Si të ushqehemi ??

[dardajan]

Kura qe do sjell me poshte nuk eshte nje kure e lehte dhe per te gjithe dhe me konkretisht kete kure nuk mund ta bejne ata individ qe vuajne nga insuficenca renale,(veshkat) insufucence epatike, rakitismo, atrite cronica , ose cdo lloj problemi tjeter i organizmit tuaj qe nuk ben te mundur transformimin e acidit citrik.
Kjo kure nuk mund te perdoret per femijet e vegjel dhe per pleqte, nuk mund ta perdorin gjithashtu edhe ata individ qe kane nje shendet te dobet.
Prandaj eshte mire qe para fillimit te saj te merret mendimi i mjekut.

Qe kjo kure te kete sukses mendoj , qe cdo individ duhet te kete kaluar fazen e tranzicionit te pershkruar ne postimet e meparshme.
Kjo kure pastron shtratin qelizor ne te gjith organizmin tuaj dhe si rrjedhim gjate kohes se kures mund tju dalin probleme te ndryshme si pasoje e futjes ne qarkullim te mucos dhe paraziteve te tjere .Gjate kohes se kures mundesisht te hani sa me pak mish, brum, dhe bulmet ose aspak.

KURA E LIMONIT

Kura zgjat 30 dite dhe dosat e percaktuara nuk duhet te shtohen.
Gjate kures nuk duhet te haet fruta te tjera me vitamina C si Kivi,portokalle mandarina etj,,, nuk duhet te haen karamele, cokollata, cumcakiz, dhe mundesisht per duhan piresit ta ulin shume sasine e cigareve te pira sepse duhani konsumon shum vitamin C.
Limonat duhet te jene te fresket dhe mundesisht nga agrikultura biollogjika Limonat e shtrydhur duhet te pihen menjeher .
Kjo kure mund te behet nje here ne gjashte muaj ose nje here ne vit.
Kura eshte shum e thjesht , cdo mengjes 30-60 min para buke duhet te pini lengun e fresket te limonit puro ose me nje filxhan uje te vaket per ata qe nuk e pin dot puro.Diten e pare pihet lengu i nje limoni te dyten lengu i dy limonave te treten tre e keshtu me rradhe deri ne 12 limona pastaj fillon uljen ne 11 limona 10 limona 9 limona derisa arrin ne nje limon , kur arrin ne nje limon duhet ta vazhdosh edhe per 6 dite te tjera

Hene1°- 1 limon
Marte 2° - 2 limona
Merkure3° -3 limona
Enjte 4° - 4 limona
Premte 5° -5 limona
Shtune 6°- 6 limona
Diel 7°- 7 limona
Hene 8° - 8 limona
Marte 9° - 9 limona
Merkure10° -10 limona
Enjte 11° -11 limona
Premte 12° -12 limona
Shtune 13° - 12 limona
Diel 14° - 11 limona
Hene15° -10 limona
Marte 16° -9 limona
Merkure 17° -8 limona
Enjte 18° -7 limona
Premte 19° -6 limona
Shtune 20° - 5 limona
Diel 21° - 4 limona
Hene22° -3 limona
Marte 23° - 2 limona
Merkure24° -1 limona

Mbajtja e gjashte diteve nga nje limon

Enjte 25° -1 limona
Premte 26° -1 limona
Shtune 27° 1 limona
Diel 28° -1 limona
Hene 29° -1 limona
Marte 30° - 1 limona

Per ata qe duan te bejne gjysmen e kures duhet te arrijne deri ne 7 limona pastaj te bejne zbritjen ditore me nje limon, dhe ne fund gjashte dite me nje limon.

[dardajan]

Pse duhet pire 30-60 min para mengjesit ?

Sepse cdo lloj lengu qe shkon ne stomak del qe andej dhe shkon ne intestino mbas 30 min deri ne 60 max.Prandaj kjo kohe duhet qe lengu i limonit te dale nga stomaku dhe te shkoj ne intestino nga ku edhe fillon te thithet dhe te shkoje ne melci e me pas ne gjak.Ne qoftese ju do hani menjeher pas pirjes se limonit ai do perzihet me ushqimin dhe nuk ben asnje efekt kurimi.

C'far ndodh ne organizmin tone gjate kesaj kure '

Imagjinoni nje makine pastrimi me 12 marshe kjo makine ndodhet brenda jush ne terrenin qelizor te cdo pjese te trupit tuaj ,kjo makine pastron terrenin me leng limoni dhe kur ju pini lengun e limonit te pare ai pastron siperfaqen me 2 limona pastron edhe pak me thell me tre akoma me thell e keshtu me rradhe derisa mbaron pastrimin .
Kur gjaku me vitamin C sprucohet ne terrenin qelizor ai shkaterron bakteriet viruset mucon etj ,ai furnizon edhe qelizen dhe kjo e fundit pas pune nxjerr jasht skoriet e mbetura nga reaksionet dhe i le ne terrenin qelizor , ne kete moment fillon sistemi limfatik qe te thith dhe pastroj terrenin nga gjith keto mbetje dhe kur keto jane te medhaja ai nuk i thith dot njehersh kashtu qe krijohen probleme te ndryshme, prandaj kura fillon me nje limon dhe shtohet dale ngadale per ti lene kohe limfes qe te pastroje terrenin.Sa me shum shtohen limonat aq me shume pune i shtohet limfes.
Limfa mbasi i thith keto mbetje i con neper nyjet limfatike qe jane fabrika te vogla te pastrimit te limfes dhe prej kendej shkone ne veshke dhe me pas melci. Ne te gjitha keto organe limfa pastrohet kullohet dhe futet perseri ne gjak pjesa e filtruar del jashte nepermjet urines prandaj ata qe kane probleme me veshkat nuk mund ta bejne dot kete kure ose mund ta bejne nen kontroll te mjekut.

Si te veprojme kur kemi probleme gjat kures ?

Supozojme se jeni ne diten e tete dhe keni pire lengun e limonit por pas 2 oresh fillojne probleme te ndryshme qe nuk mund ti duroni dot.Kjo do te thote qe sistemi limfatik ka probleme ne thithjen e mbetjeve dhe duhet lene kohe qe te kryeje kete pune.Per ta ndihmuar ne kete pastrim duhet te pini uje natyral dhe me sa me pak kripra e minerale ne permbajtje te tij.
Diten tjeter mos shtrydhni 9 limona por 7 dmth beni nje hap mbrapa dhe shikoni nese keni perseri problemet e meparshme nese jo vazhdoni kuren duke e rritur me gjysem limoni. nese problemet vazhdojne ateher beni gjithnje zbritje nga nje limon derisa te arrish nje limon te cilin vazhdoje per nje jave .

Kuren mund ta vazhdoni nje here tjeter , por mendoj se me pare duhet te kaloni periudhen e tranzicionit e cila do ta lehtesoje shum terrenin qelizor.

[dardajan]

dardajan , Ne kete makine mushkrite jane POMPA dhe ZEMRA eshte VALVOLA dhe jo e kunderta sic shpjegohet ne mjeksi keto 400 vitet e fundit. postimi nr 65

Per te vertetuar thenien e mesiperme qe ka konfirmuar PROFF Ehret ne 1922 kam sjell artikullin e meposhtem qe eshte ne anglisht nense dikush mund ta perkthej qe ta lexojne te gjithe ne Shqip do ishte me mire .
Nese shkrimi i sjelle eshte ne kundershtim me rregullat e forumit moderatori mund te vere vetem linkun qe te con ne ate artikull.

--------------------------------------------------------------------------------




(The following article was published in the Fall-Winter 1995 issue [Volume 5, #1] of "Frontier Perspectives," the journal of the Center for Frontier Sciences at Temple University in Philadelphia, Pa.)





THE HEART IS NOT A PUMP:
A REFUTATION OF THE PRESSURE PROPULSION PREMISE OF HEART FUNCTION
by
Ralph Marinelli 1; Branko Fuerst 2; Hoyte van der Zee 3; Andrew McGinn 4; William Marinelli 5

1. Rudolf Steiner Research Center, Royal Oak, MI
2. Dept. of Anesthesiology, Albany Medical College, Albany, NY
3. Dept. of Anesthesiology and Physiology, Albany Medical College, NY
4. Cardiovascular Consultants Ltd., Minneapolis, MN. Department of Medicine, University of Minnesota, MN
5. Hennipen County Medical Center and Dept. of Medicine, University of Minnesota, MN


Abstract

In 1932, Bremer of Harvard filmed the blood in the very early embryo circulating in self-propelled mode in spiralling streams before the heart was functioning. Amazingly, he was so impressed with the spiralling nature of the blood flow pattern that he failed to realize that the phenomena before him had demolished the pressure propulsion principle. Earlier in 1920, Steiner, of the Goetheanum in Switzerland had pointed out in lectures to medical doctors that the heart was not a pump forcing inert blood to move with pressure but that the blood was propelled with its own biological momentum, as can be seen in the embryo, and boosts itself with "induced" momenta from the heart. He also stated that the pressure does not cause the blood to circulate but is caused by interrupting the circulation. Experimental corroboration of Steiner's concepts in the embryo and adult is herein presented.


Introduction

The fact that the heart by itself is incapable of sustaining the circulation of the blood was known to physicians of antiquity. They looked for auxiliary forces of blood movement in various types of `etherisation' and `pneumatisation' or ensoulement of the blood on its passage through the heart and lungs. With the dawn of modern science and over the past three hundred years, such concepts became untenable. The mechanistic concept of the heart as a hydraulic pump prevailed and became firmly established around the middle of the nineteenth century.

The heart, an organ weighing about three hundred grams, is supposed to `pump' some eight thousand liters of blood per day at rest and much more during activity, without fatigue. In terms of mechanical work this represents the lifting of approximately 100 pounds one mile high! In terms of capillary flow, the heart is performing an even more prodigious task of `forcing' the blood with a viscosity five times greater than that of water through millions of capillaries with diameters often smaller than the red blood cells themselves! Clearly, such claims go beyond reason and imagination. Due to the complexity of the variables involved, it has been impossible to calculate the true peripheral resistance even of a single organ, let alone of the entire peripheral circulation. Also, the concept of a centralized pressure source (the heart) generating excessive pressure at its source, so that sufficient pressure remains at the remote capillaries, is not an elegant one.

Our understanding and therapy of the key areas of cardiovascular pathophysiology, such as septic shock, hypertension and myocardial ischemia are far from complete. The impact of spending billions of dollars on cardiovascular research using an erroneous premise is enormous. In relation to this, the efforts to construct a satisfactory artificial heart have yet to bear fruit. Within the confines of contemporary biological and medical thinking, the propulsive force of the blood remains a mystery. If the heart really does not furnish the blood with the total motive force, where is the source of the auxiliary force and what is its nature? The answer to those questions will foster a new level of understanding of the phenomena of life in the biological sciences and enable physicians to rediscover the human being which, all too often, many feel they have lost.


Overview

Implicit in the notion of pressure propulsion in the cardiovascular system are the following four major concepts.

(1) Blood is naturally inert and therefore must be forced to circulate.
(2) There is a random mix of the formed particles in the blood.
(3) The cells in the blood are under pressure at all times.
(4) The blood is amorphous and is forced to fill its vessels and thereby takes on their form.

However, there are observations that challenge these notions. It is seen that the blood has its own form, the vortex, which determines rather than conforms to the shape of the vascular lumen and circulates in the embryo with its own inherent biological momentum before the heart begins to function. Just as an inert vortex in nature pulses radially and longitudinally, we tentatively assume that blood is also free to pulse and is not subject to the pulse-restricting pressure implied in the pressure propulsion concept. The blood is not propelled by pressure but by its own biological momenta boosted by the heart.

When the heart begins to function, it enhances the blood's momentum with spiraling impulses. The arteries serve a subsidiary mimical heart function by providing spiraling boosts to the circulating blood. In so doing the arteries dilate to receive the incoming blood and contract to deliver an impulse to increase the blood's momentum.


History

The history of the pressure propulsion premise goes back to Galileo and Leonardo da Vinci. The concept of the heart functioning as a pressure pump that forces the blood, assumed to be amorphous and inanimate, into its vessels and taking on the shape of its vessels was suggested by Borelli 1, a student and a close friend of Galileo, who observed the spiraling heart and compared its function to wringing the water out of a wet cloth. Borelli did not confirm his conjecture with experiments but was supported by misleading drawings of the left ventricle found later in Leonardo's work. In Leonardo's Notebooks the left ventricle wall was shown to be of uniform thickness as one expects to find in a pressure chamber. (See Fig. 1-A.)

However, quite the contrary, the left ventricle wall thickness varies by about 1800%, as we found by dissecting bovine hearts. The thickness ranges from 0.23 cm in the apex to 4.3 cm in the equatorial area. The apex wall is so soft and weak that it can be pierced with the index finger. The peculiar variability in the ventricular wall thickness is not in keeping with the idea of the heart being a pressure generator. However, one could conceive of such a wall configuration as maximizing the moment inertia with no static pressure in the ventricle.The thin, flexible, cone shaped apex and suspension from the aorta suggest the accommodation of a twisting function especially, when taking into account the spiral orientation of the myocardial muscle layers2. (See Fig. 1-B.)

The rotary motion of the heart, arteries, and blood has been measured or detected by several investigators 2, 18, 19. With slight variations, the erroneous sketch in Leonardo's Notebooks has been used in most biology, physiology, and medical texts during the last few hundred years as well as in most modern anatomy texts in the last decades. Thus, false sketches have served to bear witness to a false premise. (See Fig. 1-C.)

William Harvey (1578-1657) attended the University of Padua while Galileo was on its Faculty. He seemed to be deciding in favor of momentum propulsion from his own experiments focusing on the blood flow and pressure propulsion probably under the influence of Borelli who focused on heart motion. At times he implied a momentum propulsion concept: "The auricle (atria) throws the blood into the ventricle" and "the ventricle projects the moving blood into the aorta." "The blood is projected by each pulsation of the heart." At other times he used expressions that imply a pressure propulsion concept. "The heart squeezes out the blood." "The blood is forced into the aorta by contraction of the ventricle." In a few cases he speaks of the pressure of the blood. However, he also used neutral terms, "the blood is transferred, transfused, transmitted, and sent" - from place to place.

Subsequent investigators who helped to firmly establish the pressure propulsion concept were as follows: Stephen Hales (1677-1761) who inserted a glass tube into the artery of a horse and assumed that the column of blood was balanced out by static pressure. Jean-Leonard-Marie Poiseuille (1799-1869) discovered that arterial dilation was in phase with ventricular ejection. Therefore, he assumed that the dilation was the passive response to the pressure in the blood. Among other things he substituted a mercury manometer for the blood manometer of Hales. Carl Ludwig (1816-1895) invented the recording manometer by adding a float with writing pen and moving chart to Poiseuille's mercury manometer, and ushered in the age of continuous pressure recording. Finally, Scipione Riva-Rocci (1896-1903) perfected the sphygmomanometer in 1903 and brought the consideration of blood pressure into clinical practice.


The Problem and Its Proposed Solution

The problematic situation in cardiovascular physiology was expressed by Berne and Levy 3 who wrote: "The problem of treating pulsatile flow through the cardiovascular system in precise mathematical terms is virtually insuperable." A fundamental aspect of this problem relates to the fact that the major portion of our knowledge of cardiac dynamics has been deduced from pressure curves. In fact our knowledge of the system has two independent sources: experimentally determined facts and logically deduced concepts from the pressure propulsion premise. The situation is so confusing that some life scientists are considering chaos theory and mathematics to try to find the order in the system. It will be shown that the chaos derives from a mix of facts and conjectures and not from the nature of the phenomenon itself.

It is our purpose to demonstrate that Borelli's premise is incorrect and to propose the concept that the blood is propelled by a unique form of momentum. First, the aortic arch does not respond as expected if the blood in it were under pressure. The aorta is a curved tube; as such it has the basic form of the widely used pressure sensitive element of the Bourdon tube gage*.

When the curved tube of the Bourdon gage is subject to positive pressure, it is forced to straighten out as one sees in a garden hose. When subject to a negative pressure, the tube's curvature is increased. During the systolic ejection (period when blood is ejected from ventricle), the aorta's curvature is seen to increase, signifying that the aorta is not undergoing a positive pressure, but rather is undergoing a negative pressure 4.

We demonstrate that this negative pressure is that associated with the vacuum center of traveling vortices of blood. Thus the motion of the aorta, when considered as nature's own pressure sensor, contradicts the pressure propulsion premise. Of course, the swirling streams of the vortex have potential pressure, so any attempt to measure pressure will result in a positive pressure reading due to interrupted momenta.

Movement without applied pressure is movement with momentum, as we observe so dramatically in the long leaps of racing cats. It is also manifest in nature in flowing water in open streams, traveling tornadoes, and jet streams which are actually horizontal spirals of air and moisture that can be thousands of miles long and move around like meandering rivers in the upper atmosphere. A thrown ball in its trajectory also moves without pressure.

What about the measured blood pressure? The concept under consideration here is the well known ratio of force to area:

pressure = force/area (force per unit area)

The pressure is an arithmetical ratio derived from the average force of the moving blood, and as such, indicates the phenomenon of the moving blood indirectly. In a momentum system the pressure is a potential while the object is in motion and becomes manifest when the velocity is impeded:

momentum (mass x velocity) = impulse (force x time)

The blood moves with various velocities in its vortex streams. At the moment of impact of an object moving with momentum, the velocity decreases while the pressure of a certain magnitude appears.

Rudolf Steiner, scientist and philosopher, pointed out on several occasions that the blood moves autonomously 5, and that the pressure is not the cause of blood flow but the result of it 6. The clinicians of old used elaborate methods of describing the nature of the arterial pulse and the ictus cordis or the apex beat, which is the impulse of the heart against the chest wall. Many descriptive terms such as thready pulse of hypovolemic shock, collapsing or water-hammer pulse of aortic incompetence and `heaving' apical impulse of left ventricular hypertrophy, convey the intuitive understanding of the real mechanism of the heart's action.

An attempt to characterize left ventricular function by indices such as the maximal velocity of contraction (Vmax) and the maximum change of left ventricular pressure with time (dP/dtmax) suggests the felt inadequacy of the simple pressure propulsion concept.


Flow and Pressure

Considerations

When fluid mass is subject to force in the form of a pressure, it will first resist movement because of its inertia and viscosity. In a pressure driven system the pressure rises faster than the fluid moves; the pressure will peak before the fluid velocity peaks. However, when one simultaneously measures pressure and flow in the aorta, the peak flow markedly precedes the peak pressure. This phenomenon was observed as early as 1860 by Chauveau and Lortet and, as reported by McDonald 7, it contradicts the law of inertia in the pressure propulsion concept. (See Fig. 2.) While this phase relationship actually confirms the momentum propulsion principle, it nevertheless remained a source of conjecture for a considerable period of time in the 1950s until it was `rescued' with the help of elaborate mathematical modeling for oscillating flow.

An observation in favor of the concept of the blood having its own momentum was reported by Noble 8 in 1968. By simultaneous pressure measurements in the left ventricle and the root of the aorta of a dog, he demonstrated that the pressure in the left ventricle exceeds the aortic pressure only during the first half of the systole and that the aortic pressure is actually higher during the second half. He found it paradoxical that the ejected blood from the ventricle continues into the aorta despite the positive pressure gradient. The erroneous concept of left ventricular pressure exceeding the aortic pressure during entire systole proposed by Wiggers in 1928 is still depicted in many modern texts of physiology. (See Fig. 3A and B.) Noble proposed that this type of pressure pattern could be a result of momentum flow; however, this idea was overshadowed by the edifice of pressure propulsion.

The concept of pressure propulsion sent physiologists and scientists from diverse fields on a crusade that resulted in numerous hypotheses and theories about the cardiovascular system mechanics. The saying that, "fluid dynamists in the nineteenth century were divided into hydraulic engineers who observed what could not be explained and mathematicians who explained things that could not be observed," still stands true to this very day.


Embryological Observations

Steiner 6 indicated that embryology provides the clues for solving the problem of the circulation. In relation to this, Bremer 9 performed a remarkable series of observations of blood circulation in the very early chick embryo before the formation of the heart valves. He described the two streams of spiraling blood with different forward velocities in the single tube stage heart. Nevertheless, the blood is noted to have a definite direction of flow within the conduits and moves without an apparent propelling mechanism.These streams spiral around their own longitudinal axes and around each other. The streams appear to be a considerable distance apart, do not fill their vessels, and appear to be in discontinuous segments.

In a movie made by Bremer of the beating embryonic heart, one observes that the spiraling blood is boosted by the pulsating heart without creating turbulence in the blood. This suggests that the momentum transfer occurring between the heart and blood is in phase; the heart must somehow sense the motion of the blood and respond to it in turn with a spiraling impulses at the same velocities as the blood, thereby combining blood and heart momenta.

It is assumed that heart muscle layers have the same velocity distribution pattern as the concentric streams of a free vortex to enable heart and blood motions to couple in multi-velocity phase. It was significant to observe that the movement of the heart occurred with minimal inward motion of the heart wall. That the streaming of the blood can be observed before the functioning of the heart is supported by observations that the circulation in the early chick embryo is maintained for around 10 minutes after the heart had been excised 10. Moreover, the inherent mobility of the blood was highlighted by Pomerance and Davies 11, who found an embryo that lived to term without a heart but was born dead and grossly disfigured. Thus, the composite view of the embryonic cardiovascular system tells us that the blood is not propelled by pressure, but rather moves with its own biological momentum and with its own intrinsic flow pattern.


Alternations of Liquid and Gas Vortices in the Blood

The existence of apparently empty space between and within the spiraling liquid stream can be explained as space filled with gas or vapor. However, this hypothesis appears absurd when considering that even small bubbles in the arterial side of circulation can result in significant embolism. Each 100 cm of arterial blood contains 0.3 ml of free physically dissolved oxygen, 2.6 ml of carbon dioxide and 1 ml of nitrogen.

The importance of the small amount of dissolved oxygen is recognized only in extreme cases of anemia when it becomes a significant alternative source of tissue oxygenation. When viewed in terms of a highly differentiated distribution of solid, liquid and vapor/gas components of the composite vortex, this amount of free gas assumes critical importance.

The fact that the gas is elusive in the escaping liquid blood is very much in accord with the finding that the blood, as individualized liquid and gas vortices, moves with pressure-free momentum. The vortex in tornadoes is a very stable cohesive configuration with a vacuum center strongly held together by a centripetal force system. It does not have the physical properties of amorphous gas under pressure that tends to expand.

To further elucidate our observations, we contrived a model ventricle with a sealed, inverted cone-shaped, 0.5 liter clear glass flask filled with water. The instrumentation consisted of installing two tubes within the flask connected to pressure transducers to record vacuum in the vortex center and the potential pressure impulse in the momentum of the swirling water. The signal of pressure versus time was displayed on the oscilloscope screen and also fed to the computer for further analysis. The `ventricle' was operated by holding it in the hand and giving it a wobble and twist simultaneously to create a vortex. To enhance visibility, we filled the canister with methylene blue colored water.

Even the most energetic operation resulted in virtually no motion of the water. With some experimenting we determined that unless the model ventricle had about 1/3 of its volume as air space, a vortex could not be formed. This led us to reason that the highly organized gas/rarified plasma is a necessary component of the blood vortex. This also raises the question of how the gas and fluid elements can express the life property of locomotion.

The idea of the composite blood cells-plasma-gas vortex is in accord with the `gaps' in the flow of the embryonic vessels. To evaluate how valid our model ventricle was, we measured its potential impulse pressure (blood pressure as it is typically measured) in the swirling water and the vacuum in its center and found them to be in the range of +130 to -180 mm Hg, respectively. (See Fig. 4.)

Furthermore, we constructed a glass `ventricle' with an attached `aorta' and showed that up to 50% of the volume of the liquid could be ejected by subjecting it to a rotary-wobbling impulse, without the inward motion of the `ventricular' wall.


A Well Known Vortex Function

It is well known that the pattern of blood flow through the heart significantly contributes to heart valve dynamics as has been shown by several studies utilizing contrast cineradiography and more recently color Doppler imaging. Taylor and Wade 12 confirmed stable vortex flow patterns behind the cusps of mitral and tricuspid valves visualizing the fine stream contrast injection. Furthermore, the vortex formation in the aortic sinus has not only been demonstrated in the model heart, but also visualized with three-directional magnetic resonance velocity mapping 13. Without the vortex formation in the aortic sinus, it is conceivable that with the blood rushing out of the left ventricular outflow tract at one to two meters per second, the coronary arteries would be ill perfused, as is the case in severe aortic stenosis (narrowing), where high velocity blood flow does not allow for formation of the normal supravalvular vortices.


Evidence of Momentum Flow in the Adult

Not only is the blood flow well maintained in the embryo before the formation of the valves; there are reports of adults in whom both infected tricuspid and pulmonary valves were surgically removed and not replaced by prosthetic valves, without significant problems 14. Werner et al. 15 using two dimensional echocardiography observed that the mitral and aortic valves were open during external chest compression and that cardiac chambers were passive and did not change in size.


The Perpetual Vortex in the Ventricle

The widely used technique of cardiac output measurement using the thermodilution method is fraught with significant deviations of individual measurements. This technique is based on the principle of warm blood mixing with the bolus of cold saline in the ventricle and detecting the rise in temperature of the resulting mixture in the pulmonary artery. A final value is obtained by averaging the results of several measurements.

By measuring electrical conductivity at various locations in the left ventricle of a dog, Irisawa 16 was unable to show uniform mixing of saline. The conductivity records showed the swirling streams of blood of different concentrations of saline within the ventricles during systole and diastole (the dilation or expansion stage of the heart muscles that allows the heart cavities to fill with blood), further supporting the concept of the highly organized vortical patterns inside the chambers of the heart.

Brecher 17 conducted an experiment on a dog that demonstrated a region of continuous negative pressure in the ventricle by observing the continuous flow of Ringer's solution from a vessel outside the heart through a cannula positioned in the left ventricle via the atrial auricle. This further confirms our concept of the persistence of the vortex in the ventricle with its negative pressure center and positive pressure impulse potential in its swirling periphery throughout the cardiac cycle. Thus the heart as a minimum functional organ consists not only of its tissue but also of the perpetual vortex of blood which provides the perpetual vacuum in its center that probably helps to pull the blood back to the heart from capillaries and veins. The persistence of the vortex explains the anomaly to engineers of a supposed pump that retains 40 % of its charge with each ejection; a pump is expected to eject close to 100 % of its charge. As a pump concept it is absurd; as presented herein it is ingenious. Pettigrew 2 found three columns of spiraling blood in the left ventricle.


Orbiting Blood Corpuscles

In contrast to the parabolic velocity profile assumed by small particle suspensions in rigid tubes of small diameter under pressure, the cellular elements in the blood arrange themselves in a flow pattern in vivo, such that the heavier red blood cells orbit nearest the center with lighter platelets in more distant orbits surrounded by a sleeve of plasma at the vessel wall. Such an ordered arrangement of blood particle configuration in a sectional view of the arteries denies an omnidirectional pressure propulsion mechanism and confirms the vortex/momenta premise.

One can demonstrate this phenomenon of differentiation by mass in the vortex by allowing spheres chosen for convenience, same size (3 mm diameter), differently colored for different weight, to swirl freely in water. It will be seen that the heaviest spheres orbit nearest the center of rotation. The vortex orbital velocities increase as the orbits approach the center of rotation. On the contrary, during the time that a force couple is applied to rotate the vessel, creating a forced vortex, all of the spheres are forced out to the periphery where the velocities are the greatest as in a centrifuge.

To further confirm the existence of the free vortex velocity pattern in vivo, we probed the blood flow in the carotid artery by positioning a Doppler transducer at 900 to the wall to sense the blood's swirling motion and processed the Doppler echoes through a variable band pass filter looking for frequency (velocity) distribution patterns. We detected echoes from groupings of particles at 400 to 650 Hz, 650 to 900 Hz and below 200 Hz Doppler-shifted frequencies. These three groupings indicate three separate orbital regions and velocities. Preliminary observations point to a highly ordered distribution of the blood's cellular and plasma components.

Also, when moving through larger arteries the red cells are in toroidal shape, with their mass at the periphery to maximize the moment of inertia, and are assumed to rotate about their individual axes due to the phenomenon of vorticity (the creation of micro-vortices between swirling layers in the main vortex moving at different velocities). Thus we can expect to find that the billions of red cells are actually traveling in their own unique space as further evidence of the extreme order of the blood motion.


The Spiral Theme

The spiral theme is also apparent in the heart and vessel form and function. The musculature of the heart and arteries all the way down to the pre-capillaries is spirally oriented, and both the heart and arteries move spirally to augment the momenta of the blood 2,(18), 19. The literature on anatomical and physiological considerations of the twisting motion of the heart and vessels is comprehensive and has recently been reviewed 2. The fact that arterial endothelial cell orientation closely follows the blood flow patterns is well established 18, (19).

In a group of patients undergoing reconstructive vascular surgery of the lower extremities, Stonebridge and Brophy observed by direct angioscopic examination that the inner surface of arteries was organized in a series of spiral folds that sometimes protruded into the lumina. They commented that the folds occur as a result of spiral blood flow, which may be more efficient, requiring less energy to drive the blood through tapering and branching arterial system 19. They also observed the vortexing blood with fiber optics in the region of the endoluminal folds. In relation to this, enthusiasts know that rifled gun barrels forcing spin on the bullet make it more stable in flight and therefore more accurate in reaching its target. In the vessels the blood "grooves" its own conduits for the purpose of enhancing its torsional impulse. However, these spiral folds are not found in excised arteries; they are dynamics of living tissue.


Physiological Conclusions

The autonomic vortex movement of the blood discussed herein is inherent to the blood motion. It is not an accidental local disturbance often explained as turbulence or eddy currents, nor a localized phenomena with a single functional purpose as in heart valve dynamics. From a broader view it is to be expected that blood should so move, considering that fluids in nature tend to move curvilinearly, which is their path of least energy. The extreme expression of this tendency in nature, in terms of order, stability and minimal expenditure of energy are tornados and "jet" streams.


Potential Clinical Consequences

These observations should foster an accelerated understanding of the cardiovascular system through a reexamination of the vast amount of valuable experimental data gathered world wide. Since we have observed that the blood has a highly ordered dynamic form and an ordered blood corpuscle motion, and orientation, we should be able to develop devices and techniques to detect small deviations from group and individual norms and thus form a basis for very early diagnosis of cardiovascular disease, which remains the number one cause of death in the U.S. Novel, more effective therapies for cardiovascular disease hopefully will also evolve from this new perspective on cardiovascular physiology.


End notes

* The Bourdon tube gage is named after its inventor, Bourdon. Its pressure sensitive element consists of a circularly bent tube that is flattened to increase its sensitivity to pressure. When the tube is subjected to an internal positive pressure it tends to straighten; when subjected to an internal negative pressure its radius of curvature is increased. The deformation of the tube is proportional to the pressure and is transmitted via links and gears to motions that turn a pointer on a scale calibrated to indicate pressure.


Acknowledgments

We thank Larry W. Stephenson, M.D., Chief of Cardiothoracic Surgery, Wayne State University School of Medicine, and Beverly Rubik, Ph.D., for their comments on this work.

References

1. Borelli, De Motu Animalium. Rome, 1681.

2. Marinelli, R., Penney, D.G., et al. 1991. Rotary motion in the heart and blood vessels: a review. Journal of Applied Cardiology 6: 421-431.

3. Berne, R., Levy, M., 1986. Cardiovascular Physiology. St. Louis, MO: C.V. Mossy Co., p. 105.

4. Rushmer, R.F., D.K. Crystal. 1951. Changes in configuration of the ventricular chambers during cardiac cycle. Circulation 4: 211-218.

5. Steiner, R., 1990. Psychoanalysis and Spiritual Psychology. Hudson, NY: Anthroposophic Press, p. 126.

6. Steiner, R., 1920. Spiritual Science and Medicine. London, England: Rudolf Steiner Press, 24-25.

7. McDonald, D.,1952. The velocity of blood flow in the rabbit aorta studied with high speed cinematography. Journal of Physiology 118: 328-329.

8. Noble, M.I., 1968. The contribution of blood momentum to left ventricular ejection in dog. Circulation Res. 26: 663-670.

9. Bremer, J. 1932. Presence and influence of spiral streams in the heart of the chick embryo. American Journal of Anatomy, 49: 409-440.

10. Manteuffel-Szoege, L., 1969. Remarks on blood flow. J. of Cardiovasc. Surg. 10: 22-30.

11. Pomerance, A., Davies, M. 1975. Pathology of the Heart London, England: Blackwell Scientific Publications, pp. 538-39.

12. Taylor, D.E.M., J.D. Wade. 1973. Pattern of blood flow in the heart. Cardiovascular Research 7:14-21.

13. Kilner P.J., Z. Y. Guang, et al. 1993. Helical and retrograde secondary flow patterns in the aortic arch studied by three-directional magnetic velocity mapping. Circulation 88: 2235-2247.

14. Arbulu, A., I. Asfaw. 1981. Tricuspid valvulectomy without prosthetic replacement. J. Thorac Cardiovasc Surg 82: 684-691.

15. Werner, J.A., H.L. Greene, et al. 1981. Visualization of cardiac valve motion in man during external chest compression using two dimensional echocardiography. Circulation 63: 1417-1421.

16. Irisawa, H., M. F., Wilson, R.F. Rushmer. 1960. Left ventricle as mixing chamber. Circulation Research 8:183-87.

17. Brecher,G.A. 1956. Experimental evidence of ventricular diastolic suction. Circulation Research 4:513-18.

18. Lowell, L.B., L.S. Adamson. 1980. Relationship between blood flow direction and endothelial cell orientation at arterial branch sites in rabbits and mice. Circ. Res. 48: 481-488.

19. Stonebridge, P.A., C. M. Brophy. 1991. Spiral flow in arteries? The Lancet 338:1360-61.

[kleos]

Përshëndetje

--------------------------------------------------------------------------------

Doja të falemnderoja njëherë për gjithë këtë material .
Kam provuar ti zbatoj ato çfarë ke shkruar , mgjth disi e vështirë , por po mundohem , deri tani përfundimi vetëm është rënie nga pesha 3 kg .
Nqs ke mundësi tju përgjigjesh disa pyetjeve të mia do të isha shumë mirënjohës .

1)Ke shkruar për disa faza që duhen kaluar për të ndërruar zakonin e të ushqyerit .Për arsye të punës dhe kushteve , pasi ktu në Shqipëri s'mund ti gjesh disa ushqime që ke përmendur dhe nuk mund ti ndjek dietat a ka ndonje problem nqs nuk i ndjek ato siç i ke përshkruar , psh nga gjithçka ngrënës kam arritur të eleminoj mishin , bulmetrat (qumësht nuk konsumoj fare) ,brumrat etj . Ushqehem me perime zarzavate te ziera dhe fruta , por ndihem i uritur tërë kohën (nuk vuaj nga ndonjë sëmundje dhe gëzoj shëndet të plotë) .

2)Pësa i përket kripës së Himalajave e cila nuk gjendet këtu(Shqipëri) , me se mund të zëvendësohet ?

3)Kurën e limonit a mund ta filloj në këtë gjendje që jam aktualisht ?

[dardajan]

Përshëndetje

--------------------------------------------------------------------------------

Doja të falemnderoja njëherë për gjithë këtë material .
Kam provuar ti zbatoj ato çfarë ke shkruar , mgjth disi e vështirë , por po mundohem , deri tani përfundimi vetëm është rënie nga pesha 3 kg .
Nqs ke mundësi tju përgjigjesh disa pyetjeve të mia do të isha shumë mirënjohës .

1)Ke shkruar për disa faza që duhen kaluar për të ndërruar zakonin e të ushqyerit .Për arsye të punës dhe kushteve , pasi ktu në Shqipëri s'mund ti gjesh disa ushqime që ke përmendur dhe nuk mund ti ndjek dietat a ka ndonje problem nqs nuk i ndjek ato siç i ke përshkruar , psh nga gjithçka ngrënës kam arritur të eleminoj mishin , bulmetrat (qumësht nuk konsumoj fare) ,brumrat etj . Ushqehem me perime zarzavate te ziera dhe fruta , por ndihem i uritur tërë kohën (nuk vuaj nga ndonjë sëmundje dhe gëzoj shëndet të plotë) .

2)Pësa i përket kripës së Himalajave e cila nuk gjendet këtu(Shqipëri) , me se mund të zëvendësohet ?

3)Kurën e limonit a mund ta filloj në këtë gjendje që jam aktualisht ?

Mund ti besh pyetjet ne kete teme qe kam hapur pikerisht per ata qe duan te ndryshojne ushqimin dhe kane veshtiresi ose edhe per sqarime te tjera :

http://www.forumishqiptar.com/showthread.php?t=92013

[dardajan]

Linku per postimin nr 123 eshte ky :

http://www.rsarchive.org/RelArtic/Marinelli/

[dardajan]

Melcia

Per melcine ka aq shume per te thene saqe duhet nje teme me vete, prandaj po ndalem vetem tek disa gjera kryesore te saj.

Melcia ka veti rigjeneruese pra edhe po te hiqet nje pjese ajo rigjenerohet brenda 4 muajve.
Melcia kryen rreth 500 lloj funksionesh.
Melcia eshte laboratori kryesor i reaksioneve me te rendesishme te organizmit tone.
Melcia kryen disintosikimin (pastrimin nga helmet ) e organizmit nepermjet pastrimit te gjakut dhe furnizimit te tij me sostanza te reja ushqimore.
Melcia eshte organi me i madh i organizmit tone.
Ajo kryen edhe shum, shum funksione te tjera qe sic e theshe edhe me lart nuk eshte vendi i pershtatshem per ti permendur, POR, POR, ajo qe dua te them eshte se gjate gjith kesaj pune kolosale ky organ fillon te degradohet, (shkaterrohet) sidomos kur ushqimet dhe helmet qe marrin jane te shumta dhe te demshme, Kanalet e ketij organi fillojne te bllokohen dhe pjese te tij mos funsionojne sic duhet kjo gje pastaj pasqyrohet ne organe te ndryshme ne forme semundje.

Pra te gjith ne pa perjashtim me ushqimet qe kemi marre gjate gjith jetes kemi bere qe ajo tashme te jete ne nje stad gjysem te bllokuar .

Melcia edhe kur eshte 80% e demtuar nuk jep probleme ne vetvete por ne organe te tjere dhe mjeket ne vend qe te kurojne melcine pra burimin merren me organe te vecanta duke perdorur ilace te cilat nga ana e tyre e rendojne akoma me shume gjendjen e mjeruar te melcise prandaj organi i pare qe duhet riaktivizuar 100% eshte melcia.

Per kete po ju jap nje recete shume te vjeter ne kohe por qe eshte zbuluar vetem vitet e fundit.
Edhe ky mjek ben pjese ne ata mjek qe njohurite e tyre duan tja u bejne te ditur mbar njerrezimit dhe jo shoqerive farmaceutike.
Sepse e drejta per dije eshte nje e drejte nderkombetare, e drejte humanitare sidomos ne fushen e mjeksise.
Me vone do flas edhe per kete mjeke qe me studimet e saja ka ndihmuar shum njerezimin.

Shpesh shum njerez me gure ne melci ose ne temth jane te detyruar te operohen duke rezikuar jeten dhe harxhuar nje sasi parash, por qe sot e tutje te mbas leximit te ketij postimi ata do te shpetojne nga operimi dhe leket do ti kursejne per femijet e tyre.

Kura: Per heqjen e gureve nga melcia dhe temthi ne rruge natyrale.

Perberesit:

Kripe e hidhur (solfat magnezi) ose ( krip angleze i thone ) 4 here 20g
Gjysem tasi me vaj ulliri 75ml
2 pompelma te kuq ose due limoni
Ornitina 3 tablete

Esence nga arra e zeze Eshte nje lloj arre qe rritet ne USA Due (Juglans nigra) emri shkencor.

Pra fillimit te kures eshte mire qe te pastrohet melcia nga parazitet per kete ka nje kure prej tre javesh me nje solucion ku jane shkrire tre lloj bimesh.
Para se te fillohet pastrimi i melcise duhet patjeter te behet me pare pastrimi i veshkave.Sepse do jene te mbingarkuara nga ky pastrim dhe krijojne probleme nese veshka nuk punon mire.
Per te bere kete kure duhen 24 ore psh e shtune dhe e diel per pushim.
Gjate ketyre 24 oreve eshte mire qe te mos merren ilace te tjera por ne raste te vecante mund te shikohet e arsyeshme marrja e tyre per kete cdo individ duhet te konsultohet me pare me mjekun nese ka ilace qe duhet ti marre pa tjeter.

Kura fillon ne 14°° te shtunen dhe mbaron ne 14°° te dielen.
Eshte mire qe nje nate me pare te mos hani yndyrna.

Mengjesi dhe dreka e dites se shtune duhet te jene te lehta dhe pa yndyre pa sheqer dhe pa qumesht. Duhet ngrene drithra e ziera. Mire do ishte psh Quinoa,ose Miglio per mengjes dhe oriz integral per dreke i ziere te pakten per nje ore ne misuren 1 me 4 pra 1 oriz dhe kater uje.Mund te perdoret kripe deti .
Orizi mund te shoqerohet me nje pjate perimesh o zarzavate te ziera si karrota spinaq, lakra etj.

Ora 14 °° duhet te keni mbaruar dreken dhe nuk do hani me deri te nesermen ne oren 14°° nuk duhet te hani asedhe nje biskote apo dicka tjeter por mund te pini vetem uje natyral ,(jo uje cesme ) .Ne qoftese nuk respektoni kete rregull gjate kures mund t,ju vije per te vjelle dhe rezultati te jete i dobet.

Ora 18°° Perzieni 20g kripe te hidhur (solfat magnezi) ne 100ml uje mund ti hidhni vitamin c ne pluhur ose gjysem limoni te shtrydhur dhe pijeni njeheresh ose me gllenka.

Ora 20°° perseriteni proceduren e ores 18 dhe pijeni ujin me kripe te hidhur.
pregatituni qe te jeni gati per gjume rreth ores 21e 45 min


Ora 21,45 Merni vajin e ullirit 75ml dhe hidheni ne nje ene prej xhami me kapak (kavanoz) .Merrni 2 pompelmat e kuq dhe shtrydhini mire ne nje ene (gote) kullojeni nga farat apo pjeset e brendshme dhe lengun e kulluar hidheni ne vazon me vaj mbyllni mire kapakun e vazos dhe tundeni fort derisa lengjet te bashkohen dhe te marrin nje ngjyre si te bardhe. nga ora 21.45 deri 22°° mund te shkoni ne banjo ose te pregatiteni per gjume.

Ora 22°° Pijeni perzierjen e pregatitur me vaj dhe pompelm e bashke me te edhe 3 kapsula ornitina, Dhe qe nga ky moment brenda 5 minutave duhet te jeni shtrire ne krevat per gjume.Eshte e rendesishme respektimi i te gjitha orareve me perpikmeri.
Duhet te shtriheni me kuriz dhe me duart siper kokes te mbeshtetura mbi jastek.
Ne kete moment guret fillojne te levizin por ju nuk ndieni asgje sepse kanlet ku ato kalojne jane hapur nga kripa e hidhur (kripa Angleze) Duhet vetem te flini deri ne mengjes.Mund te dilni edhe ne banjo gjat nates por shikoni edhe brenda ne water e mblidhini guret me nje kullese. Ornitina do t'ju vere ne gjume shume shpejt.

Ora 06°° e megjesit e dites tjeter jo me para se ora 6 pra pas ores gjashte te megjesit perzjeni 20g kripe te hidhur (solfat magnezi) ne 100ml uje dhe pijeni me limon ose me pak mjalte per te hequr shijen e hidhur.
Ne qoftese ju vjen per te dale ne banje prisni pak sa te pini dozen e ores 6 dhe pas pak minutash mund te shkoni ne banje. Dhe nese nuk ju vjen per te shkuar ne banje mbasi ta keni pire dosen e ores 6 te mengjesit shtrihuni perseri ne krevat.

Dy ore me pas pra rreth ores 8°° merrni dosen e fundit me kripe te hidhur te pregatitur si me pare dhe pijeni pastaj shkoni perseri ne krevat.

Pas dy oresh pra rreth ores 10 mund te pini leng frutash te shtrydhur vete, dhe pas 30 min mund te hani edhe fruta te nje lloji.

ora 14°° Mund te hani normalisht pa egzagjiruar dhe mundesisht vetem nje lloj ushqimi pra te nje tipi jo shum ushqime njehersh.
Mund te hani psh tave me presh pa mish dhe shum pak vaj.Ose byrek me qepe e presh te bere vete, pa shum yndyre.
Shkarkimet mund te vazhdojne gjate gjith dites prandaj mos u beni merak.


Per ata qe duan ta bejne kete kure me te forte ne oren 8°° te megjesit ne vend te ujit me kripe te hidhur, mund te pregatisin perseri vajin me pompelm si me pare dhe ta pine. Dhe vetem pas 4 oresh te pijne ujin me kripe te hidhur te pregatitur si me pare. Qe i bie ne oren 12 te drekes.

Gjate kesaj kohe sidomos ne mengjesin e dites tjeter pra ne oren 6 do shkoni shpesh ne banje mbasi te mbaroni pune mos t'ju vije neveri por shikoni ne sipefaqe te ujit dhe mblidhini me nje site te gjithe guret qe kane dale dhe verini ne diell te thahen pastaj mund edhe ti kotrolloni duke i care per te par se cfar kishit brenda ne melci dhe temth. Ato rrine ne sipefaqe te ujit edhe pas shkarkimit te ujit sepse jane te lehte .
Ato kane ngjyra dhe madhesi te ndryshme me e madhja arrin sa nje koker qershi por shume elastike dhe pa peshe .
Keto gure nuk shifen dot me radiografi.
Po ata qe kan hequr temthin mund ta bejne ?
Po mund ta bejne dhe kane bere pa asnje problem.


Kjo kure nuk eshte aspak e rrezikshme si per femije e per pleq.
Kjo kure mund te behet pa problem 2-3 here ne vit.
Shikojeni mire gjuhen tuaj para fillimit te kure gjate saj dhe ne fund ,pjesa e anshme e gjuhes ka lidhje me melcine pra pasqyron shendetin e saj.

Mbas kesaj kure do tju largohen shum alergji te ndryshme, dhimbje te shpatullave dhe shtylles kurizore.Do ndjeni gjithashtu nje permirsim te pergjithshem.


shenim
Mund te beni pyetje per kete kure por mos e filloni pa ju dhene edhe kuren per pastrimin e veshkave .
Qe kura te kete efekt me te madh duhet ne fillim nje kure prej tre javesh per ngordhjen e paraziteve.
Mire eshte qe keto kura te behen pasi te keni kaluar fazen e tranzicionit te ushqyerit sepse keto organe gjate kesaj faze mbushen perseri me gure kolesteroli dhe kristale.
Megjithate ajo eshte e vlefshme per te gjithe dhe ne cdo kohe.


Me poshte po bashkangjis edhe disa foto me gure te nxjerre nga kjo kure.

[dardajan]

Ne qoftese gjate kures ka ngritje te temperatures duhet te nderpritet kura .
Ne qoftese gjate kures ka cregullime apo dhimbje te forta te nderpritet kura.
Deri me sot kjo kure nuk ka patur asnje efekt negativ por gjithsesi duhet parashikuar cdo gje sepse jo te gjith njerzit jane njelloj .
Nese ndodh ndonje problem i tille nderpritet kura dhe behet menjeher nje klistere dhe pihet uje natyral.

[dardajan]

UNE ? jo, jo, por do me pelqente ta kisha shpikur une megjithse shpikesi i saj nuk dihet pasi kjo kure vjen nga lashtesia pra nga shkrimet e vjetra dhe e ka zbuluar Dot-sa Hulda Regehr Clark specializuar ne Biofisika dhe Fisiologjia puna e saj shkencore dhe praktike me pacientet ka filluar ne fund i viteve 70. Dhe vetem keto vitet e fundit ajo ka botuar librat e saj me punen e saj shkencore shum te perparuar si nga ana e kapjes se problemit dhe trajtimit ashtu edhe te mjeteve te punes qe ka shpikur vete per kete kerkim shkencor. Ajo ka botuar disa libra ku dallojne me shume librat me titull :
Kura e te gjitha semundjeve
Kura e te gjith kancereve te avancuar.
Dot-sa Clark i ka botuar te gjitha zbulimet e saj ne libra te ndryshem ajo i ka vene ne internet te gjitha zbulimet e saj ne menyre qe te jene te kopjueshem e lexueshem nga te gjithe ,ajo ne kundershtim me shume shkencetar te tjere nuk i ka shitur zbulimet e saja ne shoqeri farmaceutike sepse deshiron qe njerzit ti njohin dhe sherojne vet problemet e tyre te shendetit ne kete drejtim ajo eshte njesoj si Prof Ehret,MCKeith pra deshirojne qe zbulimet e tyre te mos jene vegla ne duart e disave qe abuzojne dhe perfitojne pastaj tek individet e semure.Ata duan nje bote ku emri semundje te mos egzistoje me.
Prandaj meritat per kete kure jane te saja sic jane edhe per kuren kunder parasiteve qe mund ta paraqis me vone, dhe per kuren e pastrimit te veshkave.

Per ata qe duan te dine dhe mesojne me shume per te dhe studimet e saj mund te lexojne ne websitin e saj. Aty do te gjeni edhe kurat e tjera qe un mund tja u perkthej me vone.

http://www.drclark.net/

[dardajan]

Per te kuptuar mekanizmin e kesaj kure duhet sqaruar funksioni i temthit dhe i melcise.Melcia prodhon nje leng qe ne e quajme lengu i temthit (ne mjeksi "bile") ajo prodhon nga 500 deri ne 1500 ml ne dite dhe ky leng sherben per te tretur ushqimin qe vjen nga stomaku dhe futet ne intestino ,melcia ka lidhje direkte ( tub ) me intestinon per te derdhur kete leng por kur nuk ka ushqim ne intestino dhe qe ky leng te mos shkoje dem organizmi yne e mbyll valvolen qe lejon kete kalim dhe lengu i prodhuar depozitohet ne temth aty ajo arrin nje koncentrim 10 here me te madh se masa fillestare ,keshtu qe ne momentin qe ushqimi vjen ne intestino nje hormon me emrin

(colecistochinina-pancreozimina)

qe prodhohet nga mukoza e intestinos ben kontraktimin e temthit dhe hapjen e valvoles per leshimin e ketij lengu.Dhe 95% e ketij lengu pasi kryen pune ne intestino thithet perseeri nga intestino dhe cohet ne melci per tu ricikluar.
Pse leshohet ky leng ne intestino?
Sepse ushqimi qe del nga stomaku dhe hyn ne intestino eshte shum acid keshtu qe per te mos demtuar mukozen e intestinos ky leng ka permbajtje te larte bikarbonati i cili alkalizon ushqimin dhe mbron intestinon.
Ky leng gjithashtu ka si funksion edhe shkrirjen e yndyrnave duke bere te mundur thithjen e vitaminave D, E, K e A nga intestino dhe qe gjenden ne keto yndyrna.
Ky leng ka efekt shkaterrues per bakteriet e keqia qe hyjne me ushqimin.

Kush eshte mekanizmi i kesaj kure ?
Kur ne mbarojme se ngreni ne oren 14°° ushqimi deri ne oren 18 eshte tretur dhe ka perfunduar ne intestino kripa Angleze krijon presion gjate shperberjes dhe pastron intestinon. Me pastrimin e intestinos valvola qe leshon lengun tretes nga melcia mbyllet dhe lengu qe prodhohet kalon ne temth duke e fryre ate deri ne maksimum.Kur ne pijme vajin me pompelm te perzier ai shkon ne stomak dhe pas rreth nje ore shkon ne intestino mete mberitur ketu hormoni kontrakton temthin dhe hap valvolen per leshimin e lengut drejt intestinos qe duhet per te tretur yndyren dhe ulur aciditetin kjo levizje kryhet nen presionin e boshatisjes se menjehershme te temthit nepermjet kanalit tashme te zgjeruar nga presioni i kripes.
Kjo levizje e vrullshme merr perpara edhe guret qe gjenden gjate rruges se saj dhe i con ne intestino nga ku dalin me jashteqitjen.
Nga ana e saj edhe melcia leshon lengun e saj me presion duke gjetur rruge te lire shkarkon guret e saj.

Per mendimin tim qe kura te jete e plote duhet zgjedhur varianti i dyte ai qe diten tjeter ne mengjes ne oren 8°° ne vend te dozes se trete te pish perseri perzierjen e vajit dhe 4 ore me vone kripen.

Po bashkangjis edhe foto per ta kuptuar me mire