Exam 4 (Lecture 56) - Luteal Phase Flashcards
Name the two sub-phases of the luteal phase and the concentration trends of the major hormones (P4, E2, LH and FSH) during these two sub-phases.
1) Metestrus
- P4 starts to rise after ovulation
2) Diestrus
- P4 peaks during diestrus
*The other hormones are at insignificant during these two subphases.
Describe the transitions of the follicular cells to the luteal cells; that is, which follicular cells become which luteal cells?
Granulosa cells = become the large luteal cells (LLCs)
Theca cells = become the small luteal cells (SLCs)
What are the two general facets of luteolysis? (slide 6)
1) The finite lifespan of the LLCs and SLCs
2) A hormone that kills the LLCs and SLCs
What are the CA and CH?
CA = corpus albicans
- The very small CL (CL has started to degenerate so that the cycle can restart at the follicular phase)
CH = corpus hemorrhagicum
- The early stage of the CL; named due to the blood vessels that rupture during the progression of the CL
Which cells are the major source of progesterone during the luteal phase, and why are they the major source?
Large luteal cells; LH (that normally stimulates theca cells/SLCs to synthesize P4) levels are very low during the luteal phase.
Discuss the relationship between oxytocin and PGF2-alpha in regards to the active facet of luteolysis.
The dying CL releases oxytocin (peptide hormone).
As apoptosis increases in the CL, oxytocin release also increases.
- P4 increases the number of oxytocin receptors in the endometrium (uterus)
- Oxytocin then stimulates the synthesis of PGF2-alpha in the uterus
- PGF2-alpha goes to the CL using the vascular counter-current exchange
- PGF2-alpha directly activates apoptosis by activating its cognate GPCR
- The PGF2-alpha activity speeds up the degeneration of the CL and return to the follicular phase
Discuss the five feedback mechanisms of the luteal phase.
1) P4 prevents GnRH release at the hypothalamus
2) P4 prevents GnRH activity at the anterior pituitary
3) P4 stimulates oxytocin-R synthesis in the endometrium
4) Oxytocin stimulates PGF2-alpha synthesis in the endometrium
5) PGF2-alpha stimulates oxytocin release from the CL