Stria terminalis

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Terminal stria
Gray683.png
Dissection of brain-stem. Lateral view. (Stria terminalis labeled at upper right.)
Details
Latin stria terminalis
Identifiers
Gray's p.808
NeuroNames hier-268
NeuroLex ID Stria terminalis
Dorlands
/Elsevier
s_26/12763050
TA A14.1.09.275
FMA 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 ventral medial nucleus of the hypothalamus.

Anatomy[edit]

The stria terminalis covers the 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 foramen 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.

Functions[edit]

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] It is also thought to promote behavioral inhibition in response to unfamiliar individuals, by input from the orbitofrontal cortex.[3] Bilateral disruption of this pathway has been shown to attenuate reinstatement of drug seeking behaviour in rodents.[4]

Bed nucleus of the stria terminalis (BNST)[edit]

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.[5] A sample of six male-to-female transsexuals taking estrogen were found to have female-typical number of cells in the BSTc, whereas a female-to-male transsexual taking testosterone was found to have a male-typical number.[6][7] The authors (W. Chung, G. De Vries, 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 disorder and proposed that such was determined before birth.

Criticisms of the former statement suggest[8] the study used an unrepresentative sample and did not adequately control for hormone replacement therapy, which has been shown to influence hypothalamic size,[9] 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.[6] 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.[10]

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.[11]

Additional images[edit]

References[edit]

  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. PMID 17314298. 
  3. ^ 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. 
  4. ^ 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. 
  5. ^ 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. 
  6. ^ a b 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. doi:10.1038/378068a0. PMID 7477289. 
  7. ^ 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/jc.85.5.2034. PMID 10843193. 
  8. ^ Lawrence, A. A. (2007). A critique of the brain-sex theory of transsexualism.
  9. ^ Hulshoff Pol, H. E., Cohen-Kettenis, P. T., Van Haren, N. E., Peper, J. S., Brans, R. G., 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.
  10. ^ 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. PMID 11826131. 
  11. ^ 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, 737–746.

External links[edit]