@article{monteiro-riviere_inman_hedgpeth_mosteller_piedrahita_2006, title={Dermatological effects of chronic exposure to 7,12-dimethylbenz[a]anthracene (DMBA) or N-methyl-N-nitrosoguanidine (MNNG) in swine}, volume={25}, ISSN={["1556-9527"]}, url={http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000238451100004&KeyUID=WOS:000238451100004}, DOI={10.1080/15569520600695546}, abstractNote={Purpose: To determine whether chronic exposure to DMBA or MNNG in combination with or without UVB exposure would induce skin carcinomas in swine. Methods: Eight gilts were exposed to 100 mJ of UVB in their left side, allowed to recuperate, and divided into two groups. Each gilt received identical high doses (DMBA 50 µM; MNNG 250 mM), low doses (DMBA 500 nM; MNNG 2.5 mM), carrier (DMSO), or nothing added treatments in the UVB and non-UVB sides. Animals were exposed weekly for 30 weeks and skin samples collected at 10, 20, and 30 weeks from initiation of exposure. An additional sample was collected 16 weeks following cessation of exposure. All samples were scored for dermal morphology, including intracellular epidermal edema, intercellular epidermal edema, papillary dermal edema, perivascular infiltrates, pyknotic stratum basale cells, collagen necrosis, and epidermal-dermal separation, and the data were analyzed by ANOVA. MNNG and UVB light had a significant effect on epidermal thickness and the number of cell layers. The greatest increase in epidermal thickness occurred from 20 weeks to 30 weeks in the UVB plus MNNG treatment. Treatment with MNNG resulted in intracellular and intercellular epidermal edema, dermal edema, and dermal inflammation at both the low and high doses of MNNG. In contrast, all the morphological evaluations of the DMBA treatments were less severe than the MNNG. Conclusion: Our findings show that although chronic exposure to MNNG and DMBA, with or without UVB exposure, caused severe to mild dermatopathological changes, neither resulted in the development of skin carcinomas. These results indicate that at least with respect to responses to DMBA and MNNG, the swine model mimics more closely the responses seen in human skin.}, number={2}, journal={CUTANEOUS AND OCULAR TOXICOLOGY}, author={Monteiro-Riviere, N and Inman, A and Hedgpeth, V and Mosteller, B and Piedrahita, J}, year={2006}, pages={103–119} }
 @article{boonyaprakob_gadsby_hedgpeth_routh_almond_2005, title={Expression and localization of hypoxia inducible factor-1 alpha mRNA in the porcine ovary}, volume={69}, number={3}, journal={Canadian Journal of Veterinary Research}, author={Boonyaprakob, U. and Gadsby, J. E. and Hedgpeth, V. and Routh, P. A. and Almond, G. W.}, year={2005}, pages={215–222} }
 @article{boonyaprakob_gadsby_hedgpeth_routh_almond_2003, title={Cloning of pig prostaglandin F-2 alpha(FP) receptor cDNA and expression of its mRNA in the corpora lutea}, volume={125}, DOI={10.1530/rep.0.1250053}, abstractNote={Changes in the expression and localization of luteal mRNA for PGF(2alpha) (FP) receptors may be critical in determining the luteolytic action of PGF(2alpha) in pig corpora lutea. In this study, a full-length FP receptor (FPr) cDNA was isolated and cloned from pig corpora lutea. This isolate (GenBank accession no. U91520) contains an open reading frame of 1086 bases coding for a protein of 362 amino acids with seven potential transmembrane domains. The predicted amino acid sequence of this isolate was 83% identical to the FPr amino acid sequence of other species including sheep, cattle and humans. Northern blot analysis showed the presence of an FPr message of about 5 kb in mRNA from pig corpora lutea. Relatively weak FPr mRNA expression was detected on day 4 and day 7 of the oestrous cycle. The expression was greater (P < 0.05) on days 10, 13 and 15 than on days 4 and 7. In situ hybridization analysis revealed that mRNA for FPr was expressed predominantly in the steroidogenic large luteal subtype of cell, although there was some expression in small luteal cells, with histological appearance of steroidogenic small cells. Localization of hybridization signals of FPr was observed in luteal tissue at all stages examined. These data demonstrate that FPr is expressed in pig corpora lutea throughout the oestrous cycle and that upregulation of the FPr mRNA occurs when the corpora lutea becomes sensitive to PGF(2alpha). Direct luteal targets of PGF(2alpha) appear to be primarily large steroidogenic cells in this species.}, number={1}, journal={Reproduction (Cambridge, England)}, author={Boonyaprakob, U. and Gadsby, J. E. and Hedgpeth, V. and Routh, P. and Almond, Glen}, year={2003}, pages={53–64} }
 @article{boonyaprakob_gadsby_hedgpeth_routh_almond_2003, title={Expression and localization of vascular endothelial growth factor and its receptors in pig corpora lutea during the oestrous cycle}, volume={126}, DOI={10.1530/rep.0.1260393}, abstractNote={Expression and localization of mRNAs for vascular endothelial growth factor (VEGF), VEGF receptor 1 (Flt) and VEGF receptor 2 (KDR) (VEGFR-1 and VEGFR-2, respectively) were investigated in pig corpora lutea. Northern blot analysis of total RNA indicated hybridization of pig VEGF, VEGFR-1 and VEGFR-2 cDNA probes to mRNA transcripts of approximately 3.9, 7.0 and 5.0 kb, respectively. The expression of mRNAs for VEGF and its receptors during the luteal phase (days 4, 7, 10, 13 and 15 after the onset of oestrus) were assessed by northern blot analysis, and hybridization signals were normalized to expression of pig 18S rRNA. Relative hybridization signals of expression of VEGF mRNA appeared to be constant; however, expression of VEGFR-1 mRNA was low on day 4, increased on day 7, and was higher on days 10, 13 and 15 (P<0.05, compared with day 4). In contrast, no changes in expression of mRNA for VEGFR-2 were evident on days 4-13, but a decrease was detected (P<0.05) at day 15. In situ hybridization revealed that VEGF mRNA was localized predominantly in large luteal cells, whereas both VEGFR-1 and VEGFR-2 were localized to small cells. These data indicate that the VEGF system may be involved in the regulation of luteal vasculature throughout the lifespan of the corpus luteum. Although the expression of VEGF mRNA was unchanged during the luteal phase, variations in the expression of VEGFR-1 and VEGFR-2 mRNAs indicate that differential regulation of expression of the VEGF receptors may play a role in the control of VEGF-mediated vascular growth at different phases of development and maturation of the pig corpus luteum.}, number={3}, journal={Reproduction (Cambridge, England)}, author={Boonyaprakob, U. and Gadsby, J. E. and Hedgpeth, V. and Routh, P. and Almond, Glen}, year={2003}, pages={393–405} }
 @article{ge_miller_nicholson_hedgpeth_gadsby_2003, title={Insulin-like growth factor (IGF)-I and IGF binding proteins-2,-3,-4,-5 in porcine corpora lutea during the estrous cycle; evidence for inhibitory actions of IGFBP-3}, volume={25}, ISSN={["1879-0054"]}, DOI={10.1016/S0739-7240(03)00060-2}, abstractNote={In this study we measured protein concentrations of insulin-like growth factor (IGF)-I and IGF binding proteins (IGFBPs) 2-5 in porcine corpora lutea (CLs) throughout the estrous cycle (Experiment 1), and examined the effects of IGFBP-3 and IGFBP-3 antibody (AB) on luteal progesterone (P4) secretion in vitro (Experiment 2). For Experiment 1, (CLs) and serum were collected on days (D) 4, 7, 10, 13, 15 and 16 of the estrous cycle (n = 5 animals per day). IGF-I was extracted from CLs and sera, and measured by radioimmunoassay (RIA). IGFBPs were measured in CLs by ligand blots. For Experiment 2, CLs (from Experiment 1) were enzyme dissociated and luteal cells cultured (24 h) in Medium 199 (M199) containing (0-500 ng/ml) IGFBP-3 (+/-IGF-I; 100 ng/ml), or (0-10 microg/ml) IGFBP-3 AB. P4 in media was measured by RIA. In Experiment 1, luteal IGF-I concentrations (ng/g tissue) were maximal on day 4 and gradually decreased thereafter. Serum IGF-I concentrations (ng/ml) were highest on days 4 and 7, compared with days 10-15. Peak levels of luteal IGFBP-3 were also seen on days 4 and 7 of the cycle. Luteal IGFBP-2 concentrations showed a tendency to increase on day 16 (P < 0.05 versus day 10), but no significant changes in IGFBP-4 or -5 were seen. In Experiment 2, IGFBP-3 (w IGF) inhibited the steroidogenic actions of IGF-I, but had no significant actions alone (IGFBP-3 w/o IGF). Finally, IGFBP-3 AB stimulated P4 secretion on days 4 and 7, but not on days 10-16. We conclude that IGFBP-3 inhibits IGF-I actions in the porcine CL.}, number={2}, journal={DOMESTIC ANIMAL ENDOCRINOLOGY}, author={Ge, ZP and Miller, E and Nicholson, W and Hedgpeth, V and Gadsby, J}, year={2003}, month={Aug}, pages={183–197} }
 @article{miller_ge_hedgpeth_gadsby_2003, title={Steroidogenic responses of pig corpora lutea to insulin-like growth factor I (IGF-I) throughout the oestrous cycle}, volume={125}, ISSN={["1470-1626"]}, DOI={10.1530/rep.0.1250241}, abstractNote={This study was designed to investigate the roles of insulin-like growth factor I (IGF-I), IGF-type I receptor (IGF-IR) and IGF-binding proteins (IGFBPs) in regulating progesterone secretion by pig corpora lutea during the oestrous cycle, and the signal transduction pathways involved in mediating the steroidogenic actions of IGF-I. Corpora lutea were collected on days 4, 7, 10, 13 and 15 or 16 of the oestrous cycle, enzyme dissociated and the luteal cells were cultured for 24 h in Medium 199 with IGF-I (0-100 ng ml(-1)), long R(3)-IGF-I (0-100 ng ml(-1)), anti-IGF-I (Sm 1.2B; 0-10 microg ml(-1)), anti-IGF-IR (alphaIR3; 0-2 microg ml(-1)), or IGF-I signal transduction pathway inhibitors (phosphatidylinositol (PI)-3-kinase: 100 nmol Wortmannin l(-1) and 10 micromol LY 294002 l(-1); MAP kinase: 50 micromol PD 98059 l(-1)) to investigate their effects on IGF-I (100 ng ml(-1)) stimulated progesterone secretion. Pig luteal cells displayed dose-dependent responses to IGF-I and long R(3)-IGF-I on days 4 and 7 of the oestrous cycle, but not on days 10-16. There was no difference in the ED(50) or V(max) (maximal response) values between IGF-I and long R(3)-IGF-I. Neither anti-IGF-I nor anti-IGF-IR had significant effects on progesterone secretion, at any dose or day. Wortmannin and LY 294002 blocked IGF-I stimulated progesterone secretion, but PD 98059 was without effect. Finally, IGF-I (6 microg) infused into the ovary on day 7 in vivo significantly increased progesterone secretion within 45 min of infusion. The conclusions of this study are: (1) IGF-I has steroidogenic actions only on 'young' (days 4-7) pig corpora lutea; (2) endogenous IGF-I and IGFBP are insufficient to modulate progesterone secretion in vitro; and (3) the steroidogenic actions of IGF-I are mediated via PI-3-kinase.}, number={2}, journal={REPRODUCTION}, author={Miller, EA and Ge, Z and Hedgpeth, V and Gadsby, JE}, year={2003}, month={Feb}, pages={241–249} }
 @article{cushman_desouza_hedgpeth_britt_2001, title={Alteration of activation, growth, and atresia of bovine preantral follicles by long-term treatment of cows with estradiol and recombinant bovine somatotropin}, volume={65}, ISSN={["0006-3363"]}, DOI={10.1095/biolreprod65.2.581}, abstractNote={Abstract The hypothesis was that long-term treatment of cattle with estradiol (E2) and bovine somatotropin (bST) would alter the earliest stages of folliculogenesis. Nonlactating Holstein cows (n = 26) were treated in a 2 × 2 arrangement with E2 (2 × 24 mg implants, 67.1 ± 1.4 days) and bST (Posilac, 63.6 ± 1.5 days). At Day 67 ± 1.3, one ovary was removed for morphometric and immunohistochemical analysis. For each ovary, 388 ± 38 microscopic fields (2 × 2 mm) were examined and follicles within each field were classified by histological stage. Fields that contained no follicles were classified as empty. Empty fields (n = 100 per ovary) were further classified as containing no evidence of follicles or containing atretic remnants of follicles. Approximately 30 4-μm sections per ovary were stained for proliferating cell nuclear antigen (PCNA), and 150 fields per ovary were evaluated. Additional sections (n = 10 per ovary) were assessed immunohistochemically for apoptosis, and fluorescence intensity was determined for each follicle. Treatment with bST significantly decreased percentage of empty fields containing atretic remnants. Treatment with E2 induced activation of follicles as shown by a decrease in percentage of primordial follicles and an increase in percentage of primary follicles as determined by PCNA staining. At the primary follicle stage the combination of bST + E2 decreased apoptosis as shown by decreased fluorescence intensity. Thus, E2 induced activation of follicles, bST enhanced survival, and the combination lowered atresia.}, number={2}, journal={BIOLOGY OF REPRODUCTION}, author={Cushman, RA and DeSouza, JC and Hedgpeth, VS and Britt, JH}, year={2001}, month={Aug}, pages={581–586} }
 @article{cushman_desouza_hedgpeth_britt_2001, title={Effect of long-term treatment with recombinant bovine somatotropin and estradiol on hormone concentrations and ovulatory response of superovulated cattle}, volume={55}, ISSN={["0093-691X"]}, DOI={10.1016/S0093-691X(01)00500-3}, abstractNote={The objective was to assess effects of long-term treatment with recombinant bovine somatotropin (bST) and estradiol-17β (E2) on the number of follicles that ovulated in response to FSH. Non-lactating Holstein and Jersey cows (Trial 1, n=27) and Angus cows and heifers (Trial 2, n=35) received two ear implants of E2 and biweekly injections of bST in a 2 × 2 arrangement of treatments. Estradiol implants were removed 74.6 ± 1.1 d after insertion and 18.1 ± 0.9 d after the last biweekly injection of bST. Cows were stimulated with FSH-P beginning 2 d after removal of E2 implants, and PGF2alpha (PGF) was given on the third day of FSH treatment Ovaries were collected to determine the number of CL at 1 to 2 wk after treatment with PGF. In Trial 2 only, cattle were inseminated at estrus and embryos were collected 6 to 8 d later. Implants of E2 increased (P < 0.01) serum E2 8-fold initially and E2 was still elevated 5-fold at removal of implants. Injections of bST increased (P < 0.01) serum growth hormone (GH) 15-fold and insulin-like growth factor-I (IGF-I) 3-fold. In Trial 1, number of CL was increased by the combination of bST+E2 (P < 0.01). In Trial 2, E2 increased the number of CL (P < 0.05), and bST increased the number of total ova and transferable embryos (P < 0.01). We conclude that long-term treatment with bST and E2 may interact to enhance follicular development and ovulatory response to FSH.}, number={7}, journal={THERIOGENOLOGY}, author={Cushman, RA and DeSouza, JC and Hedgpeth, VS and Britt, JH}, year={2001}, month={Apr}, pages={1533–1547} }
 @article{sinclair_squires_raeside_britt_hedgpeth_2001, title={The effect of early postnatal treatment with a gonadotropin-releasing hormone agonist on the developmental profiles of testicular steroid hormones in the intact male pig}, volume={79}, DOI={10.2527/2001.7941003x}, abstractNote={Three studies examined the effects of early postnatal treatment with a GnRH agonist on plasma concentrations of testosterone, dehydroepian-drosterone sulfate, 16-androstene steroids in fat and salivary glands, androstenone in fat and plasma, and testicular development of intact male pigs. The first study involved 45 7-d-old pigs assigned to three treatment groups: 1) boars administered 100 microg/kg of Lupron depot, 2) boars administered 200 microg/kg of Lupron depot, and 3) control boars receiving a saline carrier. The second study involved 20 7-d-old pigs assigned to two treatments: daily injection of 200 microL of 0.5 mg/mL Lupron from d 7 to 35 and controls treated with saline. The third study involved a total of 100 animals assigned to 10 groups of 10 based on their age at slaughter. These groups were subdivided into one of two treatments: 1) boars injected with 200 microL of 0.5 mg/mL of Lupron from d 3 to 35 and 2) control boars injected with saline. Testicular steroid hormone concentrations in plasma decreased (P < 0.01) within 7 d of GnRH agonist treatment. Following cessation of treatment, steroid levels increased to control levels and remained constant until the final rise at 5 mo. Plasma testosterone levels in the 100 microg/kg depot treatment group were higher (P < 0.05) than that of the 200 microg/kg and control group at 164 d of age. There were no differences between treatments (P > 0.05) in testicular steroid hormone levels at the end of study 2 or 3. There were no differences (P > 0.05) in concentrations of 16-androstene steroids in salivary glands between any of the treatment groups at market weight in studies 1 and 2. Fat androstenone levels measured in the third study ranged between 0.6 microg/g and 4.2 microg/g at 7 to 28 d of age. Treatment with GnRH agonist decreased plasma steroid levels and testicular development; however, by d 60 testicular size and weight were at control levels and remained similar until 180 d of age. The results of these studies indicate that daily administration of a GnRH agonist significantly decreased testicular development and steroidogenesis only during treatment, but testis growth and steroidogenesis had returned to control levels by 60 d of age in male pigs. Suppression of the early postnatal rise in testicular steroid hormones did not affect growth performance or steroid hormone levels at 5 to 6 mo of age.}, number={4}, journal={Journal of Animal Science}, author={Sinclair, P. A. and Squires, E. J. and Raeside, J. I. and Britt, Jack and Hedgpeth, V. G.}, year={2001}, pages={1003–1010} }
 @article{cushman_hedgpeth_echternkamp_britt_2000, title={Evaluation of numbers of microscopic and macroscopic follicles in cattle selected for twinning}, volume={78}, DOI={10.2527/2000.7861564x}, abstractNote={We hypothesized that the number of microscopic follicles present in the ovaries of cattle selected for twin births (Twinner) would be greater than in the ovaries of contemporary Controls. Ovaries were collected from seven Control and seven Twinner cows at slaughter. The number of Small (1 to 3.9 mm), Medium (4 to 7.9), and Large (> 8 mm) surface follicles was counted and one ovary was fixed for histological evaluation. Fifty to sixty consecutive 6-microm slices were taken from a piece of cortical tissue, approximately 1 cm x 1 cm in area, located between the surface follicles. Microscopic follicles were classified as primordial (oocyte surrounded by a single layer of squamous pregranulosa cells), primary (oocyte surrounded by a single layer of one or more cuboidal granulosa cells), secondary (oocyte surrounded by two or more layers of granulosa cells), or tertiary (oocyte surrounded by multiple layers of granulosa cells with initiation of antrum formation to < or = 1 mm in diameter). The total number of follicles was counted in 200 fields (2 mm x 2 mm) per ovary. A field containing no follicles was classified as empty. There were significantly more secondary follicles in Twinner compared with Control ovaries (12.9 vs 6.3; P < .05). Twinners also tended to have more small surface follicles (35.4 vs 49.0; P < 0.1). We conclude that ovaries of Control and Twinner cows do not differ in the number of primordial follicles or in the number of follicles activated into the growing pool; however, Twinner cows are able to maintain more growing follicles at the secondary and subsequent stages of development.}, number={6}, journal={Journal of Animal Science}, author={Cushman, R. A. and Hedgpeth, V. S. and Echternkamp, S. E. and Britt, Jack}, year={2000}, pages={1564–1567} }
 @article{whaley_hedgpeth_farin_martus_jayes_britt_2000, title={Influence of vitamin A injection before mating on oocyte development, follicular hormones, and ovulation in gilts fed high-energy diets}, volume={78}, DOI={10.2527/2000.7861598x}, abstractNote={Previous research revealed that treatment with vitamin A approximately 5 d before ovulation may increase litter size in weaned sows and improve embryonal survival in gilts fed high-energy diets that reduced embryonal survival. For the current study, the hypothesis was that administration of vitamin A before ovulation would alter development of follicles and oocytes in a way favorable to enhanced embryonal survival. (Landrace x Large White) x (Duroc x Hampshire) gilts (n = 44) were fed 11.0 Mcal ME x gilt(-1) x d(-1) beginning 7 d after second estrus and given (i.m.) corn oil or 1 x 10(6) IU of vitamin A (retinyl palmitate) on d 15 after second estrus. Gilts were checked for estrus every 4 h, mated naturally at third estrus, and assigned randomly to undergo midventral laparotomy beginning at 24 to 28, 28 to 32, 32 to 36, or 36 to 40 h after onset of third estrus. At laparotomy, ovulated oocytes and early-stage embryos were recovered from oviducts, and ovaries were removed for aspiration of oocytes and granulosa cells from unovulated follicles. Oocytes and embryos were stained for assessment of stage of development. Granulosa cells were cultured to assess their ability to secrete progesterone. Follicular fluid was assayed for progesterone, estradiol-17beta, IGF-I, and PGF2alpha. Treatment with vitamin A altered development of oocytes and embryos by decreasing the percentage at the germinal vesicle stage and increasing the percentage at advanced stages. Mean stage of development was increased by vitamin A, but variation in stage was decreased. Among follicles matched by meiotic stage of oocyte, follicular fluid concentrations of progesterone, IGF-I, and PGF2alpha were greater in vitamin A-treated gilts than in controls, but treatment with vitamin A in vivo did not affect LH-stimulated or unstimulated secretion of progesterone by granulosa cells in vitro. These data provide evidence that vitamin A may influence embryonic development by advancing resumption of meiosis and altering follicular hormonal environment during follicle maturation.}, number={6}, journal={Journal of Animal Science}, author={Whaley, S. L. and Hedgpeth, V. S. and Farin, C. E. and Martus, N. S. and Jayes, F. C. L. and Britt, Jack}, year={2000}, pages={1598–1607} }
 @article{cushman_desouza_hedgpeth_britt_1999, title={Superovulatory response of one ovary is related to the micro- and macroscopic population of follicles in the contralateral ovary of the cow}, volume={60}, ISSN={["1529-7268"]}, DOI={10.1095/biolreprod60.2.349}, abstractNote={We hypothesized that the ovulatory response of one ovary to FSH would be related positively to the size of the primordial and growing pools of follicles in the other ovary. Nonlactating cows (n = 26) were unilaterally ovariectomized and 2 days later were superovulated. The superovulatory response was classified as Low (< 5 corpora lutea [CL]), Medium (5-14 CL), or High (> 14 CL). Surface follicles on the ovary removed before superovulation were classified as small (1-3 mm), medium (3-7 mm), or large ( > 7 mm), and the ovary was then fixed and serially sectioned. Follicles </= 1 mm in diameter in 388 +/- 38 fields (2 x 2 mm) per cow were classified as primordial, primary, secondary, or tertiary. By classification, Suboptimal ovaries contained < 100 follicles </= 1 mm and Optimal ovaries contained > 250 follicles </= 1 mm. Number of CL was correlated positively with total number of primordial, tertiary, and medium surface follicles. Number of Empty fields (2 x 2-mm fields containing no follicles) was correlated negatively with superovulatory response and number of primordial follicles. Number of CL was related to number of tertiary follicles in a positive linear manner and the number of medium follicles in a positive quadratic manner (r 2 = 0.66). Numbers of primordial, tertiary, small surface follicles, medium surface follicles, and total surface follicles were lower (p </= 0.06) in the Low superovulatory response group than in the Medium or High group. Suboptimal ovaries had fewer small surface follicles and fewer CL than Optimal ovaries (p < 0.05). We conclude that superovulatory response in cattle is related positively to the pools of primordial and growing follicles in the bovine ovary.}, number={2}, journal={BIOLOGY OF REPRODUCTION}, author={Cushman, RA and DeSouza, JC and Hedgpeth, VS and Britt, JH}, year={1999}, month={Feb}, pages={349–354} }
 @article{cushman_davis_boonyaprakob_hedgpeth_burns_britt_1999, title={Technical note: Use of slow-release estradiol and prostaglandin F-2 alpha to induce pseudopregnancy and control estrus in gilts}, volume={77}, DOI={10.2527/1999.77112883x}, abstractNote={We determined whether a single injection of slow-release estradiol-17beta (SRE2) would induce pseudopregnancy in gilts and whether PGF2alpha would regress the corpora lutea (CL) of pseudopregnancy. Crossbred gilts (n = 40) were induced to ovulate by treatment with 400 IU of hCG + 200 IU of eCG (PG600, Intervet, Millsboro, DE) given at 180 d of age (d = 0). On d 14, gilts were injected i.m. with one of five doses (n = 8 gilts/dose) of SRE2 (0, 12.5, 25, 50, or 100 mg). Blood samples were collected before SRE2 and twice weekly until d 73 to monitor serum progesterone (P4) and estradiol (E2). On d 59, gilts received (i.m.) 10 mg of PGF2alpha (Lutalyse, Pharmacia Upjohn, Kalamazoo, MI) and were checked for estrus for 7 d. On d 62, mammary development was scored (0 = no development; 1 = some development; 2 = teat and gland development) by a neutral observer. Treatment with SRE2 increased (P < .05) peak E2 concentrations, duration of luteal function, and mammary gland score. There were no differences (chi-square, P > .05) among doses of SRE2 in the percentage of pseudopregnant gilts that showed luteolysis after PGF2alpha. We conclude that a single injection of SRE2 can induce pseudopregnancy and that the CL can be regressed with PGF2alpha, providing a simple method for controlling estrus in gilts.}, number={11}, journal={Journal of Animal Science}, author={Cushman, R. A. and Davis, P. E. and Boonyaprakob, U. and Hedgpeth, V. S. and Burns, P. J. and Britt, Jack}, year={1999}, pages={2883–2885} }
 @article{britt_cushman_hedgpeth_shaw_1999, title={Use of an ovarian biopsy to predict surface follicle numbers on the bovine ovary.}, volume={60}, number={1999}, journal={Biology of Reproduction}, author={Britt, J. H. and Cushman, R. A. and Hedgpeth, V. S. and Shaw, D. W.}, year={1999}, pages={107} }
 @article{whaley_hedgpeth_britt_1997, title={Evidence that injection of vitamin A before mating may improve embryo survival in gilts fed normal or high-energy diets}, volume={75}, DOI={10.2527/1997.7541071x}, abstractNote={The hypothesis was that administration of vitamin A before ovulation would improve embryo survival in gilts fed a high-energy diet intentionally to reduce embryo survival. Forty crossbred ([Landrace x Large White] x [Duroc x Hampshire]) gilts were fed control (5.5 Mcal ME/d) or high-energy (11.0 Mcal ME/d) diets from 7 d after second estrus until 11 to 12 d after third estrus. Gilts in each dietary group received (i.m.) corn oil or retinyl palmitate (1 x 10(6) IU, vitamin A) on d 15 after second estrus and were mated at third estrus. Blood for determination of progesterone and estradiol was collected twice daily. The uterus and ovaries were removed on d 11 or 12 after third estrus for assessment of number of CL, and number, size and aromatase activity of embryos. Neither diet nor vitamin treatment affected number of CL. The high-energy diet exerted a negative effect on number of embryos (P = .09) and embryo survival (P = .07), whereas vitamin A exerted a positive effect on number of embryos (P = .07) and embryo survival (P = .08). The high-energy diet increased variation in embryo diameter, whereas vitamin A reduced variation in diameter and increased average diameter. Neither diet nor vitamin treatment influenced aromatase activity of embryos. Diet and vitamin treatment interacted with day to influence serum progesterone, but not estradiol. Injecting vitamin A before estrus restored embryo survival to normal levels in gilts fed high-energy diets, and this may be attributable to decreased variation in size of embryos.}, number={4}, journal={Journal of Animal Science}, author={Whaley, S. L. and Hedgpeth, V. S. and Britt, Jack}, year={1997}, pages={1071–1077} }