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Umbilical cord‐derived MSC and hyperbaric oxygen therapy effectively protected the brain in rat after acute intracerebral haemorrhage

机译:脐带衍生的MSC和高压氧疗法有效地保护大鼠急性脑内出血后大鼠的大脑

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摘要

This study tested the hypothesis that combined therapy with human umbilical cord‐derived mesenchymal stem cells (HUCDMSCs) and hyperbaric oxygen (HBO) was superior to either one on preserving neurological function and reducing brain haemorrhagic volume (BHV) in rat after acute intracerebral haemorrhage (ICH) induced by intracranial injection of collagenase. Adult male SD rats (n = 30) were equally divided into group 1 (sham‐operated control), group 2 (ICH), group 3 (ICH +HUCDMSCs/1.2 × 106 cells/intravenous injection at 3h and days 1 and 2 after ICH), group 4 (ICH +HBO/at 3 hours and days 1 and 2 after ICH) and group 5 (ICH +HUCDMSCs‐HBO), and killed by day 28 after ICH. By day 1, the neurological function was significantly impaired in groups 2‐5 than in group 1 (P < .001), but it did not differ among groups 2 to 5. By days 7, 14 and 28, the integrity of neurological function was highest in group 1, lowest in group 2 and significantly progressively improved from groups 3 to 5 (all P < .001). By day 28, the BHV was lowest in group 1, highest in group 2 and significantly lower in group 5 than in groups 3/4 (all P < .0001). The protein expressions of inflammation (HMGB1/TLR‐2/TLR‐4/MyD88/TRAF6/p‐NF‐κB/IFN‐γ/IL‐1ß/TNF‐α), oxidative stress/autophagy (NOX‐1/NOX‐2/oxidized protein/ratio of LC3B‐II/LC3B‐I) and apoptosis (cleaved‐capspase3/PARP), and cellular expressions of inflammation (CD14+, F4/80+) in brain tissues exhibited an identical pattern, whereas cellular levels of angiogenesis (CD31+/vWF+/small‐vessel number) and number of neurons (NeuN+) exhibited an opposite pattern of BHV among the groups (all P < .0001). These results indicate that combined HUCDMSC‐HBO therapy offered better outcomes after rat ICH.
机译:该研究检测了与人脐带衍生的间充质干细胞(HUCDMSC)组合治疗和高压氧(HBO)的假设优于保存神经功能和降低大鼠急性脑出血后大鼠脑出血体积(BHV)的假设(颅内注射胶原酶诱导的ICH)。成年雄性SD大鼠(n = 30)被同等分为第1组(假手术控制),第2组(ICH),第3组(ICH + HUCDMSCs / 1.2×106细胞/静脉注射3小时后1和2 ICH),第4组(ICH + HBO / 3小时和第1天和第2天)和第5组(ICH + HUCDMSCS-HBO),并在ICH之后的第28天杀死。在第1天,在第2-5组中,神经功能显着损害于1族(p <.001),但第2组至5分中没有差异。在第7,14和28天,神经功能的完整性第1组中最高,第2组中最低,并从组3到5中显着改善(所有P <.001)。在第28天,BHV在第1组中最低,第2组中最高,第5组中显着低于3/4组(所有P <.0001)。炎症的蛋白表达(HMGB1 / TLR-2 / TLR-4 / MYD88 / TRAF6 / P-NF-κB/ IFN-γ/ IL-1ß/ TNF-α),氧化应激/自噬(NOX-1 / NOx- 2 /氧化蛋白/ LC3B-II / LC3B-I的蛋白/比例)和脑组织中炎症(CD14 +,F4 / 80 +)的细胞凋亡(CD14 +,F4 / 80 +)表现出相同的模式,而细胞水平血管生成(CD31 + / VWF + /小容器数)和神经元数(NeUN +)在组中表现出相反的BHV模式(所有P <.0001)。这些结果表明,大鼠ICH后,HUCDMSC-HBO治疗的组合提供了更好的结果。

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