Searchable, peer-reviewed, open-access proceedings from bioscience and biomedical conferences

bp0012cpr16 | Programmes for Controlled Reproduction | CPR1985

Control of pig reproductionin a breeding programme

Martinat-Botte Françoise , Bariteaut F. , Badouard B. , Terquit M.

Summary. Important improvements in the management of sows have been made over the past 20 years in Europe and the U.S.A. Nevertheless, annual productivity varied between 15 and 25 piglets weaned per sow per year in France for 1983. Reasons for such a difference in productivity have been analysed quantitatively.Marked differences exist between herds in the genotype of pig used and in the age of puberty. Transportation acts as a stress...

bp0014cpr9 | Ovarian and Uterine Function | CPR1993

Sources and biological actions of relaxin in pigs

Bagnell C. A. , Zhang Q. , Downey B. , Ainsworth L.

Although the major source of relaxin in pigs is the corpus luteum of pregnancy, there is now evidence for relaxin gene expression and translation into protein in the theca intema cells of the preovulatory follicle, the corpus luteum of the cycle and the uterus. The theca interna cells retain their ability to express the relaxin gene and protein following ovulation. During the early stages of development of the corpus luteum, the theca-derived small lutein cells are the so...

bp0016cpr23 | New Technologies | CPR2001

Transgenic alteration of sow milk to improve piglet growth and health

Wheeler M. B. , Bleck G. T. , Donovan S. M.

There are many potential applications of transgenic methodologies for developing new and improved strains of livestock. One practical application of transgenic technology in pig production is to improve milk production or composition. The first week after parturition is the period of greatest loss for pig producers, with highest morbidity and mortality attributed to malnutrition and scours. Despite the benefits to be gained by improving lactation performance, little prog...

bp0002rdr12 | Inhibin | REDR1990

Inhibin and secretion of FSH in oestrous cycles of cows and pigs

Taya K , Kaneko H , Watanabe G , Sasamoto S

Abstract unavailableKeywords: inhibin; oestradiol; cow; pig; FSH© 1991 Journals of Reproduction & Fertility Ltd...

bp0005rdr12 | Pre-natal Programming of Lifetime Productivity and Health | REDR2002

Gene expression in the developing embryo and fetus

Taylor J , Fairburn H , Beaujean N , Meehan R , Young L

Determining the stage- and tissue-specific patterns of gene expression shown by the embryo and fetus will provide information about the control of normal development. Identification of alterations in these patterns associated with specific abnormal phenotypes will also be informative regarding the underlying molecular mechanisms. In addition, qualitative and quantitative changes in gene expression that deviate from the norm may provide a potential marker system for predicting ...

bp0005rdr20 | Neuroendocrine Interactions | REDR2002

Stress and the control of LH secretion in the ewe

Smith RF , Ghuman SPS , Evans NP , Karsch FJ , Dobson H

Stress influences the activity of the reproductive system at several sites. One of the most significant effects is at level of the GnRH secretory system to reduce GnRH pulsatility and thus LH pulsatility. This in turn reduces the oestradiol signal that stimulates the GnRH–LH surge in the follicular phase. Three sequential phases have been identified in the induction of the GnRH–LH surge by oestradiol: (i) activation, (ii) transmission and (iii) surge secretion. There...

bp0007rdr22 | The Ruminant Corpus Luteum | REDR2010

Regulation of corpus luteum development and maintenance: specific roles of angiogenesis and action of prostaglandin F

Miyamoto A , Shirasuna K , Shimizu T , Bollwein H , Schams D

Development of the corpus luteum (CL) in ruminants occurs in a rapid and time-dependent manner within 1 week after ovulation, with morphologic and biochemical changes in the cells of the theca interna and granulosa cells of the preovulatory follicle. These changes involve luteinisation of steroidogenic cells and angiogenesis to establish normal luteal function (progesterone secretion). The CL is composed of a large number of vascular endothelial cells, large and small steroido...

bp0013cpr2 | The Hypothalamic-Pituitary-Ovarian Axis | CPR1989

Regulation and action of gonadotrophinsin pigs

Esbenshade K. L. , Ziecikt A. J. , Britt J. H.

Summary. Gonadotrophins, synthesized and secreted from the basophils of the adenohypophysis, bind to various target cells and elicit a wide variety of responses. Specific receptors for gonadotrophins have been found on plasma membranes of thecal, granulosa, luteal, endometrial and myometrial cells in the female and on Leydig and Sertoli cells in the Male. Gonadotrophins exert their effects through various intracellular second messengers and control biosyn...

bp0015cpr2 | Regulation of Reproductive Function | CPR1997

Immune-endocrine interactions affecting luteal function in pigs

Wuttke W. , Pitzel L. , Knoke L. , Theiling K. , Jarry H.

The formation, normal function and destruction of corpora lutea are essential features of normal reproduction. Although the formation of corpora lutea from follicles is largely dependent on pituitary gonadotrophins, the process of luteolysis is locally regulated and poorly understood. The corpus luteum consists of several steroidogenic and nonsteroidogenic cell types that interact with each other in a paracrine manner. Under cell culture conditions, large luteal cells tha...