THE VASCULAR STRUCTURE OF THE EXTRAPLACENTAL UTERINE MUCOSA OF THE RABBIT

1950 ◽  
Vol 7 (1) ◽  
pp. 86-99 ◽  
Author(s):  
HELEN J. PARRY

The finer vascular system of the extra-placental uterine mucosa of the rabbit during oestrus and the early stages of pregnancy and pseudopregnancy was studied by means of the benzidine-nitroprusside blood stain and by injection. In the oestrous uterus there is a marked mesometrial hyperaemia which intensifies during the early stages of pregnancy and pseudopregnancy. No spiral arteries nor arterio-venous anastomoses were found in the uterine endometrium. During the early stages of pregnancy, as the uterine mucosa proliferates, there is an intense growth of new blood vessels, accompanied by a corresponding increase in the amount of blood in the vessels. This occurs throughout the uterus at first, but after 8 days post coitum the increase continues around the conceptus but slows down and finally stops between the conceptuses and in the pseudopregnant horn. When the trophoblast of the blastocyst wall fuses with the uterine epithelium the fusion areas become well vascularized. It is suggested that this vascularization is stimulated by the invading trophoblast. The trophoblast actually breaks down the walls of the maternal capillaries and allows the maternal blood to bathe the embryonic syncytium and during the time that this is happening there is a marked leucocytosis around the fusion areas. The results are discussed in relation to the previous literature and to their possible physiological significance.

1905 ◽  
Vol s2-49 (193) ◽  
pp. 1-38
Author(s):  
RICHARD ASSHETON ◽  
THOMAS G. STEVENS

1. The full-term after-birth of the elephant consists of a chorion from which spring many much-branched villi, which spread out in all directions into plate-like branches. These end in (a) proximal foliaceous terminations, in which the fœtal blood vessels ramify, which interlace with a complicated system of much larger blood channels filled with maternal blood, having well-defined but non-nucleated walls; (b) more distal lobate terminations, which are covered by a wellmarked columnar or cubical epithelium -- presumably the trophoblast -- which are partly embedded in a kind of coagulum or detritus, and partly appear to hang loosely in irregular blood spaces without walls ; (c) the stems of still more prolonged villi, which have been torn off and probably left embedded in the walls of the uterus; (d) a few torn ends of blood-vessels. 2. The main trunks of the villi and their foliaceous terminations are everywhere separated from the maternal bloodchannels by a syncytial layer, which is continuous with the epithelium covering the lobate terminations, and is presumably trophoblastic. 3. The half-term placenta originally examined by Owen in 1850 shows, in its more central region, characters which are essentially similar to those of the full-term specimen, and goes far to prove the existence of longer villi which penetrate deeply into the uterine mucosa. The lateral areas of the zonary belt exhibit many most interesting previous conditions. We are able to see in these the simple terminations of the foetal villi covered with a single layer of trophoblast separated from the uterine tissues by a layer of matei'ial partly maternal and partly of foetal origin. There is no process of growth round existing maternal capillaries to form an angio-plasmode, nor apparently any phagocytic action on the part of the trophoblast. The vascularisation of the after-birth is effected by the invasion of the trophoblast by extravasated maternal blood, which flows at first in intercellular and intervillous passages which form the larger channels of the after-birth maternal vascular system, and then makes its way along intra-cellular or intrasyncytial canals through a plasmodium produced by the breaking down of the trophoblast of two adjoining villi. We think the evidence is in favour of considering the corpuscles floating in this invading stream, which contains no red non-nucleated corpuscles in its more advanced portions, to be of maternal rather than trophoblastic origin. 4. The tissues of the full-term placenta contain pigment granules, which are deposited chiefly in the syncytial layer. This we regard as an excretory product; it is almost quite absent from the tissues of the half-term specimen. Leucocytes, either of maternal or foetal origin, seem to be concerned in the transference of this pigment into the maternal blood stream. 5. The subcircular bodies of Owen we find as described by him and Turner, though we note the presence of minute villi on their outer surface. 6. We confirm the opinion of previous writers that the zonary band in part is a "deciduous" form of placenta, although there is not much maternal tissue except the blood. It is not correct to speak of the after-birth being composed of a "much hypertrophied mncosa layer of the uterus." 7. The placenta of the elephant shows by its long villi, which tend to remain embedded in the uterus wall, a resemblance to the condition found in the Sirenia; by the villous patches at the poles and other villi which come out from the uterus, either with or without their trophoblastic covering, but with no maternal cells attached, a resemblance to the ungulata vera of the Perissodactyl type ; by the invasion of the trophoblast--if such it is--by the maternal blood stream, a resemblance to the Discoplacental type, although the actual manner by which this invasion occnrs would seem to be--so far as our very limited material affords us opportunity of observation--unlike anything hitherto described.1 8. The resemblance, at first sight obvious enough to the zonary placenta of the carnivora, is superficial. The elephant's placenta differs from that of the carnivora in (a) consisting of three areas of attachment instead of one, two of which, are wholly in the non-deciduous type, the other partly deciduous, partly non-deciduous. (b) There is nothing formed comparable to an angio-plasmode. (c) The maternal capillaries do not directly become the maternal vessels of the after-birth.


The implantation of the blastocyst of Loxodonta , and the early development of the placenta, are described from material collected in Africa by Dr R. M. Laws. Implantation is central, the blastocyst settling in one of three or four deep longitudinal grooves in the uterine lumen. Its growth distends the uterine horn before it becomes attached to the uterine wall. As the bilaminar blastocyst continues to grow the trophoblast erodes the uterine epithelium over a zonary area and is there closely applied to the uterine stroma. It remains unattached over the embryonal and abembryonal poles, where the uterine epithelium is retained. As the yolk-sac approaches its maximum volume it is invested by mesoderm, forming an extensive trilaminar omphalopleur, the outer layer (trophoblast) of which immediately begins to invade the uterine stroma by peg-like proliferations that enter by the uterine glands. The latter undergo little change during these early stages and do not undergo extensive modification at any stage, but their basal portions become moderately distended after the gland openings are blocked by the trophoblast. As the trophoblast of the yolk-sac wall invades the stroma the allantois reaches the chorion and from this time the yolk-sac is rapidly reduced in volume. The allantois soon fills the exocoel and occupies the whole cavity of the conceptus surrounding the embryo and amnion. The allantochorionic placenta develops (over three discrete areas in the specimen described) by the growth of villi which are formed as the earliest trophoblast proliferations acquire a mesenchymal core and become vascularized. There remain areas where the trophoblast does not attach to the uterine wall and in these areas the uterine epithelium proliferates in a characteristic manner and appears to shed cellular material into the residual uterine lumen. As the allantochorionic villi develop, the underlying uterine stroma thickens, and large blood channels appear in it, lined by a shallow endothelium. These blood vessels, which have few branches, penetrate to the face of the placenta. Their investment by the advancing trophoblast leads to the ‘ vasochorial ’ condition described in an earlier account. The characteristic marginal haematomata of the elephant apparently form where an extending villous area meets an area of intact (although modified) uterine epithelium. This epithelium is undermined by lateral extension of the invading foetal tissue and some of the adventitious maternal blood vessels that reach the face of the placenta are disrupted and release blood into the uterine lumen where the stromal tissue is exposed between the advancing foetal villi and the surviving uterine epithelium. This blood is trapped in folds of the allantochorion, the trophoblast cells of which often contain maternal erythrocytes. These developmental characters are discussed with reference to their functional significance, and compared with the corresponding changes in the Carnivora, most of which are also characterized by an endotheliochorial placenta of zonary form with haematomata, marginal or otherwise. It is suggested that their occurrence is related to the intermediate position of the endotheliochorial placenta between the epitheliochorial type, in which the uterine glands contribute more importantly to embryonic nourishment, and the haemochorial type, in which transfer from the maternal circulation to the trophoblast is facilitated by the direct contact between them. The mode of implantation is shown to be very different from that in hyrax, which superficially resembles Loxodonta in the morphology of the foetal membranes. Comparison is also made with the aard-vaak and the manatee. The aard-vaak has a zonary endothelial placenta, marginal haematomata and a quadrilocular allantois, but does not resemble Loxodonta closely in detailed placental structure. The mid-term placenta of the manatee, on the other hand, bears a very striking resemblance to that of the elephant in many respects, especially in the manner in which the trophoblast is modified where it invests large maternal blood vessels. The phylogenetic significance of these similarities and differences is briefly discussed.


1872 ◽  
Vol 7 ◽  
pp. 760-762
Author(s):  
Turner

The author gave a brief sketch of the various theories which have been advanced by Velpeau, R. Lee, Braxton Hicks, the Hunters, Owen, Weber, J. Reid, J. Goodsir, Virchow, Kölliker, Van Der Kolk, Arthur Farre, and Ercolani regarding to the relations of the maternal blood-vessels to the placenta and chorionic villi. He then proceeded to state the results of his own observations on various specimens of placentæ, some of which had been separated at the full time, others prematurely, and on three specimens attached to the uterine wall.


Phlebologie ◽  
2010 ◽  
Vol 39 (03) ◽  
pp. 167-175
Author(s):  
M. Poetke ◽  
P. Urban ◽  
H.-P. Berlien

SummaryVascular malformations are structural abnormalities, errors of vascular morphogenesis, which can be localized in all parts of the vascular system. All vascular malformations by definition, are present at birth and grow proportionately with the child; their volume can change. In contrast to the haemangiomas, which only proliferate from the endothelial cells the division in stages is of clinical importance. Vascular malformations are divided from the part of vascular system, which is affected.In principle the techniques of laser application in congenital vascular tumours like haemangiomas and in vascular malformations are similar, but the aim is different. In tumours the aim is to induce regression, in vascular malformations the aim is to destroy the pathologic vascular structure because there is no spontaneous regression. This means that the parameters for treatment of vascular malformations must be more aggressive than for vascular tumours.


2016 ◽  
Vol 11 (2) ◽  
pp. 210-217 ◽  
Author(s):  
A.T. Akhmetov ◽  
A.A. Valiev ◽  
A.A. Rakhimov ◽  
S.P. Sametov ◽  
R.R. Habibullina

It is mentioned in the paper that hydrodynamic conditions of a flow in blood vessels with the stenosis are abnormal in relation to the total hemodynamic conditions of blood flow in a vascular system of a human body. A microfluidic device developed with a stepped narrowing for studying of the blood flow at abnormal conditions allowed to reveal blood structure in microchannels simulating the stenosis. Microstructure change is observed during the flow of both native and diluted blood through the narrowing. The study of hemorheological properties allowed us to determine an increasing contribution of the hydraulic resistance of the healthy part of the vessel during the stenosis formation.


Author(s):  
Lucia Dacome

Chapter 7 furthers the analysis of the role of anatomical models as cultural currencies capable of transferring value. It does so by expanding the investigation of the early stages of anatomical modelling to include a new setting. In particular, it follows the journey of the Palermitan anatomist and modeller Giuseppe Salerno and his anatomical ‘skeleton’—a specimen that represented the body’s complex web of blood vessels and was presented as the result of anatomical injections. Although Salerno was headed towards Bologna, a major centre of anatomical modelling, he ended his journey in Naples after the nobleman Raimondo di Sangro purchased the skeleton for his own cabinet of curiosities. This chapter considers the creation and viewing of an anatomical display in di Sangro’s Neapolitan Palace from a comparative perspective that highlights how geography and locality played an important part in shaping the culture of mid-eighteenth-century anatomical modelling.


1999 ◽  
Vol 5 (S2) ◽  
pp. 1192-1193
Author(s):  
H. Ditrich

The architecture of the kidney of birds (and also reptiles) is, unlike in mammalians, mainly determined by the organization of the blood vascular system. Besides arterial supply and venous drainage, the renal portal system forms a main structural component. While the latter was often regarded as a “primitive” feature in the literature, morphological and physiological data reveal its great functional importance.Microvascular corrosion casts studied in the scanning electron microscope permit the visualization of minute vessels, retaining their 3D-arrangement. Additionally, when compared with graphical reconstructions of serial sections, this method avoids several inherent artifacts like fixation and dehydration shrinkage as well as the compression of the object by the sectioning blade. Most of the studies on avian kidneys with this technique used the domestic chicken as a model. In order to provide additional material for comparative and functional studies, data on the intrarenal vascular structure of other species are required.


Author(s):  
Елизавета Александровна Молчанова ◽  
Петр Вячеславович Лужнов

В работе приведены понятия жесткости, эластичности и тонуса сосудов, а также же их взаимосвязь с общим состоянием сосудистой стенки. Описан индекс, объединяющий влияние вышеперечисленных факторов на состояние сосудистой системы и дающий представление о возрасте сосудов пациента, а также показана связь этого индекса с возрастом человека. Представлен обзор способов определения возраста сосудов с помощью контурного анализа пульсовой волны. Среди предложенных способов был выделен подход на основе контурного анализа сигнала пульсовой волны, а также ее второй производной. В данном исследовании проводилась разработка алгоритма расчета показателя возраста сосудов (VA), базирующаяся на анализе сигнала и его второй производной. При этом особое внимание уделялось физической интерпретации параметров, входящих в состав расчетной формулы. С помощью представленного алгоритма в группе из трех испытуемых был определен сосудистый возраст. Из анализа полученных результатов было выявлено влияние физиологических факторов на значение возраста сосудов. Предложены методики, позволяющие исключить влияние этих факторов на значения показателя VA и тем самым получить более точные результаты. Также представлены стратегии дальнейшего развития исследований в этом направлении In The paper presents the concepts of rigidity, elasticity and tone of blood vessels, as well as their relationship with the general state of the vascular wall. An index is described that combines the influence of the above factors on the state of the vascular system and gives an idea of the age of the patient's vessels, and also shows the relationship of this index with the age of a person. An overview of the methods for determining the age of blood vessels using the contour analysis of the pulse wave is presented. Among the proposed methods, an approach based on the contour analysis of the pulse wave signal, as well as its second derivative, was singled out. In this study, an algorithm was developed for calculating the indicator of vascular age (VA), based on the analysis of the signal and its second derivative. In this case, special attention was paid to the physical interpretation of the parameters included in the calculation formula. Using the presented algorithm, vascular age was determined in a group of three subjects. From the analysis of the results obtained, the influence of physiological factors on the value of the age of the vessels was revealed. Methods are proposed that allow to exclude the influence of these factors on the values of the VA indicator and thereby obtain more accurate results. Also presented are strategies for the further development of research in this direction


2000 ◽  
Vol 203 (11) ◽  
pp. 1659-1669 ◽  
Author(s):  
T. Schwerte ◽  
B. Pelster

The analysis of perfusion parameters using the frame-to-frame technique and the observation of small blood vessels in transparent animals using video microscopy can be tedious and very difficult because of the poor contrast of the images. Injection of a fluorescent probe (fluorescein isothiocynate, FITC) bound to a high-molecular-mass dextran improved the visibility of blood vessels, but the gray-scale histogram showed blurring at the edges of the vessels. Furthermore, injection of the fluorescent probe into the ventricle of small zebrafish (Danio rerio) embryos (body mass approximately 1 mg) often resulted in reduced cardiac activity. Digital motion analysis, however, proved to be a very effective tool for analysing the shape and performance of the circulatory system in transparent animals and tissues. By subtracting the two fields of a video frame (the odd and the even frame), any movement that occurred within the 20 ms necessary for the acquisition of one field could be visualised. The length of the shifting vector generated by this subtraction, represented a direct measure of the velocity of a moving particle, i.e. an erythrocyte in the vascular system. By accumulating shifting vectors generated from several consecutive video frames, a complete trace of the routes over which erythrocytes moved could be obtained. Thus, a cast of the vascular system, except for those tiny vessels that are not entered by erythrocytes, could be obtained. Because the gray-scale value of any given pixel or any given group of pixels increased with the number of erythrocytes passing it, digital motion analysis could also be used to visualise the distribution of blood cells in transparent tissues. This method was used to describe the development of the peripheral vascular system in zebrafish larvae up to 8 days post-fertilisation. At this stage, food intake resulted in a clear redistribution of blood between muscle tissue and the gut, and alpha-adrenergic control of peripheral blood flow was established.


1990 ◽  
Vol 259 (3) ◽  
pp. R393-R404 ◽  
Author(s):  
T. H. Adair ◽  
W. J. Gay ◽  
J. P. Montani

Prolonged imbalances between the perfusion capabilities of the blood vessels and the metabolic requirements of the tissue cells often lead to modification of the vasculature to satisfy the tissue needs. This homeostatic response appears to be bidirectional, since the vascularity of a tissue can increase or decrease in parallel with primary changes in metabolic rate. The factors that mediate the responses are not well understood, but oxygen has been implicated as a major control element, since vessel growth increases during hypoxic conditions and decreases during hyperoxic conditions. The following feedback control hypothesis may apply to many different physiological situations. Decreased oxygenation causes the tissues to become hypoxic, and this initiates a variety of signals that lead to the growth of blood vessels. The increase in vascularity promotes oxygen delivery to the tissue cells by decreasing diffusion distances, increasing capillary surface area, and increasing the maximum rate of blood flow. When the tissues receive adequate amounts of oxygen even during periods of peak activity, the intermediate effectors return to normal levels, and this negative signal, in turn, stops the further development of the vasculature. Although the effector mechanisms of the hypoxic stimulus are still being investigated, adenosine, which is produced in hypoxic tissues, appears to mediate hypoxia-induced increases in vascularity in some instances. Roles for fibroblast growth factor as well as mechanical factors associated with vasodilation and increased blood flow are postulated. Although blood vessel growth is a multifactorial process, a major influence in its regulation appears to be metabolic need. If this view is correct, it may be found that many of the quantitatively significant factors that control growth in a given vasculature are themselves modulated or controlled by metabolic signals reflecting the nutritional status of the tissues which that vasculature supplies.


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