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低甲状腺条件下成年心肌中小动脉密度的调节。

Regulation of arteriolar density in adult myocardium during low thyroid conditions.

机构信息

Cardiovascular Research Center, Sanford Research, University of South Dakota, Sioux Falls, South Dakota, USA.

出版信息

Vascul Pharmacol. 2010 Mar-Apr;52(3-4):146-50. doi: 10.1016/j.vph.2009.10.003. Epub 2009 Oct 20.

Abstract

Low thyroid function induced by either propylthiouracil (PTU) treatment or thyroidectomy surgery led to a reduction of arteriolar density in adult rat myocardium, which can be prevented by treatment with thyroxine or the thyroid hormone analogue 3,5-diiodothyropropionic acid (DITPA). However, many questions related to pathophysiological changes and the regulation of arteriolar density in the heart due to hypothyroidism remain unanswered. Sprague-Dawley rats were treated with PTU in drinking water for 1, 3, and 6weeks, or co-treated with the vasodilator dipyridamole and PTU for 6weeks, or treated with PTU for 6weeks and treatment discontinued for 2 or 4weeks. Heart mass, body mass, cardiac function and myocardial arteriolar density were determined. Arteriolar loss in hypothyroidism induced by PTU treatment progressed gradually with a 22% reduction after 3weeks treatment and 34% by 6weeks which was largely reversed after discontinuing PTU treatment for only 2weeks. Combined treatment with the vasodilator dipyridamole during the 6-week PTU treatment period prevented vessel loss indicating the mechanism of arteriolar loss from hypothyroidism may result from vasoconstriction. These results suggest that thyroid hormone is a powerful regulator of vasculature in adult myocardium, particularly in low thyroid states.

摘要

无论是丙硫氧嘧啶(PTU)治疗还是甲状腺切除术引起的甲状腺功能低下,都会导致成年大鼠心肌中小动脉密度降低,而用甲状腺素或甲状腺激素类似物 3,5-二碘甲状腺原氨酸丙酸(DITPA)治疗则可预防这种情况。然而,许多与甲状腺功能减退引起的心脏病理生理变化和小动脉密度调节相关的问题仍未得到解答。将 Sprague-Dawley 大鼠用饮用水中的 PTU 处理 1、3 和 6 周,或用血管扩张剂双嘧达莫和 PTU 共同处理 6 周,或用 PTU 处理 6 周并停药 2 或 4 周。测定心脏质量、体重、心功能和心肌小动脉密度。PTU 治疗引起的甲状腺功能低下导致的小动脉丢失逐渐进展,3 周治疗后减少 22%,6 周治疗后减少 34%,仅停药 2 周后大部分得到逆转。在 6 周的 PTU 治疗期间联合使用血管扩张剂双嘧达莫可预防血管丢失,这表明甲状腺功能低下引起的小动脉丢失的机制可能是血管收缩。这些结果表明,甲状腺激素是成年心肌中血管的强大调节剂,特别是在甲状腺功能低下的情况下。

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