Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Hung Tsung Hsiao"'
Publikováno v:
PLoS ONE, Vol 17, Iss 1 (2022)
Introduction Previous studies have demonstrated that cytokines, transforming growth factor (TGF-β1), and brain-derived neurotrophic factor (BDNF) can impact the intensity of pain in rodents. However, the roles of cytokines, TGF-β1 and BDNF in human
Externí odkaz:
https://doaj.org/article/6c5aa71c13694043ae93e3b07cebca7b
Publikováno v:
Journal of Biomedical Science, Vol 26, Iss 1, Pp 1-11 (2019)
Abstract Background Complex regional pain syndrome (CRPS) is related to microcirculation impairment caused by tissue hypoxia and peripheral cytokine overproduction in the affected human limb and chronic post-ischemic pain (CPIP) is considered as an a
Externí odkaz:
https://doaj.org/article/c1ed9b1722fb44debd651979c350056c
Publikováno v:
Biomedicines, Vol 10, Iss 6, p 1318 (2022)
Vortioxetine (VOR) is recognized to exert antidepressant actions. However, whether this drug modifies ionic currents in excitable cells remains unclear. The aim of this study was to explore the electrophysiological effects of VOR and other related co
Externí odkaz:
https://doaj.org/article/1db943c2ed8b4daebe1a2e697f96679e
Autor:
Ping-Ching Wu, Dar-Bin Shieh, Hung-Tsung Hsiao, Jeffery Chi-Fei Wang, Ya-Chi Lin, Yen-Chin Liu
Publikováno v:
Journal of Nanobiotechnology, Vol 16, Iss 1, Pp 1-9 (2018)
Abstract Background Nanoparticles have become one of the most promising among the potential materials used for biomedical applications. However, few researchers have focused on their effects on analgesia. Despite the fact that various nanoparticles h
Externí odkaz:
https://doaj.org/article/9e3b5408b7b9486d9b24752acad645b0
Publikováno v:
Membranes, Vol 11, Iss 8, p 636 (2021)
PT-2385 is currently regarded as a potent and selective inhibitor of hypoxia-inducible factor-2α (HIF-2α), with potential antineoplastic activity. However, the membrane ion channels changed by this compound are obscure, although it is reasonable to
Externí odkaz:
https://doaj.org/article/50d674b406054d828ed631eb1f7f4748
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 33, Iss 4, Pp 165-170 (2017)
Transcutaneous electrical nerve stimulators (TENSs) have been proved to be effective in muscle pain management for several decades. However, there is no consensus for the optimal TENS program. Previous research demonstrated that a 100 Hz TENS (L-TENS
Externí odkaz:
https://doaj.org/article/ade0c83a7d8e45b8a6515bb13978fec6
Publikováno v:
Membranes, Vol 11, Iss 636, p 636 (2021)
Membranes
Volume 11
Issue 8
Membranes
Volume 11
Issue 8
PT-2385 is currently regarded as a potent and selective inhibitor of hypoxia-inducible factor-2α (HIF-2α), with potential antineoplastic activity. However, the membrane ion channels changed by this compound are obscure, although it is reasonable to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c42d275370c221f7c32fb320f2147739
https://www.mdpi.com/2077-0375/11/8/636
https://www.mdpi.com/2077-0375/11/8/636
Publikováno v:
Journal of Biomedical Science, Vol 26, Iss 1, Pp 1-11 (2019)
Journal of Biomedical Science
Journal of Biomedical Science
Background Complex regional pain syndrome (CRPS) is related to microcirculation impairment caused by tissue hypoxia and peripheral cytokine overproduction in the affected human limb and chronic post-ischemic pain (CPIP) is considered as an animal mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::165a93912bd91a0b3c5629e950577624
http://link.springer.com/article/10.1186/s12929-019-0576-z
http://link.springer.com/article/10.1186/s12929-019-0576-z
Publikováno v:
Drug Development Research. 80:846-856
Nalbuphine (NAL) is recognized as a mixer with the κ-opioid receptor agonist and the μ-opioid receptor antagonist. However, whether this drug causes any modifications in neuronal ionic currents is unclear. The effects of NAL on ionic currents in mH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5741df0ad64e79811dac9a5ca97a81e
https://doi.org/10.1002/ddr.21568
https://doi.org/10.1002/ddr.21568
Publikováno v:
Brain Research Bulletin. 149:11-20
Ivabradine (IVA), a heart-rate reducing agent, is recognized as an inhibitor of hyperpolarization-activated cation current (Ih) and also reported to ameliorate inflammatory or neuropathic pain. However, to what extent this agent can perturb another t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9182c3681490095b91fb3fc84063db98
https://doi.org/10.1016/j.brainresbull.2019.03.016
https://doi.org/10.1016/j.brainresbull.2019.03.016