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在感染前很久单次皮下注射纤维素醚可使啮齿动物对朊病毒疾病产生持续保护作用。

A Single Subcutaneous Injection of Cellulose Ethers Administered Long before Infection Confers Sustained Protection against Prion Diseases in Rodents.

作者信息

Teruya Kenta, Oguma Ayumi, Nishizawa Keiko, Kawata Maki, Sakasegawa Yuji, Kamitakahara Hiroshi, Doh-Ura Katsumi

机构信息

Department of Neurochemistry, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

Division of Forest and Biomaterials Science, Graduate School of Agriculture, Kyoto University, Sakyo-ku, Kyoto, Japan.

出版信息

PLoS Pathog. 2016 Dec 14;12(12):e1006045. doi: 10.1371/journal.ppat.1006045. eCollection 2016 Dec.

Abstract

Prion diseases are fatal, progressive, neurodegenerative diseases caused by prion accumulation in the brain and lymphoreticular system. Here we report that a single subcutaneous injection of cellulose ethers (CEs), which are commonly used as inactive ingredients in foods and pharmaceuticals, markedly prolonged the lives of mice and hamsters intracerebrally or intraperitoneally infected with the 263K hamster prion. CEs provided sustained protection even when a single injection was given as long as one year before infection. These effects were linked with persistent residues of CEs in various tissues. More effective CEs had less macrophage uptake ratios and hydrophobic modification of CEs abolished the effectiveness. CEs were significantly effective in other prion disease animal models; however, the effects were less remarkable than those observed in the 263K prion-infected animals. The genetic background of the animal model was suggested to influence the effects of CEs. CEs did not modify prion protein expression but inhibited abnormal prion protein formation in vitro and in prion-infected cells. Although the mechanism of CEs in vivo remains to be solved, these findings suggest that they aid in elucidating disease susceptibility and preventing prion diseases.

摘要

朊病毒病是由朊病毒在大脑和淋巴网状系统中积累引起的致命性、进行性神经退行性疾病。在此,我们报告,单次皮下注射纤维素醚(CEs),这种物质常用作食品和药品中的非活性成分,可显著延长经脑内或腹腔内接种263K仓鼠朊病毒的小鼠和仓鼠的寿命。即使在感染前长达一年时进行单次注射,CEs仍能提供持续保护。这些作用与CEs在各种组织中的持续残留有关。更有效的CEs具有更低的巨噬细胞摄取率,并且CEs的疏水修饰消除了其有效性。CEs在其他朊病毒病动物模型中也具有显著效果;然而,其效果不如在感染263K朊病毒的动物中观察到的那么明显。动物模型的遗传背景被认为会影响CEs的作用。CEs不会改变朊病毒蛋白的表达,但在体外和朊病毒感染的细胞中可抑制异常朊病毒蛋白的形成。尽管CEs在体内的作用机制仍有待解决,但这些发现表明它们有助于阐明疾病易感性并预防朊病毒病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d4/5156379/ed915a9ac58f/ppat.1006045.g001.jpg

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