Brain proteomic modifications associated to protective effect of grape extract in a murine model of obesity

Selima Smine1, Antoine Obry2, Safwen Kadri3

  • 1Laboratoire des Substances Bioactives, Centre de Biotechnologie, Technopole Borj-Cedria, Hammam-Lif, Tunisie; Laboratoire Polymères, Biopolymères, Membranes, UMR6270 CNRS, IRIB, Normandie Université, Mont Saint Aignan, France; Université Tunis El Manar, Faculté des Sciences de Tunis, Laboratoire de Neurophysiologie et Pathologies Fonctionnelles, Tunis, Tunisie.

Insights

Grape seed and skin extract (GSSE) may offer protection against high-fat diet (HFD) induced brain changes. GSSE treatment corrected most protein disturbances in rat brains caused by HFD, suggesting therapeutic potential for metabolic disorders.

Area of Science:

  • Neuroscience
  • Biochemistry
  • Metabolic Disorders

Background:

  • The global obesity epidemic necessitates novel therapeutic strategies beyond surgery and limited pharmacotherapy.
  • Brain dysfunction associated with high-fat diets (HFD) and potential mitigation by grape seed and skin extract (GSSE) require further proteomic investigation.
  • Understanding the proteomic modifications in brain lipotoxicity is crucial for developing effective interventions.

Purpose of the Study:

  • To investigate the proteomic alterations in the brain induced by a high-fat diet (HFD) in rats.
  • To evaluate the protective effects of grape seed and skin extract (GSSE) against HFD-induced brain changes.
  • To identify specific pathways affected by HFD and potentially modulated by GSSE.

Main Methods:

  • Rats were treated for 8 weeks with HFD, GSSE (500mg/kg BW), or a combination of HFD and GSSE.
  • Differential proteomics using mass spectrometry was employed to analyze brain protein modifications.
  • Proteomic data was analyzed to identify proteins involved in key cellular processes.

Main Results:

  • HFD significantly altered brain proteins involved in oxidative stress, glycolysis, and calcium signaling.
  • Proteins associated with the cytoskeleton were also affected by HFD exposure.
  • GSSE administration reversed most of the HFD-induced protein abundance changes, indicating a protective effect.

Conclusions:

  • GSSE demonstrates a significant capacity to counteract HFD-induced proteomic disturbances in the brain.
  • These findings highlight the potential of GSSE as a therapeutic agent for managing metabolic disorders and associated neurotoxicity.
  • Further research into GSSE's mechanisms is warranted for its application in combating diet-induced brain dysfunction.

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