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History and future of leptin: Discovery, regulation and signaling.
Münzberg, Heike; Heymsfield, Steven B; Berthoud, Hans-Rudolf; Morrison, Christopher D.
Afiliación
  • Münzberg H; Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America. Electronic address: Heike.Munzberg@pbrc.edu.
  • Heymsfield SB; Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America.
  • Berthoud HR; Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America.
  • Morrison CD; Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America.
Metabolism ; 161: 156026, 2024 Sep 07.
Article en En | MEDLINE | ID: mdl-39245434
ABSTRACT
The cloning of leptin 30 years ago in 1994 was an important milestone in obesity research. Prior to the discovery of leptin, obesity was stigmatized as a condition caused by lack of character and self-control. Mutations in either leptin or its receptor were the first single gene mutations found to cause severe obesity, and it is now recognized that obesity is caused mostly by a dysregulation of central neuronal circuits. Since the discovery of the leptin-deficient obese mouse (ob/ob) the cloning of leptin (ob aka lep) and leptin receptor (db aka lepr) genes, we have learned much about leptin and its action in the central nervous system. The first hope that leptin would cure obesity was quickly dampened because humans with obesity have increased leptin levels and develop leptin resistance. Nevertheless, leptin target sites in the brain represent an excellent blueprint to understand how neuronal circuits control energy homeostasis. Our expanding understanding of leptin function, interconnection of leptin signaling with other systems and impact on distinct physiological functions continues to guide and improve the development of safe and effective interventions to treat metabolic illnesses. This review highlights past concepts and current emerging concepts of the hormone leptin, leptin receptor signaling pathways and central targets to mediate distinct physiological functions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Metabolism Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Metabolism Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos