon

AU - Jansen-Olesen, Inger

AU - Olesen, Jes

N1 - Copyright © 2017 Elsevier Ltd. All rights reserved.

PY - 2017

Y1 - 2017

N2 - Preclinical research activities in relation to pain typically involve the 'holy trinity' of nociceptive, inflammatory and neuropathic pain for purposes of target validation and defining target product profiles of novel analgesic compounds. For some reason it seems that headache or migraine are rarely considered as additional entities to explore. Frontline medications used in the treatment of, for example, inflammatory pain, neuropathic pain and migraine (NSAIDs versus pregabalin/duloxetine versus triptans) reveal distinct differences in pathophysiology that partially explain this approach. Nevertheless, for many patients enduring chronic pain, regardless of aetiology, high unmet needs remain. By focusing more on commonalities shared between neuropathic pain and headache disorders such as migraine, drug discovery efforts could be spread more efficiently across a larger indication area. Here, some of the most commonly used models and methods employed within 'pain and migraine' drug development will be presented. Recent advances within these disciplines suggest that, with the addition of a few extra carefully chosen ancillary models and/or endpoints, the relative value in terms of resources used, reciprocal flow of information and net worth of a 'typical' package could be increased substantially for the pain and migraine fields.

AB - Preclinical research activities in relation to pain typically involve the 'holy trinity' of nociceptive, inflammatory and neuropathic pain for purposes of target validation and defining target product profiles of novel analgesic compounds. For some reason it seems that headache or migraine are rarely considered as additional entities to explore. Frontline medications used in the treatment of, for example, inflammatory pain, neuropathic pain and migraine (NSAIDs versus pregabalin/duloxetine versus triptans) reveal distinct differences in pathophysiology that partially explain this approach. Nevertheless, for many patients enduring chronic pain, regardless of aetiology, high unmet needs remain. By focusing more on commonalities shared between neuropathic pain and headache disorders such as migraine, drug discovery efforts could be spread more efficiently across a larger indication area. Here, some of the most commonly used models and methods employed within 'pain and migraine' drug development will be presented. Recent advances within these disciplines suggest that, with the addition of a few extra carefully chosen ancillary models and/or endpoints, the relative value in terms of resources used, reciprocal flow of information and net worth of a 'typical' package could be increased substantially for the pain and migraine fields.

KW - Animals

KW - Chronic Pain

KW - Disease Models, Animal

KW - Drug Discovery

KW - Humans

KW - Migraine Disorders

U2 - 10.1016/j.drudis.2017.04.016

DO - 10.1016/j.drudis.2017.04.016

M3 - Review

C2 - 28476535

VL - 22

SP - 1103

EP - 1111

JO - Drug Discovery Today: BIOSILICO

JF - Drug Discovery Today: BIOSILICO

SN - 1359-6446

IS - 7

ER -

ID: 195163578