Key result
Aging in male mice was associated with a 75% decrease in pituitary GH mRNA levels after 27 months (P<0.01) and a 65% decrease in PRL mRNA levels between 12 and 27 months (P<0.01).
Aging in mice is associated with a specific, dramatic decrease in pituitary GH and PRL mRNA levels that is not driven by changes in serum T3.
Caution against extrapolating mouse pituitary aging data to humans; leaves open whether similar GH/PRL mRNA declines occur in clinical aging.
The effects of aging on pituitary GH, PRL, and alpha-tubulin messenger RNA (mRNA) levels were measured in 3-, 12-, and 27-month-old male C57BL/6J mice by dot-blot hybridization. The amount of GH and PRL mRNA in the pituitary deceased dramatically with age. However, total poly(A+) RNA (mRNA), as measured by hybridization with radioactively labeled oligo-(dT), was not altered during aging. In addition, there were no age-related changes in the level of alpha-tubulin mRNA. Thus, the effects of aging on GH and PRL mRNA levels are specific; the levels of the majority of cellular mRNAs are not altered with age. GH and mRNA levels decreased 35% between 3 and 12 months (P less than 0.05) and a total of 75% after 27 months (P less than 0.01). PRL mRNA levels decreased 65% between 12 and 27 months (P less than 0.01), although there was no significant decrease before 12 months. Whereas T3 is the most potent regulator of GH gene expression, we did not detect any significant age-related change in serum T3 levels. These results suggest that factors other than T3 play a role in the age-related decline in GH and PRL gene expression.
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Crew et al. (1987) studied Aging. Aging vs. Younger mice (3-month-old) was evaluated on Pituitary GH and PRL mRNA levels (75% decrease in GH mRNA after 27 months; 65% decrease in PRL mRNA between 12 and 27 months, p=<0.01). Aging in male mice was associated with a 75% decrease in pituitary GH mRNA levels after 27 months (P<0.01) and a 65% decrease in PRL mRNA levels between 12 and 27 months (P<0.01).
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