Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ildiko Dobos"'
Autor:
Nadine Friedrich, Krisztina Németh, Martin Tanner, Judit Rosta, Ildikó Dobos, Orsolya Oszlács, Gábor Jancsó, Karl Messlinger, Mária Dux
Publikováno v:
The Journal of Headache and Pain, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Monoclonal antibodies directed against the neuropeptide calcitonin gene-related peptide (CGRP) are effective in the prevention of chronic and frequent episodic migraine. Since the antibodies do not cross the blood brain barrier, t
Externí odkaz:
https://doaj.org/article/27face7a1c5040e98a0d9c1e885dc46c
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Frontiers in Physiology
Frontiers in Physiology
Restitution of cutaneous sensory function is accomplished by neural regenerative processes of distinct mechanisms following peripheral nerve lesions. Although methods available for the study of functional cutaneous nerve regeneration are specific and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4a6bf87966d06006ecd8e1820c8d586
https://www.frontiersin.org/article/10.3389/fphys.2020.00439/full
https://www.frontiersin.org/article/10.3389/fphys.2020.00439/full
Publikováno v:
Anesthesia & Analgesia. :420-426
UNLABELLED Recently, a series of endogenous ligands related to inhibition of sensory transduction of noxious stimuli at the spinal level has been described, including endomorphins, agmatine, and adenosine, which act on different receptors; however, l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97f85d460c02f0a99444db43b1096d56
https://doi.org/10.1213/01.ane.0000096066.26157.2a
https://doi.org/10.1213/01.ane.0000096066.26157.2a
Publikováno v:
Phytotherapy Research. 17:1032-1036
The extract of Sempervivum tectorum L. (Crassulaceae) containing several flavonoids is widely used as an antiinflammatory agent in folk medicine. Previous studies have demonstrated that various flavonoids or flavonoid-containing plant extracts produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde0f6b58500f6537255ab8e965f1053
https://doi.org/10.1002/ptr.1288
https://doi.org/10.1002/ptr.1288
Autor:
Gabriella Kekesi, Emese Csullog, Ildiko Dobos, W. Klimscha, Gyongyi Horvath, Kálmán Tóth, Gabriella Joo, György Benedek
Publikováno v:
European Journal of Pharmacology. 445:93-96
Kynurenic acid as an endogenous ligand antagonizes all types of ionotropic glutamate receptors, with preferential affinity for the glycine-binding site of the N-methyl-D-aspartate (NMDA) receptor. The purpose of the present study was to investigate t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35cc23248b62c3bcbbb6b78839a90074
https://doi.org/10.1016/s0014-2999(02)01787-9
https://doi.org/10.1016/s0014-2999(02)01787-9
Publikováno v:
Anesthesia & Analgesia. 93:1018-1024
UNLABELLED Spinal administration of the endogenous mu-opioid agonist peptide, endomorphin-1, results in antinociception in rodents, but there are few data about its interaction with other antinociceptive drugs. We investigated the antinociceptive int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2669cad5e5a926b6bb80226605123d5
https://doi.org/10.1097/00000539-200110000-00044
https://doi.org/10.1097/00000539-200110000-00044
Publikováno v:
Pain. 94:31-38
Endomorphin-1 is a novel endogenous opioid peptide with high affinity and selectivity for the mu-opioid receptor. Earlier results have shown that it causes antinociception in different pain tests, but its effect is short-lasting. The purpose of the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ddaa030890b625ca562c8e8c5d299dc
https://doi.org/10.1016/s0304-3959(01)00338-4
https://doi.org/10.1016/s0304-3959(01)00338-4
Autor:
Gabriella Joo, Gyongyi Horvath, W. Klimscha, Gabriella Kekesi, György Benedek, Margit Szikszay, Ildiko Dobos
Publikováno v:
Anesthesiology. 93:231-241
Background The spinal administration of some N-methyl-d-aspartate receptor antagonists results in antinociception and potentiates the effects of opioids and alpha2-adrenoceptor agonists, but ketamine and its enantiomers have not been examined. The pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c00b1903d58f3b2820ba1f42cf0c212
https://doi.org/10.1097/00000542-200007000-00034
https://doi.org/10.1097/00000542-200007000-00034
Publikováno v:
Pharmacological Research. 35:561-568
The antinociceptive and motor effects of the hydrophilic α2-adrenoceptor agonist ST-91 were studied after intrathecal administration to male Wistar rats in different heat–pain tests and different test settings. Intrathecal administration of ST-91
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46b559f9be548b6e49063b4fce3a0c41
https://doi.org/10.1006/phrs.1997.0188
https://doi.org/10.1006/phrs.1997.0188
Publikováno v:
PainReferences. 150(1)
Recent studies have demonstrated significant changes in the neuronal ganglioside status associated with altered functional states of nociceptive primary sensory neurons. In the present study, therefore, the effects of the inhibition of glucosylcerami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::743dde0a5ea8136c8cc8baf65e3078b5
https://pubmed.ncbi.nlm.nih.gov/20427129
https://pubmed.ncbi.nlm.nih.gov/20427129