stria terminalis#Bed nucleus of the stria terminalis

{{short description|Band of fibres along the thalamus}}

{{Infobox brain

| Name = Stria terminalis

| Latin = stria terminalis

| Image = File:Gray683.png

| Caption = Dissection of brain-stem. Lateral view (Stria terminalis labeled at upper right.).

| Image2 = File:Mouse_BNST.pdf

| Caption2 = Bed nucleus of the stria terminalis of the mouse brain

| IsPartOf =

| Components =

| Artery =

| Vein =

}}

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.

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 =

The bed nucleus of the stria terminalis (BNST) is a collection of nuclei at the base of the lateral ventricles, and in front of the septum. The BNST, hypothalamic nuclei, and septal nuclei are all in close proximity with each other and share many projections.{{cite journal |last1=Kamali |first1=A |last2=Milosavljevic |first2=S |last3=Gandhi |first3=A |last4=Lano |first4=KR |last5=Shobeiri |first5=P |last6=Sherbaf |first6=FG |last7=Sair |first7=HI |last8=Riascos |first8=RF |last9=Hasan |first9=KM |title=The Cortico-Limbo-Thalamo-Cortical Circuits: An Update to the Original Papez Circuit of the Human Limbic System. |journal=Brain topography |date=May 2023 |volume=36 |issue=3 |pages=371-389 |doi=10.1007/s10548-023-00955-y |pmid=37148369|pmc=10164017 }} It correlates with anxiety in response to threat monitoring.{{cite journal |vauthors=Somerville L, Whalen P, Kelley W |title=Human Bed Nucleus of the Stria Terminalis Indexes Hypervigilant Threat Monitoring |journal=Biol Psychiatry |volume=68 |issue=5 |pages=416–424 |year=2010 |pmid=20497902 |doi=10.1016/j.biopsych.2010.04.002 |pmc=2921460}} It is thought to act as a relay site within the hypothalamic-pituitary-adrenal axis and regulate its activity in response to acute stress.{{cite journal |vauthors=Choi D, Furay A, Evanson N, Ostrander M, Ulrich-Lai Y, Herman J |title=Bed Nucleus of the Stria Terminalis Subregions Differentially Regulate Hypothalamic–Pituitary–Adrenal Axis Activity: Implications for the Integration of Limbic Inputs |journal=J Neurosci |volume=27 |issue=8 |pages=2025–34 |year=2007 |pmid=17314298 |doi=10.1523/JNEUROSCI.4301-06.2007|pmc=6673539 }} 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.{{cite journal |vauthors=Hammack SE, Todd TP, Kocho-Schellenberg M, Bouton ME |title=Role of the Bed Nucleus of the Stria Terminalis in the Acquisition of Contextual Fear at Long or Short Context-Shock Intervals |journal=Behavioral Neuroscience|volume=129 |issue=5 |pages=673–678 |year=2015 |pmid=26348716 |doi=10.1037/bne0000088 |pmc=4586907}} It is also thought to promote behavioral inhibition in response to unfamiliar individuals, by input from the orbitofrontal cortex.{{cite journal |author=Fox A, Shelton S, Oakes T, Converse A, DavidsonR, Kalin N |title=Orbitofrontal Cortex Lesions Alter Anxiety-Related Activity in the Primate Bed Nucleus of Stria Terminalis |journal=J Neurosci |volume=30 |issue=20 |pages=7023–27 |year=2010 |pmid=20484644 |doi=10.1523/JNEUROSCI.5952-09.2010 |pmc=2915894}} Bilateral disruption of this pathway has been shown to attenuate reinstatement of drug seeking behaviour in rodents.{{cite journal |author= Suzanne Erb · Natalina Salmaso · Demetra Rodaros Jane Stewart |title=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|journal=Psychopharmacology |volume=158 |pages=360–65 |year=2001 |doi= 10.1007/s002130000642 |issue= 4 |pmid=11797056|s2cid=23284158}}

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.{{Cite journal|last1=Jennings|first1=Joshua H.|last2=Rizzi|first2=Giorgio|last3=Stamatakis|first3=Alice M.|last4=Ung|first4=Randall L.|last5=Stuber|first5=Garret D.|date=2013-09-27|title=The Inhibitory Circuit Architecture of the Lateral Hypothalamus Orchestrates Feeding|journal=Science|language=en|volume=341|issue=6153|pages=1517–1521|doi=10.1126/science.1241812|issn=0036-8075|pmid=24072922|pmc=4131546|bibcode=2013Sci...341.1517J }}

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

<span id="Sexually dimorphic"></span>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.{{cite journal |author=Swaab D |title=Sexual differentiation of the brain and behavior |journal=Best Pract Res Clin Endocrinol Metab |volume=21 |issue=3 |pages=431–44 |year=2007 |pmid=17875490 |doi=10.1016/j.beem.2007.04.003}} 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.{{cite journal |vauthors=Zhou J, Hofman M, Gooren L, Swaab D |title=A sex difference in the human brain and its relation to transsexuality |journal=Nature |volume=378 |issue=6552 |pages=68–70 |year=1995 |pmid=7477289 |doi=10.1038/378068a0|bibcode=1995Natur.378...68Z |url=https://pure.knaw.nl/portal/en/publications/a-sex-difference-in-the-human-brain-and-its-relation-to-transsexuality(9da6a0a1-f622-44f3-ac4f-fec297a7c6c2).html |hdl=20.500.11755/9da6a0a1-f622-44f3-ac4f-fec297a7c6c2 |s2cid=4344570 |hdl-access=free }}{{cite journal |vauthors=Kruijver F, Zhou J, Pool C, Hofman M, Gooren L, Swaab D |title=Male-to-female transsexuals have female neuron numbers in a limbic nucleus |journal=J. Clin. Endocrinol. Metab. |volume=85 |issue=5 |pages=2034–41 |year=2000 |pmid=10843193 |doi=10.1210/jcem.85.5.6564|doi-access=free }} 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,{{cite journal | vauthors = Hulshoff Pol HE, Cohen-Kettenis PT, Van Haren NE, Peper JS, Brans RG, Cahn W et al | year = 2006 | title = Changing your sex changes your brain: Influences of testosterone and estrogen on adult human brain structure | doi = 10.1530/eje.1.02248 | journal = European Journal of Endocrinology | volume = 155 | issue = Suppl. 1| pages = S107–S114 | doi-access = }} 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. 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.{{cite journal |vauthors=Chung W, De Vries G, Swaab D |title=Sexual differentiation of the bed nucleus of the stria terminalis in humans may extend into adulthood |journal=J Neurosci |volume=22 |issue=3 |pages=1027–33 |year=2002 |pmid=11826131|pmc=6758506 |doi=10.1523/JNEUROSCI.22-03-01027.2002 }}

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.{{cite book |title=Crash Course Psychiatry |last=Cameron |first=Alasdair |year=2004 |publisher=Elsevier Ltd |isbn=978-0-7234-3340-8}}

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.{{cite journal|last1=Dumais|first1=KM|last2=Alonso|first2=AG|last3=Immormino|first3=MA|last4=Bredewold|first4=R|last5=Veenema|first5=AH|title=Involvement of the oxytocin system in the bed nucleus of the stria terminalis in the sex-specific regulation of social recognition.|journal=Psychoneuroendocrinology|date=February 2016|volume=64|pages=79–88|doi=10.1016/j.psyneuen.2015.11.007|pmid=26630388|pmc=4698213}}

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.{{cite journal | vauthors = Schiltz K, Witzel J, Northoff G, Zierhut K, Gubka U, Fellman H, Kaufmann J, Tempelmann C, Wiebking C, Bogerts B | year = 2007 | title = Brain pathology in pedophilic offenders: Evidence of volume reduction in the right amygdala and related diencephalic structures | journal = Archives of General Psychiatry | volume = 64 | issue = 6| pages = 737–746 | doi=10.1001/archpsyc.64.6.737 | pmid=17548755| doi-access = }}

References