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The effect of hypoxia-induced intrauterine growth restriction on renal artery function

Published online by Cambridge University Press:  25 April 2012

M. T. C. Verschuren ,
J. S. Morton ,
A. Abdalvand ,
Y. Mansour ,
C. F. Rueda-Clausen ,
C. A. Compston ,
V. Luyckx  and
S. T. Davidge
M. T. C. Verschuren
Affiliation:
Department of Obstetrics and Gynaecology, University of Alberta, Edmonton, Canada Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands
J. S. Morton
Affiliation:
Department of Obstetrics and Gynaecology, University of Alberta, Edmonton, Canada Women and Children's Health Research Institute and the Cardiovascular Research Centre, Edmonton, Canada
A. Abdalvand
Affiliation:
Department of Obstetrics and Gynaecology, University of Alberta, Edmonton, Canada Women and Children's Health Research Institute and the Cardiovascular Research Centre, Edmonton, Canada
Y. Mansour
Affiliation:
Department of Obstetrics and Gynaecology, University of Alberta, Edmonton, Canada Women and Children's Health Research Institute and the Cardiovascular Research Centre, Edmonton, Canada
C. F. Rueda-Clausen
Affiliation:
Women and Children's Health Research Institute and the Cardiovascular Research Centre, Edmonton, Canada Department of Physiology, University of Alberta, Edmonton, Canada
C. A. Compston
Affiliation:
Renal Division, Department of Medicine, University of Alberta, Edmonton, Alberta
V. Luyckx
Affiliation:
Renal Division, Department of Medicine, University of Alberta, Edmonton, Alberta
S. T. Davidge*
Affiliation:
Department of Obstetrics and Gynaecology, University of Alberta, Edmonton, Canada Women and Children's Health Research Institute and the Cardiovascular Research Centre, Edmonton, Canada Department of Physiology, University of Alberta, Edmonton, Canada
*
*Address for correspondence: Dr S. T. Davidge, Departments of Obstetrics/Gynaecology and Physiology, 232 Heritage Medical Research Centre, University of Alberta, Edmonton, Alberta T6G 2S2, Canada. Email sandra.davidge@ualberta.ca
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Abstract

The risk of developing cardiovascular diseases is known to begin before birth and the impact of the intrauterine environment on subsequent adult health is currently being investigated from many quarters. Following our studies demonstrating the impact of hypoxia in utero and consequent intrauterine growth restriction (IUGR) on the rat cardiovascular system, we hypothesized that changes extend throughout the vasculature and alter function of the renal artery. In addition, we hypothesized that hypoxia induces renal senescence as a potential mediator of altered vascular function. We demonstrated that IUGR females had decreased responses to the adrenergic agonist phenylephrine (PE; pEC50 6.50 ± 0.05 control v. 6.17 ± 0.09 IUGR, P < 0.05) and the endothelium-dependent vasodilator methylcholine (MCh; E max 89.8 ± 7.0% control v. 41.0 ± 6.5% IUGR, P < 0.001). In IUGR females, this was characterised by increased basal nitric oxide (NO) modulation of vasoconstriction (PE pEC50 6.17 ± 0.09 IUGR v. 6.42 ± 0.08 in the presence of the NO synthase inhibitor N-nitro-l-arginine methyl ester hydrochloride (l-NAME; P < 0.01) but decreased activated NO modulation (no change in MCh responses in the presence of l-NAME), respectively. In contrast, IUGR males had no changes in PE or MCh responses but demonstrated increased basal NO (PE pEC50 6.29 ± 0.06 IUGR v. 6.42 ± 0.12 plus l-NAME, P < 0.01) and activated NO (E max 37.8 ± 9.4% control v. −0.8 ± 13.0% plus l-NAME, P < 0.05) modulation. No significant changes were found in gross kidney morphology, proteinuria or markers of cellular senescence in either sex. In summary, renal vascular function was altered by hypoxia in utero in a sex-dependent manner but was unlikely to be mediated by premature renal senescence.

Keywords

intrauterine growth restrictionrenalsenescencevascular function

Information

Type
Original Article
Information
Journal of Developmental Origins of Health and Disease , Volume 3 , Issue 5 , October 2012 , pp. 333 - 341
Copyright
Copyright © Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2012

Introduction

Cardiovascular diseases are a major health problem and are the leading cause of death worldwide. It is becoming increasingly clear that the risk of developing cardiovascular diseases in adult life is determined, in part, before birth (reviewed by BarkerReference Barker 1 ). In compensation for a poor intrauterine environment, the fetus develops long-lasting adaptations in cardiovascular, metabolic and endocrine function, which can lead to an enhanced susceptibility to cardiovascular disease in adult life.Reference Barker 2 – Reference Barker 4 There is a growing body of evidence suggesting that a sub-optimal in utero environment can cause conditions such as endothelial dysfunction,Reference Goodfellow, Bellamy and Gorman 5 – Reference Leeson, Whincup and Cook 8 hypertension,Reference Stein, Zybert, van der Pal-de Bruin and Lumey 9 coronary artery disease,Reference Kajantie, Barker, Osmond, Forsen and Eriksson 10 obesityReference Fall, Sachdev and Osmond 11 and diabetesReference Alastalo, Raikkonen and Pesonen 12 later in life.

Intrauterine growth restriction (IUGR) has many different causes but is most commonly due to a placental insufficiency leading to an inadequate nutrient and oxygen supply to the fetus. Animal models developed to investigate this area have utilized a decrease in the supply of nutrients, oxygen or both to the fetus; however, each model has its limitations. The fetus has some recourse to adjust for a limited nutrient supply,Reference Jobgen, Ford and Jobgen 13 however, there are few mechanisms to compensate for a limited oxygen supply; which is a common occurrence in several obstetric pathological conditions that may lead to IUGR such as pre-eclampsia, placenta previa, maternal anemia and smoking. We, and others, have previously shown that hypoxia in utero, leading to growth restricted offspring, causes endothelial dysfunction in systemic resistance arteries.Reference Goodfellow, Bellamy and Gorman 5 – Reference Leeson, Whincup and Cook 8 , Reference Morton, Rueda-Clausen and Davidge 14 – Reference Williams, Hemmings, Mitchell, McMillen and Davidge 16 Modifications in vascular function, particularly in resistance arteries, contribute to the acute regulation of blood pressure while chronic regulation of blood pressure is primarily mediated by the kidney. The early development of the kidney can be greatly affected by an adverse perinatal environment.Reference Luyckx and Brenner 17 For example, IUGR infants display disproportionately reduced fetal kidney growth and have fewer nephrons at birth compared with normal birth weight infants.Reference Latini, De Mitri and Del Vecchio 18 , Reference Manalich, Reyes, Herrera, Melendi and Fundora 19 Similarly, in animal models, uteroplacental insufficiency, prenatal dexamethasone or alterations in maternal nutrient intake have been shown to reduce nephron number in offspring, which is often associated with later development of spontaneous hypertension.Reference Marchand and Langley-Evans 20 – Reference Celsi, Kistner and Aizman 27 In addition, adverse intrauterine conditions have been shown to cause decreased glomerular filtration rate, altered expression of renal sodium transporters,Reference Dagan, Habib, Gattineni, Dwarakanath and Baum 28 – Reference Manning, Beutler, Knepper and Vehaskari 31 disturbances of the renin-angiotensin-aldosterone system (RAAS),Reference Bogdarina, Welham, King, Burns and Clark 32 – Reference Franco, Casarini and Carneiro-ramos 35 decreased levels of 11β-hydroxysteroid dehydrogenaseReference Bertram, Trowern, Copin, Jackson and Whorwood 36 , Reference Struwe, Berzl and Schild 37 and increased nephrosclerosisReference Plank, Nüsken and Menendez-Castro 38 leading, eventually, to hypertension, renal disease and other cardiovascular diseases.Reference Moritz, Dodic and Wintour 39 The early post-natal environment has been shown to further impact developmental programming. Rapid catch-up growth, for example, has been associated with premature vascular, renal and cardiac senescence, all of which likely contribute to vascular dysfunction and hypertension.Reference Tarry-Adkins, Martin-Gronert, Chen, Cripps and Ozanne 40 , Reference Luyckx, Compston, Simmen and Mueller 41 The role of cellular senescence in the effects of intrauterine hypoxia on renal vascular function is, however, unknown.

In IUGR rodent offspring, bilateral renal denervation has been found to reverse or prevent elevated blood pressure.Reference Alexander, Hendon, Ferril and Dwyer 42 , Reference Ojeda, Johnson, Dwyer and Alexander 43 In addition, circulating catecholamines have been found to be increased in growth restricted girls but not boysReference Franco, Casarini and Carneiro-ramos 35 and in IUGR rats,Reference Shaul, Cha and Oh 44 and increased sympathetic nervous system activity was found in female, but not male, IUGR rats.Reference Jansson and Lambert 45 These results suggest that growth restriction causes increased sympathetic innervation leading to enhanced vascular constriction and hypertension. More interestingly, there is a strong suggestion that these effects of IUGR may be sex-dependent. To date, few studies have investigated vascular function of renal arteries of offspring born from complicated pregnancies.Reference Sanders, Fazzi, Janssen, Blanco and De Mey 46 – Reference Sanders, Fazzi and Janssen 48 In one of these studies, intrauterine stress was induced by ligation of the uterine arteries at day 13 of pregnancy in Wistar Kyoto rats and changes in adrenoreceptor-mediated responses were found in male offspring exposed to intrauterine stress; the renal artery showed enhanced vasoconstrictor (α1 and α2) and vasodilator (β1 and β2) responses.Reference Sanders, Fazzi, Janssen, Blanco and De Mey 46 , Reference Sanders, Fazzi and Janssen 48 Although many systemic vascular effects of hypoxia-induced IUGR have been determined,Reference Morton, Rueda-Clausen and Davidge 14 – Reference Williams, Hemmings, Mitchell, McMillen and Davidge 16 , Reference Rueda-Clausen, Morton and Davidge 49 – Reference Xu, Williams, O'Brien and Davidge 51 the specific effects on renal vascular function are not known. Our own lab has shown changes in endothelium-dependent vasodilator function in mesenteric arteries from a hypoxia-induced IUGR model in response to both pharmacological agonists and the physiological stimuli of flow,Reference Morton, Rueda-Clausen and Davidge 14 , Reference Morton, Rueda-Clausen and Davidge 52 changes which were sex-dependent. We hypothesized that these changes may extend throughout the vasculature and may alter vascular function of the renal artery following growth restriction in utero, potentially in a sex-dependent manner. In addition, we hypothesized that exposure to hypoxia may induce renal senescence as a potential mediator of altered vascular function.

Materials and methods

Animals and study groups

All protocols were approved by the University of Alberta Health Sciences Animal Policy and Welfare Committee in accordance with the Canadian Council on Animal Care guidelines. As previously described,Reference Morton, Rueda-Clausen and Davidge 14 , Reference Rueda-Clausen, Morton and Davidge 49 , Reference Morton, Rueda-Clausen and Davidge 52 , Reference Rueda-Clausen, Morton, Lopaschuk and Davidge 53 female Sprague Dawley rats, 3 months old, were acclimatised in-house before breeding and maintained on a standard diet and tap water in a 12:12 h light:dark cycle. Pregnant dams were randomly allocated to control or hypoxia groups on day 15 of gestation. Maternal hypoxia was induced by placing rats into a Plexiglas chamber (A-Chamber, BioSpherix, NY, USA) where oxygen supply was reduced to 11.5% using a ProOx Oxygen Controller (BioSpherix, NY, USA) supplying a continuous infusion of an air/nitrogen mixture. Control animals were kept in a room air (21% oxygen) environment. On day 21 of pregnancy the rats were removed from the chamber and allowed to give birth in a normal oxygen environment. Litters were reduced to eight pups, four males and four females, to avoid the impact of competition for milk on the subsequent growth of the offspring. Pups were weaned at 3 weeks into standard cages and housed under standard conditions until the experimental day at 4 months of age. A total of 22 control offspring (from 10 litters) and 18 offspring from dams exposed to a hypoxic environment (IUGR, from 10 litters) were used for experimental procedures. Offspring were chosen for each experimental procedure such that no two animals in one experiment came from the same litter; hence the dam was the experimental unit.

Pressure myography

Pressure myography was used to measure physiological vascular function of renal arteries. Animals were killed by exsanguination via excision of the superior vena cava under inhaled isoflurane anesthesia and the left kidney, including the renal artery and a section of the abdominal aorta, was excised. For consistency, the left artery was always chosen for study. The tissue was placed in ice-cold physiological saline solution (PSS, composition: 10 mM HEPES, 5.5 mM glucose, 1.56 mM CaCl2, 4.7 mM KCl, 142 mM NaCl, 1.17 mM MgSO4, 1.18 mM KH2PO4, pH 7.5). The renal artery and branches were dissected free of renal, adipose and connective tissues under a stereo-microscope. Taking into account the length, diameter and branching of the vessels, third-order arteries were found to be most suitable for vascular studies. Two arteries were mounted and tied to two glass cannulae in 2.5 ml PSS-containing chambers of a pressure myograph (Living Systems, Burlington, VT, USA). Intraluminal pressure was controlled by a peristaltic pump and set to 100 mmHg to mimic the physiological in vivo pressure of this artery. The temperature of the baths was maintained at 37°C. To measure arterial lumen diameter, the myograph was placed under a microscope connected to a video dimension analyser and video monitor.

All vessels were equilibrated for 1 h with multiple changes in PSS during which time pressure was increased to 140 mmHg for 10 min and then reset to 100 mmHg. The responses (change in lumen diameter) of arteries to the adrenergic vasoconstrictor phenylephrine (PE; 0.01 nM to 1 mM) or the endothelium-dependent vasodilator methylcholine (MCh; 0.01 nM to 10 μM) were observed in the presence or absence of the nitric oxide synthase (NOS) inhibitor N-nitro-l-arginine methyl ester hydrochloride (l-NAME; 100 μM). All drugs were administered extralumenally into the bathing solution.

Nephron structure

At the time of euthanasia, right kidneys were excised and a portion fixed in 10% formalin. Histopathological preparations and hematoxylin/eosin staining were performed at the Alberta Diabetes Institute Histology Core (Edmonton, Canada). Tissue sections were examined by light microscopy.

Proteinuria

At the time of euthanasia, urine samples were aspirated from the bladder. Urine was snap frozen in liquid nitrogen and stored at −80°C until the time of analysis. Total urine albumin concentrations were measured using the AssayMax Rat Albumin ELISA Kit (AssayPro, catalog number ERA3201-1). Urine creatinine was measured using the Creatinine (Urinary) Assay Kit (Cayman Chemical Company, catalog number 500701). Proteinuria was quantified and expressed as the albumin to creatinine ratio.

Senescence markers

At the time of euthanasia, right kidneys were excised and a portion was snap frozen in liquid nitrogen and stored at −80°C until the time of analysis. Total RNA was extracted from whole kidney samples using the RNeasy Minikit (Qiagen, Mississauga, ON, Canada). Expression of senescence markers p16, p21, p53 and the mitochondrial stress marker p66shc were analyzed by real time RT-PCR as previously described.Reference Luyckx, Compston, Simmen and Mueller 41 Gene transcript levels were calculated by the ΔCT method and expressed as percent hypoxanthine-guanine phosphoribosyltransferase (HPRT).

Data collection and statistical analysis

Data were presented as mean ± s.e. Vasodilator responses were calculated as a percentage of constrictor tone. All data were normally distributed as tested using the Kolmogorov–Smirnov test for Gaussian distribution. Sources of variability considered in the model include sex (male, female) and prenatal treatment (control, IUGR), leading to four study groups. The significance of the difference in mean values of continuous variables between groups was determined by a two-way analysis of variance (ANOVA), with Bonferroni post-test for multiple comparisons. Differences between groups in physical characteristics were analyzed by Students’ t-test.

Results

Body weight

Despite a significant reduction in body weight at birth in this model (data previously shownReference Morton, Rueda-Clausen and Davidge 14 ), at 4 months of age hypoxia in utero had no effect on body weight in males (492 ± 17 g controls v. 480 ± 17 g IUGR), or females (298 ± 12 g controls v. 275 ± 11 g IUGR).

Vascular function

Maximal responses to PE in the left renal artery were unaltered by sex or hypoxia in utero, however, there was a significant effect of IUGR on sensitivity to PE in females but not males (Table 1).

Table 1

Sensitivity (pEC50) of renal arteries from 4-month-old rat offspring to PE

PE, phenylephrine; IUGR, intrauterine growth restriction; ANOVA, analysis of variance; l-NAME, N-nitro-l-arginine methyl ester hydrochloride; Int., interaction effect of two-way ANOVA. *p < 0.05, no value; p > 0.05.

In females, but not males, there was a significant effect of IUGR on the sensitivity of PE responses; data presented as mean ± s.e. (n).

Vasodilation to MCh in the renal arteries of male offspring was unaltered by hypoxia in utero; no significant change in maximal vasodilation or sensitivity between IUGR and control offspring was observed (Fig. 1a). In the control male group, there was no effect of l-NAME on vasodilation (P > 0.05, Fig. 1b), however, the IUGR male group showed a significant reduction in MCh-induced vasodilation in the presence of l-NAME (P = 0.013, Fig. 1c).

Fig. 1

Vasodilator responses to methylcholine (MCh) in the renal artery of 4-month-old male offspring exposed to hypoxia in utero (intrauterine growth restriction; IUGR) and controls (a, n = 8–10). Vasodilator responses to MCh in controls (b, n = 6–7) and IUGR offspring (c, n = 8–10) in the presence or absence (w/o inhibitor) of the nitric oxide synthase inhibitor, N-nitro-l-arginine methyl ester hydrochloride (l-NAME; *P < 0.05, two-way analysis of variance with a Bonferroni post-test).

In females, however, renal arteries from IUGR animals demonstrated a significant reduction in vasodilation to MCh compared with controls (P = 0.0005, Fig. 2a). Further, l-NAME significantly inhibited vasodilation in controls (P = 0.031, Fig. 2b), but did not inhibit vasodilation to MCh in offspring exposed to hypoxia in utero (P > 0.05, Fig. 2c).

Fig. 2

Vasodilator responses to methylcholine (MCh) in the renal artery of 4-month-old female offspring exposed to hypoxia in utero (intrauterine growth restriction; IUGR) and controls (a, n = 5–7). Vasodilator responses to MCh in controls (b, n = 5) and IUGR offspring (c, n = 5–7) in the presence or absence of the nitric oxide synthase inhibitor, N-nitro-l-arginine methyl ester hydrochloride (l-NAME; *P < 0.05, ***P < 0.001, two-way analysis of variance with a Bonferroni post-test).

Morphology

During vascular function experiments, we found no differences in renal artery diameters in either males (control 613 ± 33 μm v. IUGR 611 ± 54 μm) or females (control 549 ± 24 μm v. IUGR 476 ± 28 μm; P > 0.05). Given the observed differences in vascular function, which may lead to differences in renal perfusion, we investigated renal morphology by histopathological techniques. Examination of the gross morphology of the kidneys did not uncover any differences in renal structures (Fig. 3).

Fig. 3

Kidney sections from male control (a), male intrauterine growth restriction (IUGR) (c), female control (b) and female IUGR (d) rats. Representative images of kidney sections stained with hemotoxylin and eosin to investigate morphological characteristics.

Proteinuria

Urinary albumin excretion was examined as an early marker of glomerular hypertension and renal dysfunction. Adjusted for urine creatinine levels, there was no change in the albumin–creatinine ratio in IUGR males or females (Fig. 4).

Fig. 4

Urine albumin/creatinine ratios in 4-month-old male and female, control and intrauterine growth restriction (IUGR) offspring (P > 0.05, two-way analysis of variance, n = 5–6 per group).

Senescence markers

Expression levels of the senescence markers p53, p21 and p16 and the mitochondrial stress marker p66shc in whole kidney tissue were not significantly different in IUGR males and females (Fig. 5a–5d, P > 0.05). By two-way ANOVA analysis, expression of p16 demonstrated a non-significant tendency to be increased in both IUGR males and females compared with their respective controls (Fig. 5c, P = 0.089).

Fig. 5

Expression levels of the senescence markers p53 (a), p21 (b) and p16 (c) and the mitochondrial stress marker p66shc (d) in the kidneys of 4-month-old male and female, control and intrauterine growth restriction (IUGR) offspring (P > 0.05, two-way analysis of variance, n = 6 per group). HPRT, hypoxanthine-guanine phosphoribosyltransferase.

Discussion

Despite the well-recognised impact of growth restriction on the cardiovascular system, this study is one of the first to address the long-term impact of IUGR caused by reduced oxygen in utero on the function of the renal vasculature, an important organ in long-term blood pressure regulation. We have demonstrated that MCh-induced renal vasodilation in females at 4 months of age was reduced by hypoxia exposure in utero, while this parameter was unaffected in 4-month-old males.

Interestingly, in only male offspring, we observed a greater contribution of the nitric oxide (NO) pathway to MCh-induced vasodilation in IUGR v. controls. These data would suggest an upregulation of the NO pathway in stimulated conditions that may have been programmed by a compromised intrauterine environment and, further, may explain the unaltered vasodilation to MCh in the male IUGR group. Interestingly, contrary to the findings of previous studies performed in the renal arteries of rat models including hypertensive SHRs, diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) and Sprague Dawley rats, an NO contribution to vasodilation was absent in the male control group. In these studies renal arteries from both control and pathologic animals exhibited a dependence on both NO and endothelial derived hyperpolarizing factors (EDHF) for vasodilation.Reference Kagota, Yamaguchi, Nakamura and Kunitomo 54 – Reference Jiang, Li and Rand 59 Our data suggest that, in control males, pathways other than NO, for example, prostacyclin (PGI2) or EDHF may be more important in vasodilation. A PE-induced increase in endothelial calcium may also be responsible for a greater release of EDHF and this may represent a compensatory mechanism in male offspring exposed to hypoxia in utero. Further studies would need to be performed to investigate the endothelium-dependent mechanisms responsible for renal artery vasodilation in this group.

Conversely, in females we found that hypoxia in utero led to a significant loss of MCh-induced vasodilation in the renal arteries. In addition, in females but not in males, there was a significant effect of IUGR on the sensitivity of renal arteries to PE. Contrary to males, a MCh-induced NO component was present in control females. These data suggest that, in female offspring, hypoxia in utero results in a downregulation of normal NO-mediated vasodilator mechanisms, which have an impact on the overall ability of the vessel to dilate. In this case, females appear to be affected by growth restriction to a greater extent than males. These findings are consistent with our previous work in this model where NO-induced vasodilation was also reduced in mesenteric arteries.Reference Morton, Rueda-Clausen and Davidge 14 Given our observations of changes in NO-mediated vasodilation, it is possible that sex-specific changes in underlying NOS activity may be an explanatory factor in the different responses to the insult of IUGR. Although Franco et al. Reference Franco, Arruda and Dantas 60 have previously found there to be sex-specific changes in eNOS expression and activity in the aortae from a rat model of intrauterine undernutrition; these data would suggest a greater impact of growth restriction on the male offspring. This discrepancy may reflect vascular-bed specific alterations in NO pathways.

Interestingly, changes in the vascular function of the renal artery were not found to be associated with any changes in gross morphology or with proteinuria. The changes previously observed in the mesenteric arcade were reminiscent of an ‘early aging’ phenotype.Reference Morton, Rueda-Clausen and Davidge 14 , Reference Morton, Rueda-Clausen and Davidge 52 A study of the messenger ribonucleic acid (mRNA) expression of senescence markers did not show any significant differences between control and IUGR whole kidneys from either males or females. Analysis of whole kidney RNA may have missed a localized increase in vascular senescence. The marker, p16 represents one factor in a distinct pathway leading from environmental stressors to hypophosphorylated retinoblast protein, an indicator of accelerated or earlier senescence.Reference Luyckx, Compston, Simmen and Mueller 41 In our study we noted that p16 may be increased by IUGR and this was mirrored in both males and females. This may represent a very early indication of accelerated aging due to IUGR in these groups; however, since the animals were only studied at 4 months of age, representing young adults, these changes may be further amplified with increased age and would need to be studied at older age points to confirm or refute this observation. In addition, the levels of protein expression could also be verified to further delineate any potential changes in renal senescence.

The major strength of this study is that it is the first to describe renal artery function in this model of IUGR. To our knowledge, only three studies have previously investigated vascular function of renal arteries following a compromised pregnancy.Reference Sanders, Fazzi, Janssen, Blanco and De Mey 46 – Reference Sanders, Fazzi and Janssen 48 Sanders et al., studied renal arteries from 21-day-old males with IUGR induced by ligation of the uterine arteries at day 13 of pregnancy in Wistar Kyoto rats. The renal artery showed enhanced vasoconstrictor (α1 and α2) and vasodilator (β1 and β2) responses in these rats, but no change in adrenergic responsiveness was found in mesenteric, femoral or saphenous arteries.Reference Sanders, Fazzi, Janssen, Blanco and De Mey 46 These authors reported similar findings in male offspring at 21 days, where IUGR was induced by maternal uterine artery ligation on day 17 of gestation.Reference Sanders, Fazzi, Janssen, Blanco and De Mey 46 Intriguingly in this study, enhanced vasodilation was observed in the right, but not the left renal artery of IUGR offspring, accompanied by an upregulation of α2-adrenoreceptor expression in the right kidney only.Reference Sanders, Fazzi and Janssen 48 The cause of the asymmetry of renal artery responsiveness is not known, but sympathetic nerve fiber density was found to be greater in left renal arteries in this study. Maximal contractile responses to PE were not affected by IUGR or laterality. Vascular reactivity of the renal, uterine, mesenteric and femoral arteries was also studied in 18-month-old female rats with IUGR induced by ligation of uterine vessels at 18 days of gestation.Reference Mazzuca, Wlodek, Dragomir, Parkington and Tare 47 These females were found to have selective uterine artery endothelial dysfunction, with reduced relaxation in response to EDHF, and increased stiffness. Vascular structure and function were largely preserved in the other arteries studied, although a small decrease in renal artery stiffness was noted. The authors do not mention whether left or right arteries were studied. The variability of results between these and our study likely reflects different animal models of IUGR, ages, gender, vascular bed and size and laterality of the vessel studied. Each of the prior studies has utilized first order renal arteries, which are conduit arteries, whereas we have studied 3rd order arteries, which are resistance vessels. In addition, all three studies utilized uteroplacental insufficiency as a programming model, which in addition to inducing fetal hypoxia, also results in nutrient restriction. In our model, hypoxia may have been more severe and, therefore, differs significantly from these published studies and adds new information to the field. Future studies should include investigation of the sympathetic innervation of the kidneys in our model. In general, most studies describe a relative loss of vasodilation in the IUGR offspring, which conceivably does participate in programmed susceptibility to premature hypertension, cardiovascular and renal disease.

In summary, this study demonstrated that IUGR females had decreased sensitivity to both PE and MCh that was characterised by increased basal but decreased activated NO. In contrast, IUGR males had no changes in PE or MCh responses but demonstrated increased basal and activated NO, which may have compensated for decreased endothelial function. No changes were found in gross kidney morphology, proteinuria or markers of cellular senescence in either sex although there was a suggestion of increased expression of the senescence marker p16. In summary, renal vascular function was altered by growth restriction in utero in a sex-dependent manner but these changes were unlikely to be mediated by renal senescence.

Acknowledgments

The study was supported by grants from the Canadian Institute of Health Research. S.T. Davidge is funded by Alberta Innovates Health Solutions as an Alberta Heritage Foundation for Medical Research Scientist and is a Canada Research Chair (CRC) in Women's Cardiovascular Health. V. Luyckx is funded by the University of Alberta Hospital Foundation, Amgen Senior Research Fellowship, Western Canada.

Footnotes

a

These authors have contributed equally to the preparation of this manuscript.

References

1. Barker, DJP. Adult consequences of fetal growth restriction. Clin Obstet Gynecol. 2006; 49, 270–283.Google Scholar
2. Barker, DJ. In utero programming of chronic disease. Clin Sci (Lond). 1998; 95, 115–128.Google Scholar
3. Barker, DJ. In utero programming of cardiovascular disease. Theriogenology. 2000; 53, 555–574.Google Scholar
4. Barker, DJ. Fetal programming of coronary heart disease. Trends Endocrinol Metab: TEM. 2002; 13, 364–368.Google Scholar
5. Goodfellow, J, Bellamy, MF, Gorman, ST, et al. . Endothelial function is impaired in fit young adults of low birth weight. Cardiovasc Res. 1998; 40, 600–606.CrossRefGoogle ScholarPubMed
6. Halvorsen, CP, Andolf, E, Hu, J, et al. . Discordant twin growth in utero and differences in blood pressure and endothelial function at 8 years of age. J Inter Med. 2006; 259, 155–163.Google Scholar
7. Leeson, CPM, Kattenhorn, M, Morley, R, Lucas, A, Deanfield, JE. Impact of low birth weight and cardiovascular risk factors on endothelial function in early adult life. Circulation. 2001; 103, 1264–1268.CrossRefGoogle ScholarPubMed
8. Leeson, CPM, Whincup, PH, Cook, DG, et al. . Flow-mediated dilation in 9- to 11-year-old children: the influence of intrauterine and childhood factors. Circulation. 1997; 96, 2233–2238.Google Scholar
9. Stein, AD, Zybert, PA, van der Pal-de Bruin, K, Lumey, L. Exposure to famine during gestation, size at birth, and blood pressure at age 59 y: evidence from the dutch famine. Eur J Epidemiol. 2006; 21, 759–765.Google Scholar
10. Kajantie, E, Barker, DJP, Osmond, C, Forsen, T, Eriksson, JG. Growth before 2 years of age and serum lipids 60 years later: the Helsinki Birth Cohort Study. Int J Epidemiol. 2008; 37, 280–289.CrossRefGoogle ScholarPubMed
11. Fall, CHD, Sachdev, HS, Osmond, C, et al. Adult metabolic syndrome and impaired glucose tolerance are associated with different patterns of body mass index gain during infancy: data from the New Delhi Birth Cohort. Diabetes Care. 2008; 31, 2349–2356.Google Scholar
12. Alastalo, H, Raikkonen, K, Pesonen, A-K, et al. . Cardiovascular health of Finnish war evacuees 60 years later. Ann Med. 2009; 41, 66–72.Google Scholar
13. Jobgen, WS, Ford, SP, Jobgen, SC, et al. . Baggs ewes adapt to maternal undernutrition and maintain conceptus growth by maintaining fetal plasma concentrations of amino acids. J Anim Sci. 2008; 86, 820–826.Google Scholar
14. Morton, JS, Rueda-Clausen, CF, Davidge, ST. Mechanisms of endothelium-dependent vasodilation in male and female, young and aged offspring born growth restricted. Am J Physiol Regul Integr Comp Physiol. 2010; 298, R930–R938.CrossRefGoogle Scholar
15. Hemmings, DG, Williams, SJ, Davidge, ST. Increased myogenic tone in 7-month-old adult male but not female offspring from rat dams exposed to hypoxia during pregnancy. Am J Physiol Heart Circ Physiol. 2005; 289, H674–H682.Google Scholar
16. Williams, SJ, Hemmings, DG, Mitchell, JM, McMillen, IC, Davidge, ST. Effects of maternal hypoxia or nutrient restriction during pregnancy on endothelial function in adult male rat offspring. J Physiol. 2005; 565, 125–135.Google Scholar
17. Luyckx, VA, Brenner, BM. The clinical importance of nephron mass. J Am Soc Nephrol. 2010; 21, 898–910.Google Scholar
18. Latini, G, De Mitri, B, Del Vecchio, A, et al. . Foetal growth of kidneys, liver and spleen in intrauterine growth restriction: “programming” causing “metabolic syndrome” in adult age. Acta Paediatr. 2004; 93, 1635–1639.CrossRefGoogle Scholar
19. Manalich, R, Reyes, L, Herrera, M, Melendi, C, Fundora, I. Relationship between weight at birth and the number and size of renal glomeruli in humans: a histomorphometric study. Kidney Int. 2000; 58, 770–773.CrossRefGoogle ScholarPubMed
20. Marchand, MC, Langley-Evans, SC. Intrauterine programming of nephron number: the fetal flaw revisited. J Nephrol. 2001; 14, 327–331.Google Scholar
21. Schreuder, MF, Nyengaard, JR, Fodor, M, van Wijk, JA, Delemarre-van de Waal, HA. Glomerular number and function are influenced by spontaneous and induced low birth weight in rats. J Am Soc Nephrol. 2005; 16, 2913–2919.CrossRefGoogle ScholarPubMed
22. Sanders, MW, Fazzi, GE, Janssen, GM, et al. . Reduced uteroplacental blood flow alters renal arterial reactivity and glomerular properties in the rat offspring. Hypertension. 2004; 43, 1283–1289.Google Scholar
23. Hughson, M, Farris, AB III, Douglas-Denton, R, Hoy, WE, Bertram, JF. Glomerular number and size in autopsy kidneys: the relationship to birth weight. Kidney Int. 2003; 63, 2113–2122.Google Scholar
24. Brenner, BM, Garcia, DL, Anderson, S. Glomeruli and blood pressure. Less of one, more the other? Am J Hypertens. 1988; 1(Pt 1), 335–347.CrossRefGoogle ScholarPubMed
25. Keller, G, Zimmer, G, Mall, G, Ritz, E, Amann, K. Nephron number in patients with primary hypertension. N Engl J Med. 2003; 348, 101–108.Google Scholar
26. Vehaskari, VM, Aviles, DH, Manning, J. Prenatal programming of adult hypertension in the rat. Kidney Int. 2001; 59, 238–245.Google Scholar
27. Celsi, G, Kistner, A, Aizman, R, et al. . Prenatal dexamethasone causes oligonephronia, sodium retention, and higher blood pressure in the offspring. Pediatr Res. 1998; 44, 317–322.CrossRefGoogle ScholarPubMed
28. Dagan, A, Habib, S, Gattineni, J, Dwarakanath, V, Baum, M. Prenatal programming of rat thick ascending limb chloride transport by low-protein diet and dexamethasone. Am J Physiol Regul Integr Comp Physiol. 2009; 297, R93–RR9.Google Scholar
29. Nehiri, T, Duong Van Huyen, J-P, Viltard, M, et al. . Exposure to maternal diabetes induces salt-sensitive hypertension and impairs renal function in adult rat offspring. Diabetes. 2008; 57, 2167–2175.CrossRefGoogle ScholarPubMed
30. Franco, MdCP, Nigro, D, Fortes, ZB, et al. . Intrauterine undernutrition – renal and vascular origin of hypertension. Cardiovasc Res. 2003; 60, 228–234.Google Scholar
31. Manning, J, Beutler, K, Knepper, MA, Vehaskari, VM. Upregulation of renal BSC1 and TSC in prenatally programmed hypertension. Am J Physiol Renal Physiol. 2002; 283, F202–F206.Google Scholar
32. Bogdarina, I, Welham, S, King, PJ, Burns, SP, Clark, AJL. Epigenetic modification of the renin–angiotensin system in the fetal programming of hypertension. Circ Res. 2007; 100, 520–526.CrossRefGoogle ScholarPubMed
33. Nwagwu, MO, Cook, A, Langley-Evans, SC. Evidence of progressive deterioration of renal function in rats exposed to a maternal low-protein diet in utero. Br J Nutr. 2000; 83, 79–85.Google Scholar
34. Sahajpal, V, Ashton, N. Renal function and angiotensin AT1 receptor expression in young rats following intrauterine exposure to a maternal low-protein diet. Clin Sci. 2003; 104, 607–614.Google Scholar
35. Franco, MCP, Casarini, DE, Carneiro-ramos, MS, et al. . Circulating renin–angiotensin system and catecholamines in childhood: is there a role for birthweight? Clin Sci. 2008; 114, 375–380.Google Scholar
36. Bertram, C, Trowern, AR, Copin, N, Jackson, AA, Whorwood, CB. The maternal diet during pregnancy programs altered expression of the glucocorticoid receptor and type 2 11{beta}-hydroxysteroid dehydrogenase: potential molecular mechanisms underlying the programming of hypertension in utero. Endocrinology. 2001; 142, 2841–2853.CrossRefGoogle ScholarPubMed
37. Struwe, E, Berzl, GM, Schild, RL, et al. . Simultaneously reduced gene expression of cortisol-activating and cortisol-inactivating enzymes in placentas of small-for-gestational-age neonates. Am J Obstet Gynecol. 2007; 197, 43.e1–43.e6.Google Scholar
38. Plank, C, Nüsken, KD, Menendez-Castro, C, et al. . Intrauterine growth restriction following ligation of the uterine arteries leads to more severe glomerulosclerosis after mesangioproliferative glomerulonephritis in the offspring. Am J Nephrol. 2010; 32, 287–295.Google Scholar
39. Moritz, KM, Dodic, M, Wintour, EM. Kidney development and the fetal programming of adult disease. Bioessays. 2003; 25, 212–220.Google Scholar
40. Tarry-Adkins, JL, Martin-Gronert, MS, Chen, J-H, Cripps, RL, Ozanne, SE. Maternal diet influences DNA damage, aortic telomere length, oxidative stress, and antioxidant defense capacity in rats. FASEB J. 2008; 22, 2037–2044.Google Scholar
41. Luyckx, VA, Compston, CA, Simmen, T, Mueller, TF. Accelerated senescence in kidneys of low-birth-weight rats after catch-up growth. Am J Physiol Renal Physiol. 2009; 297, F1697–F1705.Google Scholar
42. Alexander, BT, Hendon, AE, Ferril, G, Dwyer, TM. Renal denervation abolishes hypertension in low-birth-weight offspring from pregnant rats with reduced uterine perfusion. Hypertension. 2005; 45, 754–758.Google Scholar
43. Ojeda, NB, Johnson, WR, Dwyer, TM, Alexander, BT. Early renal denervation prevents development of hypertension in growth-restricted offspring. Clin Exp Pharmacol Physiol. 2007; 34, 1212–1216.Google Scholar
44. Shaul, PW, Cha, CJ, Oh, W. Neonatal sympathoadrenal response to acute hypoxia: impairment after experimental intrauterine growth retardation. Pediatr Res. 1989; 25, 466–472.Google Scholar
45. Jansson, T, Lambert, GW. Effect of intrauterine growth restriction on blood pressure, glucose tolerance and sympathetic nervous system activity in the rat at 3–4 months of age. J Hypertens. 1999; 17, 1239–1248.Google Scholar
46. Sanders, M, Fazzi, G, Janssen, G, Blanco, C, De Mey, J. Prenatal stress changes rat arterial adrenergic reactivity in a regionally selective manner. Eur J Pharmacol. 2004; 488, 147–155.Google Scholar
47. Mazzuca, MQ, Wlodek, ME, Dragomir, NM, Parkington, HC, Tare, M. Uteroplacental insufficiency programs regional vascular dysfunction and alters arterial stiffness in female offspring. J Physiol. 2010; 588, 1997–2010.Google Scholar
48. Sanders, MW, Fazzi, GE, Janssen, GMJ, et al. . Reduced uteroplacental blood flow alters renal arterial reactivity and glomerular properties in the rat offspring. Hypertension. 2004; 43, 1283–1289.Google Scholar
49. Rueda-Clausen, CF, Morton, JS, Davidge, ST. Effects of hypoxia-induced intrauterine growth restriction on cardiopulmonary structure and function during adulthood. Cardiovasc Res. 2009; 81, 713–722.CrossRefGoogle ScholarPubMed
50. Williams, SJ, Campbell, ME, McMillen, IC, Davidge, ST. Differential effects of maternal hypoxia or nutrient restriction on carotid and femoral vascular function in neonatal rats. Am J Physiol Regul Integr Comp Physiol. 2005; 288, R360–R367.Google Scholar
51. Xu, Y, Williams, SJ, O'Brien, D, Davidge, ST. Hypoxia or nutrient restriction during pregnancy in rats leads to progressive cardiac remodeling and impairs postischemic recovery in adult male offspring. FASEB J. 2006; 20, 1251–1253.Google Scholar
52. Morton, JS, Rueda-Clausen, CF, Davidge, ST. Flow-mediated vasodilation is impaired in adult rat offspring exposed to prenatal hypoxia. J Appl Physiol. 2011; 110, 1073–1082.Google Scholar
53. Rueda-Clausen, CF, Morton, JS, Lopaschuk, GD, Davidge, ST. Long-term effects of intrauterine growth restriction on cardiac metabolism and susceptibility to ischaemia/reperfusion. Cardiovasc Res. 2011; 90, 285–294.Google Scholar
54. Kagota, S, Yamaguchi, Y, Nakamura, K, Kunitomo, M. Altered endothelium-dependent responsiveness in the aortas and renal arteries of Otsuka Long-Evans Tokushima Fatty (OLETF) rats, a model of non-insulin-dependent diabetes mellitus. Gen Pharmacol. 2000; 34, 201–209.CrossRefGoogle Scholar
55. Bussemaker, E, Popp, R, Fisslthaler, B, et al. . Aged spontaneously hypertensive rats exhibit a selective loss of EDHF-mediated relaxation in the renal artery. Hypertension. 2003; 42, 562–568.Google Scholar
56. Michel, FS, Man, GS, Man, RY, Vanhoutte, PM. Hypertension and the absence of EDHF-mediated responses favour endothelium-dependent contractions in renal arteries of the rat. Br J Pharmacol. 2008; 155, 217–226.Google Scholar
57. Orescanin, Z, Milovanovic, SR. Effect of l-arginine on the relaxation caused by sodium nitroprusside on isolated rat renal artery. Acta physiologica Hungarica. 2006; 93, 271–283.Google Scholar
58. Kagota, S, Tamashiro, A, Yamaguchi, Y, Nakamura, K, Kunitomo, M. Excessive salt or cholesterol intake alters the balance among endothelium-derived factors released from renal arteries in spontaneously hypertensive rats. J Cardiovasc Pharmacol. 1999; 34, 533–539.Google Scholar
59. Jiang, F, Li, CG, Rand, MJ. Mechanisms of nitric oxide-independent relaxations induced by carbachol and acetylcholine in rat isolated renal arteries. Br J Pharmacol. 2000; 130, 1191–1200.CrossRefGoogle ScholarPubMed
60. Franco, MdCP, Arruda, RMMP, Dantas, APV, et al. . Intrauterine undernutrition: expression and activity of the endothelial nitric oxide synthase in male and female adult offspring. Cardiovasc Res. 2002; 56, 145–153.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Sensitivity (pEC50) of renal arteries from 4-month-old rat offspring to PE

Figure 1

Fig. 1 Vasodilator responses to methylcholine (MCh) in the renal artery of 4-month-old male offspring exposed to hypoxia in utero (intrauterine growth restriction; IUGR) and controls (a, n = 8–10). Vasodilator responses to MCh in controls (b, n = 6–7) and IUGR offspring (c, n = 8–10) in the presence or absence (w/o inhibitor) of the nitric oxide synthase inhibitor, N-nitro-l-arginine methyl ester hydrochloride (l-NAME; *P < 0.05, two-way analysis of variance with a Bonferroni post-test).

Figure 2

Fig. 2 Vasodilator responses to methylcholine (MCh) in the renal artery of 4-month-old female offspring exposed to hypoxia in utero (intrauterine growth restriction; IUGR) and controls (a, n = 5–7). Vasodilator responses to MCh in controls (b, n = 5) and IUGR offspring (c, n = 5–7) in the presence or absence of the nitric oxide synthase inhibitor, N-nitro-l-arginine methyl ester hydrochloride (l-NAME; *P < 0.05, ***P < 0.001, two-way analysis of variance with a Bonferroni post-test).

Figure 3

Fig. 3 Kidney sections from male control (a), male intrauterine growth restriction (IUGR) (c), female control (b) and female IUGR (d) rats. Representative images of kidney sections stained with hemotoxylin and eosin to investigate morphological characteristics.

Figure 4

Fig. 4 Urine albumin/creatinine ratios in 4-month-old male and female, control and intrauterine growth restriction (IUGR) offspring (P > 0.05, two-way analysis of variance, n = 5–6 per group).

Figure 5

Fig. 5 Expression levels of the senescence markers p53 (a), p21 (b) and p16 (c) and the mitochondrial stress marker p66shc (d) in the kidneys of 4-month-old male and female, control and intrauterine growth restriction (IUGR) offspring (P > 0.05, two-way analysis of variance, n = 6 per group). HPRT, hypoxanthine-guanine phosphoribosyltransferase.