Arcuate nucleus

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This article is about the hypothalamic structure. For the structure in the medulla oblongata, see Arcuate nucleus (medulla).
Arcuate nucleus
HypothalamicNuclei.PNG
Arcuate nucleus is 'AR', at bottom center, in green.
Details
Part of Hypothalamus
Identifiers
Latin nucleus arcuatus hypothalami
MeSH A08.186.211.730.385.357.352.081
NeuroNames hier-378
NeuroLex ID Arcuate nucleus of hypothalamus
TA A14.1.08.923
FMA 62329
Anatomical terms of neuroanatomy

The arcuate nucleus of the hypothalamus (also known as ARH,[1] ARC,[2] or infundibular nucleus [2][3]) 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.[1][2][4] 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.[1][2][4][5]

Cell populations[edit]

Neuroendocrine neurons[edit]

Different groups of arcuate nucleus neuroendocrine neurons secrete various types or combinations of neurotransmitters, such as neuropeptide Y (NPY), Agouti-related peptide (Agrp) propiomelanocortin (POMC), kisspeptin, dopamine, substance p, growth hormone releasing hormone (GhRH), and somatostatin.[1]

Groups of neuroendocrine neurons include:

  • TIDA Neurons are Tuberofundibular dopaminergic neurons that regulate the secretion of prolactin from the pituitary gland and release GABA neurotransmitter. They are to be involved in controlling prolactin (PRL) secretion by releasing dopamine neurotransmitter. Tuberoinfundibular dopaminergic (TIDA) neurons are neurons involved in the tuberoinfundibular pathway and have nerve endings in the median eminence that release dopamine into the hypophysial portal blood.[6] In lactating females, TIDA neurons are inhibited by the stimulus of suckling. Dopamine released from their nerve endings at the median eminence is transported to the anterior pituitary gland, where it regulates the secretion of prolactin. Dopamine inhibits prolactin secretion, so when the TIDA neurons are inhibited, there is increased secretion of prolactin, which stimulates lactogenesis (milk production). Prolactin acts in a short-loop negative feedback manner to decrease its levels by stimulating the release of dopamine. Dopaminergic neurons of the arcuate also inhibit the release of gonadotropin-releasing hormone, explaining in part why lactating (or otherwise hyperprolactinemic) women experience oligomenorrhea or amenorrhea (infrequency or absence of menses).[6]
  • Kisseptin/NKB neurons within the arcuate nucleus form synaptic inputs with TIDA neurons. These neurons express estrogen receptors and also coexpress neurokinin B in female rats.[7]
  • Growth hormone releasing GHRH neurons helps to control growth hormone (GH) secretion in a mechanism with somatostatin, neuropeptide Y (NPY) and GHRH.[8]
  • NPY/AGRP neurons and POMC/CART neurons make up two groups of neurons in the arcuate nucleus that are centrally involved in the neuroendocrine function of feeding. Medial neurons utilize NPY peptides as neurotransmitters to stimulate appetite, and lateral neurons utilize POMC/CART to inhibit appetite.[2] NPY and POMC/CART neurons are sensitive to peripheral hormones such as leptin and insulin.[4]
  • Gonadotropin releasing neurons and Agouti-related peptide (AGRP) secreting neurons have also been found.[1][2] Neurons in the ARC secrete gonadotropins and metabolic histamine,[2] and regulate the secretion of lutenizing hormone (LH), which influences the activity of gonadotropin releasing hormone and steroid production.[1]
  • There are also groups of neurons expressing neurokinin b/ dynorphin that help to control reproduction.[2]

Centrally-projecting neurons[edit]

Other types of neurons have projection pathways from the arcuate nucleus to mediate different regions of the hypothalamus or to other regions outside of the hypothalamus.[2][4] Projections of these neurons extend a long distance from the arcuate nucleus to the median eminence to influence the release of hormones from the pituitary gland.[1][2] Neurons of the Arcuate nucleus have intrahypothalamic projections for neuroendrocrine circuitry.[1] such as neural projections that influence feeding behavior project to the paraventricular nucleus of the hypothalamus (PVH), the dorsomedial hypothalamic nucleus (DMH, and the lateral hypothalamic area (LHA).[1] Populations of neurons connect to the intermediate lobes of the pituitary gland, from the lateral division of the ARH to the neural and intermediate parts of the pituitary gland, and the caudal division of ARH to the median eminence.[2]

Groups of neurons that project elsewhere within the central nervous system include:

  • Centrally projecting neurons that contain neuropeptide Y (NPY), agouti-related protein (AGRP), and the inhibitory neurotransmitter GABA. These neurons, in the most ventromedial part of the nucleus, project strongly to the lateral hypothalamus and to the paraventricular nucleus of the hypothalamus, and are important in the regulation of appetite. When activated, these neurons can produce ravenous eating. These neurons are inhibited by leptin, insulin, and peptide YY and activated by ghrelin.
  • Centrally projecting neurons that contain peptide products of pro-opiomelanocortin (POMC), and cocaine- and amphetamine-regulated transcript (CART). These neurons have widespread projections to many brain areas, including to all nuclei in the hypothalamus. These cells are important in the regulation of appetite, and, when activated, they inhibit feeding. These neurons are activated by circulating concentrations of leptin and insulin, and they are directly innervated and inhibited by the NPY neurons.[9] POMC neurons that project to the medial preoptic nucleus are also involved in the regulation of sexual behavior in both males and females. The expression of POMC is regulated by gonadal steroids. The release of a POMC product, beta-endorphin is regulated by NPY.
  • Centrally projecting neurons that make somatostatin; the neurosecretory somatostatin neurons that regulate growth hormone secretion are a different population, located in the periventricular nucleus.
  • Feeding regulatory neurons also activate oxytocin-containing neurons of the periventricular nucleus (PVN), which projects to nucleus of tractus solitarus in the medulla oblongata. [2]
  • Others receive direct synaptic inputs from extra hypothalamic sites projecting into the amygdala, the hippocampus, and the Entorhinal cortex.[2]

Other neurons[edit]

Other cell populations include:

  • A small population of neurons that sensitive to ghrelin. The role of this population is not known; many neurons in the arcuate nucleus express receptors for ghrelin, but these are thought to respond mainly to blood-borne ghrelin.
  • The arcuate nucleus also contains a population of specialized ependymal cells, called tanycytes.
  • Astrocytes in the arcuate nucleus hold high capacity glucose transporters that function as nutrient sensors for appetite controlling neurons[2]
  • The diverse and specialized collections of neurons reside within a special compartment with glial cells and have their own network of capillaries and a membrane of tanycytes that help create a blood brain barrier.[2] Circulating or molecules such as hormones travel in the blood and can directly affect these neurons and their plasticity as evidence by adult neurogenesis.[2]

References[edit]

  1. ^ a b c d e f g h i Bouret, Sebastien G.; Draper, Shin J.; Simerly, Richard B. (2004-03-17). "Formation of Projection Pathways from the Arcuate Nucleus of the Hypothalamus to Hypothalamic Regions Implicated in the Neural Control of Feeding Behavior in Mice". The Journal of Neuroscience. 24 (11): 2797–2805. doi:10.1523/JNEUROSCI.5369-03.2004. ISSN 0270-6474. 
  2. ^ a b c d e f g h i j k l m n o p Dudás (2013). The Human Hypothalamus: Anatomy, Functions and Disorders. New York: Nova Science Publishers. ISBN 978-1-62081-806-0 – via Ebscohost. 
  3. ^ onderzoekinformatie.nl - Project: Does activation of neurons in the infundibular nucleus in menopause prevent the occurrence of Alzheimer changes?
  4. ^ a b c d Sapru, Hreday N. "Role of the hypothalamic arcuate nucleus in cardiovascular regulation". Autonomic Neuroscience. 175 (1-2): 38–50. doi:10.1016/j.autneu.2012.10.016. 
  5. ^ Coppari, Roberto; Ichinose, Masumi; Lee, Charlotte E.; Pullen, Abigail E.; Kenny, Christopher D.; McGovern, Robert A.; Tang, Vinsee; Liu, Shun M.; Ludwig, Thomas. "The hypothalamic arcuate nucleus: A key site for mediating leptin's effects on glucose homeostasis and locomotor activity". Cell Metabolism. 1 (1): 63–72. doi:10.1016/j.cmet.2004.12.004. 
  6. ^ a b Voogt, J. L.; Lee, Y.; Yang, S.; Arbogast, L. (2001-01-01). "Regulation of prolactin secretion during pregnancy and lactation". Progress in Brain Research. 133: 173–185. ISSN 0079-6123. PMID 11589129. 
  7. ^ Sawai, Nobuhiko; Iijima, Norio; Takumi, Ken; Matsumoto, Keisuke; Ozawa, Hitoshi (2012-09-01). "Immunofluorescent histochemical and ultrastructural studies on the innervation of kisspeptin/neurokinin B neurons to tuberoinfundibular dopaminergic neurons in the arcuate nucleus of rats". Neuroscience Research. 74 (1): 10–16. doi:10.1016/j.neures.2012.05.011. 
  8. ^ Mano-Otagiri, Asuka; Nemoto, Takahiro; Sekino, Azusa; Yamauchi, Naoko; Shuto, Yujin; Sugihara, Hitoshi; Oikawa, Shinichi; Shibasaki, Tamotsu (2006-09-01). "Growth Hormone-Releasing Hormone (GHRH) Neurons in the Arcuate Nucleus (Arc) of the Hypothalamus Are Decreased in Transgenic Rats Whose Expression of Ghrelin Receptor Is Attenuated: Evidence that Ghrelin Receptor Is Involved in the Up-Regulation of GHRH Expression in the Arc". Endocrinology. 147 (9): 4093–4103. doi:10.1210/en.2005-1619. ISSN 0013-7227. 
  9. ^ Arora and Anubhuti. Role of neuropeptides in appetite regulation and obesity--a review. Neuropeptides (2006) vol. 40 (6) pp. 375-401

Footnotes[edit]