Corpus luteum size and plasma progesterone concentration in cows

2009 ◽  
Vol 115 (1-4) ◽  
pp. 296-299 ◽  
Author(s):  
G.E. Mann
1967 ◽  
Vol 55 (1) ◽  
pp. 91-96 ◽  
Author(s):  
Benno Runnebaum ◽  
Josef Zander

ABSTRACT Progesterone was determined and identified in human peripheral blood during the preovulatory period of the menstrual cycle, by combined isotope derivative and recrystallization analysis. The mean concentration of progesterone in 1.095 ml of plasma obtained 9 days before ovulation was 0.084 μg/100 ml. However, the mean concentration of progesterone in 1.122 ml of plasma obtained 4 days before ovulation was 0.279 μg/100 ml. These data demonstrate a source of progesterone secretion other than the corpus luteum. The higher plasma-progesterone concentration 4 days before ovulation may indicate progesterone secretion of the ripening Graafian follicle of the ovary.


2003 ◽  
Vol 2003 ◽  
pp. 1-1
Author(s):  
B.V.E. Segwagwe ◽  
K.L. Macmillan ◽  
P.D. Mansell

Oestrous synchronisation involves synchronisation of ovarian follicular turnover, new wave emergence, and finally induction of ovulation which can be achieved with an injection of either GnRH (Pursley et al. 1997)or oestradiol benzoate (ODB) (Day et al. 2000). A comparative study investigating corpus luteum (CL) and follicular emergence after the administration of either GnRH or ODB at pro-oestrus has not been reported. It was hypothesised that the injection of ODB at pro-oestrus would delay emergence of the first post-ovulatory follicular wave, but that CL development and plasma progesterone concentrations would be similar in cows induced to ovulate with either GnRH or ODB.


1990 ◽  
Vol 38 (1) ◽  
pp. 45-52
Author(s):  
J. van der Meulen ◽  
F.A. Helmond ◽  
C.P.J. Oudenaarden

Progesterone profiles of 7 cycling gilts and those of 6 gilts inseminated on day 1 (1 day after the onset of oestrus) were studied. The results showed that plasma progesterone concentration in the inseminated group was higher (P


1969 ◽  
Vol 62 (1) ◽  
pp. 82-88 ◽  
Author(s):  
Elof D. B. Johansson ◽  
Leif Wide

ABSTRACT Plasma LH and progesterone levels were measured around the time of ovulation in 16 normal menstrual cycles. No increased levels of progesterone were found before the LH peak. The maximal LH peak levels lasted for 16–20 h at which time the plasma progesterone rose to a concentration of 1 to 2 ng/ml. Following the fall in the LH concentration, there was a rapid rise in the plasma progesterone concentration, indicating the formation of a corpus luteum. The lowest basal body temperature coincided with the first significant rise in LH levels.


2008 ◽  
Vol 20 (1) ◽  
pp. 237
Author(s):  
L. G. B. Siqueira ◽  
J. H. M. Viana ◽  
C. A. A. Torres ◽  
E. D. Souza ◽  
L. S. Amorim ◽  
...  

It has been suggested that ultrasound image attributes are a potential indicator of the physiological and functional status of the corpus luteum (CL). The aim of this study was to evaluate corpus luteum morphological and echotextural changes, and to correlate these changes with plasma progesterone concentration [P4] throughout the bovine estrous cycle. Crossbred heifers were scanned daily, using a B-mode, real-time ultrasound machine equipped with a 5-MHz linear-array rectal transducer, throughout a natural estrous cycle (Experiment 1; n = 12) or during a shorter estrous cycle, interrupted on the 10th day, by luteolysis induction (Experiment 2; n = 6). Blood samples were collected for further plasma [P4] analyses by RIA. Corpora lutea areas (cm2) were measured, and daily images of each CL were videotaped (VHS tapes) until digitized. Computer-assisted analyses of image attributes were performed using a custom-developed software. Daily values of luteal area, echotexture, and plasma [P4] values were analyzed by ANOVA with Tukey's test to determine differences among means of each cycle day. Pearson's correlation coefficients were calculated between luteal area, mean pixel value, pixel heterogeneity, and plasma [P4]. In the first experiment, luteal tissue area increased to a maximum on the 10th day (P < 0.05), followed by a plateau, and then declined from Day 14 to next estrus. There was a significant correlation between luteal tissue area and plasma P4 (r = 0.69; P < 0.01). In the second experiment, plasma P4 dropped to basal values 24 h after luteolysis induction. Luteal tissue area decreased at a slow rate, and reached values similar to ones from metestrus 36 h after treatment. In Experiment 1, echotexture parameters of the CL were analyzed after data adjustment to the onset of luteolysis. In both experiments, mean pixel values did not change throughout the estrous cycle and there was no correlation between mean pixel values and plasma [P4] (P > 0.10). Pixel heterogeneity changed throughout the natural estrous cycle, with maximum value on metestrus (Day 14; Day 0 = luteolysis) and minimum on diestrus (Day 2; P < 0.01). However, this parameter did not change when luteolysis was induced (Experiment 2; P > 0.10). There were significant correlations between pixel heterogeneity and plasma progesterone in both of the experiments (r = –0.69 and r = –0.48; P < 0.05). In conclusion, mean pixel values do not reflect morphological or functional changes of the CL throughout the estrous cycle. On the other hand, based on the correlations between pixel heterogeneity and systemic [P4] in both experiments, this image attribute (heterogeneity) has the potential to indicate functionality and steroidogenic capacity of the luteal gland.


1983 ◽  
Vol 97 (3) ◽  
pp. 425-436 ◽  
Author(s):  
Leigh Findlay ◽  
K. L. Ward ◽  
M. B. Renfree

Mammary gland lactose concentrations in pregnant tammar wallabies remained low at 115 ± (s.e.m.) μg/g wet weight of tissue until immediately before parturition, then increased to 1274±262 μg/g after birth. Concentrations in non-pregnant cyclic animals were generally low 143±36 μg/g), but were raised in three animals around the time of oestrus. Removal of the corpus luteum on day 18 of pregnancy or the oestrous cycle caused an increase in lactose concentrations in both lutectomized and sham-operated animals. This occurred despite a significant lowering of peripheral plasma progesterone concentration in only the lutectomized group. Plasma cortisol concentrations were high in some of these animals, but showed no consistent relationships with the raised lactose concentrations. The increased peripartum lactose concentration normally coincides with a sharp fall in peripheral plasma progesterone concentration, but artificial maintenance of high progesterone levels had no effect on the increase of mammary gland lactose at parturition. Mammary gland lactose concentrations in tammar wallabies are therefore a useful indicator of biosynthetic activity and as an index of lactogenesis but the role, if any, of progesterone withdrawal in lactogenesis remains unclear.


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