Jump to content

Hypothalamus

From Wikipedia, the free encyclopedia
(Redirected from Anterior hypothalamus)

Not to be confused with Subthalamus or Hypophthalmus.

Hypothalamus
Location of the human hypothalamus
Location of the hypothalamus (cyan) in relation to the pituitary and to the rest of the brain
Details
Part ofBrain
Identifiers
Latinhypothalamus
MeSHD007031
NeuroLex IDbirnlex_734
TA98A14.1.08.401
A14.1.08.901
TA25714
FMA62008
Anatomical terms of neuroanatomy
Look up hypothalamus in Wiktionary, the free dictionary.

The hypothalamus (pl.: hypothalami; from Ancient Greek ὑπό (hupó) 'under' and θάλαμος (thálamos) 'chamber') is a small part of the vertebrate 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.[1] It forms the basal part of the diencephalon. All vertebrate brains contain a hypothalamus.[2] In humans, it is about the size of an almond.[3]

The hypothalamus has the function of regulating certain metabolic processes and other activities of the autonomic nervous system. It synthesizes and secretes certain neurohormones, called releasing hormones or hypothalamic hormones, and these in turn stimulate or inhibit the secretion of hormones from the pituitary gland. The hypothalamus controls body temperature, hunger, important aspects of parenting and maternal attachment behaviours, thirst,[4] fatigue, sleep, circadian rhythms, and is important in certain social behaviors, such as sexual and aggressive behaviors.[5][6]

Structure

[edit]

The hypothalamus is divided into four regions (preoptic, supraoptic, tuberal, mammillary) in a parasagittal plane, indicating location anterior-posterior; and three zones (periventricular, intermediate, lateral) in the coronal plane, indicating location medial-lateral.[7] Hypothalamic nuclei are located within these specific regions and zones.[8] It is found in all vertebrate nervous systems. In mammals, magnocellular neurosecretory cells in the paraventricular nucleus and the supraoptic nucleus of the hypothalamus produce neurohypophysial hormones, oxytocin and vasopressin.[9] These hormones are released into the blood in the posterior pituitary.[10] Much smaller parvocellular neurosecretory cells, neurons of the paraventricular nucleus, release corticotropin-releasing hormone and other hormones into the hypophyseal portal system, where these hormones diffuse to the anterior pituitary.[citation needed]

Nuclei

[edit]

The hypothalamic nuclei include the following:[11][12]

List of nuclei, their functions, and the neurotransmitters, neuropeptides, or hormones that they utilize
Region Area Nucleus Function[13]
Anterior (supraoptic) Preoptic Preoptic nucleus
Ventrolateral preoptic nucleus Sleep
Medial Medial preoptic nucleus
  • Regulates the release of gonadotropic hormones from the adenohypophysis
  • Contains the sexually dimorphic nucleus, which releases GnRH, differential development between sexes is based upon in utero testosterone levels
  • Thermoregulation[14]
Supraoptic nucleus
Paraventricular nucleus
Anterior hypothalamic nucleus
Suprachiasmatic nucleus
Lateral Lateral nucleus See Lateral hypothalamus § Function – primary source of orexin neurons that project throughout the brain and spinal cord
Middle (tuberal) Medial Dorsomedial hypothalamic nucleus
Ventromedial nucleus
Arcuate nucleus
Lateral Lateral nucleus See Lateral hypothalamus § Function – primary source of orexin neurons that project throughout the brain and spinal cord
Lateral tuberal nuclei
Posterior (mammillary) Medial Mammillary nuclei (part of mammillary bodies)
Posterior nucleus
Lateral Lateral nucleus See Lateral hypothalamus § Function – primary source of orexin neurons that project throughout the brain and spinal cord
Tuberomammillary nucleus[17]
  • Cross-section of the monkey hypothalamus displays two of the major hypothalamic nuclei on either side of the fluid-filled third ventricle.
    Cross-section of the monkey hypothalamus displays two of the major hypothalamic nuclei on either side of the fluid-filled third ventricle.
  • Hypothalamic nuclei
    Hypothalamic nuclei
  • Hypothalamic nuclei on one side of the hypothalamus, shown in a 3-D computer reconstruction[18]
    Hypothalamic nuclei on one side of the hypothalamus, shown in a 3-D computer reconstruction[18]

Connections

[edit]
Further information: Lateral hypothalamus § Orexinergic projection system, and Tuberomammillary nucleus § Histaminergic outputs

The hypothalamus is highly interconnected with other parts of the central nervous system, in particular the brainstem and its reticular formation. As part of the limbic system, it has connections to other limbic structures including the amygdala and septum, and is also connected with areas of the autonomous nervous system.

The hypothalamus receives many inputs from the brainstem, the most notable from the nucleus of the solitary tract, the locus coeruleus, and the ventrolateral medulla.

Most nerve fibres within the hypothalamus run in two ways (bidirectional).

Sexual dimorphism

[edit]

Several hypothalamic nuclei are sexually dimorphic; i.e., there are clear differences in both structure and function between males and females.[19] Some differences are apparent even in gross neuroanatomy: most notable is the sexually dimorphic nucleus within the preoptic area,[19] in which the differences are subtle changes in the connectivity and chemical sensitivity of particular sets of neurons. The importance of these changes can be recognized by functional differences between males and females. For instance, males of most species prefer the odor and appearance of females over males, which is instrumental in stimulating male sexual behavior. If the sexually dimorphic nucleus is lesioned, this preference for females by males diminishes. Also, the pattern of secretion of growth hormone is sexually dimorphic;[20] this is why in many species, adult males are visibly distinct sizes from females.

Responsiveness to ovarian steroids

[edit]

Other striking functional dimorphisms are in the behavioral responses to ovarian steroids of the adult. Males and females respond to ovarian steroids in different ways, partly because the expression of estrogen-sensitive neurons in the hypothalamus is sexually dimorphic; i.e., estrogen receptors are expressed in different sets of neurons.[citation needed]

Estrogen and progesterone can influence gene expression in particular neurons or induce changes in cell membrane potential and kinase activation, leading to diverse non-genomic cellular functions. Estrogen and progesterone bind to their cognate nuclear hormone receptors, which translocate to the cell nucleus and interact with regions of DNA known as hormone response elements (HREs) or get tethered to another transcription factor's binding site. Estrogen receptor (ER) has been shown to transactivate other transcription factors in this manner, despite the absence of an estrogen response element (ERE) in the proximal promoter region of the gene. In general, ERs and progesterone receptors (PRs) are gene activators, with increased mRNA and subsequent protein synthesis following hormone exposure.[citation needed]

Male and female brains differ in the distribution of estrogen receptors, and this difference is an irreversible consequence of neonatal steroid exposure.[citation needed] Estrogen receptors (and progesterone receptors) are found mainly in neurons in the anterior and mediobasal hypothalamus, notably:

Development

[edit]
Median sagittal section of brain of human embryo of three months

In neonatal life, gonadal steroids influence the development of the neuroendocrine hypothalamus. For instance, they determine the ability of females to exhibit a normal reproductive cycle, and of males and females to display appropriate reproductive behaviors in adult life.

  • If a female rat is injected once with testosterone in the first few days of postnatal life (during the "critical period" of sex-steroid influence), the hypothalamus is irreversibly masculinized; the adult rat will be incapable of generating an LH surge in response to estrogen (a characteristic of females), but will be capable of exhibiting male sexual behaviors (mounting a sexually receptive female).[23]
  • By contrast, a male rat castrated just after birth will be feminized, and the adult will show female sexual behavior in response to estrogen (sexual receptivity, lordosis behavior).[23]

In primates, the developmental influence of androgens is less clear, and the consequences are less understood. Within the brain, testosterone is aromatized (to estradiol), which is the principal active hormone for developmental influences. The human testis secretes high levels of testosterone from about week 8 of fetal life until 5–6 months after birth (a similar perinatal surge in testosterone is observed in many species), a process that appears to underlie the male phenotype. Estrogen from the maternal circulation is relatively ineffective, partly because of the high circulating levels of steroid-binding proteins in pregnancy.[23]

Sex steroids are not the only important influences upon hypothalamic development; in particular, pre-pubertal stress in early life (of rats) determines the capacity of the adult hypothalamus to respond to an acute stressor.[24] Unlike gonadal steroid receptors, glucocorticoid receptors are very widespread throughout the brain; in the paraventricular nucleus, they mediate negative feedback control of CRF synthesis and secretion, but elsewhere their role is not well understood.

Function

[edit]

Hormone release

[edit]
Endocrine glands in the human head and neck and their hormones

The hypothalamus has a central neuroendocrine function, most notably by its control of the anterior pituitary, which in turn regulates various endocrine glands and organs. Releasing hormones (also called releasing factors) are produced in hypothalamic nuclei then transported along axons to either the median eminence or the posterior pituitary, where they are stored and released as needed.[25]

Anterior pituitary

In the hypothalamic–adenohypophyseal axis, releasing hormones, also known as hypophysiotropic or hypothalamic hormones, are released from the median eminence, a prolongation of the hypothalamus, into the hypophyseal portal system, which carries them to the anterior pituitary where they exert their regulatory functions on the secretion of adenohypophyseal hormones.[26] These hypophysiotropic hormones are stimulated by parvocellular neurosecretory cells located in the periventricular area of the hypothalamus. After their release into the capillaries of the third ventricle, the hypophysiotropic hormones travel through what is known as the hypothalamo-pituitary portal circulation. Once they reach their destination in the anterior pituitary, these hormones bind to specific receptors located on the surface of pituitary cells. Depending on which cells are activated through this binding, the pituitary will either begin secreting or stop secreting hormones into the rest of the bloodstream.[27]

Secreted hormone Abbreviation Produced by Effect
Thyrotropin-releasing hormone
(Prolactin-releasing hormone) 		TRH, TRF, or PRH Parvocellular neurosecretory cells of the paraventricular nucleus Stimulate thyroid-stimulating hormone (TSH) release from anterior pituitary (primarily)
Stimulate prolactin release from anterior pituitary
Corticotropin-releasing hormone CRH or CRF Parvocellular neurosecretory cells of the paraventricular nucleus Stimulate adrenocorticotropic hormone (ACTH) release from anterior pituitary
Dopamine
(Prolactin-inhibiting hormone) 		DA or PIH Dopamine neurons of the arcuate nucleus Inhibit prolactin release from anterior pituitary
Growth-hormone-releasing hormone GHRH Neuroendocrine neurons of the Arcuate nucleus Stimulate growth-hormone (GH) release from anterior pituitary
Gonadotropin-releasing hormone GnRH or LHRH Neuroendocrine cells of the Preoptic area Stimulate follicle-stimulating hormone (FSH) release from anterior pituitary
Stimulate luteinizing hormone (LH) release from anterior pituitary
Somatostatin[28]
(growth-hormone-inhibiting hormone) 		SS, GHIH, or SRIF Neuroendocrine cells of the Periventricular nucleus Inhibit growth-hormone (GH) release from anterior pituitary
Inhibit (moderately) thyroid-stimulating hormone (TSH) release from anterior pituitary

Other hormones secreted from the median eminence include vasopressin, oxytocin, and neurotensin.[29][30][31][32]

Posterior pituitary

In the hypothalamic–pituitary–adrenal axis, neurohypophysial hormones are released from the posterior pituitary, which is actually a prolongation of the hypothalamus, into the circulation.

Secreted hormone Abbreviation Produced by Effect
Oxytocin OXY or OXT Magnocellular neurosecretory cells of the paraventricular nucleus and supraoptic nucleus Uterine contraction
Lactation (letdown reflex)
Vasopressin
(antidiuretic hormone) 		ADH or AVP Magnocellular and parvocellular neurosecretory cells of the paraventricular nucleus, magnocellular cells in supraoptic nucleus Increase in the permeability to water of the cells of distal tubule and collecting duct in the kidney and thus allows water reabsorption and excretion of concentrated urine

It is also known that hypothalamic–pituitary–adrenal axis (HPA) hormones are related to certain skin diseases and skin homeostasis. There is evidence linking hyperactivity of HPA hormones to stress-related skin diseases and skin tumors.[33]

Stimulation

[edit]

The hypothalamus coordinates many hormonal and behavioural circadian rhythms, complex patterns of neuroendocrine outputs, complex homeostatic mechanisms, and important behaviours. The hypothalamus must, therefore, respond to many different signals, some of which are generated externally and some internally. Delta wave signalling arising either in the thalamus or in the cortex influences the secretion of releasing hormones; GHRH and prolactin are stimulated whilst TRH is inhibited.

The hypothalamus is responsive to:

Olfactory stimuli

[edit]

Olfactory stimuli are important for sexual reproduction and neuroendocrine function in many species. For instance if a pregnant mouse is exposed to the urine of a 'strange' male during a critical period after coitus then the pregnancy fails (the Bruce effect). Thus, during coitus, a female mouse forms a precise 'olfactory memory' of her partner that persists for several days. Pheromonal cues aid synchronization of oestrus in many species; in women, synchronized menstruation may also arise from pheromonal cues, although the role of pheromones in humans is disputed.

Blood-borne stimuli

[edit]

Peptide hormones have important influences upon the hypothalamus, and to do so they must pass through the blood–brain barrier. The hypothalamus is bounded in part by specialized brain regions that lack an effective blood–brain barrier; the capillary endothelium at these sites is fenestrated to allow free passage of even large proteins and other molecules. Some of these sites are the sites of neurosecretion - the neurohypophysis and the median eminence. However, others are sites at which the brain samples the composition of the blood. Two of these sites, the SFO (subfornical organ) and the OVLT (organum vasculosum of the lamina terminalis) are so-called circumventricular organs, where neurons are in intimate contact with both blood and CSF. These structures are densely vascularized, and contain osmoreceptive and sodium-receptive neurons that control drinking, vasopressin release, sodium excretion, and sodium appetite. They also contain neurons with receptors for angiotensin, atrial natriuretic factor, endothelin and relaxin, each of which important in the regulation of fluid and electrolyte balance. Neurons in the OVLT and SFO project to the supraoptic nucleus and paraventricular nucleus, and also to preoptic hypothalamic areas. The circumventricular organs may also be the site of action of interleukins to elicit both fever and ACTH secretion, via effects on paraventricular neurons.[citation needed]

It is not clear how all peptides that influence hypothalamic activity gain the necessary access. In the case of prolactin and leptin, there is evidence of active uptake at the choroid plexus from the blood into the cerebrospinal fluid (CSF). Some pituitary hormones have a negative feedback influence upon hypothalamic secretion; for example, growth hormone feeds back on the hypothalamus, but how it enters the brain is not clear. There is also evidence for central actions of prolactin.[citation needed]

Findings have suggested that thyroid hormone (T4) is taken up by the hypothalamic glial cells in the infundibular nucleus/ median eminence, and that it is here converted into T3 by the type 2 deiodinase (D2). Subsequent to this, T3 is transported into the thyrotropin-releasing hormone (TRH)-producing neurons in the paraventricular nucleus. Thyroid hormone receptors have been found in these neurons, indicating that they are indeed sensitive to T3 stimuli. In addition, these neurons expressed MCT8, a thyroid hormone transporter, supporting the theory that T3 is transported into them. T3 could then bind to the thyroid hormone receptor in these neurons and affect the production of thyrotropin-releasing hormone, thereby regulating thyroid hormone production.[35]

The hypothalamus functions as a type of thermostat for the body.[36] It sets a desired body temperature, and stimulates either heat production and retention to raise the blood temperature to a higher setting or sweating and vasodilation to cool the blood to a lower temperature. All fevers result from a raised setting in the hypothalamus; elevated body temperatures due to any other cause are classified as hyperthermia.[36] Rarely, direct damage to the hypothalamus, such as from a stroke, will cause a fever; this is sometimes called a hypothalamic fever. However, it is more common for such damage to cause abnormally low body temperatures.[36]

Steroids

[edit]

The hypothalamus contains neurons that react strongly to steroids and glucocorticoids (the steroid hormones of the adrenal gland, released in response to ACTH). It also contains specialized glucose-sensitive neurons (in the arcuate nucleus and ventromedial hypothalamus), which are important for appetite. The preoptic area contains thermosensitive neurons; these are important for TRH secretion.

Neural

[edit]

Oxytocin secretion in response to suckling or vagino-cervical stimulation is mediated by some of these pathways; vasopressin secretion in response to cardiovascular stimuli arising from chemoreceptors in the carotid body and aortic arch, and from low-pressure atrial volume receptors, is mediated by others. In the rat, stimulation of the vagina also causes prolactin secretion, and this results in pseudo-pregnancy following an infertile mating. In the rabbit, coitus elicits reflex ovulation. In the sheep, cervical stimulation in the presence of high levels of estrogen can induce maternal behavior in a virgin ewe. These effects are all mediated by the hypothalamus, and the information is carried mainly by spinal pathways that relay in the brainstem. Stimulation of the nipples stimulates release of oxytocin and prolactin and suppresses the release of LH and FSH.

Cardiovascular stimuli are carried by the vagus nerve. The vagus also conveys a variety of visceral information, including for instance signals arising from gastric distension or emptying, to suppress or promote feeding, by signalling the release of leptin or gastrin, respectively. Again this information reaches the hypothalamus via relays in the brainstem.

In addition hypothalamic function is responsive to—and regulated by—levels of all three classical monoamine neurotransmitters, noradrenaline, dopamine, and serotonin (5-hydroxytryptamine), in those tracts from which it receives innervation. For example, noradrenergic inputs arising from the locus coeruleus have important regulatory effects upon corticotropin-releasing hormone (CRH) levels.

Control of food intake

[edit]
Peptide hormones and neuropeptides that regulate feeding[37]
Peptides that increase
feeding behavior 		Peptides that decrease
feeding behavior
Ghrelin Leptin
Neuropeptide Y (α,β,γ)-Melanocyte-stimulating hormones
Agouti-related peptide Cocaine- and amphetamine-regulated transcript peptides
Orexins (A,B) Corticotropin-releasing hormone
Melanin-concentrating hormone Cholecystokinin
Galanin Insulin
Glucagon-like peptide 1

The extreme lateral part of the ventromedial nucleus of the hypothalamus is responsible for the control of food intake. Stimulation of this area causes increased food intake. Bilateral lesion of this area causes complete cessation of food intake. Medial parts of the nucleus have a controlling effect on the lateral part. Bilateral lesion of the medial part of the ventromedial nucleus causes hyperphagia and obesity of the animal. Further lesion of the lateral part of the ventromedial nucleus in the same animal produces complete cessation of food intake.

There are different hypotheses related to this regulation:[38]

  1. Lipostatic hypothesis: This hypothesis holds that adipose tissue produces a humoral signal that is proportionate to the amount of fat and acts on the hypothalamus to decrease food intake and increase energy output. It has been evident that a hormone leptin acts on the hypothalamus to decrease food intake and increase energy output.
  2. Gutpeptide hypothesis: gastrointestinal hormones like Grp, glucagons, CCK and others claimed to inhibit food intake. The food entering the gastrointestinal tract triggers the release of these hormones, which act on the brain to produce satiety. The brain contains both CCK-A and CCK-B receptors.
  3. Glucostatic hypothesis: The activity of the satiety center in the ventromedial nuclei is probably governed by the glucose utilization in the neurons. It has been postulated that when their glucose utilization is low and consequently when the arteriovenous blood glucose difference across them is low, the activity across the neurons decrease. Under these conditions, the activity of the feeding center is unchecked and the individual feels hungry. Food intake is rapidly increased by intraventricular administration of 2-deoxyglucose therefore decreasing glucose utilization in cells.
  4. Thermostatic hypothesis: According to this hypothesis, a decrease in body temperature below a given set-point stimulates appetite, whereas an increase above the set-point inhibits appetite.

Fear processing

[edit]

The medial zone of hypothalamus is part of a circuitry that controls motivated behaviors, like defensive behaviors.[39] Analyses of Fos-labeling showed that a series of nuclei in the "behavioral control column" is important in regulating the expression of innate and conditioned defensive behaviors.[40]

Antipredatory defensive behavior

Exposure to a predator (such as a cat) elicits defensive behaviors in laboratory rodents, even when the animal has never been exposed to a cat.[41] In the hypothalamus, this exposure causes an increase in Fos-labeled cells in the anterior hypothalamic nucleus, the dorsomedial part of the ventromedial nucleus, and in the ventrolateral part of the premammillary nucleus (PMDvl).[42] The premammillary nucleus has an important role in expression of defensive behaviors towards a predator, since lesions in this nucleus abolish defensive behaviors, like freezing and flight.[42][43] The PMD does not modulate defensive behavior in other situations, as lesions of this nucleus had minimal effects on post-shock freezing scores.[43] The PMD has important connections to the dorsal periaqueductal gray, an important structure in fear expression.[44][45] In addition, animals display risk assessment behaviors to the environment previously associated with the cat. Fos-labeled cell analysis showed that the PMDvl is the most activated structure in the hypothalamus, and inactivation with muscimol prior to exposure to the context abolishes the defensive behavior.[42] Therefore, the hypothalamus, mainly the PMDvl, has an important role in expression of innate and conditioned defensive behaviors to a predator.

Social defeat

Likewise, the hypothalamus has a role in social defeat: Nuclei in medial zone are also mobilized during an encounter with an aggressive conspecific. The defeated animal has an increase in Fos levels in sexually dimorphic structures, such as the medial pre-optic nucleus, the ventrolateral part of ventromedial nucleus, and the ventral premammilary nucleus.[6] Such structures are important in other social behaviors, such as sexual and aggressive behaviors. Moreover, the premammillary nucleus also is mobilized, the dorsomedial part but not the ventrolateral part.[6] Lesions in this nucleus abolish passive defensive behavior, like freezing and the "on-the-back" posture.[6]

Learning arbitrator

[edit]

Recent research has questioned whether the lateral hypothalamus's role is only restricted to initiating and stopping innate behaviors and argued it learns about food-related cues. Specifically that it opposes learning about information what is neutral or distant to food. According this view, the lateral hypothalamus is "a unique arbitrator of learning capable of shifting behavior toward or away from important events".[46]

Additional images

[edit]
  • Human brain left dissected midsagittal view
    Human brain left dissected midsagittal view
  • Location of the hypothalamus
    Location of the hypothalamus

See also

[edit]

References

[edit]
  1. ^ Boeree CG. "The Emotional Nervous System". General Psycholoty. Retrieved 18 April 2016.
  2. ^ Lemaire LA, Cao C, Yoon PH, Long J, Levine M (April 2021). "The hypothalamus predates the origin of vertebrates". Science Advances. 7 (18): eabf7452. Bibcode:2021SciA....7.7452L. doi:10.1126/sciadv.abf7452. PMC 8081355. PMID 33910896.
  3. ^ Ishii M, Iadecola C (November 2015). "Metabolic and Non-Cognitive Manifestations of Alzheimer's Disease: The Hypothalamus as Both Culprit and Target of Pathology". Cell Metabolism. 22 (5): 761–776. doi:10.1016/j.cmet.2015.08.016. PMC 4654127. PMID 26365177.
  4. ^ "NCI Dictionary of Cancer Terms". National Cancer Institute.
  5. ^ Saper CB, Scammell TE, Lu J (October 2005). "Hypothalamic regulation of sleep and circadian rhythms". Nature. 437 (7063): 1257–1263. Bibcode:2005Natur.437.1257S. doi:10.1038/nature04284. PMID 16251950. S2CID 1793658.
  6. ^ a b c d Motta SC, Goto M, Gouveia FV, Baldo MV, Canteras NS, Swanson LW (March 2009). "Dissecting the brain's fear system reveals the hypothalamus is critical for responding in subordinate conspecific intruders". Proceedings of the National Academy of Sciences of the United States of America. 106 (12): 4870–5. Bibcode:2009PNAS..106.4870M. doi:10.1073/pnas.0900939106. PMC 2660765. PMID 19273843.
  7. ^ Singh V (2014). Textbook of Clinical Neuroanatomy (2nd ed.). Elsevier Health Sciences. p. 134. ISBN 9788131229811.
  8. ^ Inderbir Singh (September 2011). Textbook of Anatomy: Volume 3: Head and Neck, Central Nervous System. JP Medical Ltd. pp. 1101–. ISBN 978-93-5025-383-0.
  9. ^ Sukhov RR, Walker LC, Rance NE, Price DL, Young WS (November 1993). "Vasopressin and oxytocin gene expression in the human hypothalamus". The Journal of Comparative Neurology. 337 (2): 295–306. doi:10.1002/cne.903370210. PMC 9883978. PMID 8277003.
  10. ^ Melmed S, Polonsky KS, Larsen PR, Kronenberg HM (2011). Williams Textbook of Endocrinology (12th ed.). Saunders. p. 107. ISBN 978-1437703245.
  11. ^ "Enlarged view of the hypothalamus". psycheducation.org. Jim Phelps. Archived from the original on 15 December 2005. Retrieved 7 February 2020.
  12. ^ "Emotion and the limbic system". utdallas.edu. Lucien T. "Tres" Thompson, The University of Texas at Dallas. Retrieved 7 February 2020.
  13. ^ Hall JE, Guyton AC (2011). Guyton and Hall Textbook of Medical Physiology (12th ed.). Saunders/Elsevier. ISBN 978-1416045748.
  14. ^ Yoshida K, Li X, Cano G, Lazarus M, Saper CB (September 2009). "Parallel preoptic pathways for thermoregulation". The Journal of Neuroscience. 29 (38): 11954–64. doi:10.1523/JNEUROSCI.2643-09.2009. PMC 2782675. PMID 19776281.
  15. ^ Chen CR, Zhong YH, Jiang S, Xu W, Xiao L, Wang Z, et al. (November 2021). Elmquist JK, Wong ML, Lazarus M (eds.). "Dysfunctions of the paraventricular hypothalamic nucleus induce hypersomnia in mice". eLife. 10: e69909. doi:10.7554/eLife.69909. PMC 8631797. PMID 34787078.
  16. ^ Wang Z, Zhong YH, Jiang S, Qu WM, Huang ZL, Chen CR (14 March 2022). "Case Report: Dysfunction of the Paraventricular Hypothalamic Nucleus Area Induces Hypersomnia in Patients". Frontiers in Neuroscience. 16: 830474. doi:10.3389/fnins.2022.830474. PMC 8964012. PMID 35360167.
  17. ^ Malenka RC, Nestler EJ, Hyman SE (2009). "Chapter 6: Widely Projecting Systems: Monoamines, Acetylcholine, and Orexin". In Sydor A, Brown RY (eds.). Molecular Neuropharmacology: A Foundation for Clinical Neuroscience (2nd ed.). New York: McGraw-Hill Medical. pp. 175–176. ISBN 9780071481274. Within the brain, histamine is synthesized exclusively by neurons with their cell bodies in the tuberomammillary nucleus (TMN) that lies within the posterior hypothalamus. There are approximately 64000 histaminergic neurons per side in humans. These cells project throughout the brain and spinal cord. Areas that receive especially dense projections include the cerebral cortex, hippocampus, neostriatum, nucleus accumbens, amygdala, and hypothalamus.  ... While the best characterized function of the histamine system in the brain is regulation of sleep and arousal, histamine is also involved in learning and memory ... It also appears that histamine is involved in the regulation of feeding and energy balance.
  18. ^ Brain Research Bulletin 35:323–327, 1994
  19. ^ a b Hofman MA, Swaab DF (June 1989). "The sexually dimorphic nucleus of the preoptic area in the human brain: a comparative morphometric study". Journal of Anatomy. 164: 55–72. PMC 1256598. PMID 2606795.
  20. ^ Quinnies KM, Bonthuis PJ, Harris EP, Shetty SR, Rissman EF (2015). "Neural growth hormone: Regional regulation by estradiol and / or sex chromosome complement in male and female mice". Biology of Sex Differences. 6: 8. doi:10.1186/s13293-015-0026-x. PMC 4434521. PMID 25987976.
  21. ^ Castañeyra-Ruiz L, González-Marrero I, Castañeyra-Ruiz A, González-Toledo JM, Castañeyra-Ruiz M, de Paz-Carmona H, et al. (2013). "Luteinizing hormone-releasing hormone distribution in the anterior hypothalamus of the female rats". ISRN Anatomy. 2013: 1–6. doi:10.5402/2013/870721. PMC 4392965. PMID 25938107.
  22. ^ Isgor C, Cecchi M, Kabbaj M, Akil H, Watson SJ (2003). "Estrogen receptor beta in the paraventricular nucleus of hypothalamus regulates the neuroendocrine response to stress and is regulated by corticosterone". Neuroscience. 121 (4): 837–45. doi:10.1016/S0306-4522(03)00561-X. PMID 14580933. S2CID 31026141.
  23. ^ a b c McCarthy MM, Arnold AP, Ball GF, Blaustein JD, De Vries GJ (February 2012). "Sex differences in the brain: the not so inconvenient truth". The Journal of Neuroscience. 32 (7): 2241–7. doi:10.1523/JNEUROSCI.5372-11.2012. PMC 3295598. PMID 22396398.
  24. ^ Romeo RD, Bellani R, Karatsoreos IN, Chhua N, Vernov M, Conrad CD, et al. (April 2006). "Stress history and pubertal development interact to shape hypothalamic–pituitary–adrenal axis plasticity". Endocrinology. 147 (4): 1664–74. doi:10.1210/en.2005-1432. PMID 16410296.
  25. ^ Bowen R. "Overview of Hypothalamic and Pituitary Hormones". Archived from the original on 1 March 2019. Retrieved 5 October 2014.
  26. ^ Melmed S, Jameson JL (2005). "Disorders of the anterior pituitary and hypothalamus". In Kasper DL, Braunwald E, Fauci AS, et al. (eds.). Harrison's Principles of Internal Medicine (16th ed.). New York, NY: McGraw-Hill. pp. 2076–97. ISBN 978-0-07-139140-5.
  27. ^ Bear MF, Connors BW, Paradiso MA (2016). "Hypothalamic Control of the Anterior Pituitary". Neuroscience: Exploring the Brain (4th ed.). Philadelphia: Wolters Kluwer. p. 528. ISBN 978-0-7817-7817-6.
  28. ^ Ben-Shlomo A, Melmed S (March 2010). "Pituitary somatostatin receptor signaling". Trends in Endocrinology and Metabolism. 21 (3): 123–33. doi:10.1016/j.tem.2009.12.003. PMC 2834886. PMID 20149677.
  29. ^ Horn AM, Robinson IC, Fink G (February 1985). "Oxytocin and vasopressin in rat hypophysial portal blood: experimental studies in normal and Brattleboro rats". The Journal of Endocrinology. 104 (2): 211–24. doi:10.1677/joe.0.1040211. PMID 3968510.
  30. ^ Date Y, Mondal MS, Matsukura S, Ueta Y, Yamashita H, Kaiya H, et al. (March 2000). "Distribution of orexin/hypocretin in the rat median eminence and pituitary". Brain Research. Molecular Brain Research. 76 (1): 1–6. doi:10.1016/s0169-328x(99)00317-4. PMID 10719209.
  31. ^ Watanobe H, Takebe K (April 1993). "In vivo release of neurotensin from the median eminence of ovariectomized estrogen-primed rats as estimated by push-pull perfusion: correlation with luteinizing hormone and prolactin surges". Neuroendocrinology. 57 (4): 760–4. doi:10.1159/000126434. PMID 8367038.
  32. ^ Spinazzi R, Andreis PG, Rossi GP, Nussdorfer GG (March 2006). "Orexins in the regulation of the hypothalamic–pituitary–adrenal axis". Pharmacological Reviews. 58 (1): 46–57. doi:10.1124/pr.58.1.4. PMID 16507882. S2CID 17941978.
  33. ^ Jung Eun Kim, Baik Kee Cho, Dae Ho Cho, Hyun Jeong Park (2013). "Expression of Hypothalamic–Pituitary–Adrenal Axis in Common Skin Diseases: Evidence of its Association with Stress-related Disease Activity". National Research Foundation of Korea. Retrieved 4 March 2014.
  34. ^ Mayer EA (July 2011). "Gut feelings: the emerging biology of gut-brain communication". Nature Reviews. Neuroscience. 12 (8): 453–66. doi:10.1038/nrn3071. PMC 3845678. PMID 21750565.
  35. ^ Fliers E, Unmehopa UA, Alkemade A (June 2006). "Functional neuroanatomy of thyroid hormone feedback in the human hypothalamus and pituitary gland". Molecular and Cellular Endocrinology. 251 (1–2): 1–8. doi:10.1016/j.mce.2006.03.042. PMID 16707210. S2CID 33268046.
  36. ^ a b c Fauci, Anthony, et al. (2008). Harrison's Principles of Internal Medicine (17 ed.). McGraw-Hill Professional. pp. 117–121. ISBN 978-0-07-146633-2.
  37. ^ Malenka RC, Nestler EJ, Hyman SE (2009). "Chapter 10: Neural and Neuroendocrine Control of the Internal Milieu – Table 10:3". In Sydor A, Brown RY (eds.). Molecular Neuropharmacology: A Foundation for Clinical Neuroscience (2nd ed.). New York: McGraw-Hill Medical. p. 263. ISBN 9780071481274.
  38. ^ Theologides A (May 1976). "Anorexia-producing intermediary metabolites". The American Journal of Clinical Nutrition. 29 (5): 552–8. doi:10.1093/ajcn/29.5.552. PMID 178168.
  39. ^ Swanson LW (December 2000). "Cerebral hemisphere regulation of motivated behavior". Brain Research. 886 (1–2): 113–164. doi:10.1016/S0006-8993(00)02905-X. PMID 11119693. S2CID 10167219.
  40. ^ Canteras, N.S. (2002). "The medial hypothalamic defensive system:Hodological organization and functional implications". Pharmacology Biochemistry and Behavior. 71 (3): 481–491. doi:10.1016/S0091-3057(01)00685-2. PMID 11830182. S2CID 12303256.
  41. ^ Ribeiro-Barbosa ER, Canteras NS, Cezário AF, Blanchard RJ, Blanchard DC (2005). "An alternative experimental procedure for studying predator-related defensive responses". Neuroscience and Biobehavioral Reviews. 29 (8): 1255–63. doi:10.1016/j.neubiorev.2005.04.006. PMID 16120464. S2CID 8063630.
  42. ^ a b c Cezario AF, Ribeiro-Barbosa ER, Baldo MV, Canteras NS (September 2008). "Hypothalamic sites responding to predator threats--the role of the dorsal premammillary nucleus in unconditioned and conditioned antipredatory defensive behavior". The European Journal of Neuroscience. 28 (5): 1003–15. doi:10.1111/j.1460-9568.2008.06392.x. PMID 18691328. S2CID 10073236.
  43. ^ a b Blanchard, D.C. (2003). "Dorsal premammillary nucleus differentially modulates defensive behaviors induced by different threat stimuli in rats". Neuroscience Letters. 345 (3): 145–148. doi:10.1016/S0304-3940(03)00415-4. PMID 12842277. S2CID 16406187.
  44. ^ Canteras NS, Swanson LW (November 1992). "The dorsal premammillary nucleus: an unusual component of the mammillary body". Proceedings of the National Academy of Sciences of the United States of America. 89 (21): 10089–93. Bibcode:1992PNAS...8910089C. doi:10.1073/pnas.89.21.10089. PMC 50283. PMID 1279669.
  45. ^ Behbehani MM (August 1995). "Functional characteristics of the midbrain periaqueductal gray". Progress in Neurobiology. 46 (6): 575–605. doi:10.1016/0301-0082(95)00009-K. PMID 8545545. S2CID 24690642.
  46. ^ Sharpe MJ (January 2024). "The cognitive (lateral) hypothalamus". Trends in Cognitive Sciences. 28 (1): 18–29. doi:10.1016/j.tics.2023.08.019. PMC 10841673. PMID 37758590.

Further reading

[edit]
[edit]
Wikimedia Commons has media related to Hypothalamus.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Hypothalamus&oldid=1243301561"