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Increase in periosteal angiogenesis through heat shock conditioning

机译:通过热休克调节增加骨膜血管生成

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Objective It is widely known that stress conditioning can protect microcirculation and induce the release of vasoactive factors for a period of several hours. Little, however, is known about the long-term effects of stress conditioning on microcirculation, especially on the microcirculation of the periosteum of the calvaria. For this reason, we used intravital fluorescence microscopy to investigate the effects of heat shock priming on the microcirculation of the periosteum over a period of several days. Methods Fifty-two Lewis rats were randomized into eight groups. Six groups underwent heat shock priming of the periosteum of the calvaria at 42.5°C, two of them (n = 8) for 15 minutes, two (n = 8) for 25 minutes and two (n = 8) for 35 minutes. After 24 hours, a periosteal chamber was implanted into the heads of the animals of one of each of the two groups mentioned above. Microcirculation and inflammatory responses were studied repeatedly over a period of 14 days using intravital fluorescence microscopy. The expression of heat shock protein (HSP) 70 was examined by immunohistochemistry in three further groups 24 hours after a 15-minute (n = 5), a 25-minute (n = 5) or a 35-minute (n = 5) heat shock treatment. Two groups that did not undergo priming were used as controls. One control group (n = 8) was investigated by intravital microscopy and the other (n = 5) by immunohistochemistry. Results During the entire observation period of 14 days, the periosteal chambers revealed physiological microcirculation of the periosteum of the calvaria without perfusion failures. A significant (p < 0.05) and continuous increase in functional capillary density was noted from day 5 to day 14 after 25-minute heat shock priming. Whereas a 15-minute exposure did not lead to an increase in functional capillary density, 35-minute priming caused a significant but reversible perfusion failure in capillaries. Non-perfused capillaries in the 35-minute treatment group were reperfused by day 10. Immunohistochemistry demonstrated an increase in cytoprotective HSP70 expression in the periosteum after a 15-minute and a 35-minute heat shock pretreatment when compared with the control group. The level of HSP70 expression that was measured in the periosteum after 25 minutes of treatment was significantly higher than the levels observed after 15 or 35 minutes of heat shock exposure. Conclusion A few days after heat shock priming over an appropriate period of time, a continuous increase in functional capillary density is seen in the periosteum of the calvaria. This increase in perfusion appears to be the result of the induction of angiogenesis.
机译:目的众所周知,压力调节可以保护微循环并诱导血管活性因子释放长达数小时。然而,对于应力调节对微循环,尤其是对颅骨骨膜的微循环的长期影响知之甚少。由于这个原因,我们使用了活体内荧光显微镜研究了几天内热激引发对骨膜微循环的影响。方法52只Lewis大鼠随机分为八组。六组在42.5°C下对颅骨骨膜进行热激灌注,其中两组(n = 8)持续15分钟,两组(n = 8)持续25分钟,两组(n = 8)持续35分钟。 24小时后,将骨膜腔植入上述两组中每组动物的头部。使用活体荧光显微镜在14天的时间内反复研究了微循环和炎症反应。在15分钟(n = 5),25分钟(n = 5)或35分钟(n = 5)24小时后,通过免疫组织化学检查了另外三个组的热休克蛋白(HSP)70的表达。热休克治疗。两组未进行灌注的用作对照。活体显微镜检查一个对照组(n = 8),免疫组织化学研究另一个对照组(n = 5)。结果在整个14天的观察期内,骨膜腔显示颅骨骨膜的生理微循环而无灌注失败。在进行25分钟的热休克灌注后,从第5天到第14天,功能性毛细血管密度显着(p <0.05)并持续增加。暴露15分钟并没有导致功能性毛细血管密度的增加,而灌注35分钟却引起了毛细血管严重但可逆的灌注失败。与对照组相比,在35分钟的治疗组中未灌注的毛细管在第10天再灌注。免疫组织化学表明,热休克预处理15分钟和35分钟后,骨膜中细胞保护性HSP70表达增加。治疗25分钟后在骨膜中测得的HSP70表达水平显着高于热休克暴露15或35分钟后观察到的水平。结论在适当的时间里,热休克引发后几天,颅骨骨膜中的功能性毛细血管密度持续增加。灌注的增加似乎是诱导血管生成的结果。

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