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仔猪生命最初 72 小时中心脏钠尿肽基因表达和血浆浓度。

Cardiac natriuretic Peptide gene expression and plasma concentrations during the first 72 hours of life in piglets.

机构信息

Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, 9 Blegdamsvej, DK-2100 Copenhagen, Denmark.

出版信息

Endocrinology. 2013 May;154(5):1864-72. doi: 10.1210/en.2012-2186. Epub 2013 Mar 28.

Abstract

Plasma measurement of cardiac natriuretic peptides constitutes promising markers of congenital heart disease. However, concentrations change rapidly and dramatically during the first days after delivery even in healthy neonates, which complicates clinical interpretation. It is unknown whether these changes in plasma concentrations are explained by corresponding changes in the cardiac gene expression. We quantified the chamber-specific mRNA levels of ANP (A-type natriuretic peptide) and BNP (B-type natriuretic peptide) and plasma pro-ANP and BNP-32 concentrations in healthy piglets during the first 72 hours of life (from 2 litters, n = 44). Chamber-specific ANP and BNP mRNA levels reflected hemodynamic neonate changes at birth but did not correlate with circulating natriuretic peptide concentrations. However, plasma pro-ANP and creatinine concentrations were closely correlated (P < .0001; r = 0.73). Plasma pro-ANP levels were highest on the day of delivery (5580 pmol/L [4320-6786] decreasing to 2484 pmol/L [1602-2898] after 72 hours, P < .0001). During the 72 hours, gel chromatography suggested that the translational products in circulation and in atrial tissue were immature, ie, unprocessed pro-ANP. In contrast to pro-ANP, BNP-32 plasma concentrations were low at delivery and peaked after 48 hours (12 [10.5-20.6] vs. 88.8 [71.7-101.4] pmol/L, P < .0001). To conclude, ANP and BNP gene expression differs considerably between cardiac chambers in the first 72 hours of life in healthy piglets, resembling the transition from fetal to neonate circulation. However, the cardiac gene expression does not explain plasma concentrations.

摘要

血浆心钠肽测量是先天性心脏病很有前途的标志物。然而,即使在健康新生儿中,其浓度在出生后最初几天也会迅速且显著地变化,这使得临床解释变得复杂。目前尚不清楚这些血浆浓度的变化是否是由心脏基因表达的相应变化引起的。我们在健康小猪出生后的前 72 小时内(来自 2 窝,n = 44),定量测量了心房型(ANP)和脑钠肽(BNP)以及血浆前 ANP 和 BNP-32 浓度的特定心室 mRNA 水平。特定心室的 ANP 和 BNP mRNA 水平反映了出生时的血液动力学新生儿变化,但与循环心钠肽浓度无关。然而,血浆前 ANP 和肌酐浓度密切相关(P <.0001;r = 0.73)。出生当天的血浆前 ANP 水平最高(5580 pmol/L [4320-6786],72 小时后降至 2484 pmol/L [1602-2898],P <.0001)。在 72 小时内,凝胶色谱法表明循环和心房组织中的翻译产物不成熟,即未加工的前 ANP。与前 ANP 相反,BNP-32 血浆浓度在出生时较低,48 小时后达到峰值(12 [10.5-20.6] vs. 88.8 [71.7-101.4] pmol/L,P <.0001)。总之,在健康小猪出生后的前 72 小时内,心房型和脑钠肽基因表达在各个心腔之间存在显著差异,类似于从胎儿循环向新生儿循环的过渡。然而,心脏基因表达并不能解释血浆浓度。

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