Ventromedial nucleus of the hypothalamus

Last updated
Ventromedial nucleus of the hypothalamus
HypothalamicNuclei.PNG
Ventromedial nucleus is 'VM', at center, in green.
Details
Part of Hypothalamus
Artery Basilar
Identifiers
Latin nucleus ventromedialis hypothalami
MeSH D014697
NeuroNames 398
NeuroLex ID birnlex_1572
TA98 A14.1.08.928
TA2 5729
FMA 62332
Anatomical terms of neuroanatomy

The ventromedial nucleus of the hypothalamus (VMN, VMH or ventromedial hypothalamus) is a nucleus of the hypothalamus. In 2007, Kurrasch et al. found that the ventromedial hypothalamus is a distinct morphological nucleus involved in terminating hunger, fear, thermoregulation, and sexual activity. [1] This nuclear region is involved in the recognition of the feeling of fullness.

Contents

Structure

It has four subdivisions:

These subdivisions differ anatomically, neurochemically, and behaviorally.

Function

The ventromedial nucleus (VMN) is most commonly associated with satiety. Early studies showed that VMN lesions caused over-eating and obesity in rats. However, the interpretation of these experiments was summarily discredited when Gold's research demonstrated that precision lesioning of the VMN did not result in hyperphagia. [2] Nevertheless, numerous studies have shown that the immediacy of hyperphagia and obesity syndrome are a consequence of VMN lesions or procaine injections, and point to the VMN's role in satiety. [3] [4] [5] [6] [7] [8] [9] A major review of the subject in 2006 concluded that, "anatomical studies done both before and after Gold's study did not replicate his results with lesions, and in nearly every published direct comparison of VMH lesions vs. PVN or VNAB lesions, the group with VMH lesions ate substantially more food and gained twice as much weight." [10] This strongly substantiates the classification of VMN as the primary satiety center in the hypothalamus.

It has also been found that lesions to the VMH in rats caused increased plasma insulin levels. Rats with a VMH lesion compared to normal rats overproduce a circulating satiety factor, to which the control rats can respond and rats with a VMH lesion cannot respond. A lesion to the VMH makes rats overproduce leptin, which they cannot respond to causing them to over eat, leading to obesity. [11]

Researchers looked at a series of twenty-one animals of various degrees of adiposity, with respect to growth appearance, fat distribution, general physical condition, and the correlation between the level of adiposity attained and the correlation of the hypothalamic lesion. Lesions in the hypothalamic area, particularly the region of the ventromedial hypothalamus interrupts a large number of the descending fibers from the hypothalamic cell groups that were found to contribute to obesity in rats. [12]

Another study found that there seems to be a higher concentration of cannabinoid receptor mRNA within the VMH in comparison to other nuclei within the hypothalamus. The cannabinoid ingestion has been linked to rewarding processes, and also with the release of dopamine in the brain. [13]

VMH is also important in mammal play behaviour. Lesions to VMH along with the hippocampus, amygdala, the cerebellum, and the lateral hypothalamus are all linked to reduced play. [14]

The VMHdm has a role in the male vocalizations and scent marking behaviors. [15] [16]

The VMHvl contains many distinct neuronal populations that contribute to varying, often distinct, functions. [17] Notably, this region plays a role in sexual behaviors in females (lordosis), thus stimulating their sexual arousal. [18] [19] [20] [21] The VMHvl has also been found to play a role in estrogen-mediated movement [22] and energy expenditure/thermogenesis. [23]

Bilateral FOS expression in the VMH after repeated seizures is associated with alteration in the severity of flurothyl induced seizures in C57BL/6J mice that are not present in DBA/2J mice. [24] [25] Moreover, bilateral lesions of the VMH are able to block the propagation of seizure discharge to enter the brainstem seizure system. [26]

Surgery

In West Germany, at least 70 men had their VMN operated on between 1962 and 1979. Most of these individuals had been involuntarily institutionalized or imprisoned for deviant sexual behavior, such as homosexuality, perceived hypersexuality among heterosexual men, and pedophilia. This surgery was not commonly performed elsewhere. [27]

Related Research Articles

<span class="mw-page-title-main">Hypothalamus</span> Area of the brain below the thalamus

The hypothalamus is a part of the brain that contains a number of small 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. In the terminology of neuroanatomy, it forms the ventral part of the diencephalon. All vertebrate brains contain a hypothalamus. In humans, it is the size of an almond.

<span class="mw-page-title-main">Arcuate nucleus</span>

The arcuate nucleus of the hypothalamus 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. 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.

<span class="mw-page-title-main">Neuropeptide Y</span> Mammalian protein found in Homo sapiens

Neuropeptide Y (NPY) is a 36 amino-acid neuropeptide that is involved in various physiological and homeostatic processes in both the central and peripheral nervous systems. It is secreted alongside other neurotransmitters such as GABA and glutamate. 

<span class="mw-page-title-main">Lordosis behavior</span> Naturally occurring body posture for sexual receptivity to copulation that present in most mammals

Lordosis behavior, also known as mammalian lordosis or presenting, is the naturally occurring body posture for sexual receptivity to copulation present in females of most mammals including rodents, elephants, and cats. The primary characteristics of the behavior are a lowering of the forelimbs but with the rear limbs extended and hips raised, ventral arching of the spine and a raising, or sideward displacement, of the tail. During lordosis, the spine curves dorsoventrally so that its apex points towards the abdomen.

<span class="mw-page-title-main">Octreotide</span> Octapeptide that mimics natural somatostatin pharmacologically

Octreotide, sold under the brand name Sandostatin among others, is an octapeptide that mimics natural somatostatin pharmacologically, though it is a more potent inhibitor of growth hormone, glucagon, and insulin than the natural hormone. It was first synthesized in 1979 by the chemist Wilfried Bauer, and binds predominantly to the somatostatin receptors SSTR2 and SSTR5.

<span class="mw-page-title-main">Ventrolateral preoptic nucleus</span> Nucleus of the anterior hypothalamus

The ventrolateral preoptic nucleus (VLPO), also known as the intermediate nucleus of the preoptic area (IPA), is a small cluster of neurons situated in the anterior hypothalamus, sitting just above and to the side of the optic chiasm in the brain of humans and other animals. The brain's sleep-promoting nuclei, together with the ascending arousal system which includes components in the brainstem, hypothalamus and basal forebrain, are the interconnected neural systems which control states of arousal, sleep, and transitions between these two states. The VLPO is active during sleep, particularly during non-rapid eye movement sleep, and releases inhibitory neurotransmitters, mainly GABA and galanin, which inhibit neurons of the ascending arousal system that are involved in wakefulness and arousal. The VLPO is in turn innervated by neurons from several components of the ascending arousal system. The VLPO is activated by the endogenous sleep-promoting substances adenosine and prostaglandin D2. The VLPO is inhibited during wakefulness by the arousal-inducing neurotransmitters norepinephrine and acetylcholine. The role of the VLPO in sleep and wakefulness, and its association with sleep disorders – particularly insomnia and narcolepsy – is a growing area of neuroscience research.

<span class="mw-page-title-main">Stria terminalis</span> Band of fibres along the thalamus

The stria terminalis is a structure in the brain consisting of a band of fibers running along the lateral margin of the ventricular surface of the thalamus. Serving as a major output pathway of the amygdala, the stria terminalis runs from its centromedial division to the ventromedial nucleus of the hypothalamus.

The sexually dimorphic nucleus (SDN) is an ovoid, densely packed cluster of large cells located in the medial preoptic area (POA) of the hypothalamus which is believed to be related to sexual behavior in animals. Thus far, for all species of mammals investigated, the SDN has been repeatedly found to be considerably larger in males than in females. In humans, the volume of the SDN has been found to be 2.2 times as large in males as in females and to contain 2.1 times as many cells. The human SDN is elongated in females and more spherical in males. No sex differences have been observed in the human SDN in either cell density or mean diameter of the cell nuclei. The volume and cell number of the human SDN considerably decreases with age, although the decrease in cell number is both sex and age-specific. In males, a substantial decrease in the cell number of the human SDN was observed between the age of 50–60 years. Cell death was more common in females than males, especially among those older than 70 years of age. The SDN cell number in females can drop to 10-15% of that found in early childhood.

<span class="mw-page-title-main">Vagotomy</span> Surgical procedure

A vagotomy is a surgical procedure that involves removing part of the vagus nerve. It is performed in the abdomen.

<span class="mw-page-title-main">Dorsomedial hypothalamic nucleus</span>

The dorsomedial hypothalamic nucleus is a nucleus of the hypothalamus. It is involved in feeding, drinking, body-weight regulation and circadian activity. More specifically, it is a necessary component for the expression of numerous behavioral and physiological circadian rhythms. The dorsomedial hypothalamic nucleus receives information from neurons and humors involved in feeding regulation, body weight and energy consumption, and then passes this information on to brain regions involved in sleep and wakefulness regulation, body temperature and corticosteroid secretion.

<span class="mw-page-title-main">Preoptic area</span> Region of the anterior hypothalamus

The preoptic area is a region of the hypothalamus. MeSH classifies it as part of the anterior hypothalamus. TA lists four nuclei in this region,.

The periventricular nucleus is a thin sheet of small neurons located in the wall of the third ventricle, a composite structure of the hypothalamus. It functions in analgesia.

In evolutionary psychology, people often speak of the four Fs which are said to be the four basic and most primal drives that animals are evolutionarily adapted to have, follow, and achieve: fighting, fleeing, feeding and mating.

Neuromedin U is a neuropeptide found in the brain of humans and other mammals, which has a number of diverse functions including contraction of smooth muscle, regulation of blood pressure, pain perception, appetite, bone growth, and hormone release. It was first isolated from the spinal cord in 1985, and named after its ability to cause smooth muscle contraction in the uterus.

<span class="mw-page-title-main">Coumestrol</span> Chemical compound

Coumestrol is a natural organic compound in the class of phytochemicals known as coumestans. Coumestrol was first identified as a compound with estrogenic properties by E. M. Bickoff in ladino clover and alfalfa in 1957. It has garnered research interest because of its estrogenic activity and prevalence in some foods, including soybeans, brussels sprouts, spinach and a variety of legumes. The highest concentrations of coumestrol are found in clover, Kala Chana, and Alfalfa sprouts.

<span class="mw-page-title-main">SB-334867</span> Chemical compound

SB-334867 is an orexin antagonist. It was the first non-peptide antagonist developed that is selective for the orexin receptor subtype OX1, with around 50x selectivity for OX1 over OX2 receptors. It has been shown to produce sedative and anorectic effects in animals, and has been useful in characterising the orexinergic regulation of brain systems involved with appetite and sleep, as well as other physiological processes. The hydrochloride salt of SB-334867 has been demonstrated to be hydrolytically unstable, both in solution and as the solid. Orexin antagonists have multiple potential clinical applications including the treatment of drug addiction, insomnia, obesity and diabetes.

Parabiosis is a laboratory technique used in physiological research, derived from the Greek word meaning "living beside." The technique involves the surgical joining of two living organisms in such a way that they develop a single, shared physiological system. Through this unique approach, researchers can study the exchange of blood, hormones, and other substances between the two organisms, allowing for the examination of a wide range of physiological phenomena and interactions. Parabiosis has been employed in various fields of study, including stem cell research, endocrinology, aging research, and immunology.

David Booth works full-time in research and research teaching as an honorary professor at the School of Psychology in the College of Life and Environmental Sciences of the University of Birmingham (UK). According to his Web page he investigates the ways in which an individual's life works. His research and teaching centre on the processes in the mind that fit acts and reactions of human beings and animals to the passing situation.

<span class="mw-page-title-main">Pathophysiology of obesity</span>

Pathophysiology of obesity is the study of disordered physiological processes that cause, result from, or are otherwise associated with obesity. A number of possible pathophysiological mechanisms have been identified which may contribute in the development and maintenance of obesity.

Dayu Lin is a neuroscientist and Associate Professor of Psychiatry, Neuroscience and Physiology at the New York University Grossman School of Medicine in New York City. Lin discovered the neural circuits in the hypothalamus that give rise to aggression in mice. Her lab at NYU now probes the neural circuits underlying innate social behaviors, with a focus on aggressive and defensive behaviors.

References

  1. Kurrasch DM, Cheung CC, Lee FY, Tran PV, Hata K, Ingraham HA (December 2007). "The neonatal ventromedial hypothalamus transcriptome reveals novel markers with spatially distinct patterning". The Journal of Neuroscience. 27 (50): 13624–34. doi: 10.1523/JNEUROSCI.2858-07.2007 . PMC   6673626 . PMID   18077674.
  2. Gold RM (November 1973). "Hypothalamic obesity: the myth of the ventromedial nucleus". Science. 182 (4111): 488–90. Bibcode:1973Sci...182..488G. doi:10.1126/science.182.4111.488. PMID   4795550. S2CID   3011420.
  3. Balagura S, Devenport LD (June 1970). "Feeding patterns of normal and ventromedial hypothalamic lesioned male and female rats". Journal of Comparative and Physiological Psychology. 71 (3): 357–64. doi:10.1037/h0029118. PMID   5480868.
  4. Becker EE, Kissileff HR (February 1974). "Inhibitory controls of feeding by the ventromedial hypothalamus". The American Journal of Physiology. 226 (2): 383–96. doi:10.1152/ajplegacy.1974.226.2.383. PMID   4811195.
  5. Berthoud HR, Jeanrenaud B (September 1979). "Changes of insulinemia, glycemia and feeding behavior induced by VMH-procainization in the rat". Brain Research. 174 (1): 184–7. doi:10.1016/0006-8993(79)90816-3. PMID   487120. S2CID   39015121.
  6. Brooks CM, Lockwood RA, Wiggins ML (December 1946). "A study of the effect of hypothalamic lesions on the eating habits of the albino rat". The American Journal of Physiology. 147 (4): 735–41. doi:10.1152/ajplegacy.1946.147.4.735. PMID   20277066.
  7. Epstein AN (December 1960). "Reciprocal changes in feeding behavior produced by intrahypothalamic chemical injections". The American Journal of Physiology. 199 (6): 969–74. doi:10.1152/ajplegacy.1960.199.6.969. PMID   13697000.
  8. Larkin RP (November 1975). "Effect of ventromedial hypothalamic procaine injections on feeding, lever pressing, and other behavior in rats". Journal of Comparative and Physiological Psychology. 89 (9): 1100–8. doi:10.1037/h0077192. PMID   1202103.
  9. Maes H (June 1980). "Time course of feeding induced by pentobarbital-injections into the rat's VMH". Physiology & Behavior. 24 (6): 1107–14. doi:10.1016/0031-9384(80)90055-4. PMID   7413790. S2CID   43051882.
  10. King BM (February 2006). "The rise, fall, and resurrection of the ventromedial hypothalamus in the regulation of feeding behavior and body weight". Physiology & Behavior. 87 (2): 221–44. doi:10.1016/j.physbeh.2005.10.007. PMID   16412483. S2CID   40880350.
  11. Satoh N, Ogawa Y, Katsuura G, Tsuji T, Masuzaki H, Hiraoka J, Okazaki T, Tamaki M, Hayase M, Yoshimasa Y, Nishi S, Hosoda K, Nakao K (March 1997). "Pathophysiological significance of the obese gene product, leptin, in ventromedial hypothalamus (VMH)-lesioned rats: evidence for loss of its satiety effect in VMH-lesioned rats". Endocrinology. 138 (3): 947–54. doi: 10.1210/endo.138.3.4989 . PMID   9048594.
  12. Hetherington AW, Ranson SW (June 1942). "The relation of various hypothalamic lesions to adiposity in the rat" (PDF). Journal of Comparative Neurology. 76 (3): 475–99. doi:10.1002/cne.900760308. S2CID   85715802.
  13. Jamshidi N, Taylor DA (November 2001). "Anandamide administration into the ventromedial hypothalamus stimulates appetite in rats". British Journal of Pharmacology. 134 (6): 1151–4. doi:10.1038/sj.bjp.0704379. PMC   1573067 . PMID   11704633.
  14. Panksepp J, Siviy S, Normansell L (1984). "The psychobiology of play: theoretical and methodological perspectives". Neuroscience and Biobehavioral Reviews. 8 (4): 465–92. doi:10.1016/0149-7634(84)90005-8. PMID   6392950. S2CID   26810046.
  15. Flanagan-Cato LM, Lee BJ, Calizo LH (June 2006). "Co-localization of midbrain projections, progestin receptors, and mating-induced fos in the hypothalamic ventromedial nucleus of the female rat". Hormones and Behavior. 50 (1): 52–60. doi:10.1016/j.yhbeh.2006.01.012. PMID   16546183. S2CID   36201218.
  16. Harding SM, McGinnis MY (October 2005). "Microlesions of the ventromedial nucleus of the hypothalamus: effects on sociosexual behaviors in male rats". Behavioral Neuroscience. 119 (5): 1227–34. doi:10.1037/0735-7044.119.5.1227. PMID   16300430.
  17. Kammel LG, Correa SM (January 2020). "Selective sexual differentiation of neurone populations may contribute to sex-specific outputs of the ventromedial nucleus of the hypothalamus". Journal of Neuroendocrinology. 32 (1): e12801. doi:10.1111/jne.12801. PMC   6982598 . PMID   31605642.
  18. Kow LM, Pfaff DW (May 1998). "Mapping of neural and signal transduction pathways for lordosis in the search for estrogen actions on the central nervous system". Behavioural Brain Research. 92 (2): 169–80. doi:10.1016/S0166-4328(97)00189-7. PMID   9638959. S2CID   28276218.
  19. Christensen LW, Nance DM, Gorski RA (1977). "Effects of hypothalamic and preoptic lesions on reproductive behavior in male rats". Brain Research Bulletin. 2 (2): 137–41. doi:10.1016/0361-9230(77)90010-7. PMID   880486. S2CID   4700161.
  20. Pfaff DW, Sakuma Y (March 1979). "Facilitation of the lordosis reflex of female rats from the ventromedial nucleus of the hypothalamus". The Journal of Physiology. 288: 189–202. doi:10.1113/jphysiol.1979.sp012690. PMC   1281421 . PMID   469715.
  21. Matsumoto T, Yamanouchi K (September 2000). "Acceleration of mounting behaviors in female rats by ibotenic acid lesions in the ventromedial hypothalamic nucleus". Neuroscience Letters. 291 (3): 143–6. doi:10.1016/S0304-3940(00)01388-4. PMID   10984627. S2CID   10334038.
  22. Correa SM, Newstrom DW, Warne JP, Flandin P, Cheung CC, Lin-Moore AT, Pierce AA, Xu AW, Rubenstein JL, Ingraham HA (January 2015). "An Estrogen-Responsive Module in the Ventromedial Hypothalamus Selectively Drives Sex-Specific Activity in Females". Cell Reports. 10 (1): 62–74. doi: 10.1016/j.celrep.2014.12.011 . PMC   4324838 . PMID   25543145.
  23. van Veen JE, Kammel LG, Bunda PC, Shum M, Reid MS, Massa MG, Arneson D, Park JW, Zhang Z, Joseph AM, Hrncir H, Liesa M, Arnold AP, Yang X, Correa SM (April 2020). "Hypothalamic estrogen receptor alpha establishes a sexually dimorphic regulatory node of energy expenditure". Nature Metabolism. 2 (4): 351–63. doi:10.1038/s42255-020-0189-6. PMC   7202561 . PMID   32377634.
  24. Kadiyala SB, Papandrea D, Tuz K, Anderson TM, Jayakumar S, Herron BJ, Ferland RJ (January 2015). "Spatiotemporal differences in the c-fos pathway between C57BL/6J and DBA/2J mice following flurothyl-induced seizures: A dissociation of hippocampal Fos from seizure activity". Epilepsy Research. 109: 183–96. doi:10.1016/j.eplepsyres.2014.11.009. PMC   4272448 . PMID   25524858.
  25. Kadiyala SB, Ferland RJ (March 2017). "Dissociation of spontaneous seizures and brainstem seizure thresholds in mice exposed to eight flurothyl-induced generalized seizures". Epilepsia Open. 2 (1): 48–58. doi:10.1002/epi4.12031. PMC   5560332 . PMID   28825051.
  26. Ferland RJ, Applegate CD (November 1998). "The role of the ventromedial nucleus of the hypothalamus in epileptogenesis". NeuroReport. 9 (16): 3623–9. doi:10.1097/00001756-199811160-00013. PMID   9858370. S2CID   29713035.
  27. Rieber, Inge; Sigusch, Volkmar (1979). "Psychosurgery on sex offenders and sexual ?deviants? in West Germany". Archives of Sexual Behavior. 8 (6): 523–527. doi:10.1007/BF01541419. PMID   391177. S2CID   41463669.

Further reading