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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Potential for endothelin-1-mediated impairment of contractile activity in hypertension.
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Potential for endothelin-1-mediated impairment of contractile activity in hypertension.

机译:内皮素-1-介导的高血压中收缩活性的损害障碍。

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1. The present study examined the potential for reduced exercise capacity observed in hypertensive patients as a result of elevated levels of endothelin (ET)-1. We have previously reported that ET-1 exerts low-dose stimulatory or high-dose inhibitory effects on the metabolism of the rat isolated perfused hindlimb from its vasoconstrictor activity. 2. Herein, we determined whether there are similar effects on tension development by the rat isolated constant-flow hindlimb during ET-1-mediated vasoconstriction. 3. The dose-dependent vasoconstrictor effects of ET-1 on metabolism in contracting muscle were the same as those observed previously in resting muscle. Highest concentrations of ET-1 gave rise to a transient stimulation followed by a marked inhibition of tension development, consistent with a decrease in aerobic capacity of the muscle. The vasoconstriction due to the higher doses of ET-1 was not dilated by electrical stimulation. 4. In conclusion, the biphasic nature of the actions of ET-1 suggeststhat although lower concentrations of ET-1 do not affect exercise capacity, higher concentrations that may occur in hypertension are inhibitory to metabolism and aerobic capacity of muscle. The inhibitory effects of ET-1 appear to result from enhanced functional shunting.
机译:本研究检测了由于内皮素水平升高(ET)-1的高血压患者中观察到的运动能力降低的可能性。我们此前报道,ET-1对来自其血管收缩剂活性的灌注后的Hindlimb分离的大鼠的代谢施加低剂量刺激或高剂量抑制作用。这里,我们确定在ET-1介导的血管收缩期间对大鼠分离的恒定流动后肢张力发育是否存在类似的效果。 3. ET-1对收缩肌肉代谢对代谢的剂量依赖性血管收缩剂效应与先前在静息肌肉中观察到的相同。最高浓度的ET-1产生了瞬时刺激,然后显着抑制张力发育,这一致一致,符合肌肉的有氧能力的降低。由于电刺激而不是较高剂量的ET-1引起的血管收缩。结果总之,ET-1 BuistSthat的行为的双相性质虽然较低浓度的ET-1不影响运动能力,高血压可能发生的更高浓度是代谢和肌肉的有氧能力的抑制作用。 ET-1的抑制作用似乎是增强的功能分流。

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