Cholesterol transport and steroidogenesis by the corpus luteum

The synthesis of progesterone by the corpus luteum is essential for the establishment and maintenance of early pregnancy. Regulation of luteal steroidogenesis can be broken down into three major events; luteinization (i.e., conversion of an ovulatory follicle), luteal regression, and pregnancy induced luteal maintenance/rescue. While the factors that control these events and dictate the final steroid end products are widely varied among different species, the composition of the corpus luteum (luteinized thecal and granulosa cells) and the enzymes and proteins involved in the steroidogenic pathway are relatively similar among all species. The key factors involved in luteal steroidogenesis and several new exciting observations regarding regulation of luteal steroidogenic function are discussed in this review

Quenching of lamellar ordering in an n-alkane embedded in nanopores

We present an X-ray diffraction study of the normale alkane nonadecane C_{19}H_{40} embedded in nanoporous Vycor glass. The confined molecular crystal accomplishes a close-packed structure by alignment of the rod-like molecules parallel to the pore axis while sacrificing one basic principle known from the bulk state, i.e. the lamellar ordering of the molecules. Despite this disorder, the phase transitions observed in the confined solid mimic the phase behavior of the 3D unconfined crystal, though enriched by the appearance of a true rotator phase known only from longer alkane chains.Comment: 7 pages, 3 figure

Molecular Cloning and Endometrial Expression of Porcine Amphiregulin

The porcine amphiregulin gene was previously reported to be within the quantitative trait locus (QTL) for uterine capacity on chromosome 8. Because amphiregulin stimulates cell proliferation, the amphiregulin gene might be responsible for this QTL. The objectives of this study were to clone amphiregulin cDNA and compare endometrial expression of its mRNA in pregnant Meishan (M) and White composite (WC) pigs. We obtained two amphiregulin cDNAs, one with 1,221 bp and another with 1,109 bp. The 112 bp difference corresponded to exon 5 of the human amphiregulin gene, which codes for the cytoplasmic domain. Endometrial mRNA expression of amphiregulin was significantly lower in M pigs than in WC pigs during early pregnancy (day 15–40 of gestation). Amphiregulin mRNA expression in the endometrium of both M and WC pigs increased (P \u3c 0.01) from days 15 to 20, decreased (P \u3c 0.01) from days 20 to 30, and did not change between days 30 and 40. This may result in reduced amphiregulin protein production leading to the slower development of M conceptuses, contributing to greater uterine capacity and litter size in prolific Chinese M pigs. Porcine genomic sequences isolated from a bacterial artificial chromosome genomic library contained exon 5, suggesting that the deletion of exon 5 in the mRNA may be due to differential splicing. The amphiregulin gene consisted of six exons and five introns spanning 10.3 kb

Lack of Effect of Metyrapone and Exogenous Cortisol on Early Porcine Conceptus Development

In many species, including swine, fetal plasma glucocorticoids such as cortisol increase as term approaches and are responsible for final maturational changes in numerous tissues (e.g. Silver, 1990; Sangild et al. 1993, 1994; Fowden et al. 1995). On the contrary, excessive exposure to glucocorticoids during gestationmay cause intra-uterine growth retardation, developmental abnormalities or death, or lead to increased incidence of certain diseases during adult life (Blackburn et al. 1965; Reinisch et al. 1978; Seckl et al. 2000). Hence, one might speculate that a closely regulated glucocorticoid exposure is necessary throughout gestation to ensure appropriate development and survival (Klemcke et al. 1999). We have previously demonstrated in pregnant and cyclic pigs that intra-uterine cortisol increases 4- to 6.7-fold between days 10 and 19 of pregnancy (Klemcke et al. 1998). At this time (days 10–19) in conceptus (embryo plus associated extra-embryonic membranes) development, the blastocyst is undergoing quite dramatic changes (Marrable, 1971; Anderson, 1978; Anderson et al. 1993). Part of this development involves the allantois, which rapidly expands between days 18 and 30 owing to water accumulation (Bazer et al. 1981) that might in part result from Na+,K+-ATPase-generated water movement (Macknight & Leaf, 1977). Corticosteroids are known to regulate Na+,K+-ATPase in various tissues (e.g. Verrey et al. 1996)

Lack of Effect of Metyrapone and Exogenous Cortisol on Early Porcine Conceptus Development

In many species, including swine, fetal plasma glucocorticoids such as cortisol increase as term approaches and are responsible for final maturational changes in numerous tissues (e.g. Silver, 1990; Sangild et al. 1993, 1994; Fowden et al. 1995). On the contrary, excessive exposure to glucocorticoids during gestationmay cause intra-uterine growth retardation, developmental abnormalities or death, or lead to increased incidence of certain diseases during adult life (Blackburn et al. 1965; Reinisch et al. 1978; Seckl et al. 2000). Hence, one might speculate that a closely regulated glucocorticoid exposure is necessary throughout gestation to ensure appropriate development and survival (Klemcke et al. 1999). We have previously demonstrated in pregnant and cyclic pigs that intra-uterine cortisol increases 4- to 6.7-fold between days 10 and 19 of pregnancy (Klemcke et al. 1998). At this time (days 10–19) in conceptus (embryo plus associated extra-embryonic membranes) development, the blastocyst is undergoing quite dramatic changes (Marrable, 1971; Anderson, 1978; Anderson et al. 1993). Part of this development involves the allantois, which rapidly expands between days 18 and 30 owing to water accumulation (Bazer et al. 1981) that might in part result from Na+,K+-ATPase-generated water movement (Macknight & Leaf, 1977). Corticosteroids are known to regulate Na+,K+-ATPase in various tissues (e.g. Verrey et al. 1996)

Mammalian oocytes are targets for prostaglandin E2 (PGE2) action

<p>Abstract</p> <p>Background</p> <p>The ovulatory gonadotropin surge increases synthesis of prostaglandin E2 (PGE2) by the periovulatory follicle. PGE2 actions on granulosa cells are essential for successful ovulation. The aim of the present study is to determine if PGE2 also acts directly at the oocyte to regulate periovulatory events.</p> <p>Methods</p> <p>Oocytes were obtained from monkeys and mice after ovarian follicular stimulation and assessed for PGE2 receptor mRNA and proteins. Oocytes were cultured with vehicle or PGE2 and assessed for cAMP generation, resumption of meiosis, and in vitro fertilization.</p> <p>Results</p> <p>Germinal vesicle intact (GV) oocytes from both monkeys and mice expressed mRNA for the PGE2 receptors EP2, EP3, and EP4. EP2 and EP4 proteins were detected by confocal microscopy in oocytes of both species. Monkey and mouse oocytes responded to PGE2 as well as agonists selective for EP2 and EP4 receptors with elevated cAMP, consistent with previous identification of EP2 and EP4 as Gαs/adenylyl cyclase coupled receptors. Incubation of mouse GV stage oocytes with PGE2 delayed oocyte nuclear maturation in vitro, but PGE2 treatment did not alter the percentage of mouse oocytes that fertilized successfully. PGE2 treatment also decreased the percentage of monkey oocytes that resumed meiosis in vitro. In contrast with mouse oocytes, the percentage of monkey oocytes which fertilized in vitro was lower after treatment with PGE2. Monkey oocytes with intact cumulus showed delayed nuclear maturation, but fertilization rate was not affected by PGE2 treatment.</p> <p>Conclusions</p> <p>Monkey and mouse oocytes express functional PGE2 receptors. PGE2 acts directly at mammalian oocytes to delay nuclear maturation. Surrounding cumulus cells modulate the effect of PGE2 to alter subsequent fertilization.</p

Measurement of CP Violation at the Υ(4S)\Upsilon(4S) without Time Ordering or Δt\Delta t

I derive the expressions for the CP-violating asymmetry arising from interference between mixed and direct decays in the Upsilon(4S) system, for the case in which only one of the B decay times is observed, integrating over the decay time of the other B. I observe that neither the difference of the decay times Delta t, nor even their time-ordering, need be detected. A technique for measurement of the CP-violating weak decay parameter sin(2beta) is described which exploits this observation.Comment: 9 pages postscript, also available through http://w4.lns.cornell.edu/public/CLN

Thermally Activated Dynamics of the Capillary Condensation

This paper is devoted to the thermally activated dynamics of the capillary condensation. We present a simple model which enables us to identify the critical nucleus involved in the transition mechanism. This simple model is then applied to calculate the nucleation barrier from which we can obtain informations on the nucleation time. We present a simple estimation of the nucleation barrier in slab geometry both in the two dimensional case and in the three dimensional case. We extend the model in the case of rough surfaces which is closer to the experimental case and allows comparison with experimental datas.Comment: 6 pages, 3 figures, Submitted to J. Phys. : Condens. Matter, Proceedings of the IV Liquid Matter Conference - Grenada(Spain) july 199

Assessment of Dose-dependent Endocrine and Immune Responses to Simulated Ionizing Radiation

The hypothalamic-pituitary-adrenal axis can regulate immune responses to counteract stressful stimuli in maintaining homeostasis within the body. Cosmic ionizing radiation is an innate risk within the space environment and it is known to cause direct DNA damage and indirectly impact cellular function, transduction, and communication processes. Assessment of different physiological systems and their interactions are important to consider for mitigation strategies in spaceflight. The degree of ionizing radiation and relative biological effectiveness is an open question as it pertains to immune and endocrine responses. Therefore, this study will assess the dose-dependent responses of immunity and adrenal function to cosmic ionizing radiation. For this, male and female C57 BL/6J mice were exposed to simulated, simplified five-ion galactic cosmic ray (GCR) radiation at 5cGy, 15cGy, and 50cGy. Blood and tissues were collected two-weeks post exposure and inflammatory biomarkers and hormone biochemical pathways were characterized by whole transcriptome RNA sequencing. Results displayed differential transcriptomic profiles for each condition and sex, indicating complex responses and networks are generated from different doses of ionizing radiation. Careful consideration of unique profiles highlights the current need for personalized medicine requirements for astronauts exposed to similar doses on exploration missions. Supported by the NASA Human Research Program (HRP) Human Factors Behavioral Performance Element Grant 18 18FLAG 2 0028 and Embry-Riddle Aeronautical University startup funding