JOE
HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


DOI: 10.1677/joe.0.1600365

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 ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (21)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kann, G
Right arrow Articles by Djiane, J
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kann, G
Right arrow Articles by Djiane, J
Journal of Endocrinology, Vol 160, Issue 3, 365-377
Copyright © 1999 by Society for Endocrinology


Articles

Demonstration of in vivo mammogenic and lactogenic effects of recombinant ovine placental lactogen and mammogenic effect of recombinant ovine GH in ewes during artificial induction of lactation

G Kann, A Delobelle-Deroide, L Belair, A Gertler, and J Djiane


The present study demonstrates that ovine placental lactogen (oPL) (ovine chorionic somatotrophin) may have an important role in the mammogenesis and/or lactogenesis of the ewe. Its effects were compared with that already described for ovine growth hormone (oGH). In the first experiment, 40 nulliparous ewes were induced to lactate by means of a 7 day (days 1-7) oestro-progestative treatment (E2+P4). The ewes from Group 1 (n=12) received no further treatment, while those of the other groups received either recombinant oGH (roGH, 28 micrograms/kg, i.m., twice daily, Group 2, n=12) or recombinant oPL (roPL, 79 micrograms/kg, i.m., twice daily, Group 3, n=12) from day 11 to 20. All ewes received 25 mg hydrocortisone acetate (HC) twice daily on days 18-20. Control Group 00 (n=2) received no steroid treatment at all, and the control Group 0 (n=2) received only the E2+P4 treatment. Thirteen ewes (three from each experimental group and the two of each control group) were slaughtered at the end of hormone treatments (day 21) before any milking stimulus. The 27 remaining ewes from Groups 1-3 were machine-milked and milk yields recorded daily from day 21 to 76. The E2+P4 treatment enhanced the plasma levels of oPRL, oGH and IGF-I between days 1 and 7 by 1.5, 2. 3 and 2.6 times respectively (P=0.002); roGH treatment induced a highly significant enhancement of IGF-I plasma levels from day 11 to 20, whereas a similar effect appeared for roPL-treated ewes only from day 17 to 20 (P<0.01). Eight weeks after the last exogenous hormone injections, milk yields of both roGH- and roPL-treated groups progressively rose to twice that of unsupplemented groups (P<0.001). The mammary DNA content on day 21 was higher for animals which received either oGH or oPL but, due to individual variations in so few samples (n=3), this difference was not significant. No beta-casein was measured in mammary tissue from control ewes, whereas steroid-treated ewes (E2+P4+HC) had higher casein concentrations regardless of subsequent hormonal treatment on days 11-20 (P<0.001). beta-Casein concentrations in mammary parenchyma of roGH-treated ewes did not differ from that of ewes which received only E2+P4+HC; roPL supplementation clearly enhanced expression of beta-casein (P<0.001). IGF-I stimulation by either roGH or roPL was more precisely examined during a second experiment, in which two twice-daily i.m. doses (58 or 116 micrograms/kg) of either roGH or roPL were administered to four groups of six ewes that were E2+P4 treated as those of Experiment 1. A control group (n=6) received no exogenous hormone from day 11 to 13. On day 13, hourly blood samples were taken from all ewes over 11 h. Both doses of roGH significantly stimulated IGF-I in a dose-dependent manner. The 58 micrograms/kg dose of roPL did not significantly stimulate IGF-I, but although being somewhat less efficient than the 58 micrograms/kg dose of roGH, the 116 micrograms/kg dose of roPL significantly stimulated IGF-I secretion (P<0. 001). These results suggest that mammogenesis and/or lactogenesis in the ewe is in part controlled by somatotrophic hormones such as oGH and oPL and that IGF-I could be one of the mediators of these hormones.


This article has been cited by other articles:


Home page
J DAIRY SCIHome page
B. R. Andrade, A. A. K. Salama, G. Caja, V. Castillo, E. Albanell, and X. Such
Response to Lactation Induction Differs by Season of Year and Breed of Dairy Ewes
J Dairy Sci, June 1, 2008; 91(6): 2299 - 2306.
[Abstract] [Full Text] [PDF]


Home page
J EndocrinolHome page
T. Braun, S. Li, T. J M Moss, J. P Newnham, J. R G Challis, P. D Gluckman, and D. M Sloboda
Maternal betamethasone administration reduces binucleate cell number and placental lactogen in sheep
J. Endocrinol., August 1, 2007; 194(2): 337 - 347.
[Abstract] [Full Text] [PDF]


Home page
Exp PhysiolHome page
C. Molinari, E. Grossini, D. A. S. G. Mary, F. Ribichini, N. Surico, and G. Vacca
The role of nitric oxide in the peripheral vasoconstriction caused by human placental lactogen in anaesthetized pigs
Exp Physiol, May 1, 2006; 91(3): 603 - 610.
[Abstract] [Full Text] [PDF]


Home page
J EndocrinolHome page
K H Al-Gubory, S Camous, G Germain, P Bolifraud, A Nicole, and I Ceballos-Picot
Reconsideration of the proposed luteotropic and luteoprotective actions of ovine placental lactogen in sheep: in vivo and in vitro studies.
J. Endocrinol., March 1, 2006; 188(3): 559 - 568.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
E. Biener, C. Martin, N. Daniel, S. J. Frank, V. E. Centonze, B. Herman, J. Djiane, and A. Gertler
Ovine Placental Lactogen-Induced Heterodimerization of Ovine Growth Hormone and Prolactin Receptors in Living Cells Is Demonstrated by Fluorescence Resonance Energy Transfer Microscopy and Leads to Prolonged Phosphorylation of Signal Transducer and Activator of Transcription (STAT)1 and STAT3
Endocrinology, August 1, 2003; 144(8): 3532 - 3540.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Herman, C. Bignon, N. Daniel, J. Grosclaude, A. Gertler, and J. Djiane
Functional Heterodimerization of Prolactin and Growth Hormone Receptors by Ovine Placental Lactogen
J. Biol. Chem., February 25, 2000; 275(9): 6295 - 6301.
[Abstract] [Full Text] [PDF]




HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the Society for Endocrinology.