HTR1B as a risk profile maker in psychiatric disorders: a review through motivation and memory

被引:29
作者
Drago, Antonio [1 ]
Alboni, Silvia [2 ]
Nicoletta, Brunello [2 ]
De Ronchi, Diana [1 ]
Serretti, Alessandro [1 ]
机构
[1] Univ Bologna, Inst Psychiat, I-40123 Bologna, Italy
[2] Univ Modena & Reggio Emilia, Dept Biomed Sci, Modena, Italy
关键词
Memory; Motivation; Receptor; Serotonin; 5-HT1B; Gene; Single nucleotide polymorphism; Psychotic disorder; Bipolar disorder; Obsessive-compulsive disorder; Substance-related disorders; Suicide; 5-HT1B RECEPTOR KNOCKOUT; OBSESSIVE-COMPULSIVE DISORDER; DORSAL RAPHE NUCLEUS; VENTRAL TEGMENTAL AREA; FAMILY-BASED ASSOCIATION; SEROTONIN REUPTAKE INHIBITORS; A-161T GENETIC-POLYMORPHISM; COCAINE-INDUCED INCREASES; PROTEIN-KINASE-A; LONG-TERM-MEMORY;
D O I
10.1007/s00228-009-0724-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose Serotonin receptor 1B (HTR1B) is involved in the regulation of the serotonin system, playing different roles in specific areas of the brain. We review the characteristics of the gene coding for HTR1B, its product and the functional role of HTR1B in the neural networks involved in motivation and memory; the central role played by HTR1B in these functions is thoroughly depicted and show HTR1B to be a candidate modulator of the mnemonic and motivationally related symptoms in psychiatric illnesses. Methods In order to challenge this assessment, we analyze how and how much the genetic variations located in the gene that codes for HTR1B impacts on the psychiatric phenotypes by reviewing the literature on this topic. Results We gathered partial evidence arising from genetic association studies, which suggests that HTR1B plays a relevant role in substance-related and obsessive compulsive disorders. On the other hand, no solid evidence for other psychiatric disorders was found. This finding is quite striking because of the heavy impairment of motivation and of mnemonic-related functions (for example, recall bias) that characterize major psychiatric disorders. Conclusions The possible reasons for the contrast between the prime relevance of HTR1B in regulating memory and motivation and the limited evidence brought by genetic association studies in humans are discussed, and some suggestions for possible future directions are provided.
引用
收藏
页码:5 / 27
页数:23
相关论文
共 191 条
[1]   Stimulation of 5-HT1B receptors decreases cocaine- and sucrose-seeking behavior [J].
Acosta, JI ;
Boynton, FA ;
Kirschner, KF ;
Neisewander, JL .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2005, 80 (02) :297-307
[2]   Behavioral functions of the mesolimbic dopaminergic system: An affective neuroethological perspective [J].
Alcaro, Antonio ;
Huber, Robert ;
Panksepp, Jaak .
BRAIN RESEARCH REVIEWS, 2007, 56 (02) :283-321
[3]  
Anthony JP, 2000, J NEUROSCI RES, V61, P82, DOI 10.1002/1097-4547(20000701)61:1<82::AID-JNR10>3.0.CO
[4]  
2-E
[5]   Regionally selective changes in neurotransmitter receptors in the brain of the 5-HT1B knockout mouse [J].
Ase, A. R. ;
Reader, T. A. ;
Hen, R. ;
Descarries, L. .
JOURNAL OF CHEMICAL NEUROANATOMY, 2008, 35 (04) :356-363
[6]   Decreased G-protein coupling of serotonin 5-HT1A receptors in the brain of 5-HT1B knockout mouse [J].
Ase, AR ;
Sénécal, J ;
Reader, TA ;
Hen, R ;
Descarries, L .
NEUROPHARMACOLOGY, 2002, 42 (07) :941-949
[7]   Regional changes in density of serotonin transporter in the brain of 5-HT1A and 5-HT1B knockout mice, and of serotonin innervation in the 5-HT1B knockout [J].
Ase, AR ;
Reader, TA ;
Hen, R ;
Riad, M ;
Descarries, L .
JOURNAL OF NEUROCHEMISTRY, 2001, 78 (03) :619-630
[8]  
BAKSHI VP, 1993, J PHARMACOL EXP THER, V265, P1253
[9]   How useful is the appetitive and consummatory distinction for our understanding of the neuroendocrine control of sexual behavior? [J].
Ball, Gregory F. ;
Balthazart, Jacques .
HORMONES AND BEHAVIOR, 2008, 53 (02) :307-311
[10]   Cross-modal semantic and homograph priming in healthy young, healthy old, and in Alzheimer's disease individuals [J].
Balota, DA ;
Watson, JM ;
Duchek, JM ;
Ferraro, FR .
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY, 1999, 5 (07) :626-640