Liu, Y., Yin, Hj. & Chen, Kj. Research on the correlation between platelet gelsolin and blood-stasis syndrome of coronary heart disease., Chin. J. Integr. Med. 17, 587 (2011). https://doi.org/10.1007/s11655-011-0814-z
Yue Liu, Hui-jun Yin, Ke-ji Chen. Research on the correlation between platelet gelsolin and blood-stasis syndrome of coronary heart disease[J]. Chinese Journal of Integrative Medicine, 2011,17(8):587-592.
Liu, Y., Yin, Hj. & Chen, Kj. Research on the correlation between platelet gelsolin and blood-stasis syndrome of coronary heart disease., Chin. J. Integr. Med. 17, 587 (2011). https://doi.org/10.1007/s11655-011-0814-zDOI:
Yue Liu, Hui-jun Yin, Ke-ji Chen. Research on the correlation between platelet gelsolin and blood-stasis syndrome of coronary heart disease[J]. Chinese Journal of Integrative Medicine, 2011,17(8):587-592. DOI: 10.1007/s11655-011-0814-z.
Research on the correlation between platelet gelsolin and blood-stasis syndrome of coronary heart disease
摘要
To study the distribution of gelsolin in human platelet and plasma
and the association with blood-stasis syndrome (BSS) of coronary heart disease (CHD). Sixty patients with CHD (30 in BSS group and 30 in non-BSS group) and 30 healthy subjects (control group) were included in this study. The classification of the syndrome was based on clinical symptoms and signs. Gelsolin concentration in platelet rich plasma (PRP)
platelet poor plasma (PPP)
filamentous actin (F-actin) and group-specific component globulin (Gc-globulin) of PPP were determined by enzyme-linked immunosorbent assay (ELISA). The fluorescence intensity of CD62p and cytoplasmic calcium ([Ca2+]i) in human platelets of patients and healthy persons was measured with flow cytometry. Compared with the control group
gelsolin in PRP of the BSS group increased significantly (P<0.01)
while that in PPP of the BSS and non-BSS groups decreased markedly (P<0.05)
the CD62p
[Ca2+]i of platelet
F-actin
and Gc-globulin of the BSS and non-BSS groups increased significantly (P<0.01). Compared with the non-BSS group
the gelsolin concentration in PRP of BSS group increased significantly (P<0.01)
the [Ca2+]i of platelet of the BSS group increased markedly (P<0.01)
while the F-actin and Gc-globulin of the BSS group had no statistical defference (P>0.05). Gelsolin concentration in PRP was increased and accompanied by the elevated [Ca2+]i of platelet in CHD with BSS
while gelsolin in PPP were lowered markedly. We speculate that plasma gelsolin may clear F-actin from circulation
thus resulting in depletion of plasma gelsolin significantly. This
in addition to the increased calcium influx of platelets
may lead to the gelsolin abnormal expression on platelets during the process of BSS in CHD. Therefore
platelet gelsolin may serve as a new potential biomarker and a therapeutic target of BSS in CHD.
Abstract
To study the distribution of gelsolin in human platelet and plasma
and the association with blood-stasis syndrome (BSS) of coronary heart disease (CHD). Sixty patients with CHD (30 in BSS group and 30 in non-BSS group) and 30 healthy subjects (control group) were included in this study. The classification of the syndrome was based on clinical symptoms and signs. Gelsolin concentration in platelet rich plasma (PRP)
platelet poor plasma (PPP)
filamentous actin (F-actin) and group-specific component globulin (Gc-globulin) of PPP were determined by enzyme-linked immunosorbent assay (ELISA). The fluorescence intensity of CD62p and cytoplasmic calcium ([Ca2+]i) in human platelets of patients and healthy persons was measured with flow cytometry. Compared with the control group
gelsolin in PRP of the BSS group increased significantly (P<0.01)
while that in PPP of the BSS and non-BSS groups decreased markedly (P<0.05)
the CD62p
[Ca2+]i of platelet
F-actin
and Gc-globulin of the BSS and non-BSS groups increased significantly (P<0.01). Compared with the non-BSS group
the gelsolin concentration in PRP of BSS group increased significantly (P<0.01)
the [Ca2+]i of platelet of the BSS group increased markedly (P<0.01)
while the F-actin and Gc-globulin of the BSS group had no statistical defference (P>0.05). Gelsolin concentration in PRP was increased and accompanied by the elevated [Ca2+]i of platelet in CHD with BSS
while gelsolin in PPP were lowered markedly. We speculate that plasma gelsolin may clear F-actin from circulation
thus resulting in depletion of plasma gelsolin significantly. This
in addition to the increased calcium influx of platelets
may lead to the gelsolin abnormal expression on platelets during the process of BSS in CHD. Therefore
platelet gelsolin may serve as a new potential biomarker and a therapeutic target of BSS in CHD.
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Blood stasis syndrome of coronary heart disease: A perspective of modern medicine
Biomedical mechanisms of blood stasis syndrome of coronary heart disease by systems biology approaches
Relationship between platelet activation related factors and polymorphism of related genes in patients with coronary heart disease of blood-stasis syndrome
Exploration on significance of platelet cd62p, cdp63 determination in type 2 diabetes mellitus patients with blood stasis syndrome
Association of platelet-activating factor receptor gene rs5938 (G/T) and rs313152 (T/C) polymorphisms with coronary heart disease and blood stasis syndrome in a Chinese Han population
相关作者
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相关机构
Department of Cardiology, Guang’anmen Hospital, China Academy of Chinese Medical Sciences
Department of Cardiology, Guang’anmen Hospital
Academy of Chinese Medical Sciences
Xiyuan Hospital, China Academy of Chinese Medical Sciences