Thromb Haemost 1981; 46(02): 507-510
DOI: 10.1055/s-0038-1653398
Original Article
Schattauer GmbH Stuttgart

Use of Chromogenic Substrate S-2251 for Determination of Plasminogen Activator in Rat Ovaries

H Shimada
The Department of Obstetrics and Gynecology, School of Medicine, Kyoto University, Kyoto Japan
,
T Mori
The Department of Obstetrics and Gynecology, School of Medicine, Kyoto University, Kyoto Japan
,
A Takada
*   The Department of Physiology, School of Medicine, Hamamatsu University, Shizuoka, Japan
,
Y Takada
*   The Department of Physiology, School of Medicine, Hamamatsu University, Shizuoka, Japan
,
Y Noda
The Department of Obstetrics and Gynecology, School of Medicine, Kyoto University, Kyoto Japan
,
I Takai
The Department of Obstetrics and Gynecology, School of Medicine, Kyoto University, Kyoto Japan
,
H Kohda
The Department of Obstetrics and Gynecology, School of Medicine, Kyoto University, Kyoto Japan
,
T Nishimura
The Department of Obstetrics and Gynecology, School of Medicine, Kyoto University, Kyoto Japan
› Author Affiliations
Further Information

Publication History

Received 17 March 1981

Accepted 05 May 1981

Publication Date:
05 July 2018 (online)

Summary

A simple, specific and reproducible method for determination of plasminogen activator activity in rat ovaries has been developed by using the chromogenic substrate S-2251. The two steps of enzymatic reactions, i. e. activation of plasminogen and subsequent hydrolysis of the substrate was performed in one step incubation. A linear relationship was observed between the amount of chromogen produced and activator activity in the range of the optical density from 0.05 to 1.20 for 30 min’s incubation. Endogenous activity of non-specific proteases, plasmin or plasmin inhibitors which might be contained in rat ovaries turned out not to interfere with the specificity of a standardized assay procedure. Reproducibility was firmly established with coefficient of variation not exceeding 10%. Using this method, a marked increase followed by a drastic decrease in the activator activity was shown with rat ovaries around the time of ovulation after the injection of human chorionic gonadotropin.

 
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