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心房利钠肽在双肾切除大鼠体内血液浓缩和降压活性的剂量依赖性及可逆性

Dose-dependence and reversibility of the hemoconcentrating and hypotensive activities of atrial natriuretic peptide in binephrectomized rats.

作者信息

Valentin J P, Sechi L A

机构信息

Department of Medicine, Centre Hospitalier Universitaire, Montpellier, France.

出版信息

Fundam Clin Pharmacol. 1994;8(3):238-45. doi: 10.1111/j.1472-8206.1994.tb00804.x.

DOI:10.1111/j.1472-8206.1994.tb00804.x
PMID:7927119
Abstract

In addition to its blood pressure lowering effect, atrial natriuretic peptide (ANP) infusion, increases hematocrit and decreases plasma volume by inducing a transfer of plasma fluid from the vascular to the interstitial compartment. We explored the dose-dependence as well as the reversibility of these actions by measuring changes in mean arterial pressure (MAP), hematocrit and plasma protein concentration (PPC) in anesthetized acutely binephrectomized Sprague-Dawley rats. Infusion of ANP (10, 100 or 1000 ng/kg/min for 45 min) dose-dependently reduced MAP (+2.3 +/- 1.8, -5.8 +/- 2.5 and -8.6 +/- 1.3%) and increased hematocrit (1.7 +/- 0.4, 8.1 +/- 0.4 and 9.0 +/- 0.6%), corresponding to calculated decreases in plasma volume of 3.0 +/- 0.6, 13.1 +/- 0.6 and 14.4 +/- 0.9% respectively. PPC increased significantly less than expected for a plasma volume reduction without proteins extravasation indicating that some loss of plasma proteins occurred in response to ANP. Both the reduction in MAP and plasma volume were reversible within 45 min after discontinuation of ANP infusion. During the recovery period, PPC decreased to values lower than baseline suggesting that the hemodilution was not associated with a detectable return of proteins into the circulation. Thus, in binephrectomized rats, infusion of ANP induced a dose-dependent and reversible reduction in arterial pressure and plasma volume through an extrarenal mechanism. Moreover, ANP dose-dependently increased the vascular permeability to proteins; the escaped proteins remained out of the vascular space for at least the duration of the experiment (ie 45 min post-infusion).

摘要

除了具有降血压作用外,输注心房利钠肽(ANP)可通过诱导血浆液体从血管腔转移至间质腔,从而增加血细胞比容并减少血浆容量。我们通过测量麻醉状态下急性双侧肾切除的Sprague-Dawley大鼠的平均动脉压(MAP)、血细胞比容和血浆蛋白浓度(PPC)的变化,探究了这些作用的剂量依赖性以及可逆性。输注ANP(10、100或1000 ng/kg/min,持续45分钟)可剂量依赖性地降低MAP(分别为+2.3±1.8、-5.8±2.5和-8.6±1.3%)并增加血细胞比容(分别为1.7±0.4、8.1±0.4和9.0±0.6%),相应地计算出的血浆容量减少分别为3.0±0.6、13.1±0.6和14.4±0.9%。在没有蛋白质外渗的情况下,PPC的增加显著低于血浆容量减少时预期的值,这表明响应ANP会发生一些血浆蛋白的丢失。MAP和血浆容量的降低在停止输注ANP后45分钟内均可逆。在恢复期,PPC降至低于基线的值,这表明血液稀释与可检测到的蛋白质回流入循环无关。因此,在双侧肾切除的大鼠中,输注ANP通过肾外机制诱导动脉压和血浆容量呈剂量依赖性且可逆的降低。此外,ANP剂量依赖性地增加血管对蛋白质的通透性;逸出的蛋白质至少在实验期间(即输注后45分钟)仍留在血管外空间。

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