Department of Molecular Biology, Faculty of Biology, University of Gdansk, Wita Stwosza, 59, 80-308, Gdansk, Poland.
Department of Molecular Biology, Faculty of Biology, University of Gdansk, Wita Stwosza, 59, 80-308, Gdansk, Poland.
Eur J Pharmacol. 2020 Dec 5;888:173534. doi: 10.1016/j.ejphar.2020.173534. Epub 2020 Aug 30.
Mucopolysaccharidoses (MPS) represent a devastating group of lysosomal storage diseases (LSD) affecting approximately 1 in 25,000 individuals, where degradation of glycosaminoglycans (GAG) by lysosomal enzymes is impaired due to mutations causing defects in one of GAG-degrading enzymes. The most commonly used therapy for MPS is enzyme replacement therapy, consisting of application of an active form of the missing enzyme. However, supply of the missing enzyme is not enough in case of MPS types whose symptoms are expressed in central nervous system (CNS), as enzyme does not cross the blood-brain barrier. Moreover, even though enzyme replacement therapy for non-neuronopathic MPS IVA type is approved, it has a limited impact on bone abnormalities, that are one of main symptoms in the disease. Therefore, research into alternative therapeutic approaches for these types of MPS is highly desirable. One such alternative strategy is accelerated degradation of GAG by induction of autophagy. Autophagy is a process of lysosomal degradation of macromolecules that become abnormal or unnecessary for cells. One of the latest discoveries is that GAGs can also be such molecules. Potential drug should also cross blood-brain barrier and be safe in long-term therapy. It seems that one of the polyphenols, resveratrol, can meet the requirements. The mechanism of its action in autophagy stimulation is pleiotropic. Therefore, in this review, we will briefly discuss potential of resveratrol treatment for mucopolysaccharidosis through autophagy stimulation based on research in diseases with similar outcome.
黏多糖贮积症(MPS)是一组破坏性的溶酶体贮积病(LSD),影响大约每 25000 人中就有 1 人,由于导致溶酶体降解糖胺聚糖(GAG)的酶缺陷的突变,导致 GAG 降解酶的缺陷,从而导致 GAG 的降解受损。MPS 的最常用治疗方法是酶替代疗法,包括应用缺失酶的活性形式。然而,在症状表现在中枢神经系统(CNS)的 MPS 类型中,由于酶不能穿过血脑屏障,因此缺失酶的供应是不够的。此外,即使批准了用于非神经病变性 MPS IVA 型的酶替代疗法,它对骨骼异常也只有有限的影响,骨骼异常是该疾病的主要症状之一。因此,非常需要对这些类型的 MPS 进行替代治疗方法的研究。一种这样的替代策略是通过诱导自噬加速 GAG 的降解。自噬是溶酶体降解大分子的过程,这些大分子对于细胞变得异常或不必要。最近的发现之一是 GAG 也可以成为这样的分子。潜在的药物还应该穿过血脑屏障,并在长期治疗中是安全的。似乎多酚中的一种,白藜芦醇,可以满足这些要求。其在自噬刺激中的作用机制是多效性的。因此,在这篇综述中,我们将根据具有相似结果的疾病的研究,简要讨论通过自噬刺激用白藜芦醇治疗黏多糖贮积症的潜力。