@article{K.2014,
abstract = {Diabetes is a crucial risk factor for stroke and is associated with increased frequency and poor prognosis. Although endothelial dysfunction is a known contributor of stroke, the underlying mechanisms have not been elucidated. The aim of this study was to elucidate the mechanism by which chronic hyperglycemia may contribute to the worsened prognosis following stroke, especially focusing on mitochondrial alterations. We examined the effect of hyperglycemia on hemorrhagic transformation at 24 hours after middle cerebral artery occlusion (MCAO) in streptozotocin (STZ) -induced diabetic mice. We also examined the effects of high-glucose exposure for 6 days on cell death, mitochondrial functions and morphology in human brain microvascular endothelial cells (HBMVECs) or human endothelial cells derived from induced pluripotent stem cells (iCell endothelial cells). Hyperglycemia aggravated hemorrhagic transformation, but not infarction following stroke. High-glucose exposure increased apoptosis, capase-3 activity, and release of apoptosis inducing factor (AIF) and cytochrome c in HBMVECs as well as affected mitochondrial functions (decreased cell proliferation, ATP contents, mitochondrial membrane potential, and increased matrix metalloproteinase (MMP)-9 activity, but not reactive oxygen species production). Furthermore, morphological aberration of mitochondria was observed in diabetic cells (a great deal of fragmentation, vacuolation, and cristae disruption). A similar phenomena were seen also in iCell endothelial cells. In conclusion, chronic hyperglycemia aggravated hemorrhagic transformation after stroke through mitochondrial dysfunction and morphological alteration, partially via MMP-9 activation, leading to caspase-dependent apoptosis of endothelial cells of diabetic mice. Mitochondria-targeting therapy may be a clinically innovative therapeutic strategy for diabetic complications in the future. {\textcopyright} 2014 Mishiro et al.},
added-at = {2019-06-18T22:58:43.000+0200},
author = {K., Mishiro and T., Imai and S., Sugitani and A., Kitashoji and Y., Suzuki and T., Takagi and H., Chen and Y., Oumi and K., Tsuruma and M., Shimazawa and H., Hara},
biburl = {https://www.bibsonomy.org/bibtex/2eee530e35ca9a6c85de33978600ba405/fcdi},
doi = {10.1371/journal.pone.0103818},
interhash = {42f08073eba98494ff6188cebaa9ce0a},
intrahash = {eee530e35ca9a6c85de33978600ba405},
issn = {1932-6203},
journal = {PLoS ONE},
keywords = {TUNEL_assay adenosine_triphosphate animal_experiment animal_model apoptosis article brain_ischemia capillary_endothelial_cell caspase_3 caspase_7 cell_death cell_proliferation cell_vacuole cerebrovascular_accident controlled_study diabetes_mellitus disorders_of_mitochondrial_functions endothelial_dysfunction endothelium_cell enzyme_activation enzyme_activity gelatinase_B glucose hemoglobin hyperglycemia male middle_cerebral_artery_occlusion mitochondrial_membrane_potential morphology mouse nonhuman pluripotent_stem_cell prognosis reactive_oxygen_metabolite risk_factor spectrophotometry streptozotocin-induced_diabetes_mellitus},
timestamp = {2019-06-18T22:58:43.000+0200},
title = {{Diabetes mellitus aggravates hemorrhagic transformation after ischemic stroke via mitochondrial defects leading to endothelial apoptosis}},
year = 2014
}