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Protection of bone marrow mesenchymal stem cells from acute lung injury induced by paraquat poisoning.

机译:百草枯中毒引起的骨髓间充质干细胞免受急性肺损伤的保护。

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OBJECTIVE. To examine the protective effect of bone marrow mesenchymal stem cell (BMSC) transplantation against lung injury induced by paraquat (PQ) poisoning. MATERIALS AND METHODS. Fifty-four female SD rats were randomly divided into four groups: a PQ group, a BMSC treatment group, a BMSC control group, and a normal control group. BMSC, isolated and cultured in vitro, were injected into the tail veins of the rats. The mortality rate, the ratio of lung wet/dry weight, plasma levels of IL-1beta, tumor necrosis factor-alpha (TNF-alpha), malonaldehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GSH-P(X)), and NF-kappaBp65 expression in the lung tissues were examined during 14 days after injection. Results. Survival in the PQ group ranged from 8 to 12 days, with an average of 9.6 days. All the rats in the BMSC treatment group survived for more than 14 days. In the BMSC treatment group, the ratio of lung wet /dry weight (P = 0.02 < 0.05), plasma IL-1beta and TNF-alpha levels (P = 0.00 < 0.01), MDA levels (P = 0.03 < 0.05), and expression of NF-kappaBp65 in the lung tissues (P = 0.00 < 0.01) were significantly lower than those in the PQ group by day 7 post-injection. However, the SOD and GSH-P(X) levels began to increase (P = 0.00 < 0.01) compared with the PQ group. There was no significant difference between the BMSC control group and the normal control group (P > 0.01). DISCUSSION AND CONCLUSION. BMSC transplantation may have the potential to protect against PQ-induced lung injury, by reducing lung edema and lipid peroxidation, inhibiting the release of inflammatory mediators. However, the protective effects require time to develop, and early BMSC transplantation may be more evident during the middle and late stages of therapy.
机译:目的。目的探讨骨髓间充质干细胞(BMSC)移植对百草枯(PQ)中毒引起的肺损伤的保护作用。材料和方法。 54只雌性SD大鼠随机分为四组:PQ组,BMSC治疗组,BMSC对照组和正常对照组。将分离并体外培养的BMSC注射到大鼠的尾静脉中。死亡率,肺干重/干重比,IL-1β血浆水平,肿瘤坏死因子-α(TNF-alpha),丙二醛(MDA),超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSH-P(X )),并在注射后14天内检查肺组织中的NF-κBp65表达。结果。 PQ组的生存时间为8到12天,平均9.6天。 BMSC治疗组中的所有大鼠存活超过14天。在BMSC治疗组中,肺干/湿重之比(P = 0.02 <0.05),血浆IL-1beta和TNF-α水平(P = 0.00 <0.01),MDA水平(P = 0.03 <0.05)和注射后第7天,肺组织中NF-κBp65的表达(P = 0.00 <0.01)显着低于PQ组。但是,与PQ组相比,SOD和GSH-P(X)的水平开始增加(P = 0.00 <0.01)。 BMSC对照组与正常对照组比较差异无统计学意义(P> 0.01)。讨论和结论。 BMSC移植可能通过减少肺水肿和脂质过氧化作用,抑制炎症介质的释放来预防PQ诱导的肺损伤。但是,保护作用需要时间才能发展,早期BMSC移植在治疗的中后期可能会更加明显。

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