thromboplastin and beta-Thalassemia

thromboplastin has been researched along with beta-Thalassemia* in 2 studies

Other Studies

2 other study(ies) available for thromboplastin and beta-Thalassemia

Article	Year
[Clinical significance of soluble E-selectin and tissue factor in β-thalassemia]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2014, Volume: 35, Issue:6 Topics: Adolescent; Adult; beta-Thalassemia; Child; E-Selectin; Female; Humans; Male; Middle Aged; Thromboplastin; Young Adult	2014
The HDAC inhibitors trichostatin A and suberoylanilide hydroxamic acid exhibit multiple modalities of benefit for the vascular pathobiology of sickle transgenic mice. Blood, 2010, Mar-25, Volume: 115, Issue:12 The vascular pathobiology of sickle cell anemia involves inflammation, coagulation, vascular stasis, reperfusion injury, iron-based oxidative biochemistry, deficient nitric oxide (NO) bioavailability, and red cell sickling. These disparate pathobiologies intersect and overlap, so it is probable that multimodality therapy will be necessary for this disease. We have, therefore, tested a histone deacetylase (HDAC) inhibitor, trichostatin A (TSA), for efficacy in reducing endothelial activation. We found that pulmonary vascular endothelial VCAM-1 and tissue factor (TF) expression (both are indicators of endothelial activation) are powerfully and significantly inhibited by TSA. This is seen both with pretreatment before the inducing stress of hypoxia/reoxygenation (NY1DD sickle transgenic mouse), and upon longer-term therapy after endothelial activation has already occurred (hBERK1 sickle mouse at ambient air). In addition, TSA prevented vascular stasis in sickle mice, it exhibited activity as an iron chelator, and it induced expression of the antisickling hemoglobin, hemoglobin F. Notably, the TSA analog SAHA (suberoylanilide hydroxaminc acid) that is already approved for human clinical use exhibits the same spectrum of biologic effects as TSA. We suggest that SAHA possibly could provide true, multimodality, salubrious effects for prevention and treatment of the chronic vasculopathy of sickle cell anemia. Topics: Anemia, Sickle Cell; Animals; beta-Thalassemia; Cells, Cultured; Disease Models, Animal; Endothelial Cells; Enzyme Inhibitors; Fetal Hemoglobin; Hemoglobin A; Hemoglobin, Sickle; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Intercellular Adhesion Molecule-1; Iron Chelating Agents; Mice; Mice, Inbred C57BL; Mice, Transgenic; Pulmonary Veins; Regional Blood Flow; Thromboplastin; Vascular Cell Adhesion Molecule-1; Venules; Vorinostat	2010

Article

Year

[Clinical significance of soluble E-selectin and tissue factor in β-thalassemia].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2014, Volume: 35, Issue:6

Topics: Adolescent; Adult; beta-Thalassemia; Child; E-Selectin; Female; Humans; Male; Middle Aged; Thromboplastin; Young Adult

2014

The HDAC inhibitors trichostatin A and suberoylanilide hydroxamic acid exhibit multiple modalities of benefit for the vascular pathobiology of sickle transgenic mice.

Blood, 2010, Mar-25, Volume: 115, Issue:12

The vascular pathobiology of sickle cell anemia involves inflammation, coagulation, vascular stasis, reperfusion injury, iron-based oxidative biochemistry, deficient nitric oxide (NO) bioavailability, and red cell sickling. These disparate pathobiologies intersect and overlap, so it is probable that multimodality therapy will be necessary for this disease. We have, therefore, tested a histone deacetylase (HDAC) inhibitor, trichostatin A (TSA), for efficacy in reducing endothelial activation. We found that pulmonary vascular endothelial VCAM-1 and tissue factor (TF) expression (both are indicators of endothelial activation) are powerfully and significantly inhibited by TSA. This is seen both with pretreatment before the inducing stress of hypoxia/reoxygenation (NY1DD sickle transgenic mouse), and upon longer-term therapy after endothelial activation has already occurred (hBERK1 sickle mouse at ambient air). In addition, TSA prevented vascular stasis in sickle mice, it exhibited activity as an iron chelator, and it induced expression of the antisickling hemoglobin, hemoglobin F. Notably, the TSA analog SAHA (suberoylanilide hydroxaminc acid) that is already approved for human clinical use exhibits the same spectrum of biologic effects as TSA. We suggest that SAHA possibly could provide true, multimodality, salubrious effects for prevention and treatment of the chronic vasculopathy of sickle cell anemia.

Topics: Anemia, Sickle Cell; Animals; beta-Thalassemia; Cells, Cultured; Disease Models, Animal; Endothelial Cells; Enzyme Inhibitors; Fetal Hemoglobin; Hemoglobin A; Hemoglobin, Sickle; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Intercellular Adhesion Molecule-1; Iron Chelating Agents; Mice; Mice, Inbred C57BL; Mice, Transgenic; Pulmonary Veins; Regional Blood Flow; Thromboplastin; Vascular Cell Adhesion Molecule-1; Venules; Vorinostat

2010