Original Article | Published:

Magnesium sulfate therapy of preeclampsia: an old tool with new mechanism of action and prospect in management and prophylaxis

Hypertension Research volume 35, pages 10051011 (2012) | Download Citation

Abstract

A disturbed balance between angiogenic and antiangiogenic growth factors is a highly accepted mechanism in the pathogenesis of pregnancy-induced hypertension and proteinuria, which is clinically known as preeclampsia (PE). We investigated the effect of magnesium sulfate (MgSO4) therapy on vascular endothelial growth factor (VEGF), placental growth factor (PlGF), nitric oxide (NO) metabolites, soluble fm-like tyrosine kinase-1 (sFlt-1) and endoglin levels in PE rats and the effect of this treatment on the feto-maternal outcome. The PE group showed hypertension, proteinuria and decreased number and weight of live pups relative to the control group. This result was associated with increased sFlt-1, VEGF receptor-2 (VEGFR-2), VEGFR-3 and endoglin levels but decreased NO metabolites. MgSO4 therapy ameliorated systolic hypertension and proteinuria and decreased sFlt-1, VEGFR-2, VEGFR-3 and endoglin levels but increased NO metabolites in the treated group. Physiological and biochemical changes and improved pup weight and viability were observed in the treated group. The vasodilator action of MgSO4 and increased NO production are expected to increase placental blood flow and help fetal nutrition and development. Relief of placental ischemia decreases the production of antiangiogenic growth factors and restores the bioavailability of angiogenic factors (PlGF and VEGF). These changes resulted in better fetal outcome and an improved clinical picture of PE. These findings are promising and encourage further study of the mechanism of action of MgSO4 to support its widespread use in the prevention and management of the etiopathological changes underlying the vast majority of the manifestations and complications of PE.

Introduction

Preeclampsia (PE) is a well-documented pregnancy-specific syndrome that complicates 5–8% of pregnancies in developed countries, reaching double this ratio in developing countries and causing 50 000–75 000 (15%) maternal deaths worldwide per year.1, 2, 3 Changes in proangiogenic and antiangiogenic factors are reported in preeclamptic pregnancies, and the disturbance in their levels is considered the main cause of the endothelial dysfunction that underlies the rest of the pathophysiological alterations of the disease.4, 5 Placental ischemia and hypoperfusion are common findings in PE.6, 7 They decrease placental growth factor (PlGF) and produce high concentrations of circulating antiangiogenic factors, such as soluble vascular endothelial growth factor receptor-1 (sVEGFR-1), known as soluble fm-like tyrosine kinase-1 (sFlt-1), and the transmembrane glycoprotein endoglin (ENG).4, 6, 7 Increased sFlt-1 and ENG production has been reported before the onset of the clinical picture of PE.6 This report supports the hypothesis that these factors are a cause and not only a result of the endothelial dysfunction in the major body organs, causing proteinuria, hypertension and the rest of the systemic manifestations of the disease.8, 9 VEGF has been reported to augment nitric oxide (NO) production through VEGFR-2/the kinase domain receptor,10 and NO was found to have an important role in the mitogenic effect of VEGF during angiogenesis.11 However, little is known about the relation between circulating VEGF and NO levels in PE. Decreased NO leads to vasospasm and hypoxia, which changes VEGF levels.12 In addition to increased lipid peroxides and impaired antioxidant defense mechanisms, these changes may have a role in the etiology of PE.12

Magnesium sulfate (MgSO4) is used in the management of severe cases of PE to prevent the progression to eclampsia.13 However, despite its low cost and clear evidence of multiple beneficial effects in the PE syndrome, the use of MgSO4 is still below the expected level in several countries, and the mechanism of action of this drug, particularly its effect on the angiogenic factors that regulate endothelial function and new blood vessel formation, in pregnancy is still unclear. We hypothesized that normalizing the balance between circulating angiogenic and antiangiogenic growth factors in PE may halt the progression of the disease and improve the chances of healthy outcome for the pregnant mothers and their fetuses. In the current study, we investigated the effect of MgSO4 treatment on balancing angiogenic (VEGF, PlGF and NO) and antiangiogenic (sFlt-1 and ENG) growth factors and the effect of this treatment on the clinical manifestations and pregnancy outcome in PE rats.

Methods

Experimental design

The study protocol was approved by the local ethics committee, and the experimental procedures were in accordance with the Guide for Care and Use of Laboratory Animals of the National Institutes of Health. All of the animals were maintained under standard laboratory conditions on a 12-h light/dark cycle with free access to food and water ad libitum. Virgin Wistar rats bred in the Laboratory Animal Care Unit of the College of Medicine, King Saud University, were caged 1:1 with mature males for mating. For confirmation of pregnancy, vaginal smears were checked in the early morning under a light microscope. The day of presence of spermatozoa was designated as day 0 of the 21–22-day gestation period. On day 13 of pregnancy, 60 pregnant and 10 non-pregnant rats (250–270 g) were randomized into the following experimental groups:

CON-NP: control non-pregnant rats with no treatment (n=10).

CON-P: control pregnant rats with no treatment (n=20).

PRE: pregnant rats with PE receiving no treatment (n=20).

PRE+MgSO4: pregnant rats with PE treated with MgSO4 (n=20).

Induction of PE and treatment

Omega nitro-L-arginine methyl ester (L-NAME) was administered orally at a dose of 60 mg kg−1 per day to induce PE in PRE and PRE+MgSO4 groups beginning at day 13 of pregnancy through term.14 From day 17 of pregnancy to day 21 (Term), the PRE+MgSO4 group received 500 mg kg−1 per day MgSO4 through s.c. osmotic mini pumps (Model 2 ml, Alzet Corp, Palo Alto, CA, USA).15 The CON-P group received saline infusion. L-NAME and MgSO4 powders were purchased from Sigma Chemical (St Louis, MO, USA). ELISA kits for mouse sFlt-1 (sVEGFR-1), VEGFR-2, rat VEGF, PlGF and nitrate/nitrite (NO2/NO3) were purchased from R&D Systems (Minneapolis, MN, USA). The ELISA kits for VEGFR-3 (Flt-4) and endoglin were purchased from USCN Life Science Inc (Missouri City, TX, USA). Colorimetric kits for urine protein and serum magnesium determination were purchased from Spinreact (Girona, Spain) and United Diagnostics Industry (Riyadh, Saudi Arabia), respectively.

Blood pressure (BP) measurement and sampling

Systolic BP was measured in all of the studied groups at days 0 and 20 of pregnancy with the non-invasive blood pressure system (NIBP) using tail–cuff plethysmography (Letica LE 5100, Panlab, Barcelona, Spain). Urine samples were collected at days 0 and 20 of pregnancy. Blood samples were collected at day 19 of pregnancy from the retro-orbital plexus in plain test tubes. At full-term (day 21 of pregnancy), animals were weighed and anesthetized with intramuscular (IM) ketamine (40 mg kg−1 body wt) and xylazine (5 mg kg−1 body wt), and intracardiac blood sampling and midline laparotomy incision were performed to expose the uterine horns. The developed fetuses were counted and removed. After delivery of the pups, their weight and condition (dead or alive) were recorded. One kidney was isolated from each rat, washed with cold saline, immediately immersed in 10% neutral-buffered formalin and reserved for histopathological examination.

Biochemical analysis

Proteinuria, NO production and serum magnesium level

Protein loss in the urine was quantified by a protein assay kit (Spinreact, Girona, Spain) according to the manufacturer’s instructions. Total NO production was evaluated by measuring the stable end products of NO metabolism (nitrate and nitrites) in serum and urine with a special kit (R&D Laboratories, Minneopolis, MN, USA) using nitrate reductase and Griess reagents with an ELISA reader.16 The mean minimum detection limit was 0.25 μmol l−1. Total serum magnesium (Mg++) concentration was measured colorimetrically using the calmagite complexometric method according to the kit manufacturer’s instructions.

Serum VEGF, sVEGFR-1, VEGF-2, VEGF-3, PlGF and ENG levels

Generally, these assays employed the quantitative sandwich enzyme immunoassay technique.17 The mean minimum detection limit of VEGF, PlGF and VEGFR-2 was 8.5 pg ml−1, 7 pg ml−1 and 0.27 ng ml−1, respectively, and the detection limits for sFlt-1, VEGFR-3 and Endoglin were 0–8000 pg ml−1, 31.2–2000 pg ml−1 and 0.78–50 ng ml−1, respectively.

Histopathological examination

The fixed kidney tissue samples were embedded in paraffin, cut into 3–5-μm sections, stained with hematoxylin and eosin and examined under an Olympus BX51 microscope and DP72 Camera (12 MG Pixel).

Statistical analysis

Data were analyzed using the computer software SPSS 17.0 (SPSS, Inc., Chicago, IL, USA) package for Windows. The comparison between several groups was performed using a one-way analysis of variance. A post-hoc least significant difference (LSD) test was used when analysis of variance showed significant differences. The comparison between samples of the same group at different time points of the study was performed by paired sample t-test. Pearson’s correlation analysis was used to study the relation between two variables. Data are presented as the mean±s.d. The results were significant at P<0.05.

Results

Systolic BP

At day 20 of pregnancy, the PRE group showed significantly higher BP relative to the CON-P group (P<0.001). MgSO4 significantly decreased the BP of the PRE+MgSO4 group in comparison with the non-treated PRE group (P<0.001), but BP remained significantly higher than the control value (P<0.001) (Table 1).

Table 1: Systolic BP, proteinuria, urine and serum nitrate/nitrite (uNO2/NO3, sNO2/NO3) levels and BW of the CON-P, preeclampsia (PRE) and PRE+MgSO4 groups of rats

Proteinuria

Table 1 shows that by day 20 of pregnancy, proteinuria was significantly higher in the PRE group in comparison with the CON-P group (P<0.001). MgSO4 treatment significantly decreased the proteinuria in the PRE+MgSO4 group compared with the PRE group (P<0.001), but it remained significantly higher than the CON-P and CON-NP groups (P<0.001 for each).

NO production

PE caused a significant decrease in serum and urinary NO2/NO3 levels in the PRE group compared with the CON-P group (P<0.001) (Table 1). MgSO4 therapy caused a significant increase in total NO2/NO3 levels in the PRE+MgSO4 group in comparison with the PRE group (P<0.001).

Serum magnesium

As Table 2 shows, pregnant animals in both the CON-P and the PRE groups had a significant decrease in Mg++ at days 19 and 21 of pregnancy in comparison with the CON-NP group (P=0.037 and 0.022, respectively). However, there was no significant difference between Mg++ levels between the CON-P and PRE groups (P>0.05). In contrast, Mg++ was significantly increased in the PRE+MgSO4 group compared with all of the other groups at days 19 and 21 of the study (P<0.001 for all).

Table 2: Serum magnesium (Mg++), sVEGFR-1 (sFlt-1), VEGFR-2, VEGFR-3 and sENG in the CON-P, preeclampsia (PRE) and PRE+MgSO4 groups of rats at day 19 and 21 of pregnancy and of the CON-NP group

Angiogenic and antiangiogenic growth factors levels

Serum VEGF and PlGF

Serum VEGF and PlGF levels of all of the groups in the current study were below the detection limits of the ELISA kits. According to the manufacturer of the VEGF kit, serum VEGF is not detected in normal rats.

Soluble VEGFR-1 (sFlt-1)

The PRE group showed a marked increase in serum sFlt-1 levels at day 19 of pregnancy compared with the CON-P group (P<0.001) (Table 2). However, at day 21 of pregnancy, the serum sFlt-1 level of the PRE group showed a significant decrease in comparison with the level at day 19 (P<0.001), but it remained significantly higher than the corresponding value in both the CON-P and CON-NP groups (P<0.001). MgSO4 decreased sFlt-1 levels in the PRE+MgSO4 group at days 19 in comparison with the PRE group (P<0.001). This decreased level was similar to the CON-P and CON-NP groups (P=0.81 and 0.92, respectively). At day 21 of pregnancy, serum sFlt-1 levels were further decreased in the MgSO4+PRE group, reaching the CON-P and CON-NP levels (P=0.54 and 0.36, respectively).

Serum ENG (sENG)

At day 19 of pregnancy, sENG levels increased significantly in the PRE group in comparison with the CON-P group (P<0.001) (Table 2). However, the PRE+MgSO4 group showed lower sENG levels than the PRE group (P<0.001), and the PRE+MgSO4 levels showed no difference from the levels in the CON-P group (P=0.49). At day 21 of pregnancy, sENG remained significantly higher in the PRE group compared with the PRE+MgSO4 group (P<0.001), but it decreased significantly in the CON-P and the PRE+MgSO4 groups, reaching the CON-NP level (P=0.81 and 0.22, respectively).

Morphometric criteria of pups

The number of viable fetuses was significantly lower in the PRE group in comparison with the CON-P group (P=0.001). However, in the PRE+MgSO4 group, the number of live births showed no significant difference from the CON-P group (P=0.061) (Table 3). The pup mortality rate (calculated as the number of dead fetuses/total number of pups × 100) was 0% in the CON-P group, 34.05% in the PRE group and 17.48% in the PRE+MgSO4 group. The number of dead pups was significantly higher in the PRE group in comparison with the CON-P group (P=0.001). MgSO4 therapy in the PRE+MgSO4 group decreased the number of dead pups in this group to a comparable level to the CON-P group (P=0.085). Furthermore, Table 3 shows that the total pup weight was significantly lower in the PRE group in comparison to the CON-P group (P<0.001). MgSO4 therapy increased the total pup weight in the PRE+MgSO4 group compared with the PRE group (P=0.028), but it remained significantly lower than the CON-P group (P<0.001). Similarly, the untreated PRE group showed decreased single pup weight compared with the CON-P group (P<0.001). MgSO4 treatment significantly increased the single pup weight in the PRE+MgSO4 group in comparison with the PRE group (P=0.015), but it remained significantly lower than the control group (P=0.003).

Table 3: Morphometric criteria of pups in the CON-P, preeclampsia (PRE) and PRE+MgSO4 groups of rats at day 21 of pregnancy

Body weight (BW)

As shown in Table 1, the final BW of the PRE group was significantly lower than the CON-P group (P<0.001). The MgSO4-treated PRE+MgSO4 group showed a final BW that was significantly higher than the PRE group (P=0.002) and comparable to the CON-P rats (P=0.35).

Correlation analysis

Pearson’s correlation analysis revealed a significant positive correlation between serum sFlt-1 and sENG at days 19 and 21 of pregnancy (r=0.43, P<0.01; r=0.456, P<0.01, respectively) (Figure 1a and b). However, the sENG level at day 19 of pregnancy was negatively correlated with the number of live births (r=−0.311, P=0.016) (Figure 1c) but positively correlated with the number of dead pups (r=0.26, P=0.04) (Figure 2d). Furthermore, sENG levels at days 19 and 21 were negatively correlated with single pup weight (r=−0.0431, P<0.01 and r=−0.473, P<0.001, respectively) (Figure 2a and b). Correspondingly, sFlt-1 was inversely correlated with the number of live births (r=−0.42, P=0.042) (Figure 1d) and single pup weight (r=−0.317, P=0.014) (Figure 2c). At day 19 of pregnancy, serum NO2/NO3 levels showed an inverse correlation with sFlt-1 (r=−0.408, P<0.001).

Figure 1
Figure 1

Positive correlation between serum endoglin and sFlt-1 levels at day 19 (a, r=0.43, P<0.01) and day 21 (b, r=0.456, P<0.01) of pregnancy. The number of live pups is negatively correlated with serum endoglin level at day 19 (c, r=−0.311, P=0.016) and sFlt-1 level at day 21 of pregnancy (d, r=−0.42, P=0.042).

Figure 2
Figure 2

Single pup weight is negatively correlated with serum endoglin level at days 19 and 21 (a, r=−0.0431, P<0.01 and b, r=−0.473, P<0.001) and sFlt-1 levels at day 19 (c, r=−0.317, P=0.014). (d) Positive correlation between serum endoglin and the number of dead pups (r=0.26, P=0.04).

Histopathology of the renal tissue

Hematoxylin and eosin staining of the renal tissue of the studied groups showed normal histological appearance of the glomeruli and tubules of the CON-NP and CON-P groups (Figure 3a and b). However, glomeruli in the PRE group showed increased cellularity and narrowed capillary lumen and Bowman’s capsule in comparison with the CON-NP and CON-P groups (Figure 3c). MgSO4 therapy in the PRE+MgSO4 group markedly abolished the histological changes induced by L-NAME, leading to decreased glomerular cellularity and recovery of the normal appearance of Bowman’s capsule and glomerular capillaries (Figure 3d).

Figure 3
Figure 3

Hematoxylin and eosin ( × 40) staining of the kidney tissue of the studied groups revealed normal appearance of the glomeruli and tubules in the CON-NP and CON-P groups (a, b). The PRE group showed crowded glomeruli with hypercellularity and narrow capillary lumen and Bowman’s capsule (c). MgSO4 therapy in the PRE+MgSO4 group abolished the glomerular changes induced by L-NAME (d).

Discussion

Over the past few years, there has been increasing interest in studying the role of angiogenic and antiangiogenic growth factors in the etiology, screening and management of PE. Correspondingly, the current study investigated the effect of MgSO4 therapy on a group of angiogenic and antiangiogenic growth factors in L-NAME-induced PE and the effect on the pregnancy outcome. Circulating antiangiogenic sFlt-1 and sENG were significantly elevated in the PRE group in the current study. This result was recently attributed to increased placental production and is considered a keystone in the pathophysiology of PE.5, 18 Elevated sENG predisposes pregnant women to PE through inhibition of capillary formation, TGF-β signaling and TGF-β-mediated NO synthase activation in endothelial cells.19

The undetectable levels of VEGF and PlGF in the pregnant rats in the current study were in agreement with other investigators, who failed to detect these angiogenic factors in a large population of pregnant women regardless of the end result of pregnancy.20, 21, 22 Furthermore, low PlGF in the presence of high sFlt-1 levels, as observed in the PRE group in the current study, increased the risk of PE in a prospective nested control study.21 The decrease in circulating VEGF and PlGF in PE could be due to decreased placental production.23 Moreover, increased sFlt-1 is suggested to bind to these angiogenic factors and decrease their free fractions.18, 24 Additionally, sFlt-1 competes with VEGFR-2 for VEGF, leading to disturbed angiogenesis, endothelial dysfunction, glomerular damage, impaired glomerular repair and increased apoptosis.17, 25 These changes contribute to the development of hypertension and proteinuria in PE.10 The changes in circulating sFlt-1 correlated positively with sENG at days 19 and 21 of pregnancy (Figure 1a and b). This result was in agreement with other animal and human studies that reported a high correlation between sENG and sFlt-1 on one hand and disease severity on the other hand.26, 27 A causal relationship between these antiangiogenic growth factors and fetal mortality in PE is strongly suggested by the observed negative correlation between sENG/sFlt-1 and the number of live pups and their birth weight (Figure 1c and d, Figure 2a–c) and the direct correlation between sENG and the number of dead pups (Figure 2d).

The role of Mg++ in the etiology of PE is still controversial. Unchanged, increased and decreased serum Mg++ levels have been reported in human PE.28, 29, 30 These variations were suggested to be due to population heterogeneity or differences in the sample size or assay techniques. In the current study, decreased serum Mg++ was observed in the CON-P and PRE groups in comparison with the CON-NP group. MgSO4 therapy significantly increased Mg++ levels in the PRE+MgSO4 group compared with the untreated PRE group. The comparable levels of Mg++ in the PRE and CON-P groups suggest that changes in feto-maternal demands and renal hemodynamics during pregnancy rather than PE caused the changes in serum Mg++.31

The introduction of MgSO4 therapy ameliorated the hypertension and proteinuria in the PRE+MgSO4 group in the current study. Magnesium has in vivo and in vitro vasodilator properties, and MgSO4 injection has been reported to reduce total peripheral resistance and counteract the vasospasm induced by vasoconstrictor substances, such as endothelin-1, in several vascular beds.32 This result could explain the preserved normal histological structure and the amelioration of hypertension in the PRE+MgSO4 group in the current study. Similarly, MgSO4 was able to relieve coronary vasospasms, increase blood flow and improve endothelial function, leading to a good response in several ischemic cardiac problems.17, 33 Similarly, MgSO4 inhibits cerebral vasospasms and prevents seizures in patients with severe PE.34 Other antihypertensive drugs, such as clonidine, diazoxide, frusemide and hydralazine, show no effect on the production of sFlt-1 and sENG from the placentas of patients with PE.35 This study, however, demonstrated the inhibitory effect of MgSO4 therapy on serum levels of antiangiogenic growth factors and its ability to increase NO metabolic end products in the serum and urine of the PRE+MgSO4 group. Although there is no clear explanation of this increase in NO production, both direct and indirect pathways could be hypothesized. MgSO4 might directly stimulate NO synthase activity or indirectly stimulate NO release through VEGF.36, 37 The latter suggestion is supported by the observed inverse correlation between NO metabolites and sFlt-1 levels in the current study. This gives the impression that decreased availability of VEGF due to its binding with sFlt-1 might decrease VEGF-enhanced NO production38 and vice versa. Additionally, the protective effect of MgSO4 on the renal structure observed in histopathology may preserve renal NO production in the treated group. However, further studies are needed to clarify the mechanism of this increase in NO production in MgSO4-treated PE rats.

The increase in VEGFR-2 and VEGFR-3 levels observed in the PRE group in the current study (Table 2) may be secondary to the decreased availability of VEGF, which increases the free unbound receptors in serum.39 However, decreased VEGFR-2 and VEGFR-3 in the MgSO4-treated group could be related to the decrease in sFlt-1, which increases the free unbound forms of VEGF and PlGF, making them more available to bind to other receptors, such as VEGFR-2 and VEGFR-3. Binding of VEGF to its functional receptors will help it to induce NO and vasodilatory prostacyclins in endothelial cells, leading to decreased vascular tone and BP.36, 37 In this case, VEGF works in association with NO to maintain normal structure and function of the glomerular basement membrane,40 stimulate glomerular repair, and inhibit proteinuria.41 This pathway could explain the amelioration of proteinuria and hypertension in the PRE+MgSO4 group in the current study. Additionally, the vasodilatory effect of NO may augment the inhibitory effect of MgSO4 on the vascular tone and peripheral vascular resistance, leading to decreased BP and increased renal blood flow.28

In addition, the NO signaling pathway, the vasodilator and antiplatelet effects of NO are expected to decrease vascular tone and increase placental blood flow, leading to better fetal nutrients and oxygen supply.42 This expectation explains the increased fetal viability and birth weight in the MgSO4-treated group. The reduction of circulating antiangiogenic factors in the PRE+MgSO4 group in the current study could be explained by the ability of MgSO4 to decrease systemic vascular resistance and counteract the vasoconstrictor substances in several vascular beds.28 Furthermore, MgSO4 was reported to decrease feto-placental perfusion pressure43 and depress the expression of caspase-3 in the placenta.44 These effects are anticipated to improve placental blood flow and relieve the ischemia and subsequently decrease the production of sFlt-1 and ENG.45 Enhanced placental circulation is likely to support its physiological functions, leading to better fetal nutrition, as reflected in fetal birth weight and viability.44

We found an inverse relationship between sFlt-1 and NO2/NO3 in the current study. This result suggests that the factors that increase sFlt-1 may concurrently decrease NO production, producing vasoconstriction and increasing vascular resistance through these two opposite effects, which start the pathophysiological process of PE.

We conclude that MgSO4 is thus a promising compound that has a mechanistic role in the inhibition of the pathophysiological process of PE. The vasodilatory effect of MgSO4 may be the primary mechanism of action that preserves placental circulation and protects it against ischemia and hypoperfusion. This effect inhibits the production of antiangiogenic growth factors. Second, MgSO4 augments NO production and maintains the balance between angiogenic and antiangiogenic growth factors, which is essential for the normal growth and development of the feto-placental unit.

References

  1. 1.

    , , , . Summary of the NHLBI Working Group on Research in Hypertension During Pregnancy. Hypertension 2003; 41: 437–445.

  2. 2.

    WHO. Global Burden of Disease for the Year 2001 by World Bank Region, for Use in Disease Control Priorities in Developing Countries. National Institutes of Health: Bethesda, MD. 2004.

  3. 3.

    WHO. Make Every Mother and Child Count. In: World Health Report. World Health Organization: Geneva. 2005.

  4. 4.

    , , , , , , , , , , . Plasma soluble vascular endothelial growth factor receptor-1 concentrations elevated prior to the clinical diagnosis of pre-eclampsia. J Matern Fetal Neonatal Med 2005; 17: 3–18.

  5. 5.

    , , , . Abnormal placentation, angiogenic factors, and the pathogenesis of preeclampsia. Obstet Gynecol Clin North Am 2010; 37: 239–253.

  6. 6.

    , , . Angiogenic factors and preeclampsia. Thromb Res 2009; 123: S93–S99.

  7. 7.

    , , , , , , , , , , , , . Circulating angiogenic factors and the risk of preeclampsia. N Engl J Med 2004; 350: 672–683.

  8. 8.

    , , , . Vascular endothelial growth factor antagonist is produced by the human placenta and released into the maternal circulation. Biol Reprod 1998; 59: 1540–1548.

  9. 9.

    , , , . Suppression of serum vascular endothelial growth factor immunoreactivity in normal pregnancy and in preeclampsia. Br J Obstetrics Gynecol 1997; 104: 223–228.

  10. 10.

    , , . Amniotic vascular endothelial growth factor (VEGF) and nitric oxide (NO) in women with subsequent preeclampsia. Eur J Obstet Gynecol Reprod Biol 2004; 113: 17–20.

  11. 11.

    , , , , . Role of nitric oxide and reactive oxygen species in the pathogenesis of preeclampsia. J Obstet Gynaecol Res 2010; 36: 239–247.

  12. 12.

    , , , . New scope in angiogenesis: role of vascular endothelial growth factor (VEGF), NO, lipid peroxidation, and vitamin E in the pathophysiology of pre- eclampsia among Egyptian females. Clin Biochem 2001; 34: 323–329.

  13. 13.

    , . Magnesium sulfate versus phenytoin for eclampsia. Cochrane Database Syst Rev 2003 CD000128.

  14. 14.

    , , , . Protective action of a hydroalcoholic extract of a vinifera grape skin on experimental preeclampsia in rats. Hypertens Pregnancy 2007; 26: 89–100.

  15. 15.

    , , , . MgSO4 prevents left ventricular dysfunction in an animal model of preeclampsia. Am J Obstet Gynecol 2006; 195: 1398–1403.

  16. 16.

    , , , , , . Analysis of nitrate&nitrite and (15N) nitrate in biological fluids. Anal Biochem 1982; 126: 131–138.

  17. 17.

    , , , , , , , , , , , , . Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsia. J Clin Invest 2003; 111: 649–658.

  18. 18.

    . Amniotic fluid- soluble vascular endothelial growth factor receptor-1 in preeclampsia. Obestet Gynecol 2000; 95: 353–357.

  19. 19.

    . Soluble endoglin (sEng) joins the soluble fms-like tyrosine kinase (sFlt) receptor as a pre-eclampsia molecule. Nephrol Dial Transplant 2006; 21: 3052–3054.

  20. 20.

    , , , , , . Expression of vascular endothelial growth factors 1, 2, and3 in placentas from normal and complicated pregnancies. Mol Hum Reprod 2011; 7: 205–210.

  21. 21.

    , , , , , , , . First trimester placental growth factor and soluble Fms-like tyrosine kinase 1 and risk for preeclampsia. J Clin Endocrinol Metab 2004; 89: 770–775.

  22. 22.

    , , , , , , , , , , , , , , . A longitudinal study of angiogenic (placental growth factor) and anti-angiogenic (soluble endoglin and soluble VEGF receptor-1) factors in normal pregnancy and patients destined to develop preeclampsia and deliver a small-for-gestational-age neonate. J Matern Fetal Neonatal Med 2008; 21: 9–23.

  23. 23.

    , , , , . Selective deficit of angiogenic growth factors characterizes pregnancies complicated by pre-eclampsia. Br J Obstet Gynaecol 1999; 106: 1019–1022.

  24. 24.

    , , , , , . Release and complex formation of soluble VEGFR1 from endothelial cells and biological fluids. Lab Invest 2000; 80: 443–454.

  25. 25.

    , , , . Placental growth factor and its receptor, vascular endothelial growth factor receptor-1: novel targets for stimulation of ischemic tissue revascularization and inhibition of angiogenic and inflammatory disorders. J Thromb Haemost 2003; 1: 1356–1370.

  26. 26.

    , , , , . The relationship of the level of circulating antiangiogenic factors to the clinical manifestations of preeclampsia. Prenat Diagn 2009; 29: 464–470.

  27. 27.

    , , , . The relationship between circulating endothelin-1, soluble fms-like tyrosine kinase-1 and soluble endoglin in preeclampsia. J Hum Hypertens 2012; 26: 236–241.

  28. 28.

    . Ca, Mg, Cu and Zn contents of the maternal and umbilical cord serum in pregnancy-induced hypertension. Zhonghua Fu Chan Ke Za Zhi 1989; 24: 212–214.

  29. 29.

    , , , , , . Intracellular and extracellular, ionized and total magnesium in pre-eclampsia and uncomplicated pregnancy. Clin Chem Lab Med 1999; 37: 55–59.

  30. 30.

    , . Serum calcium and serum magnesium in normal and preeclamptic pregnancy. Arch Gynecol Obstet 2005; 273: 12–16.

  31. 31.

    , , , . Serum ionized magnesium levels in normal and preeclamptic gestation. Obstet Gynecol 1997; 89: 24–27.

  32. 32.

    , , , , . Assessment of the effects of endothelin-1 and magnesium sulfate on regional blood flows in conscious rats, by the coloured microsphere reference technique. Br J Pharmacol 1999; 126: 621–626.

  33. 33.

    , , , . Intravenous magnesium sulfate in suspected acute myocardial infarction: results of the second leicester intravenous magnesium intervention trial (LIMIT-2). Lancet 1992; 339: 1553–1558.

  34. 34.

    , , , , , . Magnesium sulfate therapy in women with pre-eclampsia and eclampsia in Kuwait. Med Princ Pract 2008; 17: 227–232.

  35. 35.

    , , , , , , . Effects of anti-hypertensive drugs on production of soluble fms-like tyrosine kinase 1 and soluble endoglin from human normal and pre-eclamptic placentas in vitro. Clin Exp Pharmacol Physiol 2009; 36: 839–842.

  36. 36.

    , , , . Tumour vascular permeability factor stimulates endothelial cell growth and angiogenesis. J Clin Invest 1989; 84: 1470–1478.

  37. 37.

    , , , , , . Nitric oxide mediates mitogenic effect of VEGF on coronary vascular endothelium. Am J Physiol 1996; 270: H411–H415.

  38. 38.

    , , , , , . Vascular endothelial growth factor signals endothelial cell production of nitric oxide and prostacyclin through flk-1/KDR activation of c-Src. J Biol Chem 1999; 274: 25130–25135.

  39. 39.

    , , , , , . Angiogenic factors for the prediction of preeclampsia in high-risk women. Am J Obstet Gynecol 2007; 197: 244.e1–244.e8.

  40. 40.

    , , , , . Placental nitric oxide synthase (NOS) activity and nitric oxide (NO) production in normal pregnancy, pre-eclampsia and eclampsia. Int J Gynecol Obstet 2001; 72: 127–133.

  41. 41.

    . VEGF (165) mediates glomerular endothelial repair. J Clin Biol Chem 1999; 104: 913–923.

  42. 42.

    , , . Plasma nitric oxide levels in pregnant patients with preeclampsia and essential hypertension. Gynecol Obest Invest 1996; 41: 189–193.

  43. 43.

    , , , , , . Fetoplacental vascular tone is modified by magnesium sulfate in the preeclamptic ex vivo human placental cotyledon. Am J Obstet Gynecol 2003; 189: 839–842.

  44. 44.

    , . Effect of magnesium sulfate on fetal rats of fetal growth retardation and its relation with expression of caspase-3 on the placenta of maternal rat. Zhonghua Fu Chan Ke Za Zhi 2006; 41: 525–528.

  45. 45.

    , , , . High affinity VEGF binding and developmental expression suggest FLK-1 as a major regulator of vasculogenesis and angiogenesis. Cell 1993; 72: 835–846.

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Acknowledgements

I thank King Abdul-Aziz City for Science and Technology (KACST), Kingdom of Saudi Arabia, Riyadh, General Directorate of Research Grants Programs for supporting this research (grant number LGP-14-16). I also express my gratitude to Dr Maha Arafa for her help in the pathological examination of the kidney tissue in the study. I thank the technicians and workers in the animal house and the physiology department laboratory of the College of Medicine King Saud University for their help and assistance during the experimental part of the study.

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  1. Department of Physiology (29), College of Medicine, King Saud University, Riyadh, Saudi Arabia

    • Aida A Korish

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https://doi.org/10.1038/hr.2012.103

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