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Dive into the research topics where Chieko Tahara is active.

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Featured researches published by Chieko Tahara.


Thrombosis Research | 1990

Reference values of hemostasis related factors of healthy Japanese adults. I: Circadian fluctuation.

Yoshiko Akiyama; Mutsuyoshi Kazama; Chieko Tahara; Chisato Shimazu; Junko Otake; Kieko Kamei; Toshihiko Nakatake; Noriko Sakurai; Yoko Yasumuro; Setsuko Suzuki; Eiko Maeba; Toshiro Nishida

The circadian fluctuation of hemostasis related parameters was examined on 16 healthy Japanese adults (male 9, female 7). Twenty one parameters were measured in this study, i.e. fibrinogen, the activity of F.II, F.V., F.VII, F.VIII, F.IX, F.X., F.XI, F.XII, antithrombin III, plasminogen, alpha 2-antiplasmin, as well as the antigen level of F.IX, von Willebrand Factor, protein C, tissue-type plasminogen activator (tPA), plasminogen activator inhibitor-1 (PAI-1), beta-thromboglobulin, platelet factor 4, fibrinopeptide A, plasmin-alpha 2-antiplasmin complex and FDP. Fluctuation was not significant in almost all of the parameters except F.VIII, F.IX, beta-thromboglobulin, platelet factor 4, tPA and PAI-1. Although the fluctuations of F.VIII, F.IX, beta-thromboglobulin and platelet factor 4 were statistically significant, they remained within the normal ranges. On the other hand, tPA and free PAI-1 showed significant circadian fluctuation, of which levels were highest at 9:00. It was postulated that the significant circadian fluctuation of fibrinolytic activity will be regulated by the balance between tPA and PAI-1 in plasma.


Thrombosis Research | 1992

Changes in thrombomodulin level in plasma of endotoxin-infused rabbits

Kazuyoshi Sawada; Hitoshi Yamamoto; Kenji Matsumoto; Hisashi Yago; Seishi Suehiro; Chieko Tahara; Hidemi Ishii; Mutsuyoshi Kazama; Takeshi Abe

Changes in the plasma thrombomodulin (TM) level were examined in endotoxin-infused rabbits. The plasma TM level in normal rabbits was 143.8 +/- 8.4 ng/ml (n = 67) and the molecular weight of the major TM was about 55 kd. Endotoxin (lipopolysaccharide, LPS, E. Coli B8:0127) was intravenously infused. LPS infusion increased the plasma TM level dose-dependently between 0.2 mg/kg and 5 mg/kg. When 5 mg/kg LPS was infused, the plasma TM level started to increase immediately and was 2.3 times higher than the control value within 1 hr. The molecular weight of the major TM was about 75 kd. This rapid increase in TM occurred before the decrease in fibrinogen content and the prolongation of prothrombin time. To examine the effect of circulating leukocytes on the TM increase in endotoxin-infused rabbits, 5 mg/kg LPS was infused into rabbits with leukocytopenia induced by X-ray irradiation. The maximum plasma level of TM was significantly lower than in the untreated rabbits given LPS. These data suggest that the increase in plasma TM is caused by LPS-stimulated leukocytes prior to hemostaseological changes. It is well known that endothelial cells can be injured by stimulated leukocytes, so this increase in plasma TM probably reflects the deterioration of endothelial cells. This deterioration decreases the ability of endothelial cells to inhibit thrombosis, which would, in turn, contribute to the development of disseminated intravascular coagulation in endotoxin-infused rabbits.


Journal of the Japan Society of Blood Transfusion | 1989

Study of the safety of donor and efficacy of the collected plasma using membrane donor plasmapheresis.

Jun Teruya; Akemi Umejima; Yumi Saitoh; Emiko Maruyama; Yurie Shimizu; Mutsuyoshi Kazama; Machiko Morioka; Chieko Tahara

Because plasma is in much demand but very short in selfsufficiency in Japan, it is not enough to get source plasma derived only from 200ml or 400ml donations of whole blood. As a less expensive process whereby plasma is collected from a single voluntary donor, membrane plasmapheresis has been initiated.We investigated the safety of donating plasma and the efficacy of collected plasma by using a membrane plasmapheresis apparatus, KM8700 Kuraray. There were no complaints from 20 voluntary donors and no abnormal vital signs observed. And there was no activation of platelet, coagulation, fibrinolysis, and complement systems.The components in collected plasma showed little difference from fresh frozen plasma supplied by the Japanese Red Cross, except for a slightly low level of factor IX.We concluded that donor membrane plasmapheresis by using KM8700 Kuraray was safe and clinically useful.


Thrombosis and Haemostasis | 1990

Establishment of enzyme immunoassay of human thrombomodulin in plasma and urine using monoclonal antibodies

Hidemi Ishii; Masahiko Nakano; Jiro Tsubouchi; Tai-ichi Ishikawa; Hiroyuki Uchiyama; Sayuri Hiraishi; Chieko Tahara; Yukari Miyajima; Mutsuyoshi Kazama


Thrombosis Research | 1981

Abnormal plasminogen, a case of recurrent thrombosis

Mutsuyoshi Kazama; Chieko Tahara; Z. Suzuki; Kengo Gohchi; Takeshi Abe


Thrombosis and Haemostasis | 1990

Evaluation of international normalized ratios by a controlled field survey with 4 different thromboplastin reagents

Mutsuyoshi Kazama; Setsuko Suzuki; Takeshi Abe; Chieko Tahara; Chisato Shimazu; Yoshiko Akiyama; Katsumi Higashi; Izumi Ishiguro; Toshiyuki Kimura; Shigemi Motoi; Kazuo Tsukai; Masaki Kobayashi; Yoshimasa Niwa; Hisao Makita; Yoko Yasumuro; Toshihiko Nakatake


Thrombosis Research | 1988

Quantitative analysis of fibrin-binding affinity of fibrinolytic components by frontal affinity chromatography

Mutsuyoshi Kazama; Chieko Tahara; Takeshi Abe; K. Kasai


Japanese Journal of Thrombosis and Hemostasis | 1989

Circadian fluctuation of plasmatic plasminogen activator and its inhibitor PAI-1 of Japanese adults

Chieko Tahara; Mutsuyoshi Kazama; Yukari Miyajima; Takeshi Abe


Japanese Journal of Thrombosis and Hemostasis | 1988

Incidence of Abnormal Plasminogen in Healthy Adults and in Several Diseases in Japanese Population

Mutsuyoshi Kazama; Chieko Tahara; Kenji Matsumoto; Qilang Zhang; Iwao Naito; Juzo Matsuda; Takeshi Abe


Japanese journal of medical science & biology | 1977

Formation of soluble fibrinogen-fibrin complex in liquid human plasma; reflexion of coagulation process in storage.

Takeshi Abe; Mutsuyoshi Kazama; Chieko Tahara; Yasuhiro Miura; Junichi Yasuda

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