Hippocampal acetylcholine release during memory testing in rats: Augmentation by glucose

被引:264
作者
Ragozzino, ME [1 ]
Unick, KE [1 ]
Gold, PE [1 ]
机构
[1] UNIV VIRGINIA, DEPT PSYCHOL, LIFE SCI LABS, CHARLOTTESVILLE, VA 22903 USA
关键词
cholinergic; learning; hippocampus; microdialysis;
D O I
10.1073/pnas.93.10.4693
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several lines of evidence indicate that a modest increase in circulating glucose levels enhances memory. One mechanism underlying glucose effects on memory may be an increase in acetylcholine (ACh) release. The present experiment determined whether enhancement of spontaneous alternation performance by systemic glucose treatment is related to an increase in hippocampal ACh output. Samples of extracellular ACh were assessed at 12-min intervals using in vivo microdialysis with HPLC-EC. Twenty-four minutes after an intraperitoneal injection of saline or glucose (100, 250, or 1000 mg/kg), rats were tested in a four-arm cross maze for spontaneous alternation behavior combined with microdialysis collection. Glucose at 250 mg/kg, but not 100 or 1000 mg/kg, produced an increase in spontaneous alternation scores (69.5%) and ACh output (121.5% versus baseline) compared to alternation scores (44.7%) and ACh output (58.9% versus baseline) of saline controls. The glucose-induced increase in alternation scores and ACh output was not secondary to changes in locomotor activity. Saline and glucose (100-1000 mg/kg) treatment had no effect on hippocampal ACh output when rats remained in the holding chamber. These findings suggest that glucose may enhance memory by directly or indirectly increasing the release of ACh. The results also indicate that hippocampal ACh release is increased in rats performing a spatial task Moreover, because glucose enhanced ACh output only during behavioral testing, circulating glucose may modulate ACh release only under conditions in which cholinergic cells are activated.
引用
收藏
页码:4693 / 4698
页数:6
相关论文
共 47 条
[1]  
[Anonymous], 1979, A Stereotaxic Atlas of the Rat Brain
[2]   EVIDENCE FOR THE REGULATORY FUNCTION OF SYNAPTOPLASMIC ACETYL-COA IN ACETYLCHOLINE SYNTHESIS IN NERVE-ENDINGS [J].
BIELARCZYK, H ;
SZUTOWICZ, A .
BIOCHEMICAL JOURNAL, 1989, 262 (01) :377-380
[3]  
BRADFORD HF, 1986, CHEM NEUROBIOLOGY
[4]   EFFECTS OF GLUCOSE AND DIABETES ON BINDING OF NALOXONE AND DIHYDROMORPHINE TO OPIATE RECEPTORS IN MOUSE-BRAIN [J].
BRASE, DA ;
HAN, YH ;
DEWEY, WL .
DIABETES, 1987, 36 (10) :1173-1177
[5]   CHOLINERGIC ACTIVITY IN THE RAT HIPPOCAMPUS, CORTEX AND STRIATUM CORRELATES WITH LOCOMOTOR-ACTIVITY - AN INVIVO MICRODIALYSIS STUDY [J].
DAY, J ;
DAMSMA, G ;
FIBIGER, HC .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1991, 38 (04) :723-729
[6]  
DECKER MW, 1988, J NEUROSCI, V8, P90
[7]   RAISED GLUCOSE-LEVELS ENHANCE SCOPOLAMINE-INDUCED ACETYLCHOLINE OVERFLOW FROM THE HIPPOCAMPUS - AN INVIVO MICRODIALYSIS STUDY IN THE RAT [J].
DURKIN, TP ;
MESSIER, C ;
DEBOER, P ;
WESTERINK, BHC .
BEHAVIOURAL BRAIN RESEARCH, 1992, 49 (02) :181-188
[8]  
FELLOWS LK, 1992, J NEUROCHEM, V59, P2141
[9]  
Gibbs EL, 1942, J BIOL CHEM, V144, P325
[10]   IMPAIRED SYNTHESIS OF ACETYLCHOLINE IN BRAIN ACCOMPANYING MILD HYPOXIA AND HYPOGLYCEMIA [J].
GIBSON, GE ;
BLASS, JP .
JOURNAL OF NEUROCHEMISTRY, 1976, 27 (01) :37-42