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Cold Exposure and Oral Delivery of GLP-1R Agonists by an Engineered Probiotic Yeast Strain Have Antiobesity Effects in Mice.

ACS Synth Biol · 2023

Last updated 2026-05-28

In a mouse study, researchers engineered a probiotic yeast to produce a GLP-1 drug (Exendin-4) in the gut. When combined with cold exposure at 8°C, the yeast reduced appetite by 25% and led to 4 times more weight loss compared to the drug alone.

AI summary of the abstract below.

JournalACS Synth Biol, 2023
Citations29
Relative citation ratio3.63
NIH percentile88
Molecules
Conditions studied Obesity

Abstract

Advanced microbiome therapeutics (AMTs) holds promise in utilizing engineered microbes such as bacteria or yeasts for innovative therapeutic applications, including the delivery of therapeutic peptides. Glucagon-like peptide-1 receptor agonists, such as Exendin-4, have emerged as potential treatments for type 2 diabetes and obesity. However, current administration methods face challenges with patient adherence and low oral bioavailability. To address these limitations, researchers are exploring improved oral delivery methods for Exendin-4, including utilizing AMTs. This study engineered the probiotic yeast to produce Exendin-4 (Sb-Exe4) in the gastrointestinal tract of male C57BL/6 mice to combat diet-induced obesity. The biological efficiency of Exendin-4 secreted by was analyzed on isolated pancreatic islets, demonstrating induced insulin secretion. The characterization of Sb-Exe4 revealed that when combined with cold exposure (8 °C), the Sb-Exe4 yeast strain successfully suppressed appetite by 25% and promoted a 4-fold higher weight loss. This proof of concept highlights the potential of AMTs to genetically modify for delivering active therapeutic peptides in a precise and targeted manner. Although challenges in efficacy and regulatory approval persist, AMTs may provide a transformative platform for personalized medicine. Further research in AMTs, particularly focusing on probiotic yeasts such as , holds great potential for novel therapeutic possibilities and enhancing treatment outcomes in diverse metabolic disorders.

Verbatim abstract via PubMed 37827516 ↗