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We used Jones-matrix images of protein networks of blood plasma films obtained from laser autofluorescence and determined the sensitivity, specificity, accuracy, and prognostication of positive and negative results. Our study aimed (1) to develop and substantiate new approaches for the diagnosis of endometriosis by improving the methods of Jones-matrix mapping of laser-induced auto-fluorescence and (2) to develop statistical approaches for analyzing the distribution of values of the true component of Jones-matrix images of blood plasma. Biological preparations were performed for two groups: 35 samples from control group 1 (women with infertility of unknown origin) and 85 samples from group 2 with endometriosis (women with infertility and endometriosis). The strength of the Jones-matrix method of autofluorescence mapping of plasma proteins taken from both groups was maximal for the decisions determined based on the calculation of the statistical moment of the 4th order, for statistical moment Z4, characterizing the sharpness of the peak distribution of the polycrystalline component of the plasma film. Comparison with the similar informative data of the Jones-matrix laser autofluorescence method of histological sections of the endometrial biopsy under conditions of blind endometriosis diagnosis revealed this method of analysis highly informative. Therefore, this technique can be used in screening studies to form a risk group.

In humans, the composition of blood plasma can be altered in a clinical procedure called therapeutic plasma exchange, or plasmapheresis, which is currently FDA-approved in the U.S. for treating a variety of autoimmune diseases. The research team is currently finalizing clinical trials to determine if a modified plasma exchange in humans could be used to improve the overall health of older people and to treat age-associated diseases that include muscle wasting, neuro-degeneration, Type 2 diabetes and immune deregulation.

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However, in the original report, and in a more recent study , when blood was exchanged between young and old animals without physically joining them, young animals showed signs of aging. These results indicated that that young blood circulating through young veins could not compete with old blood.

As a result, the Conboys pursued the idea that a buildup of certain proteins with age is the main inhibitor of tissue maintenance and repair, and that diluting these proteins with blood exchange could also be the mechanism behind the original results. If true, this would suggest an alternative, safer path to successful clinical intervention: Instead of adding proteins from young blood, which could do harm to a patient, the dilution of age-elevated proteins could be therapeutic, while also allowing for the increase of young proteins by removing factors that could suppress them.

After finding that the neutral blood exchange significantly improved the health of old mice, the team conducted a proteomic analysis of the blood plasma of the animals to find out how the proteins in their blood changed following the procedure. The researchers performed a similar analysis on blood plasma from humans who had undergone therapeutic plasma exchange.

They found that the plasma exchange process acts almost like a molecular reset button, lowering the concentrations of a number of pro-inflammatory proteins that become elevated with age, while allowing more beneficial proteins, like those that promote vascularization, to rebound in large numbers.

Therapeutic plasma exchange in humans lasts about two to three hours and comes with no or mild side effects, said Kiprov, who uses the procedure in his clinical practice. The research team is about to conduct clinical trials to better understand how therapeutic blood exchange might best be applied to treating human ailments of aging.

The measurement of blood-plasma velocity distributions with spatial and temporal resolution in vivo is inevitable for the determination of shear stress distributions in complex geometries at unsteady flow conditions like in the beating heart. A non-intrusive, whole-field velocity measurement technique is required that is capable of measuring instantaneous flow fields at sub-millimeter scales in highly unsteady flows. Micro particle image velocimetry (muPIV) meets these demands, but requires special consideration and methodologies in order to be utilized for in vivo studies in medical and biological research. We adapt muPIV to measure the blood-plasma velocity in the beating heart of a chicken embryo. In the current work, bio-inert, fluorescent liposomes with a nominal diameter of 400 nm are added to the flow as a tracer. Because of their small dimension and neutral buoyancy the liposomes closely follow the movement of the blood-plasma and allow the determination of the velocity gradient close to the wall. The measurements quantitatively resolve the velocity distribution in the developing ventricle and atrium of the embryo at nine different stages within the cardiac cycle. Up to 400 velocity vectors per measurement give detailed insight into the fluid dynamics of the primitive beating heart. A rapid peristaltic contraction accelerates the flow to peak velocities of 26 mm/s, with the velocity distribution showing a distinct asymmetrical profile in the highly curved section of the outflow tract. In relation to earlier published gene-expression experiments, the results underline the significance of fluid forces for embryonic cardiogenesis. In general, the measurements demonstrate that muPIV has the potential to develop into a general tool for instationary flow conditions in complex flow geometries encountered in cardiovascular research.

Plasma is the liquid portion of whole blood. It is composed largely of water and proteins, and it provides a medium for red blood cells, white blood cells and platelets to circulate through the body. Platelets, also called thrombocytes, are blood cells that cause blood clots, as well as other necessary growth and healing functions.

PRP injections are prepared by taking anywhere from one to a few tubes of your own blood. It is then run ("spun down") in a centrifuge to separates the blood into its various components: red and white blood cells, plasma, platelets, etc. The platelets are collected and concentrated to anywhere from 2 to 8 times their normal number. The platelets are then mixed into a blood plasma liquid base and injected directly into the area of injury. Ultrasound imaging is sometimes used to guide the injection. The images below show a PRP injection into a patient's torn tendon. The ultrasound guidance is shown at left and the injection is shown at right.

The activation of the concentrated platelets in platelet-rich plasma releases growth factors that stimulate and increase the number of reparative cells your body produces. This significantly enhances the body's natural healing process.

Side effects of PRP injections are very limited because the injections are created from your own blood, and your body should not reject them or react in any negative way. As with any injection, there is a remote risk of infection. Otherwise, there are no significant risks apart from the variability and unpredictability of how effective the treatment will be for a particular patient.

In modern medical treatments, patients may receive a pint of whole blood or just the specific components of the blood that are needed to treat their particular condition. This approach to treatment, referred to as blood component therapy, allows several patients to benefit from one pint of donated whole blood.

The transfusable components that can be derived from donated blood are red cells, platelets, plasma, cryoprecipitated AHF (cryo), and granulocytes. An additional component, white cells, is often removed from donated blood before transfusion.

A whole blood donation requires minimal processing before it is ready to be transfused into a patient. If not needed right away, whole blood can be refrigerated for up to 35 days, depending on the type of anticoagulant used.

Red blood cells (RBCs), or erythrocytes, give blood its distinctive color. Produced in our bone marrow, they carry oxygen from our lungs to the rest of our bodies and take carbon dioxide back to our lungs to be exhaled. There are about one billion red blood cells in two to three drops of blood.

Red blood cells are prepared from whole blood by removing the plasma (the liquid portion of the blood). They have a shelf life of up to 42 days, depending on the type of anticoagulant used. They can also be treated and frozen for 10 years or more.

Leukocyte-reduced RBCs are prepared by removing leukocytes (white blood cells) by filtration shortly after donation. This is done before the RBCs are stored because over time the leukocytes can fragment, deteriorate, and release cytokines, which can trigger negative reactions in the patient who receives them. These reactions can occur during the initial transfusion or during any future transfusions.

Platelets, or thrombocytes, are small, colorless cell fragments in our blood whose main function is to stick to the lining of blood vessels and help stop or prevent bleeding. Platelets are made in our bone marrow.

Blood plasma serves several important functions in our bodies, despite being about 92% water. (Plasma also contains 7% vital proteins such as albumin, gamma globulin and anti-hemophilic factor, and 1% mineral salts, sugars, fats, hormones and vitamins.) It helps us maintain a satisfactory blood pressure and volume, and supplies critical proteins for blood clotting and immunity. It also carries electrolytes such as sodium and potassium to our muscles and helps to maintain a proper pH (acid-base) balance in the body, which is critical to cell function.

Plasma is obtained by separating the liquid portion of blood from the cells. Plasma is frozen within 24 hours of being donated in order to preserve the valuable clotting factors. It is then stored for up to one year, and thawed when needed. 006ab0faaa