Evaluation of the effects of thymoquinone on red blood cell deformability, morphology, and endothelial nitric oxide synthase (eNOS) synthesis in rat lower extremity ischemia-reperfusion injury.

Celalettin Gunay, Hakan Kartal, Ertan Demirdas, Bilgehan Savas Oz, Faruk Metin Comu, Gokhan Erol, Gokhan Arslan, Tayfun Ozdem, Tuna Demirkıran, Muharrem Emre Ozdaş, Isıl Ozdas, Yigit Tokgoz, Veli Can Ozdemir
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Abstract

Background: Erythrocyte deformability refers to the ability of erythrocytes to bend and twist as they pass through capillaries, which is crucial for tissue perfusion. This study aims to investigate the effects of Thymoquinone treatment on erythrocyte deformability in rats subjected to lower extremity ischemia-reperfusion injury.

Methods: The study was conducted on Wistar albino rats weighing 400-450 g. The rats were randomly divided into five groups: the control group (C), in which no treatment was applied; the group that received dimethyl sulfoxide (DMSO) as a solvent; the group subjected to 90 minutes of ischemia followed by 90 minutes of reperfusion in the main femoral artery of the lower extremity (IR); the Thymoquinone control group (TQ-C), in which the effects of Thymoquinone alone were examined; and the group that received intraperitoneal Thymoquinone one hour before the ischemia-reperfusion procedure (IR+TQ). At the end of the procedure, intracardiac blood was collected from the rats, and May-Grunwald and Giemsa (MGG) staining, endothelial nitric oxide synthase (eNOS), and erythrocyte deformability indexes were measured.

Results: The study results showed significant differences. Erythrocyte deformability was statistically significantly improved in the group that received Thymoquinone before ischemia-reperfusion compared to the group subjected to ischemia-reperfusion only. Mor-phological changes in erythrocytes were also statistically significantly better in the IR+TQ group than in the IR group. Immunohisto-chemical eNOS staining revealed that eNOS activity in the IR group was lower than in the IR+TQ group.

Conclusion: Our study demonstrates that Thymoquinone treatment administered before ischemia exerts protective effects against erythrocyte deformation and morphological deterioration by increasing eNOS activity.

评估胸腺醌对大鼠下肢缺血再灌注损伤中红细胞变形、形态和内皮一氧化氮合酶(eNOS)合成的影响。
背景:红细胞变形性是指红细胞通过毛细血管时弯曲和扭曲的能力,这对组织灌注至关重要。本研究旨在探讨胸腺醌治疗对下肢缺血再灌注损伤大鼠红细胞变形能力的影响:研究对象为体重400-450克的Wistar白化大鼠。大鼠随机分为五组:对照组(C),不进行任何治疗;接受二甲基亚砜(DMSO)作为溶剂的组;下肢股主干动脉缺血 90 分钟后再灌注 90 分钟的组(IR);胸腺醌对照组(TQ-C),该组只研究胸腺醌的作用;以及在缺血再灌注手术前一小时腹腔注射胸腺醌的一组(IR+TQ)。在缺血再灌注过程结束后,采集大鼠的心内血液,测定梅-格氏和吉氏(MGG)染色、内皮一氧化氮合酶(eNOS)和红细胞变形指数:结果:研究结果显示存在明显差异。缺血再灌注前服用胸腺醌的组与仅接受缺血再灌注的组相比,红细胞变形性在统计学上有明显改善。红细胞的形态学变化在统计学上也是IR+胸腺醌组明显优于IR组。免疫组化 eNOS 染色显示,IR 组的 eNOS 活性低于 IR+TQ 组:我们的研究表明,缺血前服用胸腺醌可通过提高 eNOS 活性,对红细胞变形和形态学恶化起到保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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