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将含咪唑二肽指定为药理学伴侣。

Designation of imidazole-containing dipeptides as pharmacological chaperones.

机构信息

Innovative Vision Products Inc, County of New Castle, Delaware, USA.

出版信息

Hum Exp Toxicol. 2011 Jul;30(7):736-61. doi: 10.1177/0960327110377526. Epub 2010 Jul 23.

Abstract

We review the dichotomous regulatory roles of natural imidazole-containing peptidomimetics (N-acetylcarnosine [NAC], carcinine, non-hydrolized carnosine) in maintaining skin homeostasis that determines whether keratinocytes survive or undergo apoptosis in response to various insults and in the development of skin diseases. General strategies addressing common ground techniques to improve absorption of usually active chaperone proteins or their dipeptide inducer (usually poorly absorbed) compounds include encapsulation into hydrophobic carriers, combination with penetration enhancers, active electrical transport or chemical modification to increase hydrophobicity. A growing evidence is presented that demonstrates the ability of NAC (lubricant eye drops) or carcinine to act as pharmacological chaperones, or being synergistically coupled in patented formulations with another imidazole-containing peptidomimetic (such as, Leucyl-histidylhydrazide), to decrease oxidative stress and ameliorate oxidative and excessive glycation stress-related eye disease phenotypes, suggesting that the field of chaperone therapy might hold novel treatments for age-related cataracts, glaucoma, age-related macular degeneration (AMD), and ocular complications of diabetes (OCD). Current efforts are being directed towards exploring therapeutic approaches of pharmacological targeting and human drug delivery for chaperone molecules based on innovative patented strategies.

摘要

我们回顾了天然咪唑类肽模拟物(N-乙酰肉碱[NAC]、卡尼丁、非水解肉碱)在维持皮肤稳态方面的二分法调节作用,这种稳态决定了角质细胞在各种刺激下是存活还是凋亡,以及在皮肤疾病的发展中。针对提高通常具有活性的伴侣蛋白或其二肽诱导剂(通常吸收不良)化合物的吸收的常见技术的一般策略包括封装到疏水性载体中、与渗透增强剂结合、主动电传输或化学修饰以增加疏水性。越来越多的证据表明,NAC(润眼液)或卡尼丁能够作为药理学伴侣蛋白发挥作用,或者与另一种含咪唑的肽模拟物(如亮氨酰-组氨酰酰肼)在专利配方中协同结合,以减少氧化应激并改善氧化和过度糖基化应激相关的眼病表型,这表明伴侣蛋白治疗领域可能为与年龄相关的白内障、青光眼、年龄相关性黄斑变性(AMD)和糖尿病性眼病(OCD)提供新的治疗方法。目前的努力方向是探索基于创新专利策略的药理学靶向和人类药物输送的伴侣蛋白分子的治疗方法。

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