Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-28T12:41:45.625Z Has data issue: false hasContentIssue false
  • English
  • Français

Location, architecture, and retinotopy of the anteromedial lateral suprasylvian visual area (AMLS) of the ferret (Mustela putorius)

Published online by Cambridge University Press:  18 February 2008

PAUL R. MANGER ,
GERHARD ENGLER ,
CHRISTIAN K.E. MOLL  and
ANDREAS K. ENGEL
PAUL R. MANGER
Affiliation:
School of Anatomical Sciences, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, Republic of South Africa
GERHARD ENGLER
Affiliation:
University Medical Centre Hamburg-Eppendorf, Centre of Experimental Medicine, Department of Neurophysiology and Pathophysiology, Hamburg, Germany
CHRISTIAN K.E. MOLL
Affiliation:
University Medical Centre Hamburg-Eppendorf, Centre of Experimental Medicine, Department of Neurophysiology and Pathophysiology, Hamburg, Germany
ANDREAS K. ENGEL
Affiliation:
University Medical Centre Hamburg-Eppendorf, Centre of Experimental Medicine, Department of Neurophysiology and Pathophysiology, Hamburg, Germany
Get access Rights & Permissions [Opens in a new window]

Abstract

The present paper describes the results of architectural and electrophysiological mapping observations of the medial bank of the suprasylvian sulcus of the ferret immediately caudal to somatosensory regions. The aim was to determine if the ferret possessed a homologous cortical area to the anteromedial lateral suprasylvian visual area (AMLS) of the domestic cat. We studied the architectural features and visuotopic organization of a region that we now consider to be a homologue to the cat AMLS. This area showed a distinct architecture and retinotopic organization. The retinotopic map was complex in nature with a bias towards representation of the lower visual field. These features indicate that the region described here as AMLS in the ferret is indeed a direct homologue of the previously described cat AMLS and forms part of a hierarchy of cortical areas processing motion in the ferret visual cortex. With the results of the present study and those of earlier studies a total of twelve cortical visual areas have been determined presently for the ferret, all of which appear to have direct homologues with visual cortical areas in the cat (which has a total of eighteen areas).

Keywords

Visual cortexCarnivoraCortical mapsCerebral cortexEvolution
Type
Research Article
Information
Visual Neuroscience , Volume 25 , Issue 1 , January 2008 , pp. 27 - 37
Copyright
© 2008 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Bininda-Emonds, O.R.P., Gittleman, J.L. & Purvis, A. (1999). Building large trees by combining phylogenetic information: A complete phylogeny of the extant Carnivora (Mammalia). Biological Reviews of the Cambridge Philosophical Society 74, 143–175.Google Scholar
Bishop, P.O., Kozak, W., Levick, W.R. & Vakkur, G.J. (1968). The determination of the projection of the visual field on to the lateral geniculate nucleus in the cat. Journal of Physiology 163, 503–539.Google Scholar
Bourne, J.A. & Rosa, M.G. (2006). Hierarchical development of the primate visual cortex, as revealed by neurofilament immunoreactivity: Early maturation of the middle temporal area (MT). Cerebral Cortex 16, 405–414.Google Scholar
Bourne, J.A., Warner, C.E. & Rosa, M.G. (2005). Topographic and laminar maturation of striate cortex in early postnatal marmoset monkeys, as revealed by neurofilament immunohistochemistry. Cerebral Cortex 15, 740–748.Google Scholar
Cantone, G., Xiao, J. & Levitt, J.B. (2006). Retinotopic organization of ferret suprasylvian cortex. Visual Neuroscience 23, 61–77.Google Scholar
Cantone, G., Xiao, J., McFarlane, N. & Levitt, J.B. (2005). Feedback connections to ferret striate cortex: Direct evidence for visuotopic convergence of feedback inputs. Journal of Comparative Neurology 487, 312–331.Google Scholar
Carroll, E.W. & Wong-Riley, M.T. (1984). Quantitative light and electron microscopic analysis of cytochrome oxidase-rich zones in the striate cortex of the squirrel monkey. Journal of Comparative Neurology 222, 1–17.Google Scholar
Darlington, D. (1957). The convolutional pattern of the brain and endocranial cast in the ferret. Journal of Anatomy (London) 91, 52–60.Google Scholar
Gallyas, F. (1979). Silver staining by means of physical development. Neurological Research 1, 203–209.Google Scholar
Hunt, D.L., Slutsky, D.A. & Krubitzer, L.A. (2000). The organization of somatosensory cortex in the ferret. Society for Neuroscience Abstracts 26, 243.13.Google Scholar
Jones, E.G. (1985). The Thalamus. New York: Plenum Press.
Kalil, R. (1978). Development of the dorsal lateral geniculate nucleus in the cat. Journal of Comparative Neurology 182, 265–292.Google Scholar
Kelly, J.B., Judge, P.W. & Phillips, D.P. (1986). Representation of the cochlea in primary auditory cortex of the ferret (Mustela putorius). Hearing Research 24, 111–115.Google Scholar
Law, M.I., Zahs, K.R. & Stryker, M.P. (1988). Organization of the primary visual cortex (area 17) of the ferret. Journal of Comparative Neurology 278, 157–180.Google Scholar
Linden, D.C., Guillery, R.W. & Cucchiaro, J. (1981). The dorsal lateral geniculate nucleus of the normal ferret and its postnatal development. Journal of Comparative Neurology 203, 189–211.Google Scholar
Lomber, S.G. & Payne, B.R. (2004). Cerebral areas mediating visual redirection of gaze: Cooling deactivation of 15 loci in the cat. Journal of Comparative Neurology 474, 190–208.Google Scholar
Lomber, S.G. (2001). Behavioral cartography of visual functions in cat parietal cortex: Areal and laminar dissociations. Progress in Brain Research 134, 265–284.Google Scholar
Manger, P.R. (2005). Establishing order at the systems level in mammalian brain evolution. Brain Research Bulletin 66, 282–289.Google Scholar
Manger, P.R., Engler, G., Moll, C.K. & Engel, A.K. (2005). The anterior ectosylvian visual area of the ferret: A homologue for an enigmatic visual cortical area of the cat? European Journal of Neuroscience 22, 706–714.Google Scholar
Manger, P.R., Kiper, D., Masiello, I., Murillo, L., Tettoni, L., Hunyadi, Z. & Innocenti, G.M. (2002a). The representation of the visual field in three extrastriate areas of the ferret (Mustela putorius), and the relationship of retinotopy and field boundaries to callosal connectivity. Cereberal Cortex 12, 423–437.Google Scholar
Manger, P.R., Masiello, I. & Innocenti, G.M. (2002b). Areal organization of the posterior parietal cortex of the ferret (Mustela putorius). Cerebral Cortex 12, 1280–1297.Google Scholar
Manger, P.R., Nakamura, H., Valentiniene, S. & Innocenti, G.M. (2004). Visual areas in the lateral temporal cortex of the ferret (Mustela putorius). Cerebral Cortex 14, 676–689.Google Scholar
McConnell, S.K. & LeVay, S. (1986). Anatomical organization of the visual system of the mink, Mustela vison. The Journal of Comparative Neurology 250, 109–132.Google Scholar
Ouellette, B.G., Minville, K., Faubert, J. & Casanova, C. (2004). Simple and complex visual motion response properties in the anterior medial bank of the lateral suprasylvian cortex. Neuroscience 123, 231–245.Google Scholar
Palmer, L.A., Rosenquist, A.C. & Tusa, R.J. (1978). The retinotopic organization of lateral suprasylvian visual areas in the cat. Journal of Comparative Neurology 177, 237–256.Google Scholar
Payne, B.R. (1993). Evidence for visual cortical area homologs in cat and macaque monkey. Cerebral Cortex 3, 1–25.Google Scholar
Philipp, R., Distler, C. & Hoffmann, K.P. (2005). A motion-sensitive area in ferret extrastriate visual cortex: An analysis in pigmented and albino animals. Cerebral Cortex 16, 779–790.Google Scholar
Rosa, M.G. & Manger, P.R. (2005). Clarifying homologies in the mammalian cerebral cortex: The case of the third visual area (V3). Clinical and Experimental Pharmacology and Physiology 32, 327–339.Google Scholar
Rosa, M.G. & Tweedale, R. (2005). Brain maps, great and small: Lessons from comparative studies of primate visual cortical organization. Philosophical Transactions of the Royal Society of London, Series B 360, 665–691.Google Scholar
Rosa, M.G. (1999). Topographic organisation of extrastriate areas in the flying fox: Implications for the evolution of mammalian visual cortex. The Journal of Comparative Neurology 411, 503–523.Google Scholar
Symonds, L.L. & Rosenquist, A.C. (1984). Corticocortical connections among visual areas in the cat. Journal of Comparative Neurology 299, 1–38.Google Scholar
Toyama, K., Fujii, K. & Umetani, K. (1990). Functional differentiation between the anterior and posterior Clare-Bishop cortex of the cat. Experimental Brain Research 81, 221–233.Google Scholar
Updyke, B.V. (1986). Retinotopic organization with the cat's posterior suprasylvian sulcus and gyrus. Journal of Comparative Neurology 246, 265–280.Google Scholar
Van der Gucht, E., Vandesande, F. & Arckens, L. (2001). Neurofilament protein: A selective marker for the architectonic parcellation of the visual cortex in adult cat brain. Journal of Comparative Neurology 441, 345–368.Google Scholar
Zahs, K.R. & Stryker, M.P. (1985). The projection of the visual field onto the lateral geniculate nucleus of the ferret. Journal of Comparative Neurology 241, 210–224.Google Scholar