Key result
Targeting 12(S)-HETE-induced activation of intracellular TRPV1 with the V1-cal peptide or genetic deletion ameliorated diabetes-induced endothelial dysfunction in mice.
Why the study?
Patients with diabetes rapidly develop endothelial dysfunction that progresses to vascular disease, but mechanisms linking lipid peroxidation and mitochondrial dysfunction to targetable pathways remained to be defined.
Does targeting 12(S)-HETE-induced TRPV1 activation prevent diabetes-induced endothelial dysfunction in type 1 diabetic mice?
Does targeting 12(S)-HETE-induced TRPV1 activation prevent diabetes-induced endothelial dysfunction in type 1 diabetic mice?
Pharmacological targeting of 12(S)-HETE-induced TRPV1 activation may offer a novel strategy to prevent early-stage vascular disease and endothelial dysfunction in diabetes.
Should not yet change practice; hypothesis-generating for intracellular TRPV1 targeting in diabetic endothelial dysfunction.
Patients with diabetes develop endothelial dysfunction shortly after diabetes onset that progresses to vascular disease underlying the majority of diabetes-associated comorbidities. Increased lipid peroxidation, mitochondrial calcium overload, and mitochondrial dysfunction are characteristics of dysfunctional endothelial cells in diabetic patients. We here identified that targeting the lipid peroxidation product 12(S)-hydroxyeicosatetraenoic acid-induced [12(S)-HETE-induced] activation of the intracellularly located cation channel transient receptor potential vanilloid 1 (TRPV1) in endothelial cells is a means to causally control early-stage vascular disease in type I diabetic mice. Mice with an inducible, endothelium-specific 12/15-lipoxygenase (12/15Lo) knockout were protected similarly to TRPV1-knockout mice from type 1 diabetes-induced endothelial dysfunction and impaired vascular regeneration following arterial injury. Both 12(S)-HETE in concentrations found in diabetic patients and TRPV1 agonists triggered mitochondrial calcium influx and mitochondrial dysfunction in endothelial cells, and 12(S)-HETE effects were absent in endothelial cells from TRPV1-knockout mice. As a therapeutic consequence, we found that a peptide targeting 12(S)-HETE-induced TRPV1 interaction at the TRPV1 TRP box ameliorated diabetes-induced endothelial dysfunction and augmented vascular regeneration in diabetic mice. Our findings suggest that pharmacological targeting of increased endothelial lipid peroxidation can attenuate diabetes-induced comorbidities related to vascular disease.
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Otto et al. (2020) studied Diabetes-induced endothelial dysfunction. V1-cal peptide or genetic deletion of 12/15Lo or Trpv1 vs. Vehicle, TAT linker, or wild-type diabetic mice was evaluated on Endothelium-dependent vasorelaxation and mitochondrial function (p=<0.001). Targeting 12(S)-HETE-induced activation of intracellular TRPV1 with the V1-cal peptide or genetic deletion ameliorated diabetes-induced endothelial dysfunction in mice.
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