Dg. Flood et Pd. Coleman, DENDRITIC REGRESSION DISSOCIATED FROM NEURONAL DEATH BUT ASSOCIATED WITH PARTIAL DEAFFERENTATION IN AGING RAT SUPRAOPTIC NUCLEUS, Neurobiology of aging, 14(6), 1993, pp. 575-587
As neurons are lost in normal aging, the dendrites of surviving neighb
or neurons may proliferate, regress, or remain unchanged. In the case
of age-related dendritic regression, it has been difficult to distingu
ish whether the regression precedes neuronal death or whether it is a
consequence of loss of afferent supply. The rat supraoptic nucleus (SO
N) represents a model system in which there is no age-related loss of
neurons, but in which there is an age-related loss of afferents. The m
agnocellular neurosecretory neurons of the SON, that produce vasopress
in and oxytocin for release in the posterior pituitary, were studied i
n male Fischer 344 rats at 3, 12, 20, 27, 30, and 32 months of age. Co
unts in Nissl-stained sections showed no neuronal loss with age, and c
onfirmed similar findings in other strains of rat and in mouse and hum
an. Nucleolar size increased between 3 and 12 months of age, due, in p
art, to nucleolar fusion, and was unchanged between 12 and 32 months o
f age, indicating maintenance of general cellular function in old age.
Dendritic extent quantified in Golgi-stained tissue increased between
3 and 12 months of age, was stable between 12 and 20 months, and decr
eased between 20 and 27 months. We interpret the increase between 3 an
d 12 months as a late maturational change. Dendritic regression betwee
n 20 and 27 months was probably the result of deafferentation due to t
he preceding age-related loss of the noradrenergic input to the SON fr
om the ventral medulla.