Lipid peroxidation, Total Peroxyl Radical-Trapping Ability, and Antioxidant Vitamin Levels in Maternal Venous Plasma of Preterm Premature Rupture of Membranes.
- Author:
Yoon Ha KIM
1
;
Bong Whan AHN
;
Sung Yeul YANG
;
Cheol Hong KIM
;
Moon Kyoung CHO
;
Kwang Su LEE
;
Seok Mo KIM
;
Tae Bok SONG
Author Information
1. Department of Obstetrics and Gynecology, Chonnam National University Medical School, Gwangju, Korea.
- Publication Type:Original Article
- Keywords:
Preterm premature rupture of membranes;
Lipid peroxide;
TRAP;
Ascorbic acid
- MeSH:
alpha-Tocopherol;
Antioxidants;
Ascorbic Acid;
Chromatography, Liquid;
Female;
gamma-Tocopherol;
Humans;
Lipid Peroxidation*;
Membranes*;
Plasma*;
Pregnancy;
Rupture*;
Uric Acid;
Vitamin A;
Vitamins*
- From:Korean Journal of Obstetrics and Gynecology
2004;47(2):342-348
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: Our purpose was to investigate lipid peroxide levels, total peroxyl radical-trapping antioxidative parameter (TRAP) values, and antioxidant vitamin levels in the maternal venous blood plasma of preterm premature rupture of membranes (PPROM) and to evaluate their roles of pathophysiology in PPROM. METHODS: Samples of maternal blood were obtained from women with normal pregnancy (n=23) and PPROM (n=20). Lipid peroxide levels of maternal venous blood plasma were measured by thiobarbituric acid reaction. The TRAP value of maternal venous blood plasma was measured by Wayner's method, although some reaction conditions were modified. Ascorbic acid and uric acid were measured by high performance liquid chromatography (HPLC) CoulArray detector of water-soluble antioxidants. Retinol, alpha-tocopherol, and gamma-tocopherol were measured by HPLC-CoulArray detector of fat-soluble vitamins RESULTS: Lipid peroxide levels in the maternal venous blood plasma of PPROM were significantly higher than that of normal pregnancy (3.87 +/- 0.24 vs. 3.04 +/- 0.24 nmol/mg protein, p<0.05). TRAP values in the maternal venous blood plasma of PPROM were significantly lower than that of normal pregnancy (0.33 +/- 0.02 vs. 0.40 +/- 0.02 mM, p<0.05). Ascorbic acid levels in the maternal venous blood plasma of PPROM were significantly lower than that of normal pregnancy (383.8 +/- 47.5 vs. 563.3 +/- 73.8 nmol/mg, p<0.05). There were no significant differences in maternal venous blood plasma uric acid, retinol, alpha-tocopherol, and gamma-tocopherol levels between two groups. CONCLUSION: This findings suggest that the imbalance of increased lipid peroxidation and decreased antioxidant activity in maternal blood may be involved in the pathophysiology of PPROM. Low levels of ascorbic acid in maternal blood appears to be an important determinant of PPROM.
