PRENATAL OXAZEPAM EFFECTS ON COCAINE CONDITIONED PLACE PREFERENCE IN DEVELOPING MICE

被引:9
作者
DELLOMO, G [1 ]
LAVIOLA, G [1 ]
CHIAROTTI, F [1 ]
ALLEVA, E [1 ]
BIGNAMI, G [1 ]
机构
[1] IST SUPER SANITA,BEHAV PATHOPHYSIOL SECT,FISIOPATOL ORGANO & SISTEMA LAB,VIALE REGINA ELENA 299,I-00161 ROME,ITALY
关键词
BEHAVIORAL DEVELOPMENT; LOCOMOTOR ACTIVITY; CONDITIONED PLACE PREFERENCE; COCAINE; PRENATAL OXAZEPAM; MOUSE;
D O I
10.1016/0892-0362(93)90017-I
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The positively reinforcing and activity enhancing effects of IP cocaine (0, 5, or 25 mg/kg) were assessed at three ages (14-17, 21-24, and 28-31 days) in outbred CD-1 mouse pups treated prenatally by either oxazepam (OX, 15 mg/kg PO twice/day on days 12-16 of pregnancy) or vehicle (VEH). A 4-day unbiased conditioned place preference (CPP) procedure was used with combined visual and tactile cues (white walls and wide-mesh metal floor versus black walls and narrow-mesh floor) (11). A single 25 mg/kg cocaine dose produced CPP in both prenatal groups of 28-31 day-old mice. At the two younger ages, a significant cocaine CPP was found in prenatal OX mice but not in vehicle animals; the latter apparently developed CPP less readily than the offspring of indisturbed dams in a previous experiment (11). On the other hand, prenatal OX did not produce substantial changes in the developmental profile of cocaine effects on locomotor activity, consisting of a dose-related response enhancement which is much more marked at 22 and 29 days than before weaning (11).
引用
收藏
页码:207 / 210
页数:4
相关论文
共 20 条
[1]   SHORT-TERM, MEDIUM-TERM, AND LONG-TERM EFFECTS OF PRENATAL OXAZEPAM ON NEUROBEHAVIOURAL DEVELOPMENT OF MICE [J].
ALLEVA, E ;
LAVIOLA, G ;
TIRELLI, E ;
BIGNAMI, G .
PSYCHOPHARMACOLOGY, 1985, 87 (04) :434-441
[2]   DEVELOPMENT OF MOUSE ACTIVITY, STIMULUS REACTIVITY, HABITUATION, AND RESPONSE TO AMPHETAMINE AND SCOPOLAMINE [J].
ALLEVA, E ;
BIGNAMI, G .
PHYSIOLOGY & BEHAVIOR, 1985, 34 (04) :519-523
[3]  
ALLEVA E, 1986, NEUROTOXICOLOGY, V7, P309
[4]  
ARCHER J E, 1971, Developmental Psychobiology, V4, P193, DOI 10.1002/dev.420040302
[5]   SELECTIVE CHANGES IN MOUSE BEHAVIORAL-DEVELOPMENT AFTER PRENATAL BENZODIAZEPINE EXPOSURE - A PROGRESS REPORT [J].
BIGNAMI, G ;
ALLEVA, E ;
CHIAROTTI, F ;
LAVIOLA, G .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 1992, 16 (05) :587-604
[6]   THE EFFECTS OF PERINATAL DIAZEPAM EXPOSURE ON STRESS-INDUCED ACTIVATION OF THE MESOTELENCEPHALIC DOPAMINE SYSTEM [J].
DEUTCH, AY ;
GRUEN, RJ ;
ROTH, RH .
NEUROPSYCHOPHARMACOLOGY, 1989, 2 (02) :105-114
[7]   CENTRAL AND PERIPHERAL BENZODIAZEPINE RECEPTORS - INVOLVEMENT IN AN ORGANISMS RESPONSE TO PHYSICAL AND PSYCHOLOGICAL STRESS [J].
DRUGAN, RC ;
HOLMES, PV .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1991, 15 (02) :277-298
[8]   SOME LONG-LASTING NEUROCHEMICAL EFFECTS OF PRENATAL OR EARLY POSTNATAL EXPOSURE TO DIAZEPAM [J].
FRIEDER, B ;
GRIMM, VE .
JOURNAL OF NEUROCHEMISTRY, 1985, 45 (01) :37-42
[9]   PERINATAL DIAZEPAM EXPOSURE - ALTERATIONS IN EXPLORATORY-BEHAVIOR AND MESOLIMBIC DOPAMINE TURNOVER [J].
GRUEN, RJ ;
DEUTCH, AY ;
ROTH, RH .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 36 (01) :169-175
[10]   ONTOGENY OF COCAINE HYPERACTIVITY AND CONDITIONED PLACE PREFERENCE IN MICE [J].
LAVIOLA, G ;
DELLOMO, G ;
ALLEVA, E ;
BIGNAMI, G .
PSYCHOPHARMACOLOGY, 1992, 107 (2-3) :221-228