| Preoptic area | |
|---|---|
 Preoptic area is 'PO', at left, in blue. | |
 Preoptic area of the mouse brain | |
| Details | |
| Identifiers | |
| Latin | area praeoptica |
| Acronym(s) | POA |
| MeSH | D011301 |
| NeuroNames | 377 |
| NeuroLex ID | birnlex_1706 |
| TA98 | A14.1.08.407 |
| TA2 | 5710 |
| FMA | 62313 |
| Anatomical terms of neuroanatomy | |
The preoptic area is a region of the hypothalamus. MeSH classifies it as part of the anterior hypothalamus. TA lists four nuclei in this region, (medial, median, lateral, and periventricular).
The preoptic area is responsible for thermoregulation and receives nervous stimulation from thermoreceptors in the skin, mucous membranes, and hypothalamus itself. [1]
The median preoptic nucleus is located along the midline in a position significantly dorsal to the other three preoptic nuclei, at least in the crab-eating macaque brain. It wraps around the top (dorsal), front, and bottom (ventral) surfaces of the anterior commissure.
The median preoptic nucleus generates thirst. Drinking decreases noradrenaline release in the median preoptic nucleus. [2]
The medial preoptic nucleus is bounded laterally by the lateral preoptic nucleus, and medially by the preoptic periventricular nucleus. It releases gonadotropin-releasing hormone (GnRH), controls copulation in males, and is larger in males than in females.
The medial preoptic area (mPOA) has been implicated in parental care in both males and females. In rats, oxytocin and vasopressin are associated with maintaining maternal care through local release in the mPOA and the adjacent bed nucleus of the stria terminalis (BNST). Oxytocin and vasopressin V1a receptor binding are increased in both the mPOA and the BNST in lactating rats when compared to controls. [3] The mPOA also has a high density of estradiol receptors that, when activated, can cause a male rat to show maternal-type behaviors. [4] Additionally, the mPOA is critical for the onset and expression of parental behavior, as evidenced by increases in the immediate early gene c-fos, in experienced rat mothers or fathers when compared to controls. Also in fathers, studies have shown that when they receive ultrasonic or pheromone cues from their mates, their c-fos expression in the mPOA further increased, suggestive that rat paternal behavior is mediated through the mPOA but activated by direct interactions with a mate. [5] Large lesions of the mPOA disrupt the onset of maternal behavior, nest-building, and pup retrieval, with the lateral projections being especially critical. [6]
The mPOA is sexually dimorphic, that is, it differs in function between males and females. In females, studies have examined the influence of the mPOA on precopulatory and appetitive behaviors. Precopulatory behaviors involve several brain areas, including the mPOA as well as the medial amygdala (MA) and BNST. Studies using female Syrian hamsters have shown that the mPOA is important for sexual odor preference. While control females will investigate male odors more than female odors, those with bilateral lesions to the mPOA (MPOA-X) will show no difference in odor preference, but vaginal scent marking and lordosis remained unaffected. [7] Appetitive behaviors of female rats – including hops, darts, and solicitations – have been linked to dopamine (DA) transmission in the mPOA. Since ascorbic acid (Vitamin C) enhances DA transmission in mesolimbic and nigrostriatal pathways, it has been shown that infusions of ascorbic acid into the mPOA increases appetitive behaviors compared to controls. [8]
In male rats, the mPOA affects the consummatory phase of sexual behavior, and possibly motivation, with lesions causing a complete loss of copulatory behaviors. [9] Conversely, electrical stimulation of this area triggers male copulatory behavior, as measured by decreases in the latency to ejaculate. [10] Furthermore, testosterone implanted into the mPOA of castrated males completely restores mating, as long as aromatase is not inhibited. [11]
The ventrolateral preoptic nucleus, or intermediate nucleus, is adjacent to the medial preoptic nucleus. It also mediates non-REM sleep onset.
The preoptic periventricular nucleus is located along the midline and is medial to the medial preoptic nucleus.
The hypothalamus is a small part of the brain that contains a number of nuclei with a variety of functions. One of the most important functions is to link the nervous system to the endocrine system via the pituitary gland. The hypothalamus is located below the thalamus and is part of the limbic system. It forms the ventral part of the diencephalon. All vertebrate brains contain a hypothalamus. In humans, it is the size of an almond.
The paraventricular nucleus is a nucleus in the hypothalamus. Anatomically, it is adjacent to the third ventricle and many of its neurons project to the posterior pituitary. These projecting neurons secrete oxytocin and a smaller amount of vasopressin, otherwise the nucleus also secretes corticotropin-releasing hormone (CRH) and thyrotropin-releasing hormone (TRH). CRH and TRH are secreted into the hypophyseal portal system and act on different targets neurons in the anterior pituitary. PVN is thought to mediate many diverse functions through these different hormones, including osmoregulation, appetite, and the response of the body to stress.
The arcuate nucleus of the hypothalamus is an aggregation of neurons in the mediobasal hypothalamus, adjacent to the third ventricle and the median eminence. The arcuate nucleus includes several important and diverse populations of neurons that help mediate different neuroendocrine and physiological functions, including neuroendocrine neurons, centrally projecting neurons, and astrocytes. The populations of neurons found in the arcuate nucleus are based on the hormones they secrete or interact with and are responsible for hypothalamic function, such as regulating hormones released from the pituitary gland or secreting their own hormones. Neurons in this region are also responsible for integrating information and providing inputs to other nuclei in the hypothalamus or inputs to areas outside this region of the brain. These neurons, generated from the ventral part of the periventricular epithelium during embryonic development, locate dorsally in the hypothalamus, becoming part of the ventromedial hypothalamic region. The function of the arcuate nucleus relies on its diversity of neurons, but its central role is involved in homeostasis. The arcuate nucleus provides many physiological roles involved in feeding, metabolism, fertility, and cardiovascular regulation.
The ventromedial nucleus of the hypothalamus is a nucleus of the hypothalamus. In 2007, Kurrasch et al. found that the ventromedial hypothalamus is a distinct morphological nucleus involved in terminating hunger, fear, thermoregulation, and sexual activity. This nuclear region is involved in the recognition of the feeling of fullness.
The septal area, consisting of the lateral septum and medial septum, is an area in the lower, posterior part of the medial surface of the frontal lobe, and refers to the nearby septum pellucidum.
The olfactory tubercle (OT), also known as the tuberculum olfactorium, is a multi-sensory processing center that is contained within the olfactory cortex and ventral striatum and plays a role in reward cognition. The OT has also been shown to play a role in locomotor and attentional behaviors, particularly in relation to social and sensory responsiveness, and it may be necessary for behavioral flexibility. The OT is interconnected with numerous brain regions, especially the sensory, arousal, and reward centers, thus making it a potentially critical interface between processing of sensory information and the subsequent behavioral responses.
The vascular organ of lamina terminalis (VOLT), organum vasculosum of the lamina terminalis(OVLT), or supraoptic crest is one of the four sensory circumventricular organs of the brain, the others being the subfornical organ, the median eminence, and the area postrema in the brainstem.
Vasopressin receptor 1A (V1AR), or arginine vasopressin receptor 1A is one of the three major receptor types for vasopressin, and is present throughout the brain, as well as in the periphery in the liver, kidney, and vasculature.
The sexually dimorphic nucleus (SDN) is an ovoid, densely packed cluster of large cells located in the medial preoptic area (POA) of the hypothalamus which is believed to be related to sexual behavior in animals. Thus far, for all species of mammals investigated, the SDN has been repeatedly found to be considerably larger in males than in females. In humans, the volume of the SDN has been found to be 2.2 times as large in males as in females and to contain 2.1 times as many cells. The human SDN is elongated in females and more spherical in males. No sex differences have been observed in the human SDN in either cell density or mean diameter of the cell nuclei. The volume and cell number of the human SDN considerably decreases with age, although the decrease in cell number is both sex and age-specific. In males, a substantial decrease in the cell number of the human SDN was observed between the age of 50–60 years. Cell death was more common in females than males, especially among those older than 70 years of age. The SDN cell number in females can drop to 10-15% of that found in early childhood.
INAH-3 is the short form for the third interstitial nucleus of the anterior hypothalamus, and is the sexually dimorphic nucleus of humans. The INAH-3 is significantly larger in males than in females regardless of age and larger in heterosexual males than in homosexual males and heterosexual females.
Neurotensin is a 13 amino acid neuropeptide that is implicated in the regulation of luteinizing hormone and prolactin release and has significant interaction with the dopaminergic system. Neurotensin was first isolated from extracts of bovine hypothalamus based on its ability to cause a visible vasodilation in the exposed cutaneous regions of anesthetized rats.
The periventricular nucleus is a thin sheet of small neurons located in the wall of the third ventricle, a composite structure of the hypothalamus. It functions in analgesia.
Prenatal stress is exposure of an expectant mother to psychosocial or physical stress, which can be caused by daily life events or by environmental hardships. This psychosocial or physical stress that the expectant mother is experiencing has an effect on the fetus. According to the Developmental Origins of Health and Disease (DOHaD), a wide range of environmental factors a woman may experience during the perinatal period can contribute to biological impacts and changes in the fetus that then causes health risks later in the child's life.
Sexual orientation is an enduring pattern of romantic or sexual attraction to persons of the opposite sex or gender, the same sex or gender, or to both sexes or more than one gender, or none of the aforementioned at all. The ultimate causes and mechanisms of sexual orientation development in humans remain unclear and many theories are speculative and controversial. However, advances in neuroscience explain and illustrate characteristics linked to sexual orientation. Studies have explored structural neural-correlates, functional and/or cognitive relationships, and developmental theories relating to sexual orientation in humans.
Galanin-like peptide (GALP) is a neuropeptide present in humans and other mammals. It is a 60-amino acid polypeptide produced in the arcuate nucleus of the hypothalamus and the posterior pituitary gland. It is involved in the regulation of appetite and may also have other roles such as in inflammation, sex behavior, and stress.
The anteroventral periventricular nucleus (AVPV) is a small cluster of cells located in the preoptic area of hypothalamus of the brain that is abundant in nuclear hormone receptors in a sexually dimorphic manner, strongly implicated, in rat models, as being neonatally imprinted and subsequently controlling sex-typical physiology and behaviors. This nucleus or cluster of cells is typically of bigger size in females than males, contrary to the sexually dimorphic nucleus (SDN) that is bigger in males.
Parvocellular neurosecretory cells are small neurons that produce hypothalamic releasing and inhibiting hormones. The cell bodies of these neurons are located in various nuclei of the hypothalamus or in closely related areas of the basal brain, mainly in the medial zone of the hypothalamus. All or most of the axons of the parvocellular neurosecretory cells project to the median eminence, at the base of the brain, where their nerve terminals release the hypothalamic hormones. These hormones are then immediately absorbed into the blood vessels of the hypothalamo-pituitary portal system, which carry them to the anterior pituitary gland, where they regulate the secretion of hormones into the systemic circulation.
Parental experience, as well as changing hormone levels during pregnancy and postpartum, cause changes in the parental brain. Displaying maternal sensitivity towards infant cues, processing those cues and being motivated to engage socially with her infant and attend to the infant's needs in any context could be described as mothering behavior and is regulated by many systems in the maternal brain. Research has shown that hormones such as oxytocin, prolactin, estradiol and progesterone are essential for the onset and the maintenance of maternal behavior in rats, and other mammals as well. Mothering behavior has also been classified within the basic drives.
The Organizational-Activational Hypothesis states that steroid hormones permanently organize the nervous system during early development, which is reflected in adult male or female typical behaviors. In adulthood, the same steroid hormones activate, modulate, and inhibit these behaviors. This idea was revolutionary when first published in 1959 because no other previous experiment had demonstrated that adult behaviors could be determined hormonally during early development.
Kisspeptin, neurokinin B, and dynorphin (KNDy) neurons are neurons in the hypothalamus of the brain that are central to the hormonal control of reproduction.
