Bone Structure

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Part A: Bone Tissue Structure and Repair
1. Definitions:
a. Fracture – an injury which occurs in bones due to the bone(s) being unable to withstand the stress of heavy loads, impacts or abnormal movements, causing the bone(s) to break.
b. Proximal – describes the position of a feature within a limb as closer to the limb’s origin in comparison to another feature within the same limb
c. Diaphysis – is the shaft between the proximal and distal ends of long bones consisting of an outer layer of compact bone which surrounds the medullary cavity

2. Humerus – long bone
Occipital bone – flat bone
3rd lumbar vertebral body – irregular bone

3. Majority of the vertebral body is made up of spongy bone. The matrix of spongy bone consists of thin bundles …show more content…

Osteoblasts are responsible for the process of ossification. These cells produce the organic components of the bone matrix (mostly collagen) to form osteoid (unmineralised bone matrix). Osteoblasts also stimulate an increase in calcium phosphate at the fracture so that the salts attach to the osteoid to form bone. Osteoblasts are eventually surrounded by the bone it produces and develop into osteocytes.

8. Osteoclasts are responsible for the process of bone resorption. These large multi-nucleated cells attach to the bone and release acids and enzymes which erodes the bone matrix, releasing the calcium and phosphate ions. This process is important in maintaining homeostatic levels of calcium and phosphate ions within in the blood. 9. The extracellular matrix of bone consists of both organic and inorganic components. One third of the matrix is organic (contains carbon and hydrogen) and mostly consists of collagen fibres. Two thirds of the matrix is inorganic containing salts and minerals, primarily calcium and phosphate and partly sodium, magnesium and carbonate. Both organic and inorganic components of the bone contribute to a bones strength and …show more content…

Calcium causes muscle contraction by allowing myosin heads to form cross bridges with actin by breaking the troponin-tropomyosin bond and exposing the actin active sites. Once formed, the myosin head ‘power strokes’ releasing ADP, P and energy in the form of heat, shortening the length of the sarcomere. The myosin head is then reactivated by binding to an ATP molecule and can form another cross bridge. As calcium is at an excessive level, the body repeats the process of cross bridging as fast as possible, hence the severe muscle contractions and rise in body temperature. Not only is ATP used in cross bridge formation, it is also used to return calcium back into the sarcoplasmic reticulum via active transport, however the calcium channels are unable to close due to the presence of halothane. Both these applications of ATP during an episode of malignant hyperthermia severely depletes the body of ATP, which is detrimental to a patient’s

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