The origin, course, and termination of the hippocampothalamic projections in the macaque

The projections from the hippocampal formation to the thalamus were investigated with both anterograde and retrograde tracers. Horseradish peroxidase was injected into medial and midline thalamic sites in six cases, and tritiated amino acids were injected into the hippocampal formation in nine others, five of which had prior transections of the fornix. Only the subicular and entorhinal cortices were found to project to the thalamus. From the subicular cortex, dense bilateral projections were traced through the fornix to the anterior nuclei, while lighter fornical projections terminated in other rostral midline sites, including the nuclei reuniens, centralis latocellularis, and paraventricularis. These projections arose predominantly from the polymorphic cells which are located in the deepest cellular layers of the subiculum and prosubiculum. In addition, the subicular cortex was found to project to the nucleus lateralis dorsalis. The latter projection, which showed evidence of a crude topographic organization, ran either through the fornix or, unlike the other subicular efferents, through the sublenticular limb of the internal capsule to form part of the temporopulvinar bundle of Arnold. The nonfornical projection to the nucleus lateralis dorsalis passed through the medial pulvinar, where there was some additional termination. Few, if any, projections from the entorhinal cortex to the thalamus travelled in the fornix. Rather, the entorhinal efferents were carried in the inferior thalamic peduncle to the magnocellular portion of the nucleus medialis dorsalis, and in the internal capsule and bundle of Arnold to the medial pulvinar and the nucleus lateralis dorsalis.

[1]  M. Mishkin,et al.  Further evidence that amygdala and hippocampus contribute equally to recognition memory , 1984, Neuropsychologia.

[2]  Hans J. Markowitsch,et al.  Thalamic mediodorsal nucleus and memory: A critical evaluation of studies in animals and man , 1982, Neuroscience & Biobehavioral Reviews.

[3]  Feinberg Jf The Wernicke-Korsakoff syndrome. , 1980 .

[4]  C. Poletti,et al.  Evidence for a second hippocampal efferent pathway to hypothalamus and basal forebrain comparable to fornix system: a unit study in the awake monkey. , 1980, Journal of neurophysiology.

[5]  J. DeVito,et al.  Subcortical projections to the hippocampal formation in squirrel monkey (Saimiri sciureus) , 1980, Brain Research Bulletin.

[6]  W M Cowan,et al.  Subcortical afferents to the hippocampal formation in the monkey , 1980, The Journal of comparative neurology.

[7]  R. Passingham The hippocampus as a cognitive map J. O'Keefe & L. Nadel, Oxford University Press, Oxford (1978). 570 pp., £25.00 , 1979, Neuroscience.

[8]  A. Siegel,et al.  Origin of the fornix system in the squirrel monkey , 1979, Brain Research.

[9]  L. Nadel,et al.  The Hippocampus as a Cognitive Map , 1978 .

[10]  M. Mesulam,et al.  Tetramethyl benzidine for horseradish peroxidase neurohistochemistry: a non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents. , 1978, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[11]  L. E. White,et al.  Origin of the direct hippocampus-anterior thalamic bundle in the rat: A combined horseradish peroxidase-Golgi analysis , 1977, Experimental Neurology.

[12]  G. V. Van Hoesen,et al.  Hippocampal efferents reach widespread areas of cerebral cortex and amygdala in the rhesus monkey. , 1977, Science.

[13]  A. Siegel,et al.  Thalamic projections of the hippocampal formation: Evidence for an alternate pathway involving the internal capsule , 1977, Brain Research.

[14]  C E Poletti,et al.  Fornix system efferent projections in the squirrel monkey: An experimental degeneration study , 1977, The Journal of comparative neurology.

[15]  L. Heimer,et al.  A safer and more sensitive substitute for diamino-benzidine in the light microscopic demonstration of retrograde and anterograde axonal transport of HRP , 1977, Neuroscience Letters.

[16]  K. Heilman,et al.  Korsakoff's syndrome resulting from bilateral fornix lesions , 1977, Neurology.

[17]  W. Cowan,et al.  An autoradiographic study of the organization of the efferet connections of the hippocampal formation in the rat , 1977, The Journal of comparative neurology.

[18]  D. Pandya,et al.  Some connections of the entorhinal (area 28) and perirhinal (area 35) cortices of the rhesus monkey. I. Temporal lobe afferents , 1975, Brain Research.

[19]  Deepak N. Pandya,et al.  Some connections of the entorhinal (area 28) and perirhinal (area 35) cortices of the rhesus monkey. II. Frontal lobe afferents , 1975, Brain Research.

[20]  J. Nelson,et al.  Asymptomatic destruction of the fornix in man. , 1975, Archives of neurology.

[21]  P. Gloor,et al.  The connections of the amygdala and of the anterior temporal cortex in the human brain , 1960, The Journal of comparative neurology.

[22]  W. Nauta,et al.  A Comparison of the Distribution of the fornix system in the rat, guinea pig, cat, and monkey , 1959, The Journal of comparative neurology.

[23]  W. Nauta,et al.  Subcortical projections from the temporal neocortex in Macaca mulatta , 1956 .

[24]  T. Powell,et al.  STUDIES OF THE CONNEXIONS OF THE FORNIX SYSTEM , 1954, Journal of neurology, neurosurgery, and psychiatry.

[25]  G. J. Romanes,et al.  The Neocortex of Macaca mulatta , 1948 .

[26]  M Mishkin,et al.  Projections of the amygdala to the thalamus in the cynomolgus monkey , 1984, The Journal of comparative neurology.

[27]  J. Brierley 8 – Neuropathology of Amnesic States , 1977 .

[28]  W. Sweet,et al.  Loss of recent memory following section of fornix. , 1959, Transactions of the American Neurological Association.

[29]  Sweet Wh,et al.  Loss of recent memory following section of fornix. , 1959 .