Clamping Cortisol and Testosterone Mitigates the Development
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Sleep loss in men increases cortisol and decreases testosterone, and sleep restriction by 3–4 h/night induces insulin resistance.

Researchers clamped cortisol and testosterone and determined the effect on insulin resistance in a randomized double-blind, in-laboratory crossover study.

The participants were 34 healthy young men. 4 nights of sleep restriction (SR) of 4 hours/night under two treatment conditions in random order: dual hormone clamp (cortisol and testosterone fixed), or matching placebo (cortisol and testosterone not fixed).

Fasting blood samples, and an additional 23 samples for a 3-hour oral glucose tolerance test (OGTT), were collected before and after SR under both treatment conditions. Cytokines and hormones were measured from the fasting samples. Overall insulin sensitivity was determined from the OGTT by combining complementary measures: homeostasis model assessment of insulin resistance of the fasting state; Matsuda Index of the absorptive state, and; minimal model of both fasting and absorptive states.

Results:
-- SR alone induced hyperinsulinemia, hyperglycemia and overall insulin resistance.

-- Clamping cortisol and testosterone alleviated the development of overall insulin resistance and hyperinsulinemia by 50%. Interleukin-6, high sensitivity C-reactive protein, peptide YY, and ghrelin did not change, whereas tumor necrosis factor-α and leptin changed in directions that would have mitigated insulin resistance with SR alone.

Conclusively, fixing cortisol-testosterone exposure mitigates the development of insulin resistance and hyperinsulinemia, but not hyperglycemia, from sustained SR in men. The interplay between cortisol and testosterone may be important as a mechanism by which SR impairs metabolic health.

Source: https://academic.oup.com/jcem/advance-article-abstract/doi/10.1210/clinem/dgab375/6287014?redirectedFrom=fulltext
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