不同抗血小板药物对脓毒性ARDS早期血小板活化及血小板-白细胞聚集形成的影响。

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Lu Wang, Liang-Yu Mi, Xiang-Yu Chen, Huai-Wu He, Yun Long
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引用次数: 0

摘要

背景:在脓毒症患者中,血小板被激活并粘附于中性粒细胞,形成血小板-白细胞聚集体(PLAs),导致MODS的发展。ARDS是脓毒性MODS的主要表现之一。本研究旨在探讨不同抗血小板治疗药物对脓毒性ARDS早期血小板活化及血小板-白细胞聚集物(PLA)形成的影响。方法:60只成年雄性SD大鼠随机分为:对照组;ARDS组、ARDS +阿司匹林组、ARDS +氯吡格雷组、ARDS +替罗非班组。ARDS通过5 mg/kg剂量的脂多糖(LPS)气管内注射。造模后立即灌胃阿司匹林或氯吡格雷。造模后立即腹腔注射替罗非班。各组大鼠造模后6 h采用快速断头法安乐死。采用流式细胞术和免疫荧光染色检测血小板活化和聚乳酸。苏木精、伊红染色行肺组织组织学检查。结果:阿司匹林、氯吡格雷和替罗非班可显著降低脓毒性ARDS患者CRP、IL-1和TNF-α (P < 0.05)。结论:阿司匹林、氯吡格雷和替罗非班可减轻早期脓毒性ARDS患者的炎症反应和肺水肿,降低血小板功能,减轻低氧血症。阿司匹林、氯吡格雷和替罗非班可降低脓毒性ARDS早期血小板活化和PLA形成。阿司匹林、氯吡格雷和替罗非班最终减轻了早期脓毒性ARDS的肺损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of different antiplatelet therapy drugs on platelet activation and platelet-leukocyte aggregate formation in early septic ARDS.

Background: In patients with sepsis, platelets are activated and adhere to neutrophils, forming platelet-leukocyte aggregates (PLAs) that lead to the development of MODS. ARDS is one of the main manifestations of septic MODS. We designed this study to explore the effects of different anti-plate therapy drugs on platelet activation and platelet-leukocyte aggregate (PLA) formation in the early stage of septic ARDS.

Methods: Sixty adult male SD rats were randomly divided into: Control group; ARDS group, ARDS + aspirin group, ARDS + clopidogrel group and ARDS + tirofiban group. ARDS was performed via instill lipopolysaccharide (LPS) intratracheally at a dose of 5 mg/kg. Aspirin or clopidogrel were given by gavage immediately after modeling. Tirofiban were given by intraperitoneal injection immediately after modeling. Rats in every group were euthanized by rapid decapitation 6 h after modeling. Platelet activation and PLA were assessed using flow cytometry and immunofluorescence staining. Histology of lung was performed by hematoxylin and eosin staining.

Results: Aspirin, clopidogrel and tirofiban decreased CRP, IL-1 and TNF-α significantly in septic ARDS (P < 0.05). Aspirin, clopidogrel and tirofiban decreased platelet function and ratio of wet/dry significantly in septic ARDS (P < 0.05). Aspirin, clopidogrel and tirofiban increased PaO2 significantly in septic ARDS (P < 0.05). Platelet activation and PLA in the ARDS + aspirin group, ARDS + clopidogrel group and ARDS + tirofiban group decreased significantly compared to the ARDS group (P < 0.05). At 6 h after ARDS operation, obvious histological damage was observed in the lungs. All of these histological changes were quantitatively evaluated using injury scores. Aspirin, clopidogrel and tirofiban reduced the histological damages in ARDS group (P < 0.05).

Conclusions: Aspirin, clopidogrel and tirofiban alleviated the inflammatory response and pulmonary edema, reduced platelet function, and alleviated hypoxemia in early septic ARDS. Aspirin, clopidogrel and tirofiban reduced platelet activation and PLA formation in early septic ARDS. Aspirin, clopidogrel and tirofiban ultimately alleviated lung injury in early septic ARDS.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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