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血小板裂解液可刺激中风后的血管生成、神经发生和神经保护。

Platelet lysates stimulate angiogenesis, neurogenesis and neuroprotection after stroke.

机构信息

Stroke Service and the Peritz and Chantal Cerebrovascular Research Laboratory, Hadassah Ein Kerem, Jerusalem, Israel.

出版信息

Thromb Haemost. 2013 Aug;110(2):323-30. doi: 10.1160/TH12-11-0875. Epub 2013 Jun 13.

Abstract

Platelets contain chemo-attractants and mitogens that have a major role in tissue repair. Therefore we hypothesised that tissue regeneration secondary to activation of endogenous neural stem cells (eNSC) can be enhanced by delivering platelets to the ischaemic brain. To examine these potential therapeutic effects we injected platelet-poor plasma (PPP), fibroblast growth factor (FGF2) and platelet lysate (PLT) to the lateral ventricles after permanent middle cerebral artery occlusion (PMCAO) in rats. The animals were tested with the neurological severity score, and infarct volumes were measured at 90 days post-PMCAO. Immunohistochemistry was used to determine the fate of newborn cells and to count blood vessels in the ischaemic brain. Platelets significantly increased eNSC proliferation and angiogenesis in the subventricular zone (SVZ) and in the peri-lesion cortex. Functional outcome was significantly improved and injury size was significantly reduced in rats treated with PLT suggesting additional neuroprotective effects. In conclusion, local delivery of PLT to the lateral ventricles induces angiogenesis, neurogenesis and neuroprotection and reduces behavioural deficits after brain ischaemia.

摘要

血小板含有趋化因子和有丝分裂原,在组织修复中起主要作用。因此,我们假设通过将血小板递送至缺血性大脑,可以增强内源性神经干细胞 (eNSC) 激活引起的组织再生。为了研究这些潜在的治疗效果,我们在大鼠永久性大脑中动脉闭塞 (PMCAO) 后将血小板缺乏血浆 (PPP)、成纤维细胞生长因子 (FGF2) 和血小板裂解物 (PLT) 注射到侧脑室。用神经严重程度评分对动物进行测试,并在 PMCAO 后 90 天测量梗塞体积。免疫组织化学用于确定新生细胞的命运,并计算缺血性大脑中的血管数量。血小板显著增加了侧脑室下区 (SVZ) 和损伤皮层中的 eNSC 增殖和血管生成。用 PLT 治疗的大鼠的功能结果显著改善,损伤面积显著减小,表明具有额外的神经保护作用。总之,将 PLT 局部递送至侧脑室可诱导血管生成、神经发生和神经保护,并减少脑缺血后的行为缺陷。

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