Hormonal influences on the glycogen content of normal and delayed implanting mouse blastocysts
β Scribed by Ozias, C. Blake ;Weitlauf, Harry M.
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- English
- Weight
- 392 KB
- Volume
- 177
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
β¦ Synopsis
The proportion of delayed implanting mouse blastocysts capable of normal development following transfer to pseudopregnant recipients is influenced by the length of the delay period. Thus, approximately one-third develop normally when transferred on days 5, 9 or 15 (day 1, day of vaginal plug), while only 3% do so when transferred on day 30 (Weitlauf and Greenwald, '68a). In the present experiments, the amount of glycogen in normal and delayed implanting mouse blastocysts was estimated enzymatically to determine whether it plays a limiting role in embryonic survival.
Normal blastocysts and delayed implanting blastocysts (i.e., in mice ovariectomized on day 4) contained a similar amount of glycogen on day 5. However, by day 10 the amount of glycogen in the delayed implanting blastocysts dropped to about half that found on day 5 but showed no further decrease between day 10 and day 30. Therefore, the amount of glycogen in delayed implanting mouse blastocysts does not appear to be the limiting factor in embryonic survival.
π SIMILAR VOLUMES
## Abstract The effect of continuous darkness on diurnal variation of glycogen content in pineal cells of adult mice was investigated by means of a semiquantitative histochemical method. In darkβmaintained mice, a diurnal rhythm in pineal glycogen content persisted for the first 7 days of darkness.
The industrial use of bismuth is increasing. In medicine, bismuth compounds have long been used in the treatment of gastrointestinal disorders, recently in combination with antibiotics for the treatment of Helicobacter pylori-associated peptic ulcers. Bismuth-induced encephalopathy is a known side-e
The injection of mice with 800 micrograms of an affinity-purified goat antibody to mouse IgD (GaM delta) induces early, T-independent polyclonal increases in the expression of B cell surface Ia, and B cell size and DNA synthesis, as well as later, T-dependent polyclonal increases in spleen cell numb