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SS-31 肽可实现靶向线粒体的药物递送:一种有前途的治疗性改变,可防止氨基糖苷类药物引起的毛细胞损伤。

SS-31 peptide enables mitochondrial targeting drug delivery: a promising therapeutic alteration to prevent hair cell damage from aminoglycosides.

机构信息

a School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.

出版信息

Drug Deliv. 2017 Nov;24(1):1750-1761. doi: 10.1080/10717544.2017.1402220.

Abstract

Aminoglycoside-induced hearing loss stems from damage or loss of mechanosensory hair cells in the inner ear. Intrinsic mitochondrial cell death pathway plays a key role in that cellular dysfunction for which no proven effective therapies against oto-toxicities exist. Therefore, the aim of the present study was to develop a new mitochondrial targeting drug delivery system (DDS) that provided improved protection from gentamicin. Particularly, SS-31 peptide-conjugated geranylgeranylacetone (GGA) loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles were constructed successfully via emulsion-solvent evaporation method. The zebrafish lateral line sensory system was used as an in vivo evaluating platform to investigate the protective efficiency against gentamicin. SS-31 modification significantly reduced the activity of mechanoelectrical transduction (MET) channel and gentamicin uptake in zebrafish lateral line hair cells. As expected, SS-31 conjugated nanoparticles showed mitochondrial specific accumulation in hair cells when compared with unconjugated formulations. Furthermore, intracellular SS-31 modified PLGA NPs slightly enhanced mitochondrial membrane potential (MMP, ΔΨ) and then returned to a steady-state, indicating their effect on the respiratory chain complexes in mitochondria. GGA loaded SS-31 conjugated nanoparticles demonstrated the most favorable hair cells survivals against gentamicin when compared with unconjugated groups whereas blank formulations failed to exhibit potency, indicating that the efficiency was attributed to drug delivery of GGA. These results suggest that our constructed mitochondria-targeting PLGA based DDS have potential application in protecting hair cells from ototoxic agents.

摘要

氨基糖苷类诱导的听力损失源于内耳机械感觉毛细胞的损伤或丧失。内在的线粒体细胞死亡途径在细胞功能障碍中起着关键作用,而目前尚无针对耳毒性的有效治疗方法。因此,本研究旨在开发一种新的线粒体靶向药物传递系统(DDS),以提供对抗庆大霉素的更好保护。特别地,通过乳化溶剂蒸发法成功构建了 SS-31 肽缀合的香叶基香叶基丙酮(GGA)负载的聚(乳酸-共-乙醇酸)(PLGA)纳米粒子。斑马鱼侧线感觉系统被用作体内评估平台,以研究对抗生素的保护效率。SS-31 修饰显著降低了机械电转导(MET)通道的活性和庆大霉素在斑马鱼侧线毛细胞中的摄取。正如预期的那样,与未缀合的制剂相比,SS-31 缀合的纳米颗粒在毛细胞中显示出线粒体特异性积累。此外,与未修饰的 PLGA NPs 相比,细胞内 SS-31 修饰的 PLGA NPs 略微增强了线粒体膜电位(MMP,ΔΨ),然后恢复到稳定状态,表明它们对线粒体呼吸链复合物的作用。与未缀合的组相比,负载 GGA 的 SS-31 缀合纳米颗粒对庆大霉素显示出最有利的毛细胞存活率,而空白制剂未能表现出效力,表明效率归因于 GGA 的药物传递。这些结果表明,我们构建的基于 PLGA 的线粒体靶向 DDS 具有保护毛细胞免受耳毒性药物的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b2/8241023/8d22c424ffd1/IDRD_A_1402220_F0001_B.jpg

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