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血管紧张素II受体拮抗剂CV-11974与脑血流自动调节

Angiotensin II receptor antagonist CV-11974 and cerebral blood flow autoregulation.

作者信息

Vraamark T, Waldemar G, Strandgaard S, Paulson O B

机构信息

Department of Neurology, Rigshospitalet, Copenhagen, Denmark.

出版信息

J Hypertens. 1995 Jul;13(7):755-61.

PMID:7594439
Abstract

OBJECTIVE

To investigate whether the angiotensin II (Ang II) subtype 1 receptor (AT1) antagonist CV-11974 had a similar effect to angiotensin converting enzyme inhibitors on cerebral blood flow autoregulation in normotensive Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHR).

METHODS

Sixteen WKY rats and 16 SHR were given CV-11974 0.1 mg/kg intravenously and compared with two control groups (n = 16). Their cerebral blood flow was measured with the intracarotid xenon-133 injection method and blood pressure was raised by noradrenaline infusion and lowered by controlled haemorrhage in separate groups of rats. The limits of autoregulation were determined by computed least-sum-of-squares analysis.

RESULTS

The dose of CV-11974 given lowered blood pressure but did not influence baseline cerebral blood flow. In WKY rats the lower limit of autoregulation in control rats was 60 +/- 3 mmHg, whereas after CV-11974 administration it was 48 +/- 2 mmHg (P < 0.01). In SHR the corresponding values were 85 +/- 2 and 78 +/- 2 mmHg, respectively (P < 0.05). In WKY rats the upper limit of autoregulation in control rats was 144 +/- 5 mmHg, whereas after CV-11974 administration it was 126 +/- 7 mmHg (P < 0.05). In SHR the corresponding figures were 174 +/- 8 and 144 +/- 6 mmHg, respectively (P < 0.01).

CONCLUSION

Thus, the AT1 receptor antagonist, although it did not influence baseline cerebral blood flow, shifted the autoregulation curve towards lower blood pressure. This effect is similar to that of angiotensin converting enzyme inhibitors, and might be due to release of Ang II-dependent tone in the larger cerebral resistance vessels.

摘要

目的

研究血管紧张素II(Ang II)1型受体(AT1)拮抗剂CV - 11974对正常血压的Wistar - Kyoto(WKY)大鼠和自发性高血压大鼠(SHR)脑血流自动调节的作用是否与血管紧张素转换酶抑制剂相似。

方法

给16只WKY大鼠和16只SHR静脉注射0.1 mg/kg的CV - 11974,并与两个对照组(n = 16)进行比较。采用颈内动脉注射氙-133的方法测量它们的脑血流,在不同组的大鼠中通过输注去甲肾上腺素升高血压,并通过控制性出血降低血压。通过计算最小二乘法分析确定自动调节的限度。

结果

给予的CV - 11974剂量可降低血压,但不影响基线脑血流。在WKY大鼠中,对照组自动调节的下限为60±3 mmHg,而给予CV - 11974后为48±2 mmHg(P < 0.01)。在SHR中,相应的值分别为85±2和78±2 mmHg(P < 0.05)。在WKY大鼠中,对照组自动调节的上限为144±5 mmHg,而给予CV - 11974后为126±7 mmHg(P < 0.05)。在SHR中,相应的数字分别为174±8和144±6 mmHg(P < 0.01)。

结论

因此,AT1受体拮抗剂虽然不影响基线脑血流,但使自动调节曲线向较低血压方向移动。这种作用与血管紧张素转换酶抑制剂相似,可能是由于大脑较大阻力血管中Ang II依赖性张力的释放。

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