Levels of oxidative stress and redox-related molecules in the placenta in preeclampsia and fetal growth restriction

Recent evidence suggests that oxidative stress is involved in the pathophysiology of preeclampsia. Using immunohistochemistry and Western blotting, we investigated the oxidative stress- and redox-related molecules, such as 8-hydroxy-2'-deoxyguanosine (8-OHdG), 4-hydroxynonenal (4-HNE), thioredo...

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Veröffentlicht in:Virchows Archiv : an international journal of pathology 2004, Vol.444 (1), p.49-55
Hauptverfasser: TAKAGI, Yasushi, NIKAIDO, Toshio, TOKI, Toshihiko, KITA, Naoko, KANAI, Makoto, ASHIDA, Takashi, OHIRA, Satoshi, KONISHI, Ikuo
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container_title Virchows Archiv : an international journal of pathology
container_volume 444
creator TAKAGI, Yasushi
NIKAIDO, Toshio
TOKI, Toshihiko
KITA, Naoko
KANAI, Makoto
ASHIDA, Takashi
OHIRA, Satoshi
KONISHI, Ikuo
description Recent evidence suggests that oxidative stress is involved in the pathophysiology of preeclampsia. Using immunohistochemistry and Western blotting, we investigated the oxidative stress- and redox-related molecules, such as 8-hydroxy-2'-deoxyguanosine (8-OHdG), 4-hydroxynonenal (4-HNE), thioredoxin (TRX) and redox factor-1 (ref-1) in the placenta in preeclampsia, intrauterine growth restriction (IUGR), preeclampsia + IUGR and in normal pregnancy. Using immunohistochemistry, the level of 8-OHdG was significantly higher in IUGR ( P=0.012) or preeclampsia + IUGR (P=0.0021) than in normal pregnancy, while TRX expression was significantly higher in preeclampsia (P=0.045), and ref-1 expression was significantly higher in preeclampsia (P=0.017), IUGR (P=0.016) and preeclampsia + IUGR (P=0.0038) than in normal pregnancy. The levels of 4-HNE did not differ significantly between either preeclampsia or IUGR and normal pregnancy. A significant positive correlation was observed between TRX and ref-1 expressions in both normal (rho=0.52) and complicated (rho=0.43) pregnancies. Using Western blotting, ref-1 expression tended to be higher in complicated pregnancies than in normal pregnancy (P=0.09). These results suggest that oxidative DNA damage is increased in IUGR and that redox function is enhanced in both preeclampsia and IUGR compared with normal pregnancy.
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Using immunohistochemistry and Western blotting, we investigated the oxidative stress- and redox-related molecules, such as 8-hydroxy-2'-deoxyguanosine (8-OHdG), 4-hydroxynonenal (4-HNE), thioredoxin (TRX) and redox factor-1 (ref-1) in the placenta in preeclampsia, intrauterine growth restriction (IUGR), preeclampsia + IUGR and in normal pregnancy. Using immunohistochemistry, the level of 8-OHdG was significantly higher in IUGR ( P=0.012) or preeclampsia + IUGR (P=0.0021) than in normal pregnancy, while TRX expression was significantly higher in preeclampsia (P=0.045), and ref-1 expression was significantly higher in preeclampsia (P=0.017), IUGR (P=0.016) and preeclampsia + IUGR (P=0.0038) than in normal pregnancy. The levels of 4-HNE did not differ significantly between either preeclampsia or IUGR and normal pregnancy. A significant positive correlation was observed between TRX and ref-1 expressions in both normal (rho=0.52) and complicated (rho=0.43) pregnancies. 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Using immunohistochemistry and Western blotting, we investigated the oxidative stress- and redox-related molecules, such as 8-hydroxy-2'-deoxyguanosine (8-OHdG), 4-hydroxynonenal (4-HNE), thioredoxin (TRX) and redox factor-1 (ref-1) in the placenta in preeclampsia, intrauterine growth restriction (IUGR), preeclampsia + IUGR and in normal pregnancy. Using immunohistochemistry, the level of 8-OHdG was significantly higher in IUGR ( P=0.012) or preeclampsia + IUGR (P=0.0021) than in normal pregnancy, while TRX expression was significantly higher in preeclampsia (P=0.045), and ref-1 expression was significantly higher in preeclampsia (P=0.017), IUGR (P=0.016) and preeclampsia + IUGR (P=0.0038) than in normal pregnancy. The levels of 4-HNE did not differ significantly between either preeclampsia or IUGR and normal pregnancy. A significant positive correlation was observed between TRX and ref-1 expressions in both normal (rho=0.52) and complicated (rho=0.43) pregnancies. Using Western blotting, ref-1 expression tended to be higher in complicated pregnancies than in normal pregnancy (P=0.09). These results suggest that oxidative DNA damage is increased in IUGR and that redox function is enhanced in both preeclampsia and IUGR compared with normal pregnancy.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>14574573</pmid><doi>10.1007/s00428-003-0903-2</doi><tpages>7</tpages></addata></record>
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subjects Aldehydes - analysis
Antioxidants
Biological and medical sciences
Blotting, Western
Deoxyguanosine - analogs & derivatives
Deoxyguanosine - analysis
Diseases of mother, fetus and pregnancy
DNA Damage
DNA-(Apurinic or Apyrimidinic Site) Lyase - analysis
Female
Fetal Growth Retardation - etiology
Fetal Growth Retardation - metabolism
Gestational Age
Gynecology. Andrology. Obstetrics
Humans
Immunohistochemistry
Investigative techniques, diagnostic techniques (general aspects)
Medical sciences
Oxidation-Reduction
Oxidative Stress
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Placenta - chemistry
Pre-Eclampsia - etiology
Pre-Eclampsia - metabolism
Preeclampsia
Pregnancy
Pregnancy. Fetus. Placenta
Thioredoxins - analysis
title Levels of oxidative stress and redox-related molecules in the placenta in preeclampsia and fetal growth restriction
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