M. Carnes et al., COINCIDENT PLASMA ACTH AND CORTICOSTERONE TIME-SERIES - COMPARISONS BETWEEN YOUNG AND OLD RATS, Experimental gerontology, 29(6), 1994, pp. 625-643
Senescence is accompanied by a reduced ability to respond to a variety
of physical acid behavioral stressors. A sizable literature has been
devoted to the interplay between hypothalamic-pituitary-adrenocortical
axis dysfunction and senescence; yet, the precise interactions remain
an enigma. Adrenocorticotropic hormone (ACTH) is secreted in pulsatil
e bursts generating complex signals in the plasma compartment that mus
t be ''read'' by adrenocortical cells in order to initiate appropriate
secretory responses. We have previously demonstrated subtle differenc
es between young and old rats in the pattern of fluctuations in plasma
ACTH concentrations over time, despite no difference in mean levels.
The present work addressed the physiological significance of these dif
ferences in the plasma ACTH Signal by analyzing the corresponding plas
ma corticosterone concentration time series and the relationship betwe
en these two hormones over time. Time series of integrated 10-min ACTH
and corticosterone concentrations were collected over 4 h at the time
of diurnal activation and analyzed in the time and frequency domains.
The time of onset of the diurnal surge occurred 20 min later in old r
ats, and the ratio of corticosterone to ACTH was less at the time of o
nset and peak of the diurnal surge. Corticosterone levels were lower i
n old rats and mean ACTH and corticosterone levels were correlated in
young but not old rats, as were maximum levels of the two hormones. Cr
oss-correlation of ACTH and corticosterone time series and comparison
of spectra were consistent with smoother fluctuations in plasma cortic
osterone in old animals with less variability at time scales less than
55 min. We conclude that age may be associated with a delay in diurna
l activation of the HPA axis, a loss of sensitivity of adrenal cortico
sterone secretion to plasma ACTH levels, and a relative loss of high f
requency variability in the corticosterone signal, as seen in many phy
siological systems with age.