Catalepsy induced by nitric oxide synthase inhibitors

被引:35
作者
Del Bel, EA
da Silva, CA
Guimaraes, FS
机构
[1] Sch Odontol, Dept Physiol, BR-14040904 Ribeirao Preto, Brazil
[2] Sch Med, Dept Pharmacol, BR-14040904 Ribeirao Preto, Brazil
来源
GENERAL PHARMACOLOGY | 1998年 / 30卷 / 02期
基金
巴西圣保罗研究基金会;
关键词
L-NOARG; L-NAME; L-NMMA; L-arginine; tolerance; dopamine;
D O I
10.1016/S0306-3623(97)00075-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Previous study showed that N-G-nitro-L-arginine (L-NOARG), an inhibitor of nitric oxide synthase, induces catalepsy in a dose-dependent manner in male albino Swiss mice. 2. The objective of the present work was to further investigate this effect, extending it to other NOS inhibitors. 3. Results showed that L-NOARG (40-80 mg/kg IP), N-G-nitro L-arginine methylester (L-NAME, 40-160 mg/kg IP) or N-G-monomethyl-L-arginine (L-NMMA, 80 mg/kg IP) were able to induce catalepsy in mice. The effect of L-NOARG (40 mg/kg) was antagonized by pretreatment with L-arginine (300 mg/kg), but not by D arginine (300 mg/kg). The catalepsy inducing effect of L-NOARG suffered rapid tolerance, showing a significant decrease after two days of chronic treatment (40 mg/kg IP, twice a day). 4. The results suggest that interference with the formation of nitric oxide induces significant motor effects in mice. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:245 / 248
页数:4
相关论文
共 30 条
[1]   EFFECT OF NO SYNTHASE INHIBITION ON BEHAVIORAL-CHANGES INDUCED BY A SINGLE ADMINISTRATION OF METHAMPHETAMINE [J].
ABEKAWA, T ;
OHMORI, T ;
KOYAMA, T .
BRAIN RESEARCH, 1994, 666 (01) :147-150
[2]   NITRIC-OXIDE REGULATION OF METHAMPHETAMINE-INDUCED DOPAMINE RELEASE IN CAUDATE-PUTAMEN [J].
BOWYER, JF ;
CLAUSING, P ;
GOUGH, B ;
SLIKKER, W ;
HOLSON, RR .
BRAIN RESEARCH, 1995, 699 (01) :62-70
[3]   COMPARISON OF EFFECTS OF CHRONIC AND ACUTE ADMINISTRATION OF N-G-NITRO-L-ARGININE METHYL-ESTER TO THE RAT ON INHIBITION OF NITRIC OXIDE-MEDIATED RESPONSES [J].
BRYANT, CE ;
ALLCOCK, GH ;
WARNER, TD .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (08) :1673-1679
[4]   NITRIC-OXIDE - FOE OR FRIEND TO THE INJURED BRAIN [J].
CHOI, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (21) :9741-9743
[5]   CATALEPSY, FOS PROTEIN, AND DOPAMINE-RECEPTOR OCCUPANCY AFTER LONG-TERM HALOPERIDOL TREATMENT [J].
COPPENS, HJ ;
SEBENS, JB ;
KORF, J .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1995, 51 (2-3) :175-182
[6]   TOLERANCE TO HALOPERIDOL CATALEPSY [J].
EZRINWATERS, C ;
SEEMAN, P .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1977, 41 (03) :321-327
[7]   GLUTAMATE, NITRIC-OXIDE AND CELL CELL SIGNALING IN THE NERVOUS-SYSTEM [J].
GARTHWAITE, J .
TRENDS IN NEUROSCIENCES, 1991, 14 (02) :60-67
[8]   ANXIOLYTIC EFFECT OF NITRIC-OXIDE SYNTHASE INHIBITORS MICROINJECTED INTO THE DORSAL CENTRAL GREY [J].
GUIMARAES, FS ;
DEAGUIAR, JC ;
DELBEL, EA ;
BALLEJO, G .
NEUROREPORT, 1994, 5 (15) :1929-1932
[9]  
HOKFELT T, 1994, NEUROPHARMACOLOGY, V33, P221
[10]   NITRIC-OXIDE MODULATES NMDA-INDUCED INCREASES IN INTRACELLULAR CA-2+ IN CULTURED RAT FOREBRAIN NEURONS [J].
HOYT, KR ;
TANG, LH ;
AIZENMAN, E ;
REYNOLDS, IJ .
BRAIN RESEARCH, 1992, 592 (1-2) :310-316