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Ultrasound of 10 MHz frequency as a novel strategy for skin anti-aging therapy.

机译:10 MHz频率的超声波作为皮肤抗衰老疗法的一种新策略。

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Aging is believed to be connected with accumulated damaging of cellular macromolecules in non-dividing cells as well as with reduction of the cells capability to repair this damage. Damage of the macromolecules occurs through different physical and chemical factors (e.g. different types of irradiation, heat, toxins, etc.). The fate of the damaged macromolecules is dependent on such processes as degradation of unstable proteins, refolding of misfolded proteins, controlling of regulatory proteins and prevention of protein folding. These processes are essentially regulated through activation of heat shock proteins (HSPs) [1,2]. HSP family includes different proteins classified according to their molecular weights. Among them the HSP70 and HSP90 seems to be responsible for the recognition and refolding of proteins. HSPs are present in all cell types and were found not only inside of the cells where they believed to act cyto-protectively (to prevent the cells against the second stress that would otherwise cause lethal molecular damage) but also in the cell membrane and in the extracellular space where they can show the cytotoxic effect increasing the cell death [3,4]. It is well known that HSPs are over-expressed in cancer cells as well as on outer cellular membranes of damaged cells after some aggressive treatments (e.g. [5]). There is also increasing evidence of HSPs expression in different neurodegenerative disorders, during inflammation, by trauma as well as by cerebral and cardiac ischemia. It is believed that in the most of these diseases induction of a heat shock response might be an effective prophylactic treatment to minimize the severe injuries, making HSPs activation a potential therapeutic modality.
机译:人们认为衰老与非分裂细胞中细胞大分子的累积损伤以及细胞修复这种损伤的能力降低有关。大分子的损坏是通过不同的物理和化学因素(例如不同类型的辐射,热量,毒素等)发生的。受损大分子的命运取决于诸如不稳定蛋白质的降解,错误折叠的蛋白质重新折叠,调控蛋白的控制以及蛋白质折叠的预防等过程。这些过程实质上是通过激活热激蛋白(HSP)来调节的[1,2]。 HSP家族包括根据其分子量分类的不同蛋白质。其中HSP70和HSP90似乎负责蛋白质的识别和重折叠。 HSP存在于所有细胞类型中,不仅存在于它们认为具有细胞保护作用的细胞内部(以防止细胞抵抗可能导致致命分子损伤的第二种应激),而且还存在于细胞膜和细胞中。它们可以在细胞外空间显示出细胞毒性作用,从而增加细胞死亡[3,4]。众所周知,经过一些积极的治疗后,HSPs在癌细胞以及受损细胞的外细胞膜上都过表达(例如[5])。还越来越多的证据表明,在炎症,外伤以及脑和心脏缺血中,HSPs在不同的神经退行性疾病中表达。据信,在大多数这些疾病中,诱发热休克反应可能是一种有效的预防性治疗,可最大程度地减少严重伤害,从而使HSP活化成为潜在的治疗方式。

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