Complete series of questions that demonstrate your understanding of the human muscular and skeletal system? Contents: Page 1: Title Page Page 2: Introduction page 2 – 6: Section One – The Muscular System Pages 6– 7: Section Two – The Skeletal System Pages 7- 11: Section Three – Macrophages and the Mononuclear Phagocyte Framework Page 11: Conclusion Page11-12. References Bibliography Page no 1 Introduction: This report has been arranged to show phenomenal comprehension of the capabilities and life structures of the human solid and skeletal frameworks. In segment one, a synopsis is given about the design of muscle tissue types, muscle cells and connective tissues, as well as their purposes and areas inside the body. Detail is likewise given about muscle constriction with a specific spotlight on striated muscle types. In area two, the skeletal framework is described with regards to the kinds of bone, joints, and defensive designs. In segment three, the data is assembled to show how the human body uses velocity and fixes and safeguards bones and muscles when harm happens. Section 1: The muscular system MUSCLE TISSUES & CELL TYPE: There are three principal kinds of solid tissue answerable for development inside the human body: Skeletal Muscle: Skeletal muscle is viewed as joined to the skeleton and is liable for the willful development of bones. Skeletal muscle filaments run in equal plots and are multinucleated and energetically striated. Smooth Muscle: Smooth muscle is tracked down in the covering of inward organs (GI plot, uterus, veins, eyes, and so on) It controls the compulsory choking of these areas (for example peristalsis, vasoconstriction, understudy widening). Smooth muscle strands are not striated, have a shaft shape and every fiber contains a solitary focal core. Cardiovascular Muscle: Cardiovascular muscle is tracked down in the heart and is liable for the cadenced withdrawal of the heart (for example heartbeat) Cardiovascular muscle strands are fanning, intercalated, delicately striated and have a solitary core for each fiber. Page no 2 fig No 1: Muscle tissue and cell type. MUSCLE CONNECTIVE TISSUES: Connective tissues are formed by the mesoderm of the embryo and are found throughout the entire body. Their purpose is to connect other tissues and organs, store and transport materials, and to provide support to the body’s vital systems. The three components of connective tissue are extra-cellular matrix, living cells, and fibers, which are either collagen (white fibers), elastin (yellow fibers) or reticular. Collagen fibers are the thickest elastin is thinner and stretchy and reticular are the most delicate, found in organs. Table 1 Distribution and main functions of the cells of the mononuclear phagocyte system. Page no 3 Muscles contract utilizing actin and myosin: As examined later, the engine action of myosin moves its head bunches along the actin fiber toward the in addition to end. This development slides the actin fibers from the two sides of the sarcomere toward the M line, shortening the sarcomere and bringing about muscle withdrawal. Sliding filament theory of muscle contraction: 1. Sarcoplasmic reticulum discharges calcium particles. 2. Calcium particles tie to troponin. 3. Tropomyosin moves to uncover dynamic destinations of actin. 4. ATP is parted into ADP and P. 5. Myosin head ties to actin. 6. ADP and P set free from myosin. 7. Myosin cross-spans twist, pulling actin toward focus of sarcomere. The sliding fiber hypothesis of muscle happens during the time spent muscle withdrawal (development). This likewise happens for the most part in skeletal muscles. The interaction starts with the arrival of calcium particles which ties to troponin and this limiting considers the openness of the myosin restricting site which is obstructed by tromyosin. Stretched muscle contraction: fig no 2: Stretched Muscle Contraction Image source: https://www.teachpe.com/anatomy-physiology/sliding-filament-theory Page no 4 The diagram above shows a muscle stretched. The I – bands and the H – zone is wider. The myosin and actin filaments overlap, but not by much. As a result, fewer cross bridges between Actin and Myosin form, so muscle strength is lower. Partial muscle contraction: fig no 3: Partial Muscle Contraction Image source: https://www.teachpe.com/anatomy-physiology/sliding-filament-theory With a partial muscle contraction myosin and actin overlap more. Therefore, more potential for cross bridges to form. The I – bands and H – zone shortens. Fully muscle contraction: fig no 3: fully Muscle Contraction Image source: https://www.teachpe.com/anatomy-physiology/sliding-filament-theory Page no 5 The diagram above shows a fully contracted muscle with lots of overlap between the actin and myosin. Because the thin actin filaments have overlapped there is a reduced potential for cross bridges to form again. Therefore, there will be low force production from the muscle . Section 2:Skeletal muscle: Skeletal muscle is a type of muscle tissue that is attached to bones and is responsible for voluntary movement and maintaining posture. It is made up of elongated, multinucleated cells called muscle fibers, which contract and relax to generate force. Skeletal muscles work in pairs, with one muscle contracting while its antagonist relaxes, allowing for smooth and coordinated movement. Types Of Bones: There are two main types of bones in the human body are: Long bones and short bones. Long bones, such as the femur (thigh bone) and tibia (shin bone), provide support and aid in movement. Short bones, such as the bones of the wrist, are usually cube-shaped and provide stability. Additionally, there are flat bones, such as the scapula (shoulder blade) and the pelvis, which provide protection for internal organs and serve as attachment points for muscles. There are also sesamoid bones, which are small bones embedded within tendons, and irregular bones, which don't fit into the other categories and have unique shapes. Function, types, Components, Characteristics of Connective Tissue: fig no 5: major functions &components of connective tissue. Page no 6 Bone Connective tissues: Connective tissues, delegated ligaments, tendons, and ligament, are utilized to interface muscles to bones and to link joints together. Ligaments are made areas of strength for of, collagen strands which join to a muscle and at the periosteum, which covers the bone. They should be hard to shield the muscle from tearing under pressure of customary development. Ligaments, for example, those found in the lower leg joints which are more inclined to cadenced pressure, are encircled by a ligament sheath which contains a film of synovial liquid to diminish grinding and safeguard the ligament from becoming damaged. Ligands are likewise produced using extreme strands of collagen organized in equal packs to expand their solidarity. The two closures of the tendons connect to the periosteum on bones and work to balance out joints and forestall separation. Tendons can be extracapsular (tracked down outwardly of the joint) or intracapsular (saw as inside the joint). Types Of Connective Tissue: The types of connective tissue include are: Loose connective tissue Adipose tissue Dense fibrous connective tissue Elastic connective tissue Cartilage Osseous tissue (bone) Blood. Section:3 Macrophages and the Mononuclear Phagocyte Framework: Macrophages are portrayed by their advanced phagocytic capacity and have practical experience in turnover of protein strands and evacuation of dead cells, tissue flotsam and jetsam, or other particulate material. They have a wide range of morphologic elements relating to their condition of useful action and to the tissue they possess. A commonplace macrophage estimates somewhere in the range of 10 and 30 μm in measurement and has an erratically found, oval or kidney-formed core. Macrophages are available in the connective tissue of most organs and are frequently alluded to by pathologists as "histiocytes. Page no 7 Plasma cell: Plasma cells are immune response delivering cells that are separated B lymphocytes. that intercede humoral insusceptibility by constant emission of antibodies. These cells are significant for humoral resistance and are tracked down in the bone marrow. Structure and Functions of Plasma cells: The plasma cells are large lymphocytes with dense basophilic cytoplasm, an eccentric nucleus, and a well-organized network of Golgi apparatus and Rough Endoplasmic Reticulum (RER). These cells bear specific surface markers cluster of differentiation (CD)78, CD138, and ILR-6. Plasma cells are CD27++ in contrast to naive B-cells that are CD27-. Plasma cells secrete antibodies into the circulating blood; however, unlike their precursors, they do not exhibit immunoglobulin (Ig) class switching. Also, B-cells do not act as antigenpresenting cells once differentiated into plasma cells. The short-lived plasma cells usually secrete IgM, whereas the long-lived plasma cells (LLPC) release IgG and IgA. Therefore, LLPC is the primary source of IgG in the circulating blood. These antibodies show high affinity toward their antigen as B-cell maturation, and their secretion relies on somatic hypermutation. Recent studies suggest the role of plasma cells in inhibiting follicular T-helper cell development and thus, regulating the immune response. Mast Cells: Mast cells are oval or irregularly shaped connective tissue cells, between 7 and 20 μm in diameter, whose cytoplasm is filled with basophilic secretory granules. The nucleus is centrally situated and often obscured by abundant secretory granules (Figure 5–5). These granules are electron-dense and heterogeneous (ranging from 0.3 to 2.0 μm in diameter.) Because of their high content of acidic radicals in their sulfated GAGs, mast cell granules display metachromasia, which means that they can change the color of some basic dyes (e.g., toluidine blue) from blue to purple or red. The granules are poorly preserved by common fixatives, so that mast cells are frequently difficult to identify. Page no 8 Fig no 6: Mast cell Mast cells function in the localized release of many bioactive substances with roles in the local inflammatory response, innate immunity, and tissue repair. A partial list of important molecules released from these cells’ secretory granules includes the following: Heparin, a sulfated GAG that acts locally as an anticoagulant. Histamine, which promotes increased vascular permeability and smooth muscle contraction. Serine proteases, which activate various mediators of inflammation. Eosinophil and neutrophil chemotactic factors, which attract those leukocytes. Cytokines, polypeptides directing activities of leukocytes and other cells of the immune system. Phospholipid precursors for conversion to prostaglandins, leukotrienes, and other important lipid mediators of the inflammatory response. Page no 9 fig no 6: Mast cell creation. Leukocytes: Other than macrophages and plasma cells, connective tissue typically contains different leukocytes got from cells circling in the blood. Leukocytes, or white platelets, make up a populace of meandering cells in connective tissue. They leave blood by moving between the endothelial cells lining venules to enter connective tissue by a cycle called diapedesis. This interaction increments significantly during aggravation, which is a vascular and cell cautious reaction to injury or unfamiliar substances, including pathogenic microbes or disturbing synthetic substances. Traditionally, the significant indications of aroused tissues incorporate "redness and enlarging with intensity and torment” Irritation starts with the nearby arrival of synthetic go between from different cells, the ECM, and blood plasma proteins. These substances follow up on the neighborhood microvasculature, pole cells, macrophages, and different cells to instigate occasions normal for irritation, for instance expanded blood stream and vascular penetrability, diapedesis and relocation of leukocytes, and initiation of macrophages for phagocytosis. Fiber: The fibrous components of connective tissue are elongated structures formed from proteins that polymerize after secretion from fibroblasts. The three main types of fibers include collagen, reticular, and elastic fibers. Collagen and reticular fibers are both formed by proteins of the collagen family, and elastic fibers are composed mainly of the protein elastin. These fibers are distributed unequally among the different types of connective tissue, with the predominant fiber type usually responsible for conferring specific tissue properties. Page no 10 Collagen: The collagens comprise a group of proteins chose during development for their capacity to frame various extracellular designs. The different filaments, sheets, and organizations made of collagens are areas of strength for very impervious to ordinary shearing and tearing powers. Collagen is a critical component of every single connective tissue, as well as epithelial storm cellar layers and the outside laminae of muscle and nerve cells. Collagen is the most plentiful protein in the human body, addressing 30% of its dry weight. A significant result of fibroblasts, collagens are emitted by a few other cell types and are recognizable by their sub-atomic creations, morphologic qualities, dispersion, capabilities, and pathologies. A group of 28 collagens exists in vertebrates, the most significant of which are recorded in Table 5-3. They can be gathered into the accompanying classifications as indicated by the designs shaped by their communicating subunits. Conclusion: This report takes care of how strong and skeletal frameworks capability together impeccably to empower headway and when injury or sickness happens, how our bodies can fix themselves partially. Bones are organized to take into consideration organs to be safeguarded while giving people their level and strength. Muscles contract through sliding fiber hypothesis which requires pairings of agonist and bad guy muscles and makes energy as ATP. Ligaments, tendons, ligament, and connective tissue join muscles to bones and bones to joints which is crucially significant for mellowing the effect of locomotion. References: Yin, L., Li, N., Jia, W., Wang, N., Liang, M., Yang, X. and Du, G., 2021. Skeletal muscle atrophy: From mechanisms to treatments. Pharmacological research, 172, p.105807. Yin, L., Li, N., Jia, W., Wang, N., Liang, M., Yang, X. and Du, G., 2021. Skeletal muscle atrophy: From mechanisms to treatments. Pharmacological research, 172, p.105807. Suzuki, T., Palus, S. and Springer, J., 2018. Skeletal muscle wasting in chronic heart failure. ESC heart failure, 5(6), pp.1099-1107. Kirk, B., Feehan, J., Lombardi, G. and Duque, G., 2020. Muscle, bone, and fat crosstalk: the biological role of myokines, osteokines, and adipokines. Current Osteoporosis Reports, 18(4), pp.388-400. Markus, I., Constantini, K., Hoffman, J.R., Bartolomei, S. and Gepner, Y., 2021. Exercise-induced muscle damage: Mechanism, assessment and nutritional factors to accelerate recovery. European journal of applied physiology, 121, pp.969-992. Page no 11 Kirk, B., Miller, S., Zanker, J. and Duque, G., 2020. A clinical guide to the pathophysiology, diagnosis and treatment of osteosarcopenia. Maturitas, 140, pp.27-33. Delbono, O., Rodrigues, A.C.Z., Bonilla, H.J. and Messi, M.L., 2021. The emerging role of the sympathetic nervous system in skeletal muscle motor innervation and sarcopenia. Ageing research reviews, 67, p.101305. Sciorati, C., Gamberale, R., Monno, A., Citterio, L., Lanzani, C., De Lorenzo, R., Ramirez, G.A., Esposito, A., Manunta, P., Manfredi, A.A. and Rovere-Querini, P., 2020. Pharmacological blockade of TNFα prevents sarcopenia and prolongs survival in aging mice. Aging (Albany NY), 12(23), p.23497. Zullo, A., Fleckenstein, J., Schleip, R., Hoppe, K., Wearing, S. and Klingler, W., 2020. Structural and functional changes in the coupling of fascial tissue, skeletal muscle, and nerves during aging. Frontiers in Physiology, 11, p.592. Aas, S.N., Breit, M., Karsrud, S., Aase, O.J., Rognlien, S.H., Cumming, K.T., Reggiani, C., Seynnes, O., Rossi, A.P., Toniolo, L. and Raastad, T., 2020. Musculoskeletal adaptations to strength training in frail elderly: a matter of quantity or quality?. Journal of cachexia, sarcopenia and muscle, 11(3), pp.663677. Page no 12