VASOPRESSIN INDUCTION OF LONG-LASTING POTENTIATION OF SYNAPTIC TRANSMISSION IN THE DENTATE GYRUS

被引:48
作者
CHEN, C
BRINTON, RD
SHORS, TJ
THOMPSON, RF
机构
[1] UNIV SO CALIF,SCH PHARM,DEPT MOLEC PHARMACOL & TOXICOL,1985 ZONAL AVE,LOS ANGELES,CA 90033
[2] UNIV SO CALIF,SCH PHARM,NEUROSCI PROGRAM,LOS ANGELES,CA 90033
关键词
LTP; HIPPOCAMPUS; LEARNING AND MEMORY; PEPTIDE;
D O I
10.1002/hipo.450030211
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Vasopressin receptors are present in both the developing and mature dentate gyrus of the rat brain and are of the V1 vasopressor type. Because vasopressin has been shown to influence memory function when injected into the dentate gyrus. the influence of this peptide on an electrophysiological model of learning and memory using the field excitatory postsynaptic potential (EPSP) of the dentate gyrus was investigated. Results of these studies showed that nanomolar concentrations of [Arg8]-vasopressin induced a prolonged increase in the amplitude and slope of the evoked population response in the presence of 1.5 mM calcium. Moreover, the expression of the vasopressin-induced potentiation of the EPSP persisted following removal of vasopressin from the perfusion medium. The vasopressin-induced sustained increase has been termed long-term vasopressin potentiation (LTVP). The closely related neuropeptide oxytocin had no effect upon the EPSP of the dentate gyrus. Preincubation of hippocampal slices in a selective V1 antagonist blocked the expression of LTVP. The ability of the V1 antagonist to block LTVP demonstrates that the potentiation induced by vasopressin is receptor-specific. In the presence of 2.5 mM calcium, the effect of vasopressin was opposite to that observed in 1.5 mM calcium. Under the conditions of 2.5 calcium, vasopressin induced a prolonged depression in the amplitude and slope of the EPSP. Expression of both potentiation and depression appeared within 5 minutes of application and persisted for the length of the observation, 60 minutes. These experiments demonstrate that vasopressin can induce long-lasting changes in the excitability of dentate gyrus neurons that are both calcium-dependent and receptor-specific.
引用
收藏
页码:193 / 204
页数:12
相关论文
共 57 条
[21]  
GRUENER R, 1988, FASEB J, V2, pA785
[22]   ORIGIN AND TERMINATION OF HIPPOCAMPAL PERFORANT PATH IN RAT STUDIED BY SILVER IMPREGNATION [J].
HJORTHSIMONSEN, A ;
JEUNE, B .
JOURNAL OF COMPARATIVE NEUROLOGY, 1972, 144 (02) :215-+
[23]  
JOHNSTON D, 1988, P355
[24]   REGULATION OF SYNAPTIC TRANSMISSION IN THE CENTRAL NERVOUS-SYSTEM - LONG-TERM POTENTIATION [J].
KENNEDY, MB .
CELL, 1989, 59 (05) :777-787
[25]   PHOSPHATIDYLINOSITOL METABOLISM IN RAT HEPATOCYTES STIMULATED BY VASOPRESSIN [J].
KIRK, CJ ;
MICHELL, RH ;
HEMS, DA .
BIOCHEMICAL JOURNAL, 1981, 194 (01) :155-165
[26]   REGULATION OF GLUCONEOGENESIS BY NOREPINEPHRINE, VASOPRESSIN, AND ANGIOTENSIN-II - A COMPARATIVE-STUDY IN THE ABSENCE AND PRESENCE OF EXTRACELLULAR CA-2+ [J].
KNEER, NM ;
LARDY, HA .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1983, 225 (01) :187-195
[27]   BEHAVIORAL-EFFECTS OF NEUROPEPTIDES - ENDORPHINS AND VASOPRESSIN [J].
KOOB, GF ;
BLOOM, FE .
ANNUAL REVIEW OF PHYSIOLOGY, 1982, 44 :571-582
[28]   EFFECT OF OXYTOCIN AND VASOPRESSIN ON MEMORY CONSOLIDATION - SITES OF ACTION AND CATECHOLAMINERGIC CORRELATES AFTER LOCAL MICRO-INJECTION INTO LIMBIC-MIDBRAIN STRUCTURES [J].
KOVACS, GL ;
BOHUS, B ;
VERSTEEG, DHG ;
DEKLOET, ER ;
DEWIED, D .
BRAIN RESEARCH, 1979, 175 (02) :303-314
[29]   [1-(BETA-MERCAPTO-BETA,BETA-CYCLOPENTAMETHYLENEPROPIONIC ACID),2-(O-METHYL)TYROSINE]ARGININE-VASOPRESSIN AND [1-(BETA-MERCAPTO-BETA,BETA-CYCLOPENTAMETHYLENEPROPIONIC ACID)]ARGININE-VASOPRESSIN, 2 HIGHLY POTENT ANTAGONISTS OF THE VASOPRESSOR RESPONSE TO ARGININE-VASOPRESSIN [J].
KRUSZYNSKI, M ;
LAMMEK, B ;
MANNING, M ;
SETO, J ;
HALDAR, J ;
SAWYER, WH .
JOURNAL OF MEDICINAL CHEMISTRY, 1980, 23 (04) :364-368
[30]  
LANDGRAF R, 1991, BRAIN RES, V554, P287