基础医学与临床 ›› 2009, Vol. 29 ›› Issue (10): 1092-1096.

• 研究论文 • 上一篇    下一篇

甲状腺素对犬心房电生理特征和连接蛋白Cx43的影响

高崇瀚 宋凌鲲 李凡 戴引 殷跃辉   

  1. 重庆医科大学附属第二医院心血管内科 重庆医科大学附属第二医院心血管内科
  • 收稿日期:2008-11-11 修回日期:2009-02-13 出版日期:2009-10-20 发布日期:2009-10-20
  • 通讯作者: 殷跃辉

Effect of thyroid hormone on the electrophysiological properties and Cx43 of canine atria

Chong-han GAO, Ling-kun SONG, Fan LI, Yin DAI, Yue-hui YIN   

  1. Department of Cardiology, the Second Affiliated Hospital, Chongqing Medical University Department of Cardiology, the Second Affiliated Hospital, Chongqing Medical University
  • Received:2008-11-11 Revised:2009-02-13 Online:2009-10-20 Published:2009-10-20
  • Contact: Yue-hui YIN

摘要: 目的 研究甲状腺素对犬心房电生理特征和连接蛋白Cx43表达及分布的影响,探讨甲状腺功能亢进性心脏病(甲亢性心脏病)发生房颤的机制。方法 健康成年杂种犬16只,随机分为对照组(n=6)和实验组(n=10)。给实验组犬腹腔注射左旋甲状腺素(L-Thy)80μg/(kg·d),持续8个月,以建立犬甲亢动物模型,分别于0、2、4、6和8个月测定心房有效不应期(AERP),Western blot检测心房连接蛋白Cx43表达,激光共聚焦显微镜观察Cx43表达及分布的改变。 结果 和对照组相比,L-Thy组犬第4、6、8个月AERP明显缩短(P<0.05),左右心房Cx43表达显著下降(P<0.01),两组左房Cx43的表达量的差值显著高于两组右房Cx43表达量的差值(P<0.05),左右心房分布于细胞两端的Cx43显著减少(P<0.01)。结论 甲状腺激素导致的心房电重构和连接蛋白的重构是甲状腺激素所致心房重构过程的一部分,参与促成了甲亢性心脏病房颤的发生、发展及维持。

关键词: 甲状腺功能亢进, 连接蛋白, 缝隙连接, 心房颤动

Abstract: Objective To determine whether atrial tissue shows alterations in electrophysiological proterties and in the expression and distribution of Cx43 in dogs with hyperthyroidism induced by Levothyroxine. Methods Sixteen mongrel canines of either sex weighing 12-17kg were randomized into control group (n=6) and L-thy group (n=10). Levothyroxin (80μg/kg) was administered daily by intraperitoneal injection for 8 months to all dogs in the L-thy group. Every 2 months atrial effective refractory period (AERP) was measured in both groups. Atrial tissues were collected at the 8th month. The expression of Cx43 in atria was evaluated with western blot analysis. Cx43 in atria was located by immunofluorescence and detected with Laser Scanning Confocal Microscope. Results compared with the control group, AERP of the L-thy group in the 4th, 6th and 8th month was significantly shorter (P<0.05). Levothyroxine significantly reduced the expression of Cx43 in left and right atrial (P<0.01), and the heterogeneous Cx43 down-regulation between left and right atria in the L-thy group was significant (P<0.05). Connexin43 located at the intercalated disc of atrial myocardium in the L-thy group was significantly reduced (P<0.01). Conclusions Thyroid hormone leads to atrial electrical remodeling and gap junction remodeling, involving heterogeneous reduction in Cx43 expression and disturbance in the distribution of Cx43. These changes are components of a variety of remodeling processes necessary, although not causative, for AF to become sustained.

Key words: Hyperthyrodism, connexin, gap junction, atrial fibrillation

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