P. Saldeen et al., PROSTANOID PRODUCTION IN THE UMBILICOPLACENTAL ARTERIAL TREE RELATIVETO IMPAIRED GLUCOSE-TOLERANCE, Early human development, 50(2), 1998, pp. 175-183
The purpose of this study was to investigate prostanoid synthesis in d
ifferent segments of the umbilicoplacental vascular tree and its relat
ionship to impaired maternal glucose tolerance. Segments from the umbi
lical artery and vein, allantochorionic artery branches, and the cotyl
edon artery from 21 women with diabetes or impaired glucose tolerance
and 10 healthy women were studied. Production of prostacyclin (PGI(2))
and thromboxane (TxA(2)) metabolites was determined. The Mann-Whitney
U test, Wilcoxon signed-ranks matched-pairs test, Kruskal-Wallis test
, analysis of variance, and simple linear regression analysis were use
d. A two-tailed P value of < 0.05 was considered statistically signifi
cant. From the umbilical artery distal to the cotyledon artery, the PG
I(2) synthesis decreased and the TxA(2) synthesis increased gradually
towards the periphery in normal pregnancy. The PGI(2)/TxA(2) ratio was
more than 200 times higher in the umbilical artery than in the cotyle
don artery. The TxA(2) production tended in general to be higher in th
e diabetic group than in the control group, resulting in significantly
lower PGI(2)/TxA(2) ratios in some vessels. The prostanoid production
was not significantly correlated to maternal HbA(lc) or cord C-peptid
e concentrations. The balance between vascular prostacyclin and thromb
oxane synthesis in the umbilicoplacental arterial tree changed gradual
ly towards the periphery: the more peripheral, the lower the prostacyc
lin and the higher the thromboxane production. The physiological role
of this phenomenon is unknown, but may be of importance for the equili
bration of vascular tone between arteries of different calibers. The a
ltered prostanoid balance found in diabetic pregnancy was not directly
attributable to the degree of maternal glycemic control, but may refl
ect increased free radical activity and peroxide production in diabete
s. (C) 1998 Elsevier Science Ireland Ltd.