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从单个大鼠心肌细胞中释放心房利钠肽。

Release of atrial natriuretic peptide from individual rat cardiocytes.

作者信息

Miller H A, Southerland C M

机构信息

Department of Biological Sciences, East Tennessee State University, Johnson City 37614.

出版信息

Endocr Res. 1990;16(3):347-60. doi: 10.1080/07435809009033011.

Abstract

Atrial natriuretic peptide (ANP) is released from the atria and acts to regulate blood volume and pressure. The release of ANP appears to be stimulated by atrial distension, initiated by stretch on the cardiocytes. The purpose of the present study was to develop an assay that would allow for the detection of ANP release from single, isolated cells in the absence of distension. Using the reverse hemolytic plaque assay and antibody raised against human-alpha ANP, the release of ANP was detected from trypsin dissociated rat atrial cells. The specificity of the assay was demonstrated by a 67% reduction in ANP plaque forming cells detected following preabsorption of the anti-sera with rat-alpha ANP. The assay also proved efficient in monitoring changes in ANP secreting cell populations, where an acute treatment with dexamethasone resulted in a doubling of the percentage of atrial cardiocytes detected within a 4 hour antibody incubation. Finally, the assay established that about 52% of the dispersed atrial cardiocytes release ANP. The establishment of a plaque assay for ANP release should assist in addressing questions concerning what hormones may regulate ANP secretion directly and also allow for the determination of ANP secreting cell population dynamics.

摘要

心房利钠肽(ANP)由心房释放,作用是调节血容量和血压。ANP的释放似乎是由心房扩张刺激的,这种扩张由心肌细胞的拉伸引发。本研究的目的是开发一种检测方法,能够在不存在扩张的情况下检测单个分离细胞释放的ANP。使用反向溶血空斑试验和针对人α-ANP产生的抗体,从胰蛋白酶解离的大鼠心房细胞中检测到了ANP的释放。用大鼠α-ANP预吸收抗血清后,检测到的ANP空斑形成细胞减少了67%,证明了该检测方法的特异性。该检测方法还被证明可有效监测ANP分泌细胞群体的变化,地塞米松急性处理导致在4小时抗体孵育内检测到的心房心肌细胞百分比增加了一倍。最后,该检测方法确定约52%的分散心房心肌细胞释放ANP。建立ANP释放的空斑试验应有助于解决关于哪些激素可能直接调节ANP分泌的问题,也有助于确定ANP分泌细胞群体的动态变化。

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