PLASMA OESTRADIOL AND HUMAN LUTEINIZING HORMONE DURING THE MENSTRUAL CYCLE

1969 ◽  
Vol 61 (1_Suppl) ◽  
pp. S213 ◽  
Author(s):  
C. S. Corker ◽  
F. Naftolin ◽  
D. Exley
2021 ◽  
Vol 25 ◽  
pp. e00211
Author(s):  
Ellen Anckaert ◽  
Alexander Jank ◽  
Julia Petzold ◽  
Felix Rohsmann ◽  
Rhonda Paris ◽  
...  

Endocrinology ◽  
1970 ◽  
Vol 87 (4) ◽  
pp. 658-666 ◽  
Author(s):  
VERNON C. STEVENS ◽  
SARAH J. SPARKS ◽  
JOHN E. POWELL

1972 ◽  
Vol 53 (1) ◽  
pp. 31-35 ◽  
Author(s):  
K. BROWN-GRANT ◽  
C. S. CORKER ◽  
F. NAFTOLIN

SUMMARY Plasma luteinizing hormone (LH) concentrations were already lower on Day 2 of pregnancy than at the same time after the preceding ovulation in the non-pregnant rat, and fell progressively up to Day 16 of pregnancy. No evidence was obtained of any increase at the time when the ovulatory surge of LH would have occurred if the animal had not become pregnant. Pituitary LH concentration was lower in mated rats on the morning of Day 0 of pregnancy than in unmated controls on the morning of the day of oestrus. Subsequently it increased slowly to reach a level higher than at any stage of the oestrous cycle by Day 8 of pregnancy and remained high until at least Day 16 of pregnancy. Peripheral plasma oestradiol concentration increased late on Day 2 of pregnancy and was still raised on Day 4 but was never more than about one fourth of the peak concentration seen on the morning of prooestrus during the oestrous cycle. There were similar changes in plasma LH and oestradiol concentrations in the 48 h after a single injection of 2·5mg progesterone on the morning of the day of dioestrus, a procedure that delays ovulation by 1 or 2 days. Administration of a synthetic progestational compound (medroxyprogesterone acetate) to pregnant rats delayed blastocyst implantation and the delay was associated with a marked decrease in peripheral plasma LH to levels below those of normal pregnancy.


1984 ◽  
Vol 58 (6) ◽  
pp. 1050-1058 ◽  
Author(s):  
JOHANNES D. VELDHUIS ◽  
INESE Z. BEITINS ◽  
MICHAEL L. JOHNSON ◽  
MERCEDES A. SERABIAN ◽  
MARIA L. DUFAU

BMJ ◽  
1972 ◽  
Vol 4 (5836) ◽  
pp. 333-336 ◽  
Author(s):  
K. Hillier ◽  
A. Dutton ◽  
C. S. Corker ◽  
A. Singer ◽  
M. P. Embrey

1985 ◽  
Vol 61 (1) ◽  
pp. 43-49 ◽  
Author(s):  
MICHAEL R. SOULES ◽  
ROBERT A. STEINER ◽  
NANCY L. COHEN ◽  
WILLIAM J. BREMNER ◽  
DONALD K. CLIFTON

1997 ◽  
Vol 93 (1) ◽  
pp. 29-34 ◽  
Author(s):  
G. I. Adebayo ◽  
L. Hemeryck ◽  
M. Hall ◽  
D. Gasparro ◽  
M. Sinnott ◽  
...  

1. We undertook a temporal study of external sodium-stimulated lithium efflux (sodium—lithium countertransport) in erythrocytes and blood pressure by measuring these two parameters in three phases of the menstrual cycle (menstrual, midcycle and luteal phases) in 22 healthy, non-medicated females with regular menstrual cycles. Plasma oestradiol and progesterone levels were also determined. 2. Sodium—lithium countertransport activity (activity in 140 mmol/1 external NaCl) in the midcycle phase (0.176 ± 0.017 mmol h−1 l−1 of cells) was lower than in the menstrual (0.192 ± 0.016 mmol h−1 l−1 of cells, P < 0.030) and luteal (0.203 ± 0.018 mmol h−1 l−1 of cells, P < 0.030) phases. The Vmax of the transporter changed similarly but the Km was unaltered. 3. The plasma oestradiol level was 628.9 ± 39.1 pmol/1 in the midcycle phase, higher than in the menstrual (232 ± 18.5 pmol/1, P < 0.001) and luteal (372.5 ± 28.1 pmol/1, P < 0.001) phases. The progesterone level was 28.6 ± 2.1 nmol/1 in the luteal phase, and values were lower in the menstrual (2.5 ± 0.3 nmol/1, P < 0.001) and midcycle (2.8 ± 0.4 nmol/1, P < 0.001) phases. 4. There was no correlation between plasma oestradiol and sodium—lithium countertransport activity or Vmax during the menstrual cycle, but plasma progesterone was positively correlated with sodium—lithium countertransport activity (r = 0.478, P < 0.025, n = 22) and Vmax (r = 0.551, P < 0.045, n = 14) in the luteal phase. 5. Systolic blood pressure did not change significantly during the menstrual cycle. However, the diastolic pressure showed variation similar to that in sodium—lithium countertransport activity/Vmax, its midcycle value of 66.6 ± 1.4 mmHg being lower than that in the luteal (71.6 ± 1.3 mmHg, P < 0.025) and menstrual (70.6 ± 1.4 mmHg, P < 0.025) phases. 6. We conclude that sodium—lithium countertransport activity exhibits catamenial variation. Therefore we suggest, given this observation, that blood sampling for the assessment of the state of activity of the transport system be standardized in relation to a phase of the menstrual cycle in future studies involving females.


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