Leptin inhibits basal but not gonadotrophin-stimulated testosterone production in the immature mouse and sheep testis
Muren Herrid A B , Yin Xia A C , Tim O’Shea A and James R. McFarlane A DA Centre for Bioactive Discovery in Health and Aging, University of New England, Armidale, NSW 2350, Australia.
B Present address: CSIRO Livestock Industries, Locked Bag 1, Post Office, Armidale, NSW 2350, Australia.
C Present address: Program in Membrane Biology and Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Harvard, Medical School, Boston, MA 02114, USA.
D Corresponding author. Email: jmcfarla@une.edu.au
Reproduction, Fertility and Development 20(4) 519-528 https://doi.org/10.1071/RD07062
Submitted: 3 April 2007 Accepted: 27 January 2008 Published: 11 April 2008
Abstract
The mechanisms whereby leptin regulates testosterone secretion are complex and are likely to involve actions at different levels of the hypothalamus–pituitary–gonadal axis. In the present study, the effect of leptin on testicular steroidogenesis at different developmental stages in mice and sheep was investigated. Testosterone data from testicular slice and Leydig cells of immature and adult mice testes demonstrated that the action of leptin in the regulation of steroidogenesis appears to be dependent on the developmental stage of the testis. Leptin biphasically modulates basal testosterone production in immature testicular slice cultures: at relatively low concentrations (6.25–12.5 ng mL–1) leptin exerts a significant inhibitory effect, but has less of an effect at very low (1.25 ng mL–1) or high concentrations (25 ng mL–1). However, leptin failed to modulate basal testosterone levels in Leydig cell preparations. In contrast with immature testes, leptin was unable to regulate either basal or human chorionic gonadotrophin (10 IU mL–1)-stimulated testosterone production in adult testicular slices or Leydig cell cultures. The age- and concentration-dependent regulation pattern was confirmed using sheep testicular slice culture. Leptin (1.56–25 ng mL–1) significantly inhibited basal testosterone production in the testis from birth to Day 21, but had no effect on Day 27 or older testes. However, the plasma and testicular concentrations of leptin and testosterone data in the ram indicate that such a regulatory effect of leptin on testis steroidogenesis in vitro is unable to efficiently influence testosterone concentrations in vivo. This does not exclude the possibility of a non-competitive mechanism of interaction between leptin and luteinising hormone to regulate testosterone production. Thus, we hypothesise that leptin is not an important independent regulator of testosterone concentration in the normal physiological state. The physiological significance and mechanism of leptin regulation of basal testosterone production are not known; further studies are required to elucidate these important issues.
Additional keyword: postnatal development.
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