The Effect of GnRH Agonist (Buserelin) Treatment of Awasi Ewes on Day 12 Post-mating on Plasma Oestradiol Concentrations

2006 ◽  
Vol 9 (2) ◽  
pp. 201-204
Author(s):  
Ghazi F. Basiouni
1994 ◽  
Vol 58 (2) ◽  
pp. 243-247 ◽  
Author(s):  
N. F. G. Beck ◽  
A. R. Peters ◽  
S. P. Williams

AbstractAn investigation was conducted to determine the effects of treatment with the GnRH agonist buserelin on day 12 post mating on the reproductive performance of ewes. There was a non-significant (P > 0·05) increase in nonreturn rate (control 0·76 v. buserelin 0·83) and litter size (control 1·51 v. buserelin 1·77) in three flocks. However, there was a significant (P < 0·05) increase in the number of twin lambs born (control 20 v. buserelin 40) and litter size (control 1·44 v. buserelin 1·68) in the yearling flock. There was no effect of buserelin on oestrous cycle length, although there was a tendency for treated animals to have a longer gestation length and heavier lambs. In a ewe lamb flock there was no effect of buserelin on non-return rate or litter size assessed post slaughter on day 31 of pregnancy. However, ovulation rate tended to be greater in the treated animals, which suggests that buserelin may have induced the formation of accessory corpora lutea. These results indicate that buserelin treatment improves embryo survival and that this effect is particularly evident in yearling ewes.


1969 ◽  
Vol 61 (1_Suppl) ◽  
pp. S213 ◽  
Author(s):  
C. S. Corker ◽  
F. Naftolin ◽  
D. Exley

1973 ◽  
Vol 72 (2) ◽  
pp. 330-344 ◽  
Author(s):  
Peter Doerr

ABSTRACT A hapten-radioimmunoassay for plasma oestradiol is described and information about the reliability of the method is given in detail. Oestradiol-3-hemisuccinate coupled to keyhole limpet haemocyanin is used for immunization of rabbits. The antiserum utilized for the assay is characterized by its titer, affinity and specificity. Following ether extraction and NaOH-light petroleum partition oestradiol is separated from crossreacting oestrogens by TLC. Oxidation of oestradiol on the plate is prevented by mercaptoethanol. To separate free and antibody bound ligand 250 μg dextran-coated charcoal per tube is used in the presence of bovine serum gammaglobulin (1 mg/ml). The between-assay precision based on 15 different determinations of control samples from normal adult male plasma was 9.4% (C. V.). The mean reagent blank value of 31 determinations was equivalent to 0.3 pg oestradiol and the detection limit in terms of the 99% confidence limit for a single blank value, was equivalent to 4.3 pg oestradiol. A procedure for detecting plasma blanks is described. Plasma oestradiol is separated from approximately all concomitant substances originally present in the sample by enzymatic conversion into oestrone and a second TLC. No plasma blanks could be detected with respect to normal adult male plasma. Normal values for adult males based on 51 subjects were characterized by a median of 17.2 pg/ml and the 95 percentiles of 9.5–27.6.


1982 ◽  
Vol 101 (2) ◽  
pp. 248-253 ◽  
Author(s):  
Viveca Odlind ◽  
Kerstin Elamsson ◽  
Doris E. Englund ◽  
Arne Victor ◽  
Elof D. B. Johansson

Abstract. Sex hormone binding globulin (SHBG) levels were studied for possible effects of oestradiol-17β on SHBG. No change in SHBG plasma was recorded during normal menstrual cycles or during treatment with oestradiol-17β to menopausal women. However, gonadotrophin treatment to amenorrhoeic women to induce ovulation resulted in high oestradiol concentrations and a pronounced increase in SHBG was found during the luteal phase of these cycles. A marked increase of SHBG was also recorded in a woman with pronounced fluctuations of oestradiol during treatment with levonorgestrel sc implants for contraception. In conclusion, effects on SHBG were only found when extraordinarily high levels of plasma oestradiol were recorded.


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