RECONSTRUCTIONS OF POPULATIONS OF LUTEINIZING-HORMONE-RELEASING HORMONE NEURONS IN YOUNG AND MIDDLE-AGED RATS REVEAL PROGRESSIVE INCREASES IN SUBGROUPS EXPRESSING FOS PROTEIN ON PROESTRUS AND AGE-RELATED DEFICITS
Bs. Rubin et al., RECONSTRUCTIONS OF POPULATIONS OF LUTEINIZING-HORMONE-RELEASING HORMONE NEURONS IN YOUNG AND MIDDLE-AGED RATS REVEAL PROGRESSIVE INCREASES IN SUBGROUPS EXPRESSING FOS PROTEIN ON PROESTRUS AND AGE-RELATED DEFICITS, Endocrinology, 136(9), 1995, pp. 3823-3830
Fos expression has been used as a marker of activation of neuroendocri
ne cells including LHRH neurons. In this study, Fos protein was locali
zed within LHRH neurons in young and middle-aged rats to trace the tem
poral and spatial pattern of LHRH neuronal activation associated with
the preovulatory LH surge. Animals were killed during the late morning
, afternoon, and evening of proestrus. Dual immunocytochemical protoco
ls localized LHRH and LHRH/Fos neurons, and computer-assisted methods
were used to reconstruct forebrain populations of single- and double-l
abeled LHRH neurons. Although a significant increase in the number of
LHRH/Fos neurons was noted by evening in both age groups, a greater in
crease was observed in young (12% in morning, 28% in afternoon, and 62
% by evening) compared with aging females (5% in morning, 10% in after
noon, and 40% by evening). Reconstructions of LHRH and LHRH/Fos neuron
s revealed time- and age-dependent differences in Fos expression withi
n LHRH neurons. In young females, LHRH/Fos neurons were restricted to
central regions of the population of LHRH neurons on the morning of pr
oestrus. By evening, Fos expression was also observed in more peripher
al and caudal LHRH neurons. In middle-aged females, Fos expression was
restricted to ventral subgroups of LHRH neurons on the afternoon of p
roestrus. By evening, more LHRH neurons contained Fos protein, however
, few were located in the dorsal aspect of the population. These data
trace the progressive increase in activation of LHRH neurons during th
e preovulatory LH surge in young females and reveal deficits in this p
attern of activation by middle age.