An analysis of atrophy in the medial mammillary nucleus following hippocampal and fornix lesions in humans and nonhuman primates

Citation
M. Loftus et al., An analysis of atrophy in the medial mammillary nucleus following hippocampal and fornix lesions in humans and nonhuman primates, EXP NEUROL, 163(1), 2000, pp. 180-190
Citations number
31
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EXPERIMENTAL NEUROLOGY
ISSN journal
00144886 → ACNP
Volume
163
Issue
1
Year of publication
2000
Pages
180 - 190
Database
ISI
SICI code
0014-4886(200005)163:1<180:AAOAIT>2.0.ZU;2-7
Abstract
Lesions of the hippocampal formation or transections of the fornix are foll owed by shrinkage of the medial mammillary nucleus (MMN). We determined whe ther the shrinkage of this nucleus was due to loss and/or shrinkage of neur ons in addition to the loss of neuropil. We examined the MMN in a patient ( KB) with an infarct that led to marked atrophy of the left hippocampus and subiculum, leaving the right MMN intact. Unbiased, stereological measuremen t techniques were used to compare the total cell number and individual neur onal cross-sectional areas in both left and right MMN in this patient and i n two control human brains. We also analyzed the MMN in four macaque monkey s that underwent experimental unilateral transections of the fornix. The vo lume of the MMN on the lesioned side in KB was 55% of the unlesioned side ( 2.8 mm(3) vs 5.1 mm(3)); the MMN in the monkey cases were reduced to 47-58% of the volume of the nonlesioned side. Neurons in the deafferented MMN of KB and of the monkey subjects were decreased in cross-sectional area (16-20 %, P < 0.0001). There was a trend toward decreased cell numbers (11-15%) on the lesioned side in all cases. We have estimated that the loss in cell nu mber and shrinkage of remaining cells contribute negligibly to the 45% redu ction in MMN volume. Therefore, the loss of neuropil (dendrites and afferen t and efferent axons) appears to be the major contributor to the change in MMN volume. (C) 2000 Academic Press.