Academic Thesis

Basic information

Name Toru Yamazaki
Belonging department
Occupation name
researchmap researcher code
researchmap agency

Title

Urinary thromboxane A2/prostacyclin balance reflects the pathological state of a diabetic 

Bibliography Type

Joint Author

Author

 

OwnerRoles

 

Summary

Levels of the stable urinary metabolites of thromboxane A2 and prostacyclin, 11-dehydro-thromboxane B2 (11-dehydro-TXB2) and 2,3-dinor-6-keto-prostaglandin F1alpha (2,3-dinor-6-keto-PGF1alpha) were measured in diabetics to elucidate the relation between the thromboxane A2/prostacyclin (TX/PGI) balance and pathological states of diabetes mellitus. 11-Dehydro-TXB2 and 2,3-dinor-6-keto-PGF1alpha were derivatized to methyl ester-propylamide-dimethylisopropylsilyl ether and methyl ester-methoxime-dimethylisopropylsilyl ether derivatives, respectively, and applied to a gas chromatography/selected ion monitoring. The TX/PGI ratios of diabetics were higher than those of healthy volunteers, suggesting the hypercoagulative states of this disease. The ratios showed positive correlations with the levels of blood glucose. The levels of hemoglobin A1c and triglyceride were correlated weakly with the ratio. Some of the patients who had relatively low levels of blood glucose also showed high TX/PGI ratios. Furthermore, the ratio increased in the order of the groups 1, 2, and 3; group 1 contained patients who did not take medicine for diabetes, group 2 contained those who took oral hypoglycemic agents, and group 3 contained those who received insulin therapy. These observations indicate that the TX/PGI ratio reflects the pathological conditions of diabetes and is a useful marker, having few different features from other markers that are presently used.
58(5-6):263-71.

Magazine(name)

Prostaglandins Other Lipid Mediat 

Publisher

 

Volume

 

Number Of Pages

 

StartingPage

 

EndingPage

 

Date of Issue

1999/11

Referee

 

Invited

 

Language

 

Thesis Type

 

International Journal

 

International Collaboration

 

ISSN

 

eISSN

 

DOI

 

NAID

 

Cinii Books Id

 

PMID

 

PMCID

 

URL

Format

 

Download

 

J-GLOBAL ID

 

arXiv ID

 

ORCID Put Code

 

DBLP ID

 

Subject1

 

Subject2

 

Subject3

 

Major Achivement