Probiotic Pediococcus pentosaceus ameliorates MPTP-induced oxidative stress via regulating the gut microbiota–gut–brain axis
Open accessAbstract
Recent evidence demonstrated that functional bacteria were involved in the regulation of Parkinson’s disease (PD). However, the mechanism of probiotics in improving PD was unclear. Here the antioxidant effect and the mechanism of probiotics Pediococcus pentosaceus (PP) on PD were studied by regulating the gut–brain axis. In this study, male C57BL/6J mice were injected with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) intraperitoneally to establish a PD model and were then treated with PP for 4 weeks. Subsequently, a series of neurobehavioral tests to evaluate the motor function of the mice was performed. Additionally, degeneration of dopaminergic neurons, accumulation of α-synuclein, the production of an oxidative stress response, and the expression of nuclear factor erythroid 2-related factor 2 (Nrf2) pathway-related proteins were evaluated. Moreover, the gut microbial composition and the level of metabolite γ-aminobutyric acid (GABA) were assessed. The results showed that PP treatment could improve MPTP-induced motor deficits, the degeneration of dopaminergic neurons, and the accumulation of α-synuclein. Moreover, PP treatment significantly increased the levels of SOD1, Gpx1, and Nrf2, while it decreased the levels of Keap1 in the brain of MPTP-induced mice. Notably, PP treatment improved the gut microbial dysbiosis and increased the level of GABA in MPTP-induced mice. These findings indicated that PP might represent a promising candidate, due to the metabolite of GABA, that could be used for the treatment of PD.
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Gut microbiota manipulation affects GABA levels, and probiotic Pediococcus pentosaceus and prebiotic polymannuronic acid reduce GABA levels in brains of MPTP-induced mice, ameliorating motor dysfunction and neuronal degeneration.
“The administration of probiotic Pediococcus pentosaceus and prebiotic polymannuronic acid has shown promise in alleviating gut dysbiosis and reducing GABA levels in the brains of MPTP-induced mice, resulting in the amelioration of motor dysfunction and neuronal degeneration.490,511”
From Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases (2024) · cites this paper as [511]
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Bravo, J. A., Forsythe, P., Chew, M. V., Escaravage, E., Savignac, H. M., Dinan, T. G., Bienenstock, J., & Cryan, J. F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102999108 · Cited by 3,888 · see citing works
Diagnosis and Treatment of Parkinson Disease: A Review
Armstrong, M. J., & Okun, M. S. (2020) · JAMA · doi:10.1001/jama.2019.22360 · Cited by 2,924 · see citing works
The Emerging Evidence of the Parkinson Pandemic
Dorsey, E. R., Sherer, T., Okun, M. S., & Bloem, B. R. (2018) · Journal of Parkinson s Disease · doi:10.3233/jpd-181474 · Cited by 1,995 · see citing works
NRF2, a Transcription Factor for Stress Response and Beyond
He, F., Ru, X., & Wen, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134777 · Cited by 1,820 · see citing works
NRF2 and the Hallmarks of Cancer
Rojo de la Vega, M., Chapman, E., & Zhang, D. D. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.03.022 · Cited by 1,672 · see citing works
Neurotransmitter modulation by the gut microbiota
Strandwitz, P. (2018) · Brain Research · doi:10.1016/j.brainres.2018.03.015 · Cited by 1,527 · see citing works
Psychobiotics: A novel class of psychotropic
Dinan, T. G., Stanton, C., & Cryan, J. F. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.001 · Cited by 1,287 · see citing works
Unger, M. M., Spiegel, J., Dillmann, K.-U., Grundmann, D., Philippeit, H., Bürmann, J., Faßbender, K., Schwiertz, A., & Schäfer, K.-H. (2016) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2016.08.019 · Cited by 1,159 · see citing works
Hill‐Burns, E. M., Debelius, J. W., Morton, J. T., Wissemann, W. T., Lewis, M. R., Wallen, Z. D., Peddada, S. D., Factor, S. A., Molho, E., Zabetian, C. P., et al. (2017) · Movement Disorders · doi:10.1002/mds.26942 · Cited by 874 · see citing works
Oxidative stress in the aging substantia nigra and the etiology of Parkinson's disease
Trist, B. G., Hare, D. J., & Double, K. L. (2019) · Aging Cell · doi:10.1111/acel.13031 · Cited by 778 · see citing works
Sun, M.-F., Zhu, Y.-L., Zhou, Z.-L., Jia, X.-B., Xu, Y.-D., Yang, Q., Cui, C., & Shen, Y.-Q. (2018) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2018.02.005 · Cited by 736 · see citing works
Zheng, P., Zeng, B., Liu, M., Chen, J., Pan, J., Han, Y., Liu, Y., Cheng, K., Zhou, C., Wang, H., et al. (2019) · Science Advances · doi:10.1126/sciadv.aau8317 · Cited by 704 · see citing works
Zhao, Z., Ning, J., Bao, X.-Q., Shang, M., Ma, J., Li, G., & Zhang, D. (2021) · Microbiome · doi:10.1186/s40168-021-01107-9 · Cited by 616 · see citing works
Parkinson's disease: Mechanisms, translational models and management strategies
Raza, C., Anjum, R., & Shakeel, N. U. A. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.03.057 · Cited by 604 · see citing works
Oxidative stress and cellular pathologies in Parkinson’s disease
Puspita, L., Chung, S. Y., & Shim, J. (2017) · Molecular Brain · doi:10.1186/s13041-017-0340-9 · Cited by 486 · see citing works
Altered gut microbiota and inflammatory cytokine responses in patients with Parkinson's disease
Lin, C.-H., Chen, C.-C., Chiang, H.-L., Liou, J.-M., Chang, C.-M., Lu, T.-P., Chuang, E. Y., Tai, Y.-C., Cheng, C., Lin, H.-Y., et al. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1528-y · Cited by 469 · see citing works
Determinants of dopaminergic neuron loss in Parkinson's disease
Surmeier, D. J. (2018) · FEBS Journal · doi:10.1111/febs.14607 · Cited by 455 · see citing works
An Updated Review on Pharmaceutical Properties of Gamma-Aminobutyric Acid
Ngo, D., & Vo, T. (2019) · Molecules · doi:10.3390/molecules24152678 · Cited by 405 · see citing works
Unraveling gut microbiota in Parkinson's disease and atypical parkinsonism
Barichella, M., Severgnini, M., Cilia, R., Cassani, E., Bolliri, C., Caronni, S., Ferri, V., Cancello, R., Ceccarani, C., Faierman, S., et al. (2019) · Movement Disorders · doi:10.1002/mds.27581 · Cited by 393 · see citing works
Gut microbiota in Parkinson's disease: Temporal stability and relations to disease progression
Aho, V. T. E., Pereira, P. A. B., Voutilainen, S., Paulin, L., Pekkonen, E., Auvinen, P., & Scheperjans, F. (2019) · eBioMedicine · doi:10.1016/j.ebiom.2019.05.064 · Cited by 361 · see citing works
Gut Microbiota and Metabolome Alterations Associated with Parkinson’s Disease
Vascellari, S., Palmas, V., Melis, M., Pisanu, S., Cusano, R., Uva, P., Perra, D., Madau, V., Sarchioto, M., Oppo, V., et al. (2020) · mSystems · doi:10.1128/msystems.00561-20 · Cited by 291 · see citing works
Oxidative Stress in Parkinson's Disease: A Systematic Review and Meta-Analysis
Wei, Z., Li, X., Li, X., Liu, Q., & Cheng, Y. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00236 · Cited by 290 · see citing works
Shaping the Nrf2-ARE-related pathways in Alzheimer’s and Parkinson’s diseases
Fão, L., Mota, S. I., & Rego, A. C. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.100942 · Cited by 270 · see citing works
β-glucan attenuates cognitive impairment via the gut-brain axis in diet-induced obese mice
Shi, H., Yu, Y., Lin, D., Zheng, P., Zhang, P., Hu, M., Wang, Q., Pan, W., Yang, X., Hu, T., et al. (2020) · Microbiome · doi:10.1186/s40168-020-00920-y · Cited by 264 · see citing works
sarasa, S. B., Mahendran, R., Muthusamy, G., Thankappan, B., Selta, D. R. F., & Angayarkanni, J. (2019) · Current Microbiology · doi:10.1007/s00284-019-01839-w · Cited by 240 · see citing works
Pediococcus pentosaceus, a future additive or probiotic candidate
Jiang, S., Cai, L., Lv, L., & Li, L. (2021) · Microbial Cell Factories · doi:10.1186/s12934-021-01537-y · Cited by 240 · see citing works
Parkinson’s Disease: A Review from Pathophysiology to Treatment
Marino, B. L. B., de Souza, L. R., Sousa, K. P. A., Ferreira, J. V., Padilha, E. C., da Silva, C. H. T. D. P., Taft, C. A., & Hage-Melim, L. I. D. S. (2019) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557519666191104110908 · Cited by 228 · see citing works
The benefits and mechanisms of exercise training for Parkinson's disease
Feng, Y.-S., Yang, S., Tan, Z., Wang, M., Xing, Y., Dong, F., & Zhang, F. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117345 · Cited by 222 · see citing works
Dysbiosis of gut microbiota in a selected population of Parkinson's patients
Pietrucci, D., Cerroni, R., Unida, V., Farcomeni, A., Pierantozzi, M., Mercuri, N. B., Biocca, S., Stefani, A., & Desideri, A. (2019) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2019.06.003 · Cited by 217 · see citing works
An Overview of the Nrf2/ARE Pathway and Its Role in Neurodegenerative Diseases
Zgórzyńska, E., Dziedzic, B., & Walczewska, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179592 · Cited by 207 · see citing works
Zhang, C., Zhao, M., Wang, B., Su, Z., Guo, B., Qin, L., Zhang, W., & Zheng, R. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102134 · Cited by 205 · see citing works
Wang, L., Zhao, Z., Zhao, L., Zhao, Y., Yang, G., Wang, C., Gao, L., Niu, C., & Li, S. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c07711 · Cited by 203 · see citing works
Yao, W., Lu, M., Mei, M., Wang, H., Han, Z., Chen, M., Yao, H. P., Song, N., Ding, X. L., Ding, J., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14788-x · Cited by 196 · see citing works
Zhou, Z.-L., Jia, X.-B., Sun, M.-F., Zhu, Y.-L., Qiao, C.-M., Zhang, B.-P., Zhao, L.-P., Yang, Q., Cui, C., Chen, X., et al. (2019) · Neurotherapeutics · doi:10.1007/s13311-019-00719-2 · Cited by 195 · see citing works
Ishii, T., Warabi, E., & Mann, G. E. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.09.002 · Cited by 181 · see citing works
Lai, F., Jiang, R., Xie, W., Liu, X., Tang, Y., Xiao, H., Gao, J., Jia, Y., & Bai, Q. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2620-x · Cited by 169 · see citing works
Yu, J. S., Youn, G. S., Choi, J., Kim, C., Kim, B., Yang, S., Lee, J., Park, T., Kim, B. K., Kim, Y. B., et al. (2021) · Clinical and Translational Medicine · doi:10.1002/ctm2.634 · Cited by 143 · see citing works
Heo, J. Y., Nam, M.-H., Yoon, H. H., Kim, J., Hwang, Y. J., Won, W., Woo, D. H., Lee, J. A., Park, H.-J., Jo, S., et al. (2020) · Current Biology · doi:10.1016/j.cub.2019.11.079 · Cited by 135 · see citing works
Beyond Dopamine: GABA, Glutamate, and the Axial Symptoms of Parkinson Disease
Tuura, R., Baumann, C. R., & Baumann‐Vogel, H. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00806 · Cited by 123 · see citing works
Su, Y., Deng, M., Xiong, W., Xie, A., Guo, J., Liang, Z., Hu, B., Chen, J., Zhu, X., Man, H., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.12.008 · Cited by 123 · see citing works
Systemic Activation of Nrf2 Pathway in Parkinson's Disease
Petrillo, S., Schirinzi, T., Lazzaro, G. D., D’Amico, J., Colona, V. L., Bertini, E., Pierantozzi, M., Mari, L., Mercuri, N. B., Piemonte, F., et al. (2019) · Movement Disorders · doi:10.1002/mds.27878 · Cited by 105 · see citing works
Koutzoumis, D. N., Vergara, M., Pino, J. A., Buddendorff, J., Khoshbouei, H., Mandel, R. J., & Torres, G. E. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113159 · Cited by 103 · see citing works
Dong, F., Xiao, F., Li, X., Li, Y., Wang, X., Yu, G., Zhang, T., & Wang, Y. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03235-8 · Cited by 94 · see citing works
GABAergic changes in the thalamocortical circuit in Parkinson's disease
van Nuland, A. J. M., den Ouden, H. E. M., Zach, H., Dirkx, M. F., van Asten, J. J. A., Scheenen, T. W. J., Toni, I., Cools, R., & Helmich, R. C. G. (2019) · Human Brain Mapping · doi:10.1002/hbm.24857 · Cited by 90 · see citing works
Zheng, H.-F., Wang, W.-Q., Li, X., Rauw, G. A., & Baker, G. B. (2016) · Amino Acids · doi:10.1007/s00726-016-2332-y · Cited by 83 · see citing works
Sarasso, E., Agosta, F., Piramide, N., Gardoni, A., Canu, E., Leocadi, M., Castelnovo, V., Basaia, S., Tettamanti, A., Volonté, M. A., et al. (2021) · Movement Disorders · doi:10.1002/mds.28717 · Cited by 83 · see citing works
Zhu, Z., Shi, Z., Xie, C., et al. (2018) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2018.11.018 · Cited by 76 · see citing works
Cheng, L., Chou, P.-Y., Hou, A.-T., Huang, C.-L., Shiu, W.-L., & Wang, S. (2022) · Food & Function · doi:10.1039/d2fo00165a · Cited by 57 · see citing works
NRF2 Activation and Downstream Effects: Focus on Parkinson’s Disease and Brain Angiotensin
Parga, J. A., Rodriguez-Perez, A. I., García-Garrote, M., Rodríguez‐Pallares, J., & Labandeira-García, J. L. (2021) · Antioxidants · doi:10.3390/antiox10111649 · Cited by 52 · see citing works
Lv, R., Du, L., Zhou, F., et al. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00375 · Cited by 48 · see citing works
Hao, L., Cheng, Y., Su, W., et al. (2021) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-021-11111-6 · Cited by 47 · see citing works
Yan, T., Mao, Q., Zhang, X., Wu, B., Bi, K., He, B., & Jia, Y. (2021) · Food & Function · doi:10.1039/d0fo02836c · Cited by 41 · see citing works
Xue Ming, T. A. N. G., Yu, R., Zhou, Q., Jiang, S., & Le, G. (2018) · Nutrition & Metabolism · doi:10.1186/s12986-018-0299-2 · Cited by 40 · see citing works
Lee, J. A., Son, H. J., Choi, J., Kim, J., Han, S. H., Shin, N., Kim, J. H., Kim, S., Heo, J. Y., Kim, D. J., et al. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.11.006 · Cited by 30 · see citing works
Li, C. V., Si, J., Tan, F., Park, K., & Zhao, X. (2021) · Drug Design Development and Therapy · doi:10.2147/dddt.s286104 · Cited by 28 · see citing works
Upper brainstem GABA levels in Parkinson’s disease
Song, Y., Gong, T., Saleh, M. G., Mikkelsen, M. E., Wang, G., & Edden, R. A. E. (2021) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-021-00910-7 · Cited by 28 · see citing works
Wu, Y., Hu, J. Y., Long, X., Pan, Y., Mu, J., Park, K., & Zhao, X. (2021) · Drug Design Development and Therapy · doi:10.2147/dddt.s292243 · Cited by 26 · see citing works
Choe, H., Lee, H., Lee, J., et al. (2021) · Journal of Food Biochemistry · doi:10.1111/jfbc.13639 · Cited by 20 · see citing works
Suhaibani, A. A., Bacha, A. G. B., Alonazi, M. A., Bhat, R. S., & El-Ansary, A. K. (2021) · Food Science & Nutrition · doi:10.1002/fsn3.2418 · Cited by 19 · see citing works
Tsukahara, T., Kawase, T., Yoshida, H., Bukawa, W., Kan, T., & Toyoda, A. (2019) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2019.1659717 · Cited by 15 · see citing works
Lee, H.-J., & Park, H.-J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073660 · Cited by 13 · see citing works
Tiron alleviates MPTP‐induced Parkinsonism in mice via activation of Keap‐1/Nrf2 pathway
Mohamed, S. A., El‐Kashef, D. H., & Nader, M. A. (2020) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.22685 · Cited by 11 · see citing works
Effects of Pediococcus pentosaceus LI05 on immunity and metabolism in germ-free rats
Jiang, S., Xia, J., Lv, L., et al. (2021) · Food & Function · doi:10.1039/d0fo02530e · Cited by 11 · see citing works
Gamma‐aminobutyric acid levels in cerebrospinal fluid in neuropaediatric disorders
Cortès‐Saladelafont, E., Molero-Luís, M., Cuadras, D., Casado, M., Armstrong, J., Yubero, D., Montoya, J., Artuch, R., García‐Cazorla, À., & Institut De Recerca Sant Joan De Déu Working Group (2018) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.13746 · Cited by 10 · see citing works
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Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases
Loh, J. S., Mak, W. Q., Tan, L. K. S., Ng, C. X., Chan, H. H., Yeow, S. H., Foo, J. B., Ong, Y. S., How, C. W., & Khaw, K. Y. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01743-1 · Cited by 1,193 · see citing works
- Authors
- Pan, S., Wei, H., Yuan, S., Kong, Y., Yang, H., Zhang, Y., Cui, X., Chen, W., Liu, J., & Zhang, Y.
- Affiliations
- First Affiliated Hospital of Wenzhou Medical University (CN)
- Wenzhou Medical University (CN)
- Corresponding author
- Liu, Jiaming
- Zhang, Yang
- Venue
- Frontiers in Cellular and Infection Microbiology
- Publisher
- Frontiers Media SA
- Published
- 2022-11-09
- Volume
- 12
- Pages
- 1022879-1022879
- ISSN
- 2235-2988 (ISSN-L)
- PMC
- PMC9682001
- OpenAlex
- W4308720768
- Cited by
- 51
- References
- 64
- Citations by year
- 2026: 11 · 2025: 15 · 2024: 21 · 2023: 4
- FWCI
- 5.26
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Cellular and Infection Microbiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Natural Science Foundation of Zhejiang Province
- Topics
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Keywords
- Pediococcus pentosaceus, probiotics, Parkinson's disease, MPTP-induced neurotoxicity, gut-brain axis, gut dysbiosis, oxidative stress, Nrf2 signaling, dopaminergic neuron loss, alpha-synuclein, GABA, motor impairment, antioxidant activity
- MeSH terms
- Gastrointestinal Microbiome, Pediococcus pentosaceus, Kelch-Like ECH-Associated Protein 1, Brain-Gut Axis, Animals, gamma-Aminobutyric Acid, Male, Mice, Inbred C57BL, Parkinson Disease, 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine, Oxidative Stress, Probiotics, NF-E2-Related Factor 2, Mice, alpha-Synuclein
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