Gomez-Sanchez E P
Endocrinology. 1986 Feb;118(2):819-23. doi: 10.1210/endo-118-2-819.
There is suggestive evidence for the direct participation of mineralocorticoids in the production of centrally mediated hypertension. Unilaterally nephrectomized Sprague-Dawley rats received a continuous infusion for 30 days using implanted osmotic minipumps with 1) artificial spinal fluid (CSF) intracerebroventricularly (icvt); 2) 0.005 micrograms aldosterone/h icvt; 3) 0.005 micrograms aldosterone/h sc; 4) 0.5 micrograms aldosterone/h sc. There was no significant difference between the groups in average weight gain (52 +/- 2 g) or organ weight to body weight, nor was urine volume increased above normal except in the group receiving the high sc dose of aldosterone. Blood pressure was significantly elevated only in those animals receiving 0.005 micrograms aldosterone/h icvt and 0.5 micrograms aldosterone/h sc. A second experiment was done using a specific spironolactone-type mineralocorticoid antagonist, prorenone. The rats were grouped as follows: 1) CSF icvt; 2) 0.005 micrograms/h aldosterone icvt; 3) 0.005 micrograms/h aldosterone plus 0.005 micrograms/h prorenone icvt; 4) 0.005 micrograms/h aldosterone plus 0.02 micrograms/h prorenone icvt; 5) 0.02 micrograms/h prorenone icvt. This study confirmed that this minute dose of aldosterone infused icvt produced a statistically significant increase in blood pressure with no increase in urine volume. Both the low, 0.005 micrograms/h, and high, 0.02 micrograms/h, doses of prorenone antagonized the pressor effect of aldosterone when infused with aldosterone into the lateral cerebral ventricle. The groups receiving 0.02 micrograms/h prorenone icvt or CSF icvt did not differ significantly in those parameters measured. A dose of aldosterone that was too small to produce changes in blood pressure when infused systemically was found to produce hypertension without polydypsia/polyuria when infused intrathecally. This pressor effect could be blocked by the concomitant infusion of a specific antagonist, prorenone. The study presented offers strong circumstantial evidence supporting a direct hypertensinogenic effect of aldosterone within the central nervous system.
有提示性证据表明盐皮质激素直接参与中枢介导性高血压的产生。单侧肾切除的斯普拉格 - 道利大鼠使用植入式渗透微型泵持续输注30天,输注的物质分别为:1)人工脑脊液(CSF)经脑室(icvt);2)0.005微克醛固酮/小时经脑室;3)0.005微克醛固酮/小时皮下注射;4)0.5微克醛固酮/小时皮下注射。各组在平均体重增加(52±2克)或器官重量与体重之比方面无显著差异,除接受高剂量皮下注射醛固酮的组外,尿量也未高于正常水平。仅在接受0.005微克醛固酮/小时经脑室和0.5微克醛固酮/小时皮下注射的动物中,血压显著升高。第二项实验使用了一种特异性螺内酯类盐皮质激素拮抗剂——孕烯诺龙。大鼠分组如下:1)脑脊液经脑室;2)0.005微克/小时醛固酮经脑室;3)0.005微克/小时醛固酮加0.005微克/小时孕烯诺龙经脑室;4)0.005微克/小时醛固酮加0.02微克/小时孕烯诺龙经脑室;5)0.02微克/小时孕烯诺龙经脑室。该研究证实,经脑室输注的这一微小剂量醛固酮在尿量未增加的情况下使血压产生了具有统计学意义的升高。当与醛固酮一起注入侧脑室时,低剂量(0.005微克/小时)和高剂量(0.02微克/小时)的孕烯诺龙均拮抗了醛固酮的升压作用。接受0.02微克/小时孕烯诺龙经脑室或脑脊液经脑室的组在测量的参数方面无显著差异。当经全身输注时剂量过小而无法引起血压变化的醛固酮,经鞘内输注时却能在不伴有烦渴/多尿的情况下产生高血压。这种升压作用可被同时输注特异性拮抗剂孕烯诺龙所阻断。本研究提供了有力的间接证据,支持醛固酮在中枢神经系统内具有直接的致高血压作用。