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NORs and their transcription competence during the cell cycle.

In human cells ribosomal genes are organized as clusters, NORs, situated on the short arms of acrocentric chromosomes. It was found that essential components of the RNA polymerase I transcription machinery, including UBF, can be detected on some NORs, termed "competent" NORs, during mitosis. The competent NORs are believed to be transcriptionally active during interphase. However, since individual NORs were not observed in the cell nucleus, their interphase status remains unclear. To address this problem, we detected the competent NORs by two commonly used methods, UBF immunofluorescence and silver staining, and combined them with FISH for visualization of rDNA and/or specific chromosomes. We found that the numbers of competent NORs on specific chromosomes were largely conserved in the subsequent cell cycles, with certain NOR-bearing homologues displaying a very stable pattern of competence. Importantly, those and only those NORs that were loaded with UBF incorporated bromo-uridine in metaphase after stimulation with roscovitine and in telophase, suggesting that competent and only competent NORs contain ribosomal genes transcriptionally active during interphase. Applying premature chromosome condensation with calyculin A, we visualized individual NORs in interphase cells, and found the same pattern of competence as observed in the mitotic chromosomes.

Cell Cycle↗

Using ultrasound measurements to predict body composition of yearling bulls.

Carcass traits have been successfully used to determine body composition of steers. Body composition, in turn, has been used to predict energy content of ADG to compute feed requirements of individual animals fed in groups. This information is used in the Cornell value discovery system (CVDS) to predict DM required (DMR) for the observed animal performance. In this experiment, the prediction of individual DMR for the observed performance of group-fed yearling bulls was evaluated using energy content of gain, which was based on ultrasound measurements to estimate carcass traits and energy content of ADG. One hundred eighteen spring-born purebred and crossbred bulls (BW = 288 +/- 4.3 kg) were sorted visually into 3 marketing groups based on estimated days to reach USDA low Choice quality grade. The bulls were fed a common high-concentrate diet in 12 slatted-floor pens (9 to 10 head/pen). Ultrasound measurements including back-fat (uBF), rump fat, LM area (uLMA), and intramuscular fat were taken at approximately 1 yr of age. Carcass measurements including HCW, backfat over the 12th to 13th rib (BF), marbling score (MRB), and LM area (LMA) were collected for comparison with ultrasound data for predicting carcass composition. The 9th to 11th-rib section was removed and dissected into soft tissue and bone for determination of chemical composition, which was used to predict carcass fat and empty body fat (EBF). The predicted EBF averaged 23.7 +/- 4.0%. Multiple regression analysis indicated that carcass traits explained 72% of the variation in predicted EBF (EBF = 16.0583 + 5.6352 x BF + 0.01781 x HCW + 1.0486 x MRB - 0.1239 x LMA). Because carcass traits are not available on bulls intended for use as herd sires, another equation using predicted HCW (pHCW) and ultrasound measurements was developed (EBF = 39.9535 x uBF - 0.1384 x uLMA + 0.0867 x pHCW - 0.0897 x uBF x pHCW - 1.3690). This equation accounted for 62% of the variation in EBF. The use of an equation to predict EBF developed with steer composition data overpredicted the EBF predicted in these experiments (28.7 vs. 23.7%, respectively). In a validation study with 37 individually fed bulls, the use of the ultrasound-based equation in the CVDS to predict energy content of gain accounted for 60% of the variation in the observed efficiency of gain, with 1.5% bias, and identified 3 of the 4 most efficient bulls.

Adipose Tissue↗

Local and systemic effects of intrauterine estradiol-17 beta on luteal function of nonpregnant sows.

This study was conducted to determine if intrauterine injections of estradiol-17 beta (E2 beta) could maintain luteal function in nonpregnant sows. Eight sows were assigned to surgery on d 8 or 9 of the estrous cycle (first day of estrus = d 0). At surgery, cannulas were inserted bilaterally into the uterine artery (UA) and common utero-ovarian vein (UOV), as well as into the lumen of each isolated uterine horn. Electromagnetic blood flow transducers were placed around the middle uterine artery supplying each horn of four sows. After surgery, sows were assigned randomly to receive either intrauterine injections of vehicle (.9% NaCl) into both uterine horns (control sows) or E2 beta into one uterine horn (375 ng/injection) and vehicle into the other (treated sows) every 6 h from 1200 h on d 11 to 1200 h on d 15. Uterine blood flow (UBF) was quantified, and blood was sampled from the UA and UOV, periodically, from d 11 to 18. On d 18, sows were ovariectomized and corpora lutea (CL) were weighed. Blood plasma was subsequently analyzed for progesterone (P4) and prostaglandin F (PGF) by radioimmunoassay. Control sows had smaller (P less than .05) CL than treated sows on d 18 (3,046 +/- 614 vs 4,451 +/- 324 mg). Progesterone concentrations in UOV blood of treated sows tended to increase from d 11 (469 +/- 110 ng/ml) to 18 (626 +/- 209 ng/ml) while P4 in UOV blood of control sows decreased markedly (P less than .01) from d 11 (579 +/- 79 ng/ml) to 18 (14 +/- 5 ng/ml). In addition, UOV P4 concentrations on the E2-beta-injected side of treated sows were higher (P less than .05) than those on the vehicle-injected side from d 14 to 18. The UBF of two treated sows increased eightfold to 10-fold within 12 h of the first E2 beta injection and remained elevated through d 17, while UBF of two control sows remained constant. Prostaglandin F concentrations in UOV blood of treated sows were lower (P less than .05) than in UOV blood of control sows on d 14 and 15. There was no effect of side of E2 beta injection on PGF concentrations, which were similar in UOV blood draining both uterine horns of treated sows. Thus, the local effect of E2 beta in stimulating P4 secretion by the ipsilateral ovary is not due to reduced PGF concentrations in UOV blood draining the E2 beta-injected horn.

Animals↗

Role of adrenergic receptors in mediating estradiol-17 beta-stimulated increases in uterine blood flow of cows.

This study was conducted to investigate the association between estradiol-17 beta (E2 beta) and periarterial alpha and beta-adrenergic receptors in altering blood flow to the bovine uterus. Three nonpregnant Hereford cows were ovariectomized, and an electromagnetic blood flow transducer was placed around the middle uterine artery supplying one uterine horn. A catheter was then placed into a branch of the same artery for infusion of drugs or vehicle. Beginning 3 wk after surgery, uterine blood flow (UBF) of each cow was recorded for 5 min at 20-min intervals throughout a 160-min period three times weekly for 6 wk. Vehicle (.9% NaCl), phentolamine (PHEN, 1 or 10 micrograms) or propranolol (PROP, 1 or 10 micrograms) was infused for 5 min beginning 20 min after the initial UBF measurements, while vehicle or E2 beta (1 microgram) was infused for 5 min beginning at 40 min. Within a week, the first and third 160-min periods contained the same treatment (vehicle or E2 beta), and the second period consisted of vehicle or E2 beta plus PHEN or PROP, allowing for direct comparison of periods 1 and 3 with period 2. Twenty minutes after infusion of E2 beta, UBF was elevated (26.8 +/- 5.4 ml/min; P less than .05) over baseline, reaching a maximal increase at 40 min before starting to decline by 120 min. Uterine blood flow increased (39.2 +/- 7.6 ml/min; P less than .01) during the 5-min infusion of PHEN, and thereafter the magnitude and pattern were similar to those resulting from E2 beta treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Lack of peripheral sympathetic control of uterine blood flow during acute heat stress.

Peripheral alpha- and beta-adrenergic control of uterine blood flow (UBF) during acute heat stress of the gravid ewe was investigated. An electromagnetic blood flow probe was surgically implanted around the left miduterine artery and catheters inserted in the left carotid artery and right jugular vein in ewes between d 120 and 130 of gestation. Four or more days postsurgery, ewes were fitted with instruments to measure rectal temperature (Tr), heart rate (HR), respiratory rate (RR), blood pressure (BP) and UBF. One-half hour after instrument calibration, a 15-min thermoneutral control period was initiated with carotid artery blood samples taken at 5-min intervals for pH and PCO2 determinations. Ewes were then subjected to a heat challenge that reached 40 C at 2 h. All physiological data were recorded every 5 min as 1-min mean values. In seven experiments on five ewes, an alpha-adrenergic blocking drug, phenoxybenzamine (PB) was infused at 1 mg/min for 15 min subsequent to maximum depression of UBF. A beta-adrenergic blocking drug, propranolol (PR) was infused at .35 mg/min for 15 min in eight experiments on five ewes. Analysis of variance comparisons were made between the control period and heat stress infusion periods within the PB and PR experiments. Further comparisons were made between the start and 5, 10 or 15 min of PB or PR infusion in order to test drug effects during an acute heat stress. Rectal temperature HR, RR and arterial pH were higher (P less than .05) at the start of PR and PB infusions than during the thermoneutral control period.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

[Ultrastructural localization of transcription sites of rRNA genes in the nucleolus of wheat].

There were no definite conclusions about transcription sites of rRNA genes in nucleoli of eukaryotes for a long time. We used the wheat as specimen and observed ultrastructure of chromatin in FC of nucleoli by conventional transmission electron microscope. And we employed anti-DNA antibodies to analyze the distribution of DNA in nucleoli, and found that DNA located in FC, DFC and the transitional region between them. Using anti-UBF antibodies to study localization of RNA polymerase I transcription factor UBF in nucleoli, we observed that UBF located in DFC and the transitional region between DFC and FC in wheat, but not in FC. Furthermore, with anti-RNA/DNA hybrid antibodies, we directly and selectively labeled the transcription sites of rRNA genes of nucleoli and revealed that it located in DFC and the transitional region between DFC and FC in wheat.

Cell Nucleolus↗

Affinity fractionation and characterization of chick brain synaptosomes.

Chick brain synaptosomes were fractionated by affinity chromatography on concanavalin A-Sepharose. Three subfractions were obtained. One, designated UBF, was not bound to the affinity adsorbent and represented 36% of the total synaptosomal protein treated with the beads. A second fraction, designated BF1, adhered to concanavalin A-Sepharose exclusively through its carbohydrate recognition site. The third fraction, called BF2, bound to the beads through hydrophobic interactions and represented about 20% of the total synaptosomal protein. About 20% of the total synaptosomal protein was found to be retarded on three ligand-less gels, with potential for only hydrophobic interactions. This binding can be reversed, however, by ethylene glycol, a result indicating hydrophobic binding sites on the synaptosomes. Enzyme marker studies and electron microscopy showed differences between UBF, BF1, and BF2, mainly with respect to mitochondrial contamination. Binding studies with [3H]-Con A show the absence of Con A-specific carbohydrates from the surface of UBF or BF2. As expected strong and specific binding between [3H]-Con A and [3H] BF1 was observed. These findings are discussed in relation to a model for the interior working of the synaptosomes.

Absorption↗

Comparative study of prostaglandin I2 (PG I2) and thromboxane A2 (TXA2) synthetase inhibitor (OKY-1581) on hemodynamics in pregnant dogs.

Effects of intravenous injections of prostaglandin I2 (PG I2) and thromboxane A2 (TXA2) synthetase inhibitor (OKY-1581) on mean arterial pressure (MAP), cardiac output (CO), heart rate (HR), renal blood flow (RBF), and uterine blood flow (UBF) were investigated in the anesthetized pregnant dog. A dose-dependent fall in MAP was observed with these two agents. HR was almost unchanged by both PG I2 and TXA2 synthetase inhibitor. PG I2 and TXA2 synthetase inhibitor produced increases in CO and RBF in a dose-dependent manner. PG I2 caused a dose-dependent decrease in UBF, while TXA2 synthetase inhibitor was followed by an insignificant decrease in UBF. PG I2 and TXA2 synthetase inhibitor did not induce any increase in intrauterine pressure (IUP). The possibility of treatment of pregnancy-induced hypertension with PG I2 or TXA2 synthetase inhibitor is discussed.

Acrylates↗

[Effect of nicotine on uterine blood flow and antagonistic effect of prostaglandin I2 derivative (OP-41483) in pregnant ewes].

In order to elucidate the mechanism of the detrimental effect of smoking on uteroplacental circulation in pregnant women, and to confirm the protective effect of PGI2 derivative (OP-41483) against the effect, hemodynamic responses to various doses of nicotine infusion (0.25-1.0 mg/min) were measured before and during the OP-41483 infusion in chronically instrumented pregnant ewes. Moreover, the isometric tension responses of spiral strips of sow uterine arteries to the nicotine and norepinephrine perfusion were also measured using an in vitro technique. The results were as follows: Maternal mean arterial blood pressure (MAP) and the cardiac output were increased by the intravenous infusion of various doses of nicotine; however the uterine blood flow (UBF) decreased consistently in a dose-dependent fashion, and it decreased 20.4% from the control level following the infusion of 1.0 mg/min nicotine, suggesting a detrimental effect on the fetus. During the infusion of OP-41483 (25 micrograms/min), nicotine induced MAP increases were suppressed at all test doses and the decrease in UBF was lessened by 22% of control delta UBF on doses of 1.0 mg/min nicotine. In the muscle chamber, the tension increase in uterine artery strips of nonpregnant sows to various nicotine concentrations (10(-7)-10(-4) M) were suppressed by the preliminary treatment with phentolamine (0.1 mg/min), and the responses to norepinephrine were also suppressed by the preliminary treatment with a low concentration of nicotine (10(-6) M) in the buffer bath.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Control of uterine and ovarian blood flow throughout the estrous cycle and pregnancy of ewes, sows and cows.

Current investigations strongly indicate a relationship between the function of adrenergic (vasoconstrictor) nerves innervating uterine and ovarian arteries and local concentrations of estrogen and progesterone. During the estrous cycle of ewes, cows and sows, the higher the estrogen:progesterone ratio in systemic blood, the greater is the quantity of blood flowing through the uterine vascular bed. When converted to a catechol form, estrogen may reduce uterine vasoconstriction by binding to and suppressing perivascular alpha-adrenergic receptor activity. Progesterone, in contrast to estrogen, augments the responsiveness of vascular smooth muscle to norepinephrine. Lymphatic vessels, which are in close linear apposition to the adventitia of the uterine vasculature may serve to transport steroids to the periarterial nerves. Vasodilation associated with steroid-induced changes in autonomic function appears to be modulated and amplified by estrogen-dependent changes in prostaglandin biosynthesis. During early pregnancy in ewes, cows and sows, vasodilation, mediated by the conceptus, occurs in the luteal and (or) uterine vascular beds on days critical for continuation of pregnancy in each species. In cows and sows, this vasodilatory effect of the conceptus is associated with increased concentrations of estrogens in the uterine lumen, as well as the lymph and blood draining the uterus. After the initial increase in blood flow to the uterus during early pregnancy, changes in the estrogen:progesterone ratio in fetal and maternal fluids appear to be unrelated to changes in uterine blood flow (UBF). This lack of association between the estrogen:progesterone ratio and UBF may result from a progressive reduction in number of adrenergic nerves observed in the uterus throughout pregnancy. If one accepts that the estrogen:progesterone ratio controls UBF through alterations in the function of periarterial adrenergic nerves, the impaired function of the nerves during mid and late gestation may preclude the effects of these steroids.

Animals↗

Decidua-associated changes in guinea pig uterine blood flow and volume: relation to uterine norepinephrine concentrations.

Changes in uterine blood flow (UBF) and uterine blood volume (UBV) during decidual tissue (DT) formation in the guinea pig were assessed at 2, 6, and 10 days postuterine trauma (PT). Uterine weight increased steadily between days 2 and 10 PT in DT-bearing animals as compared with the constant uterine weights observed in controls. Both UBF and UBV levels were elevated between days 2 and 10 PT in DT-bearing animals as compared with controls with the vascular changes being histologically related to the progressive stromal differentiation. Uterine norepnephrine (NE) levels were significantly (P less than or equal to 0.05-0.01) depressed in the hyperemic, DT-bearing uteri as compared with controls. These results indicate that the uterine hyperemia associated with DT formation in the guinea pig involves a sustained increase in uterine vascular volume as well as vascular perfusion rate under conditions of depressed uterine NE levels. These events are intimately associated with the support of stromal differentiation in the guinea pig.

Animals↗

Downregulation of the upstream binding factor1 by glycogen synthase kinase3beta in myeloid cells induced to differentiate.

The upstream binding factor 1 (UBF1), one of the proteins that regulate the activity of RNA polymerase I, is downregulated in 32D myeloid cells induced to differentiate into granulocytes, either by the type 1 insulin-like growth factor (IGF-1) or the granulocytic colony stimulating factor (G-CSF). Downregulation of UBF1 is largely due to protein degradation, while mRNA levels are not affected. Inhibition of UBF1 degradation by lithium chloride (LiCl)and lactacystin suggest a role of glycogen synthase kinase beta (GSK3beta) in a proteasome-dependent degradation of UBF. GSK3beta phosphorylates in vitro and in vivo the UBF protein, which has five putative motifs for phosphorylation by GSK3beta. Elimination and/or mutations of these motifs stabilize the UBF1 protein even in cells induced to differentiate. Conversely, a stably transfected, constitutively active GSK3beta accelerates the downregulation of UBF1. We show further that activation of the differentiating protein C/EPBalpha in 32D cells transformed by the oncogenic BCR/ABL protein causes downregulation of UBF1. Finally, inhibition of differentiation of myeloid cells by a dominant negative mutant of Stat3 stabilizes the UBF1 protein, while rapamycin-induced differentiation of myeloid cells downregulates UBF1 levels. Taken together, our results indicate that the induction of granulocytic differentiation in 32D murine myeloid cells causes the degradation of UBF1, via GSK3beta and the proteasome pathway.

Animals↗

Nucleolar ultrastructure and protein allocation in in vitro produced porcine embryos.

The nucleolus formation was studied as an indirect marker of the ribosomal RNA (rRNA) genes activation in porcine embryos following oocyte maturation, fertilization, and culture in vitro. Nucleologenesis was assessed by transmission electron microscopy (TEM), light microscopical autoradiography following 20 min of 3H-uridine incubation, and immunocytochemical localization of key nucleolar proteins involved in rRNA transcription (upstream binding factor (UBF), topoisomerase I, and RNA polymerase I) and processing (fibrillarin, nucleophosmin, nucleolin) by confocal laser scanning microscopy. During the first four post-fertilization cell cycles, TEM revealed spherical nucleolus precursor bodies (NPBs), consisting of densely packed fibrils, as the most prominent intra-nuclear entities of the blastomeres. Fibrillo-granular nucleoli were observed in some blastomeres in a single embryo during the 5th cell cycle, i.e., the tentative 16-cell stage, where formation of fibrillar centres (FC), a dense fibrillar component, and a granular component on the surface of the NPBs was seen. In this embryo, autoradiographic labeling was detected over the nucleoplasm and in particular over the nucleoli. Fibrillarin was immunocytochemically localized in the presumptive NPBs of the pronuclei. This protein was again localized to the presumptive NPBs together with nucleolin from late during the 3rd cell cycle, i.e., the four-cell stage in some embryos. UBF, RNA polymerase I, and nucleophosmin were localized to the presumptive NPBs in a proportion of the embryos at the 4th cell cycle, i.e., the tentative eight-cell stage and onwards. Toposiomerase I was not localized to intra-nuclear entities even during the 5th post-fertilization cell cycle. Moreover, a considerable proportion of the blastomere nuclei apparently did not show localization of other nucleolar proteins. In conclusion, porcine embryos produced in vitro display a substantial delay in or even lack of the development of functional nucleoli.

Animals↗

Maintenance of nucleolar machineries and pre-rRNAs in remnant nucleolus of erythrocyte nuclei and remodeling in Xenopus egg extracts.

The nuclear functions in erythrocytes are almost completely extinct. There is no RNA polymerase I transcription, although a remnant nucleolar structure is still present. The remnant nucleolus of Xenopus laevis erythrocytes maintains a morphologically organized structure, nearly exclusively fibrillar. In this inactive nucleolar remnant, we revealed the presence of a modified form of transcription factor UBF. Several proteins of the processing machinery such as fibrillarin, nucleolin and B23/NO38, snoRNAs U3 and U8, and partially processed preribosomal RNAs colocalized in these remnant structures. Attempts to reprogram these erythrocyte nuclei in Xenopus egg extract showed that import of several nucleolar proteins was induced while the nucleolar remnant was disorganized. UBF became abundant and showed a necklace-like distribution on the decondensed ribosomal genes. Fibrillarin, nucleolin, and snoRNAs U3 and U8, also largely imported from the extract, were associated in large prenuclear bodies scattered in the nucleoplasm. B23/NO38 was present in different small bodies formed only in the most decondensed nuclei. In these remodeled erythrocyte nuclei, there was no imported preribosomal RNA and the initial presence of a residual nucleolar structure containing several partners of ribosome biogenesis was not sufficient to promote reassembly of newly imported nucleolar machineries. These nuclei, which reproduce the early events of nucleogenesis are also transcriptionally silent and thus compare to the early embryonic nuclei of Xenopus laevis.

Animals↗

Mammalian RNA polymerase I exists as a holoenzyme with associated basal transcription factors.

Transcription initiation of ribosomal RNA genes requires RNA polymerase I (Pol I) and auxiliary factors which either bind directly to the rDNA promoter, e.g. TIF-IB/SL1 and UBF, or are assembled into productive transcription initiation complexes via interaction with Pol I, e.g. TIF-IA, and TIF-IC. Here we show that all components required for specific rDNA transcription initiation are capable of physical interaction with Pol I in the absence of DNA and can be co-immunoprecipitated with antibodies against defined subunits of murine Pol I. Sucrose gradient centrifugation and fractionation on gel filtration columns reveals that approximately 10% of cellular Pol I elutes as a defined complex with an apparent molecular mass of > 2000 kDa. The large Pol I complex contains saturating levels of TIF-IA, TIF-IB and UBF, but limiting amounts of TIF-IC. In support of the existence of a functional complex between Pol I and basal factors, the large complex is transcriptionally active after complementation with TIF-IC. The results suggest that, analogous to class II gene transcription, a pre-assembled complex, the "Pol I holoenzyme", exists that appears to be the initiation-competent form of Pol I.

Animals↗

The two isoforms of the 90-kDalton nucleolus organizer region autoantigen (upstream binding factor) bind with different avidity to DNA modified by the antitumor drug cisplatin.

It has been previously described that some proteins containing HMG boxes are able to bind more strongly to DNA modified with cis-diamminedichloroplatinum (II) (cisplatin) than to unmodified DNA. In the present study, we analyzed the interaction of cisplatin-modified DNA with the human autoantigen NOR-90 (UBF), a transcription factor that contains several HMG boxes. Using autoantibodies against NOR-90 to perform ELISA and immunoprecipitation, it was confirmed that NOR-90 (UBF) was able to bind cisplatin-modified DNA more avidly than unmodified DNA or trans-diamminedichloroplatinum(II) (transplatin) modified DNA. Moreover, by Southwestern, we observed that the 97 kDalton isoform of NOR-90 (UBF1) was able to bind cisplatin-modified DNA more strongly than the 94 kDalton isoform (UBF2); binding of unmodified DNA or transplatin-modified DNA was not detected with either isoform. Sera containing autoantibodies against NOR-90 did not inhibit, but increased the binding of NOR-90 to cisplatin-modified DNA.

Autoantigens↗

Etilefrine and amezinium reduce uterine blood flow of pregnant guinea pigs.

Etilefrine and Amezinium are used during pregnancy to prevent hypotension and fetal growth retardation. The effect of these drugs on uterine blood flow (UBF), uterine vascular resistance (UVR) and fetal growth are, however, unknown. 31 guinea pigs were injected daily with Etilefrine (3 X 0.14 mg/kg) and Amezinium (0.14 mg/kg) from day 30 to day 60. Uterine blood flow was measured with radioactive-labeled microspheres. Uterine vascular resistance was calculated from arterial blood pressure and uterine blood flow. 10 guinea pigs treated with 0.9% sodium chloride served as controls. As a response to Etilefrine and Amezinium, UBF fell by 68 and 48%, respectively, accompanied by an increase in UVR. The fetal weight decreased only slightly. It is concluded that long-term application of anti-hypotensive drugs may be hazardous to uterine blood flow and fetal growth.

Animals↗

Uterine prostaglandin and blood flow responses to estradiol-17 beta in cyclic cattle.

Normal cyclic dairy cattle (n = 7) underwent a midventral laparotomy on day 17 of the estrous cycle and were fitted, ipsilateral to the CL, with: an electromagnetic flow transducer around the uterine artery (UA; n = 5); catheters within the ovarian vein (OV; n = 7) via a uterine branch of the ovarian vein, uterine branch of the ovarian artery (UBOA; n = 5) and facial artery (FA; n = 7). On day 18, blood samples were collected at 30 min intervals for 1 h prior to injection of estradiol-17 beta (E2; 3 mg) and 12 h post-E2. Uterine blood flow (UBF) was monitored continuously and plasma samples analyzed for PGF2 alpha and PGFM. Exact locations of catheters in reproductive tracts were verified post-slaughter. Data were analyzed by method of least squares analysis of variance. Uterine blood flow (ml/min) increased above pre-E2 flow rates within 30 min post-E2 injection, peaked between 2.5 to 3.5 h and declined between 4 to 8.5 h. A small secondary rise in UBF occurred between 9 and 12 h. Regression analysis for concentrations (pg/ml) of PGF2 alpha and PGFM in the OV (i.e., [OV]-[FA]) demonstrate a similar response as PGFM concentration in the FA in that all increased at approximately 3 h, peaked between 5 and 7 h and returned to near baseline levels by 9 to 10 h post-E2. Facial artery PGFM concentrations were positively correlated with uterine production of PGF2 alpha (r = .66) and PGFM (r = .30), whereas FA PGF2 alpha concentrations were not. In three of five cows, a difference in PGF2 alpha was detected between UBOA and FA (UBOA greater than FA); supportive of a local countercurrent exchange between the uterine venous drainage and the ovarian artery.

Animals↗