Thromb Haemost 1994; 71(04): 452-455
DOI: 10.1055/s-0038-1642459
Review Article
Schattauer GmbH Stuttgart

Effects of Recombinant Human Soluble Thrombomodulin (rhs-TM) on a Rat Model of Disseminated Intravascular Coagulation with Decreased Levels of Plasma Antithrombin III

Yoshikazu Aoki
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Rika Ohishi
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Ryoichi Takei
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Osamu Matsuzaki
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Mitsunobu Mohri
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Ken-ichi Saitoh
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Komakazu Gomi
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Taisuke Sugihara
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Takao Kiyota
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Shuji Yamamoto
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Torao Ishida
The Institute for Life Science Research, Asahi Chemical Industry, Shizuoka, Japan
,
Ikuro Maruyama
1   The Department of Clinical Laboratory Medicine, Kagoshima University School of Medicine, Kagoshima, Japan
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Publikationsverlauf

Received: 17. August 1993

Accepted after revision: 14. Dezember 1993

Publikationsdatum:
06. Juli 2018 (online)

Summary

We reported that recombinant human soluble thrombomodulin (rhs- TM) is effective for disseminated intravascular coagulation (DIC) in vivo, in mice and rats. In the present work, we investigated the effects of decreased plasma antithrombin III (ATIII) levels on anticoagulant effects of rhs-TM, as compared to findings with heparin, of which effect is lowered by the decreased plasma ATIII levels in patients with DIC. Rat plasma ATIII levels decreased when we mixed plasma with anti-rat ATIII antibody and the potential of heparin to prolong APTT or PT was markedly diminished. The potential of rhs-TM to prolong APTT and PT was not affected. In rats injected with anti-rat ATIII antibody, plasma ATIII levels decreased immediately. When the rats were infused with tissue factor (TF), DIC was induced. At doses of rhs-TM and heparin which were equally effective at inhibiting the decrease in platelet count and fibrinogen level in cuntiol rats treated with TF, only rhs-TM remained effective in preventing DIC in rats with reduced ATIII levels. Heparin was not effective, when administered to these rats with reduced ATIII levels. Therefore, rhs-TM effectively inhibits coagulation independent of ATIII levels, in contrast to heparin, which depends on the ATIII level.

 
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