肌节功能障碍和klotho基因表达缺陷的小鼠的早期意外死亡
Kyosuke Takeshita1, Toshihiko Fujimori, Yoko Kurotaki
1Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Circulation
|March 24, 2004
概括
在小鼠中,克洛托基因缺陷会导致鼻腔节点功能障碍和在压力下突然死亡. 克洛托在压力期间对心脏起器功能至关重要.
科学领域:
- 心血管生理学心血管生理学
- 遗传学 是一个遗传学.
- 衰老研究研究 衰老研究
背景情况:
- 克洛托基因缺陷 (kl/kl小鼠) 会导致与年龄相关的疾病和过早死亡.
- 在kl/kl小鼠中过早死亡的根本原因尚不清楚.
研究的目的:
- 调查克洛托基因在压力诱导死亡率中的作用.
- 为了确定心脏功能和klotho在klotho缺乏小鼠的局部化.
主要方法:
- 对kl/kl小鼠和野生型 (WT) 小鼠进行束应力.
- 评估了心率,血北上腺素和自主功能.
- 执行药理阻塞和过度驱动节奏.
- 分析了孤立的鼻节准备剂.
- 使用一个klotho-null记者基因系统 (kl(-geo)) 来确定klotho定位.
主要成果:
- kl/kl小鼠在压力期间表现出高的突然死亡率,与节功能障碍有关.
- 在压力下,kl/kl小鼠的心率和北上腺素没有增加.
- kl/kl小鼠表现出明显较低的内在心率和较长的鼻节恢复时间.
- 克洛托表达完全局限于心脏中的鼻节点.
结论:
- 克洛托基因表达对于心腔节点作为压力下的起器的功能至关重要.
- 心脏的鼻节点是有关心脏起器功能的klotho表达的主要部位.
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