DIFFERENTIAL ANTINOCICEPTIVE EFFECTS OF SENDIDE, A NK1-RECEPTOR ANTAGONIST, AND MORPHINE IN THE CAPSAICIN TEST

被引:16
作者
SAKURADA, T [1 ]
YOGO, H [1 ]
KATSUMATA, K [1 ]
TANNO, K [1 ]
SAKURADA, S [1 ]
KISARA, K [1 ]
OHBA, M [1 ]
机构
[1] ASAHI GLASS CO LTD, DIV PROD RES & DEV, YOKOHAMA, KANAGAWA 221, JAPAN
关键词
SENDIDE; NK-1-RECEPTOR; MORPHINE; CAPSAICIN; SPINAL CORD; MOUSE;
D O I
10.1016/0006-8993(94)91080-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The peptide NK1-receptor antagonists, sendide and [D-Trp(7)]sendide, have been evaluated for antinociceptive activity in the capsaicin test. Both peptides, injected intrathecally (i.t.) 5 min prior to intraplantar capsaicin, produced a dose-dependent reduction of the capsaicin-induced paw licking response. Naloxone (4.0 mg/kg) pretreatment did not affect sendide- and [D-Trp(7)]sendide-induced antinociception, wherease naloxone at a dose of 0.5 mg/kg antagonized the antinociceptive effect of i.t. administered morphine. Conversely, the antinociceptive action induced by both NK1-receptor antagonists was reduced significantly by i.t. co-administration of substance P. Morphine-induced antinociception was not antagonized by co-administration of substance P. These results led us to the understanding of differential action mechanism of NK1-receptor antagonist- and morphine-induced antinociception as assayed by the capsaicin test.
引用
收藏
页码:319 / 322
页数:4
相关论文
共 23 条
[1]   INVITRO RELEASE OF SUBSTANCE-P FROM SPINAL-CORD SLICES BY CAPSAICIN CONGENERS [J].
BUCSICS, A ;
LEMBECK, F .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1981, 71 (01) :71-77
[2]   PHARMACOLOGICAL PROFILE OF A HIGH-AFFINITY DIPEPTIDE NK1-RECEPTOR ANTAGONIST, FK888 [J].
FUJII, T ;
MURAI, M ;
MORIMOTO, H ;
MAEDA, Y ;
YAMAOKA, M ;
HAGIWARA, D ;
MIYAKE, H ;
IKARI, N ;
MATSUO, M .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 107 (03) :785-789
[3]   SUBSTANCE-P RELEASE FROM SPINAL-CORD SLICES BY CAPSAICIN [J].
GAMSE, R ;
MOLNAR, A ;
LEMBECK, F .
LIFE SCIENCES, 1979, 25 (07) :629-636
[4]  
GARCES YI, 1992, LIFE SCI, V52, P353
[5]   PHARMACOLOGICAL PROPERTIES OF A POTENT AND SELECTIVE NONPEPTIDE SUBSTANCE-P ANTAGONIST [J].
GARRET, C ;
CARRUETTE, A ;
FARDIN, V ;
MOUSSAOUI, S ;
PEYRONEL, JF ;
BLANCHARD, JC ;
LADURON, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (22) :10208-10212
[6]   RELEASE OF SUBSTANCE-P FROM THE CAT SPINAL-CORD [J].
GO, VLW ;
YAKSH, TL .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 391 :141-167
[7]   CAPSAICIN AND POTASSIUM EVOKED SUBSTANCE-P RELEASE FROM THE NUCLEUS TRACTUS SOLITARIUS AND SPINAL TRIGEMINAL NUCLEUS INVITRO [J].
HELKE, CJ ;
JACOBOWITZ, DM ;
THOA, NB .
LIFE SCIENCES, 1981, 29 (17) :1779-1785
[8]  
HYLDEN J L K, 1983, European Journal of Pharmacology, V86, P95
[9]  
HYLDEN JLK, 1980, EUR J PHARMACOL, V67, P311
[10]   OPIATE ANALGESICS INHIBIT SUBSTANCE - P RELEASE FROM RAT TRIGEMINAL NUCLEUS [J].
JESSELL, TM ;
IVERSEN, LL .
NATURE, 1977, 268 (5620) :549-551