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Organization of identified fiber tracts in the rat fimbria-fornix: an anterograde tracing and electron microscopic study

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Abstract

The fimbria is a major route for afferent and efferent fibers of the hippocampal formation. However, little is known about the intrinsic organization of the fimbria-fornix complex. In this study, the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHAL) was used to analyze the ultrastructure and topography of identified fiber tracts within the fimbria-fornix. Septo-hippocampal fibers are loosely distributed throughout the fimbria-fornix. Commissural fibers cross the midline in the ventral hippocampal commissure and form a tight fiber bundle in the fimbria. Crossed entorhino-hippocampal fibers cross the midline in the ventral hippocampal commissure rostral to the commissural fiber bundle, and crossed entorhino-entorhinal fibers pass through the dorsal hippocampal commissure. This suggests a topographical organization of fiber tracts within the fimbria-fornix that reflects the laminar organization of the hippocampal target structure: fibers of the diffusely terminating septohippocampal projection are loosely distributed throughout the fimbria-fornix, while those projections that are known to terminate in specific laminae of the hippocampal formation (commissural projection, crossed entorhino-hippocampal projection) form fiber bundles within the fimbria and the ventral hippocampal commissure.

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Abbreviations

A :

Astrocyte

CA1, CA3 :

hippocampal subfields

CC :

corpus callosum

D :

dendrite

DG :

dentate gyrus

DHC :

dorsal hippocampal commissure

Fi :

fimbria

LS :

lateral septal area

LV :

lateral ventricle

O :

oligodendrocyte

SFO :

subfornical organ

VHC :

ventral hippocampal commissure

References

  • Alonso A, Köhler C (1982) Evidence for separate projections of hippocampal pyramidal and non-pyramidal neurons to different parts of the septum in the rat brain. Neurosci Lett 31:209–214

    Google Scholar 

  • Amaral DG, Witter MP (1995) The hippocampal formation. In: Paxinos G (ed) The rat nervous system, 2nd edn. Academic Press, New York London, pp 443–494

    Google Scholar 

  • Brook GA, Lawrence JM, Raisman G (1993) Morphology and migration of cultured Schwann cells transplanted into the fimbria and hippocampus in adult rats. Glia 9:292–304

    Google Scholar 

  • Buchan AM, Pulsinelli WA (1990) Septo-hippocampal deafferentation protects CA1 neurons against ischemic injury. Brain Res 512(1):7–14

    Google Scholar 

  • Deller T, Leranth C (1990) Synaptic connections of NPY-immunoreactive neurons in the rat hilar area. J Comp Neurol 300:433–447

    Google Scholar 

  • Deller T, Nitsch R (1995) Selective rostral transection of the fornix spares the hippocampal commissural pathway in the rat: a Phaseolus vulgaris-leucoagglutinin-tracing study. Exp Brain Res 104:243–248

    Google Scholar 

  • Deller T, Nitsch R, Frotscher M (1994) Associational and commissural afferents of parvalbumin-immunoreactive neurons in the rat hippocampus: a combined immunocytochemical and PHAL study. J Comp Neurol 350:612–622

    Google Scholar 

  • Deller T, Nitsch R, Frotscher M (1995) Phaseolus vulgaris-leucoagglutinin (PHAL) tracing of commissural fibers to the rat fascia dentata: evidence for a previously unknown commissural projection to the outer molecular layer. J Comp Neurol 352:55–68

    Google Scholar 

  • Deller T, Frotscher M, Nitsch R (1996) Sprouting of crossed entorhino-dentate fibers after a unilateral entorhinal lesions: anterograde tracing of fiber reorganization with Phaseolus vulgaris leucoagglutinin (PHAL). J Comp Neurol (in press)

  • Dutar P, Lamour Y, Rascol O, Jobert A (1986) Septo-hippocampal neurons in the rat: further study of their physiological and pharmacological properties. Brain Res 365:325–334

    Google Scholar 

  • Finnerty GT, Jefferys JGR (1993) Functional connectivity from CA3 to the ipsilateral and contralateral CA1 in the rat dorsal hippocampus. Neuroscience 56:101–108

    Google Scholar 

  • Freund TF, Antal M (1988) GABA-containing neurons in the septum control inhibitory interneurons in the hippocampus. Nature 336:170–173

    Google Scholar 

  • Frotscher M (1988) Neuronal elements in the hippocampus and their synaptic connections. In: Frotscher M, Kugler P, Misgeld U, Zilles K (eds) Neurotransmission in the hippocampus. Adv Anat Embryol Cell Biol 111:2–19

  • Frotscher M (1991) Target cell specificity of synaptic connections in the hippocampus. Hippocampus 1:123–130

    Google Scholar 

  • Frotscher M (1992) Specificity of interneuronal connections. Ann Anat 174:377–382

    Google Scholar 

  • Frotscher M, Zimmer J (1983) Commissural fibers terminate on non-pyramidal neurons in the guinea pig hippocampus — a combined Golgi/EM degeneration study. Brain Res 265:289–293

    Google Scholar 

  • Gaykema RPA, Kuil J van der, Hersh LB, Luiten PGM (1991) Patterns of direct projections from the hippocampus to the medial septum-diagonal band complex: anterograde tracing with Phaseolus vulgaris leucoagglutinin combined with immunocytochemistry of choline acetyltransferase. Neuroscience 43:349–360

    Google Scholar 

  • Gerfen CR, Sawchenko PE (1984) An anterograde neuroanatomical tracing method that shows the detailed morphology of neurons, their axons and terminals: immunohistochemical localization of an axonally transported plant lectin, Phaseolus vulgaris leucoagglutinin. Brain Res 290:219–238

    Google Scholar 

  • Koliatsos VE, Applegate MD, Kitt CA, Walker LC, DeLong MR, Price DL (1989) Aberrant phosphorylation of neurofilaments accompanies transmitter-related changes in rat septal neurons following transection of the fimbria-fornix. Brain Res 482:205–218

    Google Scholar 

  • Lamour Y, Dutar P, Jobert A (1984) Septo-hippocampal and other medial septum-diagonal band neurons: electrophysiological and pharmacological properties. Brain Res 309:227–239

    Google Scholar 

  • Leranth C, Frotscher M (1983) Commissural afferents to the rat hippocampus terminate on vasoactive intestinal polypeptidelike immunoreactive non-pyramidal neurons. An EM and immunocytochemical degeneration study. Brain Res 276:357–361

    Google Scholar 

  • Li YJ, Simon JR, Low WC (1992) Intrahippocampal grafts of cholinergic-rich striatal tissue ameliorate spatial memory deficits in rats with fornix lesions. Brain Res Bull 29:147–155

    Google Scholar 

  • Naumann T, Peterson GM, Frotscher M (1992) Fine structure of rat septohippocampal neurons: II. A time course analysis following axotomy. J Comp Neurol 325:219–242

    Google Scholar 

  • Nyakas C, Luiten PGM, Spencer DG, Traber J (1987) Detailed projection patterns of septal and diagonal band efferents to the hippocampus in the rat with emphasis on innervation of CA1 and dentate gyrus. Brain Res Bull 18:533–545

    Google Scholar 

  • Paxinos G, Watson C (1986) The rat brain in stereotaxic coordinates, 2nd edition. Academic Press, New York London

    Google Scholar 

  • Raisman G (1969) Neuronal plasticity in the septal nuclei of the adult rat. Brain Res 14:25–48

    Google Scholar 

  • Raisman G, Field PM (1973) A quantitative investigation of the development of collateral reinnervation after partial deafferentiation of the septal nuclei. Brain Res 50:241–264

    Google Scholar 

  • Raisman G, Lawrence JM, Brook GA (1993) Schwann cells transplanted into the CNS. Int J Dev Neurosci 11:651–669

    Google Scholar 

  • Seress L, Ribak CE (1984) Direct commissural connections to basket cells of the hippocampal dentate gyrus: anatomical evidence for feed-forward inhibition. J Neurocytol 13:215–225

    Google Scholar 

  • Steward O (1976) Topographic organization of the projections from the entorhinal area to the hippocampal formation of the rat. J Comp Neurol 167:285–314

    Google Scholar 

  • Steward O, Scoville SA (1976) Cells of origin of entorhinal cortical afferents to the hippocampus and fascia dentata of the rat. J Comp Neurol 169:347–370

    Google Scholar 

  • Suzuki M, Raisman G (1992) The glial framework of central white matter tracts: segmented rows of contiguous interfascicular oligodendrocytes and solitary astrocytes give rise to a continuous meshwork of transverse and longitudinal processes in the adult rat fimbria. Glia 6:222–235

    Google Scholar 

  • Suzuki M, Raisman G (1994) Multifocal pattern of postnatal development of the macroglial framework of the rat fimbria. Glia 12:294–308

    Google Scholar 

  • Swanson LW, Wyss JM, Cowan WM (1978) An autoradiographic study of the organization of intrahippocampal association pathways in the rat. J Comp Neurol 181:681–716

    Google Scholar 

  • Swanson LW, Sawchenko PE, Cowan WM (1980) Evidence that the commissural, associational and septal projections of the regio inferior of the hippocampus arise from the same neurons. Brain Res 197:207–212

    Google Scholar 

  • Wyss JM (1981) An autoradiographic study of the efferent connections of the entorhinal cortex in the rat. J Comp Neurol 199:495–512

    Google Scholar 

  • Wyss JM, Swanson LW, Cowan WM (1980) The organization of the fimbria, dorsal fornix and ventral hippocampal commissure in the rat. Anat Embryol 158:303–316

    Google Scholar 

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Adelmann, G., Deller, T. & Frotscher, M. Organization of identified fiber tracts in the rat fimbria-fornix: an anterograde tracing and electron microscopic study. Anat Embryol 193, 481–493 (1996). https://doi.org/10.1007/BF00185879

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