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肾脏神经导致 Schlager BPH/2J 小鼠发生高血压。

Renal nerves contribute to hypertension in Schlager BPH/2J mice.

机构信息

Neuropharmacology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Australia.

Heart Failure Research Group, Baker Heart and Diabetes Institute, Melbourne, Australia.

出版信息

Hypertens Res. 2019 Mar;42(3):306-318. doi: 10.1038/s41440-018-0147-9. Epub 2018 Dec 10.

Abstract

Schlager mice (BPH/2J) are hypertensive due to a greater contribution of the sympathetic nervous system (SNS) and renin-angiotensin system (RAS). The kidneys of BPH/2J are hyper-innervated suggesting renal nerves may contribute to the hypertension. We therefore determined the effect of bilateral renal denervation (RD) on hypertension in BPH/2J. Mean arterial pressure (MAP) was measured by radiotelemetry before and for 3 weeks after RD in BPH/2J and BPN/3J. The effects of pentolinium and enalaprilat were examined to determine the contribution of the SNS and RAS, respectively. After 3 weeks, MAP was -10.9 ± 2.1 mmHg lower in RD BPH/2J compared to baseline and -2.1 ± 2.2 mmHg in sham BPH/2J (P < 0.001, n = 8-10). RD had no effect in BPN/3J (P > 0.1). The depressor response to pentolinium was greater in BPH/2J than BPN/3J, but in both cases the response in RD mice was similar to sham. Enalaprilat decreased MAP more in RD BPH/2J compared to sham (-12 vs -3 mmHg, P < 0.001) but had no effect in BPN/3J. RD reduced renal noradrenaline in both strains but more so in BPH/2J. RD reduced renin mRNA and protein, but not plasma renin in BPH/2J to levels comparable with BPN/3J mice. We conclude that renal nerves contribute to hypertension in BPH mice as RD induced a sustained fall in MAP, which was associated with a reduction of intrarenal renin expression. The lack of inhibition of the depressor effects of pentolinium and enalaprilat by RD suggests that vasoconstrictor effects of the SNS or RAS are not involved.

摘要

施拉格鼠(BPH/2J)由于交感神经系统(SNS)和肾素-血管紧张素系统(RAS)的贡献更大而患有高血压。BPH/2J 的肾脏过度神经支配,表明肾脏神经可能有助于高血压。因此,我们确定了双侧肾去神经支配(RD)对 BPH/2J 高血压的影响。在 RD 前后 3 周,通过无线电遥测测量 BPH/2J 和 BPN/3J 的平均动脉压(MAP)。分别检查戊烷和依那普利拉特的作用,以确定 SNS 和 RAS 的贡献。3 周后,RD BPH/2J 的 MAP 比基线低 10.9±2.1mmHg,而 sham BPH/2J 为 2.1±2.2mmHg(P<0.001,n=8-10)。RD 在 BPN/3J 中没有影响(P>0.1)。与 BPN/3J 相比,BPH/2J 的戊烷降压反应更大,但在这两种情况下,RD 小鼠的反应与 sham 相似。与 sham 相比,依那普利拉特使 RD BPH/2J 的 MAP 降低更多(-12 对-3mmHg,P<0.001),但对 BPN/3J 没有影响。RD 降低了两种品系的肾去甲肾上腺素,但在 BPH/2J 中降低更多。RD 降低了 BPH/2J 的肾素 mRNA 和蛋白,但对血浆肾素没有影响,使其与 BPN/3J 小鼠相当。我们得出结论,肾脏神经有助于 BPH 小鼠的高血压,因为 RD 引起了 MAP 的持续下降,这与肾内肾素表达的减少有关。RD 对 pentolinium 和 enalaprilat 的降压作用没有抑制作用表明,SNS 或 RAS 的血管收缩作用不参与其中。

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