Department of Otolaryngology, Hannover Medical School, University of Veterinary Medicine Hannover, Germany.
Int J Nanomedicine. 2012;7:2449-64. doi: 10.2147/IJN.S29712. Epub 2012 May 15.
Sensorineural hearing loss leads to the progressive degeneration of spiral ganglion cells (SGC). Next to postoperative fibrous tissue growth, which should be suppressed to assure a close nerve-electrode interaction, the density of healthy SGC is one factor that influences the efficiency of cochlear implants (CI), the choice of treatment for affected patients. Rolipram, a phosphodiesterase-4 inhibitor, has proven neuroprotective and anti-inflammatory effects and might also reduce SGC degeneration and fibrosis, but it has to pass the cellular membrane to be biologically active.
Lipidic nanocapsules (LNC) can be used as biodegradable drug carriers to increase the efficacy of conventional application methods. We examined the biological effects of rolipram and LNC's core encapsulated rolipram on SGC and dendritic cell (DC) tumor necrosis factor-α (TNF-α) production in vitro and on SGC survival in systemically-deafened guinea pigs in vivo.
Our results prove that rolipram does not have a beneficial effect on cultured SGC. Incorporation of rolipram in LNC increased the survival of SGC significantly. In the DC study, rolipram significantly inhibited TNF-α in a dose-dependent manner. The rolipram-loaded LNC provided a significant cytokine inhibition as well. In vivo data do not confirm the in vitro results.
By transporting rolipram into the SGC cytoplasm, LNC enabled the neuroprotective effect of rolipram in vitro, but not in vivo. This might be due to dilution of test substances by perilymph or an inadequate release of rolipram based on differing in vivo and in vitro conditions. Nevertheless, based on in vitro results, proving a significantly increased neuronal survival when using LNC-rolipram compared to pure rolipram and pure LNC application, we believe that the combination of rolipram and LNC can potentially reduce neuronal degeneration and fibrosis after CI implantation. We conclude that rolipram is a promising drug that can be used in inner ear therapy and that LNC have potential as an inner ear drug-delivery system. Further experiments with modified conditions might reveal in vivo biological effects.
感音神经性听力损失导致螺旋神经节细胞(SGC)进行性退化。除了术后纤维组织生长,为了确保紧密的神经-电极相互作用,应该抑制纤维组织生长,健康的 SGC 密度是影响耳蜗植入物(CI)效率的因素之一,这是受影响患者的治疗选择。罗利普兰是一种磷酸二酯酶-4 抑制剂,已被证明具有神经保护和抗炎作用,也可能减少 SGC 退化和纤维化,但它必须穿过细胞膜才能具有生物活性。
脂质纳米胶囊(LNC)可用作生物降解性药物载体,以提高常规应用方法的功效。我们在体外研究了罗利普兰和包封在 LNC 核心中的罗利普兰对 SGC 和树突状细胞(DC)肿瘤坏死因子-α(TNF-α)产生的生物学效应,并在体内研究了罗利普兰对系统性耳聋豚鼠 SGC 存活的影响。
我们的结果证明罗利普兰对培养的 SGC 没有有益的作用。将罗利普兰掺入 LNC 中可显著提高 SGC 的存活率。在 DC 研究中,罗利普兰以剂量依赖性方式显著抑制 TNF-α。载有罗利普兰的 LNC 也提供了显著的细胞因子抑制作用。体内数据并未证实体外结果。
通过将罗利普兰输送到 SGC 细胞质中,LNC 在体外实现了罗利普兰的神经保护作用,但在体内不行。这可能是由于淋巴液稀释了测试物质,或者由于体内和体外条件的不同,罗利普兰的释放不足。尽管如此,基于体外结果,当使用 LNC-罗利普兰与纯罗利普兰和纯 LNC 应用相比时,证明神经元存活率显著增加,我们认为罗利普兰和 LNC 的组合可能会减少 CI 植入后神经元的退化和纤维化。我们得出结论,罗利普兰是一种有前途的内耳治疗药物,LNC 具有作为内耳药物递送系统的潜力。具有改良条件的进一步实验可能会揭示体内生物学效应。