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自发性高血压大鼠血浆中的哇巴因

Ouabain in plasma from spontaneously hypertensive rats.

作者信息

Doris P A

机构信息

Department of Cell Biology and Anatomy, Texas Tech University Health Sciences Center, Lubbock 79430.

出版信息

Am J Physiol. 1994 Jan;266(1 Pt 2):H360-4. doi: 10.1152/ajpheart.1994.266.1.H360.

Abstract

Ouabain has recently been identified in mammalian plasma with an apparent adrenocortical origin. The objectives of the present study were to determine whether boiled plasma supernatants (BPS) from spontaneously hypertensive rats (SHR) contained elevated levels of material able to inhibit 86Rb uptake, an indicator of sodium pump activity, compared with Wistar-Kyoto rats (WKY). Furthermore, the effect of increasing dietary calcium content from 1 to 3% on 86Rb-uptake inhibitory activity in plasma was examined. BPS from SHR and WKY consuming 1% calcium contained sodium pump inhibitory activity equivalent to 16.43 +/- 0.23 and 5.08 +/- 0.10 ng ouabain/ml, respectively (P < 0.0001). Increasing dietary calcium intake to 3% reduced plasma ouabain-like activity (OLA) to 9.97 +/- 0.20 ng/ml (P < 0.0001) in SHR but was without effect in WKY (5.39 +/- 0.05; not significant). It was then determined whether the plasma 86Rb-uptake inhibition could be attributed to authentic ouabain. In WKY plasma pools the percentage of OLA attributable to authentic ouabain was 38.0% by radioimmunoassay and 56.7% by 86Rb-uptake assay. In SHR these values were 3.8% and < 7.1%, respectively. Whereas the data in the present study provide confirmation of the presence of ouabain in rat plasma, ouabain does not account for the elevated OLA in SHR plasma reported here and elsewhere. This hypertensinogenic cardiotonic steroid appears to be appropriately downregulated in SHR rats.

摘要

哇巴因最近在哺乳动物血浆中被发现,其明显起源于肾上腺皮质。本研究的目的是确定与Wistar - Kyoto大鼠(WKY)相比,自发性高血压大鼠(SHR)的煮沸血浆上清液(BPS)中是否含有能抑制86Rb摄取(钠泵活性指标)的物质的升高水平。此外,还研究了将饮食钙含量从1%增加到3%对血浆中86Rb摄取抑制活性的影响。食用1%钙的SHR和WKY的BPS中钠泵抑制活性分别相当于16.43±0.23和5.08±0.10 ng哇巴因/毫升(P<0.0001)。将饮食钙摄入量增加到3%可使SHR血浆中的哇巴因样活性(OLA)降至9.97±0.20 ng/毫升(P<0.0001),但对WKY无影响(5.39±0.05;无显著性差异)。然后确定血浆中86Rb摄取抑制是否可归因于真正的哇巴因。在WKY血浆池中,通过放射免疫测定法,真正哇巴因占OLA的百分比为38.0%,通过86Rb摄取测定法为56.7%。在SHR中,这些值分别为3.8%和<7.1%。尽管本研究中的数据证实了大鼠血浆中存在哇巴因,但哇巴因并不能解释此处及其他地方报道的SHR血浆中OLA的升高。这种具有致高血压作用的强心甾类物质在SHR大鼠中似乎被适当下调。

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