Effect of Increasing Maternal Body Mass Index on Oxidative and Nitrative Stress in The Human Placenta

被引:98
作者
Roberts, V. H. J. [1 ]
Smith, J. [1 ]
McLea, S. A. [1 ]
Heizer, A. B. [1 ]
Richardson, J. L. [1 ]
Myatt, L. [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Obstet & Gynecol, Cincinnati, OH 45267 USA
关键词
Nitrative stress; Oxidative stress; Obesity; CATALYTIC-ACTIVITY; PEROXYNITRITE; NITROTYROSINE; INFLAMMATION; GLUTATHIONE; EXPRESSION; PREGNANCY; PROTEINS; RESIDUES; OBESITY;
D O I
10.1016/j.placenta.2008.11.019
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Maternal obesity is an increasing problem in obstetrics associated with adverse pregnancy outcomes and delivery complications. As an inflammatory state, where elevated levels of pro-inflammatory cytokines are found, obesity can lead to the increased incidence of oxidative and nitrative stress. These stresses may result in protein oxidation and protein nitration respectively, which are post- translational covalent modifications that can modify the structure and subsequently alter the function of a protein. The objective of this Study was to examine whether placental oxidative and nitrative stress increase with increasing maternal body mass index. Placental tissue was collected from three groups of patients categorized as lean, overweight and obese. The presence of nitrotyrosine residues, a marker of nitrative stress, and antioxidant enzymes, as markers of oxidative stress, were assessed by immunohistochemistry, Western blot and ELISA. Protein carbonyl formation, a specific measure of protein oxidation, was measured by OxyBlot(TM) kit. Nitrotyrosine residues were increased in obese compared to lean and overweight groups although localization was unaltered across the three groups. Superoxide dismutase enzyme expression, localization and activity was unaltered between the groups. Protein carbonyl formation was greater in the lean compared to the overweight individuals. This study demonstrates that with increasing maternal body mass index there is an increase in placental nitrative stress. There does not appear to be a corresponding increase in oxidative stress and indeed we demonstrate some evidence of a decrease in oxidative effects in these placenta samples. Potentially the formation of peroxynitrite may be consuming reactive oxygen species and reducing oxidative stress. There may be a shift in the balance between nitrative and oxidative stress, which may be a protective mechanism for the placenta. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:169 / 175
页数:7
相关论文
共 28 条
[11]   Glutathione and glutathione-related enzymes in decidua and placenta of controls and women with pre-eclampsia [J].
Knapen, MFCM ;
Peters, WHM ;
Mulder, TPJ ;
Merkus, HMWM ;
Jansen, JBMJ ;
Steegers, EAP .
PLACENTA, 1999, 20 (07) :541-546
[12]   Role of peroxynitrite in altered fetal-placental vascular reactivity in diabetes or preeclampsia [J].
Kossenjans, W ;
Eis, A ;
Sahay, R ;
Brockman, D ;
Myatt, L .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (04) :H1311-H1319
[13]   Increased nitrotyrosine in the diabetic placenta - Evidence for oxidative stress [J].
Lyall, F ;
Gibson, JL ;
Greer, IA ;
Brockman, DE ;
Eis, ALW ;
Myatt, L .
DIABETES CARE, 1998, 21 (10) :1753-1758
[14]   Oxidative stress in the placenta [J].
Myatt, L ;
Cui, XL .
HISTOCHEMISTRY AND CELL BIOLOGY, 2004, 122 (04) :369-382
[15]   Nitrotyrosine residues in placenta - Evidence of peroxynitrite formation and action [J].
Myatt, L ;
Rosenfield, RB ;
Eis, ALW ;
Brockman, DE ;
Greer, I ;
Lyall, F .
HYPERTENSION, 1996, 28 (03) :488-493
[16]  
*NIDDK WEIGHT CONT, STAT REL OV OB
[17]  
Noor Rana, 2002, Med Sci Monit, V8, pRA210
[18]  
Roberts VHJ, 2007, PLACENTA, V28, pA9
[19]   Post-translational modifications of the P2X4 purinergic receptor subtype in the human placenta are altered in preeclampsia [J].
Roberts, V. H. J. ;
Webster, R. P. ;
Brockman, D. E. ;
Pitzer, B. A. ;
Myatt, L. .
PLACENTA, 2007, 28 (04) :270-277
[20]   Role of placentally produced inflammatory and regulatory cytokines in pregnancy and the etiology of preeclampsia [J].
Rusterholz, Corinne ;
Hahn, Sinuhe ;
Holzgreve, Wolfagang .
SEMINARS IN IMMUNOPATHOLOGY, 2007, 29 (02) :151-162