Mouse genetic models for prepulse inhibition: an early review

被引:235
作者
Geyer, MA
McIlwain, KL
Paylor, R
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[3] Baylor Coll Med, Div Neurosci, Houston, TX 77030 USA
关键词
prepulse inhibition; knockout mice; transgenic mice; startle; schizophrenia;
D O I
10.1038/sj.mp.4001159
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prepulse inhibition (PPI) is the phenomenon in which a weak prepulse stimulus attenuates the response to a subsequent startling stimulus. Patients with schizophrenia and some other neuropsychiatric disorders have impaired PPI. Impaired PPI in these patient populations is thought to reflect dysfunctional sensorimotor gating mechanisms. Recently, various inbred mouse strains and genetically modified mouse lines have been examined to investigate the potential genetic basis of sensorimotor gating. This review provides a synopsis of the use of mouse models to explore genetic and neurochemical influences on PPI. Studies describing the PPI responses of various inbred strains of mice, mice with genetic mutations, and mice treated with various drugs prior to July 2001 are reviewed. The continuous nature of the distribution of PPI responses among inbred strains of mice indicates that PPI is a polygenic trait. Findings from spontaneous and gene-targeted mutants suggest that mutant mice are important tools for dissecting and studying the role of single genes and their products, and chromosomal regions in regulating PPI. Pharmacological studies of PPI have typically confirmed effects in mice that are similar to those reported previously in rats, with some important exceptions. The use of mice to study PPI is increasing at a dramatic rate and is helping to increase our understanding of the biological basis for sensorimotor gating.
引用
收藏
页码:1039 / 1053
页数:15
相关论文
共 116 条
[1]   NICOTINE INCREASES SENSORY GATING MEASURED AS INHIBITION OF THE ACOUSTIC STARTLE REFLEX IN RATS [J].
ACRI, JB ;
MORSE, DE ;
POPKE, EJ ;
GRUNBERG, NE .
PSYCHOPHARMACOLOGY, 1994, 114 (02) :369-374
[2]   NORMALIZATION BY NICOTINE OF DEFICIENT AUDITORY SENSORY GATING IN THE RELATIVES OF SCHIZOPHRENICS [J].
ADLER, LE ;
HOFFER, LJ ;
GRIFFITH, J ;
WALDO, MC ;
FREEDMAN, R .
BIOLOGICAL PSYCHIATRY, 1992, 32 (07) :607-616
[3]   Clonidine - A critical review of its role in the treatment of psychiatric disorders [J].
Ahmed, I ;
Takeshita, J .
CNS DRUGS, 1996, 6 (01) :53-70
[4]  
BAKKER CE, 1994, CELL, V78, P23
[5]   DECREASED EXPRESSION OF THE EMBRYONIC FORM OF THE NEURAL CELL-ADHESION MOLECULE IN SCHIZOPHRENIC BRAINS [J].
BARBEAU, D ;
LIANG, JJ ;
ROBITAILLE, Y ;
QUIRION, R ;
SRIVASTAVA, LK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2785-2789
[6]   Restoration of sensory gating of auditory evoked response by nicotine in fimbria-fornix lesioned rats [J].
Bickford, PC ;
Wear, KD .
BRAIN RESEARCH, 1995, 705 (1-2) :235-240
[7]   Development of commissural connections in the hippocampus of reeler mice:: Evidence of an inhibitory influence of Cajal-Retzius cells [J].
Borrell, V ;
Ruiz, M ;
Del Río, JA ;
Soriano, E .
EXPERIMENTAL NEUROLOGY, 1999, 156 (02) :268-282
[8]   PRE-STIMULUS EFFECTS ON HUMAN STARTLE REFLEX IN NORMALS AND SCHIZOPHRENICS [J].
BRAFF, D ;
STONE, C ;
CALLAWAY, E ;
GEYER, M ;
GLICK, I ;
BALI, L .
PSYCHOPHYSIOLOGY, 1978, 15 (04) :339-343
[9]  
BRAFF DL, 1990, ARCH GEN PSYCHIAT, V47, P181
[10]   Human studies of prepulse inhibition of startle: normal subjects, patient groups, and pharmacological studies [J].
Braff, DL ;
Geyer, MA ;
Swerdlow, NR .
PSYCHOPHARMACOLOGY, 2001, 156 (2-3) :234-258