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Am J Physiol Regul Integr Comp Physiol 280: R1755-R1771, 2001;
0363-6119/01 $5.00
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Vol. 280, Issue 6, R1755-R1771, June 2001

Hypothesis testing of the aging male gonadal axis via a biomathematical construct

Daniel M. Keenan1 and Johannes D. Veldhuis2,3

1 Department of Statistics and 2 Center for Biomathematical Technology, University of Virginia, Charlottesville 22903; and 3 Division of Endocrinology, Department of Internal Medicine, Health Sciences Center, General Clinical Research Center, Charlottesville, Virginia 22908

Neuroendocrine axes are feedback- and feedforward-coupled dynamic ensembles. Disruption of selected pathways in such networklike organizations may explicate loss of orderly hormonal output as observed in aging. To test this notion more explicitly, we implemented an earlier computer-assisted biomathematical model of the interlinked male hypothalamo [gonadotropin-releasing hormone (GnRH)]-pituitary [luteinizing hormone, (LH)]-testicular [Leydig cell testosterone (Te)] axis (Am J Physiol Endocrinol Metab Physiol 275: E157-E176, 1988; Keenan D., W. Sun, and J. D. Veldhuis, SIAM J Appl Math 61: 934-965, 2000). Thereby, we appraise mechanistic hypotheses for more disorderly LH and Te secretion in aging men. We compare model predictions with monitored abnormalities in the older male, namely, irregular patterns of individual and synchronous LH and Te release, reduced 24-h rhythmic Te output, and variably elevated LH secretion. Among the mechanisms examined, the most parsimonious aging hypothesis would entail impaired LH feedforward on Te without or with attenuated Te feedback on GnRH/LH secretion. This investigative strategy should aid in exploring new postulates of disrupted feedback networks in pathophysiology.

gonadotropin-releasing hormone; luteinizing hormone; Leydig cell testosterone


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