Stria terminalis

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Stria terminalis
Gray683.png
Dissection of brain-stem. Lateral view (Stria terminalis labeled at upper right.).
Mouse BNST.pdf
Bed nucleus of the stria terminalis of the mouse brain
Details
Identifiers
Latin stria terminalis
NeuroNames 286
NeuroLex ID birnlex_937
TA98 A14.1.09.275
TA2 5592
FMA 61974
Anatomical terms of neuroanatomy

The stria terminalis (or terminal stria) 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.

Contents

Anatomy

The stria terminalis covers the superior thalamostriate vein, marking a line of separation between the thalamus and the caudate nucleus as seen upon gross dissection of the ventricles of the brain, viewed from the superior aspect.

The stria terminalis extends from the region of the interventricular foramina to the temporal horn of the lateral ventricle, carrying fibers from the amygdala to the septal nuclei, hypothalamic, and thalamic areas of the brain. It also carries fibers projecting from these areas back to the amygdala.

Bed nucleus of the stria terminalis (BNST)

The activity of the bed nucleus of the stria terminalis correlates with anxiety in response to threat monitoring. [1] It is thought to act as a relay site within the hypothalamic-pituitary-adrenal axis and regulate its activity in response to acute stress. [2] However, the stress response is time related and the BNST does not activate for contextual fear. This means that a sudden scary situation that is under ten minutes long, does not activate the BNST. [3] It is also thought to promote behavioral inhibition in response to unfamiliar individuals, by input from the orbitofrontal cortex. [4] Bilateral disruption of this pathway has been shown to attenuate reinstatement of drug seeking behaviour in rodents. [5]

This nucleus is known to project inhibitory fibers to the lateral hypothalamus and participate in the control of feeding in rodents. Optogenetic activation of this inhibitory pathway rapidly produced voracious feeding behavior in well-fed mice and optogenetic inhibition of this pathway reduces food intake even in starved animals. [6]

Derangement of opioid signaling in the BNST appears to mediate chronic alcohol-induced changes in stress response.

Sexual dimorphism

The central subdivision of the bed nucleus of the stria terminalis (BSTc) is sexually dimorphic. On average, the BSTc is twice as large in men as in women and contains twice the number of somatostatin neurons. [7] A sample of six post-mortem, long-term hormone replacement therapy (HRT) treated trans women (male-to-female) were found to have a female-typical number of cells in the BSTc, whereas a trans man (female-to-male) was found to have a male-typical number. [8] [9] The authors (Jiang-Ning Zhou, Frank PM Kruijver, Dick Swaab) also examined subjects with hormone-related disorders and found no pattern between those disorders and the BSTc while the single untreated male-to-female transsexual had a female-typical number of cells. They concluded that the BSTc provides evidence for a neurobiological basis of gender identity and proposed that such was determined before birth.

Hormone replacement therapy has been shown to influence hypothalamic size, [10] even though the study tried to do this by including non-transsexual male and female controls which, for a variety of medical reasons, had experienced hormone reversal. [8] The statement about the neurobiological basis from birth has later been brought to question, though not refuted, by a follow-up study by the same group which found that the sexual dimorphism of the BSTc is not present before adulthood (approximately 22 years of age) even though transsexuals report being aware of their gender identity since childhood. [11]

Since somatostatin-expressing neurons typically block dendritic inputs to the postsynaptic neuron, thus inhibiting signals traveling through associated structures, it is believed that the larger bed nucleus of the stria terminalis found in men (including transgender men) reduce the startle response in men and may be responsible for the higher incidence of specific phobias in women, and a possible source for the stereotype of women being afraid of mice. [12]

Oxytocin receptor activity in the BNST is important for social recognition in rats. Both male and female rats that received a microinjection of oxytocin receptor antagonist had lower social recognition scores than rats that received a vehicle injection, and microinjections of oxytocin into the BNST enhanced social memory in male, but not female, rats. [13]

Reduction of the size of the bed nucleus of the stria terminalis has been observed in pedophilic male perpetrators, in addition to reductions in the right amygdala, hypothalamus and abnormalities in related structures. The authors propose that childhood deficits in the BNST and medial amygdala may cause inhibition of sexual maturity. [14]

Related Research Articles

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

The hypothalamus is a small part of the brain that contains a number of 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. 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">Olfactory system</span> Sensory system used for smelling

The olfactory system or sense of smell is the sensory system used for smelling (olfaction). Olfaction is one of the special senses, that have directly associated specific organs. Most mammals and reptiles have a main olfactory system and an accessory olfactory system. The main olfactory system detects airborne substances, while the accessory system senses fluid-phase stimuli.

<span class="mw-page-title-main">Solitary nucleus</span> Sensory nuclei in medulla oblongata

The solitary nucleus is a series of sensory nuclei forming a vertical column of grey matter in the medulla oblongata of the brainstem. It receives general visceral and/or special visceral inputs from the facial nerve, glossopharyngeal nerve and vagus nerve ; it receives and relays stimuli related to taste and visceral sensation. It sends outputs to various parts of the brain, such as the hypothalamus, thalamus, and reticular formation. Neuron cell bodies of the SN are roughly somatotopically arranged along its length according to function.

<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.

In animals, including humans, the startle response is a largely unconscious defensive response to sudden or threatening stimuli, such as sudden noise or sharp movement, and is associated with negative affect. Usually the onset of the startle response is a startle reflex reaction. The startle reflex is a brainstem reflectory reaction (reflex) that serves to protect vulnerable parts, such as the back of the neck and the eyes (eyeblink) and facilitates escape from sudden stimuli. It is found across many different species, throughout all stages of life. A variety of responses may occur depending on the affected individual's emotional state, body posture, preparation for execution of a motor task, or other activities. The startle response is implicated in the formation of specific phobias.

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

The ventromedial nucleus of the 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. This nuclear region is involved in the recognition of the feeling of fullness.

<span class="mw-page-title-main">Septal area</span> Area in the lower, posterior part of the medial surface of the frontal lobe

The septal area, consisting of the lateral septum and medial septum, is an area in the lower, posterior part of the medial surface of the frontal lobe, and refers to the nearby septum pellucidum.

<span class="mw-page-title-main">Circumventricular organs</span> Interfaces between the brain and the circulatory system

Circumventricular organs (CVOs) are structures in the brain characterized by their extensive and highly permeable capillaries, unlike those in the rest of the brain where there exists a blood–brain barrier (BBB) at the capillary level. Although the term "circumventricular organs" was originally proposed in 1958 by Austrian anatomist Helmut O. Hofer concerning structures around the brain ventricular system, the penetration of blood-borne dyes into small specific CVO regions was discovered in the early 20th century. The permeable CVOs enabling rapid neurohumoral exchange include the subfornical organ (SFO), the area postrema (AP), the vascular organ of lamina terminalis, the median eminence, the pituitary neural lobe, and the pineal gland.

<span class="mw-page-title-main">Vasopressin receptor 1A</span> Protein-coding gene in the species Homo sapiens

Vasopressin receptor 1A (V1AR), or arginine vasopressin receptor 1A is one of the three major receptor types for vasopressin, and is present throughout the brain, as well as in the periphery in the liver, kidney, and vasculature.

INAH-3 is the short form for the third interstitial nucleus of the anterior hypothalamus, and is the sexually dimorphic nucleus of humans. The INAH-3 is significantly larger in males than in females regardless of age and larger in heterosexual males than in homosexual males and heterosexual females.

The amygdalofugal pathway is one of the three major efferent pathways of the amygdala, meaning that it is one of the three principal pathways by which fibers leave the amygdala. It leads from the basolateral nucleus and central nucleus of the amygdala. The amygdala is a limbic structure in the medial temporal lobe of the brain. The other main efferent pathways from the amygdala are the stria terminalis and anterior commissure.

Gender incongruence is the state of having a gender identity that does not correspond to one's sex assigned at birth. This is experienced by people who identify as transgender or transsexual, and often results in gender dysphoria. The causes of gender incongruence have been studied for decades.

<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.

<span class="mw-page-title-main">Lateral hypothalamus</span>

The lateral hypothalamus (LH), also called the lateral hypothalamic area (LHA), contains the primary orexinergic nucleus within the hypothalamus that widely projects throughout the nervous system; this system of neurons mediates an array of cognitive and physical processes, such as promoting feeding behavior and arousal, reducing pain perception, and regulating body temperature, digestive functions, and blood pressure, among many others. Clinically significant disorders that involve dysfunctions of the orexinergic projection system include narcolepsy, motility disorders or functional gastrointestinal disorders involving visceral hypersensitivity, and eating disorders.

<span class="mw-page-title-main">Neuroscience of sex differences</span> Characteristics of the brain that differentiate the male brain and the female brain

The neuroscience of sex differences is the study of characteristics that separate brains of different sexes. Psychological sex differences are thought by some to reflect the interaction of genes, hormones, and social learning on brain development throughout the lifespan.

<span class="mw-page-title-main">HSD2 neuron</span>

HSD2 neurons are a small group of neurons in the brainstem which are uniquely sensitive to the mineralocorticosteroid hormone aldosterone, through expression of HSD11B2. They are located within the caudal medulla oblongata, in the nucleus of the solitary tract (NTS). HSD2 neurons are activated during a prolonged deficit in body sodium or fluid volume, as occurs after dietary sodium deprivation or during frank hypovolemia. They are also activated by supraphysiologic stimulation of the mineralocorticoid receptor. They are inactivated when salt is ingested. To date, HSD2 neurons have been identified and studied only in rats and mice.

<span class="mw-page-title-main">Central nucleus of the amygdala</span> Nucleus within the amygdala

The central nucleus of the amygdala is a nucleus within the amygdala. It "serves as the major output nucleus of the amygdala and participates in receiving and processing pain information."

The parafacial zone (PZ) is a brain structure located in the brainstem within the medulla oblongata believed to be heavily responsible for non-rapid eye movement (non-REM) sleep regulation, specifically for inducing slow-wave sleep.

References

  1. Somerville L, Whalen P, Kelley W (2010). "Human Bed Nucleus of the Stria Terminalis Indexes Hypervigilant Threat Monitoring". Biol Psychiatry. 68 (5): 416–424. doi:10.1016/j.biopsych.2010.04.002. PMC   2921460 . PMID   20497902.
  2. Choi D, Furay A, Evanson N, Ostrander M, Ulrich-Lai Y, Herman J (2007). "Bed Nucleus of the Stria Terminalis Subregions Differentially Regulate Hypothalamic–Pituitary–Adrenal Axis Activity: Implications for the Integration of Limbic Inputs". J Neurosci. 27 (8): 2025–34. doi:10.1523/JNEUROSCI.4301-06.2007. PMC   6673539 . PMID   17314298.
  3. Hammack SE, Todd TP, Kocho-Schellenberg M, Bouton ME (2015). "Role of the Bed Nucleus of the Stria Terminalis in the Acquisition of Contextual Fear at Long or Short Context-Shock Intervals". Behavioral Neuroscience. 129 (5): 673–678. doi:10.1037/bne0000088. PMC   4586907 . PMID   26348716.
  4. Fox A, Shelton S, Oakes T, Converse A, DavidsonR, Kalin N (2010). "Orbitofrontal Cortex Lesions Alter Anxiety-Related Activity in the Primate Bed Nucleus of Stria Terminalis". J Neurosci. 30 (20): 7023–27. doi:10.1523/JNEUROSCI.5952-09.2010. PMC   2915894 . PMID   20484644.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. Suzanne Erb · Natalina Salmaso · Demetra Rodaros Jane Stewart (2001). "A role for the CRF-containing pathway from central nucleus of the amygdala to bed nucleus of the stria terminalis in the stress-induced reinstatement of cocaine seeking in rats". Psychopharmacology. 158 (4): 360–65. doi:10.1007/s002130000642. PMID   11797056. S2CID   23284158.
  6. Jennings, Joshua H.; Rizzi, Giorgio; Stamatakis, Alice M.; Ung, Randall L.; Stuber, Garret D. (2013-09-27). "The Inhibitory Circuit Architecture of the Lateral Hypothalamus Orchestrates Feeding". Science. 341 (6153): 1517–1521. Bibcode:2013Sci...341.1517J. doi:10.1126/science.1241812. ISSN   0036-8075. PMC   4131546 . PMID   24072922.
  7. Swaab D (2007). "Sexual differentiation of the brain and behavior". Best Pract Res Clin Endocrinol Metab. 21 (3): 431–44. doi:10.1016/j.beem.2007.04.003. PMID   17875490.
  8. 1 2 Zhou J, Hofman M, Gooren L, Swaab D (1995). "A sex difference in the human brain and its relation to transsexuality". Nature. 378 (6552): 68–70. Bibcode:1995Natur.378...68Z. doi:10.1038/378068a0. hdl: 20.500.11755/9da6a0a1-f622-44f3-ac4f-fec297a7c6c2 . PMID   7477289. S2CID   4344570.
  9. Kruijver F, Zhou J, Pool C, Hofman M, Gooren L, Swaab D (2000). "Male-to-female transsexuals have female neuron numbers in a limbic nucleus". J. Clin. Endocrinol. Metab. 85 (5): 2034–41. doi: 10.1210/jcem.85.5.6564 . PMID   10843193.
  10. Hulshoff Pol HE, Cohen-Kettenis PT, Van Haren NE, Peper JS, Brans RG, Cahn W, et al. (2006). "Changing your sex changes your brain: Influences of testosterone and estrogen on adult human brain structure". European Journal of Endocrinology. 155 (Suppl. 1): S107–S114. doi:10.1530/eje.1.02248.
  11. Chung W, De Vries G, Swaab D (2002). "Sexual differentiation of the bed nucleus of the stria terminalis in humans may extend into adulthood". J Neurosci. 22 (3): 1027–33. doi:10.1523/JNEUROSCI.22-03-01027.2002. PMC   6758506 . PMID   11826131.
  12. Cameron, Alasdair (2004). Crash Course Psychiatry. Elsevier Ltd. ISBN   978-0-7234-3340-8.
  13. Dumais, KM; Alonso, AG; Immormino, MA; Bredewold, R; Veenema, AH (February 2016). "Involvement of the oxytocin system in the bed nucleus of the stria terminalis in the sex-specific regulation of social recognition". Psychoneuroendocrinology. 64: 79–88. doi:10.1016/j.psyneuen.2015.11.007. PMC   4698213 . PMID   26630388.
  14. Schiltz K, Witzel J, Northoff G, Zierhut K, Gubka U, Fellman H, Kaufmann J, Tempelmann C, Wiebking C, Bogerts B (2007). "Brain pathology in pedophilic offenders: Evidence of volume reduction in the right amygdala and related diencephalic structures". Archives of General Psychiatry. 64 (6): 737–746. doi:10.1001/archpsyc.64.6.737. PMID   17548755.