首页> 美国卫生研究院文献>Physiological Genomics >Systems Biology and Polygenic Traits: Elevated K+ channel activity opposes vasoconstrictor response to serotonin in cerebral arteries of the Fawn Hooded Hypertensive rat
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Systems Biology and Polygenic Traits: Elevated K+ channel activity opposes vasoconstrictor response to serotonin in cerebral arteries of the Fawn Hooded Hypertensive rat

机译:系统生物学和多基因性状:K +通道活性升高与小鹿派生的高血压大鼠脑动脉中对5-羟色胺的血管收缩反应相反。

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摘要

Previous studies suggest that middle cerebral arteries (MCAs) of Fawn Hooded Hypertensive (FHH) rats exhibit impaired myogenic response and introgression of a small region of Brown Norway chromosome 1 containing 15 genes restored the response in FHH.1BN congenic rat. The impaired myogenic response in FHH rats is associated with an increase in the activity of the large conductance potassium (BK) channel in vascular smooth muscle cells (VSMCs). The present study examined whether the increased BK channel function in FHH rat alters vasoconstrictor response to serotonin (5-HT). Basal myogenic tone and spontaneous myogenic response of the MCA was attenuated by about twofold and about fivefold, respectively in FHH compared with FHH.1BN rats. 5-HT (0.1 μM)-mediated vasoconstriction was about twofold lower, and inhibition of the BK channel increased the vasoconstrictor response by about threefold in FHH compared with FHH.1BN rats. 5-HT (3 μM) decreased BK channel and spontaneous transient outward currents in VSMCs isolated from FHH.1BN but had no effect in FHH rats. 5-HT significantly depolarized the membrane potential in MCAs of FHH.1BN than FHH rats. Blockade of the BK channel normalized 5-HT-induced depolarization in MCAs of FHH rats. The 5-HT-mediated increase in cytosolic calcium concentration was significantly reduced in plateau phase in the VSMCs of FHH relative to FHH.1BN rats. These findings suggest that sequence variants in the genes located in the small region of FHH rat chromosome 1 impairs 5-HT-mediated vasoconstriction by decreasing its ability to inhibit BK channel activity, depolarize the membrane and blunt the rise in cytosolic calcium concentration.
机译:先前的研究表明,小鹿头型高血压(FHH)大鼠的中脑动脉(MCA)表现出生肌反应受损,布朗挪威1号染色体小区域的渗入恢复了FHH中的反应。1 BN 同基因大鼠。 FHH大鼠的肌源性反应受损与血管平滑肌细胞(VSMC)中大电导钾(BK)通道活性的增加有关。本研究检查了FHH大鼠中增加的BK通道功能是否改变了对5-羟色胺(5-HT)的血管收缩反应。与FHH.1 BN 大鼠相比,FHH的MCA的基础肌张力和自发肌反应分别减弱了约两倍和约五倍。与FHH.1 BN 大鼠相比,5-HT(0.1μM)介导的血管收缩降低了约两倍,并且BK通道的抑制使FHH的血管收缩反应增加了约三倍。 5-HT(3μM)降低了从FHH.1 BN 分离的VSMC中的BK通道和自发的瞬时外向电流,但对FHH大鼠没有影响。 5-HT显着使FHH.1 BN 的MCA细胞膜电位去极化。在FHH大鼠的MCA中,BK通道的阻滞使5-HT诱导的去极化归一化。与FHH.1 BN 大鼠相比,FHH VSMC中5-HT介导的胞质钙浓度增加明显减少。这些发现表明,位于FHH大鼠1号染色体小区域的基因中的序列变异体通过降低其抑制BK通道活性,使膜去极化和抑制胞质钙浓度升高的能力而损害了5-HT介导的血管收缩。

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