The various hypothalamic nuclei show very different patterns of change
in ageing. These patterns are a basis for changes in biological rhyth
ms, hormones, autonomous functions or behavior. The suprachiasmatic nu
cleus (SCN) coordinates circadian and circannual rhythms. A marked sea
sonal and circadian variation in the vasopressin (AVP) cell number of
the SCN was observed in relation to the variation in photoperiod. Duri
ng normal ageing, the circadian variation and number of AVP-expressing
neurons in the SCN decreases. The sexually dimorphic nucleus (SDN), i
ntermediate nucleus or INAH-1 is localized between the supraoptic and
paraventricular nucleus (PVN). In adult men the SDN is twice as large
as in adult women. In girls, the SDN shows a first period of decreasin
g cell numbers during prepubertal development, leading to sexual dimor
phism. During ageing a decrease in cell number is found in both sexes.
The cells of the supraoptic nucleus and PVN produce AVP or oxytocin a
nd coexpress tyrosine hydroxylase. These nuclei are examples of neuron
populations that seem to stay perfectly intact in ageing. Parvicellul
ar corticotropin-releasing-hormone (CRH)-containing neurons are found
throughout the PVN. CRH neurons in the PVN are activated in the course
of ageing, as indicated by their increase in number and AVP coexpress
ion. Part of the infundibular (or arcuate) nucleus, the subventricular
nucleus, contains hypertrophic neurons in postmenopausal women. The h
ypertrophied neurons contain neurokinin-B (NKB), substance P and estro
gen receptors and probably act on LHRH neurons as interneurons. The NK
B neurons may also be involved in the initiation of menopausal flushes
. The nucleus tuberalis lateralis might be involved in feeding behavio
r and metabolism. It does not show any decrease in neuronal numbers in
ageing. It is remarkable that the majority of the hypothalamic nuclei
do not show signs of degeneration during ageing, but rather activatio
n with the exception of the SDN and SCN.