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Factors that contribute to wound healing
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Wound healing is a complex process that involves sequential phases that overlap in time. It would be necessary to understand the normal wound healing process before look into the biological mechanisms of scar formation. Once a normal tissue is injured, a series of cellular activity will be triggered in order to restore the original structure and function. The process of wound healing can be classified into four phases, hemostasis, inflammation, proliferation and remodeling.
Once a normal tissue is injured, hemostasis will get started. This process is aims to protect the vascular system, so that the vital organ such as heart, brain and kidneys are able to remain its function. Platelets will begin to aggregate at the wound site and it will release clotting factors which prevent excessive bleeding. On the other hand, the cytoplasm of platelets which contain alpha-granules that filled with growth factors and cytokines
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Fibroblast is located at the dermis layer of skin. The fibroblasts surrounded at the wound site will get stimulated and attracted by TGF beta and PDGF that are released by inflammatory cells and platelets. Fibroblasts are responsible to produce collagens and extracellular matrix component that are needed for tissue restoration. The reasons that made collagen an important component in wound healing especially the remodeling phase is because it would affect the integrity and strength of the tissue. Out of all the collagens secreted, collagen type 1 has been identified as the most abundant type of collagen in scar tissue formation. Around 7 to 8 days later, fibroblasts will have differentiated into myofibroblasts. Myofibroblasts contains alpha-smooth muscle actin (alpha-SMA) can help to close the wound by contraction. In normal case, after healing is completed, myofibroblasts will undergo apoptosis. If this mechanism is failed to work, hypertrophic or keloids scars will
Carlton suffered an acute tissue injury on his foot after stepping on a sharp edge shell, which disrupted the layers of the skin. Immediately after an injury occurs, an inflammatory response begins, which serves to control and eliminate altered tissue/cells, microorganism, and antigens. This takes place in two phases. 1) The vascular phase, in which small vessels(arterioles, venules) at the site of injury undergo changes. Beginning, with
Haemolytic colonies were classified by a white ring around the patched colony, indicating that haemolysis of the blood agar occurred. Conversely, non-haemolytic colonies were classified by a lack of a white ring, which indicated that no haemolysis took place.
Acne damages the skin. The bacteria and oil cause damage to the pores, skin, and underlying tissue. In response, the body sends white blood cells and other treatment molecules called collagen to the area in an attempt to heal the damaged tissues. Most acne scars only affect the outer layers of skin. Depending on how much collagen one’s body produces affects the scar type, if the scars are depressed the body does not produce enough collagen, if the scars are raised the body produced too much collagen (American Association of Dermatology 2011).
Each system, as noted early, contributes to reversing cause of shock in this phase. The first of this will be seen when cause of shock is from hemorrhage and significant blood loss from the body, and all components of the hematologic system, or from blood, has its own function as a response (Kolecki “Pathophysiology”). The body’s process of quickly locating and slowing down bleeding within the body is called hemostasis. As soon as a blood vessel is broken, both the liquid and solid components within the blood effect how the body responds (Tortura 703).
Not all attributes are obvious for every situation. The lion's share of instances of OI (conceivably 85-90 %) are created by a predominant change in a quality coding for sort I collagen (Types I, II, III, and IV in the accompanying rundown). Sorts VII and VIII are recently recognized structures that are acquired in a passive way. The qualities bringing about these two sorts have been recognized. Sorts V and VI don't have a sort 1 collagen change, however the qualities bringing about them have not yet been recognized. The general components of each referred to sort of OI are as per the
Regeneration is a process in which tissue molds itself into an exact replica of an injured or severed part. The process of regeneration depends on different factors such as the environment and the development of the organism in question (Br, 1955). Regeneration occurs in several steps and the organism must have the ability to perform each one for successful regeneration with minimal loss of necessary function. First, after a wound is made muscular contraction closes up the wound (Pellettieri et al., 2010). Next a blastema, a group of undifferentiated cells, forms and will differentiate into the missing parts. Lastly the undifferentiated cells go through epimorphosis where the lost parts are formed by the blastema (Reddien & Sánchez Alvarado, 2004).
Inflammation: the response to injured tissue that stops bleeding and causes swelling and warmth as the tissue prepares to repair itself
Repair after a muscle is damaged happens through the division of certain cells who then fuse to existing, undamaged muscle fibers to correct the damage. Different muscle types take different amounts of time to heal and regenerate after it has been damaged. Smooth muscle cells can regenerate with the greatest capacity due to their ability to divide and create many more cells to help out. While cardiac muscle cells hardly regenerate at all due to the lack of specialized cells that aid in repair and regeneration. In skeletal muscle, satellite cells aid in helping restoration after injury. Along with muscles, tendons are very important structures within the human body, and they to can be damaged. However, tendon repair involves fibroblast cells cross-linking collagen fibers that aid in not only reinforcing structural support, but also mechanical support as well (“Understanding Tendon Injury,” 2005). While quite different from muscle repair, tendon repair involves the similarity of reestablishing d...
Two major types of dressing that are used for covering third degree burns and are FDA approved and recognized, Biobrane and Integra. Both of these dressings are laid and kept in place until autographing can be possible. Growing a patients skin in a lab, which is called cultured skin, is a process that helps eliminate the donor site and scarring from auto grafting. Taking a skin sample about the size of a quarter can be grown into enough skin to nearly cover all the body in about 2 to 3 weeks. The only problem with this method is that something has to cover the wounds in the meantime. This is when the Integra and Biobrane take effect. The wound could be covered with Integra or Biobrane acting as the epidermal layer of the skin until the new grown skin is ready for grafting.
The solution to this problem is located in the lab. Researchers across the country are working day in and day out to come up with a solution to accelerate the healing of soft tissues. They have come up with many solutions, from vibration therapy, to personalized rehab plans, but none of these are yielding truly significant results. I believe the solution lies at the molecular level. I believe that we can observe the healing of these soft connective tissues and learn from it. Then we can design a method from the observations to accelerate the production of the fibrils and collagen that will go on to make up the soft connective tissue. I have begun to take the beginning steps in solving this problem through my mentorship with Dr. Weinhold. Our research goals go hand in hand, which has led us to beginning research on the release of an angiogenic growth factor through a gelatin that will coat sutures. In theory, this angiogenic growth factor, once released from the crosslinking with the gelatin will stimulate the development of blood vessels around the recently repaired collagenous tissue. This, in turn, will allow the tendon/ligament to have a better oxygen supply and allow for quicker
In septic patients, increased levels of PAI-1 inhibit plasminogen activator (t-PA), which converts plasminogen to plasmin. Release of fibrin inhibits fibrinolysis by activation of thrombin-activatable fibrinolysis inhibitor (TAFI). In addition, the release of PAF causes platelet aggregation. This combination of inhibition of fibrinolysis, fibrin strand production and platelet aggregation contribute to a state of coagulopathy. This can lead to microcirculatory dysfunction with isolated or multiple organ dysfunction and cell death. Mr Hertz’s coagulation profile showed a fibrinogen level of 5.6 g/L, indicating that coagulopathies were underway in his system.
The cytoskeleton is made up of three different types of filaments, actin filaments, intermediate filaments and microtubules. Actin filaments are the thinnest, they are also known as microfilaments. They create a band under the plasma membrane, this gives strength to the cell and links transmembrane proteins such as cell surface receptors to cytoplasmic proteins. Intermediate filaments include keratins, lamins, neurofilaments and vimentins. Keratins form hooves, horns and hair and are found in epithelial cells. Lamins form a type of mesh that ‘stabilizes the inner membrane of the nuclear envelope’ (Biology Pages). Neurofilaments bring strength to the axons of neurons and vimentins provide mechanical support to cells – particularly muscles. The cytoskeleton is also involved in cell
Platelets, which are also produced in the bone barrow, are checked on a Complete Blood Count with Differential. Platelets help stop bleeding from injury by creating clots. If your CBC blood test shows low platelet levels, you might be more susceptible to bleeding. High platelet levels could mean that you have an increased risk of internal clots.
Our approach in managing wounds was far from being optimal in our own setting. After having read the article of Sibbald et al (1) and assisting to presentations during the first residential week-end, our approach at St. Mary 's Hospital Center 's Family Medicine Clinic must change. We were not classifying wounds as healable, maintenance or non-healable. We were always considering the wounds in our practice as healable despite considering the system 's restraints or the patients ' preferences. In the following lines, I will define and summarize the methods one should use in order to initial management of wounds and how to integrate it better to our site. The first goal we need to set is to determine its ability to heal. In order to ascertain if a wound is healable, maintenance or a non-healable wound.
The white blood cells destroy any unfamiliar pathogens in the bloodstream and can cause inflammation. Therefore, the inflammation causes a surplus of white blood cells to clot the wound for healing.