Metformin, a “Wonder Drug”, Targets METC for Pulmonary Protection

E. Ros
{"title":"Metformin, a “Wonder Drug”, Targets METC for Pulmonary Protection","authors":"E. Ros","doi":"10.20455/ros.2023.n801","DOIUrl":null,"url":null,"abstract":"Metformin, a widely used antidiabetic drug, possesses other beneficial activities, including cardiovascular protection, anti-tumorigenesis, antiaging, and weight control. This Cutting-Edge Research Highlights outlines some latest basic research discoveries on metformin’s suppression of mitochondrial electron transport chain (METC) in the intervention of pulmonary inflammatory disorders, including tuberculosis and acute respiratory distress syndrome in animal models. These novel discoveries further support metformin as a pleiotropic drug for treating diverse diseases.\n(First online: February 19, 2023)\nREFERENCES\n\nForetz M, Guigas B, Bertrand L, Pollak M, Viollet B. Metformin: from mechanisms of action to therapies. Cell Metab 2014; 20(6):953–66. doi: https://dx.doi.org/10.1016/j.cmet.2014.09.018\nVasan K, Werner M, Chandel NS. Mitochondrial metabolism as a target for cancer therapy. Cell Metab 2020; 32(3):341–52. doi: https://dx.doi.org/10.1016/j.cmet.2020.06.019\nKulkarni AS, Gubbi S, Barzilai N. Benefits of metformin in attenuating the hallmarks of aging. Cell Metab 2020; 32(1):15–30. doi: https://dx.doi.org/10.1016/j.cmet.2020.04.001\nDay EA, Ford RJ, Smith BK, Mohammadi-Shemirani P, Morrow MR, Gutgesell RM, et al. Metformin-induced increases in GDF15 are important for suppressing appetite and promoting weight loss. Nat Metab 2019; 1(12):1202–8. doi: https://dx.doi.org/10.1038/s42255-019-0146-4\nColl AP, Chen M, Taskar P, Rimmington D, Patel S, Tadross JA, et al. GDF15 mediates the effects of metformin on body weight and energy balance. Nature 2020; 578(7795):444–8. doi: https://dx.doi.org/10.1038/s41586-019-1911-y\nRoca FJ, Whitworth LJ, Prag HA, Murphy MP, Ramakrishnan L. Tumor necrosis factor induces pathogenic mitochondrial ROS in tuberculosis through reverse electron transport. Science 2022; 376(6600):eabh2841. doi: https://dx.doi.org/10.1126/science.abh2841\nXian H, Liu Y, Rundberg Nilsson A, Gatchalian R, Crother TR, Tourtellotte WG, et al. Metformin inhibition of mitochondrial ATP and DNA synthesis abrogates NLRP3 inflammasome activation and pulmonary inflammation. Immunity 2021; 54(7):1463–77 e11. doi: https://dx.doi.org/10.1016/j.immuni.2021.05.004\nZhong Z, Liang S, Sanchez-Lopez E, He F, Shalapour S, Lin XJ, et al. New mitochondrial DNA synthesis enables NLRP3 inflammasome activation. Nature 2018; 560(7717):198–203. doi: https://dx.doi.org/10.1038/s41586-018-0372-z\nBillingham LK, Stoolman JS, Vasan K, Rodriguez AE, Poor TA, Szibor M, et al. Mitochondrial electron transport chain is necessary for NLRP3 inflammasome activation. Nat Immunol 2022; 23(5):692–704. doi: https://dx.doi.org/10.1038/s41590-022-01185-3\nGuo H, Wang Q, Ghneim K, Wang L, Rampanelli E, Holley-Guthrie E, et al. Multi-omics analyses reveal that HIV-1 alters CD4+ T cell immunometabolism to fuel virus replication. Nat Immunol 2021; 22(4):423–33. doi: https://dx.doi.org/10.1038/s41590-021-00898-1\n","PeriodicalId":91793,"journal":{"name":"Reactive oxygen species (Apex, N.C.)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reactive oxygen species (Apex, N.C.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20455/ros.2023.n801","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Metformin, a widely used antidiabetic drug, possesses other beneficial activities, including cardiovascular protection, anti-tumorigenesis, antiaging, and weight control. This Cutting-Edge Research Highlights outlines some latest basic research discoveries on metformin’s suppression of mitochondrial electron transport chain (METC) in the intervention of pulmonary inflammatory disorders, including tuberculosis and acute respiratory distress syndrome in animal models. These novel discoveries further support metformin as a pleiotropic drug for treating diverse diseases. (First online: February 19, 2023) REFERENCES Foretz M, Guigas B, Bertrand L, Pollak M, Viollet B. Metformin: from mechanisms of action to therapies. Cell Metab 2014; 20(6):953–66. doi: https://dx.doi.org/10.1016/j.cmet.2014.09.018 Vasan K, Werner M, Chandel NS. Mitochondrial metabolism as a target for cancer therapy. Cell Metab 2020; 32(3):341–52. doi: https://dx.doi.org/10.1016/j.cmet.2020.06.019 Kulkarni AS, Gubbi S, Barzilai N. Benefits of metformin in attenuating the hallmarks of aging. Cell Metab 2020; 32(1):15–30. doi: https://dx.doi.org/10.1016/j.cmet.2020.04.001 Day EA, Ford RJ, Smith BK, Mohammadi-Shemirani P, Morrow MR, Gutgesell RM, et al. Metformin-induced increases in GDF15 are important for suppressing appetite and promoting weight loss. Nat Metab 2019; 1(12):1202–8. doi: https://dx.doi.org/10.1038/s42255-019-0146-4 Coll AP, Chen M, Taskar P, Rimmington D, Patel S, Tadross JA, et al. GDF15 mediates the effects of metformin on body weight and energy balance. Nature 2020; 578(7795):444–8. doi: https://dx.doi.org/10.1038/s41586-019-1911-y Roca FJ, Whitworth LJ, Prag HA, Murphy MP, Ramakrishnan L. Tumor necrosis factor induces pathogenic mitochondrial ROS in tuberculosis through reverse electron transport. Science 2022; 376(6600):eabh2841. doi: https://dx.doi.org/10.1126/science.abh2841 Xian H, Liu Y, Rundberg Nilsson A, Gatchalian R, Crother TR, Tourtellotte WG, et al. Metformin inhibition of mitochondrial ATP and DNA synthesis abrogates NLRP3 inflammasome activation and pulmonary inflammation. Immunity 2021; 54(7):1463–77 e11. doi: https://dx.doi.org/10.1016/j.immuni.2021.05.004 Zhong Z, Liang S, Sanchez-Lopez E, He F, Shalapour S, Lin XJ, et al. New mitochondrial DNA synthesis enables NLRP3 inflammasome activation. Nature 2018; 560(7717):198–203. doi: https://dx.doi.org/10.1038/s41586-018-0372-z Billingham LK, Stoolman JS, Vasan K, Rodriguez AE, Poor TA, Szibor M, et al. Mitochondrial electron transport chain is necessary for NLRP3 inflammasome activation. Nat Immunol 2022; 23(5):692–704. doi: https://dx.doi.org/10.1038/s41590-022-01185-3 Guo H, Wang Q, Ghneim K, Wang L, Rampanelli E, Holley-Guthrie E, et al. Multi-omics analyses reveal that HIV-1 alters CD4+ T cell immunometabolism to fuel virus replication. Nat Immunol 2021; 22(4):423–33. doi: https://dx.doi.org/10.1038/s41590-021-00898-1
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“灵丹妙药”二甲双胍靶向肺保护METC
二甲双胍是一种广泛使用的降糖药,具有其他有益活性,包括心血管保护、抗肿瘤、抗衰老和控制体重。本前沿研究重点概述了二甲双胍抑制线粒体电子传递链(METC)干预肺部炎症性疾病(包括结核病和急性呼吸窘迫综合征)动物模型的一些最新基础研究发现。这些新发现进一步支持二甲双胍作为治疗多种疾病的多效性药物。[参考文献]foretz M, Guigas B, Bertrand L, Pollak M, Viollet B.二甲双胍:从作用机制到治疗。Cell Metab 2014;20(6): 953 - 66。doi: https://dx.doi.org/10.1016/j.cmet.2014.09.018Vasan K, Werner M, Chandel NS。线粒体代谢作为癌症治疗的靶点。Cell Metab 2020;32(3): 341 - 52。doi: https://dx.doi.org/10.1016/j.cmet.2020.06.019Kulkarni AS, Gubbi S, Barzilai N.二甲双胍在减缓衰老特征方面的益处。Cell Metab 2020;32(1): 15 - 30。doi: https://dx.doi.org/10.1016/j.cmet.2020.04.001Day EA, Ford RJ, Smith BK, Mohammadi-Shemirani P, Morrow MR, Gutgesell RM,等。二甲双胍诱导的GDF15增加对抑制食欲和促进体重减轻很重要。Nat Metab 2019;1(12): 1202 - 8。doi: https://dx.doi.org/10.1038/s42255-019-0146-4Coll AP, Chen M, Taskar P, Rimmington D, Patel S, Tadross JA,等。GDF15介导二甲双胍对体重和能量平衡的影响。自然2020;578(7795): 444 - 8。doi: https://dx.doi.org/10.1038/s41586-019-1911-yRoca FJ, Whitworth LJ, Prag HA, Murphy MP, Ramakrishnan L.肿瘤坏死因子通过反向电子传递诱导结核致病性线粒体ROS。科学2022;376 (6600): eabh2841。doi: https://dx.doi.org/10.1126/science.abh2841Xian H, Liu Y, Rundberg Nilsson A, Gatchalian R, Crother TR, Tourtellotte WG,等。二甲双胍抑制线粒体ATP和DNA合成可消除NLRP3炎性体激活和肺部炎症。免疫2021;e11 54(7): 1463 - 77。doi: https://dx.doi.org/10.1016/j.immuni.2021.05.004Zhong Z, Liang S, Sanchez-Lopez E, He F, Shalapour S,林晓军,等。新的线粒体DNA合成使NLRP3炎性体激活。自然2018;560(7717): 198 - 203。doi: https://dx.doi.org/10.1038/s41586-018-0372-zBillingham LK, Stoolman JS, Vasan K, Rodriguez AE, Poor TA, Szibor M,等。线粒体电子传递链是NLRP3炎性小体激活的必要条件。Nat Immunol 2022;23(5): 692 - 704。doi: https://dx.doi.org/10.1038/s41590-022-01185-3Guo H, Wang Q, Ghneim K, Wang L, Rampanelli E, Holley-Guthrie E,等。多组学分析表明,HIV-1改变CD4+ T细胞免疫代谢以促进病毒复制。Nat Immunol 2021;22(4): 423 - 33所示。doi: https://dx.doi.org/10.1038/s41590 - 021 - 00898 - 1
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