Published May 17, 2024
| Version v1
Publication
Chemical and biological characterization of the DPP-IV inhibitory activity exerted by lupin (Lupinus angustifolius) peptides: From the bench to the bedside investigation
Contributors
Others:
- Universidad de Sevilla. Departamento de Bioquímica Médica y Biología Molecular e Inmunología
- Instituto de Biomedicina de Sevilla (IBIS)
- Consejeria de Salud
- Consejeria de Transformacion Economica, Industria, Conocimiento y Universidades, Junta de Andalucia
- Erasmus+ Mobility Programme
- Ministerio de Economia y Competitividad, Gobierno de Espana
- Ministerio de Educacion, Cultura y Deporte, Gobierno de Espana
- PAIDI Program from Junta de Andalucia
- Universidad de Sevilla
Description
Dipeptidyl peptidase IV (DPP-IV) is considered a key target for the diabetes treatment, since it is involved in glucose metabolism. Although lupin protein consumption shown hypoglycemic activity, there is no evidence of its effect on DPP-IV activity. This study demonstrates that a lupin protein hydrolysate (LPH), obtained by hydrolysis with Alcalase, exerts anti-diabetic activity by modulating DPP-IV activity. In fact, LPH decreased DPP-IV activity in a cell-free and cell-based system. Contextually, Caco-2 cells were employed to identify LPH peptides that can be intestinally trans-epithelial transported. Notably, 141 different intestinally transported LPH sequences were identified using nano- and ultra-chromatography coupled to mass spectrometry. Hence, it was demonstrated that LPH modulated the glycemic response and the glucose concentration in mice, by inhibiting the DPP-IV. Finally, a beverage containing 1 g of LPH decreased DPP-IV activity and glucose levels in humans.
Abstract
Premio Mensual Publicación Científica Destacada de la US. Facultad de MedicinaAdditional details
Identifiers
- URL
- https://idus.us.es/handle//11441/158518
- URN
- urn:oai:idus.us.es:11441/158518
Origin repository
- Origin repository
- USE