Paraventricular nucleus of hypothalamus

Paraventricular nucleus of hypothalamus

Human paraventricular nucleus (PVN) in this coronal section is indicated by the shaded area. Dots represent vasopressin (AVP) neurons (also seen in the supraoptic nucleus, SON). The medial surface is the 3rd ventricle (3V).

Magnocellular neurons of the PVN and SON project to the posterior "lobe" of the pituitary
Details
Identifiers
Latin Nucleus paraventricularis hypothalami
MeSH A08.186.211.730.385.357.342.400
NeuroNames hier-370
NeuroLex ID Paraventricular nucleus of hypothalamus
Dorlands
/Elsevier
n_11/12582324
TA A14.1.08.909
FMA 62320

Anatomical terms of neuroanatomy

The paraventricular nucleus (PVN, PVA, or PVH) is a neuronal nucleus in the hypothalamus. It contains groups of neurons that can be activated by stressful and/or physiological changes. Many PVN neurons project directly to the posterior pituitary where they release oxytocin or vasopressin into the general circulation. Other PVN neurons control various anterior pituitary functions, while still others directly regulate appetite and autonomic functions in the brainstem and spinal cord.

Location

The paraventricular nucleus lies adjacent to the third ventricle. It lies within the periventricular zone and is not 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 neurons extend to sites (in the median eminence and in the posterior pituitary) beyond the blood–brain barrier.

Neurons

The PVN contains magnocellular neurosecretory cells whose axons extend into the posterior pituitary, parvocellular neurosecretory (neuroendocrine) cells that project to the median eminence, and several populations of peptide-containing 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.

Parvocellular neurosecretory (Neuroendocrine) 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 (Preautonomic) 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 to the PVN

The PVN receives afferent inputs from many brain regions.

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.[3]

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.[4][5][6]

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 .

References

  1. Giuliano F, Allard J (August 2001). "Dopamine and sexual function". International Journal of Impotence Research. 13 Suppl 3: S18–28. doi:10.1038/sj.ijir.3900719. PMID 11477488. Retrieved 2014-12-30.
  2. Argiolas A, Melis MR (May 2005). "Central control of penile erection: role of the paraventricular nucleus of the hypothalamus". Progress in Neurobiology 76 (1): 1–21. doi:10.1016/j.pneurobio.2005.06.002. PMID 16043278. Retrieved 2014-12-30.
  3. Russell JA, Blackburn RE, Leng G (June 1988). "The role of the AV3V region in the control of magnocellular oxytocin neurons". Brain Research Bulletin 20 (6): 803–10. doi:10.1016/0361-9230(88)90095-0. PMID 3044525.
  4. Beck B (July 2006). "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. doi:10.1098/rstb.2006.1855. PMC 1642692. PMID 16874931. Retrieved 2014-12-30.
  5. Konturek PC, Konturek JW, Cześnikiewicz-Guzik M, Brzozowski T, Sito E, Konturek SJ (December 2005). "Neuro-hormonal control of food intake: basic mechanisms and clinical implications" (PDF). Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society. 56 Suppl 6: 5–25. PMID 16340035. Retrieved 2014-12-30.
  6. Nillni EA (April 2010). "Regulation of the hypothalamic thyrotropin releasing hormone (TRH) neuron by neuronal and peripheral inputs". Frontiers in Neuroendocrinology 31 (2): 134–56. doi:10.1016/j.yfrne.2010.01.001. PMC 2849853. PMID 20074584. Retrieved 2014-12-30.

External links

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