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黏液溶解剂N-乙酰半胱氨酸和厄多司坦对人体止血的影响。

The Effects of Mucolytic Agents N-Acetylcysteine and Erdosteine on Hemostasis in Humans.

作者信息

Oktar S, Doğru S, Motor S, Demirköse M, Erden E Ş

机构信息

MD, PhD, Associate Professor in Pharmacology, Department of Pharmacology; University of Health Sciences, Beyhekim Training and Research Hospital, Konya, Turkey.

MD, Assistant Professor in Chest Diseases, Department of Chest Diseases; Gaziantep University, Medical School, Gaziantep, Turkey.

出版信息

Sovrem Tekhnologii Med. 2024;16(4):55-60. doi: 10.17691/stm2024.16.4.06. Epub 2024 Aug 30.

DOI:10.17691/stm2024.16.4.06
PMID:39881835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11773143/
Abstract

UNLABELLED

There are some indications in a few studies on animals and humans that the mucolytic agents N-acetylcysteine and erdosteine have a disruptive effect on the coagulation cascade. This study to examine the effects of both erdosteine and N-acetylcysteine on the coagulation pathway.

MATERIALS AND METHODS

The research was conducted on patients treated with N-acetylcysteine (600 mg/day) or erdosteine (600 mg/day) for 7-14 days. To evaluate the coagulation and hemogram parameters, blood samples were taken from patients before treatment and on days 7-14 after starting the treatment. Hemogram and coagulation parameters were measured in the venous blood samples.

RESULTS

The levels of factor II significantly decreased, and the platelet count significantly increased in patients treated with erdosteine. D-dimer levels reduced and factor VII levels increased in patients treated with N-acetylcysteine, but these changes were not significant (p=0.069 and p=0.062, respectively). Other coagulation and hemogram values did not change in both groups. Erdosteine may have a dualistic effect on the coagulation cascade through its different metabolites.

摘要

未标注

在一些针对动物和人类的研究中有迹象表明,黏液溶解剂N-乙酰半胱氨酸和厄多司坦对凝血级联反应有破坏作用。本研究旨在考察厄多司坦和N-乙酰半胱氨酸对凝血途径的影响。

材料与方法

对接受N-乙酰半胱氨酸(600毫克/天)或厄多司坦(600毫克/天)治疗7至14天的患者进行研究。为评估凝血和血常规参数,在治疗前以及开始治疗后第7至14天采集患者的血样。在静脉血样本中测量血常规和凝血参数。

结果

接受厄多司坦治疗的患者中,凝血因子II水平显著降低,血小板计数显著升高。接受N-乙酰半胱氨酸治疗的患者中,D-二聚体水平降低,凝血因子VII水平升高,但这些变化不显著(分别为p = 0.069和p = 0.062)。两组的其他凝血和血常规值均未改变。厄多司坦可能通过其不同代谢产物对凝血级联反应产生二元效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6155/11773143/e38e36b87bc5/STM-16-4-06-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6155/11773143/f0a90a0f6f77/STM-16-4-06-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6155/11773143/e38e36b87bc5/STM-16-4-06-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6155/11773143/f0a90a0f6f77/STM-16-4-06-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6155/11773143/e38e36b87bc5/STM-16-4-06-f2.jpg

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本文引用的文献

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N-Acetyl Cysteine Prevents Arterial Thrombosis in a Dose-Dependent Manner In Vitro and in Mice.N-乙酰半胱氨酸以剂量依赖的方式在体外和小鼠中预防动脉血栓形成。
Arterioscler Thromb Vasc Biol. 2024 Feb;44(2):e39-e53. doi: 10.1161/ATVBAHA.123.319044. Epub 2023 Dec 21.
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The Effect of Perioperative N-acetylcysteine on the Short and Long Term Outcomes in Pediatrics Undergoing Living-Donor Liver Transplantation.围手术期N-乙酰半胱氨酸对接受活体肝移植的儿科患者短期和长期预后的影响。
Int J Organ Transplant Med. 2021;12(1):12-20.
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Understanding the Role of the Antioxidant Drug Erdosteine and Its Active Metabolite on Methicillin Resistant Biofilm Formation.
了解抗氧化药物厄多司坦及其活性代谢产物在耐甲氧西林生物膜形成中的作用。
Antioxidants (Basel). 2021 Nov 29;10(12):1922. doi: 10.3390/antiox10121922.
4
Multifaceted Beneficial Effects of Erdosteine: More than a Mucolytic Agent.厄多司坦的多方面有益作用:不仅仅是黏液溶解剂。
Drugs. 2020 Nov;80(17):1799-1809. doi: 10.1007/s40265-020-01412-x.
5
Efficacy and safety profile of mucolytic/antioxidant agents in chronic obstructive pulmonary disease: a comparative analysis across erdosteine, carbocysteine, and N-acetylcysteine.黏液溶解/抗氧化剂在慢性阻塞性肺疾病中的疗效和安全性:厄多司坦、卡博司坦和乙酰半胱氨酸的比较分析。
Respir Res. 2019 May 27;20(1):104. doi: 10.1186/s12931-019-1078-y.
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Potent Thrombolytic Effect of -Acetylcysteine on Arterial Thrombi.-乙酰半胱氨酸对动脉血栓的强效溶栓作用。
Circulation. 2017 Aug 15;136(7):646-660. doi: 10.1161/CIRCULATIONAHA.117.027290. Epub 2017 May 9.
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Increased homocysteine plasma level is associated with shortened prothrombin time in HIV-infected patients.
HIV Clin Trials. 2016 Sep;17(5):218-23. doi: 10.1080/15284336.2016.1220712. Epub 2016 Aug 16.
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Front Immunol. 2014 Dec 18;5:649. doi: 10.3389/fimmu.2014.00649. eCollection 2014.
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Respir Res. 2014 Feb 7;15(1):14. doi: 10.1186/1465-9921-15-14.
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