(Boston)— Regulation of thyroid hormone (TH) levels is a complex multilevel phenomenon. The paraventricular nucleus (PVN) of the hypothalamus (the region of the brain that controls the involuntary nervous system) has been identified as a direct regulator of thyrotropin (a hormone secreted by the pituitary gland that regulates the production of thyroid hormones). The PVN is a key regulator of TH levels, integrating multiple signaling systems.
Now for the first time, researchers from Boston University Chobanian & Avedisian School of Medicine, have shown that in addition to being critical for regulating thyroid hormone levels, thyrotropin-releasing hormone (TRH) neurons play a major role in the response to fasting and weight loss.
To test this function, the researchers used a chemogenetic approach (engineering of protein receptors to respond to previously unrecognized small molecules) to either stimulate or inhibit specific neuronal populations. They injected an experimental model with an adeno-associated virus (AAV) coding for a mutant receptor activated exclusively by an exogenous compound into specific areas of the brain.
According to the researchers, by controlling the activity of these neurons they were able to change the entire endocrine system related to the thyroid. "Probing deeper into these findings will lead to new knowledge with potential application to metabolic and thyroid-related diseases, such as obesity and central hypothyroidism," adds Hollenberg, who also is physician-in-chief at Boston Medical Center.
These findings appear online in the journal Thyroid.
This work was supported in part by K01 DK091403 and RO1 grants DK056123 and DK117940 from the NIDDK and Research Grant from the American Thyroid Association to K.R.V. R.R. was supported by a research fellowship 2014/ 20704-5 from FAPESP (Brazil).
