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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Role of brain ouabainlike compound in central nervous system-mediated natriuresis in rats.
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Role of brain ouabainlike compound in central nervous system-mediated natriuresis in rats.

机译:脑哇巴因样化合物在大鼠中枢神经系统介导的利尿作用中的作用。

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摘要

Intracerebroventricular infusion of artificial sodium-rich cerebrospinal fluid induces increases in blood pressure and urinary sodium excretion. To examine the role of brain ouabainlike compound in these central nervous system-mediated responses, we evaluated the effects of prior intracerebroventricular injection of the Fab fragments of digoxin-specific antibody (Digibind, 10 mg/mL, 10 microL) on changes in blood pressure and urinary sodium excretion after intracerebroventricular infusion of high-sodium (323 mmol/L, 150 microL/kg per 15 minutes) cerebrospinal fluid in anesthetized rats. Antiouabain action of Digibind was revealed by the inhibition of a contractile response to ouabain in guinea pig aorta. Similar significant increases in blood pressure were found in rats that received preinjection of Digibind (n = 14) compared with control rats that received injection of saline (n = 5) or normal sheep IgG (n = 8). In rats pretreated with Digibind the natriuretic responses to central high sodium were significantly diminished by 68% (P < .05) or 82% (P < .05) compared with rats treated with saline or normal IgG, respectively. In contrast, Digibind did not affect either pressor or natriuretic responses to intracerebroventricular angiotensin II (600 ng/30 microL per 10 minutes). These data indicate that Digibind significantly inhibits increases in renal sodium excretion in response to high central sodium and suggest that brain ouabainlike compound may be involved in central nervous system-mediated natriuresis with nonpressor mechanisms.
机译:脑室内注入富含钠的人工脑脊液会导致血压升高和尿钠排泄增加。为了检查脑哇巴因样化合物在这些中枢神经系统介导的反应中的作用,我们评估了事先脑室内注射地高辛特异性抗体(Digibind,10 mg / mL,10 microL)的Fab片段对血压变化的影响麻醉大鼠脑室内输注高钠(323 mmol / L,150 microL / kg每15分钟)的脑脊液后尿液和尿钠排泄。 Digibind的抗哇巴因作用是通过抑制豚鼠主动脉中对哇巴因的收缩反应来揭示的。与注射盐水(n = 5)或正常羊IgG(n = 8)的对照大鼠相比,预先注射Digibind的大鼠(n = 14)的血压有相似的显着升高。与用生理盐水或正常IgG处理的大鼠相比,用Digibind预处理的大鼠的利钠钠对中枢高钠的反应分别显着降低了68%(P <.05)或82%(P <.05)。相反,Digibind既不影响对脑室内血管紧张素II(每10分钟600 ng / 30 microL)的升压或利钠反应。这些数据表明,Digibind可显着抑制对高中枢钠的反应而引起的肾钠排泄的增加,并表明脑哇巴因样化合物可能以非加压机制参与中枢神经系统介导的钠尿。

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