Paraventricular nucleus of hypothalamus explained

Paraventricular nucleus of hypothalamus should not be confused with Periventricular nucleus.

Paraventricular nucleus of hypothalamus
Latin:nucleus paraventricularis hypothalami

The paraventricular nucleus (PVN, PVA, or PVH) 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).[1] CRH and TRH are secreted into the hypophyseal portal system and act on different targets neurons in the anterior pituitary. Dysfunctions of PVN can cause hypersomnia in mice,[2] and dysfunction of the paraventricular nucleus can lead to drowsiness for up to 20 hours per day in humans.[3] PVN is thought to mediate many diverse functions through different hormones, including osmoregulation, appetite,wakefulness, and the response of the body to stress.[4] [5]

Location

The paraventricular nucleus lies adjacent to the third ventricle. It lies within the periventricular zone and is not to be confused with the periventricular nucleus, which occupies a more medial position, beneath the third ventricle. The PVN is highly vascularised and is protected by the blood–brain barrier, although its neuroendocrine cells extend to sites (in the median eminence and in the posterior pituitary) beyond the blood–brain barrier. PVN is accounting for only about 1% of the brain volume.In the rat, the PVN consists of approximately 100,000 neurons located in a volume of about 0.5 cubic millimetre.[6]

Neurons

The PVN contains magnocellular neurosecretory cells whose axons extend into the posterior pituitary, parvocellular neurosecretory cells that project to the median eminence, ultimately signalling to the anterior pituitary, and several populations of other cells that project to many different brain regions including parvocellular preautonomic cells that project to the brainstem and spinal cord.

Magnocellular neurosecretory neurons

The magnocellular cells in the PVN elaborate and secrete two peptide hormones: oxytocin and vasopressin.

These hormones are packaged into large vesicles, which are then transported down the unmyelinated axons of the cells and released from neurosecretory nerve terminals residing in the posterior pituitary gland.

Similar magnocellular neurons are found in the supraoptic nucleus which also secrete vasopressin and a smaller amount of oxytocin.

Parvocellular neurosecretory neurons

The axons of the parvocellular neurosecretory neurons of the PVN project to the median eminence, a neurohemal organ at the base of the brain, where their neurosecretory nerve terminals release their hormones at the primary capillary plexus of the hypophyseal portal system. The median eminence contains fiber terminals from many hypothalamic neuroendocrine neurons, secreting different neurotransmitters or neuropeptides, including vasopressin, corticotropin-releasing hormone (CRH), thyrotropin-releasing hormone (TRH), gonadotropin-releasing hormone (GnRH), growth hormone-releasing hormone (GHRH), dopamine (DA) and somatostatin (growth hormone release inhibiting hormone, GIH) into blood vessels in the hypophyseal portal system. The blood vessels carry the peptides to the anterior pituitary gland, where they regulate the secretion of hormones into the systemic circulation. The parvocellular neurosecretory cells include those that make:

Centrally-projecting neurons

As well as neuroendocrine neurons, the PVN contains interneurons and populations of neurons that project centrally (i.e., to other brain regions). The centrally-projecting neurons include

Afferent inputs

The PVN receives afferent inputs from many brain regions and different parts of the body, by hormonal control.[4]

Among these, inputs from neurons in structures adjacent to the anterior wall of the third ventricle (the "AV3V region") carry information about the electrolyte composition of the blood, and about circulating concentrations of such hormones as angiotensin and relaxin, to regulate the magnocellular neurons.[9]

Inputs from the brainstem (the nucleus of the solitary tract) and the ventrolateral medulla carry information from the heart and stomach. Inputs from the hippocampus to the CRH neurones are important regulators of stress responses.

Inputs from neuropeptide Y-containing neurons in the arcuate nucleus coordinate metabolic regulation (via TRH secretion) with regulation of energy intake.[10] [11] [12] Specifically, the projections from the arcuate nucleus seem to exert their effect on appetite via MC4R-expressing oxytocinergic cells of the PVN.[13]

Inputs from suprachiasmatic nucleus about levels of lighting (circadian rhythms).

Inputs from glucose sensors within the brain stimulate release of vasopressin and corticotropin-releasing hormone from parvocellular neurosecretory cells.

Further reading

Notes and References

  1. Ferguson AV, Latchford KJ, Samson WK . The paraventricular nucleus of the hypothalamus - a potential target for integrative treatment of autonomic dysfunction . Expert Opinion on Therapeutic Targets . 12 . 6 . 717–27 . June 2008 . 18479218 . 2682920 . 10.1517/14728222.12.6.717 .
  2. Chen . Chang-Rui . Zhong . Yu-Heng . Jiang . Shan . Xu . Wei . Xiao . Lei . Wang . Zan . Qu . Wei-Min . Huang . Zhi-Li . 2021-11-17 . Elmquist . Joel K . Wong . Ma-Li . Lazarus . Michael . Dysfunctions of the paraventricular hypothalamic nucleus induce hypersomnia in mice . eLife . 10 . e69909 . 10.7554/eLife.69909 . free . 34787078 . 8631797 . 2050-084X.
  3. Wang . Zan . Zhong . Yu-Heng . Jiang . Shan . Qu . Wei-Min . Huang . Zhi-Li . Chen . Chang-Rui . 2022-03-14 . Case Report: Dysfunction of the Paraventricular Hypothalamic Nucleus Area Induces Hypersomnia in Patients . Frontiers in Neuroscience . English . 16 . 10.3389/fnins.2022.830474 . free . 35360167 . 1662-453X. 8964012 .
  4. Book: Fox, Stuart Ira . vanc . Human Physiology . Twelfth . McGraw Hill . 2011 . 665 .
  5. Chen . Chang-Rui . Zhong . Yu-Heng . Jiang . Shan . Xu . Wei . Xiao . Lei . Wang . Zan . Qu . Wei-Min . Huang . Zhi-Li . 2021-11-17 . Elmquist . Joel K . Wong . Ma-Li . Lazarus . Michael . Dysfunctions of the paraventricular hypothalamic nucleus induce hypersomnia in mice . eLife . 10 . e69909 . 10.7554/eLife.69909 . free . 34787078 . 8631797 . 2050-084X.
  6. Grassi . D. . Marraudino . M. . Garcia-Segura . L. M. . Panzica . G. C. . 2022-04-01 . The hypothalamic paraventricular nucleus as a central hub for the estrogenic modulation of neuroendocrine function and behavior . Frontiers in Neuroendocrinology . 65 . 100974 . 10.1016/j.yfrne.2021.100974 . 34995643 . 0091-3022.
  7. Giuliano F, Allard J . Dopamine and sexual function . International Journal of Impotence Research . 13 Suppl 3 . S18-28 . August 2001 . 11477488 . 10.1038/sj.ijir.3900719 . free .
  8. Argiolas A, Melis MR . 24929538 . Central control of penile erection: role of the paraventricular nucleus of the hypothalamus . Progress in Neurobiology . 76 . 1 . 1–21 . May 2005 . 16043278 . 10.1016/j.pneurobio.2005.06.002 .
  9. Russell JA, Blackburn RE, Leng G . 4762486 . The role of the AV3V region in the control of magnocellular oxytocin neurons . Brain Research Bulletin . 20 . 6 . 803–10 . June 1988 . 3044525 . 10.1016/0361-9230(88)90095-0 .
  10. Beck B . Neuropeptide Y in normal eating and in genetic and dietary-induced obesity . Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences . 361 . 1471 . 1159–85 . July 2006 . 16874931 . 1642692 . 10.1098/rstb.2006.1855 .
  11. Konturek PC, Konturek JW, Cześnikiewicz-Guzik M, Brzozowski T, Sito E, Konturek SJ . Neuro-hormonal control of food intake: basic mechanisms and clinical implications . Journal of Physiology and Pharmacology . 56 Suppl 6 . 5–25 . December 2005 . 16340035 .
  12. Nillni EA . Regulation of the hypothalamic thyrotropin releasing hormone (TRH) neuron by neuronal and peripheral inputs . Frontiers in Neuroendocrinology . 31 . 2 . 134–56 . April 2010 . 20074584 . 2849853 . 10.1016/j.yfrne.2010.01.001 .
  13. Qin C, Li J, Tang K . The Paraventricular Nucleus of the Hypothalamus: Development, Function, and Human Diseases . Endocrinology . 159 . 9 . 3458–3472 . September 2018 . 30052854 . 10.1210/en.2018-00453 . free .