Oral delivery of a therapeutic gene encoding glucagon-like peptide 1 to treat high fat diet-induced diabetes

J Control Release. 2017 Dec 28:268:305-313. doi: 10.1016/j.jconrel.2017.08.035. Epub 2017 Aug 30.

Abstract

The number of people suffering from insulin-independent type 2 diabetes mellitus (T2DM) is ever increasing on a yearly basis. Current anti-diabetic medications often result in adverse weight gain and hypoglycemic episodes. Hypoglycemia can be avoided with glucagon-like peptide (GLP)-1 receptor agonists, which are expensive and require daily injections that may result immune activation. This study demonstrates the use of non-viral vector based oral delivery of GLP-1 gene through enterohepatic recycling pathways of bile acids. Oral administration of the plasmid DNA (pDNA) encoding GLP-1 decreased diabetic glucose levels to the normoglycemic range with significant weight reduction in a high-fat diet (HFD) induced diabetic mouse model and a genetically engineered T2DM rat model. This novel oral GLP1 delivery system is an attractive alternative to treat late-stage T2DM conditions that require repeated insulin injection and can potentially minimize the occurrence of hypoglycemic anomalies.

Keywords: Anti-obesity; Diabetes; Hypoglycemia; Oral delivery; Peptide nanoparticle.

MeSH terms

  • Animals
  • Cell Line
  • DNA / administration & dosage*
  • DNA / chemistry
  • Diabetes Mellitus, Type 2 / therapy*
  • Diet, High-Fat
  • Female
  • Gene Transfer Techniques*
  • Genetic Therapy
  • Glucagon-Like Peptide 1 / genetics*
  • Heparin / administration & dosage
  • Heparin / chemistry
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Rats, Sprague-Dawley
  • Rats, Zucker
  • Taurocholic Acid / administration & dosage
  • Taurocholic Acid / chemistry

Substances

  • Taurocholic Acid
  • Glucagon-Like Peptide 1
  • Heparin
  • DNA