Disruption of the Melanin-Concentrating Hormone Receptor 1 (MCH1R) Affects Thyroid Function

• Published in: Endocrinology (Philadelphia) 2012-12, Vol.153 (12), p.6145-6154
• Main Authors: Chung, Shinjae, Liao, Xiao-Hui, Di Cosmo, Caterina, Van Sande, Jacqueline, Wang, Zhiwei, Refetoff, Samuel, Civelli, Olivier
• Format: Article
• Language: English
• Subjects: Animals; Biological activity; Biological and medical sciences; Crosses, Genetic; Disruption; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation; Hormones; Hypothalamus; Hypothyroidism; Iodine Radioisotopes - pharmacology; Kinetics; Male; Melanin; Melanin-concentrating hormone; Mice; Mice, Knockout; mRNA; Peptides - chemistry; Physiological effects; Physiological responses; Pituitary; Receptors; Receptors, Somatostatin - genetics; Receptors, Somatostatin - physiology; Secretion; Thyrocytes; Thyroid; Thyroid gland; Thyroid Gland - metabolism; Thyroid hormones; Thyroid-stimulating hormone; Thyroid-TRH-TSH; Thyrotropin-releasing hormone; Thyroxine; Thyroxine - metabolism; Triiodothyronine; Triiodothyronine - metabolism; Vertebrates: endocrinology; Zona incerta
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/en.2011-1435

Melanin-concentrating hormone (MCH) is a peptide produced in the hypothalamus and the zona incerta that acts on one receptor, MCH receptor 1 (MCH1R), in rodents. The MCH system has been implicated in the regulation of several centrally directed physiological responses, including the hypothalamus-pituitary-thyroid axis. Yet a possible direct effect of the MCH system on thyroid function has not been explored in detail. We now show that MCH1R mRNA is expressed in thyroid follicular cells and that mice lacking MCH1R [MCH1R-knockout (KO)] exhibit reduced circulating iodothyronine (T4, free T4, T3, and rT3) levels and high TRH and TSH when compared with wild-type (WT) mice. Because the TSH of MCH1R-KO mice displays a normal bioactivity, we hypothesize that their hypothyroidism may be caused by defective thyroid function. Yet expression levels of the genes important for thyroid hormones synthesis or secretion are not different between the MCH1R-KO and WT mice. However, the average thyroid follicle size of the MCH1R-KO mice is larger than that of WT mice and contained more free and total T4 and T3 than the WT glands, suggesting that they are sequestered in the glands. Indeed, when challenged with TSH, the thyroids of MCH1R-KO mice secrete lower amounts of T4. Similarly, secretion of iodothyronines in the plasma upon 125I administration is significantly reduced in MCH1R-KO mice. Therefore, the absence of MCH1R affects thyroid function by disrupting thyroid hormone secretion. To our knowledge, this study is the first to link the activity of the MCH system to the thyroid function.