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Angiotensin-(1-12) is an alternate substrate for angiotensin peptide production in the heart

机译:血管紧张素-(1-12)是心脏中血管紧张素肽产生的另一种底物

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Identification of angiotensin-(1-12) as an intermediate precursor derived directly from angiotensinogenled us to explore whether the heart has the capacity to process angiotensin-(1-12) into biologically active angiotensin peptides. The generation of angiotensin I, angiotensin II, and angiotensin-(1-7) from exogenous angiotensin-(1-12) was evaluated in the effluent of isolated perfused hearts mounted on a Langendorff apparatus in three normotensiveand two hypertensive strains: Sprague-Dawley, Lewis, congenicmRen2.Lewis, Wistar-Kyoto, and spontaneously hypertensive rats. Hearts were perfused with Krebs solution for 60 min before and after the addition of angiotensin-(1-12) (10 nmol/l). Angiotensin-(1-12)caused the rapid appearance of both angiotensin I and angiotensin II in the perfusate that peaked between 30 and 60 min of recirculation. Production of angiotensin-(1-7) from exogenous angiotensin-(1-12) rose steadily over the course of the 60-min experiment. These data directly demonstrate that angiotensin-(1-12) is a substrate for the formation of angiotensin peptides in cardiac tissue. This finding further suggests that this angiotensinogen-derived product is a previously unrecognized important precursor peptide to the renin-angiotensinsystem cascade.
机译:血管紧张素-(1-12)作为直接从血管紧张素衍生的中间前体的鉴定使我们探索心脏是否具有将血管紧张素-(1-12)加工成生物活性血管紧张素肽的能力。在安装在Langendorff装置上的三个正常血压和两个高血压菌株中的分离灌注心脏的流出物中,评估了外源性血管紧张素(1-12)生成血管紧张素I,血管紧张素II和血管紧张素(1-7)的情况:Sprague-Dawley ,Lewis,congenicmRen2,Lewis,Wistar-Kyoto和自发性高血压大鼠。在添加血管紧张素-(1-12)(10 nmol / l)之前和之后,用Krebs溶液灌注心脏60分钟。血管紧张素-(1-12)在灌注液中迅速出现血管紧张素I和血管紧张素II,在循环30至60分钟之间达到峰值。在60分钟的实验过程中,外源性血管紧张素-(1-12)产生的血管紧张素-(1-7)稳定增长。这些数据直接证明血管紧张素-(1-12)是在心脏组织中形成血管紧张素肽的底物。该发现进一步表明,该血管紧张素原来源的产物是肾素-血管紧张素系统级联的先前未被识别的重要前体肽。

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