Olfactory tract

Summary

The olfactory tract is a bilateral bundle of afferent nerve fibers from the mitral and tufted cells of the olfactory bulb that connects to several target regions in the brain, including the piriform cortex, amygdala, and entorhinal cortex. It is a narrow white band, triangular on coronal section, the apex being directed upward.

Olfactory tract
Olfactory tract lying in olfactory sulcus and olfactory striae labelled
Details
SystemOlfactory system
LocationBrain
Identifiers
Latintractus olfactorius
NeuroNames283
NeuroLex IDbirnlex_1663
TA98A14.1.09.431
TA25539
FMA77626
Anatomical terms of neuroanatomy
[edit on Wikidata]

Structure edit

The olfactory tract and olfactory bulb lie in the olfactory sulcus[1] a sulcus formed by the medial orbital gyrus on the inferior surface of each frontal lobe. The olfactory tracts lie in the sulci which run closely parallel to the midline. Fibers of the olfactory tract appear to end in the antero-lateral part of the olfactory tubercle, the dorsal and external parts of the anterior olfactory nucleus, the frontal and temporal parts of the prepyriform area, the cortico-medial group of amygdala nuclei and the nucleus of the stria terminalis.[2]

The olfactory tract divides posteriorly into a medial and a lateral stria.[1] Caudal to this is the olfactory trigone, and the anterior perforated substance.[1]

Medial olfactory stria edit

The medial olfactory stria turns medially behind the parolfactory area and ends in the subcallosal gyrus; in some cases a small intermediate stria is seen running backward to the anterior perforated substance.

Lateral olfactory stria edit

The lateral olfactory stria is directed across the lateral part of the anterior perforated substance and then bends abruptly medially toward the uncus of the parahippocampal gyrus.

Clinical significance edit

Destruction to the olfactory tract results in ipsilateral anosmia (loss of the ability to smell). Anosmia either total or partial is a symptom of Kallmann syndrome a genetic disorder that results in disruption of the development of the olfactory tract.[3][4] The depth of the olfactory sulcus is an indicator of such congenital anosmia.[5]

Additional images edit

References edit

  1. ^ a b c Carpenter, Malcolm B. (1985). Core text of neuroanatomy (3rd ed.). Baltimore: Williams & Wilkins. p. 29. ISBN 0683014552.
  2. ^ Allison, A. C. (1954). "The secondary olfactory areas in the human brain". Journal of Anatomy, 88 (Pt 4), 481–488.2.
  3. ^ Purves, Dale (2012). Neuroscience (5th ed.). Sunderland, Mass. p. 515. ISBN 9780878936953.{{cite book}}: CS1 maint: location missing publisher (link)
  4. ^ "Kallmann syndrome". Genetics Home Reference. US Library of Medicine. National Institutes for Health. Genetic and Rare Diseases Information. June 26, 2016. Retrieved November 15, 2021.
  5. ^ Huart, C.; Meusel, T.; Gerber, J.; Duprez, T.; Rombaux, P.; Hummel, T. (November 2011). "The Depth of the Olfactory Sulcus Is an Indicator of Congenital Anosmia". American Journal of Neuroradiology. 32 (10): 1911–1914. doi:10.3174/ajnr.A2632. PMC 7966015. PMID 21868619.

  This article incorporates text in the public domain from page 826 of the 20th edition of Gray's Anatomy (1918)

External links edit