Whitten, W. K. (1957). The effect of progesterone on the development of mouse eggs in vitro. The Journal of endocrinology, 16(1), 80-85. https://doi.org/10.1677/joe.0.0160080
Whitten WK. The effect of progesterone on the development of mouse eggs in vitro. J Endocrinol. 1957;16(1):80-85. doi:10.1677/joe.0.0160080
Whitten, W. K. "The effect of progesterone on the development of mouse eggs in vitro." The Journal of endocrinology, vol. 16, no. 1, 1957, pp. 80-85.
For EndNote, Zotero or Mendeley:
License
No open license is recorded for this paper. Reuse terms are set by the publisher.
Abstract
Summary
1. The action of progesterone on the development of the mouse ovum from the eight-celled stage to the blastula has been studied in vitro . 2. Concentrations of progesterone below 2 μg/ml. produced no observable effect, whereas some toxicity was observed at 4 μg/ml. and few ova survived higher concentrations. 3. Herniation of the zona pellucida by the developing blastula is described; this process was inhibited by 4 μg/ml., but not by 2 μg/ml. of progesterone. 4. Blastulae appear to be more sensitive to the action of progesterone than are earlier stages. 5. Oestrogens afforded no demonstrable protection against the toxic action of progesterone when added to the culture medium. 6. The possible physiological significance of these findings is discussed.
Summary. The manner whereby progesterone acts as an inhibitor of cleavage of mammalian ova was studied using rabbit ova in vitro. Progesterone blocked cleavage when it was present in the culture medium at concentrations of 10 µg/ml more, and exerted this same effect on all stages up to the morula. The growth of blastocysts was not affected. The action was reversible: ova resumed cleavage within 2 to 3 hr after removal to progesterone-free media. The reversal was time-specific and was used to phase the subsequent cleavage of ova inhibited for varying periods of time. The inhibition was overcome by increasing the concentrations of amino acids or of the serum component in the medium. Supplementing the progesterone media with oestradiol did not reverse the inhibition. Autoradiographs of sections of ova that were kept in C-labelled progesterone for 8 hr, showed silver grains concentrated on the surface of the ovum and the zona pellucida. It is concluded that progesterone blocks cleavage by limiting the supply of protein or amino acids and thus inhibiting protein synthesis within the ovum. Presumably this is done by the progesterone aggregating on the surface of the cell or its protective coating. The inhibitory action appears to be timed in relation to some event that precedes mitosis by an hour or two. It is therefore suggested that the protein synthesis involved is related to formation of the mitotic apparatus or to chromosome condensation.
DeMayo FJ et al., 2020·Journal of molecular endocrinology·Free full text on PubMed Central
Progesterone's ability to maintain pregnancy in eutherian mammals highlighted this steroid as the 'hormone of pregnancy'. It was the unique 'pro-gestational' bioactivity of progesterone that enabled eventual purification of this ovarian steroid to crystalline form by Willard Myron Allen in the early 1930s. While a functional connection between normal progesterone responses ('progestational proliferation') of the uterus with the maintenance of pregnancy was quickly appreciated, an understanding of progesterone's involvement in the early stages of pregnancy establishment was comparatively less well understood. With the aforementioned as historical backdrop, this review focuses on a selection of key advances in our understanding of the molecular mechanisms by which progesterone, through its nuclear receptor (the progesterone receptor), drives the development of endometrial receptivity, a transient uterine state that allows for embryo implantation and the establishment of pregnancy. Highlighted in this review are the significant contributions of advanced mouse engineering and genome-wide transcriptomic and cistromic analytics which reveal the pivotal molecular mediators and modifiers that are essential to progesterone-dependent endometrial receptivity and decidualization. With a clearer understanding of the molecular landscape that underpins uterine responsiveness to progesterone during the periimplantation period, we predict that common gynecologic morbidities due to abnormal progesterone responsiveness will be more effectively diagnosed and/or treated in the future.
Intrauterine pressure was monitored in vivo in oestrogen-treated ovariectomized ewes before, during and after treatment with progesterone (50 mg s.c./day for 3 days). Progesterone reversibly reduced the frequency and amplitude of myometrial activity and abolished uterine reactivity to oxytocin (i.v.) and PGF-2alpha (intrauterine infusion). The rate of rise of intrauterine pressure during active pressure cycles was significantly reduced. These results confirm that the action of progesterone on the ovine myometrium is comparable to the classic progesterone 'block'. The intrauterine infusion of PGF-2alpha (10 microgram/min), which elicited a marked mechanical response in the control animals, failed to stimulate the progesterone-'blocked' uterus, suggesting that the inhibition produced by progesterone is due to a direct action of the hormone on the uterine muscle and not to an indirect mechanism operating through endometrial prostaglandin output.
Progesterone, the naturally-occurring 21-carbon steroid produced by the corpus luteum of the ovary and by the placenta, plays an important role in re-production. It is not surprising, then, that it has been used extensively as a supplement in the treatment of disorders of fertility and pregnancy. For example, progesterone is necessary for maintenance of pregnancy in mammals, including humans, and has been given for threatened or habitual miscarriage. The relaxant effect of progesterone on smooth muscle, including that of the uterus, has led to administration of this agent for preterm labor. The effect of progesterone in preparing the endometrium for implantation of the blastocyst has given rise to use of this hormone after natural or induced ovulation to supplement the function of the corpus luteum. How well such treatments work has been argued for many years; however, the fact remains that large numbers of women of reproductive age have received this hormone. It is pertinent, then, to consider whether progesterone or similar agents exert adverse effects on embryo development.
PMID 13491736 13491736 DOI 10.1677/joe.0.0160080 10.1677/joe.0.0160080 Whitten et al. 1957, Whitten 1957
Cite this article
Whitten, W. K. (1957). The effect of progesterone on the development of mouse eggs in vitro. The Journal of endocrinology, 16(1), 80-85. https://doi.org/10.1677/joe.0.0160080
Whitten WK. The effect of progesterone on the development of mouse eggs in vitro. J Endocrinol. 1957;16(1):80-85. doi:10.1677/joe.0.0160080
Whitten, W. K. "The effect of progesterone on the development of mouse eggs in vitro." The Journal of endocrinology, vol. 16, no. 1, 1957, pp. 80-85.
Keywords
Animals, In Vitro Techniques, Mice, Ovum/drug Effects, Progesterone/pharmacology, Progesterone, OVUM/effect of Drugs On, PROGESTERONE/effects