Biol Reprod Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

BOR - Papers in Press, published online ahead of print February 6, 2008.
Biol Reprod 2008, 10.1095/biolreprod.107.065532
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow [Supplemental Data]
Right arrow All Versions of this Article:
78/6/1049    most recent
biolreprod.107.065532v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow My Folders
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gassmann, M.
Right arrow Articles by Vogel, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gassmann, M.
Right arrow Articles by Vogel, J.
Agricola
Right arrow Articles by Gassmann, M.
Right arrow Articles by Vogel, J.
BIOLOGY OF REPRODUCTION 78, 1049–1057 (2008)
DOI: 10.1095/biolreprod.107.065532
© 2008 by the Society for the Study of Reproduction, Inc.

Pregnancy; 

Abortion in Mice with Excessive Erythrocytosis Is Due to Impaired Arteriogenesis of the Uterine Arcade1

Max Gassmann 3, Annamaria Manini 3, Thomas Stallmach 4, Bianca Saam 3, Gisela Kuhn 3, Beat Grenacher 3, Anna Y. Bogdanova 3, and Johannes Vogel 2 3

Institute of Veterinary Physiology,3 Vetsuisse Faculty and Zürich Center for Integrative Human Physiology (ZIHP), and Department of Pathology,4 University of Zürich, CH-8057 Zürich, Switzerland

ABSTRACT

We postulate that repeated pregnancy loss, intrauterine growth restriction, and preeclampsia are caused by impaired elevation of uterine blood flow due to disturbed arteriogenesis of the uterine arcade. This hypothesis is based on the observation that pregnant human erythropoietin-overexpressing (plasma levels elevated 12-fold) mice (termed tg6 mice) suffering from excessive erythrocytosis generally abort at midgestation unless their hematocrit of 0.85 is drastically lowered. Transgenic mice show placental malformations that parallel those observed in pregnant women suffering from impaired uterine perfusion. Shear stress, a key factor inducing arteriogenesis, was 5-fold lower in tg6 mice compared with wildtype (WT) littermates. Consequently, uterine artery growth was reduced, and dramatically fewer viable pups (1.63 ± 2.20 vs. 8.10 ± 0.74 in WT) of lower weight (1.29 ± 0.07 g vs. 1.62 ± 0.12 g in WT) were delivered in first pregnancies. Only in subsequent pregnancies did tg6 deliver approximately the expected number of pups. Birth weights of tg6 offspring, however, remained reduced. As the spleen is a major site of extramedullary erythropoiesis in tg6 animals, splenectomy reduced the hematocrit to 0.6–0.7. In turn, shear stress increased to normal values, and splenectomized primiparous tg6 showed normal uterine artery growth and delivery of pups similar in number and weight compared with WT. We conclude that poor arteriogenesis is a previously unappreciated cause for clinically important pregnancy complications.

arteriogenesis, erythropoietin, female reproductive tract, fertility, intrauterine growth restriction, intrauterine growth retardation, polycythemia, preeclampsia, pregnancy, repeated pregnancy loss, uterine artery

INTRODUCTION

Spontaneous abortion, intrauterine growth restriction (IUGR), and/or preeclampsia are all associated with and impaired pregnancy-induced increase in uterine artery (UA) blood flow [1–4]. However, the primary cause and secondary effect of lower UA blood flow in these conditions are unknown. All three conditions are more frequent in nulliparous women. Spontaneous abortion affects 10%–15% of pregnant women, and in 85% of these cases, abortion occurs in the first trimester of pregnancy [5]. Miscarriage occurs in about 25% of all cases [6]. The risk of pregnancy loss decreases as the number of pregnancies rises [7], paralleled by an increase in the birth weight of babies from second and subsequent gestations [8].

At high altitudes, babies usually have a reduced birth weight, and the incidence of IUGR or preeclampsia is higher [9, 10]. This was observed even centuries ago by the Spanish conquistadors, who asked their pregnant wives to leave Cuzco, the Inca capital located about 3400 m above sea level, and to return to Lima (sea level) during pregnancy and delivery [11]. Reduced UA blood flow rather than lower arterial oxygen content—that is, elevated compared with women living at low altitude [12]—appears causal. In addition, pregnant women at high altitudes have a smaller UA diameter than those at low altitudes [12] and have fewer uteroplacental vessels in placental deciduas with impaired vascular remodeling [13]. Elevated hematocrit values due to reasons other than high altitude also result in poor pregnancy outcome but are treatable by reducing the hematocrit [14]. Interestingly, in a subgroup of subfertile women with unexplained repeated pregnancy loss, the only abnormal parameter detected was an insufficient increase in blood flow of the UA during pregnancy [15, 16]. Disturbed uterine perfusion correlates with defects in placental development, predominantly at the maternal-fetal interface, that ultimately might cause pregnancy loss, IUGR, or preeclampsia [17, 18].

Despite the obvious clinical significance, the etiology of the insufficient rise in uterine perfusion during pregnancy in these pathologies has not been fully investigated. We propose that poor arteriogenesis (length and diameter growth) of the UA during pregnancy plays a key role in unexplained repeated pregnancy loss, IUGR and, presumably, in preeclampsia too. This hypothesis arose from observations in our transgenic mice (tg6 mice) that overexpress human erythropoietin, resulting in a 12-fold elevation of erythropoietin plasma levels and, consequently, hematocrit levels as high as 0.80–0.90 [19]. Between Days 9 and 10 of pregnancy, tg6 mice usually lose their fetuses unless their hematocrit is reduced. In analogy to the observations in humans with impaired uterine perfusion [3, 13, 20], our transgenic mice failed to develop the labyrinth layer at Day 9.5. Moreover, the decidual arteries are much smaller in tg6 mice compared with wildtype (WT) littermates (supplemental figures available online at www.biolreprod.org).

To study the impact of arteriogenesis on pregnancy outcome, we recorded the number and weight of pups born and measured the UA luminal area, wall area, and the number of endothelial cells (ECs) and smooth muscle cells (SMCs) of the arterial wall in WT, tg6, and splenectomized (Splx) tg6 mice (note that in tg6 mice, extramedullary erythropoiesis occurs in the spleen [21]). Shear stress was estimated from measurements of mean circulating time, whole-blood viscosity, and the radius of the UA. Plasma nitrate/nitrite and erythropoietin levels were also measured. Finally, to test whether impaired arteriogenesis due to low shear stress is causative for the pregnancy complications in our tg6 mice, we measured both capillary density and capillary:fiber ratio in hind limb muscles 3 wk after femoral artery occlusion. The resulting data revealed impaired arteriogenesis also in this experimental setup, making pregnancy-associated hormonal disturbances or other problems [22] an unlikely cause of the poor pregnancy outcome in tg6 mice.

MATERIALS AND METHODS

Animals

All animal experiments conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85–23, revised 1996) and institutional guidelines and were approved by the Kantonales Veterinäramt Zürich.

The transgenic mouse line Tg(PDGFB-EPO)321Gass (genetic background C57BL/6, termed tg6) was generated by pronuclear microinjection of the full-length human erythropoietin cDNA driven by the human platelet-derived growth factor B-chain promoter, as previously described [19]. Compared with WT littermates, tg6 mice exhibit a 12-fold elevation of plasma erythropoietin levels, resulting in hematocrit values as high as 0.85 [19, 21, 23–25]. Wild-type C57BL/6 females were used as controls.

Experimental Design

The prerequisite of the present study was a normal fertility of tg6 oocytes. Therefore, we first performed embryo transfer to pseudopregnant surrogate mothers (WT) from tg6 females previously mated with either WT or tg6 males.

In the next set of experiments, the reproductive outcome (number of fetuses at different gestational ages; Table 1) and the pregnancy-induced changes of the UA luminal and wall area as well as the numbers of ECs and SMCs present were assessed at gestational age 0 (nulligravida), Days 7, 9–10, 11, 15, 17, and after parturition. These measurements were performed in four experimental groups: WT mice, splenectomized tg6 mice (Splx), primiparous tg6 mice, and multiparpous tg6 mice. Because only 25% of our normal breeding offspring could be used for the study and tg6 mice usually abort between Days 9 and 10, untreated tg6 mice were investigated only for the gestational ages 0, Days 7, 10, and after parturition (n = 5 for each gestational age and for all groups, except for Splx Embryonic Day 7 (E7) [n = 3] and Splx E9 [n = 3] mice, where cell counting failed due to insufficient tissue preservation).


View this table:
[in this window]
[in a new window]
[Download PPT slide]
  		TABLE 1. Number of fetuses at different gestational ages; pregnancy outcome of WT, Splx, primiparous, and multiparous tg6 mice; and weight of live pups.*

As we hypothesized that the poor pregnancy outcome of tg6 mice is due to impaired arteriogenesis, we estimated arterial wall shear stress in the UA. Considering that arteriogenesis is induced by endothelial shear stress ({tau}) [26], we determined all parameters necessary for shear stress calculation according to the equation:


Formula 78

This equation indicates that shear stress in all vessels is proportional to blood viscosity ({eta}) and mean blood flow velocity (v), and inversely proportional to the vessel radius (r). Blood flow velocity itself is dependent on blood volume (BV) and cardiac output (CO), since it is inversely proportional to mean circulating time (mCT) that is given by [27]:


Formula 78

Previous data showed that tg6 mice have a 2.5 times higher BV and a slightly lower CO compared with WT mice [21, 23]. In addition, tg6 mice exhibit chronic vasodilation mediated by elevated production of nitric oxide [19]. Finally, blood viscosity is increased to a lesser extent than expected (4-fold rather than 8-fold) due to increased red cell flexibility [21]. (Greater erythrophagocytosis lowers erythrocyte life span, resulting in elevated red cell flexibility [24].) Thus, we determined mCT (WT: n = 3, Splx: n = 5, and untreated tg6: n = 7), blood viscosity (n = 6 each), and diameter of the UA (see above). In addition, we measured plasma nitrite/nitrate levels in each of these groups (WT: n = 5, Splx: n = 6, untreated tg6: n = 8).

Recently, we demonstrated that arteriogenesis of the UA is irreversible in WT C57BL/6 mice [28]. We hypothesized that arteriogenesis, although insufficient in the initial pregnancies, might be additive in repeated pregnancies, finally allowing all tg6 females to deliver pups. To this end, WT (n = 10), Splx (n = 14), and untreated tg6 (n = 14) mice were mated until all of them delivered at least one viable pup. The number of pregnancies required to be successful was determined for each individual female. The tg6 mice from this set of experiments (n = 7) were killed directly after delivery for UA examination, as described above.

Apart from the UA, we investigated the effect of excessive erythropoietin and hematocrit on the functional outcome of arteriogenesis in another vascular bed independent of pregnancy. To this end, we used the hind limb occlusion model and measured capillary density and capillary:fiber ratio in both lower legs of WT, Splx, and untreated tg6 mice (n = 3 each) 3 wk after femoral artery occlusion. For each single leg, we analyzed 712-1498 capillaries.

Surgical Procedures

Anesthesia for all surgical procedures was induced with a gas mixture containing 4% isoflurane, 30% O2, and 70% N2O and maintained with 1.5% isoflurane. Temgesic (0.05 mg/kg, subcutaneously) was administered for postoperative analgesia.

Embryo transfer. Twelve-week-old tg6 females were superovulated by injection (intraperitoneal) of eCG (5 IU; Folligon; Intervet, Boxmeer, The Netherlands), followed 48 h later by hCG (5 IU; Pregnyl; Organon AG, Pfäffikon, Switzerland). Upon the second injection, tg6 females were mated with C57BL/6 WT males, and 44 h after the second injection, the females were killed. The two-cell embryos were flushed from the excised oviducts using M2 medium (Sigma-Aldrich, Buchs, Switzerland) and cultured in M16 medium (37°C, 5% CO2 in air) until use.

Surrogate mothers were prepared as described previously [29], and embryo transfer was performed exactly as described therein. A total of 10–16 embryos (half in each uterus horn) were transferred to a single surrogate mother.

Splenectomy. Since extramedullary erythropoiesis in tg6 mice occurs mainly in the spleen [21], this organ was removed at an age of 14 ± 1.32 wk in tg6 mice through a midline laparatomy. Two weeks later, hematocrit was measured one to two times per week, and the mice were mated when the hematocrit value was between 0.60 and 0.75.

Hind limb occlusion. To analyze arteriogenesis and its functional outcome in tg6 mice independently of pregnancy, we used the hind limb occlusion model [26]. The left femoral artery was ligated twice and transected in between. Thereafter, the mice were housed under standard conditions for 3 wk and then killed by cervical dislocation, and both hind limbs were harvested, frozen, and stored at –20°C.

Breeding

Virgin females at an age of 19 ± 2.45 wk were housed together with an NMRI or (C57BL/6 x DBA/2)F1/Crl male for up to four nights and were checked twice a day for vaginal sperm plugs. The females were separated from males after four nights or when a plug was detected (defined as Day 1 of pregnancy). Three days after separation, vaginal smear analysis [30] was performed daily for 5 days. If no estrus cycle occurred, the female was considered to be pregnant; conversely, if an estrus cycle occurred, it was considered "failed conception," and the animal was remated. Pregnant mice that had been separated from the male without being scored plug positive were killed after delivery, as the exact day of conception was unknown.

To ensure that the hormonal influence of the cycle on the UA was kept to a minimum [31] in mice assigned to gestational age 0, we used either virgin or mated females that exhibited an empty uterus on laparotomy and showed evidence of diestrus (as determined by instant vaginal smear analysis) following killing at Day 7, 9, 10, or 11. Diestrus was selected because it is the estrus cycle stage of longest duration (50–60 h) and lowest estrogen levels.

Reproductive Outcome

At laparotomy on the scheduled day of pregnancy, the number of fetuses in each uterine horn was recorded. For females killed on the day of delivery, numbers and weights of delivered pups were determined.

Furthermore, the number of pregnancies required by each individual female to deliver pups for the first time ("pregnancy order") was determined by performing a series of vaginal smear analyses during the 4–5 days after mating, as described above. If a previously virgin mouse showed no estrus cycle after mating, it was considered to be pregnant, having the pregnancy order 1. If the same female did not deliver, it was mated again. For each subsequent pregnancy until first delivery of at least one live pup, a corresponding higher number of pregnancies was assigned.

Histology and Morphometry

At the scheduled day of pregnancy (0, 7, 9–10, 11, 15, 17, or after parturition), anesthetized mice were perfusion fixed at an arterial pressure of 115 mm Hg according to Forssmann et al. [32]. Mice were then postfixed for at least 1 day in the second Forssmann-Ito solution. Subsequently, the uterus, including mesometrium and UAs, was cryoprotected in 10% sucrose in PBS for 1 day.

Each uterine horn with its corresponding UA was sectioned into 10 µm slices at –30°C using a cryomicrotome (Leica CM3050 S). The uterine horn was divided into equal thirds (proximal, middle, and distal), and at least four slices were taken from each third. Slides were dried at room temperature, defatted in acetone, and photographed in bright field with the 10 x 10 objective of a Zeiss Axiovert 200M microscope equipped with a CCD camera (Zeiss Axio Cam HRm).

Luminal area, wall thickness, and wall area of the most circular cross sections of the proximal, middle, and distal segments of the left and right UA were measured using the ImageJ 1.30v software (http://rsb.info.nih.gov/ij/), as described [28]. Thereafter, the slides were stained with hematoxylin and eosin, and the number of SMC nuclei in as well as the nuclei of ECs in the UA were counted using a Zeiss Axioskop 2 microscope, as described [28]. Some uteri of WT and tg6 mice of gestational ages 9–10 were not frozen but embedded in paraffin, sectioned, stained with hematoxylin and eosin and examined by a blinded pathologist (T.S.).

Capillary density and capillary:fiber ratio in the hind limbs (n = 3) were determined in 10 µm cryosections of the lower leg using the unspecific alkaline phosphatase staining [33]. Then, the numbers of capillaries per area as well as the number of capillaries in direct contact to single muscle fibers were counted.

Measurement of Mean Circulation Time

Mean circulating time was calculated using equation 2 (see above). Cardiac output and plasma volume were measured as described [21, 34]. Total BV was calculated using plasma volume and hematocrit.

Blood Viscosity

Blood viscosity was measured with a rotation viscosimeter (DVIII+ Rheometer; Brookfield Engineering Laboratories, Middlebrow, MA) in heparinized blood at 37°C and shear rates between 2 s–1 and 450 s–1, as described previously [21].

Nitrite/Nitrate Levels in Plasma

To determine the plasma nitrate/nitrite concentration, plasma samples were deproteinized and centrifuged, and the nitrate in the supernatants was reduced to nitrite using the Nitralyzer kit from World Precision Instruments (Berlin, Germany). The reduced samples were further reduced to nitric oxide using a Brown solution (1.62 g KJ, 0.57g J2 dissolved in 202 ml acetic acid and 15 ml H2O) heated to 60°C and continuously bubbled with helium. The helium transferred the produced nitric oxide to a chemiluminescence detector (CLD88 Exhalyzer; ECO-Medical, Dürten, Switzerland) through a washing bottle containing 1 M NaOH at 4°C. The resulting nitric oxide peaks were analyzed using the software supplied with the chemiluminescence detector.

Statistical Analysis

The data are expressed as means ± SD and were compared with one-way ANOVA with a Tukey-Kramer post hoc test using GraphPad Instat Software (version 3.05). Percentage data were log-transformed before calculation of the statistics. In cases of negative percentage values in a data set, prior to analyses the minimum of all values plus one was added to all percentage values. Uterine artery histological differences between gestational ages within an experimental group and between experimental groups within a gestational age (Figs. 1 and 2), differences in mean circulation time, nitrate:nitrite ratios, between experimental groups (Fig. 3), and differences between capillary density and capillary:fiber ratio between experimental groups and between legs with occluded and nonoccluded femoral artery were determined (Fig. 4). A P value < 0.05 was considered significant.


Figure 01
View larger version (32K):
[in this window]
[in a new window]
[Download PPT slide]
  		FIG. 1. Luminal area (A, B) and wall area (C, D) of the UA before (E0) and during pregnancy and after parturition in wild-type (wt), splenectomized tg6 mice (splx), primiparous, and multiparous tg6 mice. A) Compared with E0, luminal area increased within each group of mice. B) On a percentage basis, luminal area increased similarly in wt and splx (2.6-fold), whereas in tg6 mice, luminal area increased only 1.5 times. There was no significant difference between primiparous and multiparous tg6 mice. C) Wall area increased in all groups until the day of delivery. D) Increase of wall area on a percentage basis was highest in wt mice and lowest in tg6 mice. Multiparous tg6 had a larger wall area compared with primiparous tg6, although this difference was not significant. Data in B and D are shown as percentage difference between indicated gestational age and mean of E0 within each group. Means ± SD (A, C) or SEM (B, D). Hct, Hematocrit. Single symbols, P < 0.05; double symbols, P < 0.01; triple symbols, P < 0.001; *, vs. E0 within the same experimental group; #, vs. wt; $, vs. splx within the same time point.


Figure 02
View larger version (36K):
[in this window]
[in a new window]
[Download PPT slide]
  		FIG. 2. Changes in EC (A, B) and SMC (C, D) numbers in the UA wall during pregnancy in wild-type (wt), splenectomized tg6 (splx), primiparous, and multiparous tg6 mice. Wt and splx increased both EC and SMC numbers, whereas primiparous tg6 mice did not. On a percentage basis, the effect on endothelial cell number was highest in wt (B) followed by splx, whereas SMCs increased similarly in wt and splx (D). Only after subsequent pregnancies did multiparous tg6 mice show a moderate but significant increase in both cell numbers. Means ± SD (A, C) or SEM (B, D). Single symbols, P < 0.05; double symbols, P < 0.01; triple symbols, P < 0.001. *, vs. E0 within the same experimental group; #, vs. wt; $, vs. splx within the same time point; &, vs. primiparous after parturition.


Figure 03
View larger version (15K):
[in this window]
[in a new window]
[Download PPT slide]
  		FIG. 3. Mean circulating time (mCT) of blood (A) and plasma nitrate/nitrite levels (B) in virgin wild-type (wt) mice, splenectomized tg6 (splx) mice with a Hct < 0.75, and tg6 mice (tg6) with Hct > 0.8. A) In untreated tg6 mice, the mCT was about 12-fold higher than in wt. Splenectomy restored mCT to close to wt values. B) Tg6 showed 2.76 times higher nitrate/nitrite plasma levels than wt, which decreased significantly to values between that of tg6 and wt mice after splenectomy. Data shown as means ± SD. ###P < 0.001 vs. wt; $$$P < 0.001 vs. splx.


Figure 04
View larger version (16K):
[in this window]
[in a new window]
[Download PPT slide]
  		FIG. 4. Capillary density (A) and capillary:fiber ratio (B) of the lower leg in wild-type (wt), splenectomized tg6 (splx) mice with a Hct < 0.75, and tg6 mice with Hct > 0.8 after femoral artery occlusion. A) Capillary density of the occluded left leg as a percentage of the nonoccluded right leg, which was set to 100% (dashed line). Tg6 mice had reduced capillary density after occlusion, whereas splx and wt showed no changes. Data are shown as means ± SD. B) Capillary:fiber ratio of the occluded (left leg) and nonoccluded (right leg) sides. Capillary:fiber ratio after occlusion (left) was significantly reduced in tg6, whereas in wt and splx the ratio was only slightly and not significantly decreased. Data are shown as means ± SD. Single symbols, P < 0.05; double symbols, P < 0.01; triple symbols, P < 0.001; #, vs. wt; $, vs. splx within the same group of columns; a, P < 0.001 vs. tg6 left; d, P < 0.01; dd, P < 0.001 vs. splx left.

RESULTS

Excessive Erythrocytosis Leads to Impaired Fertility in tg6 Females but Not Males

We bred the transgenic mouse line with excessive erythrocytosis, termed "tg6" [19], by mating transgenic males to WT C57BL/6 females, since successful breeding using tg6 females was a rare event. Histological examination of plug-positive tg6 females revealed that the developing fetuses died around Embryonic Day 9.5, and no labyrinth layer was established. Moreover, at midgestation the decidual arteries had much smaller diameters in tg6 mice compared with WT littermates (supplemental figures available online at www.biolreprod.org). To ensure that oocytes derived from tg6 females had the potential to give rise to normal litters, embryo transfer was performed. To this end, we harvested two-cell embryos from tg6 females previously mated with either WT or tg6 males. Subsequently, 62 embryos were transferred to pseudopregnant surrogate mothers, and 51 viable pups were born, confirming that transgenic embryos isolated from tg6 females were capable of developing to term. Of note, mating between hemizygous tg6 males and tg6 females also gave rise to viable offspring homozygous for the human erythropoietin cDNA (our unpublished observation). Assuming that excessive erythrocytosis directly or indirectly caused the observed subfertility, we reduced the tg6 female's hematocrit by splenectomy, because the spleen is the main organ for extramedullary erythropoiesis [21]. Approximately 2–3 wk after surgery, tg6 females reached hematocrit levels between 0.6 and 0.75 and were successfully mated to WT males. Note that the high erythropoietin plasma levels in tg6 females were not reduced upon splenectomy (RIA; DiaSorin, Stillwater, MN; in mU/ml: WT, 30.3 ± 7.5; tg6, 457.8 ± 172.2; splenectomized tg6, 915.6 ± 229.2), implying that high levels of circulating human erythopoietin was not likely a direct cause of subfertility.

Next, we determined the number of fetuses in each uterine horn at different days of pregnancy in WT, splenectomized tg6, and untreated tg6 mice in their first pregnancy. Within the first 10 days of development, the number of implanted fetuses was similar in all three groups (Table 1). At pregnancy's end, WT and splenectomized tg6 mice delivered a similar number of living pups (8.1 ± 0.74 and 7.86 ± 1.68, respectively). In contrast, most tg6 females aborted during their first pregnancy, and the few that had successful pregnancies delivered a very small number of pups, only some of which (1.63 ± 2.20) were viable. Moreover, the birth weight of the viable pups was significantly lower (1.26 ± 0.05 g) compared with those delivered by WT (1.66 ± 0.09 g) and splenectomized tg6 (1.56 ± 0.07 g) mice (Table 1, bottom). Interestingly, tg6 female mice that had aborted their fetuses during their first pregnancies improved the outcome in the next pregnancies and delivered significantly more viable pups (6.00 ± 2.58) compared with the few tg6 females with successful first pregnancies. Although the number of pups was not significantly different from that of splenectomized tg6 mice, the weight of the pups (1.36 ± 0.12 g)—although slightly elevated—remained significantly lower.

Furthermore, the number of pregnancies within which 100% of the experimental group achieved viable pups was least in WT mice (two pregnancies), slightly higher in splenectomized tg6 mice (three pregnancies), and highest in tg6 mice (four pregnancies; Table 2). Thus, in the first pregnancy, WT mice had the highest success rate, followed by the splenectomized tg6 mice, whereas tg6 mice were considerably less successful.


View this table:
[in this window]
[in a new window]
[Download PPT slide]
  		TABLE 2. Percentage of females that delivered viable pups at different pregnancies.*

Impaired UA Growth in Pregnant tg6 Mice

As shown in Figure 1A, the luminal areas of the UA at gestational age E0 were similar in WT and splenectomized tg6 mice, both being significantly smaller than those of tg6 females without splenectomies. This is in line with the significantly lower numbers of endothelial as well as smooth muscle cells at gestational age E0 in WT compared with untreated tg6 mice (Fig. 2, A and C).

The luminal area of the UA of WT and splenectomized tg6 mice progressively increased throughout the pregnancy (Fig. 1, A and B). Compared with Day 0, the percentage of UA increase in luminal area was significant at Day 9 in WT mice and at Day 11 in splenectomized tg6 animals. In primiparous tg6 females, a significant increase in the luminal area was not observed before Day 10 and, surprisingly, no further growth was seen at the end of pregnancy. In contrast, compared with E0 values, WT and splenectomized tg6 mice had a similar increase in UA luminal area (168% and 177%, respectively) at the end of the pregnancy (Fig. 1B). However, primiparous and multiparous tg6 females modestly increased the luminal area of the UA from fertilization to the day of delivery by 53% and 59%, respectively.

Correspondingly, in WT and splenectomized tg6 mice, the UA wall area progressively increased until the day of delivery (97% and 69%, respectively), whereas in tg6 mice its growth increased only until Day 10 by 36% in the first pregnancy and by 53% in subsequent ones (Fig. 1, C and D). Thus, tg6 mice showed a tendency to enhance wall growth after at least one previous pregnancy. This growth, however, was still significantly lower than that of WT mice.

In all three groups, growth of the UA wall was further examined by counting the ECs and SMCs. Wildtype and splenectomized tg6 mice showed a progressive increase in both ECs and SMCs during pregnancy (Fig. 2). In particular, the percent increase in EC number became significant at Day 9 in WT (35%) and at Day 11 in Splx (27%), whereas the increase in SMC number became significant on Day 11 in WT (23%) and Day 9 in Splx (18%). In contrast, EC and SMC numbers did not change in primiparous tg6 mice during pregnancy as well as on the day of delivery. Wildtype and splenectomized tg6 mice had significantly (56%–78%) higher EC and SMC numbers at the end of pregnancy. Following two or more pregnancies in tg6 mice, numbers of ECs and SMCs at the day of delivery were significantly higher (22% and 34%, respectively) compared with primiparous tg6. However, the total increase in ECs and SMCs remained dramatically lower compared with WT and splenectomized tg6 mice. Taken together, these observations show impaired growth of the UA during pregnancy of tg6 mice suffering from excessive erythrocytosis. As this effect is especially pronounced during the first pregnancy, and the growth of the UA is irreversible after the first pregnancy in mice [28], poor arteriogenesis of the UA is most likely the major cause of abortion in tg6 mice.

Reduced Endothelial Shear Stress in tg6 Mice

As mentioned in the Introduction and explained in Materials and Methods, arteriogenesis is induced by endothelial shear stress that, in turn, is proportional to blood viscosity and mean blood flow velocity and inversely proportional to the vessel radius. Knowing that nulligravida tg6 mice have an increased radius of the UA (Fig. 1A, E0), we determined blood viscosity and mean blood flow velocity.

At physiological shear rates between 11 and 115 sec–1 [35], Splx had an apparent blood viscosity of 9.78–5.51 mPa/sec. This value is 45%–52% higher compared with WT, but 50%–54% lower compared with tg6 mice [21].

As shown in Figure 3A, the mean blood circulating time in virgin mice—calculated from BV and CO [27]—was about 12-fold higher in tg6 compared with WT mice (85.01 sec vs. 7.17 sec) and 7-fold higher than in Splx (11.58 sec). Assuming that the length of the vasculature is not altered following splenectomy, the drop in mean circulating time was equivalent to a 7-fold acceleration of the mean blood flow velocity.

In accordance with our previous results [19], nitrite/nitrate plasma levels (Fig. 3B) were significantly higher in tg6 mice (156.90 ± 28.49 µmol/ml) compared with WT animals (56.75 ± 10.65 µmol/ml). Upon splenectomy and subsequent hematocrit reduction, plasma nitrite/nitrate levels decreased significantly (109.57 ± 16.92 µmol/ml), reaching a value between those of WT and tg6 mice. Because plasma nitrite and nitrate are accepted as indirect measures of nitric oxide, we conclude that the elevated nitric oxide level in tg6 was reduced after splenectomy, resulting in an overall reduction in vessel diameter. This is in accordance with the fact that the lumens of UA at Day 0 were similar in WT and splenectomized tg6 mice, but both were significantly smaller than those of untreated tg6 mice (Fig. 1A, E0).

According to equation 1 mentioned in Materials and Methods, we calculated a 4- to 5-fold lower endothelial shear stress in tg6 mice suffering from excessive erythrocytosis compared with splenectomized tg6 and WT mice, respectively.

Impaired Arteriogenesis in tg6 Mice after Occlusion of the Femoral Artery

To provide further evidence that shear stress is causal for impaired arteriogenesis in tg6 mice suffering from excessive erythrocytosis, we made use of the hind limb occlusion model. After ligation of the femoral artery, blood is forced to pass through collateral vessels to bypass the occlusion. This leads to increased shear stress in the collateral vessels, stimulating outward remodeling [26]. Following occlusion of the left femoral artery in tg6 mice, the muscle capillary density in the occluded left leg was 47% of that of the nonoccluded right leg (Fig. 4A), suggesting a loss of capillaries as a consequence of insufficient blood supply through collateral arteries. Similarly, the capillary:fiber ratio was significantly reduced to about 50% (Fig. 4B). After splenectomy, tg6 mice showed no significant differences in muscle capillary density (Fig. 4A) and capillary:fiber ratio (Fig. 4B) between occluded and nonoccluded legs, paralleling the findings in WT mice. This indicates that after splenectomy of tg6 mice, the functional result of collateral vessel growth is similar to that of WT mice.

Taken together, our data obtained from the uterine and femoral arteries provide convincing evidence for overall impaired arteriogenesis due to reduced shear stress in tg6 mice suffering from excessive erythrocytosis. Accordingly, during pregnancy, this inefficient arterial outward remodeling most probably causes abortion.

DISCUSSION

Unexplained repeated pregnancy loss, IUGR, and preeclampsia are associated with insufficient increases in uterine blood flow during pregnancy [2, 9, 16, 36]. Here, we present evidence that a previously unappreciated reason for these pathologies may be insufficient arteriogenesis of the UA, a process that follows fetal growth with delay. Because arteriogenesis is dependent on vessel wall shear stress [26], we studied transgenic mice that presumably altered this parameter due to erythropoietin-induced excessive erythrocytosis. Female transgenic mice usually abort around midgestation. Maternal problems are causal, as embryo transfer from tg6 females mated with either tg6 or WT males to WT pseudopregnant surrogate mothers results in normal delivery of both hemizygous and homozygous pups.

The subfertility phenotype of tg6 mice was rescued by different approaches that increased uterine blood supply by stimulating arteriogenesis of the uterine arcade. The first strategy was to use a "natural" rescue occurring in response to multiple pregnancies in a single animal. In many mammals, including humans, reproductive outcome improves with subsequent pregnancies [8, 37, 38], most probably because arteriogenesis of the UA is irreversible, as we showed recently in C57BL/6 mice [28]. However, others reported partial regression of the pregnancy-induced outward remodeling of the UA in mice [39, 40]. This difference might be due to a varying genetic background and/or fixation procedure in situ (as we did [28]) or ex situ [39, 40]. Apart from these quantitative differences, there is no doubt that arteriogenesis of the UA is at least not completely reversible. For untreated tg6 mice, this suggests that limited growth of the UA induced by (insufficient) arteriogenesis is additive during subsequent pregnancies, finally resulting in successful pregnancies of all tg6 females.

Another possible way to improve pregnancy outcome in tg6 mice is by splenectomy that does not lower plasma erythropoietin levels but considerably reduces the amount of hematopoietic tissue and, consequently, the hematocrit to levels below 0.75. This, in turn, increases endothelial shear stress by a factor of 4 and is paralleled by enhanced arteriogenesis of the UA, as evident from the enlarged diameter and wall area of the UA along with a corresponding gain in wall cell number. In keeping with this, cell proliferation during the first pregnancy was observed in WT and splenectomized tg6 mice, but not in untreated tg6 mice. Subsequent pregnancies of untreated tg6 females were necessary to induce significant cell proliferation in the UA wall. Apart from the UA, delayed and insufficient arteriogenesis was also observed in virgin tg6 mice following femoral artery occlusion, as indicated by a reduced muscle capillary density and capillary:fiber ratio. In analogy to the improvement in pregnancy outcome, splenectomy in tg6 mice reduced capillary loss in the lower leg muscle close to WT values. These results show that arteriogenesis in tg6 mice is impaired locally not just in the UA but also in the entire systemic vascular bed, making pregnancy-associated hormonal differences an unlikely cause for the poor pregnancy outcome in tg6 mice. Thus, the best explanation for improved arteriogenesis in both the UA and collateral arteries of the leg is that wall shear stress is increased by hematocrit reduction.

Unfortunately, wall shear stress in the UA cannot be measured directly. Therefore, by measuring the parameters that determine wall shear stress (Materials and Methods), including mean circulation time (a measure for average blood flow velocity), whole-blood viscosity, and vessel radius, an estimate was calculated. Splenectomy in tg6 mice reduced whole-blood viscosity to 50%–54% of that of untreated tg6 mice [21, 25]. However, the most prominent effect of the splenectomy-induced hematocrit reduction in tg6 mice was the decrease in mean circulation time by about 86%—close to values found in WT mice and equivalent to a 7-fold acceleration of mean blood flow velocity. Moreover, the diameter of the UA in splenectomized tg6 compared with untreated tg6 mice was significantly smaller and similar to that of WT mice (Fig. 1A, E0). This parallels the significantly reduced plasma nitrate/nitrite levels seen in splenectomized tg6 mice compared with untreated tg6 mice. Taken together, when introducing these parameters into equation 2 mentioned in Materials and Methods, we obtained an estimated 4-fold increase in wall shear stress in the UA of tg6 mice following splenectomy. Calculated wall shear stress in splenectomized tg6 mice is then quite close to that found in WT animals, in which shear stress is nearly 5-fold higher than in untreated tg6 mice.

Although the present results strongly argue for impaired arteriogenesis being the underlying cause for miscarriage in tg6 mice, hormonal factors should be considered. Nienartowicz et al. [41] postulated that UA growth might be induced by hormones from the placenta (e.g., estrogen) via direct diffusion between the UA and vein. However, in light of our data there are some inconsistencies with this hypothesis. First, in virgin tg6 mice, arteriogenesis is also altered in systemic arteries of nonpregnant animals, hence independent of pregnancy-induced hormonal changes. Second, pregnancy hormones should be particularly important in the first third of pregnancy. In tg6 mice, the embryos develop normally in this trimester of pregnancy (Table 1, histological indication of abortion observed only after Day 9; supplemental figures available online at www.biolreprod.org). Thus, pregnancy-associated hormonal changes might be the predominant mechanism in the first trimester of pregnancy in outward remodeling, whereas shear stress may play a more prominent role thereafter. This hypothesis is in line with a previous study demonstrating that UA remodeling in pseudopregnancy is comparable to that in early pregnancy [42]. In that study, the authors found similar, although less pronounced, structural changes within the UA in the first 14 days of pseudopregnancy compared with "normal" pregnant mice. The effect was gone at Day 17 of pseudopregnancy. The latter results support a role for the endocrine changes of early pregnancy and the effect of shear stress in later pregnancy.

A number of studies suggest that endothelial nitric oxide synthase (NOS3) is involved in uterine vascular adaptation. During pregnancy, levels of NOS3 in the UA and nitric oxide in the blood plasma rise [43], inducing vasodilation and increased blood flow. Inhibition of NOS3 during pregnancy causes decreased uterine perfusion [44] and fetal growth restriction [45]. Furthermore, NOS3-deficient mice show impaired remodeling of the UA and deliver 1.6 times fewer viable pups than WT mice [46]. The most important factors stimulating NOS3 synthesis in the UA are estrogens [47, 48] and shear stress [49–51]. As mentioned above, tg6 mice have chronically elevated plasma nitric oxide levels. Thus, early in pregnancy, tg6 might be unable to further increase nitric oxide production under the influence of high estrogen levels. This could impair UA dilation early in the pregnancy, a hypothesis supported by our results: In the first trimester of pregnancy, increase of UA luminal area in tg6 mice is only half of that measured in splenectomized tg6 and WT mice. Consequently, without the initial vasodilation in early pregnancy, blood flow fails to increase, thus further reducing the already low arteriogenic stimulus in the UA of tg6 mice. Therefore, nitric oxide may contribute to the impaired remodeling of the UA in tg6 mice, but other mechanisms must also be involved. This idea is in accordance with the fact that NOS3-deficient mice have only 1.6 times smaller litter sizes [46], whereas tg6 mice have a litter size 5 times smaller, both compared with WT animals. As in tg6 mice, subfertility in women suffering from polycythemia vera or erythrocytosis can be markedly improved just by reducing hematocrit to normal values [14], and patients with severe preeclampsia have significantly elevated hematocrit and hemoglobin values [52]. Pregnancy enhances the (uterine) artery vasodilator response to flow [51, 53], presumably by estrogen-dependent NOS3 induction, as stated above. In turn, small arteries of women suffering from unexplained repeated pregnancy loss, IUGR, or preeclampsia have a blunted shear stress-induced dilation [49, 54]. For UA adaptation, pregnancy-associated hormonal changes may be more important at the beginning of pregnancy, whereas later—during rapid fetal growth—shear stress-induced outward remodeling might be the predominant mechanism. This hypothesis is in line with the fact that the above-mentioned pathologies usually occur in the second half of pregnancy, when fetal growth accelerates considerably.

We also analyzed the impact of impaired shear stress in the UA on the expression level of selected shear stress-regulated genes [55, 56] that are thought to play a role in arteriogenesis [26, 57]. Expression level of the diestrus state in virgin mice was compared to that measured instantly after parturition for the following genes: inhibitor of metalloproteinase 1 (Timp1), endothelial nitric oxide synthase (Nos3), colony-stimulating factor 2 (Csf2), and matrix metalloproteinases 2 and 9 (Mmp2 and Mmp9), all normalized to the endothelial cell marker Tie2. Unfortunately, these experiments failed to provide clear and significant results, although a trend in normalization of shear stress-regulated gene expression was observed after splenectomy in tg6. On one hand, this might be due to the limited amount of tissue that can be obtained from the murine UA. On the other hand a recent study on functional genomics of flow-induced inward and outward remodeling suggests that there is quite little gene regulation in outward remodeling [58]. In that study, at different time points after induction of outward remodeling, maximally 1% of 14 633 cDNAs were differentially regulated more than two times. This, the largest effect during outward remodeling, was seen after 32 days—at earlier time points, maximally 0.5% genes were differentially expressed. The pregnancy of the mouse, however, lasts only 21 days. Moreover, this study shows that for selected genes that had been tested in RT-PCR a large scatter and inconsistent expression pattern among individual animals (upregulation as well as downregulation in different animals for the same gene under the same conditions). We have observed exactly the same with our samples. This, together with minor expression changes, might explain why we could not obtain significant results.

Our data suggest an important role for shear stress-induced outward remodeling (arteriogenesis) in successful pregnancy outcome in mice. Assuming that our observations parallel the situation in women, impaired arteriogenesis of the UA due to abnormal flow mechanics may be a previously unrecognized cause for unexplained repeated pregnancy loss, IUGR—especially at high altitudes or in other cases of (excessive) erythrocytosis [14, 59]—and, possibly, also preeclampsia. This appears to apply particularly to the first pregnancy that could act as a physiological stimulus for complete maturation of the uterine arcade [28] through arteriogenesis, explaining the higher incidence of these pathologies in first pregnancies.

ACKNOWLEDGMENTS

The authors thank J. Schenkel for his useful advice in mouse breeding, Th. Rülicke for his advice in embryo transfer, O. Baum for his advice on the unspecific alkaline phosphatase staining, M. Hässig for advice concerning the biostatistics, and M. Tissot van Patot for proofreading the manuscript.

FOOTNOTES

1Supported by the Swiss National Science Foundation (3100A0–104242), Stiftung für wissenschaftliche Forschung an der Universität Zürich, and University Research Priority Program "Integrative Human Physiology" at the ZIHP to J.V. Back

Correspondence: 2Johannes Vogel, Institute of Veterinary Physiology, Vetsuisse Faculty, University of Zürich, Winterthurerstr. 260, CH-8057 Zürich, Switzerland. FAX: 41 44 6358932; e-mail: jvogel{at}vetphys.uzh.ch

Received: 12 September 2007.

First decision: 29 October 2007.

Accepted: 25 January 2008.

REFERENCES

  1. Han V. Intrauterine growth restriction and mechanism of fetal growth. In: Knobill E, Neill JD (eds.), Encyclopedia of Reproduction. New York:: Academic Press; 1998:877–892.
  2. Konje JC, Howarth ES, Kaufmann P, Taylor DJ. Longitudinal quantification of uterine artery blood volume flow changes during gestation in pregnancies complicated by intrauterine growth restriction. BJOG 2003; 110:301–305.[CrossRef][Medline]
  3. Aardema MW, Oosterhof H, Timmer A, van RI, Aarnoudse JG. Uterine artery Doppler flow and uteroplacental vascular pathology in normal pregnancies and pregnancies complicated by pre-eclampsia and small for gestational age fetuses. Placenta 2001; 22:405–411.[CrossRef][Medline]
  4. Kliman HJ. Uteroplacental blood flow. The story of decidualization, menstruation, and trophoblast invasion. Am J Pathol 2000; 157:1759–1768.[Free Full Text]
  5. Coulam CB. Epidemiology of recurrent spontaneous abortion. Am J Reprod Immunol 1991; 26:23–27.[Medline]
  6. Huang DY, Usher RH, Kramer MS, Yang H, Morin L, Fretts RC. Determinants of unexplained antepartum fetal deaths. Obstet Gynecol 2000; 95:215–221.[CrossRef][Medline]
  7. Roman E, Doyle P, Beral V, Alberman E, Pharoah P. Fetal loss, gravidity, and pregnancy order. Early Hum Dev 1978; 2:131–138.[CrossRef][Medline]
  8. Khong TY, Adema ED, Erwich JJ. On an anatomical basis for the increase in birth weight in second and subsequent born children. Placenta 2003; 24:348–353.[CrossRef][Medline]
  9. Zamudio S. High-altitude hypoxia and preeclampsia. Front Biosci 2007; 12:2967–2977.[CrossRef][Medline]
  10. Moore LG. Fetal growth restriction and maternal oxygen transport during high altitude pregnancy. High Alt Med Biol 2003; 4:141–156.[CrossRef][Medline]
  11. Gonzales GF. Peruvian contributions to the study on human reproduction at high altitude: From the chronicles of the Spanish conquest to the present. Respir Physiol Neurobiol 2007; 158:172–179.[CrossRef][Medline]
  12. Zamudio S, Palmer SK, Droma T, Stamm E, Coffin C, Moore LG. Effect of altitude on uterine artery blood flow during normal pregnancy. J Appl Physiol 1995; 79:7–14.[Abstract/Free Full Text]
  13. Tissot van Patot M, Grilli A, Chapman P, Broad E, Tyson W, Heller DS, Zwerdlinger L, Zamudio S. Remodelling of uteroplacental arteries is decreased in high altitude placentae. Placenta 2003; 24:326–335.[CrossRef][Medline]
  14. Robinson S, Bewley S, Hunt BJ, Radia DH, Harrison CN. The management and outcome of 18 pregnancies in women with polycythemia vera. Haematologica 2005; 90:1477–1483.[Abstract/Free Full Text]
  15. Goswamy RK, Williams G, Steptoe PC. Decreased uterine perfusion–a cause of infertility. Hum Reprod 1988; 3:955–959.[Abstract/Free Full Text]
  16. Nakatsuka M, Habara T, Noguchi S, Konishi H, Kudo T. Impaired uterine arterial blood flow in pregnant women with recurrent pregnancy loss. J Ultrasound Med 2003; 22:27–31.[Abstract/Free Full Text]
  17. Dokras A, Hoffmann DS, Eastvold JS, Kienzle MF, Gruman LM, Kirby PA, Weiss RM, Davisson RL. Severe feto-placental abnormalities precede the onset of hypertension and proteinuria in a mouse model of preeclampsia. Biol Reprod 2006; 75:899–907.[Abstract/Free Full Text]
  18. Madazli R, Somunkiran A, Calay Z, Ilvan S, Aksu MF. Histomorphology of the placenta and the placental bed of growth restricted foetuses and correlation with the Doppler velocimetries of the uterine and umbilical arteries. Placenta 2003; 24:510–516.[CrossRef][Medline]
  19. Ruschitzka FT, Wenger RH, Stallmach T, Quaschning T, de Wit C, Wagner K, Labugger R, Kelm M, Noll G, Rulicke T, Shaw S, Lindberg RL, et al. Nitric oxide prevents cardiovascular disease and determines survival in polyglobulic mice overexpressing erythropoietin. Proc Natl Acad Sci U S A 2000; 97:11609–11613.[Abstract/Free Full Text]
  20. Stallmach T, Hebisch G. Placental pathology: its impact on explaining prenatal and perinatal death. Virchows Arch 2004; 445:9–16.[Medline]
  21. Vogel J, Kiessling I, Heinicke K, Stallmach T, Ossent P, Vogel O, Aulmann M, Frietsch T, Schmid-Schonbein H, Kuschinsky W, Gassmann M. Transgenic mice overexpressing erythropoietin adapt to excessive erythrocytosis by regulating blood viscosity. Blood 2003; 102:2278–2284.[Abstract/Free Full Text]
  22. Caniggia I, Mostachfi H, Winter J, Gassmann M, Lye SJ, Kuliszewski M, Post M. Hypoxia-inducible factor-1 mediates the biological effects of oxygen on human trophoblast differentiation through TGFbeta(3). J Clin Invest 2000; 105:577–587.[Medline]
  23. Wagner KF, Katschinski DM, Hasegawa J, Schumacher D, Meller B, Gembruch U, Schramm U, Jelkmann W, Gassmann M, Fandrey J. Chronic inborn erythrocytosis leads to cardiac dysfunction and premature death in mice overexpressing erythropoietin. Blood 2001; 97:536–542.[Abstract/Free Full Text]
  24. Bogdanova A, Mihov D, Lutz H, Saam B, Gassmann M, Vogel J. Enhanced erythro-phagocytosis in polycythemic mice overexpressing erythropoietin. Blood 2007; 110:762–769.[Abstract/Free Full Text]
  25. Frietsch T, Maurer MH, Vogel J, Gassmann M, Kuschinsky W, Waschke KF. Reduced cerebral blood flow but elevated cerebral glucose metabolic rate in erythropoietin overexpressing transgenic mice with excessive erythrocytosis. J Cereb Blood Flow Metab 2007; 27:469–476.[CrossRef][Medline]
  26. Schaper W, Scholz D. Factors regulating arteriogenesis. Arterioscler Thromb Vasc Biol 2003; 23:1143–1151.[Abstract/Free Full Text]
  27. Juchems R. Hämodynamische Korrelation von Teilgröβen der Indikatorverdünnungskurve unter besonderer Berücksichtigung der mittleren Kreislaufzeit. Verh Dtsch Ges Kreislaufforsch 1966; 32:261–266.[Medline]
  28. Wassel K, Kuhn G, Gassmann M, Vogel J. Permanently increased conductance of the murine uterine arcade after the first pregnancy. Eur J Morphol 2006; 42:225–232.[CrossRef]
  29. Rulicke T, Haenggli A, Rappold K, Moehrlen U, Stallmach T. No transuterine migration of fertilised ova after unilateral embryo transfer in mice. Reprod Fertil Dev 2006; 18:885–891.[CrossRef][Medline]
  30. Miyazaki S, Tanebe K, Sakai M, Michimata T, Tsuda H, Fujimura M, Nakamura M, Kiso Y, Saito S. Interleukin 2 receptor gamma chain (gamma(c)) knockout mice show less regularity in estrous cycle but achieve normal pregnancy without fetal compromise. Am J Reprod Immunol 2002; 47:222–230.[CrossRef][Medline]
  31. Markee JE. Rhythmic vascular uterine changes. Am J Physiol 1932; 256:E690–E698.
  32. Forssmann WG, Ito S, Weihe E, Aoki A, Dym M, Fawcett DW. An improved perfusion fixation method for the testis. Anat Rec 1977; 188:307–314.[CrossRef][Medline]
  33. Da Silva-AL, Baum O, Zakrzewicz A, Pries AR. Vascular endothelial growth factor is expressed in endothelial cells isolated from skeletal muscles of nitric oxide synthase knockout mice during prazosin-induced angiogenesis. Biochem Biophys Res Commun 2002; 297:1270–1276.[CrossRef][Medline]
  34. Vogel J. Measurement of cardiac output in small laboratory animals using recordings of blood conductivity. Am J Physiol Heart Circ Physiol 1997; 273:H2520–H2527.[Abstract/Free Full Text]
  35. Erslev AJ, Caro J, Besarab A. Why the kidney? Nephron 1985; 41:213–216.[Medline]
  36. Jirous J, Diejomaoh M, Al-Othman S, Al-Abdulhadi F, Al-Marzouk N, Sugathan T. A correlation of the uterine and ovarian blood flows with parity of nonpregnant women having a history of recurrent spontaneous abortions. Gynecol Obstet Invest 2001; 52:51–54.[CrossRef][Medline]
  37. van der Steen HAM. Maternal influence mediated by litter size during the suckling period on reproduction traits in pigs. Livest Prod Sci 1985; 13:147–153.[CrossRef]
  38. Robinson R, Cox HW. Reproductive performance in a cat colony over a 10-year period. Lab Anim 1970; 4:99–112.[Abstract/Free Full Text]
  39. Hilgers RH, Schiffers PM, Aartsen WM, Fazzi GE, Smits JF, De Mey JGR. Tissue angiotensin-converting enzyme in imposed and physiological flow-related arterial remodeling in mice. Arterioscler Thromb Vasc Biol 2004; 24:892–897.[Abstract/Free Full Text]
  40. Hilgers RH, Bergaya S, Schiffers PM, Meneton P, Boulanger CM, Henrion D, Levy BI, De Mey JGR. Uterine artery structural and functional changes during pregnancy in tissue kallikrein-deficient mice. Arterioscler Thromb Vasc Biol 2003; 23:1826–1832.[Abstract/Free Full Text]
  41. Nienartowicz A, Link S, Moll W. Adaptation of the uterine arcade in rats to pregnancy. J Dev Physiol 1989; 12:101–108.[Medline]
  42. van der Heijden OW, Essers YP, Spaanderman ME, De Mey JGR, van Eys GJ, Peeters LL. Uterine artery remodeling in pseudopregnancy is comparable to that in early pregnancy. Biol Reprod 2005; 73:1289–1293.[Abstract/Free Full Text]
  43. Magness RR, Sullivan JA, Li Y, Phernetton TM, Bird IM. Endothelial vasodilator production by uterine and systemic arteries. VI. Ovarian and pregnancy effects on eNOS and NO(x). Am J Physiol Heart Circ Physiol 2001; 280:H1692–H1698.[Abstract/Free Full Text]
  44. Miller SL, Jenkin G, Walker DW. Effect of nitric oxide synthase inhibition on the uterine vasculature of the late-pregnant ewe. Am J Obstet Gynecol 1999; 180:1138–1145.[CrossRef][Medline]
  45. Molnar M, Suto T, Toth T, Hertelendy F. Prolonged blockade of nitric oxide synthesis in gravid rats produces sustained hypertension, proteinuria, thrombocytopenia, and intrauterine growth retardation. Am J Obstet Gynecol 1994; 170:1458–1466.[Medline]
  46. van der Heijden OW, Essers YP, Fazzi G, Peeters LL, De Mey JGR, van Eys GJ. Uterine artery remodeling and reproductive performance are impaired in endothelial nitric oxide synthase-deficient mice. Biol Reprod 2005; 72:1161–1168.[Abstract/Free Full Text]
  47. Vagnoni KE, Shaw CE, Phernetton TM, Meglin BM, Bird IM, Magness RR. Endothelial vasodilator production by uterine and systemic arteries. III. Ovarian and estrogen effects on NO synthase. Am J Physiol 1998; 275:H1845–H1856.[Medline]
  48. Chen DB, Bird IM, Zheng J, Magness RR. Membrane estrogen receptor-dependent extracellular signal-regulated kinase pathway mediates acute activation of endothelial nitric oxide synthase by estrogen in uterine artery endothelial cells. Endocrinology 2004; 145:113–125.[Abstract/Free Full Text]
  49. Cockell AP, Poston L. Flow-mediated vasodilatation is enhanced in normal pregnancy but reduced in preeclampsia. Hypertension 1997; 30:247–251.[Abstract/Free Full Text]
  50. Joyce JM, Phernetton TM, Shaw CE, Modrick ML, Magness RR. Endothelial vasodilator production by uterine and systemic arteries. IX. eNOS gradients in cycling and pregnant ewes. Am J Physiol Heart Circ Physiol 2002; 282:H342–H348.[Abstract/Free Full Text]
  51. Cockell AP, Poston L. 17Beta-estradiol stimulates flow-induced vasodilatation in isolated small mesenteric arteries from prepubertal femal rats. Am J Obstet Gynecol 1997; 177:1432–1438.[CrossRef][Medline]
  52. Heilmann L, Rath W, Pollow K. Hemorheological changes in women with severe preeclampsia. Clin Hemorheol Microcirc 2004; 31:49–58.[Medline]
  53. Mateev S, Sillau AH, Mouser R, McCullough RE, White MM, Young DA, Moore LG. Chronic hypoxia opposes pregnancy-induced increase in uterine artery vasodilator response to flow. Am J Physiol Heart Circ Physiol 2003; 284:H820–H829.[Abstract/Free Full Text]
  54. Yoshida A, Nakao S, Kobayashi H, Kobayashi M. Noninvasive assessment of flow-mediated vasodilation with 30-MHz transducer in pregnant women. Hypertension 1998; 31:1200–1201.[Free Full Text]
  55. Bongrazio M, Da Silva AL, Bergmann EC, Baum O, Hinz B, Pries AR, Zakrzewicz A. Shear stress modulates the expression of thrombospondin-1 and CD36 in endothelial cells in vitro and during shear stress-induced angiogenesis in vivo. Int J Immunopathol Pharmacol 2006; 19:35–48.[Medline]
  56. Baum O, Da Silva-AL, Willerding G, Wockel A, Planitzer G, Gossrau R, Pries AR, Zakrzewicz A. Endothelial NOS is main mediator for shear stress-dependent angiogenesis in skeletal muscle after prazosin administration. Am J Physiol Heart Circ Physiol 2004; 287:H2300–H2308.[Abstract/Free Full Text]
  57. De Mey JGR, Schiffers PM, Hilgers RH, Sanders MM. Toward functional genomics of flow-induced outward remodeling of resistance arteries. Am J Physiol Heart Circ Physiol 2005; 288:H1022–H1027.[Abstract/Free Full Text]
  58. Wesselman JP, Kuijs R, Hermans JJ, Janssen GM, Fazzi GE, van EH, Evelo CT, Struijker-Boudier HA, De MJG. Role of the Rhoa/Rho kinase system in flow-related remodeling of rat mesenteric small arteries in vivo. J Vasc Res 2004; 41:277–290.[CrossRef][Medline]
  59. Kametas NA, Krampl E, McAuliffe F, Rampling MW, Nicolaides KH. Pregnancy at high altitude: a hyperviscosity state. Acta Obstet Gynecol Scand 2004; 83:627–633.[CrossRef][Medline]




This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow [Supplemental Data]
Right arrow All Versions of this Article:
78/6/1049    most recent
biolreprod.107.065532v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow My Folders
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gassmann, M.
Right arrow Articles by Vogel, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gassmann, M.
Right arrow Articles by Vogel, J.
Agricola
Right arrow Articles by Gassmann, M.
Right arrow Articles by Vogel, J.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS