First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
J Vasc Surg. 2011 Mar;53(3):743-53. doi: 10.1016/j.jvs.2010.09.017. Epub 2010 Nov 20.
Proanthocyanidins are abundantly found in grape seeds and have been suggested to inhibit the pathogenesis of systemic diseases. We investigated the antithrombotic effects of proanthocyanidins in a rat model of deep vein thrombosis (DVT) and examined the underlying mechanisms.
DVT was induced in rat model by inferior vena cava (IVC) ligation. Grape seed proanthocyanidins extract (GSPE, 400 mg/kg/d) dissolved in saline (2 mL) was orally administered to the experimental rats. Control rats were administrated saline (2 mL) only. The thrombi were harvested and weighed. The IVC was analyzed histologically and by transmission electron microscopy. The cytokines interleukin (IL)-6, IL-8, and tumor necrosis factor-α (TNF-α) were detected by enzyme-linked immunosorbent assay. Expression of cellular adhesion molecules (CAMs) in thrombi was examined by Western blot.
GSPE significantly reduced thrombus length and weight (P < .01) and protected the integrity of the endothelium. GSPE inhibited thrombogenesis-promoting factors P-selectin, von Willebrand factor, and CAMs, and promoted thrombogenesis-demoting factors CD34, vascular endothelial growth factor receptor-2, and ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type one motif, member 13). Compared with the control, GSPE significantly lowered the cytokines IL-6 (74.19 ± 13.86 vs 189.54 ± 43.76 pg/mL; P < .01), IL-8 (80.71 ± 21.42 vs 164.56 ± 39.54 pg/mL; P < .01), and TNF-α (43.11 ± 17.58 vs 231.84 ± 84.11 pg/mL; P < .01).
GSPE significantly inhibited the propagation of thrombus induced by IVC ligation in a rat model. The antithrombotic properties of proanthocyanidins are likely to be directly associated with endothelial protection and regeneration, platelet aggregation, and inhibition of inflammatory cell and thrombus adhesion. Thus, proanthocyanidins may have a clinical application in DVT treatment.
原花青素大量存在于葡萄籽中,已被证明可抑制全身性疾病的发病机制。本研究旨在通过大鼠深静脉血栓形成(DVT)模型来研究原花青素的抗血栓作用,并探讨其潜在机制。
通过下腔静脉(IVC)结扎在大鼠模型中诱导 DVT。将葡萄种子原花青素提取物(GSPE,400mg/kg/d)溶解在生理盐水(2mL)中,通过口服给予实验组大鼠。对照组大鼠仅给予生理盐水(2mL)。采集血栓并称重。通过组织学和透射电子显微镜分析 IVC。通过酶联免疫吸附试验检测细胞因子白细胞介素(IL)-6、IL-8 和肿瘤坏死因子-α(TNF-α)。通过 Western blot 检测血栓中细胞黏附分子(CAM)的表达。
GSPE 显著降低血栓长度和重量(P<.01),并保护内皮完整性。GSPE 抑制促血栓形成因子 P-选择素、血管性血友病因子和 CAMs,促进促血栓形成因子 CD34、血管内皮生长因子受体-2 和 ADAMTS13(一种含有血小板反应蛋白 1 型基序的金属蛋白酶 13)。与对照组相比,GSPE 显著降低细胞因子 IL-6(74.19±13.86 与 189.54±43.76pg/mL;P<.01)、IL-8(80.71±21.42 与 164.56±39.54pg/mL;P<.01)和 TNF-α(43.11±17.58 与 231.84±84.11pg/mL;P<.01)。
GSPE 显著抑制大鼠模型中 IVC 结扎引起的血栓形成。原花青素的抗血栓特性可能与内皮保护和再生、血小板聚集以及抑制炎症细胞和血栓黏附直接相关。因此,原花青素可能在 DVT 治疗中有临床应用。