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慢性肾衰竭大鼠脑肾素-血管紧张素系统的上调

Upregulation of the brain renin-angiotensin system in rats with chronic renal failure.

作者信息

Nishimura M, Takahashi H, Yoshimura M

机构信息

Cardiovascular Division, Toujinkai Hospital, Iga, Kyoto, Japan.

出版信息

Acta Physiol (Oxf). 2007 Apr;189(4):369-77. doi: 10.1111/j.1748-1716.2006.01663.x.

Abstract

AIM

We investigated how the brain renin-angiotensin system is involved in regulation of the sympathetic activity and arterial pressure in rats with chronic renal failure.

METHODS

Systolic arterial pressure, heart rate and diurnal urinary noradrenaline excretion were measured for 12 weeks in spontaneously hypertensive rats (SHR) with or without subtotal nephrectomy. Expression of mRNAs related to the brain renin-angiotensin system was measured using polymerase chain reaction. Effects of a 6-day intracerebroventricular infusion of a type 1 angiotensin II receptor antagonist (candesartan) or bilateral dorsal rhizotomy on these variables were also investigated.

RESULTS

Systolic arterial pressure and urinary excretion of noradrenaline were consistently higher in subtotally nephrectomized SHR than in sham-operated SHR (262 +/- 5 vs. 220 +/- 3 mmHg, P < 0.001; 2.71 +/- 0.22 vs. 1.69 +/-0.19 ng g(-1) body weight day(-1), P < 0.001). Expression of renin, angiotensin-converting enzyme and type 1 angiotensin II receptor mRNAs in the hypothalamus and lower brainstem was greater in subtotally nephrectomized SHR than in sham-operated SHR. Continuous intracerebroventricular infusion of candesartan attenuated hypertension and the increase in urinary noradrenaline excretion in subtotally nephrectomized SHR. Dorsal rhizotomy decreased arterial pressure, urinary excretion of noradrenaline and expression of renin-angiotensin system-related mRNAs in brains of subtotally nephrectomized SHR.

CONCLUSION

The brain renin-angiotensin system in subtotally nephrectomized SHR appears to be activated via afferent nerves from the remnant kidney, resulting in sympathetic overactivity and hypertension in this chronic renal failure model.

摘要

目的

我们研究了脑肾素 - 血管紧张素系统如何参与慢性肾衰竭大鼠交感神经活动和动脉血压的调节。

方法

对有或无次全肾切除术的自发性高血压大鼠(SHR)测量收缩动脉压、心率和昼夜尿去甲肾上腺素排泄量,为期12周。使用聚合酶链反应测量与脑肾素 - 血管紧张素系统相关的mRNA表达。还研究了脑室内连续输注1型血管紧张素II受体拮抗剂(坎地沙坦)6天或双侧背根切断术对这些变量的影响。

结果

次全肾切除的SHR的收缩动脉压和去甲肾上腺素尿排泄量始终高于假手术的SHR(262±5 vs. 220±3 mmHg,P < 0.001;2.71±0.22 vs. 1.69±0.19 ng g⁻¹体重日⁻¹,P < 0.001)。次全肾切除的SHR下丘脑和低位脑干中肾素、血管紧张素转换酶和1型血管紧张素II受体mRNA的表达高于假手术的SHR。脑室内连续输注坎地沙坦可减轻次全肾切除的SHR的高血压和尿去甲肾上腺素排泄增加。背根切断术降低了次全肾切除的SHR的动脉压、去甲肾上腺素尿排泄量以及脑中肾素 - 血管紧张素系统相关mRNA的表达。

结论

次全肾切除的SHR中的脑肾素 - 血管紧张素系统似乎通过来自残余肾脏的传入神经被激活,导致该慢性肾衰竭模型中的交感神经过度活跃和高血压。

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