Related Experiment Videos
Effect of altered thyroid hormone levels on hypothalamic-pituitary-adrenal function.
T C Kamilaris1, C R DeBold, S N Pavlou
1Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
The Journal of Clinical Endocrinology and Metabolism
|November 1, 1987
Summary
Thyroid hormone deficiency increases pituitary sensitivity to corticotropin-releasing hormone (CRH) and may alter the adrenocorticotropic hormone (ACTH) response to metyrapone. This suggests reduced hypothalamic CRH release in hypothyroidism.
Area of Science:
- Endocrinology
- Neuroendocrinology
- Thyroid and Adrenal Axis Physiology
Background:
- Thyroid hormones significantly influence the hypothalamic-pituitary-adrenal (HPA) axis.
- The impact of short-term thyroid hormone deficiency on HPA axis responsiveness requires further elucidation.
Purpose of the Study:
- To investigate the effects of temporary thyroid hormone withdrawal on HPA axis function.
- To assess changes in adrenocorticotropic hormone (ACTH) and cortisol responses to ovine corticotropin-releasing hormone (oCRH) and metyrapone in hypothyroid patients.
Main Methods:
- Evaluated 10 athyreotic patients during thyroxine (T4) treatment and after T4 withdrawal (biochemical hypothyroidism).
- Measured plasma ACTH and cortisol responses to intravenous oCRH.
- Assessed plasma ACTH, cortisol, and 11-deoxycortisol responses to oral metyrapone.
Main Results:
- Serum TSH significantly increased, while total T4 and free T4 index decreased after T4 withdrawal.
- Peak and integrated ACTH and cortisol responses to oCRH were significantly greater after T4 withdrawal.
- ACTH response to metyrapone was not significantly different, and 11-deoxycortisol response was similar, suggesting maximal adrenal stimulation.
Conclusions:
- Short-term thyroid hormone deficiency enhances corticotroph sensitivity to oCRH.
- Hypothyroidism may reduce the ACTH response to metyrapone-induced hypocortisolemia.
- These findings suggest a potential decrease in hypothalamic CRH release during hypothyroidism.