Genetic predisposition and the development of Posttraumatic stress disorder in an animal model

被引:45
作者
King, JA
Abend, S
Edwards, E
机构
[1] Univ Massachusetts, Sch Med, Dept Psychiat, Med Ctr, Worcester, MA 01655 USA
[2] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
基金
美国国家科学基金会;
关键词
PTSD; learned helplessness; footshock stress; animal model; corticosterone; analgesia;
D O I
10.1016/S0006-3223(01)01071-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Exposure to extremely stressful events can lead to Posttraumatic stress disorder (PTSD). Due to the complexity of PTSD, animal models have been designed and advanced to address the role of psychosocial stressors in the etiology; however, the apparent role of genetics in susceptibility to PTSD-like behaviors in animals remains unexplored. Methods: An animal model of congenital learned helpless (cLH) behavior has been used to study the effects of genetic disposition as a risk factor for the development of PTSD-like behaviors. Animals were monitored for changes in pain tolerance, spatial memory and hypothalamic-pituitary-adrenal functioning after re-exposure to intermittent stress in the presence and absence of situational cues. Results: Exposure to stress resulted in an increase in pain tolerance in the cLH animals. In the spatial memory test 80% of the cLH animals manifested a decrease in performance after exposure to stress. These animals also had a blunted poststress corticosterone response. Conclusions: The genetic learned helpless animal model exhibited physiologic symptoms of analgesia, cognitive deficits and hyporesponsivity of the hypothalainic-pituitan-adrenal axis similar to those observed in human Subjects with PTSD. It is proposed that the cLH model may be a valuable tool for exploring the role of genetic predisposition in the etiology of PTSD. (C) 2001 Society of Biological Psychiatry.
引用
收藏
页码:231 / 237
页数:7
相关论文
共 52 条
[1]   Cerebrospinal fluid and plasma beta-endorphin in combat veterans with post-traumatic stress disorder [J].
Baker, DG ;
West, SA ;
Orth, DN ;
Hill, KK ;
Nicholson, WE ;
Ekhator, NN ;
Bruce, AB ;
Wortman, MD ;
Keck, PE ;
Geracioti, TD .
PSYCHONEUROENDOCRINOLOGY, 1997, 22 (07) :517-529
[2]  
Baker DG, 1999, AM J PSYCHIAT, V156, P585
[3]   A 3-YEAR FOLLOW-UP OF CHILDREN WITH AND WITHOUT BEHAVIORAL-INHIBITION [J].
BIEDERMAN, J ;
ROSENBAUM, JF ;
BOLDUCMURPHY, EA ;
FARAONE, SV ;
CHALOFF, J ;
HIRSHFELD, DR ;
KAGAN, J .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 1993, 32 (04) :814-821
[4]   The effects of stress on memory and the hippocampus throughout the life cycle: Implications for childhood development and aging [J].
Bremner, JD ;
Narayan, M .
DEVELOPMENT AND PSYCHOPATHOLOGY, 1998, 10 (04) :871-885
[5]  
Bremner JD, 1999, AM J PSYCHIAT, V156, P1787
[6]  
BREMNER JD, 1995, AM J PSYCHIAT, V152, P973
[7]  
BREMNER JD, 1993, AM J PSYCHIAT, V150, P235
[8]   Trauma and posttraumatic stress disorder in the community -: The 1996 Detroit Area Survey of Trauma [J].
Breslau, N ;
Kessler, RC ;
Chilcoat, HD ;
Schultz, LR ;
Davis, GC ;
Andreski, P .
ARCHIVES OF GENERAL PSYCHIATRY, 1998, 55 (07) :626-632
[9]   Evidence for opiate-activated NMDA processes masking opiate analgesia in rats [J].
Célèrier, E ;
Laulin, JP ;
Larcher, A ;
Le Moal, M ;
Simonnet, G .
BRAIN RESEARCH, 1999, 847 (01) :18-25
[10]   NEUROCHEMICAL AND BEHAVIORAL CONSEQUENCES OF MILD, UNCONTROLLABLE SHOCK - EFFECTS OF PCPA [J].
EDWARDS, E ;
JOHNSON, J ;
ANDERSON, D ;
TURANO, P ;
HENN, FA .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1986, 25 (02) :415-421