APAngélica Estrada Pacheco

Angélica Estrada Pacheco

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Angélica Estrada Pacheco has a total of 10 co-authors. Here are the top co-authors by number of shared publications:

  • Alicia Molina Kautzman

    Wound Healing and Cytoprotection Group, Department of Pharmaceuticals, Biomedical Research Direction, Center for Genetic Engineering and Biotechnology, Havana, Cuba

    1 shared publication
  • Ariana García Ojalvo

    Wound Healing and Cytoprotection Group, Department of Pharmaceuticals, Biomedical Research Direction, Center for Genetic Engineering and Biotechnology, Havana, Cuba

    1 shared publication
  • Calixto Valdés Pérez

    Diabetic Foot Ulcer Service, National Institute of Angiology and Vascular Surgery, Salvador Allende Hospital, Havana, Cuba

    1 shared publication
  • David G. Armstrong

    Department of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA

    1 shared publication
  • Eduardo Álvarez Seijas

    National Center for Integral Diabetes Care, Havana, Cuba

    1 shared publication
  • Ileydis Iglesias Marichal

    National Center for Integral Diabetes Care, Havana, Cuba

    1 shared publication

Latest Publications

  • Healing enhancement of diabetic wounds by locally infiltrated epidermal growth factor is associated with systemic oxidative stress reduction

    by Ariana García Ojalvo, Jorge Berlanga Acosta, Yssel Mendoza Marí, Maday Fernández Mayola, Calixto Valdés Pérez, William Savigne Gutiérrez, Ileydis Iglesias Marichal, Eduardo Álvarez Seijas, Alicia Molina Kautzman, Angélica Estrada Pacheco, et al.

    The diabetic foot ulcer (DFU) is the leading cause of lower extremity amputation worldwide and is directly associated with comorbidity, disability and mortality. Oxidative stress mechanisms have been implicated in the pathogenesis of these wounds. Intra‐lesional infiltration of epidermal growth factor has emerged as a potential therapeutic alternative to allow for physiological benefit while avoiding the proteolytic environment at the centre of the wound. The aim of this study was to characterise the response of patients with DFUs to epidermal growth factor treatment in terms of redox status markers. Experimental groups included patients with DFUs before and 3–4 weeks after starting treatment with epidermal growth factor; compensated and non‐compensated diabetic patients without ulcers; and age‐matched non‐diabetic subjects. Evaluations comprised serum levels of oxidative stress and antioxidant reserve markers. Patients with DFUs exhibited the most disheveled biochemical profile, with elevated oxidative stress and low antioxidant reserves, with respect to non‐ulcerated diabetic patients and to non‐diabetic subjects. Epidermal growth factor intra‐lesional administration was associated with a significant recovery of oxidative stress and antioxidant reserve markers. Altogether, our results indicate that epidermal growth factor intra‐ulcer therapy contributes to restore systemic redox balance in patients with DFUs.