Memoirs: Notes on the Structure and the Development of the Elephant's Placenta

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.

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.


It is customary for Croonian lecturers, after expressing their thanks to the President and Council for the honour that they have received in being asked to give this lecture, to devote some time to a justification of their subject in terms of Mrs Croone’s suggestion that the lecture should deal with the advancement of natural knowledge on local motion. The first of these tasks, Mr President, I perform humbly and with deep gratitude, but at the same time with some surprise that Council in its wisdom should have chosen one so ill-fitted for the honour you have laid upon him. The second task is easier since my lecture will deal with the nerves which control the muscles surrounding the hollow organs of the body, blood vessels and bowels, and further justification as a theme dealing with local motion the most captious critic could not desire. Three years ago my former colleague Bernard Katz gave the Croonian Lecture on ‘ Transmission of impulses from nerve to muscle’ in which he described our present knowledge of the mechanism of the chemical mediation interposed between nerve and skeletal muscle and summarized his own brilliant contributions to this, to me, fascinating subject. Today I am dealing again with transmission from nerve to muscle, but in a different system and, I am afraid, at a quite different and lower intellectual level than that of Katz. The idea of chemical transmission from nerve to effector cell came first to T. R. Elliott in 1904 as a result of his observation, in an extensive comparative study, of the close similarities between the actions of adrenaline injected intravenously and the effects of stimulating nerves belonging to the sympathetic system. These nerves we should now call in Dale’s (1933) terminology the adrenergic nerves, those transmitting their effects whether excitatory or inhibitory by the liberation at their endings of a ‘minute charge’ of the catecholamine adrenaline or one of its analogues. The cells upon which these nerves exert their action are the smooth muscle cells controlling the movements of the hollow viscera, intestines, reproductive tract and so on, and of the muscle cells of the vascular system that regulate the diameter of the blood vessels. These are processes that do not demand high precision of timing nor do they apparently require the instant turning on and off of transmitter action with which we have grown familiar in the junction between nerve and skeletal muscle. At this junction, as Katz showed, liberation and action of acetylcholine and its inactivation by the specific enzyme cholinesterase are over in a few milliseconds, and there is no reason to believe that the liberated transmitter in the untreated junction can ever diffuse more than a few microus from its site of action. It is hemmed in by barriers of specific cholinesterase, and these are reinforced by barriers of the non-specific enzyme in blood and tissue fluids. This narrow coarctation of the transmitter acetylcholine in space and time seems, however, to be confined to places where precise timing is required, such as at the neuromuscular junction and in the ganglionic and central nervous synapse. When it is liberated as the transmitter from nerves to blood vessels, or to secretory glands, it can escape some way from its site of liberation and persist long enough to be detected by skeletal muscles sensitized by denervation, as is seen in the Sherrington, Rogowitz and Vulpian-Heidenhain phenomena. I have laboured a little this question of diffusion and action at a distance of transmitter because it constitutes prima facie one of the most striking differences between the adrenergic and the cholinergic transmitters in at least the mammalian body. It was indeed because the liberated adrenergic transmitter escaped into the blood stream and could be detected by another tissue or organ, sometimes, but not necessarily, specially sensitized, that W. B. Cannon and his colleagues in the 30’s were able to add so much to our knowledge of sympathetic innervation. Nevertheless, in spite of the relative stability of the adrenergic transmitter and its ready detection in the blood stream, little had been discovered about the quantitative aspects of its liberation and metabolism some 50 years after its existence had been postulated, whereas we now have, and have had for 30 years, quite reasonably complete information about the liberation, storage and metabolism of the unstable and ephemeral acetylcholine.


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.


2016 ◽  
Vol 2 (1) ◽  
pp. 689-693 ◽  
Author(s):  
Daniel Laqua ◽  
Carina Brieskorn ◽  
Jan Hannes Koch ◽  
Markus Rothmayer ◽  
Steve Zeiske ◽  
...  

AbstractThe fetal oxygen saturation is an important parameter to determine the health status of a fetus, which is until now mostly acquired invasively. The transabdominal, fetal pulse oximetry is a promising approach to measure this non-invasively and continuously. The fetal pulse curve has to be extracted from the mixed signal of mother and fetus to determine its oxygen saturation. For this purpose efficient algorithms are necessary, which have to be evaluated under constant and reproducable test conditions. This paper presents the improved version of a phantom which can generate artificial pulse waves in a synthetic tissue phantom. The tissue phantom consists of several layers that mimic the different optical properties of the fetal and maternal tissue layers. Additionally an artificial vascular system and a dome, which mimics the bending of the belly of a pregnant woman, are incorporated. To obtain data on the pulse waves, several measurement methods are included, to help understand the behavior of the signals gained from the pulse waves. Besides pressure sensors and a transmissive method we integrated a capacitive approach, that makes use of the so called “Pin Oscillator” method. Apart from the enhancements in the tissue phantom and the measurements, we also improved the used blood substitute, which reproduces the different absorption characteristics of fetal and maternal blood. The results show that the phantom can generate pulse waves similar to the natural ones. Furthermore, the phantom represents a reference that can be used to evaluate the algorithms for transabdominal, fetal pulse oximetry.


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.


Anaesthesia ◽  
2012 ◽  
Vol 67 (8) ◽  
pp. 936-936 ◽  
Author(s):  
P. Kundra ◽  
J. Velraj ◽  
U. Amirthalingam ◽  
S. Habeebullah ◽  
K. Yuvaraj ◽  
...  

1962 ◽  
Vol 6 (1) ◽  
pp. 88-106 ◽  
Author(s):  
Johannes A.G. Rhodin ◽  
John Terzakis
Keyword(s):  

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