Literature DB >> 2234284

The supraoptic and paraventricular nuclei of the human hypothalamus in relation to sex, age and Alzheimer's disease.

E Goudsmit1, M A Hofman, E Fliers, D F Swaab.   

Abstract

Volume and total cell number were determined in the supraoptic (SON) and paraventricular (PVN) nuclei of 14 male and 16 female subjects ranging in age from 10 to 93 years. In addition, 4 male and 6 female subjects suffering from Alzheimer's disease (AD) and ranging in age from 46 to 97 years were studied. Subjects were divided into two age groups, viz., "young" for subjects up to 60 years, and "old" for subjects older than 60. No sex differences in volume and in total cell number were observed in the SON and PVN in either age group. In addition, no significant correlation was found between total cell number in the SON and PVN and brain weight. No significant differences in volume and total cell number were found in either the SON or PVN between young and old control subjects or between AD cases and controls, indicating that these nuclei are spared from degenerative changes in senescence and AD. Determination of neuron numbers in the SON supported this view. In contrast, volume and total cell counts in the suprachiasmatic decreased in senescence and were dramatically reduced in AD. The present results indicate the occurrence of differential patterns of cell loss within the human hypothalamus with aging and in AD, which are proposed to be related to functional differences between the hypothalamic nuclei.

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Year:  1990        PMID: 2234284     DOI: 10.1016/0197-4580(90)90114-f

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  14 in total

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Review 4.  Development of the human hypothalamus.

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9.  A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus.

Authors:  U Bahnsen; P Oosting; D F Swaab; P Nahke; D Richter; H Schmale
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10.  Age-related changes in core body temperature and activity in triple-transgenic Alzheimer's disease (3xTgAD) mice.

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