Insulin-induced vascular redox dysregulation in human atherosclerosis is ameliorated by dipeptidyl peptidase 4 inhibition

Author:

Akoumianakis Ioannis1ORCID,Badi Ileana1ORCID,Douglas Gillian1ORCID,Chuaiphichai Surawee1,Herdman Laura1ORCID,Akawi Nadia1ORCID,Margaritis Marios1ORCID,Antonopoulos Alexios S.1ORCID,Oikonomou Evangelos K.1ORCID,Psarros Costas1,Galiatsatos Nikolaos2ORCID,Tousoulis Dimitris3ORCID,Kardos Attila4,Sayeed Rana5ORCID,Krasopoulos George5ORCID,Petrou Mario5,Schwahn Uwe6ORCID,Wohlfart Paulus6ORCID,Tennagels Norbert6ORCID,Channon Keith M.1ORCID,Antoniades Charalambos1ORCID

Affiliation:

1. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 9DU, UK.

2. Biochemistry Department, Hippokration General Hospital, Athens 115 27, Greece.

3. First Cardiology Clinic, Athens University Medical School, Athens 115 27, Greece.

4. Milton Keynes University Hospital NHS Foundation Trust and Faculty of Life Sciences, University of Buckingham, Buckingham MK6 5LD, UK.

5. Cardiothoracic Surgery Department, Oxford University Hospitals NHS Foundation Trust, Oxford OX3 9DU, UK.

6. Sanofi Aventis Deutschland GmbH, Frankfurt D-65926, Germany.

Abstract

Vascular oxidative stress in human atherosclerosis is reversed by restoring vascular insulin sensitivity using a dipeptidyl peptidase 4 inhibitor.

Funder

National Institute for Health Research

British Heart Foundation

Sanofi Aventis Deutshcland GmbH

Oxford Biomedical Research Centre

Alexandros S Onassis Public Benefit Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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