Mechanisms and regulations of endometrial angiogenesis

2002 ◽  
Vol 10 (1) ◽  
pp. 45-61 ◽  
Author(s):  
C Gargett ◽  
G Weston ◽  
PAW Rogers

Angiogenesis is defined as the formation of new blood vessels from the existing vasculature. Angiogenesis occurs regularly in the endometrium throughout the reproductive life of females as part of the rapid growth and regression of this tissue that occurs during the menstrual cycle. It is now clearly evident that angiogenesis plays a key role in reproductive processes such as embryo implantation, placentation, endometrial regeneration after menstruation, and in the ovary during folliculogenesis and corpus luteum formation. Given the complexity and continual change of the endometrial milieu, it seems highly likely that aberrations in the angiogenic process may contribute to various disorders, including endometrial cancer, endometriosis, menorrhagia and breakthrough bleeding – all significant and common gynaecological pathologies. This review provides an update on the mechanisms and regulation of endometrial angiogenesis, with particular reference to the role of angiogenesis in implantation and placentation, as well as two endometrial pathologies – endometriosis and breakthrough bleeding.

Reproduction ◽  
2014 ◽  
Vol 148 (5) ◽  
pp. R85-R95 ◽  
Author(s):  
François Fabi ◽  
Eric Asselin

The three isoforms of AKT: AKT1, AKT2, and AKT3, are crucial regulators of both normal and pathological cellular processes. Each of these isoforms exhibits a high level of homology and functional redundancy with each other. However, while being highly similar and structurally homologous, a rising amount of evidence is showing that each isoform possesses specific targets as well as preferential subcellular localization. The role of AKT has been studied extensively in reproductive processes, but isoform-specific roles are yet to be fully understood. This review will focus on the role of AKT in the uterus and its function in processes related to cell death and proliferation such as embryo implantation, decidualization, endometriosis, and endometrial cancer in an isoform-centric manner. In this review, we will cover the activation of AKT in various settings, localization of isoforms in subcellular compartments, and the effect of isoform expression on cellular processes. To fully understand the dynamic molecular processes taking place in the uterus, it is crucial that we better understand the physiological role of AKT isoforms as well as their function in the emergence of diseases.


1979 ◽  
Vol 11 (S6) ◽  
pp. 19-35 ◽  
Author(s):  
Barry M. Sherman ◽  
Robert B. Wallace ◽  
Alan E. Treloar

The human menstrual cycle is characterized by a series of dynamic hormonal relationships that result in the regular maturation of ovarian follicles, ovulation and corpus luteum formation. As methodology has changed and improved, it has become possible to examine these events in greater detail. The simple analysis of menstrual cycle length, when done with care in a large number of women over long time spans, has revealed much about the fundamental biological rhythm of the menstrual cycle. Of particular interest are the predictable changes in cycle length and variability that occur at different stages of reproductive life (Treloar et al., 1967; Vollman, 1977). Basal body temperature records add another dimension to the analyses of menstrual cycle length because they permit estimation of the length of the pre- and post-ovulatory phases of the menstrual cycle and provide some index of the integrity of corpus luteum function.


1974 ◽  
Vol 63 (1) ◽  
pp. 201-212 ◽  
Author(s):  
D. T. BAIRD ◽  
P. E. BURGER ◽  
G. D. HEAVON-JONES ◽  
R. J. SCARAMUZZI

SUMMARY The site of secretion of androstenedione in women was investigated by measuring the concentration of androstenedione in peripheral and ovarian venous plasma by radioimmunoassay at different stages of the menstrual cycle. The concentration in peripheral plasma rose from 1·45 ± 0·11 (s.e.m.) ng/ml on day 1 to a peak on the 7 days around mid-cycle (2·29 ± 0·08) before declining gradually during the luteal phase. The concentration of androstenedione in plasma draining ovaries containing the pre-ovulatory follicle or a corpus luteum (33·2 ± 9·0) was significantly higher than in plasma draining the contralateral ovary (10·1 ± 1·6, P < 0·001). In women in whom ovulation was induced with gonadotrophins the concentration of androstenedione in peripheral plasma rose from 1·42 ± 0·21 before treatment to reach maximum levels (2·5–4·5 ng/ml) in the luteal phase. There was a significant (P < 0·001) correlation between the concentration of androstenedione and oestradiol-17β in peripheral (r = 0·50) and ovarian (r = 0·79) venous plasma. These findings indicate that all three cellular compartments in the ovary secrete significant amounts of androstenedione in women during their reproductive life.


2020 ◽  
pp. 247-249
Author(s):  
V.O. Potapov

Background. At the menstrual cycle beginning there is a proliferation of endometrial cells under the influence of oestrogen, and in the second half, after ovulation there is a differentiation and hypertrophy of cells under the influence of corpus luteum progesterone. Lutein phase deficiency (LPD) can be divided into 3 types: lack of progesterone production (corpus luteum is absent), low progesterone level (corpus luteum hypofunction), and reduction of progesterone production period (short period of corpus luteum existence, luteal phase duration <11 days). Objective. To describe the role of nitric oxide (NO) donors in women with LPD. Materials and methods. Analysis of literature data on this issue. Results and discussion. The main adverse outcome of LPD is the absence or defective transformation and reception of the endometrium required for successful fertilization of the egg. In case of progesterone deficiency, the depth of trophoblast invasion decreases, resulting in abnormal placental development and inadequate uteroplacental blood flow. The latter can further lead to antenatal foetal death and miscarriage, preeclampsia and eclampsia, placental dysfunction. LPD should be suspected in patients with infertility, abnormal uterine bleeding, severe premenstrual syndrome, endometrial hyperplasia, and habitual miscarriage. Ultrasound signs of LPD include the absence of a dominant follicle, absence of ovulation in the presence of a mature follicle (persistence), absence of corpus luteum in the 2nd phase of the cycle, endometrial thickness in the secretion phase <9 mm, increased echogenicity only in the peripheral parts of the endometrium or three-layered endometrium. Functional tests for the detection of LPD include the basal temperature measurement and examination of smears (hypolutein type of smear, preservation of the symptom of cervical mucus crystallization in the 2nd phase of the cycle). A key element of pregravid preparation for women with LPD is the progesterone donation (in oil solution, in etiloleate or micronized). The therapeutic efficacy of different commercial progesterone drugs is the same. Progesterone helps to prepare the endometrium for trophoblast invasion and promotes uterine hypotension. Incomplete secretory transformation of the endometrium during the treatment with progesterone drugs occurs in case of inadequate blood supply to the endometrium due to low density of functional vessels or insufficient content of NO in the endometrium. Back in the late 90’s of last century, it was shown that NO acts as a powerful uterine relaxant, and reduction of its concentration leads to miscarriage. In humans, NO is produced from L-arginine, however, obtaining the required dose of the latter with food is not always possible. When L-arginine (Tivortin aspartate, “Yuria-Pharm”) is used as a NO donor, peripheral vascular dilatation and neoangiogenesis occur, which improves blood supply and endometrial trophic processes; stimulation of gene transcription and cell cycle, which increases the cell population and physiological thickness of the endometrium; regulation of sex hormone synthesis and expression of their receptors, which increases the receptivity of the endometrium. The regimen of Tivortin aspartate administration is the following: 5 ml (1 g) 6 times per day during the menstrual cycle. According to the results of our own study, L-arginine increases the biological effect of progesterone on the endometrium, promotes a more successful restoration of its physiological structure and thickness in women with LPD. The inclusion of L-arginine in the pregravid preparation of women with LPD showed a 1.9-fold decrease in the infertility incidence, a 3.3-fold increase in the number of pregnancies and births, and a 3.4-fold decrease in the number of miscarriages. Conclusions. 1. The main adverse outcome of LPD is the absence or defective transformation and reception of the endometrium required for successful fertilization of the egg. 2. Usage of L-arginine (Tivortin aspartate) as a donor of NO promotes dilatation of peripheral vessels and neoangiogenesis, stimulation of the cell cycle, regulation of the synthesis of sex hormones. 3. Inclusion of L-arginine in the pregravid preparation of women with LPD leads to the decrease in infertility, to the increase in the number of pregnancies and births and to the decrease in the number of miscarriages.


Angiology ◽  
2008 ◽  
Vol 60 (2) ◽  
pp. 242-253 ◽  
Author(s):  
Mehmet ßahin ◽  
Emel ßahin ◽  
Saadet Gümüşlü

Tumor angiogenesis is a process where new blood vessels are formed from preexisting ones, resulting in several pathologies. Solid tumors induce angiogenesis to obtain the required nutrients and oxygen. Otherwise, tumors do not grow beyond 2 to 3 mm in diameter. Cyclooxygenase-2, an inducible enzyme important in inflammation, catalyzes the production of prostanoids from arachidonic acid. Cyclooxygenase-2 plays an important role in several cancer types, including colorectal, gastric, prostate, breast, lung, and endometrial cancer. Besides, cyclooxygenase-2 has been implicated in the progression and angiogenesis of cancers. Cyclooxygenase-2 inhibitors have been used to block angiogenesis and tumor proliferation. In this review, the recent studies related to the role of cyclooxygenase-2 in several cancer types and tumor-induced angiogenesis were compiled.


1992 ◽  
Vol 37 (1) ◽  
pp. 75-78
Author(s):  
T. Oda ◽  
R. Aoki ◽  
Y. Yoshimura ◽  
S. Kohriyama ◽  
J. Yoshida ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Yuxin Luo ◽  
Yanbin Zhu ◽  
Wangdui Basang ◽  
Xin Wang ◽  
Chunjin Li ◽  
...  

Nitric oxide (NO) has attracted significant attention as a stellar molecule. Presently, the study of NO has penetrated every field of life science, and NO is widely distributed in various tissues and organs. This review demonstrates the importance of NO in both male and female reproductive processes in numerous ways, such as in neuromodulation, follicular and oocyte maturation, ovulation, corpus luteum degeneration, fertilization, implantation, pregnancy maintenance, labor and menstrual cycle regulation, spermatogenesis, sperm maturation, and reproduction. However, the mechanism of action of some NO is still unknown, and understanding its mechanism may contribute to the clinical treatment of some reproductive diseases.


2015 ◽  
Vol 93 (5) ◽  
Author(s):  
Cecily V. Bishop ◽  
Fuhua Xu ◽  
Theodore A. Molskness ◽  
Richard L. Stouffer ◽  
Jon D. Hennebold

1955 ◽  
Vol 3 (1) ◽  
pp. 44 ◽  
Author(s):  
GB Sharman

Setonix brachyurus Quoy and Gaimard is polyoestrous, the length of the cycle being about 28 days. In the wild and in the newly domesticated female, oestrous cycles are resumed in late January after an anoestrous period of 3-5 months. During this period oestrus does not occur and ovary and uterus are shrunken and quiescent. Domestication for periods exceeding 1 yr results in a greatly shortened anoestrous period, culminating in a condition in which oestrus is repeated at regular monthly intervals throughout the year. Pro-oestrus is accompanied by rapid growth of one Graafian follicle, mitotic activity in the uterus, and usually by the onset of cornification in the vaginae and appearance of partly cornified cells in the smear. At oestrus the largest follicle reaches a diameter of almost 3.0 mm. Behavioural oestrus lasts about 12 hr. Ovulation follows 12-24 hr after oestrus and is independent of the act of copulation. Invasion of the collapsed follicle by blood vessels and the growth of a corpus luteum takes place after ovulation. Under the influence of the corpus luteum a luteal phase occurs in the uterus and lasts until about 18 days after oestrus. During the period of activity of the corpus luteum the vaginal smear is almost entirely composed of non-cornified cells and leucocytes. Following the cessation of the luteal phase degenerative changes occur in the uterus and the uterine glands are invaded by leucocytes. The changes during the oestrous cycle in Setonix are compared with those occurring in Didelphis and in other marsupials.


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