High glucose levels modulate eicosanoid production in uterine and placental tissue from non-insulin-dependent diabetic rats during late pregnancy

Prostaglandins Leukotrienes and Essential Fatty Acids

Volumn 58, Issue 6, 1998, Pages 389-393

  Jawerbaum, A ^a   Novaro, V ^a   Franchi, A M ^a   Gimeno, M ^a   Gonzalez E ^a  

^a Facultad de Ciencias Naturales e Instituto M Lillo   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

6 OXOPROSTAGLANDIN F1 ALPHA; GLUCOSE; ICOSANOID; PHOSPHOLIPASE A2; PROSTAGLANDIN E2; PROSTAGLANDIN F2 ALPHA; THROMBOXANE B2;

ANIMAL TISSUE; ARACHIDONIC ACID METABOLISM; ARTICLE; CONTROLLED STUDY; FEMALE; HYPERGLYCEMIA; IN VITRO STUDY; ISOTOPE LABELING; LIQUID SCINTILLATION COUNTING; NON INSULIN DEPENDENT DIABETES MELLITUS; NONHUMAN; PLACENTA; PREGNANCY; PRIORITY JOURNAL; RADIOIMMUNOASSAY; RAT; UTERUS;

ANIMALIA;

EID: 0031827493     PISSN: 09523278     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0952-3278(98)90158-2     Document Type: Article

References (25)

1. Portha B., Picon L., Rosellini G. Chemical diabetes in the adult rat as the spontaneous evolution of neonatal diabetes. Diabetologia 1979; 17: 371-377.
2. Tridan N., Portha B., Picon L., Rosselin G. Experimental chemical diabetes and pregnancy in the rat. Diabetes 1982; 31: 75-79.
3. Jawerbaum A., Roselló-Catafau J., González E., et al. Eicosanoid production by uterine strips and by embryos obtained from diabetic pregnant rats. Prostaglandins 1993; 45: 487-495.
4. 2 activity in uterine tissue from castrated rats with non-insulin-dependent diabetes mellitus. Prostaglandins, Leukot Essent Fatty Acids 1996; 53: 341-345.
5. Fuchs A. R., Fuchs F. Endocrinology of human parturition: a review. Br J Obstet Gynaecol 1984; 91: 948-967.
6. 2 with gestational age in the rat. Biol Reprod 1982; 27: 1207-1215.
7. Björk O., Persson B. Placental changes in relation to the degree of metabolic control in diabetes mellitus. Placenta 1982; 3: 367.
8. Singer D. B., Widnes J. A., Liu C. T., Ellis R. A. Placentas in pregnancies complicated by maternal diabetes. Surv Synth Pathol Res 1984; 3: 333-341.
9. Asmussen I. Vascular morphology in diabetic placentas. Contrib Gynecol Obstet 1982; 9: 76-85.
10. Kuhn D., Crawford M., Stuart M., Botti J., Demers L. Alterations in transfer and lipid distribution of arachidonic acid in placentas of diabetic pregnancies. Diabetes 1990; 39: 914-918.
11. Jawerbaum A., Rosello-Catafau J., Gonzalez E. T., et al. Glucose metabolism, triglyceride and glycogen levels, as well as eicosanoid production in isolated uterine strips and in embryos in a rat model of non-insulin-dependent diabetes mellitus during pregnancy. Prostaglandins 1994; 47: 81-95.
12. 2 en páncreas de rata. Quimica Analítica 1991; 10: 221-225.
13. 2 production during late pregnancy in streptozotocin-induced diabetic rats. Prostaglandins 1989; 37: 695-706.
14. González E., Roselló-Catafau J. Suburo A., et al. Effect of HOE 140 and L-NAME in metabolic impairment due to streptozotocin diabetes in the rat. Med Sci Res 1997; 25: 133-136.
15. González E., Roselló-Catafau J., Xaus C., et al. Influence of nitric oxide synthase and kinin antagonists on metabolic parameters in chronic streptozotocin-induced diabetes mellitus. Prostaglandins 1997; 53: 321-36.
16. 2 in isolated rat uteri. Prostaglandins 1995; 50: 47-56.
17. Jawerbaum A., Roselló-Catafau J., González E., et al. Eicosanoid production, metabolism and contractile activity in the isolated uterus from non-insulin-dependent diabetic rats during late pregnancy. Prostaglandins 1996; 51: 307-320.
18. Rosen, Hohl. Prostaglandins and diabetes. Ann Clin Res 1984; 16: 300-313.
19. Tesfamarian B., Brown M., Deykin D., Cohen R. J. Elevated glucose promotes generation of endothelium-derived vasoconstrictor prostanoids in rabbit aorta. J Clin Invest 1990; 85: 929.
20. Williamson J., Chang K., Frangos M., et al. Hyperglycemic pseudohypoxia and diabetic complications. Diabetes 1993; 42: 801-813.
21. Tesfamariam B., Cohen R. A. Free radicals mediate endothelial cell dysfunction caused by elevated glucose. Am J Physiol 1992; 263: H 321-326.
22. Warso M. A., Lands W. E. M. Lipid peroxidation in relation to prostacyclin and thromboxane physiology and pathophysiology. Br Med Bull 1983; 39: 277-280.
23. Kuhn D. C., Botti J. J., Cherouny P. H., Demers L. M. Eicosanoid production and transfer in the placenta of the diabetic pregnancy. Prostaglandins 1975; 40: 205-215.
24. Moncada S. R., Gryglewski R. J., Bunting S., Vane J. R. A lipid peroxide inhibits the enzyme in blood vessel microsomes that generates from prostaglandin endoperoxide the substance (PGX) which prevents platelet agregation. Prostaglandins 1976; 12: 715-23.
25. Stuart M., Elrad H., Graeber J., Hakanson D., Sunderji Sh., Barvinchak M. Increased synthesis of prostaglandin endoperoxides and platelet hyperfunction in infants of mothers with diabetes mellitus. J Lab Clin Med 1979; 94: 12-23.