Publications by authors named "Jenaro A Espitia-Corredor"

Article Synopsis
  • Cardiac fibroblasts (CFs) can become senescent due to stress, contributing to poor outcomes in heart disease, particularly from cardiotoxic drugs like doxorubicin (Doxo), which also triggers inflammation through IL-1β.
  • Research shows that Doxo leads to CFs senescence as indicated by increased markers of aging and changes in their secretions, but this process can be countered by Resolvin E1 (RvE1), which has anti-inflammatory properties.
  • The study also suggests that the NLRP3 inflammasome and IL-1 receptor pathways are involved in Doxo-induced senescence, and by inhibiting these pathways or using RvE1, the negative effects of Doxo on CF
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Angiotensin II (Ang-II) is a widely studied hypertensive, profibrotic, and pro-inflammatory peptide. In the heart, cardiac fibroblasts (CF) express type 1 angiotensin II receptors (AT1R), Toll-like receptor-4 (TLR4), and the NLRP3 inflammasome complex, which play important roles in pro-inflammatory processes. When activated, the NLRP3 inflammasome triggers proteolytic cleavage of pro-IL-1, resulting in its activation.

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Article Synopsis
  • Endothelial cell senescence leads to chronic inflammation and cardiovascular issues, and can be triggered by various stressors, including cancer drugs like Doxorubicin (Doxo).
  • Doxo has been shown to increase markers of senescence in human endothelial cells, linked to the activation of the NLRP3 inflammasome and the release of interleukin-1β.
  • Resolvins, specifically resolvin E1 (RvE1), may help mitigate Doxo-induced endothelial senescence by inhibiting key inflammatory pathways, suggesting new therapeutic possibilities for reducing cardiovascular toxicity from Doxo.
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