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心房肽对慢性肾衰竭患者的影响。

The effects of atrial peptide in humans with chronic renal failure.

作者信息

Windus D W, Stokes T J, Morgan J R, Klahr S

机构信息

Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Am J Kidney Dis. 1989 Jun;13(6):477-84. doi: 10.1016/s0272-6386(89)80005-8.

Abstract

The role of atrial peptide in humans with chronic renal insufficiency is uncertain. Therefore, the effects of synthetic atrial peptide (atriopeptin III, 24 amino acids) infusion on renal function and solute excretion were examined in 16 subjects with chronic renal insufficiency of diverse etiologies. After a two-hour baseline period, atrial peptide was infused for four hours in doses ranging from 0.005 to 0.1 micrograms/kg/min. When all doses were combined, absolute and fractional excretions of sodium increased significantly from baseline values (130 +/- 15 to 231 +/- 28 microEq/min and 3.57 +/- 0.57 to 6.03 +/- 1.26%, respectively, P less than 0.05). Significant increases in urinary excretion of chloride, calcium, and phosphorus were also seen during atrial peptide infusion. Increased absolute and fractional phosphorus excretion persisted during the two-hour postinfusion period, while excretion of other solutes returned to baseline. Glomerular filtration rate (GFR) increased by greater than 20% in five of 16 subjects. Two subjects with severe renal insufficiency (GFR = 9 and 12 mL/min) had no apparent response to atrial peptide infusion. Subjects receiving doses of 0.05 and 0.1 microgram/kg/min had significant falls of mean arterial pressure by the last hour of infusion. A dose-dependent effect of atrial peptide on sodium excretion was suggested, but not statistically significant. No apparent dose-dependent effect was seen on GFR or other solute excretions. Despite the presence of chronic renal insufficiency, atrial peptide increased renal solute excretion in most subjects. The demonstration that atrial peptide retains its diuretic and natriuretic effect in the presence of renal insufficiency supports the hypothesis that atrial peptide plays an important adaptive role in sodium homeostasis of the failing kidney.

摘要

心房肽在慢性肾功能不全患者中的作用尚不确定。因此,我们对16例病因各异的慢性肾功能不全患者进行了研究,观察合成心房肽(心房肽III,24个氨基酸)输注对肾功能和溶质排泄的影响。在两小时的基线期后,以0.005至0.1微克/千克/分钟的剂量输注心房肽4小时。当所有剂量合并计算时,钠的绝对排泄量和分数排泄量较基线值显著增加(分别从130±15增加至231±28微当量/分钟,以及从3.57±0.57%增加至6.03±1.26%,P<0.05)。在输注心房肽期间,氯化物、钙和磷的尿排泄量也显著增加。输注后两小时内,磷的绝对排泄量和分数排泄量持续增加,而其他溶质的排泄量恢复至基线水平。16例患者中有5例的肾小球滤过率(GFR)增加超过20%。两名严重肾功能不全患者(GFR分别为9和12毫升/分钟)对心房肽输注无明显反应。接受0.05和0.1微克/千克/分钟剂量的患者在输注最后一小时平均动脉压显著下降。提示心房肽对钠排泄有剂量依赖性作用,但无统计学意义。未观察到心房肽对GFR或其他溶质排泄有明显的剂量依赖性作用。尽管存在慢性肾功能不全,但大多数患者输注心房肽后肾溶质排泄增加。心房肽在肾功能不全时仍保留其利尿和利钠作用,这一发现支持了心房肽在衰竭肾脏的钠稳态中起重要适应性作用的假说。

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