Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lan Ji Huang"'
Publikováno v:
Experimental and Therapeutic Medicine
In the present study, the ability of baicalin to relieve neuropathic pain due to spinal nerve ligation in rats was explored, and the relationship between baicalin and α2-adrenoceptors (α2-AR) was determined. The neuropathic pain model was establish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::762ad6f53249fb026d6f09bb667c4ecd
https://pubmed.ncbi.nlm.nih.gov/32765762
https://pubmed.ncbi.nlm.nih.gov/32765762
Publikováno v:
The Journal of Microbiology. 48:663-667
Cytolysin A (ClyA) is a pore-forming hemolytic protein encoded by the clyA gene. It has been identified in Salmonella enterica serovars Typhi and Paratyphi A. To identify and characterize the clyA genes in various Salmonella enterica strains, 21 diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1107fd8cb0a4324b18f8953501dead55
https://doi.org/10.1007/s12275-010-9268-9
https://doi.org/10.1007/s12275-010-9268-9
Autor:
Hyung Gon Lee, Myung Ha Yoon, Tae Hoon An, Lan Ji Huang, Woong Mo Kim, Chang Mo Kim, Yeo Ok Kim
Publikováno v:
Pharmacology Biochemistry and Behavior. 92:583-588
Spinal sildenafil (phosphodiesterase 5 inhibitor) and clonidine (alpha-2 adrenoceptor agonist) have shown antinociception. The author examined the properties of drug interaction after concurrent administration of intrathecal sildenafil-clonidine, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24f5c89609261cde30ba4c98bd7431c
https://doi.org/10.1016/j.pbb.2009.02.007
https://doi.org/10.1016/j.pbb.2009.02.007
Publikováno v:
British journal of anaesthesia. 106(3)
We defined the nature of the pharmacological interaction after intrathecal co-administration of ginsenosides with clonidine, and clarified the contribution of the α-2 adrenoceptors on the effect of ginsenosides.Pain was evoked by injection of a form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c32ac8e4e1eda5ebaefcefde87da658
https://pubmed.ncbi.nlm.nih.gov/21169610
https://pubmed.ncbi.nlm.nih.gov/21169610
Autor:
Woong Mo Kim, Cui Jin Hua, Yeo Ok Kim, Kyung Deok Park, Hyung Gon Lee, Lan Ji Huang, Myung Ha Yoon, Tae Hoon An
Publikováno v:
Journal of Korean medical science, vol 23, iss 6
Journal of Korean Medical Science
Journal of Korean Medical Science
The possible characteristics of spinal interaction between sildenafil (phosphodiesterase 5 inhibitor) and morphine on formalin-induced nociception in rats was examined. Then the role of the opioid receptor in the effect of sildenafil was further inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1a4644e8ec0b11ee8003aca96ec877
https://escholarship.org/uc/item/2kj4r5pg
https://escholarship.org/uc/item/2kj4r5pg
Publikováno v:
Life sciences. 83(25-26)
Aims We examined the nature of pharmacological interaction after coadministration of melatonin with clonidine or neostigmine on formalin-induced nociception at the spinal level. Further, the role of melatonin receptor subtypes in melatonin-induced an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c4a251adcc455bfbc1ad80f40f908c
https://pubmed.ncbi.nlm.nih.gov/19000700
https://pubmed.ncbi.nlm.nih.gov/19000700
Publikováno v:
Neuroscience letters. 441(1)
Recently, it has been known that the antinociception of sildenafil, a phosphodiesterase 5 inhibitor, is mediated through the opioid receptors. There are common three types of opioid receptors mu, delta, and kappa. We characterized the role of subtype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e95c9c2cc89cdf105a6e499a585d6a2
https://pubmed.ncbi.nlm.nih.gov/18585861
https://pubmed.ncbi.nlm.nih.gov/18585861
Publikováno v:
Yonsei medical journal, vol 51, iss 1
Yonsei Medical Journal
Yonsei Medical Journal
Purpose: The inhibition of phosphodiesterase 5 produces an antinociception through the increase of cyclic guanosine monophosphate (cGMP), and increasing cGMP levels enhance the release of γ-aminobutyric acid (GABA). Furthermore, this phosphodiestera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f730614d2726c3bbec990993c47d5612
https://doi.org/10.3349/ymj.2010.51.1.82
https://doi.org/10.3349/ymj.2010.51.1.82
Publikováno v:
Chonnam Medical Journal. 44:104
Green tea is being widely consumed as a health beverage. Recently, green tea polyphenols have been shown to possess potent anti-inflammatory property by inhibiting the production of prostaglandins; in particular, systemic green tea is shown to produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::393909564f90f0f60d29ae23d6b7077e
https://doi.org/10.4068/cmj.2008.44.2.104
https://doi.org/10.4068/cmj.2008.44.2.104
Autor:
Jin Hua Cui, Woong Mo Kim, Lan Ji Huang, Myung Ha Yoon, Hyung Gon Lee, Jae Dam Lee, Se Yeol Kim, Yeo Ok Kim
Publikováno v:
The Korean Journal of Pain. 21:27
Background: Experimental evidence indicates that ginseng modulate the nociceptive transmission. Authorsexamined the role of adrenergic and cholinergic receptors on the antinociceptive action of Korean red ginsengagainst the formalin-induced pain at t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff9cc6bbecfb41c970b3938cdb5324aa
https://doi.org/10.3344/kjp.2008.21.1.27
https://doi.org/10.3344/kjp.2008.21.1.27