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诱导热休克蛋白以抵御氧化应激。

Induction of heat shock proteins for protection against oxidative stress.

作者信息

Kalmar Bernadett, Greensmith Linda

机构信息

Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, Queen Square, London, UK.

出版信息

Adv Drug Deliv Rev. 2009 Apr 28;61(4):310-8. doi: 10.1016/j.addr.2009.02.003. Epub 2009 Feb 25.

Abstract

Heat shock proteins (Hsps) have been studied for many years and there is now a large body of evidence that demonstrates the role of Hsp upregulation in tissue and cell protection in a wide variety of stress conditions. Oxidative stress is known to be involved in a number of pathological conditions, including neurodegeneration, cardiovascular disease and stroke, and even plays a role in natural aging. In this review we summarize the current understanding of the role of Hsps and the heat shock response (HSR) in these pathological conditions and discuss the therapeutic potential of an Hsp therapy for these disorders. However, although an Hsp based therapy appears to be a promising approach for the treatment of diseases that involve oxidative damage, there are some significant hurdles that must be overcome before this approach can be successful. For example, to be effective an Hsp based therapy will need to ensure that the upregulation of Hsps occurs in the right place (i.e. be cell specific), at the right time and to a level and specificity that ensures that all the important binding partners, namely the co-chaperones, are also present at the appropriate levels. It is therefore unlikely that strategies that involve genetic modifications that result in overexpression of specific Hsps will achieve such sophisticated and coordinated effects. Similarly, it is likely that some pharmaceutical inducers of Hsps may be too generic to achieve the desired specific effects on Hsp expression, or may simply fail to reach their target cells due to delivery problems. However, if these difficulties can be overcome, it is clear that an effective Hsp based therapy would be of great benefit to the wide range of depilating conditions in which oxidative stress plays a critical role.

摘要

热休克蛋白(Hsps)已被研究多年,现在有大量证据表明,在多种应激条件下,Hsp上调在组织和细胞保护中发挥作用。已知氧化应激与多种病理状况有关,包括神经退行性疾病、心血管疾病和中风,甚至在自然衰老过程中也起作用。在本综述中,我们总结了目前对Hsps和热休克反应(HSR)在这些病理状况中的作用的理解,并讨论了Hsp疗法对这些疾病的治疗潜力。然而,尽管基于Hsp的疗法似乎是治疗涉及氧化损伤疾病的一种有前景的方法,但在这种方法取得成功之前,还有一些重大障碍必须克服。例如,为了有效,基于Hsp的疗法需要确保Hsps在正确的位置(即细胞特异性)、在正确的时间上调,并且上调到一定水平和特异性,以确保所有重要的结合伴侣,即共伴侣,也以适当的水平存在。因此,涉及基因修饰导致特定Hsps过表达的策略不太可能实现如此复杂和协调的效果。同样,一些Hsps的药物诱导剂可能过于通用,无法对Hsp表达产生所需的特定效果,或者可能由于递送问题而根本无法到达其靶细胞。然而,如果这些困难能够克服,显然有效的基于Hsp的疗法将对氧化应激起关键作用的广泛脱毛状况大有裨益。

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