Diurnal progesterone rhythms in the female mouse

1987 ◽  
Vol 112 (1) ◽  
pp. 15-21 ◽  
Author(s):  
K. J. Bailey
Keyword(s):  
Murine Models ◽  
Intact Mouse ◽  
Plasma Progesterone ◽  
Peripheral Plasma ◽  
Ovariectomized Mice ◽  
Oestradiol Benzoate ◽  
Adrenalectomized Mouse ◽  
Adrenal Secretion ◽  
Similar Rhythm

ABSTRACT The patterns of peripheral progesterone concentrations were investigated in a number of murine models on a 13 h light: 11 h darkness lighting regime. The pattern in the intact mouse at dioestrus was compared with that in the ovariectomized mouse. A diurnal pattern was recorded in both, maxima occurring around the end of the light period; no conspicuous nadir was recorded, levels of progesterone remaining relatively constant over a 14-h period. Adrenalectomized mice displayed no such rhythm, indicating that the adrenal is responsible for any diurnal rhythm in peripheral plasma progesterone concentrations at dioestrus. At pro-oestrus in intact animals a similar rhythm was observed, but the maximum levels of progesterone were approximately five times greater than at dioestrus and, moreover, persisted in adrenalectomized mice, indicating that the rhythm of adrenal secretion of progesterone is masked by ovarian secretion. Ovariectomized mice with implants of oestradiol-17β displayed a similar rhythm to that of intact mice at dioestrus, but had significantly higher plasma progesterone levels around the time of the maxima although not over the total 24-h period. An s.c. injection of oestradiol benzoate superimposed on oestrogen levels produced by implants had no significant effect on plasma progesterone levels. Also at pro-oestrus the pattern of peripheral LH concentration was investigated in both the intact and the adrenalectomized mouse. For both, maxima were recorded just before darkness, at 19.00 h, in advance of the progesterone surge. In adrenalectomized mice this surge at 19.00 h was attenuated. The possible role of adrenal progesterone in ovulation and the mechanisms by which endogenous oestrogens might enhance adrenal progesterone output are considered. J. Endocr. (1987) 112, 15–21

scholarly journals The role of progesterone in endometrial angiogenesis in pregnant and ovariectomised mice

Reproduction ◽  
2005 ◽  
Vol 129 (6) ◽  
pp. 765-777 ◽  
Author(s):  
Lisa M Walter ◽  
Peter A W Rogers ◽  
Jane E Girling
Keyword(s):  
Cell Proliferation ◽  
Endothelial Cells ◽  
Endothelial Cell ◽  
Endothelial Cell Proliferation ◽  
Vascular Endothelial ◽  
Plasma Progesterone ◽  
Ovariectomized Mice ◽  
Pregnant Mice ◽  
Endothelial Growth Factor

The role of progesterone (and oestrogen) in endometrial angiogenesis remains controversial. The aims of this study were to quantify endometrial angiogenesis in pregnant mice and to investigate the role of progesterone in promoting endothelial cell proliferation in ovariectomized mice. Uteri were collected on days 1 to 4 of pregnancy when circulating progesterone concentrations were increasing, prior to implantation. Before dissection, mice were injected with bromodeoxyuridine (BrdU) enabling proliferating endothelial cells to be quantified with CD31/BrdU double-immunohistochemistry. There was a significant increase in proliferating endothelial cells on day 3 of pregnancy when plasma progesterone also increased. To determine if this endothelial cell proliferation was due to progesterone, an experiment was performed on ovariectomised mice. One group was treated with a single oestradiol injection on day 8 after ovariectomy, followed by a no-treatment day and three consecutive daily injections of progesterone. Other groups were treated with either the vehicle, oestradiol or progesterone injections only; all were dissected on day 13 following ovariectomy. Unexpectedly, mice treated with progesterone-only had the highest amount of endothelial cell proliferation and oestrogen priming was found to significantly reduce this progesterone-induced endothelial cell proliferation. To determine if this proliferation is mediated by vascular endothelial growth factor (VEGF), a further experiment in which VEGF anti-serum was administered concurrently with the progesterone injections was performed. Endothelial cell proliferation was reduced but not abolished suggesting progesterone-induced endometrial angiogenesis is only partly mediated by VEGF. Results indicate that oestrogen priming is not required for progesterone to stimulate endometrial endothelial cell proliferation and that oestrogen inhibits progesterone-induced angiogenesis in ovariectomised mice.

Role of plasma progesterone concentration in early pregnancy of the ewe

1981 ◽  
Vol 21 (113) ◽  
pp. 562 ◽  
Author(s):  
FD Brien ◽  
IA Cumming ◽  
IJ Clarke ◽  
CS Cocks
Keyword(s):  
Early Pregnancy ◽  
Progesterone Level ◽  
Progesterone Concentration ◽  
Plasma Progesterone ◽  
Peripheral Plasma

Eighty-eight maiden and 125 mature Merino ewes were grazed on green irrigated pasture or given dry hay on a fallow area with or without a lupin grain supplement just before and during mating. Progesterone concentrations in peripheral plasma were measured at 12 d after coitus. Progesterone concentration was lower (2.27 vs 2.87 ng/ml, P < 0.001 ) when lupins were fed, and maiden ewes had higher progesterone concentrations than mature ewes (2.75 vs 2.36 ng/ml, P < 0.05). Pregnant ewes had higher progesterone concentrations than non-pregnant ewes (2.77 vs 2.36 ng/ml, P < 0.05), and ewes with two ovulations had higher progesterone concentrations than ewes with a single ovulation (3.13 vs 2.08 ng/ml, P < 0.001). There was an interaction between pasture type and lupin supplement, with lupins depressing progesterone level more on green irrigated pasture (lupins 2.11 ng/ml, no lupins 3.00 ng/ml, P < 0.05) than on dry pasture (lupins 2.45 ng/ml, no lupins 2.74 ng/ml, P < 0.05). The results confirm that a high plane of nutrition at mating lowers progesterone levels in plasma and suggest that this may be a factor in the increase in embryo deaths when ewes are fed lupin grain supplements.

The acute effect of placentectomy and hysterectomy on peripheral plasma progesterone levels and ovarian progesterone secretion in the pregnant rat

1983 ◽  
Vol 98 (1) ◽  
pp. 71-77 ◽  
Author(s):  
J. K. Olynyk ◽  
N. W. Bruce ◽  
B. J. Waddell
Keyword(s):  
Acute Effect ◽  
Initial Experiment ◽  
Direct Role ◽  
Pregnant Rats ◽  
Pregnant Rat ◽  
Plasma Progesterone ◽  
Peripheral Plasma ◽  
Progesterone Secretion ◽  
And Control

The role of placental luteotrophins in modulating plasma progesterone concentrations and ovarian progesterone secretion was examined in 16-day pregnant rats. In an initial experiment rats were placentectomized and their plasma progesterone concentrations monitored for 24 h; the rats were conscious within 30 min of placentectomy. Relative to control values, progesterone concentrations fell significantly within 0·5 h. A venous outflow technique was then used to monitor rates of progesterone secretion from ovaries of hysterectomized and control rats maintained under anaesthesia. Hysterectomy had no apparent effect on either progesterone secretion or plasma progesterone concentrations for at least 2 h. A final experiment was carried out to compare the effects of hysterectomy on plasma progesterone concentrations in conscious rats with those of placentectomized rats of the first experiment. Progesterone concentrations did not change significantly in hysterectomized rats for 4 h but fell to very low values by 24 h. These results suggest that placental luteotrophins do not have an acute, direct role in the control of plasma progesterone levels but are needed to maintain progesterone secretion in the longer term and possibly inhibit uterine luteolysin release.

PROPRANOLOL-BLOCKADE OF VASOPRESSIN INDUCED INCREASE IN PLASMA PROGESTERONE IN EARLY HUMAN PREGNANCY

1971 ◽  
Vol 66 (2) ◽  
pp. 283-288 ◽  
Author(s):  
Petter Fylling
Keyword(s):  
Cyclic Amp ◽  
Uterine Cervix ◽  
Adenosine Monophosphate ◽  
First Trimester ◽  
Blocking Agent ◽  
Simultaneous Administration ◽  
Plasma Progesterone ◽  
Human Pregnancy ◽  
Peripheral Plasma ◽  
Early Human

ABSTRACT Following continuous dilation of the uterine cervix or intravenous infusion of vasopressin during the first trimester of human pregnancy, a marked increase in the peripheral plasma progesterone levels was observed. This effect was blocked by simultaneous administration of propranolol (Inderal®), a β-blocking agent. It is suggested that both these stimulating and inhibiting effects might be related to 3′, 5′-adenosine monophosphate (cyclic AMP). The results indicate the existence of β-receptors in steroid producing tissues.

Role of irisin in effects of chronic exercise on muscle and bone in ovariectomized mice

2021 ◽  
Author(s):  
Naoyuki Kawao ◽  
Shunki Iemura ◽  
Miku Kawaguchi ◽  
Yuya Mizukami ◽  
Yoshimasa Takafuji ◽  
...  
Keyword(s):  
Chronic Exercise ◽  
Ovariectomized Mice

scholarly journals Targeting HSPA1A in ARID2-deficient lung adenocarcinoma

2021 ◽  
Author(s):  
Xue Wang ◽  
Yuetong Wang ◽  
Zhaoyuan Fang ◽  
Hua Wang ◽  
Jian Zhang ◽  
...  
Keyword(s):  
Lung Cancer ◽  
Lung Adenocarcinoma ◽  
Genetically Engineered ◽  
Malignant Progression ◽  
Murine Models ◽  
Rna Seq ◽  
Potential Therapeutic Target ◽  
Lung Cancers ◽  
Integrative Analyses

Abstract Somatic mutations of the chromatin remodeling gene ARID2 are observed in about 7% of human lung adenocarcinoma (LUAD). However, the role of ARID2 in the pathogenesis of LUAD remains largely unknown. Here we find that ARID2 expression is decreased during the malignant progression of both human and mice LUAD. Using two KrasG12D-based genetically engineered murine models (GEMM), we demonstrate that ARID2 knockout significantly promotes lung cancer malignant progression and shortens the overall survival. Consistently, ARID2 knockdown significantly promotes cell proliferation in human and mice lung cancer cells. Through integrative analyses of Chip-Seq and RNA-Seq data, we find that Hspa1a is up-regulated by Arid2 loss. Knockdown of Hspa1a specifically inhibits malignant progression of Arid2-deficient but not Arid2-wt lung cancers in both cell lines as well as animal models. Treatment with Hspa1a inhibitor could significantly inhibit the malignant progression of lung cancer with Arid2 deficiency. Together, our findings establish ARID2 as an important tumor suppressor in LUAD with novel mechanistic insights, and further identify HSPA1A as a potential therapeutic target in ARID2-deficient LUAD.

Murine models of inflammation: role of CD23

Allergy ◽  
2000 ◽  
Vol 55 (suppl 61) ◽  
pp. 21-26 ◽  
Author(s):  
Y. Riffo-Vasquez ◽  
S. Pitchford ◽  
D. Spina
Keyword(s):  
Murine Models

Progesterone levels in peripheral plasma of Rocky Mountain bighorn ewes (Ovis canadensis) during the estrous cycle and pregnancy

1980 ◽  
Vol 58 (6) ◽  
pp. 1105-1108
Author(s):  
P. E. Whitehead ◽  
E. H. McEwan
Keyword(s):  
Estrous Cycle ◽  
Rocky Mountain ◽  
Ovis Canadensis ◽  
Rapid Decline ◽  
Plasma Progesterone ◽  
Peripheral Plasma

Plasma progesterone levels of three Rocky Mountain bighorn ewes (Ovis canadensis) were determined during anestrus, estrus, and pregnancy. Eighteen-month-old ewes had "silent" heats with peak progesterone levels ranging from 1.0 to 2.2 ng/mL. At [Formula: see text] years of age, luteal activity preceded behavioural estrus and successful breeding. During the first 50 days of gestation, plasma progesterone levels increased to 8.5 ng/mL (8.0–9.2 ng/mL). From 50 to 80 days, progesterone levels decreased, followed by an increase to peak values of 13.3 to 23.2 ng/mL. A rapid decline in progesterone levels occurred about the time of parturition.

scholarly journals The role of cyclooxygenase-2 on endurance exercise training in female LDL-receptor knockout ovariectomized mice

2013 ◽  
Vol 85 (3) ◽  
pp. 1157-1164 ◽  
Author(s):  
FLAVIA DE OLIVEIRA ◽  
LAURA B.M. MAIFRINO ◽  
GUSTAVO P.P. DE JESUS ◽  
JULIANA G. CARVALHO ◽  
CLAUDIA MARCHON ◽  
...  
Keyword(s):  
Cardiovascular Risk ◽  
Exercise Training ◽  
Ldl Receptor ◽  
Density Lipoprotein ◽  
Cyclooxygenase 2 ◽  
Sedentary Control ◽  
Down Regulation ◽  
Ovariectomized Mice ◽  
Cox 2

Estrogen deprivation in postmenopausal women increases cardiovascular risk. Cardiovascular risk as a result of atherosclerosis is able to induce an inflammatory disease as far as cyclooxygenase-2 ( COX-2) expression. The purpose of the study was to investigate the role of COX-2 on exercise training in female mice low-density lipoprotein receptor knockout ( LDL-KO) with or without ovariectomy. A total of 15 female C57BL/6 mice and 15 female LDL-KO mice were distributed into 6 groups: sedentary control, sedentary control ovariectomized, trained control ovariectomized, LDL-KO sedentary, LDL-KO sedentary ovariectomized and LDL-KO trained ovariectomized. The ascending part of the aorta was stained with H&E and COX-2 expression was assessed by immunohistochemistry. Results revealed that ovariectomy as well as exercise training were not able to induce histopathological changes in mouse aorta for all groups investigated. LDL-KO mice demonstrated plaque containing cholesterol clefts, foamy histiocytes and mild inflammatory process for all groups indistinctly. Ovariectomy induced a strong immunoexpression in atherosclerosis lesion of LDL-KO mice. Nevertheless, a down-regulation of COX-2 expression was detected in LDL-KO trained ovariectomized when compared to LDL-KO sedentary. Our results are consistent with the notion that exercise training is able to modulate COX-2 expression in LDL-KO mice as a result of COX-2 down-regulation.

Sign in / Sign up

Export Citation Format

Share Document