首页> 外文期刊>Mechanisms of Ageing and Development >Ro5-4864, a synthetic ligand of peripheral benzodiazepine receptor, reduces aging-associated myelin degeneration in the sciatic nerve of male rats.
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Ro5-4864, a synthetic ligand of peripheral benzodiazepine receptor, reduces aging-associated myelin degeneration in the sciatic nerve of male rats.

机译:Ro5-4864是外周苯二氮卓类受体的合成配体,可减少雄性大鼠坐骨神经中与衰老相关的髓磷脂变性。

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摘要

The peripheral-type benzodiazepine receptor (PBR) is a protein predominantly located in the mitochondrial outer membrane that plays an important role in the regulation of cell survival and proliferation. Previous studies have shown an enhanced expression of PBR in the regenerating sciatic nerve, suggesting that this protein may be involved in the regenerative response. The rat sciatic nerve suffers important structural alterations with aging, including alterations in the morphology of myelin sheaths and a decrease in the number of myelinated fibers. In this study, we have assessed the effect of two PBR ligands, Ro5-4864 and PK-11195, to determine whether PBR may influence aging-associated morphological changes in the sciatic nerve. The treatment of 23-month-old, Sprague-Dawley male rats for 1 month with Ro5-4864 significantly reduced the percentage of fibers with myelin decompaction and increased the total number of myelinated fibers. In contrast, PK-11195, a PBR ligand that binds to a different site than Ro5-4864 in the PBR molecule, did not significantly affect any of the parameters analyzed. These findings support the potential role of PBR ligands to prevent aging-associated peripheral nerve degeneration.
机译:外周型苯二氮卓受体(PBR)是一种主要位于线粒体外膜中的蛋白质,在调节细胞存活和增殖中起着重要作用。先前的研究表明,再生坐骨神经中PBR的表达增强,表明该蛋白可能参与了再生反应。随着年龄的增长,大鼠坐骨神经遭受重要的结构改变,包括髓鞘的形态改变和髓鞘纤维数量的减少。在这项研究中,我们评估了两个PBR配体Ro5-4864和PK-11195的作用,以确定PBR是否可能影响坐骨神经衰老相关的形态变化。用Ro5-4864治疗23个月大的Sprague-Dawley雄性大鼠1个月,可显着降低髓磷脂分解引起的纤维百分比,并增加髓鞘纤维的总数。相反,PK-11195是一种PBR配体,与PBR分子中的Ro5-4864结合的位点不同,它不会显着影响所分析的任何参数。这些发现支持PBR配体在预防与衰老相关的周围神经变性中的潜在作用。

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