Response-inhibition capacity in spontaneously hypertensive and Wistar rats: acquisition of fixed minimum interval performance and responsiveness to D-amphetamine

被引:3
作者
Rojas-Leguizamon, Maryed [1 ,3 ]
Baroja, Jose L. [1 ]
Sanabria, Federico [2 ]
Orduna, Vladimir [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Dept Psychol, Mexico City, DF, Mexico
[2] Arizona State Univ, Dept Psychol, Tempe, AZ 85287 USA
[3] Univ Guadalajara, Univ Ctr Valleys, Dept Hlth Sci, Ameca, Jalisco, Mexico
来源
BEHAVIOURAL PHARMACOLOGY | 2018年 / 29卷 / 08期
关键词
animal models; attention-deficit hyperactivity disorder; d-amphetamine; impulsivity; response inhibition; spontaneous hypertensive rat; DEFICIT HYPERACTIVITY DISORDER; ANIMAL-MODEL; KYOTO RATS; BEHAVIORAL-INHIBITION; REINFORCER MAGNITUDE; SCHEDULE; METHYLPHENIDATE; IMPULSIVITY; NICOTINE; DRUGS;
D O I
10.1097/FBP.0000000000000411
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Reduced response-inhibition capacity is a defining feature of attention-deficit hyperactivity disorder. The fixed minimum interval (FMI) schedule has been systematically validated to assess such capacity in rats. On each FMI trial, the first lever press initiates an inter-response time (IRT); a potentially consummatory response terminates the IRT; only IRTs longer than a target interval result in access to food. Despite task validity, steady-state FMI performance in the most common animal model of attention-deficit hyperactivity disorder, the spontaneously hypertensive rat (SHR), is similar to normotensive control performance, even though SHR performs at lower levels, especially during acquisition, in similar response-withholding tasks. To determine whether such limitations of the model are specific to stable-state performance, this experiment compared FMI 6-s performance in SHR and Wistar rats during acquisition and in steady state, and assessed the effect of acute D-amphetamine (AMP) administration (0.1, 0.5, and 1.0 mg/kg) on steady-state performance. Median latencies to first lever press were consistently shorter in SHR than in Wistar rats; IRTs were shorter for SHR than for Wistar rats during acquisition, but substantially less so during asymptotic performance. AMP dose-dependently reduced latencies, shortened IRTs, and, at the highest dose, increased the proportion of IRTs under schedule control. These results suggest that, relative to Wistar rats, SHR have a reduced capacity to learn to withhold a reinforced response; once the FMI is acquired, high doses of D-AMP disrupt withholding performance in both strains, but they also enhance the responsiveness of both strains to reinforcement contingencies. Copyright (C) 2018 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:668 / 675
页数:8
相关论文
共 50 条
[1]  
American Psychiatric Association (APA), 2013, DIAGNOSTIC STAT ANUA
[2]   The effects of clinically relevant doses of amphetamine and methylphenidate on signal detection and DRL in rats [J].
Andrzejewski, Matthew E. ;
Spencer, Robert C. ;
Harris, Rachel L. ;
Feit, Elizabeth C. ;
McKee, Brenda L. ;
Berridge, Craig W. .
NEUROPHARMACOLOGY, 2014, 79 :634-641
[3]   Dissociable effects of monoamine reuptake inhibitors on distinct forms of impulsive behavior in rats [J].
Baarendse, Petra J. J. ;
Vanderschuren, Louk J. M. J. .
PSYCHOPHARMACOLOGY, 2012, 219 (02) :313-326
[4]   Comparison of the validity of the use of the spontaneously hypertensive rat as a model of attention deficit hyperactivity disorder in males and females [J].
Bayless, Daniel W. ;
Perez, Maria C. ;
Daniel, Jill M. .
BEHAVIOURAL BRAIN RESEARCH, 2015, 286 :85-92
[5]   Sex differences in operant discrimination behaviour in an animal model of attention-deficit hyperactivity disorder [J].
Berger, DF ;
Sagvolden, T .
BEHAVIOURAL BRAIN RESEARCH, 1998, 94 (01) :73-82
[6]   Influence of gender on attention deficit hyperactivity disorder in children referred to a psychiatric clinic [J].
Biederman, J ;
Mick, E ;
Faraone, SV ;
Braaten, E ;
Doyle, A ;
Spencer, T ;
Wilens, TE ;
Frazier, E ;
Johnson, MA .
AMERICAN JOURNAL OF PSYCHIATRY, 2002, 159 (01) :36-42
[7]   Insights into the neural basis of response inhibition from cognitive and clinical neuroscience [J].
Chambers, Christopher D. ;
Garavan, Hugh ;
Bellgrove, Mark A. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2009, 33 (05) :631-646
[8]   Extinction under a behavioral microscope: Isolating the sources of decline in operant response rate [J].
Cheung, Timothy H. C. ;
Neisewander, Janet L. ;
Sanabria, Federico .
BEHAVIOURAL PROCESSES, 2012, 90 (01) :111-123
[9]   The effect of d-amphetamine on performance an two operant timing schedules [J].
Chiang, TJ ;
Al-Ruwaitea, ASA ;
Mobini, S ;
Ho, MY ;
Bradshaw, CM ;
Szabadi, E .
PSYCHOPHARMACOLOGY, 2000, 150 (02) :170-184
[10]   THE EFFECTS OF DEPRIVATION UPON TEMPORALLY SPACED RESPONDING [J].
CONRAD, DG ;
SIDMAN, M ;
HERRNSTEIN, RJ .
JOURNAL OF THE EXPERIMENTAL ANALYSIS OF BEHAVIOR, 1958, 1 (01) :59-65