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[热休克HSP70蛋白在体外出血性中风模型中的保护和抗水肿作用]

[Protective and antiedema effect of heat shock HSP70 protein in hemorrhagic stroke model in vitro].

作者信息

Khama-Murad A Kh

出版信息

Eksp Klin Farmakol. 2011;74(2):19-22.

PMID:21476280
Abstract

An in vitro model of hemorrhagic stroke in live olfactory cortex slices under long-term influence of autoblood has been used and the development of edema in the samples has been studied with simultaneous monitoring of bioelectric activity of the nervous cells. Protection of the nervous cells in the olfactory cortex slices of the spontaneously hypertensive (SHR) rats from consequences of the hemorrhagic stroke was achieved by incubating brain slices for 20 min in glass vials with 1 ml of incubation solution containing heat shock protein HSP70 at a concentration of 10 mg/ml. Then the incubation medium was replaced by 3 ml of autoblood, the action of which on the nervous cells modeled the hemorrhagic stroke. After 360-min incubation in autoblood, the slices were extracted, placed in a perfusion chamber, and washed from autoblood in a flow of pure incubation solution. Then the amplitudes of separate components of the focal potentials (FPs) evoked by electrostimulation of the slices were measured and their changes analyzed. A comparison of the FP amplitudes after the action of HSP70 and autoblood to those in control group of slices showed the degree of injury and the possibility of recovery. The antiedema effects of HSP70 on the hemorrhagic stroke model was evaluated by weighing brain slices with and without the preincubation with protein, and after the subsequent exposure in autoblood. The slices were weighed on a torsion balance. The difference in weights before and after the exposure in autoblood characterized the extent of swelling and edema development in brain slices. It was established that HSP70 produced a pronounced protective antiedema effect on the slices kept in autoblood.

摘要

采用了在自体血长期影响下的活体嗅皮质切片出血性中风体外模型,研究了样本中水肿的发展情况,同时监测神经细胞的生物电活动。通过将自发性高血压(SHR)大鼠的嗅皮质切片在装有1毫升浓度为10毫克/毫升热休克蛋白HSP70的孵育溶液的玻璃瓶中孵育20分钟,实现了对其嗅皮质切片神经细胞免受出血性中风后果的影响。然后将孵育培养基换成3毫升自体血,其对神经细胞的作用模拟出血性中风。在自体血中孵育360分钟后,取出切片,放入灌流室,用纯孵育溶液冲洗掉自体血。然后测量电刺激切片诱发的局灶电位(FPs)各成分的幅度,并分析其变化。将HSP70和自体血作用后的FPs幅度与切片对照组的幅度进行比较,以显示损伤程度和恢复的可能性。通过对预孵育蛋白和未预孵育蛋白的脑切片在随后暴露于自体血前后进行称重,评估HSP70对出血性中风模型的抗水肿作用。切片在扭力天平上称重。暴露于自体血前后的重量差异表征了脑切片肿胀和水肿发展的程度。结果表明,HSP70对置于自体血中的切片产生了显著的保护性抗水肿作用。

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