Effect of isatin, an endogenous MAO inhibitor, on acetylcholine and dopamine levels in the rat striatum.

被引:0
作者
Hamaue, N [1 ]
Yamazaki, N
Minami, M
Endo, T
Hirafuji, M
Monma, Y
Togashi, H
Saito, H
Parvez, SH
机构
[1] Hlth Sci Univ Hokkaido, Fac Pharmaceut Sci, Dept Pharmacol, Ishikari, Hokkaido 06102, Japan
[2] Hlth Sci Univ Hokkaido, Fac Pharmaceut Sci, Dept Clin Pharmacol, Ishikari, Hokkaido 06102, Japan
[3] Hokkaido Univ, Coll Med Technol, Sapporo, Hokkaido 060, Japan
[4] Hokkaido Univ, Sch Med, Dept Pharmacol, Sapporo, Hokkaido 060, Japan
[5] CNRS, Inst Alfred Fossard Neurosci, F-75700 Paris, France
关键词
isatin; endogenous MAO inhibitor; dopamine; acetylcholine; striatum;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isatin, an endogenous inhibitor of monoamine oxidase (MAO), has several physiological properties for stress and anxiety following extensive experimental and clinical investigations. We previously identified isatin in the urine and brain of stroke-prone spontaneously hypertensive rats (SHRSP) using gas chromatography mass spectrometry. Lately, isatin was reported to have an inhibitory effect on acetylcholinesterase (AChE). This study elucidated the effect of isatin administered exogenously on the acetylcholine (ACh), choline (Ch) and dopamine (DA) levels of brain tissues in rats. Two hours after intraperitoneal administration of isatin (50 mg or 200 mg), striatal ACh, Ch and DA levels significantly increased Isatin (10(-6) M or 10(-4) M) administration through microdialysis also induced a significant increase in the ACh and DA concentration of perfusate from the rat striatum in a concentration-dependent manner. We were the first to show that isatin significantly increased ACh and DA levels in the rat striatum. These results suggest that endogenous isatin may play a role in regulating the brain levels of ACh with increasing the level of DA.
引用
收藏
页码:367 / 377
页数:11
相关论文
共 46 条
  • [1] BIOCHEMICAL-EVIDENCE OF SELECTIVE NERVE-CELL CHANGES IN THE NORMAL AGING HUMAN AND RAT-BRAIN
    ALLEN, SJ
    BENTON, JS
    GOODHARDT, MJ
    HAAN, EA
    SIMS, NR
    SMITH, CCT
    SPILLANE, JA
    BOWEN, DM
    DAVISON, AN
    [J]. JOURNAL OF NEUROCHEMISTRY, 1983, 41 (01) : 256 - 265
  • [2] STRESS INCREASES ENDOGENOUS BENZODIAZEPINE RECEPTOR LIGAND-MONOAMINE OXIDASE INHIBITORY ACTIVITY (TRIBULIN) IN RAT-TISSUES
    ARMANDO, I
    LEVIN, G
    BARONTINI, M
    [J]. JOURNAL OF NEURAL TRANSMISSION, 1988, 71 (01) : 29 - 37
  • [3] BANSAL R C, 1988, Research Bulletin of the Panjab University Science, V39, P71
  • [4] URINARY CATECHOLAMINE METABOLITE AND TRIBULIN OUTPUT DURING LACTATE INFUSION
    CLOW, A
    GLOVER, V
    WEG, MW
    WALKER, PL
    SHEEHAN, DV
    CARR, DB
    SANDLER, M
    [J]. BRITISH JOURNAL OF PSYCHIATRY, 1988, 152 : 122 - 126
  • [5] PERGOLIDE CAN INDUCE SOLUBLE SUPEROXIDE-DISMUTASE IN RAT STRIATA
    CLOW, A
    HUSSAIN, T
    GLOVER, V
    SANDLER, M
    WALKER, M
    DEXTER, D
    [J]. JOURNAL OF NEURAL TRANSMISSION-GENERAL SECTION, 1992, 90 (01) : 27 - 31
  • [6] DIFFERENTIAL EFFECT OF SYSTEMIC ADMINISTRATION OF BROMOCRIPTINE AND L-DOPA ON THE RELEASE OF ACETYLCHOLINE FROM STRIATUM OF INTACT AND 6-OHDA-TREATED RATS
    DEBOER, P
    ABERCROMBIE, ED
    HEERINGA, M
    WESTERINK, BHC
    [J]. BRAIN RESEARCH, 1993, 608 (02) : 198 - 203
  • [7] ENDO T, 1989, BIOGENIC AMINES, V6, P571
  • [8] ISATIN - IDENTITY WITH THE PURIFIED ENDOGENOUS MONOAMINE-OXIDASE INHIBITOR TRIBULIN
    GLOVER, V
    HALKET, JM
    WATKINS, PJ
    CLOW, A
    GOODWIN, BL
    SANDLER, M
    [J]. JOURNAL OF NEUROCHEMISTRY, 1988, 51 (02) : 656 - 659
  • [9] GLOVER V, 1991, INDIAN J EXP BIOL, V29, P1
  • [10] MONO-AMINE OXIDASE INHIBITOR IN HUMAN-URINE
    GLOVER, V
    REVELEY, MA
    SANDLER, M
    [J]. BIOCHEMICAL PHARMACOLOGY, 1980, 29 (03) : 467 - 470