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Thyroid hormone is required for hypothalamic neurons regulating cardiovascular functions
Jens Mittag, … , Anders Arner, Björn Vennström
Jens Mittag, … , Anders Arner, Björn Vennström
Published December 21, 2012
Citation Information: J Clin Invest. 2013;123(1):509-516. https://doi.org/10.1172/JCI65252.
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Research Article

Thyroid hormone is required for hypothalamic neurons regulating cardiovascular functions

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Abstract

Thyroid hormone is well known for its profound direct effects on cardiovascular function and metabolism. Recent evidence, however, suggests that the hormone also regulates these systems indirectly through the central nervous system. While some of the molecular mechanisms underlying the hormone’s central control of metabolism have been identified, its actions in the central cardiovascular control have remained enigmatic. Here, we describe a previously unknown population of parvalbuminergic neurons in the anterior hypothalamus that requires thyroid hormone receptor signaling for proper development. Specific stereotaxic ablation of these cells in the mouse resulted in hypertension and temperature-dependent tachycardia, indicating a role in the central autonomic control of blood pressure and heart rate. Moreover, the neurons exhibited intrinsic temperature sensitivity in patch-clamping experiments, providing a new connection between cardiovascular function and core temperature. Thus, the data identify what we believe to be a novel hypothalamic cell population potentially important for understanding hypertension and indicate developmental hypothyroidism as an epigenetic risk factor for cardiovascular disorders. Furthermore, the findings may be beneficial for treatment of the recently identified patients that have a mutation in thyroid hormone receptor α1.

Authors

Jens Mittag, David J. Lyons, Johan Sällström, Milica Vujovic, Susi Dudazy-Gralla, Amy Warner, Karin Wallis, Anneke Alkemade, Kristina Nordström, Hannah Monyer, Christian Broberger, Anders Arner, Björn Vennström

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Figure 2

Reduced number of pv cells in the anterior hypothalamus of Thra1+/m mice.

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Reduced number of pv cells in the anterior hypothalamus of Thra1+/m mice...
(A) Immunohistochemistry for pv in the anterior hypothalamus, as overview (left; scale bar: 250 μm) and high magnification (right; scale bar: 50 μm) in wild-type and Thra1+/m mice (middle; scale bar: 250 μm). fx, fornix; mt, mamillothalamic tract; PVN, paraventricular nucleus of the hypothalamus; 3V, 3rd ventricle; opt, optic tract. (B) Double immunohistochemistry for GFP (green) and pv (red) in the AHA of a mouse strain expressing a chimeric TRα1-GFP protein. Yellow indicates overlapping staining. Scale bar: 25 mm. (C) pv neurons in T3-treated wild-type and Thra1+/m mice or crossings with hyperthyroid Thrb–/– mice. Scale bar: 250 μm. (D) Quantification of pv neurons in the AHA of the different animal models. All values are mean ± SEM; n = 4–9. *P < 0.05 to untreated wild type; ***P < 0.001 to untreated wild type; #P < 0.05 to untreated Thra1+/m.

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