Thromb Haemost 1996; 75(06): 965-970
DOI: 10.1055/s-0038-1650402
Original Article
Schattauer GmbH Stuttgart

A Novel Platelet Activating Factor Antagonist, SM-12502, Attenuates Endotoxin-induced Disseminated Intravascular Coagulation and Acute Pulmonary Vascular Injury by Inhibiting TNF Production in Rats

Kazunori Murakami
1   The Department of Medicine, Kumamoto University Medical School, Kumamoto, Japan
,
Kenji Okajima
2   The Department of Laboratory Medicine and Kumamoto University Medical School, Kumamoto, Japan
,
Mitsuhiro Uchiba
1   The Department of Medicine, Kumamoto University Medical School, Kumamoto, Japan
,
Masayoshi Johno
3   The Department of Dermatology, Kumamoto University Medical School, Kumamoto, Japan
,
Hiroaki Okabe
2   The Department of Laboratory Medicine and Kumamoto University Medical School, Kumamoto, Japan
,
Kiyoshi Takatsuki
1   The Department of Medicine, Kumamoto University Medical School, Kumamoto, Japan
› Author Affiliations
Further Information

Publication History

Received 20 October 1995

Accepted after resubmission 27 February 1996

Publication Date:
27 July 2018 (online)

Summary

Adult respiratory distress syndrome and disseminated intravascular coagulation are important pathologic conditions affecting the outcome of patients with sepsis. To elucidate the possible therapeutic efficacy of SM-12502, a novel platelet activating factor antagonist, on acute lung injury and disseminated intravascular coagulation in sepsis, we investigated the effect of SM-12502 on an endotoxin (ET)-induced septic model in rats. SM-12502 prevented ET-induced increases in pulmonary vascular permeability and ET-induced histologic changes, such as leukocyte infiltration and pulmonary interstitial edema, 6 h following the administration of ET (5 mg/kg). SM-12502 also inhibited the decrease in fibrinogen and the increase in fibrin and fibrinogen degradation products observed following ET administration. SM-12502 prevented increases in the serum concentration of tumor necrosis factor (TNF) 90 min following ET administration in vivo, and significantly inhibited the production of TNF-α by ET-stimulated monocytes in vitro.

These findings suggest that SM-12502 attenuates the actions of endotoxin by the inhibition of TNF production

 
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