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Intrauterine undernutrition plays a role in the development of adult hypertension. Most studies are done in male offspring to delineate the mechanisms whereby blood pressure may be raised; however, the vascular mechanisms involved in female offspring are unclear. Female offspring of pregnant Sprague-Dawley rats fed either a control (C; 18%) or a low-protein (LP; 6%) diet during pregnancy were used. Birth weight and later growth were markedly lower in LP than in C offspring. LP offspring exhibited impaired estrous cyclicity with increased mean arterial pressure. Hypotensive response to acetylcholine (ACh) and the hypertensive response to phenylephrine (PE) were greater in LP than in C rats. N-nitro-L-arginine methyl ester (L-NAME) induced greater hypertensive responses in C than in LP rats. Endothelium-intact mesenteric arteries from LP offspring exhibited increased contractile responses to PE and reduced vasodilation in response to ACh. In endothelium-denuded arteries, relaxation responses to sodium nitroprusside were similar in both groups. Basal and ACh-induced increase in vascular nitrite/nitrate production was lower in LP than in C offspring. L-NAME or 1H-1,2,4-oxadiazolo-4,3-quinoxalin-1-one inhibited ACh relaxations and enhanced PE contractions in C offspring, but had minimal effect in LP rats. The decreasedNO-mediated vascular response might explainthe increased vascular contraction and arterial pressure infemale offspring with low birth weight.
Epidemiologic studies have shown that low birth weight is associated with increased risk of cardiovascular (CV) disease in adulthood and have led to the hypothesis that the fetal CV system undergoes programming in utero in response to unbalanced maternal nutrition [1,2,3,4,5,6]. These human studies are strongly supported by animal experiments showing that a severe but balanced limitation of fetal substrate supply retards fetal growth and induces CV dysfunction and hypertension [7,8,9,10]. The hypothesis of developmental origins of disease proposes that maternal undernutrition causes permanent changes in structure and function of tissues and organs, resulting in CV and related disorders in the offspring [11, 12].
The mechanisms involved in the programming of adult hypertension have remained unknown, although a significant correlation between adverse intrauterine environments and alterations of vascular or endothelial function has been reported [10, 13, 14]. In addition, a possible role for the renin-angiotensin system [15, 16], the kidney [17, 18] and stress-induced stimulation of the hypothalamic-pituitary-adrenal axis [19,20,21] has been identified. Studies of fetal programming have shown that there are gender-related differences in the occurrence of CV dysfunction in humans at various ages . Some animal studies have also demonstrated that hypertension or vascular dysfunction induced by a maternal low-protein diet is more pronounced in males than in females [13, 23, 24]. Most studies have used male animals to explain the potential mechanisms through which hypertension may be initiated by fetal undernutrition. The reasons for the paucity of studies in females may be that females develop moderate and less consistent postnatal hypertension . It is shown that the severity of hypertension in females depends on the extent of maternal protein restriction and the age at which the offspring are examined [25, 26]. Our laboratory has shown that 66% maternal protein restriction consistently results in development of hypertension at ≥6 months of age in female offspring while the males are hypertensive as early as 2 months . The delay in development of hypertension in the females is attributed to the presence of sex steroid, e.g. estrogen . It is well known that adequate levels of estrogen are essential in modulating vascular function through the release of endothelium-derived relaxant factors such as nitric oxide (NO) [28,29,30]. We and others have shown that there is a reduction in estrogen levels in the hypertensive female offspring [13, 27]. Endothelial dysfunction consequent to decreased estrogen levels or due to other factors may play a role in the development of hypertension in the female offspring of nutritionally restricted dams. Previous studies have reported that endothelium-dependent relaxation was blunted in conduit arteries (aorta) from the adult female offspring of pregnant rat dams fed a globally restricted diet . Also, the endothelial NO synthase (eNOS) activity was shown to be reduced in these animals . However, the functional consequences of low protein on resistance vessels, which are the actual determinants of blood pressure, in female offspring are currently not known. The purpose of this study was to test the hypothesis that intrauterine fetal growth restriction due to protein restriction results in low-birth-weight offspring, female offspring having impaired estrous cyclicity and exhibiting reduced endothelium-dependent vascular relaxation, enhanced vascular contraction and hypertension, specifically during their late adult life. To test this hypothesis, we studied vascular function in vivo and contraction and relaxant (endothelium-dependent and -independent) responses ex vivo in small mesenteric arteries from rat female offspring at 1 year of age.
All procedures were approved by the Animal Care and Use Committee at the University of Texas Medical Branch and were in accordance with those published by the US National Institutes of Health Guide for the Care and Use of Laboratory Animals (NIH Publication No. 85-23, revised 1996). Virgin female Sprague-Dawley rats (Harlan Sprague Dawley, Houston, Tex., USA) weighing between 175 and 225 g (4 months old) were mated with male Sprague-Dawley rats; conception was confirmed by observation of a vaginal copulation plug or the presence of sperm in the vaginal flush. Pregnant rats were randomly divided into two dietary groups, housed individually and fed a control (C, 18% casein) or low protein (LP, 6% casein) diet throughout pregnancy. The isocaloric low-protein and normal-protein diets were obtained from Harlan Teklad (Madison, Wisc., USA). The composition of the diets for the 2 groups, except for the protein content, was identical as previously described . All pregnant rats were allowed to deliver at term. At delivery, all dams were placed on the normal diet and the pups were weaned to the normal diet at 21 days of age and maintained on that diet thereafter. Offspring of C and LP pregnant rats were referred to as the C group and LP group, respectively. The litter sizes and birth weights of C and LP pups were recorded within 12 h after delivery and weighed once a week thereafter. The animals were housed in a room with a controlled temperature and a 12-hour:12-hour light-dark cycle.
Estrous cyclicity in both groups of rats was assessed by daily vaginal lavages (smears). Monitoring began on postnatal day 150 and continued for 17 days. Smears were taken between 09.00 and 11.00 h each morning, examined unstained, by light microscopy (×20), and assessed for relative abundance of leukocytes, nucleated epithelial cells and cornified epithelial cells. Six animals each from the C and LP groups were assessed for estrous cyclicity. Cyclicity was assessed by calculating the average number of estrous cycles observed in each group over the monitoring period (i.e. total number of estrous cycles divided by the number of rats in that group).
Mean arterial pressure (MAP) was determined in conscious rats at 1 year of age. Rats were anesthetized with ketamine (45 mg/kg body weight; Burns Veterinary Supply, Westbury, N.Y., USA) and xylazine (5 mg/kg body weight; Burns Veterinary Supply). The jugular vein and carotid artery were cannulated with polyethylene tubing (PE-50; Becton Dickinson, Sparks, Md., USA). After the animals had recovered from anesthesia, the carotid cannula that was filled with heparinized saline (50 U·ml–1) was connected to a pressure transducer to record MAP using the DBP001 direct blood pressure system (Kent Scientific, Litchfield, Conn., USA). The jugular vein cannula was used to administer drugs as an intravenous (i.v.) bolus. MAP was monitored continuously for 30 min before administration of any drugs. Dose-dependent hypotensive responses to acetylcholine (ACh; 0.03, 0.1, 0.3, 1, 3 μg·kg–1 i.v.) and hypertensive responses to phenylephrine (PE; 1, 3, 10, 30 μg·kg–1 i.v.) were obtained in both C and LP rats. eNOS was inhibited with the administration of N-nitro-L-arginine methyl ester (L-NAME, 50 mg·kg–1 i.v.) to rats in both groups to determine the relative contribution of the endothelium in maintaining the basal MAP. Enough time was allowed between responses for MAP to recover to the resting level.
The rats were sacrificed by CO2 inhalation and the mesenteric arcade was excised and immersed in oxygenated Krebs physiological salt solution (KPSS) : NaCl, 119; KCl, 4.7; CaCl2, 2.5; MgSO4, 1.17; NaHCO3, 25; KH2PO4, 1.18; EDTA, 0.026; and D-glucose, 5.5. Small mesenteric arteries were dissected free of connective tissue and mounted using tungsten wires on a wire myograph (Kent Scientific) to record isometric tension. The tissues were incubated for 15 min in KPSS at37°C, which was gassed with 95% O2 and 5% CO2 to maintain pH7.4. The segments were initially loaded to an optimum stretch, which was previously determined by using high-K+ physiological solution (80 mmol/l) as the contracting agent after applying different passive tensions. The initial stretch and the length of the segments (2 mm) were consistently maintained across all arterial rings of either group. For endothelium-intact mesenteric rings, extreme care was taken to avoid injury to the endothelium. For endothelium-denuded mesenteric rings, the endothelium was removedby gently rubbing the ring interior with tungsten wire. Removal of the endothelium was verified by the absence of AChrelaxation in tissues precontracted by a submaximal concentrationof PE.
Endothelium-intact mesenteric arterial rings were stimulated with increasing concentrationsof PE, and concentration-contraction curves were constructed. The PE concentration used for precontraction was that required to produce 80% of the maximal response (pEC80). Endothelium-dependent relaxation was assessed by ACh (10–9–10–5 mol/l)-induced relaxation in PE-precontracted arteries. Endothelium-independent relaxation was determined by sodium nitroprusside (SNP, 10–9–10–6 mol/l)- induced relaxation in PE-precontracted endothelium-denuded arteries. In otherexperiments, the tissues were pretreated for 30 min withL-NAME (10–4 mol/l) to inhibiteNOS or with 1H-1,2,4-oxadiazolo-4,3-quinoxalin-1-one(ODQ, 10–5 mol/l, Sigma) to inhibit cGMP production in smooth muscle and the effects on PE contraction and ACh-induced relaxationof PE contraction were measured.
Endothelium-intact mesenteric rings were placed in wells of 24-well plates containing500 μl KPSS aerated with 95% O2 and 5% CO2 at 37°C. Samples for basal accumulation of nitrite (NO2–) formed fromreleased NO were first taken. The KPSS was replacedand the arterial rings were stimulated with ACh (10–7 or 10–5) for 5 min. The ringswere rapidly removed, dabbed dry with filter paper and weighed. The incubation solutions were assayed for the stable end productof NO, NO2–. In brief, samples of incubation solution (80 μl) were mixed in a 96-well microtiter plate with100 μl of the Griess reagent (Sigma). The chromophore generatedby the reaction with NO2– was detected spectrophotometrically(540 nm) on a microtiter plate reader (Spectramax, MolecularDevices, Sunnyvale, Calif., USA). The concentration of NO2– was calculated from a calibrationcurve constructed with known concentrations of NaNO2.
Stock solutions of PE, ACh, SNP, and L-NAME(Sigma) were prepared in distilled water. ODQ wasdissolved in dimethylsulfoxide. The final concentration ofdimethylsulfoxide in solution was <0.1%. All other chemicalswere of reagent grade or better.
Data are presented as means ± SEM. Statistical analysis was performed using a two-way ANOVA followed by the Bonferroni post hoc test on all dose-response curves and the unpaired Student's t test for comparison of single observation between the C and LP groups. Because the baseline MAPs were different in the C and LP groups, the hypotensive/hypertensive responses were calculated as percent decrease/increase in MAP with respect to the baseline MAP before each response. We and others have shown that the dose-dependent percent change in MAP after agonists is not related to the baseline MAP [32, 33]. Contraction responses to PE were calculated as percent of its maximal contraction. Relaxant responses to ACh were calculated as percent inhibition of the PE-induced contraction. Maximal responses and half maximal effective concentration values were then obtained. Half maximal effective concentrations were determined by regression analysis and expressed as negative log-molar concentration. Data analysis was done using GraphPad Prism for Windows (GraphPad Software, San Diego, Calif., USA). Data from several vascular rings of thesame rat were averaged and presented as the datum for 1 rat, with the n value representing the number ofrats. Differences are considered statistically significantat p < 0.05.
The birth weight of C rats was 6.7 ± 0.08 g and wassignificantly reduced in LP rats (4.7 ± 0.1 g). Both C and LP offspring showed significant increases inbody weight with age. However, the growth curves of the two groups were significantly different and were parallel through adulthood (fig. (fig.1).1). The body weight at the time of terminal study (1 year) was significantly lower in LP offspring than in C rats (266.0 ± 4.2 vs. 277.1 ± 2.7 g). The length of gestation and number of pups per litter were not different among groups (table (table11).
Assessment of estrous cyclicity revealed a significantdecrease in the number of observed estrous cycles over a 17-dayperiod in the LP group compared to C rats (table (table1).1). The 6 rats in the C group totaled 18 estrous cycles (average = 3), while in the LP group only a total of 3 estrous cycles were observed (average = 0.5) (table (table1).1). Although few animals showed extended cycle length, most rats had already stopped cycling in the LP group.
Baseline MAP measured in 1-year-old rats was significantly higher in LP rats when compared with the C group (133.9 ± 4.05 vs. 104.7 ± 3.13 mm Hg). We found that ACh evoked a concentration-dependent decrease in MAP that was attenuated in LP rats (fig. (fig.2a).2a). Administration of PE evoked a concentration-dependent hypertensive response that was more pronounced in LP offspring compared to C rats (fig. (fig.2b).2b). Acute administration of the eNOS inhibitor, L-NAME, induced significantly greater hypertensive responses in C (60.0 ± 2.64%) than in LP offspring (30.6 ± 3.00%).
In endothelium-intact mesenteric rings from both groups of rats, PE caused concentration-dependent increases in contraction. When the PE responsewas presented as the percentage of maximum PE contraction, the median effective concentration (ED50) of PE in C ratswas greater than that in LP rats (5.4 ± 0.05 vs. 5.8 ± 0.12 mol/l; fig. fig.3,3, table table2).2). This shows that PE was more potentin producing contractions in LP rats than in C animals.
Pretreatment with L-NAME for 30 min to inhibit eNOS activity significantly enhanced the maximal PE-induced contraction in LP rats (116.6 ± 2.54%; fig. fig.4b,4b, table table2)2) and to a greater extent in C rats (136.6 ± 5.95%; fig. fig.4a,4a, table table2).2). Also, plotting the PE response asa percentage of maximum and calculation of the PE ED50 showedthat PE was slightly more potent (but the difference was not statistically significant, p = 0.46) in causing contraction in L-NAME-pretreatedthan in nontreated arterial rings of LP rats (fig. (fig.4b,4b, table table2).2). PE was far more potent in causing contraction in L-NAME-treatedthan non-treated vascular rings of C rats (fig. (fig.4a,4a, table table22).
Similarly, in endothelium-intact vascular rings, pretreatmentwith ODQ for 30 min to inhibit cGMP productionin smooth muscle significantly enhanced the maximal PE-induced contraction in LP rats (119.7 ± 3.18%; fig. fig.4b,4b, table table2)and2)and to a greater extent in C rats (136.5 ± 5.73%; fig. fig.4a,4a, table table2).2). PE was slightly more potent (but the difference is not statistically significant, p = 0.27) in producing contractions in ODQ-treated arterial rings of LP rats than in C animals (fig. (fig.4a,4a, table table22).
In endothelium-intact vascular rings of C rats, ACh causedconcentration-dependent relaxation of PE-mediated (3 × 10–6 mol/l)contraction. The ACh-induced relaxation of the PEcontraction was significantly less in LP rats than in C animals (fig. (fig.5a).5a). ED50 of ACh in mesenteric arterial rings of LP rats (6.1 ± 0.11 mol/l) was significantly different from that inarterial rings of C rats (6.7 ± 0.18 mol/l) (table (table2).2). Becausethe mesenteric arterial rings of LP rats showed greatervascular contraction compared to C rats, control experiments were performed on rings from LP rats in which the initial PE concentration was loweredto 1 × 10–6 mol/l to produce a submaximal contraction that wasroughly equal in magnitude to the contraction observed in rings of C rats precontracted with 3 × 10–6 mol/l PE. Theseexperiments showed that the ED50 of ACh in mesenteric arterial rings of LP rats precontracted with 1 × 10–6 mol/l PE (6.2 ± 0.12mol/l) was not significantly different from that inarterial rings precontracted with 3 × 10–7 mol/l PE (6.1 ± 0.11 mol/l). This shows that ACh relaxation does not vary with the amplitude of PE contractions.
Pretreatment of endothelium-intact rings with L-NAME to inhibit eNOS or ODQ to inhibitcGMP production in smooth muscle inhibited ACh-inducedrelaxation significantly in LP and C rats (fig. 5b, c, table table2).2). Removal of the endotheliumcompletely inhibited the ACh-induced relaxation to PE contractionin all groups of rats (data not shown).
In endothelium-intact vascular rings, the basal nitrite/nitrate(NOx) production was 83.9 ± 12.51 pmol/mg tissue weight inC rats and this was significantly lower in the LP rats (28.2 ± 6.37pmol/mg tissue weight) (fig. (fig.6).6). Similarly, NOx production in response to ACh was also significantly reducedin the LP group compared with the C group (fig. (fig.66).
In endothelium-denuded vascular rings of both LP and C groups, SNP, an exogenous NO donor and a standard guanylate cyclaseactivator, caused concentration-dependent relaxation of submaximalPE contractions. The SNP-induced relaxation to PE contractionswas not significantly different in vascular rings from C and LP rats (7.7 ± 0.07 vs. 7.7 ± 0.09 mol/l; fig. fig.7,7, table table22).
The goal of the present study was to determine whether dietary protein restriction during gestation resulted in hypertensivefemale offspring that exhibit impaired endothelium-dependent vascularrelaxation and enhanced vascular contraction. Terminal studies were done in female offspring at 1 year of age. The main findings are as follows: (1) birth weight and later growth are significantly lower in LP offspring compared to the C group; (2) LP offspring have extended estrous cycle lengths with a reduced number of animals cycling; (3) MAPis elevated in the offspring of LP compared to C rats; (4) PE-inducedcontraction is enhanced in vivo and in vitro in mesenteric arteries from LP rats;(5) the endothelium-dependent vascular relaxation is reducedin LP compared with C rats, and (6) the reduced vascularrelaxation and enhanced vascular contraction in LP rats appear to involve dysfunction of the endothelium.
CV disorders such as hypertension and coronary heart disease have been related to low birth weight or smallness at birth. In the present study, feeding dams on a low-protein diet during pregnancy gave birth to offspring with a significantly reduced birth weight compared with controls. Previous studies on dietary restriction produced variable results on birth weight. In some investigations, birth weight was reduced [34, 35], in others unchanged [7, 10, 14, 36] and in some even increased . The discrepancies may be due to factorsthat may alter response of the mother and fetus to nutrientrestriction such as strain, maternal age and differencesin the diets.
Similar to previous studies using protein restriction during pregnancy [13, 27],MAP was found to be significantly elevated in LP compared with C offspring in the present study. However, in contrast to our findings, some studies reported that female offspring do not develop hypertension [24, 25]. Differences in protocols, e.g. severity and duration of undernutrition or vascular bed studied, may account for the variable results obtained for each model. In some instances, vascular dysfunction may not be accompanied with increased pressor responses as observed in female offspring of global diet-restricted pregnant rats . In view of the differences in the protocols used, direct comparisons between models should be treated with caution. For example, Woods et al.  used 50% protein restriction that resulted in a reduction of about 10% in birth weight, whereas we used a diet with 66% protein restriction that resulted in a reduction of 30% in birth weight. It is possible that a severer or amore extended maternal dietary restriction (i.e. into the lactationperiod, during which nephrogenesis continues) would leadto consistent hypertension in female offspring. In agreement with our findings, there are reports of hypertension and reduced nephron number in female offspringof more severely protein-restricted dams [25, 31]. Indeed, in one study inwomen, the inverse association between birth weight and adulthypertension or cardiovascular disease was marked only in thelowest birth weight category, which represented birth weightsmore than 25% below average [39, 40]. Thus, it appearsthat the resistance of females to the hypertensive effects ofperinatal insults breaks down when the insults are severer.
In order to investigate alterations of vascular function in the female offspring of protein-restricted dams, responses to ACh, an endothelium-dependent vasodilator, to SNP, an endothelium-independent vasodilator, and to PE, a vasoconstrictor whose effects are modulated by the endothelium, were investigated. Hypotensive responses and mesenteric vasorelaxation to ACh were reduced in LP offspring compared to C rats, but no differences could be detected to SNP. These observations suggest that it is not the smooth-muscle vasodilating capability that is reduced in LP offspring but some function related to the endothelium. Reports of impaired endothelial function in female offspring have been shown in previous studies using excess fat [41, 42] and global food restriction during pregnancy . In fact, Goodfellow et al.  and Leeson et al.  demonstrated that growth restriction in human pregnancy is associated with endothelial dysfunction.
Considering that NO is the main agonist responsible for endothelial-dependent relaxation, we characterized the relative contribution of NO in vasodilation of mesenteric arteries isolated from LP and C offspring. Besides NO, ACh also induces vasorelaxation through NO-independent mechanisms [45,46,47,48]. This is evident in this study by the observation that L-NAME and ODQ did not completely inhibit ACh-induced relaxation. However, this L-NAME/ODQ-resistant component was shown to contribute equally to vasodilation in both C and LP offspring, indicating that only the NO component may be impaired, thereby contributing to the observed difference in pressor response in these groups. Although endothelium-derived hyperpolarizing factor is known to compensate for loss of NO function in arteries , such a response was not observed in this study.
Impaired NO function may be due to decreased NO synthesis and/or bioavailability. The finding that L-NAME induced a greater increase in MAP in C than in LP offspring indicates that NO-mediated control of vascular tone is certainly compromised in female offspring exposed to protein restriction in utero. Consistent with this finding, pretreatment of the isolated mesenteric arteries from C rats with L-NAME inhibited ACh-induced vascular relaxation to a greater extent than in LP offspring. These results indicate that NO synthesis by endothelial cells may be impaired in LP rats. This conceptis supported by the observation that both basal and ACh-inducedNOx productions were significantly reduced in arteriesfrom the LP compared with C rats. There are similar reports of reduced basal and agonist-induced NO release in pregnant rat dams fed a protein-restricted diet  and also in the offspring of patients with essential hypertension . The decreased levels of NO may be associated with decreased expression/activity of eNOS as previously reported by us and others [13, 51], or due to rapid degradation by superoxide . However, our attempt to determine eNOS activity in mesenteric arteries of LP rats in this study showed varied responses and was less conclusive, necessitating further investigation.
It is well known that the endothelium modulates the vasoconstrictor response to PE, probably by releasing NO. Reduced NO function may lead to increased responses to PE. The fact that the LP offspring were hyperresponsive to PE and that the mesenteric arteries with endothelium from LP rats were more responsive to PE led us to suggest that the modulatory role of the endothelium on the vascular responses has been lost in rats submitted to intrauterine protein restriction. The findings that L-NAME and ODQ pretreatment potentiated PE-induced contraction in mesenteric arteries from C rats but had minimal effects in LP offspring also suggest that the vascular smooth muscle responses to PE have been preserved in LP offspring, reinforcing the hypothesis that protein restriction in utero mainly affects the endothelium.
The factors that contribute to endothelial dysfunction in LP offspring remain unclear. In LP offspring, the reproductive performance was shown to be impaired during adult life (i.e. after 6 months) as evident by increased estrous cycle length and decreased number of cycling animals. Similar findings of reduced reproductive function associated with delayed vaginal opening, onset of first estrous and impaired endocrine function in offspring of nutrient-restricted dams were reported . We and others have reported that, consistent with the impaired reproductive function, the serum estrogen levels in rats exposed to intrauterine undernutrition are only half of those of controls [13, 27, 54]. Estrogen is known to have a vasoprotective effect on endothelium via an NO-mediated mechanism. It was shown that long-term treatment of cultured human and bovine endothelial cells with estrogen upregulates eNOS activity [30, 55]. In addition, deficiency of estrogen (following ovariectomy) in spontaneously hypertensive rats causes a reduction in endothelial function . Since females from dams submitted to protein restriction during pregnancy exhibited reduced estrogen levels, we suggested that the vasoprotective role of the estrogen on the vascular responses may be lost, leading to decreased endothelial function. Not only physiologically relevant concentrations of estrogen are important, but also having active estrogen receptors (ERs; including ERα and ERβ) is essential for botha rapid and long-term positive CV effect [57,58,59,60]. We have previously demonstrated a decrease in ERα and ERβ in the thoracic aorta of protein-restricted female offspring . In fact, preliminary studies from our laboratory have shown that ovariectomy exacerbates hypertension in the offspring of protein-restricted dams, indicating a role for estrogen in the normalization of blood pressure. Further studies are under way to delineate the vasoprotective mechanisms of estrogen.
Several previous studies have demonstrated that essential hypertensionis associated with impaired endothelium-dependent vascularrelaxation [61,62,63]. However, whether this is a primary or secondaryabnormality is unknown. Certain previous investigations havesuggested that endothelial dysfunction is a primary defectin essential hypertension, present even before the clinicaldocumentation of elevated blood pressure . On the other hand, certain observations suggest that endothelialdysfunction may occur as a consequence rather than a causeof elevated blood pressure. In particular, human studies and several animal modelsof induced hypertension, including suprarenal coarctation ofthe abdominal aorta in rabbits , salt-induced hypertensionin Dahl salt-sensitive rats , and pressure increases in cat cerebral  and dog coronary arteries , have all shown a selectiveimpairment of endothelium-dependent vasodilation after elevationsin blood pressure. It is important to emphasize the following cautionary remarksregarding the aforementioned interpretations. First, althoughwe hypothesized that the decreased endothelial cell function and increased vascularcontraction in LP rats could contribute to the observed elevation in arterialpressure, the reverse is also plausible. Further analysis of the time course ofthe changes in vascular functions and the increase in arterialpressure in rats <1 yearof age should help determine whether the relation between thesetwo parameters is causal or associative. Second, although thereduction in vascular relaxation and increase in vascular contractionin the LP group could explain in part the increase in arterial pressure, otherfactors such as renal, neural and hormonal control mechanismsof arterial pressure could also be involved. Third, as the vascularendothelium also releases contracting factors such as thromboxane and endothelin, we cannot exclude a role for these factors in the endothelial dysfunction induced by intrauterine undernutrition. Therefore, analysis of the role of other endothelium-derivedrelaxing factors in the vasculature and blood pressure changesobserved in LP ratsshould be carefully examined in future studies.
In summary, the present study has shown thatan endothelium-dependent vascular relaxation pathway involvingthe release of NO from endothelial cells, but not the smoothmuscle response to NO, is inhibited in systemic vessels of LP offspring of pregnant rats with reduced protein intake. The decreasedNO-mediated vascular relaxation pathway in LP rats might explainthe increased vascular contraction and arterial pressure inyoung adult rats with low birth weight.
Financial support from National Institutes of Health through grants No. HL-58144 and HL-72650 is greatly appreciated.