Manipulation of Nitric Oxide Levels via a Modified Hydroxyethyl Starch Molecule

被引:0
|
作者
Aksu, Ugur [1 ]
Ince, Can [2 ,3 ]
Baasner, Silke [4 ]
Hermle, Johannes [4 ]
Lupp, Corinna [4 ]
Heckmann, Dominik [4 ]
Nocken, Frank [4 ]
Westphal, Martin [4 ]
机构
[1] Istanbul Univ, Fac Sci, Dept Biol, Istanbul, Turkiye
[2] Univ Amsterdam, Acad Med Ctr, Dept Translat Physiol, Amsterdam, Netherlands
[3] Erasmus MC, Univ Med Ctr, Dept Intens Care Med, Rotterdam, Netherlands
[4] Fresenius Kabi Deutschland GmbH, Bad Homburg, Germany
关键词
Hydroxyethyl starch; Langendorff-perfused heart; Nitric oxide donor; Vasodilation; N-ACETYLPENICILLAMINE SNAP; RENAL OXYGENATION; HEMORRHAGIC-SHOCK; CRYSTALLOID RESUSCITATION; DONOR SIN-1; BLOOD-FLOW; HEART-RATE; RAT MODEL; MICROCIRCULATION; SEPSIS;
D O I
10.1016/j.jss.2022.08.005
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction: Although the improving effect of nitric oxide (NO) donors has experimentally been demonstrated in shock, there are still no NO donor medications clinically available. Thiol-nitrosothiol-hydroxyethyl starch (S-NO-HES) is a novel molecule consisting of NO coupled to a thiolated derivative of hydroxyethyl starch (HES). It was aimed to assess the ability of S-NO-HES to serve as an NO donor under a variety of in vitro simulated physiologic conditions, which might be the first step to qualify this molecule as a novel type of NO donor-fluid. Methods: We studied the effect of temperature on NO-releasing properties of S-NO-HES in blood, at 34 degrees C, 37 degrees C, and 41 degrees C. Ascorbic acid (Asc) and amylase were also tested in a medium environment. In addition, we evaluated the activity of S-NO-HES in the isolated aortic ring and Langendorff-perfused heart setup. Results: The NO release property of S-NO-HES was found at any temperature. Asc led to a significant increase in the production of NO compared to S-NO-HES incubation (P < 0.05). The addition of amylase together with Asc to the medium further increased the release of NO (P < 0.05). S-NO-HES exerted significant vasodilatory effects on phenylephrine precontracted aortic rings that were dose-dependent (P < 0.01). Furthermore, S-NO-HES significantly increased the heart rate and additionally reduced the duration of the cardiac action potential, as indicated by a reduction of QTc-B values (P < 0.01). Conclusions: We demonstrated for the first time that the S-NO-HES molecule exhibited its NO-releasing effects. The effectiveness of this new NO donor to substitute NO deficiency under septic conditions or in other indications needs to be studied. (C) 2022 Elsevier Inc. All rights reserved.
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页码:1 / 12
页数:12
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