J. Anim Sci.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J. Anim Sci. 1984. 58:1262-1270.
© 1984 American Society of Animal Science

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Diekman, M. A.
Right arrow Articles by Trout, W. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Diekman, M. A.
Right arrow Articles by Trout, W. E.

Serum Profiles of Progesterone, LH, FSH and Prolactin Immediately Preceding Induced Puberty in Gilts1,2,

Mark A. Diekman and William E. Trout

Purdue University3, West Lafayette, IN 47907

Abstract

Two experiments were conducted to determine if the secretory patterns of luteinizing hormone (LH), follicle stimulating hormone (FSH) and prolactin (PRL) and serum concentrations of progesterone change immediately preceding induced puberty in gilts. To help predict when prepubertal gilts would attain puberty, gilts were induced into puberty by relocation from confinement housing to an outdoor lot and exposure to mature boars. In Exp. 1, 17 prepubertal gilts were bled on two successive days from 0800 to 1200 h before relocation and boar exposure and until the second day of estrus or for 8 d in gilts that failed to exhibit estrus. Blood samples were collected from indwelling cannulas at 20-min intervals for 4 h. In Exp. 2, blood samples were collected from 20 prepubertal gilts at 20-min intervals from 0800 to 1200 h and from 2000 to Z400 h until the second day of estrus or for 6 d if the gilt failed to exhibit estrus. In each experiment, 11 gilts exhibited pubertal estrus 3 to 6 d after relocation and boar exposure. When the frequency of LH spikes in each gilt was normalized to the day of her preovulatory surge of LH (d 0), a decline in the frequency of LH secretory spikes was observed as gilts approached puberty. However, neither the average magnitude of LH spikes nor mean LH concentrations were different among these days. Mean serum concentrations, frequency of spikes or average magnitude of secretory spikes of FSH or PRL did not change on the days preceding the preovulatory peak of LH. In Exp. 1, 8 of 11 gilts that exhibited estrus had higher (P<.05) serum concentrations of progesterone on d –1 and 0 than on d –3 and –2. In Exp. 2, 7 of 11 gilts that achieved estrus had greater (P<.05) serum concentrations of progesterone on d –.5 than on d –1.5, –1.0 and 0. No increases in serum progesterone were observed in the gilts that failed to exhibit estrus in either experiment. In both experiments, serum concentrations of estradiol-17ß were elevated as gilts approached puberty. Serum concentrations of Cortisol remained unchanged on the days immediately preceding the preovulatory surge of LH. These results indicate that the frequency of LH secretory spikes decreased in gilts immediately preceding puberty induced by relocation and boar exposure. Of the 22 gilts that attained puberty, only 15 had a prepubertal rise of serum progesterone. Thus, it appears that a preovulatory rise in serum progesterone is not a necessary event for estrus or ovulation to occur in gilts.


Footnotes

1 Journal Paper No. 9506, Purdue Univ. Agr. Exp. Sta.

2 Presented in part at the 14th Annu. Meet, of the Soc. for the Study of Reprod., Corvallis, OR, Abstr. No. 88. The authors gratefully acknowledge Dr. G. D. Niswender, Colorado State Univ., for supplying antisera to progesterone and luteinizing hormone, Dr. N. R. Mason, Eli Lilly Co., for supplying antisera to estradiol-17ß, Dr. L. E. Reichert, Jr., Albany Medical College, for supplying purified porcine luteinizing hormone, Dr. R. J. Ryan, Mayo Clinic, for supplying purified porcine follicle stimulating hormone and Dr. P. V. Malven, Purdue Univ., for supplying antisera to porcine prolactin. The technical assistance of D. Elftman, D. Blair and K. Brandt is greatly appreciated.

3 Dept. of Anim. Sci.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1984 by the American Society of Animal Science.