Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Ulrike Holzer-Petsche"'
Autor:
Peter Holzer, Ulrike Holzer-Petsche
Publikováno v:
Frontiers in Physiology, Vol 12 (2022)
The development of small-molecule calcitonin gene-related peptide (CGRP) receptor antagonists (gepants) and of monoclonal antibodies targeting the CGRP system has been a major advance in the management of migraine. In the randomized controlled trials
Externí odkaz:
https://doaj.org/article/1dea75acc6754c8b98b057a91addb692
Autor:
Peter Holzer, Ulrike Holzer-Petsche
Publikováno v:
Frontiers in Physiology, Vol 12 (2022)
The development of small-molecule calcitonin gene-related peptide (CGRP) receptor antagonists (gepants) and of monoclonal antibodies targeting the CGRP system has been a major advance in the management of migraine. In the randomized controlled trials
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48b737712fc3e9df70b6c5ff4857e58c
https://pubmed.ncbi.nlm.nih.gov/36523559
https://pubmed.ncbi.nlm.nih.gov/36523559
Autor:
Ulrike Holzer-Petsche, Peter Holzer
Publikováno v:
Digestive Diseases. 27:24-30
Background: Inflammation is commonly associated with hyperalgesia. Ideally, this change should abate once inflammation is resolved, but this is not necessarily the case because phenotypic changes in the tissue can persist, as appears to be the case i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc5d5c4a74f8a615aef5561845bd6b67
https://doi.org/10.1159/000268118
https://doi.org/10.1159/000268118
Autor:
Örs Péter Horváth, Loránd Barthó, László Illényi, Riccardo Patacchini, Ulrike Holzer-Petsche, Gábor Petho, Andras Antal, Zsófia Lázár, Rita Benkó, Peter Holzer, Sarolta Undi
Publikováno v:
European Journal of Pharmacology. 500:143-157
Studying the visceral effects of the sensory stimulant capsaicin is a useful and relatively simple tool of neurotransmitter identification and has been used for this purpose for approximately 25 years in the authors' and other laboratories. We believ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aed84a712fdefc96c8adeb226d15a92b
https://doi.org/10.1016/j.ejphar.2004.07.020
https://doi.org/10.1016/j.ejphar.2004.07.020
Autor:
Ulrike Holzer-Petsche, Peter Holzer, Anaid Shahbazian, Helmut Schmidhammer, Eckhard Beubler, Akos Heinemann
Publikováno v:
British Journal of Pharmacology. 135:741-750
Opiates inhibit gastrointestinal propulsion, but it is not clear which opioid receptor types are involved in this action. For this reason, the effect of opioid receptor - selective agonists and antagonists on intestinal peristalsis was studied. Peris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5657413aa2f357f01246f9402fa8ad0
https://doi.org/10.1038/sj.bjp.0704527
https://doi.org/10.1038/sj.bjp.0704527
Publikováno v:
Neuroscience letters. 577
Longitudinal muscle-myenteric plexus strips of the guinea-pig ileum were used to investigate the nature of the hexamethonium-induced augmentation of the twitch response. All preparations were set up in Tyrode solution and intermittent longitudinal tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75d103b3bcad845e63991bbdcdb33e1f
https://pubmed.ncbi.nlm.nih.gov/24933535
https://pubmed.ncbi.nlm.nih.gov/24933535
Autor:
Ulrike Holzer-Petsche, Peter Holzer
Publikováno v:
Pharmacology & Therapeutics. 73:173-217
The preprotachykinin-A gene-derived peptides substance P and neurokinin (NK) A are expressed in distinct neural pathways of the mammalian gut. When released from intrinsic enteric or extrinsic primary afferent neurons, tachykinins have the potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9e896343c66f97776ee435e9025960d
https://doi.org/10.1016/s0163-7258(96)00195-7
https://doi.org/10.1016/s0163-7258(96)00195-7
Publikováno v:
British Journal of Pharmacology. 115:486-490
1. Many studies indicate an involvement of substance P in the transmission of nociceptive stimuli, without, however, presenting any conclusive evidence as to its exact site and mode of action. The present experiments tested the involvement of substan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e798b9bf7ee682ad3d94f6e2f9423b05
https://doi.org/10.1111/j.1476-5381.1995.tb16359.x
https://doi.org/10.1111/j.1476-5381.1995.tb16359.x
Autor:
Ulrike Holzer-Petsche
Publikováno v:
Regulatory Peptides. 57:19-42
For a long time research on the action of TKs on gastrointestinal tissue has been demonstrating the importance of the TKs as non-cholinergic stimulators of motility in most parts of the mammalian gastrointestinal tract. The past years witnessed the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad58a8a2d9dd7d82d5af5c3f49ea64e3
https://doi.org/10.1016/0167-0115(95)00019-8
https://doi.org/10.1016/0167-0115(95)00019-8
Autor:
Thomas A. Hinterleitner, Eckhard Beubler, Wolfgang Petritsch, Ulrike Holzer-Petsche, A. J. Eherer, Guenter J. Krejs
Publikováno v:
European Journal of Clinical Investigation. 24:664-668
In rats, the combined administration of the 5-HT2 antagonist ketanserin and the 5-HT3 antagonist tropisetron inhibits cholera toxin-induced intestinal secretion. We investigated whether these agents and the 5-HT3 antagonist ondansetron can inhibit ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b93d6088d4072bbab14bfbc17e851b5
https://doi.org/10.1111/j.1365-2362.1994.tb01058.x
https://doi.org/10.1111/j.1365-2362.1994.tb01058.x