Low birth weight (LBW) due to intrauterine growth restriction (IUGR) in humans is associated with increased blood pressure (BP) in adulthood. In Western countries, IUGR is based on uteroplacental dysfunction. We used an animal model of uteroplacental dysfunction to evaluate this correlation. We hypothesize that IUGR increases baseline BP and alters the BP response to acute stress, which may explain BP differences in previous studies using stressful methods to obtain BP. IUGR was induced by bilateral uterine artery ligation in pregnant Wistar rats according to a modified method of Wigglesworth. BP was measured in the offspring using telemetry, allowing for unstressed measurements in conscious animals. Cardiovascular data were obtained at the age of 12 wk during baseline and acute olfactory stress induced by an ammonia gauze. Rats born after IUGR had a lower birth weight versus controls and did not completely catch up in weight. At baseline, systolic BP (SBP), mean arterial pressure (MAP), and pulse pressure (PP) were elevated in IUGR rats versus controls, by 8, 6, and 5 mm Hg, respectively. There was a strong negative correlation between birth weight and SBP and between birth weight and PP. During acute stress, there was a tendency to reach a higher peak in SBP and to need a longer period to recover in IUGR animals. We conclude that IUGR is associated with increased baseline BP. I UGR leads to LBW, which is linked to an increased risk of various chronic diseases in adulthood (1-4). Numerous studies have described the association between LBW and hypertension (for review, see Huxley et al. (5)). The pathways that may lead to a rise in BP are not fully understood (6 -18).Several previous authors have studied BP in growthrestricted animals (19). In these studies, BP is commonly measured indirectly using the tail-cuff method. This method entails restraining and preheating the animal, which leads to increased BP, heart rate (HR), and plasma levels of epinephrine and norepinephrine (20). In fact, restraints on laboratory animals have been used as a stressor (21). Results obtained from these studies should therefore be interpreted with caution. The described raised BP in IUGR animals might reflect a different stress response rather than a raised baseline BP.BP can be measured both directly as in a nonstressed manner by telemetry (20). Previously, only two reports using telemetry have addressed the effect of IUGR on BP in rats. Tonkiss et al. (22) found a small rise in baseline diastolic BP (DBP) but not in SBP in IUGR rats. They also described a marked difference in the response to acute stress with a greater increase in DBP and SBP in IUGR rats. Jansson and Lambert (23) found no evidence for BP elevation after IUGR. In these studies, different models for IUGR were used. For a review of currently applied IUGR models, see Holemans et al. (19). Tonkiss et al. (24) applied an IUGR model based on prenatal protein restriction, which might not be representative of the human situation. In Western countries, the lead...