Zobrazeno 1 - 10
of 133
pro vyhledávání: '"KANETO, Hiroshi"'
Autor:
Takahashi, Masakatsu 1, *, Fukunaga, Hiroko 1, Kaneto, Hiroshi 2, Fukudome, Shin-ichi 3, Yoshikawa, Masaaki 4
Publikováno v:
In Japanese Journal of Pharmacology 2000 84(3):259-265
Publikováno v:
Chemical & Pharmaceutical Bulletin. 42(9):1859-1863
Hybrids of amino-poly(ethylene glycol) (a PEG) and [D-Ala2, (N-Me)Phe4]enkephalin analogs, H-Tyr-D-Ala-Gly-(Me)Phe-aPEG, H-Tyr-D-Ala-Gly-(Me)Phe-Leu-aPEG and H-Tyr-D-Ala-Gly-(Me)Phe-D-Leu-aPEG, were prepared by the solution method and their antinocic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cf9bfe8fd41a072223ce3e58992fbbcf
http://hdl.handle.net/10069/38845
http://hdl.handle.net/10069/38845
Publikováno v:
日本神経精神薬理学雑誌. 14(4):195-214
Extensive evidence suggests that opioid influences on the immune response are mediated through opioid receptors on the surface of immune cells. In addition, the binding of opioid agonists to centrally located opioid receptors appears also to alter im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::87bc287a215f56d556ab624c253f9df7
https://nagasaki-u.repo.nii.ac.jp/records/1584
https://nagasaki-u.repo.nii.ac.jp/records/1584
Publikováno v:
European Journal of Pharmacology. 200:293-297
The site of action of the k opioid receptor agonist, U-50,488H in suppressing the development of tolerance to morphine antinociception was examined by local application, either intrathecal (i.t., spinal) or intracerebroventricular (i.c.v., supraspina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1297fd180778e8ea86f758282de32ce3
https://doi.org/10.1016/0014-2999(91)90585-e
https://doi.org/10.1016/0014-2999(91)90585-e
Publikováno v:
Japanese journal of pharmacology. 60(2)
Based on the data that diazepam, a benzodiazepine (BZP) receptor agonist, antagonized psychological (PSY)-stress induced analgesia (SIA) without prominent action on footshock (FS)- and forced swimming (SW)-SIA and that BZP receptors are coupled with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d42b70e769a28270fb631096efab3a70
https://pubmed.ncbi.nlm.nih.gov/1336079
https://pubmed.ncbi.nlm.nih.gov/1336079
Autor:
KAWASAKI, Koichi, MAEDA, Mitsuko, YAMASHIRO, Yuko, MAYUMI, Tadanori, TAKAHASHI, Masakatsu, KANETO, Hiroshi
Publikováno v:
Chemical & Pharmaceutical Bulletin. 41(11):2053-2054
The poly(ethylene glycol) hybrid of Leu-enkephalin (Tyr-Gly-Gly-Phe-Leu) was prepared and its analgesic activity was examined. Poly(ethylene glycol) #4000 was converted to amino-poly(ethylene glycol) and coupled with the Nα-protected pentapeptide, f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::92587a9251988dc96326582d11708d3b
http://hdl.handle.net/10069/38843
http://hdl.handle.net/10069/38843
Publikováno v:
Biological & Pharmaceutical Bulletin. 16(8):806-807
Intraperitoneal administration of lauric acid (C12) at the high doses, 100-1000μmol/kg, showed weak but dose-dependent antinociceptive effect in mice. Pretreatment of the animals with 0.1μmol/kg of i.p. C12 tended to suppress the antinociceptive ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::1bdc33a3e111461471927c02be31752d
http://hdl.handle.net/10069/38835
http://hdl.handle.net/10069/38835
Publikováno v:
Psychopharmacology; 1993, Vol. 112 Issue 1, p134-141, 8p
Facilitation of memory retrieval by pretest morphine mediated by μ but not δ and κ opioid receptors.
Publikováno v:
Psychopharmacology; 1990, Vol. 102 Issue 3, p329-332, 4p
Publikováno v:
Psychopharmacology; 1990, Vol. 100 Issue 1, p27-30, 4p