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Neuroendocrinology of Male Reproductive Behavior

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Handbook of Neurochemistry and Molecular Neurobiology
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Abstract:

Berthold, working in the mid-nineteenth century, first published data linking the endocrine secretions of the rooster testes to the display of masculine courtship behavior. Since then hundreds of experiments have been published showing that testosterone is the endocrine signal produced by the Leydig cells of the testes, which in male mammals contributes both to the activation of mating behavior in adulthood and to the organization during perinatal life of neural mechanisms that control this behavior. The broader topic of the neural basis of male sex behavior has recently been reviewed (Hull et al., 2002). Therefore, the present review will concentrate selectively on neuroendocrine variables that control the adult activation as well as the perinatal development of brain mechanisms controlling male-typical sexual motivation, courtship, penile erection, and coital behaviors, with an emphasis on common mammalian models including the rat, mouse, hamster, ferret, and monkey. A common theme to all of these studies is that testosterone exerts its actions in the neural systems controlling male-typical sexual behavior both by acting directly via neural androgen receptors and after neural aromatization to estradiol or 5α−reduction to dihydrotestosterone. Estradiol, in turn, affects neural morphology and function via estradiol receptors of the alpha- or beta-subtypes, whereas dihydrotestosterone, like testosterone, acts via androgen receptors. The evidence reviewed indicates that there are many similarities and a few differences among mammalian species, including higher primates, in the principles of neuroendocrine regulation that control the development and expression of male sexual behavior.

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Abbreviations

AOB:

accessory olfactory bulb

AR:

androgen receptor

ArKO:

aromatase knockout (mouse)

ATD:

1,4,6-androstatriene-3,17-dione (aromatase blocker)

BNST:

bed nucleus of the stria terminalis

CA:

cyproterone acetate

CBP:

cAMP response element binding protein

COX-2:

cyclooxygenase 2

CPP:

conditioned place preference

DA:

dopamine

DHT:

dihydrotestosterone

DHTP:

dihydrotestosterone propionate

DNA:

deoxyribonucleic acid

DOPAC:

3,4-dihydroxy-phenylacetic acid

E:

estradiol

E25:

embryonic day 25

EB:

estradiol benzoate

ER:

estrogen receptor

F1:

first generation

GABA:

gamma amino butyric acid

GnRH:

gonadotrophin releasing hormone

HIV/AIDS:

human immunodeficiency virus/acquired immunodeficiency syndrome

INA-3:

third interstitial nucleus of the anterior hypothalamus

IR:

immunoreactivity

LS:

lumbar spinal cord

MeA:

anterior amygdaloid nucleus

MN-POA/AH:

(sexually dimorphic) male nucleus of the preoptic area/anterior hypothalamus (ferret)

MPOA/AH:

medial preoptic area/anterior hypothalamus

mRNA:

messenger ribonucleic acid

MSH:

melanocyte stimulating hormone

NO:

nitric oxide

NOS:

nitric oxide synthase

OHF:

hydroxyflutamide

P:

progesterone

PGE2:

prostaglandin E2

POE:

parent of origin effect

POM:

sexually dimorphic medial preoptic nucleus (quail)

PR:

progesterone receptor

sc:

subcutaneous

SDN:

sexually dimorphic nucleus

SPFp:

subparafascicular nucleus

SRC-1:

steroid receptor co-activator 1

Sry:

sex determining region of the Y chromosome

T:

testosterone

Tfm:

testicular feminization

TH:

tyrosine hydroxylase

TP:

testosterone propionate

VMH:

ventromedial hypothalamic nucleus

VNO:

vomeronasal organ

WT:

wild type

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Acknowledgment

Preparation of this review was supported in part by funding from NIH grants HD21094 and HD44897.

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Baum, M.J. (2007). Neuroendocrinology of Male Reproductive Behavior. In: Lajtha, A., Blaustein, J.D. (eds) Handbook of Neurochemistry and Molecular Neurobiology. Springer, New York, NY. https://doi.org/10.1007/978-0-387-30405-2_1

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