Increased adenylyl cyclase type 1 mRNA, but not adenylyl cyclase type 2 in the rat hippocampus following antidepressant treatment

被引:25
作者
Jensen, JB
Mikkelsen, JD
Mork, A
机构
[1] Bispebjerg Hosp, Dept Clin Biochem, DK-2400 Copenhagen NV, Denmark
[2] H Lundbeck & Co AS, Dept Neurobiol Res & Dev, DK-2500 Copenhagen, Denmark
关键词
adenylyl cyclase; citalopram; lithium; serotonin reuptake inhibitor; mRNA; cAMP;
D O I
10.1016/S0924-977X(99)00064-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The adenylyl cyclase (AC) system is affected by several types of antidepressant treatments, and increased activity in this system is linked to the therapeutic action of antidepressants. The present study was undertaken to compare the effects: of single-dose acid long-term treatment with the selective serotonin reuptake inhibitor, citalopram (10 mg/kg, i.p.), on the AC system in the male rat brain of Wistar rats. Furthermore, we compared the effects of long-term citalopram and lithium treatments on the AC system. Long-term citalopram, but not single-dose administration, increased the AC type 1 mRNA in the hippocampus, whereas type 2 mRNA was unaffected. Long-term lithium treatment also increased AC1 in the hippocampus. However, lone-term citalopram treatment did not increase AC type 1 protein, basal or forskolin-stimulated AC activity, but CTP increased AC activity in the hippocampus. This may indicate enhanced AC/G protein coupling. Thus, citalopram may increase cAMP signalling by acting on components of the AC system without affecting the protein level of the AC type 1. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 111
页数:7
相关论文
共 36 条
[1]   A preliminary study of possible psychoactive effects of intravenous forskolin in depressed and schizophrenic patients - Short communication [J].
Bersudsky, Y ;
Kotler, M ;
Shifrin, M ;
Belmaker, RH .
JOURNAL OF NEURAL TRANSMISSION, 1996, 103 (12) :1463-1467
[2]  
CHEN J, 1995, J PHARMACOL EXP THER, V275, P509
[3]  
CHEN JA, 1995, J NEUROCHEM, V64, P724
[4]   CHRONIC LITHIUM REGULATES THE EXPRESSION OF ADENYLATE-CYCLASE AND GI-PROTEIN ALPHA-SUBUNIT IN RAT CEREBRAL-CORTEX [J].
COLIN, SF ;
CHANG, HC ;
MOLLNER, S ;
PFEUFFER, T ;
REED, RR ;
DUMAN, RS ;
NESTLER, EJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) :10634-10637
[5]   ADENYLYL-CYCLASE ACTIVITY AND G-PROTEIN SUBUNIT LEVELS IN POSTMORTEM FRONTAL-CORTEX OF SUICIDE VICTIMS [J].
COWBURN, RF ;
MARCUSSON, JO ;
ERIKSSON, A ;
WIEHAGER, B ;
ONEILL, C .
BRAIN RESEARCH, 1994, 633 (1-2) :297-304
[6]   SELECTIVE ADENYLATE-CYCLASE INCREASE IN THE LIMBIC AREA OF LONG-TERM IMIPRAMINE-TREATED RATS [J].
DEMONTIS, GM ;
DEVOTO, P ;
GESSA, GL ;
PORCELLA, A ;
SERRA, G ;
TAGLIAMONTE, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 180 (01) :169-174
[7]   DISTRIBUTION OF TYPE-II ADENYLYL-CYCLASE MESSENGER-RNA IN THE RAT-BRAIN [J].
FURUYAMA, T ;
INAGAKI, S ;
TAKAGI, H .
MOLECULAR BRAIN RESEARCH, 1993, 19 (1-2) :165-170
[8]   CLONING AND EXPRESSION OF AN ADENYLYL CYCLASE LOCALIZED TO THE CORPUS STRIATUM [J].
GLATT, CE ;
SNYDER, SH .
NATURE, 1993, 361 (6412) :536-538
[9]   Adenylyl cyclases: Structure, regulation and function in an enzyme superfamily [J].
Hanoune, J ;
Pouille, Y ;
Tzavara, E ;
Shen, TS ;
Lipskaya, L ;
Miyamoto, N ;
Suzuki, Y ;
Defer, N .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1997, 128 (1-2) :179-194
[10]  
HOROWSKI R, 1985, CURR THER RES CLIN E, V38, P23