| Citation: | Lei Xu, Tao Zhang, Baojie Zhu, Honglin Tao, Yue Liu, Xianfeng Liu, Yi Zhang, Xianli Meng. Mitochondrial quality control disorder in neurodegenerative disorders: Potential and advantages of traditional Chinese medicines[J]. Journal of Pharmaceutical Analysis, 2025, 15(4): 101146. doi: 10.1016/j.jpha.2024.101146 |
| [1] |
D.M. Teleanu, A.G. Niculescu, I.I. Lungu, et al., An overview of oxidative stress, neuroinflammation, and neurodegenerative diseases, Int. J. Mol. Sci. 23 (2022), 5938.
|
| [2] |
World Health Organization. Parkinson’s disease: A public health approach: Technical brief. https://www.who.int/publications/i/item/9789240050983/. (Accessed 24 June 2022).
|
| [3] |
R. Al-Kharboosh, J.J. Perera, A. Bechtle, et al., Emerging point-of-care autologous cellular therapy using adipose-derived stromal vascular fraction for neurodegenerative diseases, Clin. Transl. Med. 12 (2022), e1093.
|
| [4] |
R. Hussain, H. Zubair, S. Pursell, et al., Neurodegenerative diseases: Regenerative mechanisms and novel therapeutic approaches, Brain Sci. 8 (2018), 177.
|
| [5] |
M. Mistretta, A. Farini, Y. Torrente, et al., Multifaceted nanoparticles: Emerging mechanisms and therapies in neurodegenerative diseases, Brain 146 (2023) 2227-2240.
|
| [6] |
M.A. Eldeeb, R.A. Thomas, M.A. Ragheb, et al., Mitochondrial quality control in health and in Parkinson’s disease, Physiol. Rev. 102 (2022) 1721-1755.
|
| [7] |
G.E. Choi, H.J. Han, Glucocorticoid impairs mitochondrial quality control in neurons, Neurobiol. Dis. 152 (2021), 105301.
|
| [8] |
P. Cilleros-Holgado, D. Gomez-Fernandez, R. Pinero-Perez, et al., Mitochondrial quality control via mitochondrial unfolded protein response (mtUPR) in ageing and neurodegenerative diseases, Biomolecules 13 (2023), 1789.
|
| [9] |
H. Xu, Y. Liu, L. Li, et al., Sirtuins at the crossroads between mitochondrial quality control and neurodegenerative diseases: Structure, regulation, modifications, and modulators, Aging Dis. 14 (2023) 794-824.
|
| [10] |
X. Yan, B. Wang, Y. Hu, et al., Abnormal mitochondrial quality control in neurodegenerative diseases, Front. Cell. Neurosci. 14 (2020), 138.
|
| [11] |
A. Roca-Portoles, S.W.G. Tait, Mitochondrial quality control: From molecule to organelle, Cell. Mol. Life Sci. 78 (2021) 3853-3866.
|
| [12] |
P. Mensah-Kane, N. Sumien, The potential of hyperbaric oxygen as a therapy for neurodegenerative diseases, Geroscience 45 (2023) 747-756.
|
| [13] |
F. Duraes, M. Pinto, E. Sousa, Old drugs as new treatments for neurodegenerative diseases, Pharmaceuticals (Basel) 11 (2018), 44.
|
| [14] |
J. Koschel, K. Ray Chaudhuri, L. Tonges, et al., Implications of dopaminergic medication withdrawal in Parkinson’s disease, J. Neural Transm. (Vienna) 129 (2022) 1169-1178.
|
| [15] |
P. Sivanandy, T.C. Leey, T.C. Xiang, et al., Systematic review on Parkinson’s disease medications, emphasizing on three recently approved drugs to control Parkinson’s symptoms, Int. J. Environ. Res. Public Health 19 (2021), 364.
|
| [16] |
J. Dong, Y. Cui, S. Li, et al., Current pharmaceutical treatments and alternative therapies of Parkinson’s disease, Curr. Neuropharmacol. 14 (2016) 339-355.
|
| [17] |
I. Solanki, P. Parihar, M.S. Parihar, Neurodegenerative diseases: From available treatments to prospective herbal therapy, Neurochem. Int. 95 (2016) 100-108.
|
| [18] |
X. Chen, W. Pan, The treatment strategies for neurodegenerative diseases by integrative medicine, Integr. Med. Int. 1 (2015) 223-225.
|
| [19] |
C. Ricci, Neurodegenerative disease: From molecular basis to therapy, Int. J. Mol. Sci. 25 (2024), 967.
|
| [20] |
N. Pfanner, B. Warscheid, N. Wiedemann, Mitochondrial proteins: From biogenesis to functional networks, Nat. Rev. Mol. Cell Biol. 20 (2019) 267-284.
|
| [21] |
D.H. Mendelsohn, K. Schnabel, A. Mamilos, et al., Structural analysis of mitochondrial dynamics-from cardiomyocytes to osteoblasts: A critical review, Int. J. Mol. Sci. 23 (2022), 4571.
|
| [22] |
M. Krols, B. Asselbergh, R. De Rycke, et al., Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution, Hum. Mol. Genet. 28 (2019) 615-627.
|
| [23] |
D. Larrea, M. Pera, A. Gonnelli, et al., MFN2 mutations in Charcot-Marie-Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics, Hum. Mol. Genet. 28 (2019) 1782-1800.
|
| [24] |
J.E. Lee, L.M. Westrate, H. Wu, et al., Multiple dynamin family members collaborate to drive mitochondrial division, Nature 540 (2016) 139-143.
|
| [25] |
A.M. Labrousse, M.D. Zappaterra, D.A. Rube, et al., C. elegans dynamin-related protein DRP-1 controls severing of the mitochondrial outer membrane, Mol. Cell 4 (1999) 815-826.
|
| [26] |
O.C. Loson, Z. Song, H. Chen, et al., Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission, Mol. Biol. Cell 24 (2013) 659-667.
|
| [27] |
M. Zerihun, S. Sukumaran, N. Qvit, The Drp1-mediated mitochondrial fission protein interactome as an emerging core player in mitochondrial dynamics and cardiovascular disease therapy, Int. J. Mol. Sci. 24 (2023), 5785.
|
| [28] |
J. Hu, Y. Zhang, X. Jiang, et al., ROS-mediated activation and mitochondrial translocation of CaMKII contributes to Drp1-dependent mitochondrial fission and apoptosis in triple-negative breast cancer cells by isorhamnetin and chloroquine, J. Exp. Clin. Cancer Res. 38 (2019), 225.
|
| [29] |
H. Otera, N. Miyata, O. Kuge, et al., Drp1-dependent mitochondrial fission via MiD49/51 is essential for apoptotic cristae remodeling, J. Cell Biol. 212 (2016) 531-544.
|
| [30] |
T. Song, X. Song, C. Zhu, et al., Mitochondrial dysfunction, oxidative stress, neuroinflammation, and metabolic alterations in the progression of Alzheimer’s disease: A meta-analysis of in vivo magnetic resonance spectroscopy studies, Ageing Res. Rev. 72 (2021), 101503.
|
| [31] |
J. Balog, S.L. Mehta, R. Vemuganti, Mitochondrial fission and fusion in secondary brain damage after CNS insults, J. Cereb. Blood Flow Metab. 36 (2016) 2022-2033.
|
| [32] |
J. Gao, L. Wang, J. Liu, et al., Abnormalities of mitochondrial dynamics in neurodegenerative diseases, Antioxidants (Basel) 6 (2017), 25.
|
| [33] |
H. Grel, D. Woznica, K. Ratajczak, et al., Mitochondrial dynamics in neurodegenerative diseases: Unraveling the role of fusion and fission processes, Int. J. Mol. Sci. 24 (2023), 13033.
|
| [34] |
C. Larrue, S. Mouche, S. Lin, et al., Mitochondrial fusion is a therapeutic vulnerability of acute myeloid leukemia, Leukemia 37 (2023) 765-775.
|
| [35] |
A.H. Pham, S. Meng, Q.N. Chu, et al., Loss of Mfn2 results in progressive, retrograde degeneration of dopaminergic neurons in the nigrostriatal circuit, Hum. Mol. Genet. 21 (2012) 4817-4826.
|
| [36] |
H. Chen, S.A. Detmer, A.J. Ewald, et al., Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development, J. Cell Biol. 160 (2003) 189-200.
|
| [37] |
C. Brooks, S.G. Cho, C. Wang, et al., Fragmented mitochondria are sensitized to Bax insertion and activation during apoptosis, Am. J. Physiol. Cell Physiol. 300 (2011) C447-C455.
|
| [38] |
V. Del Dotto, P. Mishra, S. Vidoni, et al., OPA1 isoforms in the hierarchical organization of mitochondrial functions, Cell Rep. 19 (2017) 2557-2571.
|
| [39] |
R. Gilkerson, P.D.L. Torre, S. St Vallier, Mitochondrial OMA1 and OPA1 as gatekeepers of organellar structure/function and cellular stress response, Front. Cell Dev. Biol. 9 (2021), 626117.
|
| [40] |
R. Sanchez-Rodriguez, C. Tezze, A.H.R. Agnellini, et al., OPA1 drives macrophage metabolism and functional commitment via p65 signaling, Cell Death Differ. 30 (2023) 742-752.
|
| [41] |
Y. Yu, H.C. Lee, K.C. Chen, et al., Inner membrane fusion mediates spatial distribution of axonal mitochondria, Sci. Rep. 6 (2016), 18981.
|
| [42] |
T. Misgeld, T.L. Schwarz, Mitostasis in neurons: Maintaining mitochondria in an extended cellular architecture, Neuron 96 (2017) 651-666.
|
| [43] |
A. Mandal, H.C. Wong, K. Pinter, et al., Retrograde mitochondrial transport is essential for organelle distribution and health in zebrafish neurons, J. Neurosci. 41 (2021) 1371-1392.
|
| [44] |
B. Sharma, D. Pal, U. Sharma, et al., Mitophagy: An emergence of new player in Alzheimer’s disease, Front. Mol. Neurosci. 15 (2022), 921908.
|
| [45] |
J. Wang, C. Xu, Astrocytes autophagy in aging and neurodegenerative disorders, Biomed. Pharmacother. 122 (2020), 109691.
|
| [46] |
A. Fleming, M. Bourdenx, M. Fujimaki, et al., The different autophagy degradation pathways and neurodegeneration, Neuron 110 (2022) 935-966.
|
| [47] |
W. Li, P. He, Y. Huang, et al., Selective autophagy of intracellular organelles: Recent research advances, Theranostics 11 (2021) 222-256.
|
| [48] |
J.D. Magalhaes, L. Fao, R. Vilaca, et al., Macroautophagy and mitophagy in neurodegenerative disorders: Focus on therapeutic interventions, Biomedicines 9 (2021), 1625.
|
| [49] |
D. Glick, S. Barth, K.F. MacLeod, Autophagy: Cellular and molecular mechanisms, J. Pathol. 221 (2010) 3-12.
|
| [50] |
M. Onishi, K. Yamano, M. Sato, et al., Molecular mechanisms and physiological functions of mitophagy, EMBO J. 40 (2021), e104705.
|
| [51] |
D.A. Chistiakov, T.P. Shkurat, A.A. Melnichenko, et al., The role of mitochondrial dysfunction in cardiovascular disease: A brief review, Ann. Med. 50 (2018) 121-127.
|
| [52] |
L.E. Fritsch, M.E. Moore, S.A. Sarraf, et al., Ubiquitin and receptor-dependent mitophagy pathways and their implication in neurodegeneration, J. Mol. Biol. 432 (2020) 2510-2524.
|
| [53] |
Z.D. Zhou, S. Sathiyamoorthy, D.C. Angeles, et al., Linking F-box protein 7 and parkin to neuronal degeneration in Parkinson’s disease (PD), Mol. Brain 9 (2016), 41.
|
| [54] |
A. Hamacher-Brady, N.R. Brady, Mitophagy programs: Mechanisms and physiological implications of mitochondrial targeting by autophagy, Cell. Mol. Life Sci. 73 (2016) 775-795.
|
| [55] |
J.S. Kerr, B.A. Adriaanse, N.H. Greig, et al., Mitophagy and Alzheimer’s disease: Cellular and molecular mechanisms, Trends Neurosci. 40 (2017) 151-166.
|
| [56] |
A. Rakovic, J. Ziegler, C.U. Martensson, et al., PINK1-dependent mitophagy is driven by the UPS and can occur independently of LC3 conversion, Cell Death Differ. 26 (2019) 1428-1441.
|
| [57] |
Q. Cai, P. Tammineni, Alterations in mitochondrial quality control in Alzheimer’s disease, Front. Cell. Neurosci. 10 (2016), 24.
|
| [58] |
K. Kaarniranta, J. Blasiak, P. Liton, et al., Autophagy in age-related macular degeneration, Autophagy 19 (2023) 388-400.
|
| [59] |
L.P. Poole, K.F. MacLeod, Mitophagy in tumorigenesis and metastasis, Cell. Mol. Life Sci. 78 (2021) 3817-3851.
|
| [60] |
M. Di Rienzo, A. Romagnoli, F. Ciccosanti, et al., AMBRA1 regulates mitophagy by interacting with ATAD3A and promoting PINK1 stability, Autophagy 18 (2022) 1752-1762.
|
| [61] |
L.P. Wilhelm, J. Zapata-Munoz, B. Villarejo-Zori, et al., BNIP3L/NIX regulates both mitophagy and pexophagy, EMBO J. 41 (2022), e111115.
|
| [62] |
J. Sassone, C. Colciago, P. Marchi, et al., Mutant Huntingtin induces activation of the Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3), Cell Death Dis. 1 (2010), e7.
|
| [63] |
A. Di Rita, P. D’Acunzo, L. Simula, et al., AMBRA1-mediated mitophagy counteracts oxidative stress and apoptosis induced by neurotoxicity in human neuroblastoma SH-SY5Y cells, Front. Cell. Neurosci. 12 (2018), 92.
|
| [64] |
B. Khalil, N. El Fissi, A. Aouane, et al., PINK1-induced mitophagy promotes neuroprotection in Huntington’s disease, Cell Death Dis. 6 (2015), e1617.
|
| [65] |
Z. Wu, A. Wu, J. Dong, et al., Grape skin extract improves muscle function and extends lifespan of a Drosophila model of Parkinson’s disease through activation of mitophagy, Exp. Gerontol. 113 (2018) 10-17.
|
| [66] |
S.M. Raefsky, M.P. Mattson, Adaptive responses of neuronal mitochondria to bioenergetic challenges: Roles in neuroplasticity and disease resistance, Free Radic. Biol. Med. 102 (2017) 203-216.
|
| [67] |
R.C. Scarpulla, Metabolic control of mitochondrial biogenesis through the PGC-1 family regulatory network, Biochim. Biophys. Acta 1813 (2011) 1269-1278.
|
| [68] |
P.A. Li, X. Hou, S. Hao, Mitochondrial biogenesis in neurodegeneration, J. Neurosci. Res. 95 (2017) 2025-2029.
|
| [69] |
H.S. Hillen, D. Temiakov, P. Cramer, Structural basis of mitochondrial transcription, Nat. Struct. Mol. Biol. 25 (2018) 754-765.
|
| [70] |
B. Leaw, S. Nair, R. Lim, et al., Mitochondria, bioenergetics and excitotoxicity: New therapeutic targets in perinatal brain injury, Front. Cell. Neurosci. 11 (2017), 199.
|
| [71] |
Y. Kang, L.F. Fielden, D. Stojanovski, Mitochondrial protein transport in health and disease, Semin. Cell Dev. Biol. 76 (2018) 142-153.
|
| [72] |
P. Guedes-Dias, B.R. Pinho, T.R. Soares, et al., Mitochondrial dynamics and quality control in Huntington’s disease, Neurobiol. Dis. 90 (2016) 51-57.
|
| [73] |
S. Kaushik, A.M. Cuervo, Proteostasis and aging, Nat. Med. 21 (2015) 1406-1415.
|
| [74] |
P. Chopade, N. Chopade, Z. Zhao, et al., Alzheimer’s and Parkinson’s disease therapies in the clinic, Bioeng. Transl. Med. 8 (2022), e10367.
|
| [75] |
M. Fakhoury, Microglia and astrocytes in Alzheimer’s disease: Implications for therapy, Curr. Neuropharmacol. 16 (2018) 508-518.
|
| [76] |
J. Wang, W. Liu, H. Shi, et al., A role for PGC-1a in the control of abnormal mitochondrial dynamics in Alzheimer’s disease, Cells 11 (2022), 2849.
|
| [77] |
J. Xing, L. Qi, X. Liu, et al., Roles of mitochondrial fusion and fission in breast cancer progression: A systematic review, World J. Surg. Oncol. 20 (2022), 331.
|
| [78] |
M. de la Cueva, D. Antequera, L. Ordonez-Gutierrez, et al., Amyloid-β impairs mitochondrial dynamics and autophagy in Alzheimer’s disease experimental models, Sci. Rep. 12 (2022), 10092.
|
| [79] |
V.K. Medala, B. Gollapelli, S. Dewanjee, et al., Mitochondrial dysfunction, mitophagy, and role of dynamin-related protein 1 in Alzheimer’s disease, J. Neurosci. Res. 99 (2021) 1120-1135.
|
| [80] |
J. Grohm, S.W. Kim, U. Mamrak, et al., Inhibition of Drp1 provides neuroprotection in vitro and in vivo, Cell Death Differ. 19 (2012) 1446-1458.
|
| [81] |
L.Y. Shields, H. Li, K. Nguyen, et al., Mitochondrial fission is a critical modulator of mutant APP-induced neural toxicity, J. Biol. Chem. 296 (2021), 100469.
|
| [82] |
M.E. Ahmed, G.P. Selvakumar, D. Kempuraj, et al., Synergy in disruption of mitochondrial dynamics by Aβ(1-42) and glia maturation factor (GMF) in SH-SY5Y cells is mediated through alterations in fission and fusion proteins, Mol. Neurobiol. 56 (2019) 6964-6975.
|
| [83] |
X. Wang, B. Su, H.G. Lee, et al., Impaired balance of mitochondrial fission and fusion in Alzheimer’s disease, J. Neurosci. 29 (2009) 9090-9103.
|
| [84] |
S.H. Baek, S.J. Park, J.I. Jeong, et al., Inhibition of Drp1 ameliorates synaptic depression, Aβ deposition, and cognitive impairment in an Alzheimer’s disease model, J. Neurosci. 37 (2017) 5099-5110.
|
| [85] |
X. Wang, Y. Xue, Y. Yao, et al., PINK1 regulates mitochondrial fission/fusion and neuroinflammation in β-amyloid-induced Alzheimer’s disease models, Neurochem. Int. 154 (2022), 105298.
|
| [86] |
P.H. Reddy, M. Manczak, X. Yin, Mitochondria-division inhibitor 1 protects against amyloid-β induced mitochondrial fragmentation and synaptic damage in Alzheimer’s disease, J. Alzheimers Dis. 58 (2017) 147-162.
|
| [87] |
S.E. Lee, D. Kwon, N. Shin, et al., Accumulation of APP-CTF induces mitophagy dysfunction in the iNSCs model of Alzheimer’s disease, Cell Death Discov. 8 (2022), 1.
|
| [88] |
L. Vaillant-Beuchot, A. Mary, R. Pardossi-Piquard, et al., Accumulation of amyloid precursor protein C-terminal fragments triggers mitochondrial structure, function, and mitophagy defects in Alzheimer’s disease models and human brains, Acta Neuropathol. 141 (2021) 39-65.
|
| [89] |
E. Zenaro, G. Piacentino, G. Constantin, The blood-brain barrier in Alzheimer’s disease, Neurobiol. Dis. 107 (2017) 41-56.
|
| [90] |
X. Liu, M. Ye, L. Ma, The emerging role of autophagy and mitophagy in tauopathies: From pathogenesis to translational implications in Alzheimer’s disease, Front. Aging Neurosci. 14 (2022), 1022821.
|
| [91] |
M. Eshraghi, A. Adlimoghaddam, A. Mahmoodzadeh, et al., Alzheimer’s disease pathogenesis: Role of autophagy and mitophagy focusing in microglia, Int. J. Mol. Sci. 22 (2021), 3330.
|
| [92] |
P.H. Reddy, X. Yin, M. Manczak, et al., Mutant APP and amyloid beta-induced defective autophagy, mitophagy, mitochondrial structural and functional changes and synaptic damage in hippocampal neurons from Alzheimer’s disease, Hum. Mol. Genet. 27 (2018) 2502-2516.
|
| [93] |
E.F. Fang, Y. Hou, K. Palikaras, et al., Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer’s disease, Nat. Neurosci. 22 (2019) 401-412.
|
| [94] |
E.F. Fang, Mitophagy and NAD+ inhibit Alzheimer disease, Autophagy 15 (2019) 1112-1114.
|
| [95] |
S. Kshirsagar, N. Sawant, H. Morton, et al., Mitophagy enhancers against phosphorylated Tau-induced mitochondrial and synaptic toxicities in Alzheimer disease, Pharmacol. Res. 174 (2021), 105973.
|
| [96] |
J.A. Pradeepkiran, A. Hindle, S. Kshirsagar, et al., Are mitophagy enhancers therapeutic targets for Alzheimer’s disease? Biomed. Pharmacother. 149 (2022), 112918.
|
| [97] |
C. Chen, C. Yang, J. Wang, et al., Melatonin ameliorates cognitive deficits through improving mitophagy in a mouse model of Alzheimer’s disease, J. Pineal Res. 71 (2021), e12774.
|
| [98] |
K. Zeng, X. Yu, Y.A.R. Mahaman, et al., Defective mitophagy and the etiopathogenesis of Alzheimer’s disease, Transl. Neurodegener. 11 (2022), 32.
|
| [99] |
L. Zhang, Y. Fang, X. Zhao, et al., BRUCE silencing leads to axonal dystrophy by repressing autophagosome-lysosome fusion in Alzheimer’s disease, Transl. Psychiatry 11 (2021), 421.
|
| [100] |
L. Zhang, Y. Fang, X. Cheng, et al., Interaction between TRPML1 and p62 in regulating autophagosome-lysosome fusion and impeding neuroaxonal dystrophy in Alzheimer’s disease, Oxid. Med. Cell. Longev. 2022 (2022), 8096009.
|
| [101] |
A. Adlimoghaddam, G.G. Odero, G. Glazner, et al., Nilotinib improves bioenergetic profiling in brain astroglia in the 3xTg mouse model of Alzheimer’s disease, Aging Dis. 12 (2021) 441-465.
|
| [102] |
W. Li, L. Kui, T. Demetrios, et al., A glimmer of hope: Maintain mitochondrial homeostasis to mitigate Alzheimer’s disease, Aging Dis. 11 (2020) 1260-1275.
|
| [103] |
R. Grewal, M. Reutzel, B. Dilberger, et al., Purified oleocanthal and ligstroside protect against mitochondrial dysfunction in models of early Alzheimer’s disease and brain ageing, Exp. Neurol. 328 (2020), 113248.
|
| [104] |
M.P. Singulani, C.P.M. Pereira, A.F.F. Ferreira, et al., Impairment of PGC-1α-mediated mitochondrial biogenesis precedes mitochondrial dysfunction and Alzheimer’s pathology in the 3xTg mouse model of Alzheimer’s disease, Exp. Gerontol. 133 (2020), 110882.
|
| [105] |
Z. Zhu, L. Xu, D. Cao, et al., Effect of orexin-A on mitochondrial biogenesis, mitophagy and structure in HEK293-APPSWE cell model of Alzheimer’s disease, Clin. Exp. Pharmacol. Physiol. 48 (2021) 355-360.
|
| [106] |
B. Li, Y. Chen, Y. Zhou, et al., Neural stem cell-derived exosomes promote mitochondrial biogenesis and restore abnormal protein distribution in a mouse model of Alzheimer’s disease, Neural Regen. Res. 19 (2024) 1593-1601.
|
| [107] |
L. Katsouri, Y.M. Lim, K. Blondrath, et al., PPARγ-coactivator-1α gene transfer reduces neuronal loss and amyloid-β generation by reducing β-secretase in an Alzheimer’s disease model, Proc. Natl. Acad. Sci. USA 113 (2016) 12292-12297.
|
| [108] |
J. Wang, M. Guo, Z. Liu, et al., PGC-1α reduces amyloid-β deposition in Alzheimer’s disease: Effect of increased VDR expression, Neurosci. Lett. 744 (2021), 135598.
|
| [109] |
B. Chen, J. Wu, S. Hu, et al., Apelin-13 improves cognitive impairment and repairs hippocampal neuronal damage by activating PGC-1α/PPARγ signaling, Neurochem. Res. 48 (2023) 1504-1515.
|
| [110] |
Y.J. Kang, S.J. Hyeon, A. McQuade, et al., Neurotoxic microglial activation via IFNγ-induced Nrf2 reduction exacerbating Alzheimer’s disease, Adv. Sci. (Weinh) 11 (2024), e2304357.
|
| [111] |
B.N. Lizama, C.T. Chu, Neuronal autophagy and mitophagy in Parkinson’s disease, Mol. Aspects Med. 82 (2021), 100972.
|
| [112] |
Z. Zhu, C. Yang, A. Iyaswamy, et al., Balancing mTOR signaling and autophagy in the treatment of Parkinson’s disease, Int. J. Mol. Sci. 20 (2019), 728.
|
| [113] |
A. Sarkar, R. Hameed, A. Mishra, et al., Genetic modulators associated with regulatory surveillance of mitochondrial quality control, play a key role in regulating stress pathways and longevity in C. elegans, Life Sci. 290 (2022), 120226.
|
| [114] |
E.J. Shin, J.H. Jeong, Y. Hwang, et al., Methamphetamine-induced dopaminergic neurotoxicity as a model of Parkinson’s disease, Arch. Pharm. Res. 44 (2021) 668-688.
|
| [115] |
R. MacDonald, K. Barnes, C. Hastings, et al., Mitochondrial abnormalities in Parkinson’s disease and Alzheimer’s disease: Can mitochondria be targeted therapeutically? Biochem. Soc. Trans. 46 (2018) 891-909.
|
| [116] |
E. Chernivec, J. Cooper, K. Naylor, Exploring the effect of rotenone-a known inducer of Parkinson’s disease-on mitochondrial dynamics in Dictyostelium discoideum, Cells 7 (2018), 201.
|
| [117] |
B. Zhou, M. Wen, X. Lin, et al., Alpha lipoamide ameliorates motor deficits and mitochondrial dynamics in the Parkinson’s disease model induced by 6-hydroxydopamine, Neurotox. Res. 33 (2018) 759-767.
|
| [118] |
Q. Zhang, C. Hu, J. Huang, et al., ROCK1 induces dopaminergic nerve cell apoptosis via the activation of Drp1-mediated aberrant mitochondrial fission in Parkinson’s disease, Exp. Mol. Med. 51 (2019) 1-13.
|
| [119] |
M. Adebayo, S. Singh, A.P. Singh, et al., Mitochondrial fusion and fission: The fine-tune balance for cellular homeostasis, FASEB J. 35 (2021), e21620.
|
| [120] |
F. Zhao, W. Wang, C. Wang, et al., Mfn2 protects dopaminergic neurons exposed to paraquat both in vitro and in vivo: Implications for idiopathic Parkinson’s disease, Biochim. Biophys. Acta Mol. Basis Dis. 1863 (2017) 1359-1370.
|
| [121] |
S. Ahmed, M. Kwatra, S. Ranjan Panda, et al., Andrographolide suppresses NLRP3 inflammasome activation in microglia through induction of parkin-mediated mitophagy in in-vitro and in-vivo models of Parkinson disease, Brain Behav. Immun. 91 (2021) 142-158.
|
| [122] |
G. Ashrafi, J.S. Schlehe, M.J. LaVoie, et al., Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin, J. Cell Biol. 206 (2014) 655-670.
|
| [123] |
D.A. Madsen, S.I. Schmidt, M. Blaabjerg, et al., Interaction between parkin and α-synuclein in PARK2-mediated Parkinson’s disease, Cells 10 (2021), 283.
|
| [124] |
Q. Gao, R. Tian, H. Han, et al., PINK1-mediated Drp1S616 phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission, Signal Transduct. Target. Ther. 7 (2022), 103.
|
| [125] |
Y. Wang, W. Chen, Y. Han, et al., Neuroprotective effect of engineered Clostridium butyricum-pMTL007-GLP-1 on Parkinson’s disease mice models via promoting mitophagy, Bioeng. Transl. Med. 8 (2023), e10505.
|
| [126] |
F. De Lazzari, F. Agostini, N. Plotegher, et al., DJ-1 promotes energy balance by regulating both mitochondrial and autophagic homeostasis, Neurobiol. Dis. 176 (2023), 105941.
|
| [127] |
H. Liu, P.W. Ho, C.T. Leung, et al., Aberrant mitochondrial morphology and function associated with impaired mitophagy and DNM1L-MAPK/ERK signaling are found in aged mutant Parkinsonian LRRK2R1441G mice, Autophagy 17 (2021) 3196-3220.
|
| [128] |
L.D. Osellame, A.A. Rahim, I.P. Hargreaves, et al., Mitochondria and quality control defects in a mouse model of Gaucher disease: Links to Parkinson’s disease, Cell Metab. 17 (2013) 941-953.
|
| [129] |
M. Elstner, C.M. Morris, K. Heim, et al., Expression analysis of dopaminergic neurons in Parkinson’s disease and aging links transcriptional dysregulation of energy metabolism to cell death, Acta Neuropathol. 122 (2011) 75-86.
|
| [130] |
A. Bender, K.J. Krishnan, C.M. Morris, et al., High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease, Nat. Genet. 38 (2006) 515-517.
|
| [131] |
Q. Zheng, H. Liu, H. Zhang, et al., Ameliorating mitochondrial dysfunction of neurons by biomimetic targeting nanoparticles mediated mitochondrial biogenesis to boost the therapy of Parkinson’s disease, Adv. Sci. (Weinh) 10 (2023), e2300758.
|
| [132] |
Y.L. Hsu, H.J. Chen, J. Gao, et al., Chiisanoside mediates the parkin/ZNF746/PGC-1α axis by downregulating miR-181a to improve mitochondrial biogenesis in 6-OHDA-caused neurotoxicity models in vitro and in vivo: Suggestions for prevention of Parkinson’s disease, Antioxidants (Basel) 12 (2023), 1782.
|
| [133] |
Z. Sun, X. Ma, H. Yang, et al., Characterization of age-dependent behavior deficits in the PGC-1α knockout mouse, in relevance to the Parkinson’s disease model, Neuroscience 440 (2020) 39-47.
|
| [134] |
R. Aviner, T.-T. Lee, V.B. Masto, et al., Polyglutamine-mediated ribotoxicity disrupts proteostasis and stress responses in Huntington’s disease, Nat. Cell Biol. 26 (2024) 892-902.
|
| [135] |
S. Tyebji, A.J. Hannan, Synaptopathic mechanisms of neurodegeneration and dementia: Insights from Huntington’s disease, Prog. Neurobiol. 153 (2017) 18-45.
|
| [136] |
U. Shirendeb, A.P. Reddy, M. Manczak, et al., Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington’s disease: Implications for selective neuronal damage, Hum. Mol. Genet. 20 (2011) 1438-1455.
|
| [137] |
J. Kim, J.P. Moody, C.K. Edgerly, et al., Mitochondrial loss, dysfunction and altered dynamics in Huntington’s disease, Hum. Mol. Genet. 19 (2010) 3919-3935.
|
| [138] |
A.J. Roe, X. Qi, Drp1 phosphorylation by MAPK1 causes mitochondrial dysfunction in cell culture model of Huntington’s disease, Biochem. Biophys. Res. Commun. 496 (2018) 706-711.
|
| [139] |
V. Costa, M. Giacomello, R. Hudec, et al., Mitochondrial fission and cristae disruption increase the response of cell models of Huntington’s disease to apoptotic stimuli, EMBO Mol. Med. 2 (2010) 490-503.
|
| [140] |
W. Song, J. Chen, A. Petrilli, et al., Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity, Nat. Med. 17 (2011) 377-382.
|
| [141] |
N. Okada, T. Yako, S. Nakamura, et al., Reduced mitochondrial complex II activity enhances cell death via intracellular reactive oxygen species in STHdhQ111 striatal neurons with mutant huntingtin, J. Pharmacol. Sci. 147 (2021) 367-375.
|
| [142] |
M.E. Solesio, S. Saez-Atienzar, J. Jordan, et al., 3-Nitropropionic acid induces autophagy by forming mitochondrial permeability transition pores rather than activating the mitochondrial fission pathway, Br. J. Pharmacol. 168 (2013) 63-75.
|
| [143] |
A. Jurcau, Molecular pathophysiological mechanisms in Huntington’s disease, Biomedicines 10 (2022), 1432.
|
| [144] |
A. Johri, A. Chandra, M. Flint Beal, PGC-1α, mitochondrial dysfunction, and Huntington’s disease, Free Radic. Biol. Med. 62 (2013) 37-46.
|
| [145] |
T.A. Intihar, E.A. Martinez, R. Gomez-Pastor, Mitochondrial dysfunction in Huntington’s disease; interplay between HSF1, p53 and PGC-1α transcription factors, Front. Cell. Neurosci. 13 (2019), 103.
|
| [146] |
A. Sharma, T. Behl, L. Sharma, et al., Mitochondrial dysfunction in Huntington’s disease: Pathogenesis and therapeutic opportunities, Curr. Drug Targets 22 (2021) 1637-1667.
|
| [147] |
R. Li, L. Wang, H.-X. Duan, et al., Regulation of mitochondrial dysfunction induced cell apoptosis is a potential therapeutic strategy for herbal medicine to treat neurodegenerative diseases, Front. Pharmacol. 13 (2022), 937289.
|
| [148] |
Y. Dong, T. Li, S. Wang, et al., Bu Zhong Yiqi Decoction ameliorates mild cognitive impairment by improving mitochondrial oxidative stress damage via the SIRT3/MnSOD/OGG1 pathway, J. Ethnopharmacol. 331 (2024), 118237.
|
| [149] |
H.S. Lim, Y.J. Kim, E. Sohn, et al., Bojungikgi-Tang, a traditional herbal formula, exerts neuroprotective effects and ameliorates memory impairments in Alzheimer’s disease-like experimental models, Nutrients 10 (2018), 1952.
|
| [150] |
Q. Xiao, H. Liu, C. Yang, et al., Bushen-Yizhi formula exerts neuroprotective effect via inhibiting excessive mitophagy in rats with chronic cerebral hypoperfusion, J. Ethnopharmacol. 310 (2023), 116326.
|
| [151] |
X. Hou, D. Wu, C. Zhang, et al., Bushen-Yizhi formula ameliorates cognition deficits and attenuates oxidative stress-related neuronal apoptosis in scopolamine-induced senescence in mice, Int. J. Mol. Med. 34 (2014) 429-439.
|
| [152] |
Y. Zhang, H. Sun, X. He, et al., Da-Bu-Yin-Wan and Qian-Zheng-San, two traditional Chinese herbal formulas, up-regulate the expression of mitochondrial subunit NADH dehydrogenase 1 synergistically in the mice model of Parkinson’s disease, J. Ethnopharmacol. 146 (2013) 363-371.
|
| [153] |
C. Gai, W. Feng, T. Qiang, et al., Da-bu-Yin-Wan and Qian-Zheng-San ameliorate mitochondrial dynamics in the Parkinson’s disease cell model induced by MPP, Front. Pharmacol. 10 (2019), 372.
|
| [154] |
S. Su, G. Chen, M. Gao, et al., Kai-Xin-San protects against mitochondrial dysfunction in Alzheimer’s disease through SIRT3/NLRP3 pathway, Chin. Med. 18 (2023), 26.
|
| [155] |
Z. Song, D. Luo, Y. Wang, et al., Neuroprotective effect of Danggui Shaoyao San via the mitophagy-apoptosis pathway in a rat model of Alzheimer’s disease, Evid Based Complement Alternat Med. 2021 (2021), 3995958.
|
| [156] |
G.S. Chai, J. Gong, J.J. Wu, et al., Danggui Buxue decoction ameliorates mitochondrial biogenesis and cognitive deficits through upregulating histone H4 lysine 12 acetylation in APP/PS1 mice, J. Ethnopharmacol. 313 (2023), 116554.
|
| [157] |
H. An, C. Lin, C. Gu, et al., Di-Huang-Yi-Zhi herbal formula attenuates amyloid-β-induced neurotoxicity in PC12 cells, Exp. Ther. Med. 13 (2017) 3003-3008.
|
| [158] |
I.J. Lee, C. Chao, Y. Yang, et al., Huang Lian Jie Du Tang attenuates paraquat-induced mitophagy in human SH-SY5Y cells: A traditional decoction with a novel therapeutic potential in treating Parkinson’s disease, Biomed. Pharmacother. 134 (2021), 111170.
|
| [159] |
Z. Ji, Y. Shi, X. Li, et al., Neuroprotective effect of Taohong Siwu Decoction on cerebral ischemia/reperfusion injury via mitophagy-NLRP3 inflammasome pathway, Front. Pharmacol. 13 (2022), 910217.
|
| [160] |
Q. Long, T. Li, Q. Zhu, et al., SuanZaoRen decoction alleviates neuronal loss, synaptic damage and ferroptosis of AD via activating DJ-1/Nrf2 signaling pathway, J. Ethnopharmacol. 323 (2024), 117679.
|
| [161] |
S. Wen, L. Wang, T. Wang, et al., Puerarin alleviates cadmium-induced mitochondrial mass decrease by inhibiting PINK1-Parkin and Nix-mediated mitophagy in rat cortical neurons, Ecotoxicol. Environ. Saf. 230 (2022), 113127.
|
| [162] |
Y. Bian, Y. Chen, X. Wang, et al., Oxyphylla A ameliorates cognitive deficits and alleviates neuropathology via the Akt-GSK3β and Nrf2-Keap1-HO-1 pathways in vitro and in vivo murine models of Alzheimer’s disease, J. Adv. Res. 34 (2021) 1-12.
|
| [163] |
H. Khan, H. Ullah, M. Aschner, et al., Neuroprotective effects of quercetin in Alzheimer’s disease, Biomolecules 10 (2019), 59.
|
| [164] |
M. Ay, J. Luo, M. Langley, et al., Molecular mechanisms underlying protective effects of quercetin against mitochondrial dysfunction and progressive dopaminergic neurodegeneration in cell culture and MitoPark transgenic mouse models of Parkinson’s disease, J. Neurochem. 141 (2017) 766-782.
|
| [165] |
D. Lee, N. Kim, S.H. Jeon, et al., Hesperidin improves memory function by enhancing neurogenesis in a mouse model of Alzheimer’s disease, Nutrients 14 (2022), 3125.
|
| [166] |
S. Kesh, R.R. Kannan, A. Balakrishnan, Naringenin alleviates 6-hydroxydopamine induced Parkinsonism in SHSY5Y cells and zebrafish model, Comp. Biochem. Physiol. C. Toxicol. Pharmacol. 239 (2021), 108893.
|
| [167] |
N. Wang, H. Wang, Q. Pan, et al., The combination of β-asarone and icariin inhibits amyloid-β and reverses cognitive deficits by promoting mitophagy in models of Alzheimer’s disease, Oxid. Med. Cell. Longev. 2021 (2021), 7158444.
|
| [168] |
B. Lee, B. Sur, S.G. Cho, et al., Wogonin attenuates hippocampal neuronal loss and cognitive dysfunction in trimethyltin-intoxicated rats, Biomol. Ther. (Seoul) 24 (2016) 328-337.
|
| [169] |
Y. Zhu, J. Wang, Wogonin increases β-amyloid clearance and inhibits tau phosphorylation via inhibition of mammalian target of rapamycin: Potential drug to treat Alzheimer’s disease, Neurol. Sci. 36 (2015) 1181-1188.
|
| [170] |
D. Wang, S. Li, W. Wu, et al., Effects of long-term treatment with quercetin on cognition and mitochondrial function in a mouse model of Alzheimer’s disease, Neurochem. Res. 39 (2014) 1533-1543.
|
| [171] |
Z. He, X. Li, Z. Wang, et al., Protective effects of luteolin against amyloid beta-induced oxidative stress and mitochondrial impairments through peroxisome proliferator-activated receptor γ-dependent mechanism in Alzheimer’s disease, Redox Biol. 66 (2023), 102848.
|
| [172] |
O.A. Ahmedy, T.M. Abdelghany, M.E.A. El-Shamarka, et al., Apigenin attenuates LPS-induced neurotoxicity and cognitive impairment in mice via promoting mitochondrial fusion/mitophagy: Role of SIRT3/PINK1/Parkin pathway, Psychopharmacology (Berl) 239 (2022) 3903-3917.
|
| [173] |
X. Yao, J. Zhang, Y. Lu, et al., Myricetin restores Aβ-induced mitochondrial impairments in N2a-SW cells, ACS Chem. Neurosci. 13 (2022) 454-463.
|
| [174] |
H. Fan, Y. Li, M. Sun, et al., Hyperoside reduces rotenone-induced neuronal injury by suppressing autophagy, Neurochem. Res. 46 (2021) 3149-3158.
|
| [175] |
H. Bai, Y. Ding, X. Li, et al., Polydatin protects SH-SY5Y in models of Parkinson’s disease by promoting Atg5-mediated but parkin-independent autophagy, Neurochem. Int. 134 (2020), 104671.
|
| [176] |
X. Song, H. Zhou, Y. Sun, et al., Inhibitory effects of curcumin on H2O2-induced cell damage and APP expression and processing in SH-SY5Y cells transfected with APP gene with Swedish mutation, Mol. Biol. Rep. 47 (2020) 2047-2059.
|
| [177] |
P.H. Reddy, M. Manczak, X. Yin, et al., Protective effects of a natural product, curcumin, against amyloid ? induced mitochondrial and synaptic toxicities in Alzheimer’s disease, J. Investig. Med. 64 (2016) 1220-1234.
|
| [178] |
F. Firdaus, M.F. Zafeer, M. Waseem, et al., Ellagic acid mitigates arsenic-trioxide-induced mitochondrial dysfunction and cytotoxicity in SH-SY5Y cells, J. Biochem. Mol. Toxicol. 32 (2018), e22024.
|
| [179] |
J. He, X. Li, S. Yang, et al., Gastrodin extends the lifespan and protects against neurodegeneration in the Drosophila PINK1 model of Parkinson’s disease, Food Funct. 12 (2021) 7816-7824.
|
| [180] |
Q. Zhao, Z. Tian, G. Zhou, et al., SIRT1-dependent mitochondrial biogenesis supports therapeutic effects of resveratrol against neurodevelopment damage by fluoride, Theranostics 10 (2020) 4822-4838.
|
| [181] |
M.F. Zafeer, F. Firdaus, E. Anis, et al., Prolong treatment with Trans-ferulic acid mitigates bioenergetics loss and restores mitochondrial dynamics in streptozotocin-induced sporadic dementia of Alzheimer’s type, Neurotoxicology 73 (2019) 246-257.
|
| [182] |
D. Wang, L. Cao, X. Zhou, et al., Mitigation of honokiol on fluoride-induced mitochondrial oxidative stress, mitochondrial dysfunction, and cognitive deficits through activating AMPK/PGC-1α/Sirt3, J. Hazard. Mater. 437 (2022), 129381.
|
| [183] |
R. Li, J. Chen, Salidroside protects dopaminergic neurons by enhancing PINK1/parkin-mediated mitophagy, Oxid. Med. Cell. Longev. 2019 (2019), 9341018.
|
| [184] |
Y. Tian, Y. Qi, H. Cai, et al., Senegenin alleviates Aβ1-42 induced cell damage through triggering mitophagy, J. Ethnopharmacol. 295 (2022), 115409.
|
| [185] |
Y. Li, J. Li, L. Yang, et al., Ginsenoside Rb1 protects hippocampal neurons in depressed rats based on mitophagy-regulated astrocytic pyroptosis, Phytomedicine 121 (2023), 155083.
|
| [186] |
M. Rashedinia, J. Saberzadeh, T. Khosravi Bakhtiari, et al., Glycyrrhizic acid ameliorates mitochondrial function and biogenesis against aluminum toxicity in PC12 cells, Neurotox. Res. 35 (2019) 584-593.
|
| [187] |
C. Yang, Y. Mo, E. Xu, et al., Astragaloside IV ameliorates motor deficits and dopaminergic neuron degeneration via inhibiting neuroinflammation and oxidative stress in a Parkinson’s disease mouse model, Int. Immunopharmacol. 75 (2019), 105651.
|
| [188] |
J. Du, J. Liu, X. Huang, et al., Catalpol ameliorates neurotoxicity in N2a/APP695swe cells and APP/PS1 transgenic mice, Neurotox. Res. 40 (2022) 961-972.
|
| [189] |
L.F.R. Qi, S. Liu, Y. Liu, et al., Ganoderic acid A promotes amyloid-β clearance (in vitro) and ameliorates cognitive deficiency in Alzheimer’s disease (mouse model) through autophagy induced by activating axl, Int. J. Mol. Sci. 22 (2021), 5559.
|
| [190] |
L. Chen, L.Y. Horng, C.L. Wu, et al., Activating mitochondrial regulator PGC-1α expression by astrocytic NGF is a therapeutic strategy for Huntington’s disease, Neuropharmacology 63 (2012) 719-732.
|
| [191] |
J. Geng, W. Liu, J. Gao, et al., Andrographolide alleviates Parkinsonism in MPTP-PD mice via targeting mitochondrial fission mediated by dynamin-related protein 1, Br. J. Pharmacol. 176 (2019) 4574-4591.
|
| [192] |
C. Wang, Q. Zou, Y. Pu, et al., Berberine rescues D-ribose-induced Alzheimer’s pathology via promoting mitophagy, Int. J. Mol. Sci. 24 (2023), 5896.
|
| [193] |
Y. Zhang, J. Wang, C. Wang, et al., Pharmacological basis for the use of evodiamine in Alzheimer’s disease: Antioxidation and antiapoptosis, Int. J. Mol. Sci. 19 (2018), 1527.
|
| [194] |
F. Meng, J. Wang, F. Ding, et al., Neuroprotective effect of matrine on MPTP-induced Parkinson’s disease and on Nrf2 expression, Oncol. Lett. 13 (2017) 296-300.
|
| [195] |
L. Cui, Y. Cai, W. Cheng, et al., A novel, multi-target natural drug candidate, matrine, improves cognitive deficits in Alzheimer’s disease transgenic mice by inhibiting Aβ aggregation and blocking the RAGE/Aβ axis, Mol. Neurobiol. 54 (2017) 1939-1952.
|
| [196] |
Y. Lei, L. Yang, C.Y. Ye, et al., Involvement of intracellular and mitochondrial Aβ in the ameliorative effects of huperzine A against oligomeric Aβ42-induced injury in primary rat neurons, PLoS One 10 (2015), e0128366.
|
| [197] |
R. Li, Y. Lu, Q. Zhang, et al., Piperine promotes autophagy flux by P2RX4 activation in SNCA/α-synuclein-induced Parkinson disease model, Autophagy 18 (2022) 559-575.
|