Arcuate nucleus: Difference between revisions

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* A small population of neurons that make the potent appetite-stimulating peptide [[ghrelin]]. The role of this population is not known; many neurons in the arcuate nucleus have receptors for ghrelin, but these are thought to respond mainly to blood-borne ghrelin, secreted by the empty stomach.<ref>Elmquist JK ''et al.'' 2005 Identifying hypothalamic pathways controlling food intake, body weight, and glucose homeostasis. ''J Comp Neurol''  493:63-71 PMID 16254991</ref>  
* A small population of neurons that make the potent appetite-stimulating peptide [[ghrelin]]. The role of this population is not known; many neurons in the arcuate nucleus have receptors for ghrelin, but these are thought to respond mainly to blood-borne ghrelin, secreted by the empty stomach.<ref>Elmquist JK ''et al.'' 2005 Identifying hypothalamic pathways controlling food intake, body weight, and glucose homeostasis. ''J Comp Neurol''  493:63-71 PMID 16254991</ref>  


* Neurons that synthesise [[kisspeptin]], a peptide that is a major regulator of the secretion of luteinizing hormone releasing hormone (LHRH).
* Neurons that synthesise [[kisspeptin]], a peptide that is a major regulator of the secretion of luteinizing hormone releasing hormone (LHRH). These neurones co-express the opi0d peptide [[dynorphin]] and neurokinin, and appear to be specifically involved in the regulation of pulsatile LHRH release.


The arcuate nucleus also contains a population of specialized [[astrocytes]], called [[tanycytes]].
The arcuate nucleus also contains a population of specialized [[astrocytes]], called [[tanycytes]].

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Schematic view of the ventral surface of the brain, at the level of the hypothalamus. The median eminence is at the bottom, and receives projections from the neuroendocrine neurons of the arcuate nucleus

The arcuate nucleus is a small part of the hypothalamus that plays an extremely important role in the regulation of hormone secretion from the pituitary gland, and in the regulation of appetite and body weight.

The arcuate nucleus is located in the mediobasal hypothalamus at the base of the brain, it lies on either side of the third ventricle and just above the median eminence. It includes several important populations of neurons, including neuroendocrine neurones, and appetite-regulating neurones.

Neuroendocrine Neurons

Schematic cross section of the mediobasal hypothalamus, with the median eminence at the bottom, showing the neuroendocrine neurons of the arcuate nucleus

The arcuate nucleus contains two important populations of neuroendocrine neurons with nerve endings in the median eminence. One population releases dopamine into the hypophysial portal blood to regulate the secretion of the hormone prolactin, which in turn controls the production of milk (lactogenesis). These are sometimes called the "tuberoinfundibular dopamine" (TIDA) neurons. 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 inhibits prolactin secretion, so, when the TIDA neurons are inhibited, prolactin secretion is increased. Dopamine 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).[1]

A second population of neuroendocrine neurons, mainly in the ventrolateral part of the arcuate nucleus, make growth hormone-releasing hormone (GHRH). Like the TIDA neurons, these neurons have nerve endings in the median eminence. GHRH released into the hypophysial portal blood is transported to the anterior pituitary gland, where it stimulates the secretion of growth hormone. [2].


Appetite-regulating neurones

LeptinactiononPOMCneurones.jpg

The arcuate nucleus has a key role in the regulation of feeding behaviour, through two important populations of centrally projecting neurons:

  • Neurons that contain neuropeptide Y (NPY); another peptide, 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. NPY and AGRP are both very potent stimulators of feeding behaviour. The expression of NPY and AgRP is strongly increased after a period of fasting, and when activated, these neurons can produce ravenous eating when food is available. These neurons are regulated by circulating concentrations of leptin (a hormone secreted from fat cells (adipose tissue) and ghrelin (a hormone secretd from the stomach when it is empty). Destruction of these neurons leads to severe loss of appetite in experimental animals [3][4][5]
  • Neurons that contain peptide products of pro-opiomelanocortin (POMC), notably including the appetite suppressing peptide alpha-melanocyte stimulating hormone (alpha-MSH) and the opioid peptide beta-endorphin; they also express another appetite-inhibiting peptide, cocaine-and-amphetamine-regulating transcript (CART), and some make the neurotransmitter acetylcholine. These neurons project to many brain areas, including to all parts of the hypothalamus. They are also very important in the regulation of appetite, and, when activated, they inhibit feeding, mainly via the effects of alpha MSH. These neurons are also regulated by circulating concentrations of leptin and ghrelin. They are directly innervated by the NPY/AGRP neurons, which inhibit them mainly via the release of GABA. POMC neurons that project to the medial preoptic nucleus are also involved in the regulation of sexual behavior in both males and females. [6][7]

Other neuronal cell types

The arcuate nucleus contains some other neuronal cell types the function of which is still not fully known. In particular, it contains:

  • Centrally-projecting neurons that make somatostatin; the neurosecretory somatostatin neurons that regulate growth hormone secretion are a different population, located in the periventricular nucleus.[8]
  • A small population of neurons that make the potent appetite-stimulating peptide ghrelin. The role of this population is not known; many neurons in the arcuate nucleus have receptors for ghrelin, but these are thought to respond mainly to blood-borne ghrelin, secreted by the empty stomach.[9]
  • Neurons that synthesise kisspeptin, a peptide that is a major regulator of the secretion of luteinizing hormone releasing hormone (LHRH). These neurones co-express the opi0d peptide dynorphin and neurokinin, and appear to be specifically involved in the regulation of pulsatile LHRH release.

The arcuate nucleus also contains a population of specialized astrocytes, called tanycytes.

References

  1. Voogt JL et al (2001) Regulation of prolactin secretion during pregnancy and lactation. Prog Brain Res 133:173-85 PMID 11589129
  2. Bluet-Pajot MT et al (1998) Hypothalamic and hypophyseal regulation of growth hormone secretion. Cell Mol Neurobiol 18:101-23 PMID 9524732
  3. Sawchenko PE (1998) Toward a new neurobiology of energy balance, appetite, and obesity: the anatomists weigh in. J Comp Neurol 402:435-41 PMID 9862319
  4. Bouret SG, Simerly RB (2006) Developmental programming of hypothalamic feeding circuits. Clin Genet 70:295-301 PMID 16965320
  5. van den Top M, Spanswick D (2006) Integration of metabolic stimuli in the hypothalamic arcuate nucleus. Prog Brain Res 153:141-54 PMID 16876573
  6. Cone RD et al. (2001) The arcuate nucleus as a conduit for diverse signals relevant to energy homeostasis. Int J Obes Relat Metab Disord 25 Suppl 5:S63-7 PMID 11840218
  7. Cone RD (2005) Anatomy and regulation of the central melanocortin system. Nat Neurosci 8:571-8 PMID 15856065
  8. Kawano H, Daikoku S (1988). "Somatostatin-containing neuron systems in the rat hypothalamus: retrograde tracing and immunohistochemical studies". J Comp Neurol 271: 293–9. PMID 2897982.
  9. Elmquist JK et al. 2005 Identifying hypothalamic pathways controlling food intake, body weight, and glucose homeostasis. J Comp Neurol 493:63-71 PMID 16254991