Effects of acute ethanol or amphetamine administration on the acoustic startle response and prepulse inhibition in adolescent and adult rats

被引:35
作者
Brunell, Steven Craig [1 ]
Spear, Linda Patia [1 ]
机构
[1] SUNY Binghamton, Dept Psychol, Ctr Dev Psychobiol, Binghamton, NY 13902 USA
关键词
adolescence; development; ethanol; amphetamine; prepulse inhibition; acoustic startle response; rats;
D O I
10.1007/s00213-006-0380-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adolescents differ from adults in their sensitivity to a variety of psychoactive drugs. For example, adolescent rats are less sensitive to locomotor stimulant and stereotypic effects of amphetamine as well as to motor-impairing and hypnotic effects of ethanol while more sensitive to ethanol-induced disruption of brain plasticity. The current study further explored age differences in psychopharmacological sensitivity by examining the effects of d-amphetamine (1.0 and 4.0 mg/kg) or ethanol (0.5, 1.0 and 1.5 g/kg) given interperitoneally on the acoustic startle response (ASR) and prepulse inhibition (PPI) in male adolescent and adult Sprague-Dawley rats. The animals were given five startle trials (120 dB for 40 ms) before semi-randomized presentation of 12 startle trials interspersed with ten trials at each prepulse intensity (40 ms pulse of 5, 10, or 20 dB above background; 100 ms before the startle stimulus). Adolescent controls showed significantly less PPI than adults, replicating previous ontogenetic findings. The higher dose of amphetamine disrupted PPI in adult but not in adolescent animals, extending previous reports of an adolescent insensitivity to amphetamine to include this measure of sensorimotor gating. Ethanol exposure failed to alter PPI at either age, although both the 1.0 and 1.5 g/kg doses of ethanol significantly suppressed the magnitude of the ASR at both ages, potentially reflecting sedative or anxiolytic effects. These data provide further evidence of the relative insensitivity of adolescent animals to amphetamine, although no age effects were found in terms of ethanol sensitivity using these measures of startle and sensorimotor gating.
引用
收藏
页码:579 / 586
页数:8
相关论文
共 53 条
[31]   Prepulse inhibition in fawn-hooded rats:: increased sensitivity to 5-HT1A receptor stimulation [J].
Martin, S ;
Lawrence, AJ ;
van den Buuse, M .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2004, 14 (05) :373-379
[32]   Typical but not "atypical" antipsychotic effects on startle gating deficits in prepubertal rats [J].
Martinez, ZA ;
Platten, A ;
Pollack, E ;
Shoemaker, J ;
Ro, H ;
Pitcher, L ;
Geyer, MA ;
Swerdlow, NR .
PSYCHOPHARMACOLOGY, 2002, 161 (01) :38-46
[33]   NEUROTRANSMITTER AND NEUROMODULATORY MECHANISMS INVOLVED IN ALCOHOL-ABUSE AND ALCOHOLISM [J].
NEVO, I ;
HAMON, M .
NEUROCHEMISTRY INTERNATIONAL, 1995, 26 (04) :305-336
[34]   Age-specific behavioral responses to psychostimulants in mice [J].
Niculescu, M ;
Ehrlich, ME ;
Unterwald, EM .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2005, 82 (02) :280-288
[35]   STARTLE RESPONSE IN RATS - EFFECT OF ETHANOL [J].
POHORECKY, LA ;
CAGAN, M ;
BRICK, J ;
JAFFE, LS .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1976, 4 (03) :311-316
[36]   RESPONDING TO ACOUSTIC STARTLE DURING CHRONIC ETHANOL INTOXICATION AND WITHDRAWAL [J].
RASSNICK, S ;
KOOB, GF ;
GEYER, MA .
PSYCHOPHARMACOLOGY, 1992, 106 (03) :351-358
[37]   CONDITIONED PLEASURE ATTENUATES THE STARTLE RESPONSE IN RATS [J].
SCHMID, A ;
KOCH, M ;
SCHNITZLER, HU .
NEUROBIOLOGY OF LEARNING AND MEMORY, 1995, 64 (01) :1-3
[38]   Amphetamine dose dependently disrupts prepulse inhibition of the acoustic startle response in rats within a narrow time window [J].
Sills, TL .
BRAIN RESEARCH BULLETIN, 1999, 48 (04) :445-448
[39]   Decreased sensitivity to the hypnotic effects of ethanol early in ontogeny [J].
Silveri, MM ;
Spear, LP .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1998, 22 (03) :670-676
[40]   The effects of NMDA and GABAA pharmacological manipulations on ethanol sensitivity in immature and mature animals [J].
Silveri, MM ;
Spear, LP .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2002, 26 (04) :449-456