Analysis of Neonatal Hemostatic and Thrombotic Mechanism, and Exploring of the New Therapeutic Approach.
Analysis of Neonatal Hemostatic and Thrombotic Mechanism, and Exploring of the New Therapeutic Approach.
批准号:
12671067
负责人:
TAKAHASHI Yukihiro
金额:
$2.37万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2001
中文摘要
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英文摘要
Neonatal hemoatatic mechanism was studied using thrombelastgram (TEG). In the early neonatal period, the r and k values of TEG in neonatal whole blood shortened and the ma value of TEG enlarged rather than these values in adult's whole blood. This characterized hypercoagulation prophile of TEG in neonate was able to be recreated by the addition of activated coagulation factors, such as thrombin, activated factor VIIa, ADP or epinephrine into normal adult whole blood. One of data, the results of activated factor VIIa, was recently submitted to the journal " Thrombosis and Haemostatic" enclosed in the booklet. And another paper concerning about the relationship between the hyper coagulation and anti-thrombotic drugs was recently subscribed. The bleeding time and coagulation time were almost normal in neonate despite the low function of platelets and the low concentrations of vitamin K dependent coagulation factors in neonate compared with adults. But, in pathological state, the thrombosis is more frequent in neonate than in children after neonate. The knowledge of the haemostatic mechanism is still obscure in neonate. From our recent study, von Willebrand factor (vWF) was relatively high and von Willebrand factor-cleaving protease was low in cord bloods of low birth weight to full term neonate. Furthermore, the higher multimer of vWF was detected. This higher multimer of vWF is more potent in hemostasis. And it may be suggested that it is related to be near normal bleeding time in neonate. We have also studied on the shear dependent platelet aggregation in cord bloods. And the low and high shear stress platelet aggregation were low, this mechanism were analyzed by the recreated blood components and the measurement of ecto-ATP activity. Ecto-ATPase in cord bloods was higher than that in adult blood. It may be suggested that ecto-ATP ase is related to the anti-thrombotic mechanism.
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高橋幸博, 吉岡章: "先天性α2-PI欠乏症"血小板血栓形成の分子機構. 353-356 (2002)
Yukihiro Takahashi、Akira Yoshioka:“先天性 α2-PI 缺乏”血小板血栓形成的分子机制 353-356 (2002)。
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高橋幸博, 吉岡章: "新生児期のvWF/vWF-CPase"血小板血栓形成の分子機構. 167-171 (2002)
Yukihiro Takahashi、Akira Yoshioka:“新生儿期的 vWF/vWF-CPase”血小板血栓形成的分子机制 167-171 (2002)。
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Yoshida K., Kamisue K., Tanaka I., Shima M., Takahashi Y., Oostuka H., Ura R., Yoshioka A.: "Vitamin K deficiency associated with intracranial bleeding due to cytomegarovirus hepatictis in a breast fed Infant despite the oral prophylavtic administration"J
Yoshida K.、Kamisue K.、Tanaka I.、Shima M.、Takahashi Y.、Oostuka H.、Ura R.、Yoshioka A.:“维生素 K 缺乏与母乳喂养婴儿因巨细胞病毒性肝炎引起的颅内出血有关,尽管
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Takahashi Y., Yoshioka A.: "Congenital PAI-Ideficiency. Molecular mechanism of platelet thrombotic formation. Fujirnura Y ed"Kansai Thrombotic Forum Nara. 353-356 (2002)
Takahashi Y.,Yoshioka A.:“先天性 PAI 缺陷。血小板血栓形成的分子机制。Fujirnura Y 编”关西血栓论坛奈良。
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高橋幸博 他7名: "Thrombelastographyを用いた新生児の血液凝固亢進機序の解析"日本産婦人科・新生児血液学会誌. 10. 45-46 (2000)
高桥幸宏等7人:“利用血栓弹力图分析新生儿血液凝固高凝机制”日本妇产科新生儿血液学会杂志10. 45-46(2000)。
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共 19 条
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财政年份:2006
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依托单位:
Analysis on the etiology and patho-physiology of neonatal thrombosis and the development of their therapy
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Evaluation of the effects of global lightining activity on the middle/upper atmosphere and atmosphere and the ionosphere/magnetosphere
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Patho-physiological analysis for the mechanism of neonatal haemostatic and neonatal thrombosis, and exploration of the new therapeutic approach
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依托单位:
STUDY ON THE FUNCTIONAL DOMAINS OF VON WILLEBRAND FACTOR IN PATIENTS WITH VON WILLEBRAND DISEASE
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批准号:06670820
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资助金额:$1.15万
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财政年份:1994
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负责人:TAKAHASHI Yukihiro
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依托单位:
Study on functinal domains of von Willebrand (vW) factor in patients with vW disease.
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资助金额:$1.34万
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负责人:TAKAHASHI Yukihiro
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依托单位:
海外基金