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Biomedical subjects

W F Pope

Publications and source records attributed to W F Pope.

53 records · Page 3Linked to original sources
PubMed1989

Effect of season and lactation on postpartum fertility of Polypay, Dorset, St. Croix and Targhee ewes.

The objective of this study was to compare rebreeding activities of spring- vs fall-lambing Polypay, Dorset, St. Croix and Targhee ewes that either suckled their lambs for 40 d or had lambs weaned at birth. Seasonal effects of male fertility were reduced by utilizing an excess number of fertile rams in the spring. Plasma concentrations of progesterone were monitored to assess days to the first normal ovulation, days to conception and estrous vs anestrous activity. Breed, season and lactation affected the rebreeding performance. Dorset ewes had similar conception rates between spring and fall but a shorter interval from lambing to first ovulation in the fall. Polypay and Targhee ewes were the opposite; they had higher conception rates in fall than in spring matings with no seasonal influence on postpartum interval. Postpartum ewes in the fall had higher conception rates, and fewer of these ewes became anestrous or had estrous cycles of abnormal duration than of those ewes lambing in the spring. Ewes that suckled for 40 d in the spring had delayed estrous activity, but when these ewes became estrual they had higher conception rates than ewes whose lambs were weaned at birth. Lactation had no inhibitory affect on the postpartum interval of fall lambing ewes. These data suggest that the response of different breeds to various components of postpartum fertility varies with season and management of the flock.

Animals↗
PubMed1989

Effects of the oviduct and wheat germ agglutinin on enzymatic digestion of porcine zona pellucidae.

Seventy-two crossbred gilts were utilized to examine whether the oviduct rendered zona pellucidae resistant to protease digestion, whether the uterus reversed this resistance and whether such a uterine reversal was necessary for hatching. Oocytes were aspirated from follicles 22 to 28 h after onset of estrus (d 0); oviductal and uterine oocytes or embryos were collected on d 1 to 6. These oocytes and embryos were subjected to a solution containing .1% trypsin and .1% pronase (37 degrees C) for observation of zona pellucidae digestion. Zonae of oviductal oocytes were more (P less than .001) resistant to digestion than were follicular oocytes. Placement of follicular oocytes in oviducts for 30 min rendered zona pellucidae more (P less than .001) resistant to protease digestion than oocytes not exposed to oviductal secretions. Resistance of zona pellucidae to proteases, however, decreased (P less than .001) after entry into the uterus. Zonae of morulae retained in oviducts took longer (P less than .001) to digest than those recovered from the uterus. Blastocysts also were treated with wheat germ agglutinin (WGA; 50 micrograms/ml) for 40 min to determine whether artificial induction of zona resistance to enzymatic digestion affected the ability of embryos to hatch. Though WGA treatment delayed (P less than .001) enzymatic digestion of zona pellucidae, time from collection to hatching was not affected. This experiment indicated that the oviduct delayed enzymatic digestion of the zona pellucidae, whereas the uterus reversed this delay. The re-establishment of enzyme susceptibility after uterine entry, however, appeared to be unrelated to the subsequent ability of blastocysts to hatch.

Animals↗
PubMed1988

Survival of small and large littermate blastocysts in swine after synchronous and asynchronous transfer procedures.

Thirty-two crossbred sows were assigned to synchronous and asynchronous embryo transfer procedures to determine if, within a litter, small blastocysts were as viable as large blastocysts. Synchronous embryo transfers were established when donors and recipients displayed the onset of estrus (Day 0) within 6 h of each other. Asynchronous transfers were established when recipients displayed the onset of estrus 18 to 24 h after that of donors. An equal number (four or five) of the smallest and largest diameter blastocysts, from a Day 7 donor, were transferred to separate uterine horns of a Day 7 (synchronous) or a Day 6 (asynchronous) recipient. Each recipient's uterine horns were ligated at the external bifurcation to prevent transuterine embryonic migration. The percentage of blastocysts surviving was determined 300 h (12.5 d) after donors exhibited estrus. Small as well as large Day 7 blastocysts survived following asynchronos transfer to a Day 6 recipient. However, fewer (P<0.01) small blastocysts survived synchronous transfer than large blastocysts. These data suggested that small blastocysts were lost due to asynchrony with the uterine environment; however, when transferred to a less advanced environment, small blastocysts were equally viable as large blastocysts.

Journal Article↗
PubMed1988

A uterine cell mitogen distinct from epidermal growth factor in porcine uterine luminal fluids: characterization and partial purification.

Uterine luminal fluids (ULF) from early (Days 10 and 12)-pregnant sows contain factors that stimulate DNA synthesis in a variety of cell lines. The major growth factor component in these fluids has been partially purified 200-fold by heat treatment, anion-exchange chromatography, and gel filtration using mouse embryo-derived AKR-2B fibroblasts as an indicator cell line. The ULF mitogen (ULFM) is a polypeptide with an apparent molecular weight of 4800; it is extremely heat stable and resistant to treatment with urea. This mitogen is also present in ULF from cycling sows but is not detectable in uterine cytosolic extracts or in serum isolated from pigs at Day 12 of pregnancy. The addition of this factor to medium containing 0.5% calf serum results in a 50% increase in final cell density of AKR-2B cells. ULFM appears biologically distinct from mouse and human epidermal growth factor (EGF), since its activity is not inhibited by antibody to mouse EGF and it does not compete for binding to human (A431) EGF receptors. In addition, the ULF factor stimulates DNA synthesis in human A431 epidermoid carcinoma cells, whereas EGF is inhibitory. Partially purified ULFM also stimulates DNA synthesis in primary cultures of pig uterine stromal cells. This mitogen activity is dose-dependent and is not inhibited by antibody to mouse EGF. Thus ULFM may act in concert with other peptide growth factors in regulating uterine growth and/or differentiation.

Animals↗
PubMed1988

Effect of electrocautery of nonovulated day 1 follicles on subsequent morphological variation among day 11 porcine embryos.

One hundred and thirteen crossbred gilts were used in three experiments to examine the relationship between the pattern or sequence of ovulation and subsequent variation in the morphology of Day 11 embryos. In the first experiment, the percentage of follicles that had ovulated was determined in individual gilts at 26, 30, 34, or 38 h after the onset of estrus (n = 20) and 39, 41, 43, 45, or 47 h post-injection of human chorionic gonadotropin (n = 25; hCG, 1000 IU). The second experiment consisted of observing the percentage of follicles ovulated in 52 additional gilts at 34 h after the onset of estrus (Day 0). In the third experiment, the morphological variation among littermate embryos was compared on Day 11 between sham-operated control gilts (n = 8) and gilts whose nonovulated follicles were destroyed by electrocautery (n = 8) on Day 1. Results of these experiments indicated that the pattern of ovulation in gilts was skewed (p less than 0.01). Ovulation, induced with hCG, appeared to occur in a majority of follicles during a short period of time, whereas the remaining ovulations occurred over a longer interval. Of the 57 gilts observed at 34 h after natural estrus, ovaries of 25 gilts contained corpora hemorrhagica (CH) and follicles; one gilt had 1 CH and 17 follicles, and 24 others had 10-17 CH with 1-4 follicles remaining. Destruction of these nonovulated follicles resulted in a more (p less than 0.01) uniform group of Day 11 embryos and with fewer (p less than 0.05) small embryos. These data demonstrated that the pattern of ovulation may affect morphological variation in embryonic development such that some of the later ovulating follicles may represent smaller embryos within a litter.

Animals↗
PubMed1988

Uterine asynchrony: a cause of embryonic loss.

During early gestation, hormonal events associated with corpora lutea formation and embryonic synthesis of proteins, prostaglandins, and steroids result in synthesis and release of endometrial secretory products into the uterine lumen. The embryo, inherently and in response to secretory products of the uterus, develops and grows. However, considerable embryonic mortality occurs when uterine secretions become altered in such a manner that they are asynchronous to the developing embryo. Factors that advance or retard development of the uterus and embryo have been utilized to document utero-embryonic asynchrony, and it has been observed that the uterus will not "wait" for embryos to become synchronous. However, the reverse is possible: embryonic development can be accelerated or decelerated. Furthermore within the uterus, localized areas might also exist that favor development of some embryos at the expense of others. This review will consider causes of utero-embryonic asynchrony and offer models of embryonic loss associated with an asynchronous environment in cattle, sheep, and swine.

Animals↗
PubMed1987

The effect of exogenous estradiol on litter size in a typical swine herd.

Fifty-six female pigs (12 gilts, 26 primiparous and 18 multiparous sows) were bred and assigned to receive either corn oil (vehicle; n=28) or estradiol-17beta (2 mg/day; i.m.; n=28) on Days 12 and 13 (Day 0=first day of estrus) to determine if exogenous estradiol could improve litter size in swine. Though litter size of the females farrowing was not increased with estradiol treatment (vehicle versus estradiol, 9.7+/-0.8 versus 10.1+/-1.8 live pigs born, respectively), more females in this group remained pregnant (vehicle versus estradiol, 6 versus 1 recycled, respectively; P<0.05). Litter size, expressed as the number of pigs born per-female-bred, was therefore increased with exogenous estradiol (vehicle versus estradiol, 7.6+/-0.8 versus 9.8+/-0.7 live pigs born, respectively; P<0.05). Some of these estradiol- treated females produced smaller (P<0.05) litters and this may be of concern in herds experiencing low fertilization/conception rates. Overall 60 more pigs were born alive to females in the estradiol-treated group than to the control group females. This experiment demonstrated that supplemental estradiol treatment on Days 12 and 13 assisted in maintenance of pregnancy and thereby increased litter size on a per-female-bred basis.

Journal Article↗
PubMed1986

Effect of asynchronous superinduction on embryo survival and range of blastocyst development in swine.

The importance of uniform development of blastocysts was examined by comparing the effects of asynchronous superinduction (Day 6 embryos into Day 7 pregnant recipients and Day 7 embryos into Day 6 pregnant recipients) on the range of embryo development at Days 12 and 13 to subsequent survival to Day 30. Twenty gilts were used to produce five Day 7 recipients that received Day 6 embryos and five Day 6 recipients that received Day 7 embryos. Embryos from the Day 7 and Day 6 recipients were examined 6 days later. Recovered embryos ranged morphologically from spherical to filamentous blastocysts. This range of embryos was within the limits of that previously observed for naturally mated sows. However, recovered blastocysts from the Day 6 embryos transferred into Day 7 recipients were morphologically more variable and proportionately less developed than the blastocysts from the Day 7 embryos transferred into Day 6 recipients. Forty additional gilts were subsequently utilized to generate 20 recipients (10 recipients per transfer group) that were examined on Day 30. More Day 7 embryos transferred into Day 6 recipients survived (p less than 0.05) than Day 6 embryos transferred into Day 7 recipients. These experiments suggested that greater variation in early development of embryos, within litters, subsequently resulted in greater mortality of embryos.

Animals↗
PubMed1986

Intrauterine migration of the porcine embryo: coordination of bead migration with estradiol.

Forty crossbred gilts were used in three experiments to examine the effects of estradiol on embryo migration. Small, spherical beads of Silastic glue containing either cholesterol or estradiol-17 beta were used to mimic embryo migration. In the first experiment, 10 cholesterol- and 10 estradiol-impregnated beads were injected into the tip of the uterine horns, either on the same side (n = 5) or opposite from each other (n = 5). The second experiment consisted of a localized release of cholesterol or estradiol and observing migration of cholesterol-containing beads inserted 10 cm anterior and posterior to this site (n = 5). In the third experiment, 10 cholesterol-impregnated beads were injected into either the tip or base of one uterine horn. Additionally, these gilts were exposed to vehicle or exogenous estradiol in a 2 X 2 factorial arrangement of treatments (n = 5). Results of these experiments indicated that cholesterol-impregnated beads migrated further (P less than .05) when adjacent to estradiol-containing beads than when in an opposite uterine horn. Localized release of estradiol failed to induce movement of beads away from the site of steroid release. Finally, beads inserted at the base of the uterus moved anteriorly following treatment of gilts with estradiol. We suggest from these experiments that the porcine uterine horn cannot discriminate between estradiol- and cholesterol-releasing beads and, further, lacks a coordinated ability to displace adjacent beads. A site-dose dependent mechanism(s) of estrogenic induction of migration may exist such that porcine embryos become bilaterally intermixed following posterior, then anterior, waves of uterine contractions.

Animals↗
PubMed1986

Dose-response shift in the ability of gilts to remain pregnant following exogenous estradiol-17 beta exposure.

Sixty mated gilts were assigned to a 2 X 6 factorial arrangement (n = 5) of day of injection (d 9 and 10 vs 12 and 13; d 0 = first day of estrus) and dose of estradiol-17 beta (0, .125, .5, 2, 8 and 32 mg X gilt-1 X d-1). Gilts were subsequently slaughtered on d 30; pregnancy was verified and percent embryonic survival calculated. A 64-fold shift in the dose-response curve for percent embryonic survival illustrated that the adverse effects of exogenous estradiol-17 beta were less when administered on d 12 and 13 as compared with d 9 and 10 (day X dose, P less than .01). This experiment demonstrated that the uterine-embryonic environment of d 12 and 13 pregnant gilts was more tolerant of exogenous estrogen alterations than that of d 9 and 10 pregnant gilts.

Animals↗
PubMed1982

Distribution of progesterone in the uterus, broad ligament, and uterine arteries of beef cows.

Samples of uterine horn, broad ligament (mesosalpinx and mesometrium), and uterine artery of ten unilaterally ovulating cows, 12-15 days after mating, were examined for differences in concentration of progesterone. Tissues (mesosalpinx, branches of the uterine artery, anterior uterine horn) adjacent to the ovary bearing the corpus luteum contained significantly greater quantities of progesterone than more distal tissues (mesometrium, uterine artery, posterior uterine horn) on the same side and all tissues on the contralateral side. In tissues on the side ipsilateral to the corpus luteum, a gradient of progesterone existed. Differences in tissue concentrations of progesterone may be the cause of observed differences in uterine physiology in the cow and ewe.

Animals↗
PubMed1982

Intrauterine migration of the porcine embryo: influence of estradiol-17 beta and histamine.

The role of estradiol-17 beta (E2) in migration of the porcine embryo was examined (Experiment 1) by observing the distribution of Silastic (polydimethyl siloxane, Medical Adhesive Silicone Type A, Dow Corning) beads impregnated with cholesterol or E2 (n=5 gilts per treatment) after 5 days in utero (Day 12 of the estrous cycle, Day 0=1st day of estrus). Beads impregnated with E2 migrated farther (P less than 0.05) than those impregnated with cholesterol. Twenty additional gilts and sows were used to determine if histamine was involved with intrauterine migration (Experiment 2). On Day 6 of gestation the tip of each uterine horn was exposed and the subserosa of each of 5 gilts was injected with either vehicle, 8 mg of cromolyn sodium (an inhibitor of histamine release) or 8 mg of cromolyn sodium plus 1 mg of histamine. Four days later (Day 10), the excised uterus was examined for migration of embryos. An additional group of 5 gilts received 8 mg of cromolyn sodium on Days 6 and 10 and were examined on Day 12. Results from the second experiment demonstrated that cromolyn sodium treatment alone restricted (P less than 0.05) Day 10 embryos to the tip of the uterine horn but by Day 12 embryos had overcome this restriction. Injection of histamine overcame the inhibitory effects of cromolyn sodium and restored migration of Day 10 embryos. These experiments suggest that both E2 and histamine are involved in intrauterine migration of the porcine embryo. The extent to which these hormones might be interrelated during migration is not fully understood at this time.

Animals↗
PubMed1982

Intrauterine migration of the porcine embryo--interaction of embryo, uterine flushings and indomethacin on myometrial function in vitro.

Twenty-four pregnant Landrace and Yorkshire gilts were utilized to examine the relationship between myometrial activity and intrauterine embryo migration. On d 2 (1st day of estrus = d 0), embryos were flushed from one oviduct and transferred to the opposite oviduct. Uterine horns were ligated at the uterotubal junction on the flushed side and 40 and 50 cm posterior to the uterotubal junction on each side. On d 6, 9 or 12 (n = 8), embryo migration was determined by flushing segments of the excised uterus. Strips of myometrium from the pregnant and nonpregnant horn of each gilt were subsequently removed and assigned to one of the three in vitro experiments to examine the effects of the embryo and uterine flushings on myometrial contractility. Myometrial contractility increased concomitantly with embryo migration through the uterine ligations (day x side interaction, P less than .10). Uterine flushings from pregnant horns contained a short-acting substance that mimicked, in part, the stimulatory influence(s) of the in situ embryo on in vitro myometrial contractility. However, only flushings from the uterine segment containing the d 12 embryos could overcome the in vitro inhibitory effects of indomethacin (P less than .01) on myometrial contractility. The porcine embryo coincubated with myometrial strips could not directly stimulate contractions of the myometrium. Results of these experiments indicate that in gilts the stimulatory influence(s) of the migrating embryo on myometrial function may involve a "hormonal" factor of short half-life that does not directly affect the smooth muscle cell.

Animals↗
PubMed1981

In-vitro binding of prostaglandin F-2 alpha to uterine luminal proteins of pregnant and non-pregnant ewes.

Pregnant and non-pregnant ewes were utilized to determine whether the presence of the embryo affected the binding of prostaglandin (PG) F-2 alpha to a uterine luminal protein. The uterine horn adjacent to the corpus luteum was flushed on Day 13 of gestation or the oestrous cycle. Flushings were incubated with [3H]PGF-2 alpha and subsequently eluted through a Sephadex column. Uterine luminal proteins of pregnant and non-pregnant ewes eluted with the void volume and failed to bind PGF-2 alpha.

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