Open Access

Maternal diabetes impairs oxidative and inflammatory response in murine placenta

  • Mohamed I. Saad1, 2Email author,
  • Taha M. Abdelkhalek3,
  • Moustafa M. Saleh3,
  • Maha M. Haiba1,
  • Shady H. Tawfik4 and
  • Maher A. Kamel1
Contributed equally
SpringerPlus20165:532

https://doi.org/10.1186/s40064-016-2180-y

Received: 21 January 2016

Accepted: 19 April 2016

Published: 26 April 2016

Abstract

Placenta is the major exchange surface between mother and fetus and plays a pivotal role in fetal development. A better understanding of the mechanisms by which diabetes alters placental function may allow better management of diabetes pregnancies. In this study, we attempt to investigate the effect of diabetic milieu with and without malformation on placental function. In order to investigate the impact of diabetic pregnancy on oxidative stress, endothelial and vascular functions of placental tissue, we mated diabetic and non-diabetic female rats with normal male rats. At gestational day 17, we terminated pregnancy, assessed fetuses for malformations and isolated placenta for measurement of various parameters of placental function. Our results show that maternal diabetes induced a state of oxidative stress in placenta, which disrupts normal signaling, activating apoptosis, as well as perturbing endothelial and vascular placental functions. The coalescence of these insults on various levels of placental function could contribute to the pleiotropic nature of diabetes-induced placental stress.

Keywords

Diabetes Placenta Embryopathy Birth defects Oxidative stress

Background

Placenta is an evolutionary conserved organ present in almost all female mammal pregnancies (Wildman 2011). Placenta is essential for consummate pregnancy, and serves several roles including: secretion of hormones, interface to allow exchange of metabolites, oxygen and nutrients between maternal and fetal circulation, as well as modulating maternal immune system and fetal growth (John and Hemberger 2012). Placentogenesis is initiated early during mammalian pregnancy due to differentiation of trophoblasts from early embryonic stem cells. Nevertheless, complete layers of rats’ placenta are discerned from as early as gestational day (GD) 12 (De Rijk et al. 2002). Placental function increases during the late phase of pregnancy to compensate for the increase in fetal circulation (De Rijk et al. 2002). Therefore, GD 17 was chosen to assess placental function in its peak and to decrease confounding factors such as normal increase in placenta oxidative stress that occurs in later days of gestation.

Placenta secretes several growth factors including placenta growth factor (PIGF2), which promotes proliferation of placental vasculature and has an affinity to vascular endothelial growth factor (VEGF) receptors (Hauser and Weich 1993). PlGF-2 is a growth factor isoform that is secreted exclusively by umbilical cord endothelial cells and placenta (Hauser and Weich 1993). Soluble VEGF receptor1 (sVEGFR1) or soluble fms-like tyrosine kinase-1 (sFlt-1) is a splice variant of VEGFR1 and act as receptor for PIGF-2 expressed on endothelial cells and have several anti-angiogenic functions through several mechanisms (Wu et al. 2010).

Diabetes and/or hyperglycemia during pregnancy perturbs placental and fetal development (Castori 2013); however, the mechanism and contribution of defects introduced by diabetic milieu on placenta is not well established. Diabetes-induced embryopathy and malformations were established since early twentieth century (Castori 2013). The abnormal milieu instigated by diabetes and/or abnormal placental function may disturb the fetus on short term, but also may contribute to the development of disease later on in life (fetal origins of disease) (Calkins and Devaskar 2011). In order to better control and manage diabetic pregnancies to reduce embryopathies and possible adult effects, we need deeper understanding of the cellular and molecular mechanisms underlying diabetic sabotage of fetal development. Basic research using animal models has contributed a considerable amount of information about the manifestations of fetal abnormalities, but the effect of diabetes on placenta has not been thoroughly investigated.

Several cellular mechanisms contribute to the pathology of diabetic malformations including impaired endothelial function, increased apoptosis, and oxidative stress that disrupt organelle function as well as protein folding and processing (Gareskog et al. 2007). These apoptotic activities are mediated by increased expression and activity of cleaved caspase-3, which is regulated by high caspase-8 activity under hyperglycemic conditions (Yang et al. 2008). Moreover, hyperglycemia alters normal placental function by reducing expression of VEGF-A, VEGFR-1/Flt-1 and PIGF in placenta and serum of diabetic mothers. These perturbations might mediate the negative effects of diabetes on placental vasculature (Helske et al. 2001).

Hyperglycemia induces oxidative stress mainly through increased flux of NADH and FADH2 to electron transport chain that promote mitochondrial dysregulation and generation of superoxide radicals (Saad et al. 2015). Also, it impairs intracellular antioxidant defense by decreasing levels of reduced glutathione (GSH) and increasing oxidized glutathione (GSSG). Since glutathione system, the predominant intracellular antioxidant mechanism, is impaired and reactive oxygen species (ROS) production is increased; this imbalance induces a state of oxidative stress, which disrupts normal cellular signaling and leads to metabolic adverse effects of diabetic pregnancy (Sakamaki et al. 1999). Although ROS is involved in several physiological functions, the term of oxidative stress is reserved mainly for the pathological mechanism or effects (Sies 2015). One major direct effect of oxidative stress is oxidation of nitric oxide—a critical vasodilator and signaling molecule in early development—by reacting with ROS to form nitroperoxides, which in turn induce nitrosative stress. A proxy for nitrosative stress that may reflect levels of protein nitrosylation is nitrous and nitric oxides levels in tissues, collectively known as nitric oxide end products (NOx) (Jawerbaum et al. 2005). 8-Oxo-7,8-dihydro-2′-deoxyguanosine (8-oxo-dG) is a major biomarker of DNA damage induced by oxidative stress. It is formed by the reaction of OH radical with the DNA guanine base and usually result in point mutations (Cooke and Evans 2007a).

Cyclooxygenase enzymes COX-1 and COX-2 convert arachidonic acid into prostaglandins such as prostaglandin E2 (PGE2), while free radicals convert arachidonic acid into PGE2-like isoprostanes. In embryos of diabetic pregnancy, COX-2 activity and expression are reduced, which decrease PGE2 significantly and shift arachidonic acid metabolism into production of PGE2-like isoprostanes by ROS (El-Bassiouni et al. 2005). PGE2 protect embryos from the damages due to hyperglycemic conditions (Goto et al. 1992), while PGE2-like isoprostanes have damaging effects in animal models of diabetic pregnancy and embryos exposed to high glucose in culture (Wentzel and Eriksson 2002).

In this study, we investigate the impact of diabetic milieu on placental function of malformed and non-malformed fetuses, to study the effect of diabetes with and without malformations on placental function in late gestation. We assessed the impact of maternal diabetes through several parameters of vascular and oxidative processes in placenta. Our hypothesis is that diabetes affects placenta vascular, inflammatory and oxidative function during late gestation.

Methods

Experimental animals

The animal protocol was approved by the Institutional Animal Care and Use Committee at the Medical Research Institute—Alexandria University. Thirty female Local Wistar-derived strain rats were included in the experiment and had an initial average weight of 180 ± 20 g. Rats were given tap water and commercial pellet diet ad libitum. Animals were housed individually on a 12-h light/dark cycle and were kept at constant humidity and temperature (20 ± 5 °C).

Induction of experimental diabetes

Diabetes was induced in adult female rats group (n = 15) through intraperitoneal injection of 55 mg/kg Streptozotocin (STZ; Sigma-Aldrich Chemical Co., Poole, UK) dissolved in sodium citrate buffer (0.01 M, pH 4.5) given daily over two successive days. An equivalent volume of buffer was administered to the control group (n = 15). Glucometer (Elite) was used for measuring glucose levels. Diabetes was confirmed by a blood glucose level >11 mmol/l measured 1 week after Streptozotocin injections.

Mating

Female rats of both groups were mated with healthy non-diabetic males overnight. The presence of sperm mucus plug in the vagina the following morning signified pregnancy (GD 0).

Sample collection and preparation

Female rats of both groups were culled by cervical dislocation on GD 17. In each sacrificed rat, the uterus was exposed by cesarean section and the number of implantations and resorptions were noted. The live embryos and their placentae were dissected out of the uterine horns, rinsed carefully in phosphate buffered saline (PBS). Overall growth and differentiation of the embryos were quantified by direct measurement of crown-to-rump length (CRL). The embryos were examined with regard to general morphology, and embryo and placentae were weighed. The occurrence of disturbed embryonic development was noted such as open neural tube, growth retardation and appearance of specific organs (head, ear, heart, legs, tail, and body rotation). Embryos were denoted as “malformed” if one or more of these structures exhibited an apparent anomaly. The weights of embryos and placentae were recorded. The placentae were snap-frozen in liquid nitrogen for subsequent analysis. Placenta was homogenized in 3 mL of 0.1 M Tris-HCl buffer, pH 7.4 containing 1 mM EDTA. Then the homogenates were centrifuged at 10,000g for 15 min at 4 °C. The supernatant was removed and stored at −80 °C for subsequent assays.

Sample assays

COX enzymes activity assays were determined according to the procedure used by Kargman et al. (1996). Briefly, the activity of COX-1 was assessed in the standard and placental (control and diabetic) supernatants treated with COX-2 inhibitor, and compared with the activity of a mixture of both standard COX-1 and placental supernatant treated with COX-2 inhibitor. The kit (Cayman Chemical Company; Ann Arbor, MI, USA) includes isozyme-specific inhibitors for distinguishing COX-2 from COX-1 activity.

The concentration of PlGF-2 was determined quantitatively using EIA kit (R & D systems, Inc., Minneapolis, MN, USA) with a sensitivity of 8.38 pg/mL. The intra- and inter-assay coefficients of variation were 8 and 13 %, respectively. Placenta level of sVEGFR1/sFlt-1 was determined by competitive ELISA kit (Kamiya Biomedical Company, Seattle, WA, USA) according to manufacturer instructions. Caspase-3 activity was assayed by a method described by Thornberry (1994). Briefly, a fluorescently labeled substrate for caspase 3 was added and the rate of its degradation was assessed by ELISA. Oxidative stress parameters measured included thiobarbituric acid reactive substances (TBARS), which represents lipid peroxidation end-products and quantified as malondialdehyde (MDA). TBARS was assayed by a protocol developed by Draper and Hadley (1990). Briefly, this involves the reaction between thiobarbituric acid and MDA, which gives off a colored product assayed by colorimetry. While glutathione oxidation parameters were assayed by an enzymatic recycling assay developed by Griffith (1980). Shortly, GSH is oxidized by 5,5′-dithio-bis(2-nitrobenzoic acid) (DNTB) to from a product detected by colorimetry. Total glutathione level is detected by reducing all the GSSG resulting from the previous reaction using (NADPH and glutathione reductase) and repeating the initial assay again. Tissue content of vitamin C was assayed by colorimetry using Folin phenol reagent (Jagota and Dani 1982), vitamin E using HPLC (McCormick and Green 1996) and selenium by atomic absorption spectroscopy (AAS) (Herber and Stoeppler 1994) were also assayed in the placentae of all study groups. Protein content was determined using a modification of the method of Lowry et al. (1951). The specific activity of each enzyme was determined by dividing its activity by the protein concentration in the sample (U/mg protein).

Isolated DNA was washed twice with 70 % ethanol, dried, and dissolved in 200 μl of 10 mM Tris/HCl, 0.1 mM EDTA and 100 mM NaCl (pH 7.0). For enzymatic digestion, 100 units of DNase I were added per 200 μg DNA at 37 °C for 1 h. Then, 5 units of nuclease P1 and 30 μl of 10 mM ZnSO4 were added, and the mixture was incubated for 1 h. After re-adjusting the pH with 100 μl of 0.4 M Tris/HCl (pH 7.8) followed by the addition of three units alkaline phosphatase, the samples were incubated for 30 min. Enzymes were precipitated with acetone (5 vol), removed by centrifugation, and the supernatant was evaporated to dryness. The DNA hydrolysates were evaluated for 8-oxo-dG content using HT 8-oxo-dG ELISA Kit II (Trevigen, USA).

The nitrite and nitrate (NOx) concentration was determined by simple Griess reaction (Guevara et al. 1998). Briefly the assay consists of two steps: diazotization of sulphanilic acid with nitrite ion and coupling of this product with diamine, which results in a measurable pink metabolite that measured at 540 nm. Before diazotization reaction, all nitrate ions present in tissue were converted to nitrite ions by the action of NADPH-dependent nitrate reductase.

Statistical analysis

All data are presented as mean ± SD. A one-way analysis of variance (ANOVA) with post hoc test (LSD) was performed on each normally distributed variable to compare the mean values. Differences were considered significant at P < 0.05. For pregnancy outcome, results were analyzed by Fisher’s exact test. All statistical analyses were performed using SPSS statistical software version 18 (SPSS, Chicago, IL, USA).

Results

In this study, we investigated several parameters of oxidative stress, endothelial function, angiogenesis and apoptosis to get a better understanding of diabetes-induced pathological processes during late gestation.

Diabetes has profoundly negative effects on pregnancy outcome. Diabetic female rats had significantly higher number of resorptions and malformations but a lower number of viable fetuses, while normal females had no malformations and only two resorptions (Table 1). Various malformations were observed in fetuses of diabetic females; most commonly, growth retardation followed by mal-rotations and short mandible as well as head mal-development, absence of tail and open neural tube (Table 3). Moreover, crown rump length was significantly decreased in diabetic embryos regardless of their malformation status (Table 2). Placental weight was significantly higher in diabetic malformed and non-malformed fetuses relative to control pregnancies. On the contrary, embryo weight was significantly lower in diabetic malformed embryos compared to diabetic non-malformed and control embryos (Table 2).
Table 1

Pregnancy outcome of diabetic and control rats

Parameters

Control

Diabetic

No. of litters

9

13

Malformed litters

0

11*

% of malformed litters

0

85

Total no. of implantations

102

123

No. of implantations/litter

11

9

No. of viable embryos

100

98*

No. of resorption

2

25

% of resorption

2

20

No. of malformations

0

40

* Significantly different from control rats (P < 0.05) by Fisher’s exact test

Table 2

Fetal parameters and placental weight at gestational day 17

Parameters

Embryos from control mothers

Embryos from diabetic mothers

Non-malformed

Malformed

CRL (mm)

12.65 ± 0.21

10.89 ± 0.18*

9.76 ± 0.19*

Embryo weight (mg)

288.6 ± 4.21

222.3 ± 4.97*

209.5 ± 4.42*

Placental weight (mg)

187.8 ± 3.79

223.1 ± 3.23*

241.5 ± 3.66#

* Significantly different from embryos of control mothers (P < 0.05)

#Significantly different from non-malformed embryos of diabetic mothers (P < 0.05), by ANOVA

Table 3

The apparent malformation types in embryos of experimental diabetic pregnanacy

Malformation

Number of embryos

%

Growth retardation

21

52.5

Open neural tube

3

7.5

Maldevelopment of head

5

12.5

Absence of tail

4

10

Malrotation

13

32.5

Short mandible

6

15

At GD 17, non-malformed placentae from diabetic mothers had significantly lower levels of antioxidant vitamins (vitamins C and E), as well as antioxidant trace element, Selenium (cofactor of glutathione peroxidase and thioredoxin reductase) compared with controls. Placentae of malformed fetuses of diabetic mothers had even more significant decrease in the levels of vitamin C, vitamin E and Selenium compared with non-malformed diabetic and controls (Fig. 1). Markers of oxidative stress levels and ROS production were higher in placenta of diabetic mothers than controls. TBARS levels were significantly elevated in placentae of malformed diabetic compared to placentae of non-malformed embryos from diabetic mothers, and both were significantly elevated compared to controls (Fig. 1).
Fig. 1

Impact of maternal diabetes on oxidative stress and antioxidants in placenta. Data are presented as mean ± SD (n = 15). *Statistically significant difference from controls, # statistically significant difference from diabetic non-malformed, by ANOVA (P < 0.05)

Levels of GSSG were significantly increased in placentae of malformed when compared with non-malformed diabetic fetuses, in which GSSG was higher than controls. The ratio of GSH/GSSG is a powerful indicator of the ROS production inside the cell and the ability of the cell to counteract oxidative stress. Both GSH and GSH/GSSG ratio were significantly diminished in placentae of malformed fetuses of diabetic mothers compared to both non-malformed and controls. Furthermore, non-malformed placentae of diabetic mothers had significantly reduced levels of GSH and GSH/GSSG ratio compared with controls (Fig. 1).

We found significantly elevated levels of NOx in placentae of malformed fetuses of diabetic mothers compared with non-malformed and controls. Moreover, NOx were increased in non-malformed diabetic placenta compared to controls (Fig. 2). Higher levels of NOx could indicate oxidative stress and endothelial dysfunction. 8-oxo-dG levels were significantly higher in placentae of malformed and non-malformed fetuses (Fig. 3).
Fig. 2

Levels of nitric oxide end products NOx (nitrates and nitrites) as markers of nitrosative stress in placenta. Data are presented as mean ± SD (n = 15). *Statistically significant difference from controls, #statistically significant difference from diabetic non-malformed, by ANOVA (P < 0.05)

Fig. 3

Levels of 8-oxo dG (DNA oxidation adduct) and cleaved caspase-3 activity as a measure of activated apoptosis in placenta. Data are presented as mean ± SD (n = 15). *Statistically significant difference from controls, #statistically significant difference from diabetic non-malformed, by ANOVA (P < 0.05)

Placental growth factor 2 (PlGF-2) levels were significantly reduced in placentae of fetuses of diabetic mothers compared with controls regardless of malformation status. Placental levels of sFlt-1 were significantly higher in diabetic fetuses placenta regardless of malformation status (Fig. 4).
Fig. 4

PIGF-2 and sFlt-1/sVEGFR1 expression in placenta indicate vascular and endothelial functions. Data are presented as mean ± SD (n = 15). *Statistically significant difference from controls, #statistically significant difference from diabetic non-malformed, by ANOVA (P < 0.05)

Caspase-3 is a critical death protease, indispensable for apoptotic chromatin condensation and DNA fragmentation. Caspase-3 activity is significantly increased in placentae of malformed compared with that of non-malformed diabetic offspring, which have higher caspase-3 activity compared with controls (Fig. 3). The cyclooxygenase isoenzymes, COX-1 and COX-2, catalyze the oxidative cyclization of the central 5 carbons within 20 carbon polyunsaturated fatty acid (arachidonic acid) to form prostaglandins, thromboxane, and levuloglandins. COX-1 is produced constitutively while COX-2 is inducible (e.g. by inflammation). COX-1 enzyme activity did not differ significantly between malformed, non-malformed or control fetuses’ placentae. However, inducible COX-2 enzyme activity was significantly diminished in malformed compared to non-malformed fetuses of diabetic mothers and controls. COX-2 activity was also significantly reduced in non-malformed fetuses’ placenta when compared with controls (Fig. 5).
Fig. 5

Activity of cyclooxygenases (COX-1 and COX-2) in placenta to assess inflammatory response and prostaglandin production in placenta. Data are presented as mean ± SD (n = 15). *Statistically significant difference from controls, #statistically significant difference from diabetic non-malformed, by ANOVA (P < 0.05)

Discussion

Diabetes mellitus during pregnancy affects the developmental milieu, jeopardizes the normal fetal development and increases the risk of various adult onset morbidities (Calkins and Devaskar 2011). We have previously demonstrated that diabetes during pregnancy increases oxidative stress in various fetal tissues including placenta (Kamel et al. 2014). However, the effect of maternal diabetes on placental inflammation, vascular and oxidative stress markers specifically, was not studied thoroughly. In this study we demonstrate that oxidative stress is significantly elevated in placenta of diabetic pregnancies regardless of malformation status of the fetus.

Our results show clearly that diabetic pregnancy placentae exhibit increased oxidative stress. Moreover, the intra-cellular antioxidant defense mechanisms, as characterized by Glutathione oxidation parameters, were diminished in placentae from diabetic pregnancies. Normal placentae show a significant increase in oxidative stress that is instrumental to their normal development (Schafer and Buettner 2001). However, as pregnancy proceeds, the level of oxidative stress decrease and anti-oxidant levels increase (Basu et al. 2015). This suggests that diabetes may disturb normal milieu of placenta through increasing oxidative stress.

Other anti-oxidant systems were also diminished in placentae of diabetic pregnancies regardless of their malformation status. Moreover, anti-oxidant vitamins levels in tissues further corroborate the findings indicating increased oxidative stress in placentae of diabetic pregnancies. Whether the observed increase in oxidative stress is caused by the diminished anti-oxidants levels in placenta or vice versa cannot be elucidated form our work. However, it must be noted that normal pregnancies exhibit reduced serum levels of vitamin E compared to non-pregnant mothers, as pregnancy is a physiological condition associated with increased oxidative burden (Yoshioka et al. 1987). Moreover, the level of vitamin E in fetal tissues is related to that in corresponding maternal tissues and is amenable to the type of diet ingested by the mother (Yoshioka et al. 1987).

The increase in oxidative stress might have caused several deleterious effects on various cellular targets. TBARS levels were significantly elevated in a similar pattern as glutathione compounds, which illustrate the increased peroxidation of lipids in the affected placentae. Moreover, markers of DNA oxidation in diabetic placentae were also significantly increased indicating that the increased oxidative stress was high enough to cause such damage. DNA oxidation may hinder normal function of cells, which may be explained by the effect of these modifications in increasing mutation rate of affected cells, specifically transversions (Cooke and Evans 2007b).

Furthermore, nitric oxide levels show a similar pattern of elevation as that observed in 8-oxo-dG, which may reflect increased protein nitrosylation in placenta. Nitrative stress or increased protein nitrosylation is a hallmark of complicated pregnancies such as those with pre-eclampsia or gestational diabetes, and the nitrosylation of DNA and proteins hamper the normal function of placenta (Lyall et al. 1998; Myatt 2010). Furthermore, the increased damage inflicted by the increased oxidative stress was also evident by the increased activity of the apoptosis marker Caspase-3 observed in our results. Our results hint to the possibility that disturbed placental milieu may induce fetal programming of adult disease. At late gestation, several important physiological changes occur that may be affected by the disturbed milieu.

In addition to the parameters of oxidative stress and anti-oxidant measured, we also measured the activity of various enzymes and growth factors in placenta. Our results are in concordance with previous studies that demonstrated association of sFlt-1 elevation with diabetes or pre-eclampsia (Salim et al. 2009; Wu et al. 2010). Given the known functions of PIGF-2 and sFlt-1, we can hypothesize that the observed pattern reflect an abnormality in the fetal or placental vasculature. However, to confirm such a hypothesis, thorough analysis of fetal vasculature must be conducted.

The downstream effects of the observed increase in placental oxidative stress were also observed. The content of cyclooxygenase isozymes was altered in placentae of diabetic malformed and non-malformed fetuses. Our results are in concordance with previous work published (Al-Matubsi et al. 2010) were COX-2 was significantly reduced in malformed diabetic compared to non-malformed diabetic placentae; however, these measurements were conducted on placentae extracted in earlier day of gestation. A major discrepancy between both results is that in our measurements COX-1 and COX-2 levels were comparable, while in Al-Matubsi and colleagues work, COX-1 levels were relatively small compared to COX-2. In absence of diabetes, oxidative stress induces expression of COX-2 in murine placenta (Burdon et al. 2007). However, in our results despite increased oxidative stress, COX-2 expression was significantly reduced in placenta, which may suggest that diabetes might have disrupted normal response to oxidative stress.

Our results are in harmony with previous observations conducted during different times of gestation. Diabetes in pregnancy regardless of malformation status is associated with increased oxidative stress and disturbed placental function. The exact mechanism by which oxidative stress disrupts normal placental function is not known but may be a result of a complex menagerie of cellular insults such as DNA mutation, protein oxidation and nitrosylation as well as apoptosis. Moreover, other conditions related to diabetes such as obesity, may contribute to the observed placental dysfunction. Although absence of fetal malformation does not rule out placental alteration, we did not observe any placental alteration in diabetic embryos (malformed and non-malformed). However, to confirm or delineate the contribution of these factors, further studies should be conducted.

Conclusion

Maternal diabetes is associated with a state of oxidative stress, sparseness of various antioxidants and growth factors that are critical for endothelial and vascular functions, and increased apoptotic activity in placenta. Whether theses perturbations are causally related or just coincidental with the effects of high glucose on placental function is still unclear. Further studies are needed to confirm and illustrate the molecular mechanisms of these abnormalities.

Notes

Abbreviations

T2DM: 

type 2 diabetes mellitus

GSH: 

glutathione

ROS: 

reactive oxygen species

RNS: 

reactive nitrogen species

8-oxo-dG: 

8-oxo-7,8-dihydro-2′-deoxyguanosine

TBARS: 

thiobarbituric acid reactive substances

MDA: 

malondialdehyde

CRL: 

crown-rump length

VEGF-A: 

vascular endothelial growth factor-A

VEGFR-1/Flt-1: 

vascular endothelial growth factor receptor

PIGF: 

placenta growth factor

NOx: 

nitric oxide end products

COX-1: 

cyclooxygenase isoenzyme-1

COX-2: 

cyclooxygenase isoenzyme-2

PGE2

prostaglandin E2

NADH2

nicotinamide adenine dinucleotide

FADH2

flavin adenine dinucleotide

Declarations

Authors’ contributions

MAK has conceived and designed the study, contributed to the analysis of the data, and to the writing and revising the manuscript. MIS, TMA, MMS and MMH have conducted most of the laboratory investigations, and contributed to the writing and revising of the manuscript. SHT has carried out the statistical analysis of the data, and helped in data assembly. All authors read and approved the final manuscript.

Acknowledgements

None.

Competing interests

The authors declare that they have no competing interests.

Ethical statement

The Institutional Animal Care and Use Committee at the Medical Research Institute—Alexandria University, Alexandria, Egypt, has approved the animal protocol.

Informed consent

The study did not involve participation of humans and formal consent is not required.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors’ Affiliations

(1)
Department of Biochemistry, Medical Research Institute
(2)
The Ritchie Centre, Hudson Institute of Medical Research, Monash University
(3)
Department of Human Genetics, Medical Research Institute, Alexandria University
(4)
Department of Molecular Medicine, University of Padova

References

  1. Al-Matubsi HY, Salim MD, El-Sharaky AS, Kamel MA, Oriquat GA, Helmy MH, El-Bassiouni EA, Shourbaji M (2010) Activities of cyclooxygenases, and levels of prostaglandins E2 and F2alpha, in fetopathy associated with experimental diabetic gestation. Diabetes Metab 36:43–50View ArticleGoogle Scholar
  2. Basu J, Bendek B, Agamasu E, Salafia CM, Mishra A, Benfield N, Patel R, Mikhail M (2015) Placental oxidative status throughout normal gestation in women with uncomplicated pregnancies. Obstetrics Gynecol Int 2015:276095View ArticleGoogle Scholar
  3. Burdon C, Mann C, Cindrova-Davies T, Ferguson-Smith AC, Burton GJ (2007) Oxidative stress and the induction of cyclooxygenase enzymes and apoptosis in the murine placenta. Placenta 28:724–733View ArticleGoogle Scholar
  4. Calkins K, Devaskar SU (2011) Fetal origins of adult disease. Curr Probl Pediatr Adolesc Health Care 41:158–176View ArticleGoogle Scholar
  5. Castori M (2013) Diabetic embryopathy: a developmental perspective from fertilization to adulthood. Mol Syndromol 4:74–86Google Scholar
  6. Cooke MS, Evans MD (2007a) 8-Oxo-deoxyguanosine: reduce, reuse, recycle? Proc Natl Acad Sci 104:13535–13536View ArticleGoogle Scholar
  7. Cooke MS, Evans MD (2007b) 8-Oxo-deoxyguanosine: reduce, reuse, recycle? Proc Natl Acad Sci USA 104:13535–13536View ArticleGoogle Scholar
  8. De Rijk EP, Van Esch E, Flik G (2002) Pregnancy dating in the rat: placental morphology and maternal blood parameters. Toxicol Pathol 30:271–282View ArticleGoogle Scholar
  9. Draper HH, Hadley M (1990) Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol 186:421–431View ArticleGoogle Scholar
  10. El-Bassiouni EA, Helmy MH, Rawash NA, El-Zoghby SM (2005) Embryopathy in experimental diabetic gestation: assessment of oxidative stress and antioxidant defence. Br J Biomed Sci 62(2):71Google Scholar
  11. Gareskog M, Cederberg J, Eriksson UJ, Wentzel P (2007) Maternal diabetes in vivo and high glucose concentration in vitro increases apoptosis in rat embryos. Reprod Toxicol 23:63–74View ArticleGoogle Scholar
  12. Goto MP, Goldman AS, Uhing MR (1992) PGE2 prevents anomalies induced by hyperglycemia or diabetic serum in mouse embryos. Diabetes 41:1644–1650View ArticleGoogle Scholar
  13. Griffith OW (1980) Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal Biochem 106:207–212View ArticleGoogle Scholar
  14. Guevara I, Iwanejko J, Dembinska-Kiec A, Pankiewicz J, Wanat A, Anna P, Golabek I, Bartus S, Malczewska-Malec M, Szczudlik A (1998) Determination of nitrite/nitrate in human biological material by the simple Griess reaction. Clin Chim Acta 274:177–188View ArticleGoogle Scholar
  15. Hauser S, Weich HA (1993) A heparin-binding form of placenta growth factor (PlGF-2) is expressed in human umbilical vein endothelial cells and in placenta. Growth Factors 9:259–268View ArticleGoogle Scholar
  16. Helske S, Vuorela P, Carpén O, Hornig C, Weich H, Halmesmäki E (2001) Expression of vascular endothelial growth factor receptors 1, 2 and 3 in placentas from normal and complicated pregnancies. Mol Hum Reprod 7:205–210View ArticleGoogle Scholar
  17. Herber RFM, Stoeppler M (1994) Trace element analysis in biological specimens. Elsevier, AmsterdamGoogle Scholar
  18. Jagota SK, Dani HM (1982) A new colorimetric technique for the estimation of vitamin C using Folin phenol reagent. Anal Biochem 127:178–182View ArticleGoogle Scholar
  19. Jawerbaum A, Higa R, White V, Capobianco E, Pustovrh C, Sinner D, Martinez N, Gonzalez E (2005) Peroxynitrites and impaired modulation of nitric oxide concentrations in embryos from diabetic rats during early organogenesis. Reproduction 130:695–703View ArticleGoogle Scholar
  20. John R, Hemberger M (2012) A placenta for life. Reprod Biomed Online 25:5–11View ArticleGoogle Scholar
  21. Kamel MaherA, Helmy MadihaH, Hanafi MervatY, Mahmoud ShimaaA, Elfetooh HA (2014) Effect of maternal diabetes on pre- and post-natal redox status of F1 rat offspring. Open J Endocr Metab Dis 4:111–127View ArticleGoogle Scholar
  22. Kargman S, Wong E, Greig GM, Falgueyret JP, Cromlish W, Ethier D, Yergey JA, Riendeau D, Evans JF, Kennedy B, Tagari P, Francis DA, O’Neill GP (1996) Mechanism of selective inhibition of human prostaglandin G/H synthase-1 and -2 in intact cells. Biochem Pharmacol 52:1113–1125View ArticleGoogle Scholar
  23. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275Google Scholar
  24. Lyall F, Gibson JL, Greer IA, Brockman DE, Eis AL, Myatt L (1998) Increased nitrotyrosine in the diabetic placenta: evidence for oxidative stress. Diabetes Care 21:1753–1758View ArticleGoogle Scholar
  25. McCormick DB, Green HL (1996) Vitamins. In: Burtis CA, Ashwood ER (eds) Clinical chemistry. Saunders, Philadeliphia, pp 473–484Google Scholar
  26. Myatt L (2010) Review: reactive oxygen and nitrogen species and functional adaptation of the placenta. Placenta 31(Suppl.):S66–S69View ArticleGoogle Scholar
  27. Saad MI, Abdelkhalek TM, Saleh MM, Kamel MA, Youssef M, Tawfik SH, Dominguez H (2015) Insights into the molecular mechanisms of diabetes-induced endothelial dysfunction: focus on oxidative stress and endothelial progenitor cells. Endocrine 50(3):537–567View ArticleGoogle Scholar
  28. Sakamaki H, Akazawa S, Ishibashi M, Izumino K, Takino H, Yamasaki H, Yamaguchi Y, Goto S, Urata Y, Kondo T, Nagataki S (1999) Significance of glutathione-dependent antioxidant system in diabetes-induced embryonic malformations. Diabetes 48:1138–1144View ArticleGoogle Scholar
  29. Salim MD, Al-Matubsi HY, El-Sharaky AS, Kamel MA, Oriquat GA, Helmy MH, El-Bassiouni EA (2009) The levels of vascular endothelial growth factor-A and placental growth factor-2 in embryopathy associated with experimental diabetic gestation. Growth Factors 27:32–39View ArticleGoogle Scholar
  30. Schafer FQ, Buettner GR (2001) Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple. Free Radic Biol Med 30:1191–1212View ArticleGoogle Scholar
  31. Sies H (2015) Oxidative stress: a concept in redox biology and medicine. Redox Biol 4:180–183View ArticleGoogle Scholar
  32. Thornberry NA (1994) Interleukin-1 beta converting enzyme. Methods Enzymol 244:615–631View ArticleGoogle Scholar
  33. Wentzel P, Eriksson UJ (2002) 8-Iso-PGF(2alpha) administration generates dysmorphogenesis and increased lipid peroxidation in rat embryos in vitro. Teratology 66:164–168View ArticleGoogle Scholar
  34. Wildman DE (2011) Review: toward an integrated evolutionary understanding of the mammalian placenta. Placenta 32(Suppl. 2):S142–S145View ArticleGoogle Scholar
  35. Wu FT, Stefanini MO, Mac Gabhann F, Kontos CD, Annex BH, Popel AS (2010) A systems biology perspective on sVEGFR1: its biological function, pathogenic role and therapeutic use. J Cell Mol Med 14:528–552Google Scholar
  36. Yang P, Zhao Z, Reece EA (2008) Activation of oxidative stress signaling that is implicated in apoptosis with a mouse model of diabetic embryopathy. Am J Obstet Gynecol 198(130):e131–e137Google Scholar
  37. Yoshioka T, Motoyama H, Yamasaki F, Ando M, Takehara Y, Yamasaki M (1987) Lipid peroxidation and vitamin E levels during pregnancy in rats. Neonatology 52:223–231View ArticleGoogle Scholar

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