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. 2009 Jun 15;587(Pt 12):2977-85.
doi: 10.1113/jphysiol.2008.168393. Epub 2009 Apr 29.

Organizational role for pubertal androgens on adult hypothalamic-pituitary-adrenal sensitivity to testosterone in the male rat

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Organizational role for pubertal androgens on adult hypothalamic-pituitary-adrenal sensitivity to testosterone in the male rat

O Evuarherhe et al. J Physiol. .

Abstract

The inhibitory effect of androgens on the hypothalamic-pituitary-adrenal (HPA) axis in basal and stress conditions in adult male rats is well documented. Major sex-related neuroendocrine changes take place during puberty. There is a robust rise in production and secretion of gonadal steroids, which is thought to underlie numerous neural and behavioural changes brought on after puberty. The present study investigated the effect of the pubertal rise in gonadal steroid levels on the subsequent adult corticosterone profile, particularly the sensitivity of the adult HPA axis to testosterone. Animals were castrated either prepubertally (28 days) or in adulthood (11 weeks) and adult animals were subsequently treated with subcutaneous implants containing either testosterone or cholesterol. Using an automated blood sampling system, blood was collected from each freely moving, conscious rat every 10 min (i) over a 24 h period; (ii) in response to 10 min of noise stress, and (iii) following an immunological challenge with lipopolysaccharide (LPS). Analysis revealed that testosterone treatment did not significantly affect overall corticosterone release over the 24 h period in adult animals castrated before puberty in contrast to animals castrated in adulthood in which testosterone significantly suppressed corticosterone secretion. Following either a noise stress or LPS injection, testosterone treatment did not affect the hypothalamic or adrenal stress response in animals castrated prepubertally. Testosterone significantly suppressed the corticotrophin-releasing hormone and arginine vasopressin mRNA as well as the corticosterone response to LPS in castrated animals that had had their testes intact over puberty. These data provide evidence that puberty is a critical organizational period during which rising levels of gonadal steroids programme the sensitivity of the adult HPA axis to gonadal steroids in adulthood.

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Figures

Figure 2
Figure 2. Example 24 h profiles of corticosterone concentrations in single rats from each treatment group
Animals were maintained on a 14–10 h light dark regimen; the dark phase of the cycle is shown by the filled bar.
Figure 1
Figure 1. Summary statistics (area under curve, pulse amplitude and pulse frequency) for corticosterone release profiles in each treatment group
n= 4–7 per group; Bonferroni's post hoc analysis: *significant decrease in the area-under-curve (P < 0.001), pulse frequency (P < 0.01) and pulse amplitude (P < 0.001) in adult CSX/testosterone-replaced animals compared to adult CSX/cholesterol treated animals. +Significantly higher number of pulses over a 24 h period in prepubertal CSX/cholesterol treated compared to prepubertal CSX/testosterone-replaced males (P < 0.05).
Figure 3
Figure 3. The effect of 10 min of noise stress administration (110 dB, noise stress from 0700–0710 h, indicated by hatch bar)(A) and LPS administration (LPS administered at 0900, indicated by arrow) (B) on plasma corticosterone concentration in testosterone-replaced and cholesterol-treated male rats castrated before or after puberty
Data presented as mean plasma corticosterone concentration ±s.e.m. Two-way ANOVA: *P < 0.05 compared with adult CSX/testosterone-replaced rats (n= 4–6 rats per group).
Figure 4
Figure 4. Average percentage change in CRH (A) and parvocellular AVP (B) mRNA levels in the PVN 3 h following LPS administration in testosterone or cholesterol-treated adult males castrated prepubertally or in adulthood
Testosterone significantly reduced the CRH and parvocellular AVP mRNA response to LPS only in animals CSX in adulthood. Two-way ANOVA: *P < 0.05 (n= 4–6 rats per group).

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