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有氧运动与酶替代疗法相结合可恢复线粒体-溶酶体轴的功能,并缓解庞贝病中的自噬障碍。

Combined aerobic exercise and enzyme replacement therapy rejuvenates the mitochondrial-lysosomal axis and alleviates autophagic blockage in Pompe disease.

作者信息

Nilsson M I, MacNeil L G, Kitaoka Y, Suri R, Young S P, Kaczor J J, Nates N J, Ansari M U, Wong T, Ahktar M, Brandt L, Hettinga B P, Tarnopolsky M A

机构信息

Department of Pediatrics and Medicine, Neuromuscular Clinic, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.

Department of Pediatrics, Division of Medical Genetics/Duke University Medical Center, Durham, NC, USA.

出版信息

Free Radic Biol Med. 2015 Oct;87:98-112. doi: 10.1016/j.freeradbiomed.2015.05.019. Epub 2015 May 19.

Abstract

A unifying feature in the pathogenesis of aging, neurodegenerative disease, and lysosomal storage disorders is the progressive deposition of macromolecular debris impervious to enzyme catalysis by cellular waste disposal mechanisms (e.g., lipofuscin). Aerobic exercise training (AET) has pleiotropic effects and stimulates mitochondrial biogenesis, antioxidant defense systems, and autophagic flux in multiple organs and tissues. Our aim was to explore the therapeutic potential of AET as an ancillary therapy to mitigate autophagic buildup and oxidative damage and rejuvenate the mitochondrial-lysosomal axis in Pompe disease (GSD II/PD). Fourteen weeks of combined recombinant acid α-glucosidase (rhGAA) and AET polytherapy attenuated mitochondrial swelling, fortified antioxidant defense systems, reduced oxidative damage, and augmented glycogen clearance and removal of autophagic debris/lipofuscin in fast-twitch skeletal muscle of GAA-KO mice. Ancillary AET potently augmented the pool of PI4KA transcripts and exerted a mild restorative effect on Syt VII and VAMP-5/myobrevin, collectively suggesting improved endosomal transport and Ca(2+)- mediated lysosomal exocytosis. Compared with traditional rhGAA monotherapy, AET and rhGAA polytherapy effectively mitigated buildup of protein carbonyls, autophagic debris/lipofuscin, and P62/SQSTM1, while enhancing MnSOD expression, nuclear translocation of Nrf-2, muscle mass, and motor function in GAA-KO mice. Combined AET and rhGAA therapy reactivates cellular clearance pathways, mitigates mitochondrial senescence, and strengthens antioxidant defense systems in GSD II/PD. Aerobic exercise training (or pharmacologic targeting of contractile-activity-induced pathways) may have therapeutic potential for mitochondrial-lysosomal axis rejuvenation in lysosomal storage disorders and related conditions (e.g., aging and neurodegenerative disease).

摘要

衰老、神经退行性疾病和溶酶体贮积症发病机制中的一个共同特征是,细胞废物处理机制(如脂褐素)无法催化的大分子碎片逐渐沉积。有氧运动训练(AET)具有多效性,可刺激多个器官和组织中的线粒体生物合成、抗氧化防御系统和自噬通量。我们的目的是探索AET作为辅助疗法的治疗潜力,以减轻自噬积累和氧化损伤,并使庞贝病(糖原贮积病II型/PD)中的线粒体-溶酶体轴恢复活力。联合重组酸性α-葡萄糖苷酶(rhGAA)和AET进行十四周的联合治疗,可减轻GAA-KO小鼠快肌骨骼肌中的线粒体肿胀,增强抗氧化防御系统,减少氧化损伤,并增加糖原清除以及自噬碎片/脂褐素的清除。辅助性AET可有效增加PI4KA转录本库,并对突触结合蛋白VII和VAMP-5/肌微管蛋白产生轻度恢复作用,共同表明内体运输和Ca(2+)介导的溶酶体胞吐作用得到改善。与传统的rhGAA单一疗法相比,AET和rhGAA联合疗法可有效减轻蛋白羰基、自噬碎片/脂褐素和P62/SQSTM1的积累,同时增强GAA-KO小鼠中MnSOD的表达、Nrf-2的核转位、肌肉质量和运动功能。联合AET和rhGAA疗法可重新激活细胞清除途径,减轻线粒体衰老,并增强糖原贮积病II型/PD中的抗氧化防御系统。有氧运动训练(或对收缩活动诱导途径进行药理学靶向)可能对溶酶体贮积症及相关病症(如衰老和神经退行性疾病)中线粒体-溶酶体轴的恢复具有治疗潜力。

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