Chapter 6 pt 2) Bones/ Skeletal Tissues Flashcards
1
Q
Ossidication
A
- Process of bone tissue formation.
- Formation of the bony skeleton Begins at 2 months of develpoment.
- Bone remodiling and repair is a lifelong process.
2
Q
Endochondral Ossification
A
- Development of bones from cartlidge (called cartlidge bones). All of the bones below the skull develop this way.
- Begins at 2 months of development.
- Hylane cartlidge is perviouly made and serves as a template for bone development. Cartlidge breaks down prior to ossification
- Primary Ossification Center)
- Blood vessels inflitrate pericondrium making it periosteum.
- Mesenchymal cells specialize into osteoblasts.
3
Q
Five Steps of Endocondral Ossification
A
- Bone Collar forms around Hyaline Cartlidge
- Cartlidge calcifies in the Diaphysis (shaft) center and cavities develop.
- Periostial Bud invades the structure and forms spongy bone.
- Diaphysis elongates and medulary cavity forms.
- Epiphsyes Calcify leaving Hyaline Cartlidge only in Epiphesyal Growth Plate.
4
Q
Intramembranous Ossification (and 4 Steps)
A
- Mescenchymal cells form the frontal, parietal, occiptial, temporal, and clavicle bones.
- 4 Major Steps
- Meschenymal cells cluster together and differentiate into osteoblasts. This develops an Ossification center in a Fibrous Membrane
- Osteoblasts scerete osteoid and calcify. They then become Osteoclasts.
- Spongy Bone and primative Periostium Form. Osteoid is laid down to make spongy bone and Meschymal cells become Periostium
- Compact Spongy Bone replace spongy bone just deep of Periostium. The spongy bone then fills with marrow.
5
Q
Postnatal Bone Growth
A
- Long Bones grow Lengthwise due to Insterstitial Growth in Epiphyseal Plate.
- Bone increases in Thickness through Appositional Growth.
6
Q
Interstitial Growth
A
- Growth in the Epiphysial Plate. Has Five Zones.
- Resting Zone (at the top of the bone) Area of cartlidge in epiphyeal plate that is inactive
- Proliferation Zone) Area of cartlidge on daiphyseal side which is rapidly dividing. New cells push away which causes lengthening.
- Hypertonic Zone) Older Cartlidge cells enlarge and form interconnecting spaces.
- Calification Zone) Cells calcify and condrocytes die.
- Ossification Zone) Spincules of cartlidge (leftovers of dead condrocytes) are eroded by osteoclasts and reformed by osteoblsts into New Bone.
7
Q
Interstital Growth (Near the End of Adolescnese)
A
- Condrocytes divide less often
- Epiphyseal plate thins and eventually closes (epiphyseal plate closure)
- This process stops around 18 in females and 21 in males.
8
Q
Appositional Growth
A
- Growth in Widness of a bone. Can occur anytime throuought life as response to stress.
- Osteoblasts Secrete Bone matrix under Periostium on External Bone
- Osteoclasts Remove Bone on Endosteal Surface
- Leads to bone that is generally thicker and stronger because building occurs faster than breaking down.
9
Q
Horomes that Regulate Bone Growth
A
- Growth Hormone) Most improtant hormone in stimulating epiphesial plate growth during childhood.
- Thyroid Hormone) Modulates growth to ensure propper propeotions,
- Testosterone (males) and Estrogen (females) activate at pruberty and cause adolesant growth spurts.
- Also end the epiphesial plate growth (stimualte closeure at the end of aolesanse)
10
Q
Bone Remodeling
A
- About 5-7% of bone mass is replaced each week.
- Spongy bone) fully replaced every 3-4 year
- Compact Bone) every 10 years
- Remodeling is the replacment of old bone tissue with new bone tissue. Takes place at diffrent rates at diffrent sections of bone.
- Occurs on both the periostum and endostum.
11
Q
Bone Homeostasis (Bone Remodeling)
A
- Resoprtion) Function of Osteoclasts.
- Secrete lysosomal enzymes and protons (H+) that digest Matrix.
- Acidity converts calcium salts to soluable material.
- Bone Deposite) New bone matrix is secreted by osteoclasts.
- Osteoid seam) band of unamterized matrix (Ostoid) that becomes calcified.
12
Q
Conrol of Bone Remodeling
A
- Two ways
- Hormonal Controls) The need to release calcium into the blood
- Response to mechanical stress
13
Q
Hormonal Control of Blood Ca+
A
- Parathyroid hormone (PTH) produced by parathyroid glands in response to low levels of Ca+.
- Stimulates osteoclasts to reobsorb bone and release Ca+ into blood.
- Secretion stops when Ca+ levels are reached.
- Calcitonin) Produced by parapholicular cells of thyroid in response to high calcium levels.
- Effects are negligable but can cause calcium reorbstion at pharmacutical levels.
14
Q
Homeostatic Imbalance (Calcium Levels)
A
- Small changes in blood calcium can cause problems in nervous funtion
- Hypocalcemia) low Ca+ levels cause nerve excitability
- Hypercalcima) High Ca+ levels cause nonresponsivness
15
Q
Response to Mechanical Stress (Bones)
A
- Bones Reflect mechanical stress put on them. Bones recive stress from weight or muscle pulls.
- Wolfs Law) Bones grow/remodel in accordance with the stress put on them
- This stress is usually off center so bones tend to curve.
- Diaphysis is thickest where the bending stress is the greates.
- Bone can be hallow because compression and tenion cancel eachother out (Normal force is 0)