Differential activation of ERK, p38, and JNK MAPK by nociceptin/orphanin FQ in the potentiation of prostaglandin cerebrovasoconstriction after brain injury-Reference-Cited by-同舟云学术

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Differential activation of ERK, p38, and JNK MAPK by nociceptin/orphanin FQ in the potentiation of prostaglandin cerebrovasoconstriction after brain injury

Published:2006-01 Issue:1-3 Volume:529 Page:129-135
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Armstead William M.

Publisher

Elsevier BV

Subject

Pharmacology

Reference30 articles.

1. Altered release of prostaglandins by opioids contributes to impaired cerebral hemodynamics following brain injury;Al-Turki;Crit. Care Med.,1998

2. Role of endothelin in pial artery vasoconstriction and altered responses to vasopressin following brain injury;Armstead;J. Neurosurg.,1996

3. Role of opioids in the physiologic and pathophysiologic control of the cerebral circulation;Armstead;Proc. Soc. Exp. Biol. Med.,1997

4. Brain injury impairs prostaglandin cerebrovasodilation;Armstead;J. Neurotrauma,1998

5. Role of nociceptin/orphanin FQ in age dependent cerebral hemodynamic effects of brain injury;Armstead;J. Neurotrauma,2000

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1. Traumatic Brain Injury Induces Nociceptin/Orphanin FQ and Nociceptin Opioid Peptide Receptor Expression within 24 Hours;International Journal of Molecular Sciences;2024-01-29

2. A Systematic Review on Traumatic Brain Injury Pathophysiology and Role of Herbal Medicines in its Management;Current Neuropharmacology;2023-12

3. The Nociceptin/Orphanin FQ peptide receptor antagonist, SB-612111, improves cerebral blood flow in a rat model of traumatic brain injury;Frontiers in Pharmacology;2023-10-18

4. Paradigm Shift in Materials for Skull Reconstruction Facilitated by Science and Technological Integration;Cureus;2022-09-03

5. Therapeutic potential of nociceptin/orphanin FQ peptide (NOP) receptor modulators for treatment of traumatic brain injury, traumatic stress, and their co-morbidities;Pharmacology & Therapeutics;2022-03

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