Endogenous digitalis-like compounds in essential and experimental hypertension.

M. Devynck, M. Pernollet, P. Meyer
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引用次数: 10

Abstract

The hypothesis that endogenous digitalis-like compounds might participate in body sodium and water homeostasis have led us to investigate the presence in plasma of compounds interacting with digoxin antibodies in man and rats. The apparent levels of digoxin-equivalents in plasma of control subjects (n = 21) and patients with essential hypertension (n = 48) or end-stage renal failure (n = 13) were 24.7 +/- 3.2, 34.4 +/- 4.4 and 98.7 +/- 17.4 pg/ml, p less than 0.05 and p less than 0.01 respectively. Positive correlations were observed between systolic and diastolic blood pressure and the apparent immunoreactivity of plasma. No relationship was found with the renal Na+ excretion or the plasma renin activity. The apparent digoxin-like immunoreactivity of the plasma was correlated with its ability to inhibit ouabain binding to the erythrocyte Na+ pump and to reduce the renal Na+,K+-ATPase activity. In rats with experimental hypertension, the plasma cross-reactivity with antidigoxin antibodies was also enhanced when compared to control rats (71.6 +/- 10.2 pg/ml, n = 12 and 57.3 +/- 5.0 pg/ml, n = 33 in Na+ loaded rats and in rats with reduced renal mass respectively compared to 43.4 +/- 3.7 pg/ml, n = 36, p less than 0.05). In spontaneously hypertensive rats (SHR), the apparent levels of digoxin- equivalents were higher than that of age-matched WKY normotensive rats. This increase was already present in prehypertensive SHR (3 week-old) (105.8 +/- 12.4 vs 40.0 +/- 6.5 pg/ml, n = 9 and 8, p less than 0.001) and persisted after hypertension has developed (134 +/- 12.6 vs 85 +/- 7.9 pg/ml, n = 7 and 8, p less than 0.005 in 30 week-old rats). The apparent affinity of the erythrocyte Na+,K+ cotransport for intracellular Na+ and the maximal rate of the Na+ pump were correlated with the plasma digoxin-like levels. These results confirm the presence in plasma of compounds possessing some of the functional and structural properties of cardioactive steroids, associated with a rise in blood pressure.
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内源性洋地黄样化合物在原发性和实验性高血压中的作用。
内源性洋地黄样化合物可能参与体内钠和水稳态的假设使我们研究了在人和大鼠血浆中与地高辛抗体相互作用的化合物的存在。对照组(n = 21)、原发性高血压(n = 48)和终末期肾衰竭(n = 13)患者血浆地高辛等效物表观水平分别为24.7 +/- 3.2、34.4 +/- 4.4和98.7 +/- 17.4 pg/ml, p < 0.05和p < 0.01。收缩压和舒张压与血浆表观免疫反应性呈正相关。与肾Na+排泄和血浆肾素活性无相关性。血浆中明显的地高辛样免疫反应性与其抑制乌阿巴因与红细胞Na+泵结合和降低肾Na+,K+- atp酶活性的能力相关。在实验性高血压大鼠中,与对照大鼠相比,血浆抗地高辛抗体的交叉反应性也有所增强(Na+负荷大鼠和肾块减少大鼠分别为71.6 +/- 10.2 pg/ml, n = 12和57.3 +/- 5.0 pg/ml, n = 33,而肾块减少大鼠分别为43.4 +/- 3.7 pg/ml, n = 36, p < 0.05)。在自发性高血压大鼠(SHR)中,地高辛等价物的表观水平高于年龄匹配的WKY正常大鼠。这种增加在高血压前期(3周龄)SHR中已经存在(105.8 +/- 12.4 vs 40.0 +/- 6.5 pg/ml, n = 9和8,p < 0.001),并在高血压发生后持续存在(134 +/- 12.6 vs 85 +/- 7.9 pg/ml, n = 7和8,30周龄大鼠中p < 0.005)。红细胞Na+、K+共转运对胞内Na+的表观亲和力和Na+泵的最大速率与血浆地高辛样水平相关。这些结果证实,血浆中存在具有心脏活性类固醇某些功能和结构特性的化合物,这些化合物与血压升高有关。
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