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Metformin Improves Autonomic Nervous System Imbalance and Metabolic Dysfunction in Monosodium L-Glutamate-Treated Rats.
Franco, Claudinéia Conationi da Silva; Previate, Carina; Trombini, Amanda Bianchi; Miranda, Rosiane Aparecida; Barella, Luiz Felipe; Saavedra, Lucas Paulo Jacinto; de Oliveira, Júlio Cezar; Prates, Kelly Valério; Tófolo, Laize Peron; Ribeiro, Tatiane Aparecida; Pavanello, Audrei; Malta, Ananda; Martins, Isabela Peixoto; Moreira, Veridiana Motta; Matiusso, Camila Cristina Ianoni; Francisco, Flávio Andrade; Alves, Vander Silva; de Moraes, Ana Maria Praxedes; de Sant Anna, Juliane Rocha; de Castro Prado, Marialba Avezum Alves; Gomes, Rodrigo Mello; Vieira, Elaine; de Freitas Mathias, Paulo Cezar.
Affiliation
  • Franco CCDS; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Previate C; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Trombini AB; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Miranda RA; Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Barella LF; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Saavedra LPJ; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • de Oliveira JC; Institute of Health Sciences, Federal University of Mato Grosso-Sinop, Sinop, Brazil.
  • Prates KV; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Tófolo LP; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Ribeiro TA; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Pavanello A; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Malta A; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Martins IP; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Moreira VM; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Matiusso CCI; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Francisco FA; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • Alves VS; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • de Moraes AMP; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
  • de Sant Anna JR; Laboratory of Mutagenesis & Genetics, Department of Cell Biology and Genetics, State University of Maringá, Maringá, Brazil.
  • de Castro Prado MAA; Laboratory of Mutagenesis & Genetics, Department of Cell Biology and Genetics, State University of Maringá, Maringá, Brazil.
  • Gomes RM; Department of Physiological Sciences, Federal University of Goiás, Goiânia, Brazil.
  • Vieira E; Postgraduate Program on Physical Education, University Católica of Brasília, Brasília, Brazil.
  • de Freitas Mathias PC; Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, Brazil.
Front Endocrinol (Lausanne) ; 12: 660793, 2021.
Article in En | MEDLINE | ID: mdl-34149616
Metformin is an antidiabetic drug used for the treatment of diabetes and metabolic diseases. Imbalance in the autonomic nervous system (ANS) is associated with metabolic diseases. This study aimed to test whether metformin could improve ANS function in obese rats. Obesity was induced by neonatal treatment with monosodium L-glutamate (MSG). During 21-100 days of age, MSG-rats were treated with metformin 250 mg/kg body weight/day or saline solution. Rats were euthanized to evaluate biometric and biochemical parameters. ANS electrical activity was recorded and analyzed. Metformin normalized the hypervagal response in MSG-rats. Glucose-stimulated insulin secretion in isolated pancreatic islets increased in MSG-rats, while the cholinergic response decreased. Metformin treatment normalized the cholinergic response, which involved mostly the M3 muscarinic acetylcholine receptor (M3 mAChR) in pancreatic beta-cells. Protein expression of M3 mAChRs increased in MSG-obesity rats, while metformin treatment decreased the protein expression by 25%. In conclusion, chronic metformin treatment was effective in normalizing ANS activity and alleviating obesity in MSG-rats.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autonomic Nervous System / Hypoglycemic Agents / Metformin / Obesity Limits: Animals Language: En Journal: Front Endocrinol (Lausanne) Year: 2021 Document type: Article Affiliation country: Brazil Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autonomic Nervous System / Hypoglycemic Agents / Metformin / Obesity Limits: Animals Language: En Journal: Front Endocrinol (Lausanne) Year: 2021 Document type: Article Affiliation country: Brazil Country of publication: Switzerland