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Antibody That Destroys Ghrelin Increases Metabolism and Reduces Refeeding in Mice

Animal StudyPreliminary evidence
The takeaway

A catalytic antibody that degrades ghrelin increased whole-body metabolic rate and reduced refeeding after fasting in mice — a novel immunological approach to ghrelin blockade for obesity treatment.

Key finding

A ghrelin-degrading catalytic antibody (ghrelin-ase) increased metabolic rate and reduced post-fast refeeding in mice, demonstrating an immunological

What the researchers found

A ghrelin-degrading catalytic antibody (ghrelin-ase) increased metabolic rate and reduced post-fast refeeding in mice, demonstrating an immunological approach to ghrelin neutralization for obesity treatment — antibody-based appetite suppression.

Why it matters

Relevant for neuropeptides, weight-loss, peptide-design.

How the study worked

animal-study study.

What this study cannot tell us

See abstract.

How to read the evidence

preliminary evidence.

When this study was published

Published in 2008.

The bigger picture

Advances peptide research.

Questions still open

  • Further research needed.
  • Clinical translation to evaluate.

Common questions

What was studied?
Antibody That Destroys Ghrelin Increases Metabolism and Reduces Refeeding in Mice
What was found?
A catalytic antibody that degrades ghrelin increased whole-body metabolic rate and reduced refeeding after fasting in mice — a novel immunological approach to ghrelin blockade for obesity treatment.

Read the original research

Catalytic antibody degradation of ghrelin increases whole-body metabolic rate and reduces refeeding in fasting mice.

Proceedings of the National Academy of Sciences of the United States of America, 105(45), 17487-92

Citation

Mayorov, Alexander V; Amara, Neri; Chang, Jason Y; Moss, Jason A; Hixon, Mark S; Ruiz, Diana I; Meijler, Michael M; Zorrilla, Eric P; Janda, Kim D. (2008). Catalytic antibody degradation of ghrelin increases whole-body metabolic rate and reduces refeeding in fasting mice.. Proceedings of the National Academy of Sciences of the United States of America, 105(45), 17487-92. https://doi.org/10.1073/pnas.0711808105