Abstract
The anterior commissure (AC) has an anterior and posterior limb. Despite comprehensive information about the posterior limb, there is limited and conflicting information about the anterior limb in the literature. We aimed to show the anatomical relationships of the AC with neighboring structures by using white matter microdissection and magnetic resonance (MR) tractography, primarily on the anterior limb of the AC. Twenty cadaveric human brains and three sheep brains were prepared according to Klingler’s method. White matter fiber microdissections were performed. MR tractography was done in 20 specimens. This study defined the body and anterior and posterior limbs of the AC. The anterior limb leaves the body from the inferior side at the level of the anterior perforated substance and olfactory tract. It then courses anteroinferolaterally, curves towards the orbital gyri, and terminates at the olfactory trigone. The posterior limb of the AC divides into rostral (anterolateral) and caudal (posterolateral) parts. The anterior limb was more prominent in sheep than in human brains. This study accurately delineates the anatomy and variations of the anterior limb of the AC in human and sheep brains for the first time in the literature to the best of our knowledge. The anterior limb of the AC is larger in sheep than in humans. An increased importance of olfaction could be the evolutionary explanation for this difference. The MR tractography results shown are unique for this delicate anatomy.
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Abbreviations
- 1n:
-
Olfactory nerve
- 2n:
-
Optic nerve
- ac:
-
Anterior commissure
- aic:
-
Anterior limb of the internal capsule
- Amg:
-
Amygdala
- alv:
-
Alveus of the hippocampus
- bfx:
-
Body of the fornix.
- scc:
-
Splenium of the corpus callosum
- Cd:
-
Caudate nucleus
- cfx:
-
Column of the fornix
- chpx:
-
Choroid plexus of the lateral ventricle
- crfx:
-
Crus of the fornix
- CP:
-
Cerebral peduncle
- cr:
-
Corona radiate
- dB:
-
Diagonal band
- ec:
-
External capsule
- gic:
-
Genu of the internal capsule
- HCd:
-
Head of caudate nucleus
- Ins:
-
Insula
- MB:
-
Mamillary body
- OB:
-
Olfactory bulb
- opt:
-
Optic tract
- OrG:
-
Orbital gyrus
- ox:
-
Optic chiasma
- pic:
-
Posterior limb of the internal capsule
- PHG:
-
Parahippocampal gyrus
- slic:
-
Sublenticular part of the internal capsule
- SC:
-
Superior colliculus
- SG:
-
Straight gyrus
- sstr:
-
Sagittal stratum
- Th:
-
Thalamus
- tp:
-
Temporal pole
- Un:
-
Uncus
References
Allen LS, Gorski RA (1991) Sexual dimorphism of the anterior commissure and Massa intermedia of the human brain. J Comp Neurol 312(1):97–104. https://doi.org/10.1002/cne.903120108
Allen LS, Gorski RA (1992) Sexual orientation and the size of the anterior commissure in the human brain. Proc Natl Acad Sci USA 89(15):7199–7202. https://doi.org/10.1073/pnas.89.15.7199
Ashwell KWS (2016) Anterior commissure versus corpus callosum: A quantitative comparison across mammals. Zoology 119(2):126–136. https://doi.org/10.1016/j.zool.2016.02.004
Barrett RLC, Dawson M, Dyrby TB, Krug K, Ptito M, D’Arceuil H, Croxson PL, Johnson PJ, Howells H, Forkel SJ, Dell’Acqua F, Catani M (2020) Differences in frontal network anatomy across primate species. J Neurosci 40(10):2094–2107. https://doi.org/10.1523/JNEUROSCI.1650-18.2019
Baudo MC, Colombo EE, Pérez MA, Rahn SI, Domenech NC, Chuang J, Forlizzi V, Buosi P, Baldoncini M, Bendersky M (2022) Three-dimensional anatomy of the anterior commissure: a tractography and anatomical study. World Neurosurg 159:e365–e374. https://doi.org/10.1016/j.wneu.2021.12.059
Baydin S, Yagmurlu K, Tanriover N, Gungor A, Rhoton AL Jr (2016) Microsurgical and fiber tract anatomy of the nucleus accumbens. Operative Neurosurg (Hagerstown Md) 12(3):269–288. https://doi.org/10.1227/NEU.0000000000001133
Brunert D, Quintela M, R., Rothermel M (2023) The anterior olfactory nucleus revisited - an emerging role for neuropathological conditions? Prog Neurobiol 228:102486. https://doi.org/10.1016/j.pneurobio.2023.102486
Brunjes PC (2013) The mouse olfactory peduncle. 2.The anterior limb of the anterior commissure. Front Neuroanat 6:51. https://doi.org/10.3389/fnana.2012.00051
Carpenter MB (1976) Human Neuroanatomy (7th ed.). Williams and Wilkins (p. 32)
Catani M (2022) The connectional anatomy of the Temporal lobe. Handb Clin Neurol 187:3–16. https://doi.org/10.1016/B978-0-12-823493-8.00001-8
Catani M, Howard RJ, Pajevic S, Jones DK (2002) Virtual in vivo interactive dissection of white matter fasciculi in the human brain. NeuroImage 17(1):77–94. https://doi.org/10.1006/nimg.2002.1136
Çavdar S, Aydın AE, Algın O, Aydın S (2021) The complex structure of the anterior white commissure of the human brain: fiber dissection and tractography study. World Neurosurgery 147:e111–e117. https://doi.org/10.1016/j.wneu.2020.11.157
Cho KH, Murakami G, Rodríguez-Vázquez JF (2013) Early fetal development of the anterior commissure. Pediatr Neurol 48(1):56–58. https://doi.org/10.1016/j.pediatrneurol.2012.09.007
Choi MH, Kim JH, Yeon HW, Choi JS, Park JY, Jun JH, Lee BY, Kim HJ, Tack GR, Chung SC (2011) Effects of gender and age on anterior commissure volume. Neurosci Lett 500(2):92–94. https://doi.org/10.1016/j.neulet.2011.06.010
Dalal T, Gupta N, Haddad R (2020) Bilateral and unilateral odor processing and odor perception. Commun Biology 3(1):150. https://doi.org/10.1038/s42003-020-0876-6
Di Virgilio G, Clarke S, Pizzolato G, Schaffner T (1999) Cortical regions contributing to the anterior commissure in man. Exp Brain Res 124(1):1–7. https://doi.org/10.1007/s002210050593
Fernández-Miranda JC, Rhoton AL Jr., Alvarez-Linera J, Kakizawa Y, Choi C, de Oliveira EP (2008) Three-dimensional microsurgical and tractographic anatomy of the white matter of the human brain. Neurosurgery 62(6 Suppl 3):989–1028. https://doi.org/10.1227/01.neu.0000333767.05328.49
Goga C, Türe U (2015) The anatomy of meyer’s loop revisited: changing the anatomical paradigm of the Temporal loop based on evidence from fiber microdissection. J Neurosurg 122(6):1253–1262. https://doi.org/10.3171/2014.12.JNS14281
Gülsuna B, Güngör A, Yazgan P, Erol G, Middlebrooks EH, Börcek AÖ, Weninger WJ, Türe U (2024) Revisiting the microsurgical anatomy of the sagittal stratum and surgical implications: fiber microdissection and tractography study. J Neurosurg 141(5):1433–1446. https://doi.org/10.3171/2024.2.JNS232671
Güngör A, Baydin S, Middlebrooks EH, Tanriover N, Isler C, Rhoton AL Jr. (2017) The white matter tracts of the cerebrum in ventricular surgery and hydrocephalus. J Neurosurg 126(3):945–971. https://doi.org/10.3171/2016.1.JNS152082
Hallam TM, Floyd CL, Folkerts MM, Lee LL, Gong QZ, Lyeth BG, Muizelaar JP, Berman RF (2004) Comparison of behavioral deficits and acute neuronal degeneration in rat lateral fluid percussion and weight-drop brain injury models. J Neurotrauma 21(5):521–539. https://doi.org/10.1089/089771504774129865
Heimer L (1983) The human brain and spinal cord functional neuroanatomy and dissection guide. Springer, p 75
Kappers C, Huber GC, Crosby EC (1936) The comparative anatomy of the nervous system of vertebrates (1st ed. vol 2). Macmillan (pp. 1465–1466)
Kermen F, Lal P, Faturos NG, Yaksi E (2020) Interhemispheric connections between olfactory bulbs improve odor detection. PLoS Biol 18(4):e3000701. https://doi.org/10.1371/journal.pbio.3000701
Klingler J (1935) Erleichterung der Makroskopischen praeparation des gehrins durch Den gefrierprozess. Schweiz Archiv Fur Neurologie Und Psychiatrie 36:247–256
Klingler J, Gloor P (1960) The connections of the amygdala and of the anterior Temporal cortex in the human brain. J Comp Neurol 115:333–369. https://doi.org/10.1002/cne.901150305
Kosugi K, Yoshitomi M, Takayama Y, Iijima K, Kimura Y, Kaneko Y, Toda M, Iwasaki M (2023) Safety, feasibility, and efficacy of additional extraventricular anterior commissurotomy with corpus callosotomy. Operative Neurosurg (Hagerstown Md) 24(2):e68–e74. https://doi.org/10.1227/ons.0000000000000478
Lavrador JP, Ferreira V, Lourenço M, Alexandre I, Rocha M, Oliveira E, Kailaya-Vasan A, Neto L (2019) White-matter commissures: A clinically focused anatomical review. Surg Radiol Anat 41(6):613–624. https://doi.org/10.1007/s00276-019-02218-7
Letzner S, Simon A, Güntürkün O (2016) Connectivity and neurochemistry of the commissura anterior of the pigeon (Columba livia). J Comp Neurol 524(2):343–361. https://doi.org/10.1002/cne.23858
Liu X, Kinoshita M, Shinohara H, Hori O, Ozaki N, Nakada M (2022) A fiber dissection study of the anterior commissure: correlations with diffusion spectrum imaging tractography and clinical relevance in gliomas. Brain Topogr 35(2):232–240. https://doi.org/10.1007/s10548-021-00879-5
Lohman AH, Mentink GM (1969) The lateral olfactory tract, the anterior commissure and the cells of the olfactory bulb. Brain Res 12(2):396–413. https://doi.org/10.1016/0006-8993(69)90008-0
Moldrich RX, Gobius I, Pollak T, Zhang J, Ren T, Brown L, Mori S, De Juan Romero C, Britanova O, Tarabykin V, Richards LJ (2010) Molecular regulation of the developing commissural plate. J Comp Neurol 518(18):3645–3661. https://doi.org/10.1002/cne.22445
Nieuwenhuys R (1998) The central nervous system of vertebrates, vol 3. Springer, p 1615
Nolte J (2009) The human brain: an introduction to its functional anatomy. Elsevier
Noonan M, Smith MA, Kelleher K, Sanfilippo MA (1998) Sex differences in anterior commissure size in the rat. Brain Res Bull 45(1):101–104. https://doi.org/10.1016/s0361-9230(97)00314-6
Paxinos G (1990) The human nervous system. Academic
Peltier J, Verclytte S, Delmaire C, Pruvo JP, Godefroy O, Le Gars D (2010 ) Microsurgical anatomy of the Temporal stem: clinical relevance and correlations with diffusion tensor imaging fiber tracking. J Neurosurg 112(5):1033–1038. https://doi.org/10.3171/2009.6.JNS08132
Peltier J, Verclytte S, Delmaire C, Pruvo JP, Havet E, Le Gars D (2011 ) Microsurgical anatomy of the anterior commissure: correlations with diffusion tensor imaging fiber tracking and clinical relevance. J Neurosurg 112(5):1033–1038. https://doi.org/10.1227/NEU.0b013e31821bc822
Pescatori L, Tropeano MP, Manfreda A, Delfini R, Santoro A (2017) Three-dimensional anatomy of the white matter fibers of the Temporal lobe: surgical implications. World Neurosurg 100:144–158. https://doi.org/10.1016/j.wneu.2016.12.120
Raybaud C (2010) The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformation. Neuroradiology 52(6):447–477. https://doi.org/10.1007/s00234-010-0696-3
Schmahmann JD, Pandya DN (2006) Fiber pathways of the brain. Oxford University Press (pp. 479–484), pp 479–484
Sturrock RR (1976) Changes in the total number of neuroglia, mitotic cells and necrotic cells in the anterior limb of the mouse anterior commissure following hypoxic stress. J Anat 122(2):447–453
Türe U, Yaşargil MG, Friedman AH, Al-Mefty O (2000) Fiber dissection technique: lateral aspect of the brain. Neurosurgery 47(2):417–427. https://doi.org/10.1097/00006123-200008000-00028
Van Alphen HA (1969) The anterior commissure of the rabbit. Acta Anat Suppl 57:1–112
Warren JE, Crinion JT, Lambon Ralph MA, Wise RJ (2009) Anterior Temporal lobe connectivity correlates with functional outcome after aphasic stroke. Brain 132(12):3428–3442. https://doi.org/10.1093/brain/awp270
Weiss A, Di Carlo DT, Di Russo P, Weiss F, Castagna M, Cosottini M, Perrini P (2021) Microsurgical anatomy of the amygdaloid body and its connections. Brain Struct Function 226(3):861–874. https://doi.org/10.1007/s00429-020-02214-3
Wilde EA, Bigler ED, Haider JM, Chu Z, Levin HS, Li X, Hunter JV (2006) Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. J Child Neurol 21(9):769–776. https://doi.org/10.1177/08830738060210090201
Yagmurlu K, Vlasak AL, Rhoton AL Jr (2015) Three-dimensional topographic fiber tract anatomy of the cerebrum. Neurosurgery 11:274–305. https://doi.org/10.1227/NEU.0000000000000704
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The authors thank CC Medical Arts (en.ccmedicalarts.com) for medical illustrations, Julie A. Yamamoto, MA, and Yuna Yamamoto for language and other editorial assistance.
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P.K.B. wrote the main manuscript text and prepared figures and videos. S.R., S.C.C., Z.F., and F.P. contributed figures and videos. E.C., W.J.W., U.T. and A.G. revised the manuscript. U.T. and A.G. supervised the study and made critical revisions to the manuscript. All authors reviewed the manuscript.
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Kuru Bektaşoğlu, P., Rahmanov, S., Güngör, A. et al. Microsurgical anatomy of the anterior commissure with special emphasis on the anterior limb: a comparative white matter fiber microdissection and tractography study. Brain Struct Funct 230, 143 (2025). https://doi.org/10.1007/s00429-025-03006-3
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DOI: https://doi.org/10.1007/s00429-025-03006-3