Effects of oleamide on choline acetyltransferase and cognitive activities

被引:83
作者
Heo, HJ
Park, YJ
Suh, YM
Choi, SJ
Kim, MJ
Cho, HY
Chang, YJ
Hong, B
Kim, HK
Kim, E
Kim, CJ
Kim, BG
Shin, DH [1 ]
机构
[1] Korea Univ, Grad Sch Biotechnol, Seoul 136701, South Korea
[2] Hanseo, Dept Food & Biotechnol, Seosan 356820, South Korea
[3] Inha Univ, Dept Biol Engn, Inchon 402751, South Korea
[4] Kyung Hee Univ, Dept Physiol, Seoul 130701, South Korea
[5] Seoul Natl Univ, Sch Chem Engn, Seoul 151742, South Korea
[6] Seoul Natl Univ, Inst Mol Biol & Genet, Seoul 151742, South Korea
关键词
choline acetyltransferase; Zityphus jujuba; oleamide; Alzheimer's disease; cognitive impairment;
D O I
10.1271/bbb.67.1284
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We screened 50 Korean traditional natural plants to measure the activation effect on choline acetyltransferase and attenuation of scopolamine-induced amnesia. The methanolic extracts from Zizyphus jujuba among the tested 50 plants, showed the highest activatory effect (34.1%) on choline acetyltransferase in vitro. By sequential fractionation of Zizyphus jujuba, the active component was finally identified as cis-9-octadecenoamide (oleamide). After isolation, oleamide showed a 65% activation effect. Administration of oleamide (0.32%) to mice significantly reversed the scopolamine-induced memory and/or cognitive impairment in the passive avoidance test and Y-maze test. Injection of scopolamine to mice impaired performance on the passive avoidance test (31% decrease in step-through latency), and on the Y-maze test (16% decrease in alternation behavior). In contrast, mice treated with oleamide before scopolamine injection were protected from these changes (12-25% decrease in step-through latency; 1-10% decrease in alternation behavior). These results suggest that oleamide should be a useful chemo-preventive agent against Alzheimer's disease.
引用
收藏
页码:1284 / 1291
页数:8
相关论文
共 23 条
[1]
Alzheimer's disease and oxidative stress: Implications for novel therapeutic approaches [J].
Behl, C .
PROGRESS IN NEUROBIOLOGY, 1999, 57 (03) :301-323
[2]
ACETYLATION OF CHOLINE AND HOMOCHOLINE BY MEMBRANE-BOUND CHOLINE-O-ACETYLTRANSFERASE IN MOUSE FOREBRAIN NERVE-ENDINGS [J].
BENISHIN, CG ;
CARROLL, PT .
JOURNAL OF NEUROCHEMISTRY, 1981, 36 (02) :732-740
[3]
BIEDLER JL, 1978, CANCER RES, V38, P3751
[4]
ALZHEIMERS-DISEASE - CHOLINE-ACETYLTRANSFERASE ACTIVITY IN BRAIN-TISSUE FROM CLINICAL AND PATHOLOGICAL SUBGROUPS [J].
BIRD, TD ;
STRANAHAN, S ;
SUMI, SM ;
RASKIND, M .
ANNALS OF NEUROLOGY, 1983, 14 (03) :284-293
[5]
The sleep inducing factor oleamide is produced by mouse neuroblastoma cells [J].
Bisogno, T ;
Sepe, N ;
DePetrocellis, L ;
Mechoulam, R ;
DiMarzo, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 239 (02) :473-479
[6]
SERUM-PROTEINS BYPASS THE BLOOD-BRAIN FLUID BARRIERS FOR EXTRACELLULAR ENTRY TO THE CENTRAL-NERVOUS-SYSTEM [J].
BROADWELL, RD ;
SOFRONIEW, MV .
EXPERIMENTAL NEUROLOGY, 1993, 120 (02) :245-263
[7]
Carr D. B., 1997, American Journal of Medicine, V103, p3S, DOI 10.1016/S0002-9343(97)00262-3
[8]
CHOLINERGIC FUNCTION AND INTELLECTUAL DECLINE IN ALZHEIMERS-DISEASE [J].
COLLERTON, D .
NEUROSCIENCE, 1986, 19 (01) :1-28
[9]
CHEMICAL CHARACTERIZATION OF A FAMILY OF BRAIN LIPIDS THAT INDUCE SLEEP [J].
CRAVATT, BF ;
PROSPEROGARCIA, O ;
SIUZDAK, G ;
GILULA, NB ;
HENRIKSEN, SJ ;
BOGER, DL ;
LERNER, RA .
SCIENCE, 1995, 268 (5216) :1506-1509
[10]
AMNESTIC EFFECTS IN MICE OF 4 SYNTHETIC PEPTIDES HOMOLOGOUS TO AMYLOID BETA-PROTEIN FROM PATIENTS WITH ALZHEIMER-DISEASE [J].
FLOOD, JF ;
MORLEY, JE ;
ROBERTS, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (08) :3363-3366