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Metformin: Experimental and Clinical Evidence for a Potential Role in Emphysema Treatment.
Polverino, Francesca; Wu, Tianshi David; Rojas-Quintero, Joselyn; Wang, Xiaoyun; Mayo, Jonathan; Tomchaney, Michael; Tram, Judy; Packard, Samuel; Zhang, Duo; Cleveland, Kristan H; Cordoba-Lanus, Elizabeth; Owen, Caroline A; Fawzy, Ashraf; Kinney, Greg L; Hersh, Craig P; Hansel, Nadia N; Doubleday, Kevin; Sauler, Maor; Tesfaigzi, Yohannes; Ledford, Julie G; Casanova, Ciro; Zmijewski, Jaroslaw; Konhilas, John; Langlais, Paul R; Schnellmann, Rick; Rahman, Irfan; McCormack, Meredith; Celli, Bartolome.
Afiliação
  • Polverino F; Asthma and Airway Disease Research Center and.
  • Wu TD; Section of Pulmonary, Critical Care, and Sleep Medicine, Baylor College of Medicine, Houston, Texas.
  • Rojas-Quintero J; Center for Innovations in Quality, Effectiveness, and Safety, Michael E. DeBakey VA Medical Center, Houston, Texas.
  • Wang X; Division of Pulmonary and Critical Care Medicine and.
  • Mayo J; Clinical and Experimental Therapeutics, College of Pharmacy, University of Georgia and Charlie Norwood VA Medical Center, Augusta, Georgia.
  • Tomchaney M; Asthma and Airway Disease Research Center and.
  • Tram J; Asthma and Airway Disease Research Center and.
  • Packard S; Asthma and Airway Disease Research Center and.
  • Zhang D; Asthma and Airway Disease Research Center and.
  • Cleveland KH; College of Pharmacy, and.
  • Cordoba-Lanus E; College of Pharmacy, and.
  • Owen CA; Servicio de Neumología, Unidad de Investigación, Hospital Universitario La Candelaria, Santa Cruz de Tenerife, Tenerife, Spain.
  • Fawzy A; Division of Pulmonary and Critical Care Medicine and.
  • Kinney GL; Division of Pulmonary and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Hersh CP; Department of Epidemiology, Colorado School of Public Health, Aurora, Colorado.
  • Hansel NN; Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Doubleday K; Division of Pulmonary and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Sauler M; Division of Endocrinology, Department of Medicine.
  • Tesfaigzi Y; Pulmonary Division, School of Medicine, Yale University, New Haven, Connecticut.
  • Ledford JG; Division of Pulmonary and Critical Care Medicine and.
  • Casanova C; Asthma and Airway Disease Research Center and.
  • Zmijewski J; Servicio de Neumología, Unidad de Investigación, Hospital Universitario La Candelaria, Santa Cruz de Tenerife, Tenerife, Spain.
  • Konhilas J; Pulmonary and Critical Care Medicine, Department of Medicine, University of Alabama, Birmingham, Alabama; and.
  • Langlais PR; Department of Physiology, University of Arizona, Tucson, Arizona.
  • Schnellmann R; Division of Endocrinology, Department of Medicine.
  • Rahman I; College of Pharmacy, and.
  • McCormack M; Department of Environmental Medicine, University of Rochester Medical Center, Rochester, New York.
  • Celli B; Division of Pulmonary and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Am J Respir Crit Care Med ; 204(6): 651-666, 2021 09 15.
Article em En | MEDLINE | ID: mdl-34033525
ABSTRACT
Rationale Cigarette smoke (CS) inhalation triggers oxidative stress and inflammation, leading to accelerated lung aging, apoptosis, and emphysema, as well as systemic pathologies. Metformin is beneficial for protecting against aging-related diseases.

Objectives:

We sought to investigate whether metformin may ameliorate CS-induced pathologies of emphysematous chronic obstructive pulmonary disease (COPD).

Methods:

Mice were exposed chronically to CS and fed metformin-enriched chow for the second half of exposure. Lung, kidney, and muscle pathologies, lung proteostasis, endoplasmic reticulum (ER) stress, mitochondrial function, and mediators of metformin effects in vivo and/or in vitro were studied. We evaluated the association of metformin use with indices of emphysema progression over 5 years of follow-up among the COPDGene (Genetic Epidemiology of COPD) study participants. The association of metformin use with the percentage of emphysema and adjusted lung density was estimated by using a linear mixed model. Measurements and Main

Results:

Metformin protected against CS-induced pulmonary inflammation and airspace enlargement; small airway remodeling, glomerular shrinkage, oxidative stress, apoptosis, telomere damage, aging, dysmetabolism in vivo and in vitro; and ER stress. The AMPK (AMP-activated protein kinase) pathway was central to metformin's protective action. Within COPDGene, participants receiving metformin compared with those not receiving it had a slower progression of emphysema (-0.92%; 95% confidence interval [CI], -1.7% to -0.14%; P = 0.02) and a slower adjusted lung density decrease (2.2 g/L; 95% CI, 0.43 to 4.0 g/L; P = 0.01).

Conclusions:

Metformin protected against CS-induced lung, renal, and muscle injury; mitochondrial dysfunction; and unfolded protein responses and ER stress in mice. In humans, metformin use was associated with lesser emphysema progression over time. Our results provide a rationale for clinical trials testing the efficacy of metformin in limiting emphysema progression and its systemic consequences.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enfisema Pulmonar / Substâncias Protetoras / Doença Pulmonar Obstrutiva Crônica / Metformina Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enfisema Pulmonar / Substâncias Protetoras / Doença Pulmonar Obstrutiva Crônica / Metformina Idioma: En Ano de publicação: 2021 Tipo de documento: Article