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Published on: November 20, 2015
Lifelong alterations in endocrine function resulting from brief perinatal hypothyroidism in the rat
Insights
Brief perinatal hypothyroidism in rats, induced by propylthiouracil (PTU), caused developmental delays and hormonal imbalances. This highlights potential risks of antithyroid drugs during pregnancy.
Area of Science:
- Endocrinology
- Developmental Biology
- Reproductive Science
Background:
- Perinatal hypothyroidism can impact long-term physiological development.
- Antithyroid drugs like propylthiouracil (PTU) are used to manage maternal thyroid conditions during pregnancy.
Purpose of the Study:
- To investigate the late consequences of a short period of perinatal hypothyroidism in rats.
- To assess the effects of prenatal and/or neonatal exposure to PTU on rat development and endocrine function.
Main Methods:
- Rats were exposed to PTU either prenatally to dams or neonatally to pups for 5 days.
- Evaluated developmental milestones (eye opening, weaning weight, puberty, estrus cycles).
- Assessed thyroid gland size, and concentrations of thyroid-stimulating hormone (TSH), luteinizing hormone-releasing hormone (LH-RH), and thyrotropin-releasing hormone (TRH).
Main Results:
- Perinatal hypothyroidism led to delayed eye opening, reduced weaning weight, delayed puberty, and prolonged estrus cycles.
- Neo-PTU rats exhibited enlarged thyroid glands with elevated TSH levels.
- Adult male neo-PTU rats showed a blunted response to TRH, indicating secondary/tertiary hypothyroidism.
Conclusions:
- Brief perinatal hypothyroidism has significant long-term developmental and endocrine consequences.
- Caution is advised regarding antithyroid drug use in pregnant women.
- Pregnant hypothyroid women require comprehensive replacement therapy.
Abstract:
The late consequences of a brief period of perinatal hypothyroidism were studied in the rat by giving propylthiouracil (PTU) prenatally to the mothers and/or neonatally for 5 days to the pups. Perinatal hypothyroidism produced a delay in eye opening, a diminution in weaning weight, a delay in puberty and first estrus, and a prolongation of estrus cycles. The neo-PTU rats usually had a persistently enlarged thyroid gland associated with an elevated pituitary, hypothalamic, and serum thyroid-stimulating hormone (TSH) concentration. The metabolic clearance rate of TSH and response to luteinizing hormone-releasing hormone (LH-RH) were normal. The response to thyrotropin-releasing hormone (TRH) stimulation was significantly blunted in adult neo-PUT males, suggesting secondary or tertiary hypothyroidism. As a result of these studies, serious thought should be given to the possible consequences of antithyroid drug therapy of pregnant women, and certainly all pregnant hypothyroid women should receive full replacement therapy.
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