Administration of cholecystokinin sulphated octapeptide (CCK-8S) induces changes on rat amino acid tissue levels and on a behavioral test for anxiety

被引:23
作者
Acosta, GB [1 ]
机构
[1] CONICET, Consejo Nacl Invest Cient & Tecn, Inst Invest Farmacol, RA-1113 Buenos Aires, DF, Argentina
来源
GENERAL PHARMACOLOGY | 1998年 / 31卷 / 04期
关键词
amino acids; CCK-8S; PD 135,158; light/dark transition test; brain;
D O I
10.1016/S0306-3623(98)00075-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The effect of the intraperitoneal administration of cholecystokinin sulphated octa peptide (CCK 8S) (10 nmol/kg i.p.) on endogenous levels of several amino acids in five areas of the rat brain was analyzed. The olfactory bulb, hypothalamus, hippocampus, cerebral frontal cortex, and corpus striatum were evaluated. In addition, the effects of CCK-8S and PD 135,158 (1 mg/kg), a selective CCKB antagonist, on the performance of rats submitted to a dark/light transition test were also studied. 2. Upon administration of CCK-8S, the concentration of glutamate was reduced (27%) in the olfactory bulb. The same was observed when the levels of glycine (31%) or alanine (43%) were determined. No significant effects were produced by CCK-8S on cortical and hypothalamic levels. In the hippocampus, the concentration of both glutamate (27%) and taurine (29%) were reduced, whereas the levels of GABA in the striatum (29%) were increased. 3. After a single injection of CCK-8S, the time spent by the rats in the illuminated site of the dark/light transition test box, was not changed. On the contrary, the administration of PD 135,158 increased the time spent in the lighted compartment. 4. These results show that systemic administration of CCK 8S produced regional specific changes in brain amino acids, without producing any significant behavioral modification in the rat exposed to a dark/light box. In contrast, the selective CCKB receptor antagonist, PD 135,158, induces anxiolytic-like action in an animal model of anxiety. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:637 / 641
页数:5
相关论文
共 36 条
[21]  
Hokfelt T, 1988, J Chem Neuroanat, V1, P11
[22]  
HOMMER DW, 1986, J NEUROSCI, V6, P3039
[23]   DEVELOPMENT OF A CLASS OF SELECTIVE CHOLECYSTOKININ TYPE-B RECEPTOR ANTAGONISTS HAVING POTENT ANXIOLYTIC ACTIVITY [J].
HUGHES, J ;
BODEN, P ;
COSTALL, B ;
DOMENEY, A ;
KELLY, E ;
HORWELL, DC ;
HUNTER, JC ;
PINNOCK, RD ;
WOODRUFF, GN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6728-6732
[24]   A hormone mechanism for gall-bladder contraction and evacuation [J].
Ivy, AC ;
Oldberg, E .
AMERICAN JOURNAL OF PHYSIOLOGY, 1928, 86 (03) :599-613
[25]  
KATSUURA G, 1981, EXPERIENTIA, V30, P60
[26]   REVERSAL OF ANTINOCICEPTIVE EFFECT OF CHOLECYSTOKININ BY BENZODIAZEPINES AND A BENZODIAZEPINE ANTAGONIST, RO-15-1788 [J].
KUBOTA, K ;
SUGAYA, K ;
MATSUDA, I ;
MATSUOKA, Y ;
TERAWAKI, Y .
JAPANESE JOURNAL OF PHARMACOLOGY, 1985, 37 (01) :101-105
[27]   A FLUORIMETRIC METHOD FOR DETERMINATION OF GABA IN TISSUES FOLLOWING CATION-EXCHANGE CHROMATOGRAPHY AND CONDENSATION WITH ORTHO-PHTHALALDEHYDE [J].
LINDGREN, S ;
ANDEN, NE ;
GRABOWSKAANDEN, M .
JOURNAL OF NEURAL TRANSMISSION, 1982, 55 (03) :243-252
[28]   CHANGES IN CENTRAL GABAERGIC FUNCTION FOLLOWING ACUTE AND REPEATED STRESS [J].
LOSADA, MEO .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 93 (03) :483-490
[29]   CHOLECYSTOKININ-INDUCED SUPPRESSION OF LOCOMOTION IS ATTENUATED IN CAPSAICIN PRETREATED RATS [J].
RITTER, RC ;
KALIVAS, P ;
BERNIER, S .
PEPTIDES, 1986, 7 (04) :587-590
[30]  
SCHNEIDER LH, 1986, PEPTIDES, V4, P749