EFFECTS OF AGE AND LONG-TERM OVARIECTOMY ON THE ESTROGEN-RECEPTOR CONTAINING SUBPOPULATIONS OF BETA-ENDORPHIN-IMMUNOREACTIVE NEURONS IN THEARCUATE NUCLEUS OF FEMALE C57BL 6J MICE/

We have reported a decrease in the number of arcuate nucleus (ARC)-imm unoreactive beta-endorphin neurons in old (24 months) female C57BW6J m ice versus young (5 months) mice. Here, we have tested by immunocytoch emistry whether age-related changes in beta-endorphin neuron numbers a re selective for beta-endorphin neurons which do or do not contain est rogen receptors (E(2)R). We also compared beta-endorphin neuron number in mice with short- (S) and long-duration (L) ovariectomy (OVX), sinc e the latter may protect against neuroendocrine aging. Mice were studi ed at 5 (young), 12 (middle-aged), or 23-24 months (old). When the mea n number of neurons per tissue section(15 sections per animal) was exa mined, there were no significant differences between young and middle- aged S-OVX females for either beta-endorphin, E(2)R, or beta-endorphin /E(2)R neuron number. However, there were significant decreases in bet a-endorphin-containing neurons in the oldest age group versus young fe males (young S-OVX: 74.4 +/- 11 (+/- SD) immunopositive neurons per ti ssue section, n = 10 mice; young L-OVX: 61.6 +/- 6.9, n = 6; old S-OVX : 45.7 +/- 9.9, n = 7; and old L-OVX: 37.5 +/- 7.3, n = 7). There were also decreases in P-endorphin neurons which contained E(2)R in the ol dest animals (young S-OVX: 16.6 +/- 6.4; young L-OVX: 13.7 +/- 1.3; ol d S-OVX: 9.2 +/- 1.8; L-OVX: 6.0 +/- 1.5) (p < 0.05 ANOVA). Both age ( p less than or equal to 0.001, two-way ANOVA) and ovarian status (p le ss than or equal to 0.05) independently affected neuron number for bot h the beta-endorphin and beta-endorphin/E(2)R populations versus young mice. We tested whether the observed age and/or ovarian-related decre ases were proportionally greater in the subpopulation of beta-endorphi n neurons which contained E(2)R compared to the total beta-endorphin n euron population. In the oldest age group, there was no significant di fference in the decrease with age in the population of beta-endorphin neurons which contained E(2)R and the total beta-endorphin population (p = 0.208). When we examined the E(2)R neuron population as compared to the beta-endorphin neuron populations, age-related decreases in the beta-endorphhin neuronal population tended to be greater than the dec reases seen in the E(2)R neuron population (p = 0.054 repeated measure s ANOVA). The tyrosine hydroxylase (TH) neuron population was studied to test whether there were changes in another ARC neuron population. T here was no age-related change in either TH neuron number (young S-OVX : 35.8 +/- 6.2, n = 4; middle-aged S-OVX: 33.1 +/- 2.8, n = 4; old S-O VX: 33.4 +/- 3.4, n = 4) or in the number of TH neurons which containe d E(2)R (young S-OVX: 7.6 +/- 1.0; middle-aged S-OVX: 7.2 +/- 0.8; old S-OVX: 6.9 +/- 1.2). These data demonstrate that ARC beta-endorphin-c ontaining perikarya are sensitive to alterations associated both with age and ovarian status; these effects are independent of one another. Our findings fail to support the hypothesis that L-OVX has a protectiv e effect on hypothalamic neurons in older females. The subpopulation o f beta-endorphin neurons that contain E(2)R are not affected to any gr eater degree by age or ovarian status than the beta-endorphin neuron p opulation as a whole in the old animal.