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清醒大鼠基础状态及容量扩张刺激后的血浆心房钠尿肽浓度与血流动力学:内肽酶抑制剂SCH 39.370及清除受体配体C-ANF-(4-23)的作用

Basal and volume expansion-stimulated plasma atrial natriuretic peptide concentrations and hemodynamics in conscious rats: effects of SCH 39.370, an endopeptidase inhibitor, and C-ANF-(4-23), a clearance receptor ligand.

作者信息

Kukkonen P, Vuolteenaho O, Ruskoaho H

机构信息

Department of Pharmacology, University of Oulu, Finland.

出版信息

Endocrinology. 1992 Feb;130(2):755-65. doi: 10.1210/endo.130.2.1531129.

Abstract

The effects of a neutral endopeptidase (NEP) inhibitor, SCH 39.370, and a clearance receptor ligand, C-atrial natriuretic factor-(4-23) [C-ANF-(4-23)] on the plasma concentration of atrial natriuretic peptide (ANP) and hemodynamics under basal conditions and during increased circulating ANP levels produced by acute volume loading in conscious rats were studied. Measurements of plasma immunoreactive N-terminal fragment of pro-ANP (IR-NT-ANP) concentrations were used to characterize the endogenous secretion of the biologically active peptide in response to drug infusions and volume expansion. Infusion of SCH 39.370 increased plasma IR-ANP levels dose-dependently in conscious normotensive Wistar rats; maximal increases of 17% (P less than 0.02) after the dose of 3 mg/kg, iv, and 67% (P less than 0.002) after the dose of 10 mg/kg, iv, SCH 39.370 were noted. Similarly, infusion of C-ANF-(4-23) alone (30 micrograms/kg, iv bolus, followed by infusion of 3 micrograms/kg.min for 30 min) increased plasma IR-ANP levels by 37% (P less than 0.001). Given in combination, SCH 39.370 and C-ANF-(4-23) produced a greater increase in plasma IR-ANP concentration (83%; P less than 0.001) than when either substance was infused alone. Neither SCH 39.370 nor C-ANF-(4-23), alone or in combination, had any effect on basal plasma IR-NT-ANP concentrations. The combination reduced mean arterial pressure (8 +/- 2 mm Hg; P less than 0.01) and right atrial pressure (0.67 +/- 0.20 mm Hg; P less than 0.01), while administration of SCH 39.370 or C-ANF-(4-23) alone had no effect on mean arterial pressure, heart rate, or right atrial pressure in conscious rats. Acute volume expansion with 0.9% saline (1.1 ml/100 g BW) resulted in an increase in right atrial pressure (2.7 +/- 0.2 mm Hg; P less than 0.001) as well as in plasma IR-ANP (55%; P less than 0.001) and IR-NT-ANP concentrations (24%; P less than 0.03). Volume expansion in rats pretreated with SCH 39.370 resulted in a greater increase in plasma IR-ANP concentrations than in control animals; the relative ANP increases corresponding to the 2.5-mm Hg increase in right atrial pressure were 1.48-, 1.69-, and 2.28-fold in control, 3 mg/kg SCH 39.370-treated, and 10 mg/kg SCH 39.370-treated groups, respectively. When the relation between changes from control in plasma IR-ANP and right atrial pressure in response to acute volume expansion was analyzed in the presence of C-ANF-(4-23), no difference was noted between control and treated rats.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

研究了中性内肽酶(NEP)抑制剂SCH 39.370和清除受体配体C型心房利钠肽(4-23)[C-ANF-(4-23)]对清醒大鼠基础状态下以及急性容量负荷导致循环中ANP水平升高时心房利钠肽(ANP)血浆浓度和血流动力学的影响。通过测量血浆中前ANP的免疫反应性N端片段(IR-NT-ANP)浓度,来表征生物活性肽在药物输注和容量扩张时的内源性分泌。在清醒的正常血压Wistar大鼠中,静脉注射SCH 39.370剂量依赖性地增加血浆IR-ANP水平;静脉注射3 mg/kg剂量后最大增加17%(P<0.02),静脉注射10 mg/kg剂量后最大增加67%(P<0.002)。同样,单独静脉注射推注C-ANF-(4-23)(30μg/kg),随后以3μg/(kg·min)输注30分钟,可使血浆IR-ANP水平升高37%(P<0.001)。联合使用时,SCH 39.370和C-ANF-(4-23)使血浆IR-ANP浓度升高幅度(83%;P<0.001)大于单独输注任何一种物质时。单独或联合使用SCH 39.370和C-ANF-(4-23)对基础血浆IR-NT-ANP浓度均无影响。联合用药降低了平均动脉压(8±2 mmHg;P<0.01)和右心房压(0.67±0.20 mmHg;P<0.01),而单独给予SCH 39.370或C-ANF-(4-23)对清醒大鼠的平均动脉压、心率或右心房压均无影响。用0.9%生理盐水(1.1 ml/100 g体重)进行急性容量负荷导致右心房压升高(2.7±0.2 mmHg;P<0.001),同时血浆IR-ANP升高(55%;P<0.001)和IR-NT-ANP浓度升高(24%;P<0.03)。用SCH 39.370预处理的大鼠容量负荷后血浆IR-ANP浓度升高幅度大于对照动物;对照、3 mg/kg SCH 39.370处理和10 mg/kg SCH 39.370处理组中,对应于右心房压升高2.5 mmHg时的相对ANP升高倍数分别为1.48倍、1.69倍和2.28倍。当在C-ANF-(4-23)存在的情况下分析急性容量负荷时血浆IR-ANP变化与右心房压变化之间的关系时,对照大鼠和处理大鼠之间未发现差异。(摘要截断于400字)

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