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肾交感神经张力在大鼠去氧皮质酮盐性高血压发生发展中的重要性。

Importance of renal sympathetic tone in the development of DOCA-salt hypertension in the rat.

作者信息

Katholi R E, Naftilan A J, Oparil S

出版信息

Hypertension. 1980 May-Jun;2(3):266-73. doi: 10.1161/01.hyp.2.3.266.

Abstract

In many experimental models, acute increases in sympathetic nervous system activity produce disproportionately greater vasoconstriction in the renal vascular bed than occurs in most other vascular beds. Since increased sympathetic nervous system activity has been implicated in the pathogenesis of DOCA-salt hypertension in the rat, we hypothesized that an attenuation of renal sympathetic tone would delay the development of this form of hypertension. Renal denervation was carried out in 5-week-old uninephrectomized male Sprague-Dawley rats 1 week before beginning DOCA-salt treatment. Systolic blood pressures using the tailcuff method in 32 sham-operated rats were significantly (p less than 0.05) elevated above control by Day five (115 +/- 3 vs 128 +/- 3 mm Hg) of DOCA-salt administration and continued to rise, reaching a plateau by Day 21 (192 +/- 5 mm Hg). In contrast, DOCA-salt administration in 32 renal denervated rats did not result in a significant elevation of blood pressure above control until Day 17 (121 +/- 3 vs 135 +/- 3 mm Hg, p less than 0.05). During the first 2 weeks of DOCA-salt treatment, fractional urinary sodium excretion was significantly greater (p less than 0.05) in renal denervated rats than in sham animals. During the third week of DOCA-salt administration, renal denervated rats had a rapid rise in blood pressure and a fall in fractional urinary sodium excretion to the level of the sham-operated animals. Coincident with the development of hypertension was a threefold increase in renal norepinephrine content (5.3 +/- 0.4 ng/g on Day 14 vs 17.7 +/- 3.0 ng/g on Day 24, p less than 0.01), suggesting reinnervation. These data suggest that increased renal sympathetic tone in the DOCA-salt rat facilitates sodium retention and is necessary for the development of the hypertension.

摘要

在许多实验模型中,交感神经系统活动的急性增加在肾血管床中产生的血管收缩程度,比在大多数其他血管床中发生的情况要大得多。由于交感神经系统活动增加与大鼠去氧皮质酮 - 盐性高血压的发病机制有关,我们推测肾交感神经张力的减弱会延迟这种高血压形式的发展。在开始去氧皮质酮 - 盐治疗前1周,对5周龄单肾切除的雄性斯普拉格 - 道利大鼠进行肾去神经支配。在32只假手术大鼠中,使用尾袖法测量的收缩压在去氧皮质酮 - 盐给药的第5天(115±3 vs 128±3 mmHg)显著(p小于0.05)高于对照组,并持续上升,在第21天达到平台期(192±5 mmHg)。相比之下,在32只肾去神经支配的大鼠中,去氧皮质酮 - 盐给药直到第17天(121±3 vs 135±3 mmHg,p小于0.05)才导致血压显著高于对照组。在去氧皮质酮 - 盐治疗的前2周,肾去神经支配的大鼠尿钠排泄分数显著高于假手术动物(p小于0.05)。在去氧皮质酮 - 盐给药的第三周,肾去神经支配的大鼠血压迅速升高,尿钠排泄分数降至假手术动物的水平。与高血压发展同时发生的是肾去甲肾上腺素含量增加了三倍(第14天为5.3±0.4 ng/g,第24天为17.7±3.0 ng/g,p小于0.01),提示再神经支配。这些数据表明,去氧皮质酮 - 盐大鼠肾交感神经张力增加促进钠潴留,并且是高血压发展所必需的。

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