Pathways of Sexual Desire

被引:431
作者
Pfaus, James G. [1 ]
机构
[1] Concordia Univ, Dept Psychol, Ctr Studies Behav Neurobiol, Montreal, PQ H4B 1R6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Sexual Desire; Hypoactive Sexual Desire Disorder; Neuropharmacology; Treatment; Libido; MEDIAL PREOPTIC AREA; MU-OPIOID RECEPTORS; BRAIN MONOAMINERGIC CONTROL; MALE REPRODUCTIVE-BEHAVIOR; CONDITIONED PARTNER PREFERENCE; NUCLEUS-ACCUMBENS DOPAMINE; LATERAL HYPOTHALAMIC AREA; VENTRAL TEGMENTAL AREA; NITRIC-OXIDE SYNTHASE; MALE-RAT;
D O I
10.1111/j.1743-6109.2009.01309.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Sexual desire is controlled by brain systems involved in sexual excitation and inhibition. Hypoactive sexual desire disorder (HSDD) may result from hypofunctional excitation, hyperfunctional inhibition, or some mix of the two. This study aimed to identify neurochemical and neuroanatomical systems involved in sexual excitation and inhibition, their role during normal, and hypoactive sexual expressions. A comprehensive review of the human and animal literature is made, and a theory surrounding the ways that HSDD can be manifested and treated is presented. Drug effects and neural systems derived largely from rat studies that are involved in the stimulation of sexual desire (excitatory system) vs. the stimulation of sexual reward, sedation, and satiety (inhibitory system). Brain dopamine systems (incertohypothalamic and mesolimbic) that link the hypothalamus and limbic system appear to form the core of the excitatory system. This system also includes melanocortins, oxytocin, and norepinephrine. Brain opioid, endocannabinoid, and serotonin systems are activated during periods of sexual inhibition, and blunt the ability of excitatory systems to be activated. Drugs that stimulate the activation of hypothalamic dopamine or that blunt endocannabinoid or serotonin release and/or postsynaptic binding may be effective in stimulating sexual desire in animals and humans. The characterization of how those drugs work will help generate a rational approach to drug development in the treatment of HSDD. Pfaus JG. Pathways of sexual desire. J Sex Med 2009;6:1506-1533.
引用
收藏
页码:1506 / 1533
页数:28
相关论文
共 243 条
[1]   A REVIEW OF ALCOHOLS EFFECTS ON SEX AND REPRODUCTION [J].
ABEL, EL .
DRUG AND ALCOHOL DEPENDENCE, 1980, 5 (05) :321-332
[2]   Activation of μ-opioid receptors inhibits lordosis behavior in estrogen and progesterone-primed female rats [J].
Acosta-Martinez, M ;
Etgen, AM .
HORMONES AND BEHAVIOR, 2002, 41 (01) :88-100
[3]   The role of δ-opioid receptors in estrogen facilitation of lordosis behavior [J].
Acosta-Martinez, M ;
Etgen, AM .
BEHAVIOURAL BRAIN RESEARCH, 2002, 136 (01) :93-102
[4]   SEXUAL REINFORCEMENT IS BLOCKED BY INFUSION OF NALOXONE INTO THE MEDIAL PREOPTIC AREA [J].
AGMO, A ;
GOMEZ, M .
BEHAVIORAL NEUROSCIENCE, 1993, 107 (05) :812-818
[5]   REINFORCING PROPERTIES OF EJACULATION IN THE MALE-RAT - ROLE OF OPIOIDS AND DOPAMINE [J].
AGMO, A ;
BERENFELD, R .
BEHAVIORAL NEUROSCIENCE, 1990, 104 (01) :177-182
[6]   NALOXONE INHIBITS THE FACILITATORY EFFECTS OF 8-OH-DPAT ON MALE-RAT SEXUAL-BEHAVIOR [J].
AGMO, A ;
FERNANDEZ, H ;
PICKER, Z .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1989, 166 (01) :115-116
[7]   EFFECTS OF A NEW TYPE OF 5-HT RECEPTOR AGONIST ON MALE-RAT SEXUAL-BEHAVIOR [J].
AHLENIUS, S ;
LARSSON, K ;
SVENSSON, L ;
HJORTH, S ;
CARLSSON, A ;
LINDBERG, P ;
WIKSTROM, H ;
SANCHEZ, D ;
ARVIDSSON, LE ;
HACKSELL, U ;
NILSSON, JLG .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1981, 15 (05) :785-792
[8]   Central nervous system agents in the treatment of erectile dysfunction: How do they work? [J].
Allard J. ;
Giuliano F. .
Current Urology Reports, 2001, 2 (6) :488-494
[9]   PARGYLINE-INDUCED INCREASE IN SEROTONIN LEVELS - CORRELATION WITH INHIBITION OF LORDOSIS IN RATS [J].
ALLEN, DL ;
RENNER, KJ ;
LUINE, VN .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1993, 45 (04) :837-841
[10]  
ANASTASOPOULOS G, 1958, Psychiatr Neurol (Basel), V136, P85