05/02/2023
Goncharenko A.I. - The Heart Space as the Basis of Superconsciousness.
A case in an experiment revealed previously unknown phenomena in the work of the heart, which led to its inevitable reinterpretation. It turned out that, pumping blood into all the body's vessels, the heart simultaneously divides it into portions of different composition, which it directs only to certain organs. This mechanism is performed by "mini-hearts" located on the inner surface of the heart's ventricles. They have affinities with certain organs and parts of the body.
These hearts have all the necessary set of "hemodynamics" for the formation of the ventricles of the heart of wreath-like "packets" of erythrocytes. The output channels of the heart in the moment of systole give these packages the target direction to the associated organ. The contracting function of the heart muscle is launched by the magnetic impulse that arises in the volume of the ventricle of the heart in the moment of its shock compression. It is established that the cardiovascular system is a separate highly organized structure of our body. It has its own brain (heart brain), its own heart (heart of a heart), and its own wave-hemodynamic connection, which controls the trajectory of the movement of information-energy packets of erythrocytes through the vessels. In addition, it materializes and distributes all forms of time in the body and serves as a system of pre-consciousness.
These statements were secondary conclusions of an experiment whose initial goal was to study a model of myocardial infarction in monkeys. As a result of a deliberately created stressful situation in the family of monkeys, the male gibbon died. At the morphological autopsy of his heart, necrotic changes were noted on the anterior-lateral surface of the apex of the heart. At the opening of the left ventricle, a thrombus was found above the site of the infarction (Fig. 1). The scientific task was thus fulfilled and confirmed with morphology. However, during the revision of all the major vessels of the animal, six more thrombi were found sitting one after another only in the left femoral artery. All of them had signs of intramural origin.
Such pathology is usually the result of a myocardial infarction. However, it was surprising that out of the entire vascular network of the monkey's body, they were laid in a single chain.
Naturally, the assumption arose that the thrombi had the same pathway out of the ventricle. And since the formation of them in the heart was repeated for a long time, it could be assumed that the unidirectionality of their movement was not random. This suggested the thought that blood from the apex of the ventricle was entering the femoral artery in portions, from the place where the thrombus was found. The dissection of the animal objectively demonstrated this relationship, as well as how the infarction of one part of the heart disconnected the femoral artery basin.
Does the feedback work if the animal's blood flow is blocked in the same femoral artery? Will we get a heart apex infarct?
In the clinic, it is known that the intersection of vessels or "syndrome of their compression" is also accompanied by a myocardial infarct [1]. Such phenomena are not rare in surgery and cardiovascular pathology, but researchers do not link them together, seeing them as only pathological anatomists' finds [2]. We, however, considered these phenomena as a regularity, which led us to the conclusion: if the pool of one artery has its representation in the heart, then the others should not be an exception. Further, animals had the arteries leading to various organs tied, and after 1-2 days the morphology of the heart was studied, and then the areas of heart damage were systematized.
Every time the blood flow was stopped, infarct-like lesions of the ventricles appeared only in places associated with the tied arteries, over which there was usually a blood clot.
The peculiarity of the histological studies of the heart was that the myocardial slices were taken simultaneously with the clot of blood located on it. As a result, under low magnification, it was possible to see the picture of the connection of the structure of the clot of blood with the inner surface of the heart. On the sections, in the place of the infarct, trabecular cells of a mesh-like shape were detected, from which in the cavity of the heart a frozen stream of erythrocytes in the form of a snail (Fig. 2) protruded.
The repetition of this picture forced us to turn to the little-known works of Kolomatsky [3]. In his studies of the heart and, in particular, the functions of the vessels of the tebezia, he (shown by arrows in the figures) used filming inside the cavity of the ventricles (Fig. 3, 4). For the first time in the world, the moment of ejection of microstreams of erythrocytes from the mouths of the vessels of Tebezia to the trabecular cell against the flow of blood from the atria during diastole was fixed on film. As a result of the collision of these flows, a local twist of the blood portion was formed above the trabecular cell.
Unfortunately, these studies were not in demand by physiology. Now, however, the countercurrent effect, discovered by Kolomatsky, explained the essence of the mechanism of formation of the pathology, frozen under the microscope.
Tebesium trabecular cells with their associated vessels resembled miniature hearts in terms of their observable characteristics. They can contract and relax independently, alter their volume, and regulate the inflow and outflow of blood portions. Miniature hearts can be disconnected from work by contracture of their lumen or by formation of a blood clot above them, as was observed in our experiments.
On the inner surface of the heart ventricles, there are around a hundred of such mini-heart cells, but their functional purpose was unknown. It was assumed that they serve as an adaptation for "uniform mixing of blood" in the ventricles [4]. It is now clear that they have exactly the opposite purpose: by vortex swirling they fill the ventricles with individual blood portions with different properties.
Experimenters know that simultaneous measurement of local pressure, oxygen saturation, temperature in different parts of the ventricle and analysis of blood composition yield different results. The spread can be so distinct that in laboratories an average error coefficient is even accepted, although this is the result of the work of miniature hearts.
In acute experiments using occlusions of peripheral arteries, the inner surface of the left ventricle was marked and a scheme of the heart's connection with certain areas of the organism was compiled. It resembled the Fesch disc spiral, but with acupuncture points of the ear, palm, or sole of the foot (Fig. 5).
This means that the inner surface of the ventricles is a multitude of hearts, each of which serves a specific organ.
Direct evidence that the miniature heart supplies blood only to the organ connected to it was obtained when a globulin solution with a radioactive label was introduced into the trabecular sinus. When the solution was introduced into the apex of the heart, the level of radioactive radiation in the blood increased tenfold at the base of the tail or hind limb (Fig. 6, B). When it was introduced to the right of the apex, it increased in the liver area (Fig. 6, A), and introduction into the base of the ventricle increased radioactivity of the brain, etc. (Fig. 6, B).
These experiments showed that target selection of blood by organs is carried out by miniature hearts.
What is the physical essence of the target blood flow distribution? It is known that the most stable form of liquid movement in the real world is a structure of an ordered vortex. To prove that in the animal and human bodies, the target blood flow is exactly a vortex, a hydrodynamic model was created. In it, Pinto tubes were connected to the liquid pressure source, not with a rigid but with an elastic hose. When its configuration changed, vortex water flows were formed that could be directed to a chosen manometric tube at will. This device proves that liquid movement in a vortex state can be directed purposefully.
Such a mechanism has been operating in the animal world for millions of years. In bilaterians, the streams of arterial and venous blood in the cavity of the same ventricle first transform into vortex "packages", which are then expelled in different directions: venous blood to the gills, and arterial to the brain. The same mechanism of separation of blood flows also works in the human fetus. Arterial and venous blood of the trabecular system of the left ventricle is twisted into separate vortices, the arterial vortex is thrown into the brain, and the deoxygenated one is thrown to the internal organs and placenta.
This mechanism is preserved throughout a person's life. Pathological cyanosis of body parts observed in people [5] is known. The localization of them in the body depends on the place of the unclosed Botallo channel in the interventricular septum. From here, the streams of venous blood flow consistently only to the same parts of the body, maintaining their cyanosis, thus revealing the location of the pathology in the heart (Fig. 7).
The next experiment was aimed at finding out: do vortex structures of blood really form in the heart? And if so, are they preserved throughout the arterial flow?
Animals were injected with dye intravenously, then instantly frozen in liquid nitrogen, after which a layered histogram of artery and heart chamber slices was made. By comparing photographs of artery and heart slices, a picture of the structural movements of erythrocytes was reconstructed. The chambers of the heart and arteries along their entire length were filled with complex formations of blood balls (Fig. 8, resembling a lattice architecture.
These experiments confirmed the hypothesis of Chizhevsky and Ahudja that erythrocytes in arterial flows move in structured "conglomerates" (Fig. 9) [6, 7].
To create such stable vortex packages of blood and control them, the heart has all the necessary means of "hemodynamics": specific musculature, trabecular cells, valves, a coronar-tebic vessel system (Fig. 10), and an electromagnetic field control mechanism.
As a result of the interaction of the counter-current of micro streams from the Tebesian vessels with the flow of blood from the atria, the streams are twisted, and the contractions of the sinuses fix their location in the chambers of the ventricles.
Thanks to the fact that the emergence of vortex volumes of erythrocytes is determined by the topographical position of the mini-heart, the spiral muscles of McCallum give each of them in the moment of systole its own target movement vector.
The question remains unclear: how do the vortex packages find their intended target and how do they determine their path of movement in the branching of vessels?
Blood circulation control is traditionally linked to the physiology of the nervous system. For over a hundred years, researchers have been looking for adaptations that would allow the central and peripheral nervous systems to regulate the amount of blood flow, and its speed, sort blood cells by age, and oxygen content, and direct them according to their purpose, but their search has not yielded the expected results.
Many studies have shown that regional blood flow is possible without the participation of the nervous system [10]. Hypotheses about the existence of a peripheral arterial heart [II], chemical regulation [12], and a centrifugal pump [6] do not provide answers to phenomena found in blood flows.
This leads to the assumption of the existence of some real, intravascular connection. Its actions allow each organ to independently request a portion of the blood of the necessary composition and volume and deliver it to its destination to meet the needs of local homeostasis.
In recent years, it has been definitely proven that there are high-frequency resonant emissions between related tissue cells [13]. Therefore, mini-hearts, which include tissues related to the associated organ, must have frequency-resonance coincidences with them. The basis for such an assumption is given by facts of embryonic heart development. It forms the organism, and the mini-hearts themselves participate in the formation of related tissues [5].
The specific musculature serves as the material carrier of each minisercum's representation in the associated organ. This musculature creates a morphological, functional, and immunological mosaic of the heart and continues the communication of the heart with smooth muscle fibers of the vessels, entering the organs, and branches there in the capillaries. It was necessary to prove that these fibers are the conductors of the high-frequency radiation of the heart monitoring system for the structural-informational-energy distribution of the blood flow. If a genetic relationship is detected between the associated organ and the mini-hearts, then a disruption of the smooth muscle connection between them should lead to a change in the architecture of moving erythrocytes. In the phase fluorometer, histochemists were able to observe a plausible uniform glow of DNA and RNA preparations from the heart and associated organ tissues, confirming their relationship. The left carotid artery [14] was chosen as the site of intervention in the smooth muscle fiber connection. Assuming that the brain bio-tokens registered by us already processed information, we assumed that the introduction of it into the hypothetical fiber communication channel heart-brain can lead to the emergence of "noise" in it, which should lead to changes in the structure of erythrocytes in this vessel.
In the experiment, bio-toxins were launched from 16 points of the brain through a semiconductor to a coil of wire with magnetostrictive properties, wound in the form of a sheath around the carotid artery. After 15-20 minutes of exposure to the test animal's own brain currents, it was submerged in liquid nitrogen. As in previous experiments, a series of carotid slices were made and the flow architecture was reconstructed. Compared to the right carotid artery, the recreated schematics lacked erythrocyte-like structures. This fact was interpreted by us as an indirect confirmation of the existence of its own fiber connection to the heart.
In order to mark the contours of the heart and organ surveillance system and track the vortex packaging along the vascular flow, it was necessary to localize the source of the heart's electrical excitation. So far, its location has not been specified [15]. But it is known that a few thousandths of a second before the appearance of electric currents in the heart, a magnetic impulse appears somewhere in the center of the ventricle [16].
The working hypothesis suggested that this impulse could be born in the blood itself. Its paramagnetic properties and non-Newtonian behavior provided grounds for this. In the in vitro experiment, 30.0 to 50.0 ml of arterial blood were subjected to a sharp compression, which was recorded as a "magnetic burst". In vivo control was provided by the parenchymatous organs of animals. In particular, the shock compression of the renal blood flow in the rhythm of the pulse provoked the appearance of electric potentials, like cardiac ones. This confirmed the assumption that physical deformation of the blood leads to excitation of the magnetic impulse, which apparently induces ionic currents on cell membranes of the endocardium, thus launching the electrical system of the heart. These wonderful properties of blood force the heart to perform its functions and carry out its electromagnetic connections beyond its limits. The pulse wave, passing through the vessels, deforms their walls and thus repolarizes the liquid crystalline proteins of the smooth muscle fibers, causing the movement of directed currents.
Her impact on the erythrocyte packaging arouses a magnetic field within it. Each package comes from a specific mini-heart, strictly dosed, individual, and the impulse arising in it has a certain frequency that is peculiar only to this vortex. The electrical impulse of the polarized smooth muscle fiber of the vessel and the magnetic radiation of the vortex package moving in its stream coincide in frequency. The pulse wave, always ahead of the vortex movement, serves as a source of high-frequency waveguide communication excitation, revealing coherence, which leads the package to the intended organ.
The plasma of the arterial vascular stream is filled with hundreds of protein fractions, the structure of whose molecules is in a folded state. Unfolding only at certain frequencies, they provide the advantage of sliding in the blood flow of the erythrocyte package, which coincides with them in frequency.
This is one of the channels of the heart's own communication. Through it, for example, an organ that requests a portion of blood receives an impulse of direct communication about the movement of nutrients to it, and the heart receives a reverse one that the portion of the blood is still on its way and has not yet been absorbed by the organ, and therefore it is not necessary to form an additional package. Blood from the heart to the organs goes 6-20 s, so the aorta and large vessels have a time reserve to take a portion of blood intended for other organs at this moment. Thus, the heart monitoring system saves up to 5-6 times the amount of blood needed by our body.
The conclusions of these experiments actually only confirm the evolution of the heart. Flatworms have dozens of individual heart members, which can be accommodated in four hearts in complex organisms and one heart in mammals. Although multiple hearts have merged into one, they continue to supply blood to the same organs that were once connected to them. When the left ventricle is filled with plaster, the output channels (Fig. II) are visible. They spiral from the top to the base, along which there are dozens of mini-hearts whose arrangement resembles a primitive worm curled into a heart (Fig. 12). The map of the zones of myocardial conduction with organs and body parts of this figure shows connections with the regions of the head (7); neck (2); upper limbs (3); spleen, stomach, and liver (4), kidneys (5); pelvic organs (6); lower limbs (7). Since there is a genetic relationship between the mini heart and the organ associated with it, it will not be surprising if it turns out that the human genome repeats the spiral of mini hearts and the latter serves as its reading device. The conclusions of the experiments change our views on the heart and circulation and explain many physiological phenomena that have been inexplicable for centuries.
For example:
- How different nutrient juices are distributed from the same aorta [18];
- How the body gets by with five liters of blood instead of the twenty required by calculation [19];
- How only old erythrocytes are selected to the spleen, and warm blood with a high content of oxygen, glucose, and young erythrocytes - to the brain [6];
- The pregnant uterus receives blood with a high content of nutrients than at the same time in the femoral artery, etc.
The cardiovascular system, knowing the program of development of other systems, lays the material basis for their development and growth and, in a literal sense, lays the foundation, in essence, predetermining our development.
In the embryonic period, the heart grows our brain. This is one of the arguments that put the reasonableness of the heart system above our consciousness.
In addition, the heart has its own brain and it is enough for the body to live. Cases are known when the body existed with a destroyed brain for many years.
The action of the cardiovascular system covers a space of trillions of living cells. Billions of capillaries serve as the devices that receive information for the heart. Their total length is about 100 thousand kilometers [20]. These thinnest vascular sensors form a boundary of interaction with the external and internal worlds. The heart does not allow the nervous system to them. All information from the Universe is absorbed through the capillaries by mobile structures of erythrocytes. Blood circulation serves as a reservoir for storing information in the heart system.
It is quite amazing how this information is materialized into forms of time. The present is a venous system, the past is lymphatic, and the future is an arterial system. The present flows out of the capillaries as real streams. Erythrocytes are the carriers of information in them. They move along the veins in the form of "coin" columns, similar to a volumetric magnetic tape, which enters the right atrium and is read there by the heart's brain.
Before discussing the formation of the past tense, it must be noted that the lymphatic system is the oldest in the circulatory system. It has its hearts, vessels, and a branched network of communication with many control centers. It is also appropriate to mention its participation in the curious coincidence. The same number of ten thousand heart contractions per day corresponds to the number of dying brain cells. In other words, every heart contraction associates a brain cell with its own cell. And one must think that these cells do not die, as it is usually assumed, but go to memory storage.
This is confirmed by the fact that the brain releases mitochondria and lysosomes into the lymphatic system through nerve fibers. They are matrix carriers of the switches of the past (memory). The future tense begins to be prepared in the right atrium from the merger of the present (venous blood) and the past (lymph). They combine in the pulmonary chamber of the processor. This is a sequence of interrelated events that represent and organize the formation of the past tense.
At the epicenter of this fusion is the brain of the heart. Located above the right ear, at the upper venous confluence on the lateral side, the brain of the heart is exposed at the entrance to the right atrium. Here it controls the entry of blood elements and forms vortical packages from them. Not a single erythrocyte passes its field of vision because the brain uses the effect of bio-location. The locator is located next to the brain, in the form of a crescent fold. Its periodic electromagnetic pulses scan information from blood balls and mitochondria.
Materializing the future, the left heart transforms laminar streams from the pulmonary veins into chaotic motion, submerging erythrocytes into the diastolic vacuum.
The heart is the only organ that interacts with a structure that fills the blood with unknown information to us. The mini-hearts of the left ventricle translate this information into packages of red blood cells and fill the arterial system with them. It must be taken into account that the packages take a path from the ventricles to the arterioles of the brain in 6-8 seconds. This interval is the moment of rupture in the perception of time between two systems: the cardiovascular and nervous systems. From the heart's brain, the information has already gone, and it will reach the brain only after several seconds. The heart's brain, returning mitochondria to the brain, includes images, feelings, and events in memory. This moment in consciousness appears as the present. But for the heart brain, it is already in the past, since in this period the heart has already contracted several times and sent new information to the central nervous system, the contents of which the brain does not yet know.
Thus, the heart system anticipates consciousness, weaves in it the three forms of time, and forms a new ability to interact with the world. The sound physiology confirms the validity of this statement. Even before we pronounce the word, the chord timpani already tightens the eardrum to the degree of sound loudness that we are about to pronounce. It turns out that our speech, its meaning, and emotionality are not spontaneous. The word has already occurred in the anticipatory superconsciousness of the heart, and the brain only realizes its meaning.
In this connection, the lines from the Gospel come to mind: "But I say to you that everyone who looks at a woman with lust has already committed adultery with her in his heart" (Matthew 5:28).
The interval of transmission of hemodynamic information from the heart to the brain shifts the forms of time in consciousness. We combine two bodily tissues: the nervous and the cardiac, two consciousnesses: one - the consciousness of the heart, the other - the consciousness of the brain. They are separated by a period of time which is the most vulnerable moment for alien pe*******on if it does not have spiritual protection.
And now we can try to understand why Jesus gave the prayer in which we address: "Our Father...", Is it not because in each of us, at least two consciousnesses live? And as soon as we pronounce "my" or "I", we deceive and there is a separation in us.
All executive organs have their representation in the heart, and the heart itself is also an executor relative to its brain. Therefore, it is necessary to assume that the heart, like the other organs, must have its own heart. But the functions of this heart of the heart are even more subtle and perfect. Based on the knowledge of the great heart, we can predict the conditions to which the heart of the heart must comply: - the capacity of its cavity will correspond to the volume of the coronary arteries; - the flows of its blood must precede the flows of the great heart; - the magnetic impulse of the great heart can be included with the systolic ejection of the heart of the heart; - its musculature is able to control the flows of blood and contain related tissues of the great heart.
Amazingly, such an organ exists. It is located in the heart and looks like an anatomical anomaly with an unknown physiological purpose. This organ is the BNA (auricula cordis). It fits all of these criteria, including its structure includes specific muscles which are not present in the surrounding cardiac tissues. Just as with the large heart, BNA can also suffer infarcts. And similarly to the large heart, clots from the auricula cordis, reaching the coronary arteries can disconnect the large heart. The BNA hides a riddle of sudden death. But does the BNA has its own heart and consciousness?
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