Impact of methimazole-induced hypothyroidism on postnatal swine

• Published in: Physiological reports 2024-04, Vol.12 (8), p.e16007-e16007
• Main Authors: Fazioli, James C, Mulligan, Margaret K, Ison, Erin K, Pasternak, J Alex
• Format: Article
• Language: English
• Subjects: Animals; Antithyroid Agents - adverse effects; Antithyroid Agents - toxicity; Apoptosis; CD36 antigen; Cell cycle; Corn syrup; Environmental conditions; Epithelium; Female; Goiter; Hogs; Homeostasis; Hormones; Hypothalamus; Hypothyroidism; Hypothyroidism - chemically induced; Hypothyroidism - metabolism; Iodine; Leukocytes (eosinophilic); Liver - drug effects; Liver - metabolism; Liver - pathology; Male; Metabolic rate; Metabolism; methimazole; Methimazole - adverse effects; Methimazole - toxicity; Nutrient utilization; Original; p53 Protein; Physiology; Pituitary; Regulation; Swine; thyroid Axis regulation; Thyroid diseases; Thyroid Gland - drug effects; Thyroid Gland - metabolism; Thyroid Gland - pathology; Thyroid hormones; Thyroxine; Thyroxine - blood; Triiodothyronine; Triiodothyronine - blood
• ISSN: 2051-817X
• DOI: 10.14814/phy2.16007

Thyroid hormones regulate metabolic rate, nutrient utilization, growth, and development. Swine are susceptible to thyroid suppression in response to disease or environmental conditions, but the physiological impact of such disruption has not been established. The objective of this study was to evaluate the impact of hypothyroidism induced with the antithyroid medication methimazole (MMI). 10 mg/kg MMI significantly decreased circulating triiodothyronine (T3) for the duration of treatment but had only a transient effect on circulating thyroxine (T4). Thyroid tissue weight was significantly increased by more than 3.5-fold in response to MMI treatment. Histologically, the eosinophilic colloid was largely absent from the thyroid follicle which displayed a disorganized columnar epithelium consistent with goiter. MMI induced hypothyroidism has no effect on growth rate over 28 days. Hepatic expression of genes associated with thyroid metabolism (DIO1, DIO2, and DIO3), lipid utilization (CD36, FASN, and ACACA), apoptosis (TP53, PERP, SIVA1, and SFN) and proliferation (CDK1, CDK2, CDK4, and CDKN1A) were unaffected by treatment. Collectively these results demonstrate that MMI induces mild systemic hypothyroidism and pronounced goiter, indicating a strong homeostatic central regulation within the hypothalamic pituitary thyroid axis. This combined with limited peripheral effects, indicates resilience to hypothyroidism in modern swine.