Difference between revisions of "Bone Response to Damage"
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− | + | <big><center>[[Bones|'''BACK TO BONES''']]</center></big> | |
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− | Circumferential incision (e.g. during [[Bones | + | |
− | *Longitudinal bone growth results | + | ===Normal structure=== |
− | *May be only on one side where periosteum is damaged | + | [[Image:Bone micro structure.jpg|right|thumb|100px|<small><center>Microscopic bone (Courtesy of RVC Histology images)</center></small>]] |
− | **Used by surgeons to treat [[Angular | + | |
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+ | **Damage to periosteum: | ||
+ | ***Invokes a hyperplastic reaction of the inner layer | ||
+ | ***Is painful | ||
+ | ***Exostoses can remodel or remain | ||
+ | **Lifting of periosteum causes new bone formation below | ||
+ | **Circumferential incision (e.g. during [[Bones - fractures|fracture]]) | ||
+ | ***Longitudinal bone growth results | ||
+ | ***May be only on one side where periosteum is damaged | ||
+ | ****Used by surgeons to treat [[Bones - developmental#Angular limb deformity|angular limb deformities]] | ||
+ | *'''Blood vessels''' | ||
+ | |||
+ | ===Bone development=== | ||
+ | |||
+ | *Two main types of bone development: | ||
+ | **'''Endochondral ossification''' (cartilage model) | ||
+ | ***Long bones mainly - physis and metaphysis | ||
+ | ***Mesenchymal cells differentiate into chondroblasts | ||
+ | ****Produce scaffold of mineralised cartilage on which osteoblasts deposit bone | ||
+ | ***Vascularised | ||
+ | ***Developed centres of ossification | ||
+ | ****Primary (diaphyseal) | ||
+ | ****Secondary (epiphyseal) | ||
+ | **'''Intramembranous ossification''' | ||
+ | ***Flat bones mainly (e.g. skull), shaft of long bones | ||
+ | ***Mesenchymal cells differentiate into osteoblasts | ||
+ | ***No cartilage precursor template | ||
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===Physis (Growth plate)=== | ===Physis (Growth plate)=== | ||
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+ | [[Image:Growth plate.jpg|left|thumb|100px|<small><center>Growth plate (Image sourced from Bristol Biomed Image Archive with permission)</center></small>]] | ||
+ | [[Image:Growth plate closer.jpg|right|thumb|100px|<small><center>Growth plate magnified(Image sourced from Bristol Biomed Image Archive with permission)</center></small>]] | ||
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+ | *Originates from the cartilage model that remains only at the junction of the diaphyseal and epiphyseal centres | ||
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+ | *Cartilage of metaphyseal growth plate is divided into: (from right to left on the magnified image) | ||
+ | ** - Resting (reserve) zone | ||
+ | ** - Proliferative zone | ||
+ | ** - Hypertrophic zone | ||
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*Site of many '''congenital''' or '''nutritional''' bone diseases in the growing animal | *Site of many '''congenital''' or '''nutritional''' bone diseases in the growing animal | ||
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*If growth teporarily stops -> layer of bone seals the growth plate -> moves into metaphysis when growth resumes -> forms '''Harris lines''' | *If growth teporarily stops -> layer of bone seals the growth plate -> moves into metaphysis when growth resumes -> forms '''Harris lines''' | ||
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− | [[ | + | ===Bone resorption=== |
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+ | *Mediated by two [[Parathyroid Pathology#Hormonal Control|hormones]]: | ||
+ | **'''Parathyroid hormone (PTH)''' | ||
+ | ***Produced by <u>chief cells in the parathyroid glands</u> in response to <u>decreased</u> serum calcium | ||
+ | ***In response, osteoclasts increase in number and resorb mineralised matrix - increase Ca in blood | ||
+ | **'''Calcitonin''' | ||
+ | ***Produced by <u>C-cells in the thyroid glands</u> in response to <u>increased</u> serum calcium | ||
+ | ***Inhibits osteoclasts | ||
+ | |||
+ | ===Bone dynamics=== | ||
+ | |||
+ | *Bone growth and maintenance of normal structure are directly related to mechanical forces | ||
+ | *Mechanical forces generate bioelectrical potentials (piezoelectricity) | ||
+ | **These potentials strengthen bone | ||
+ | **Inactivity reduces the potentials -> bone loss | ||
+ | |||
+ | *In neonates: | ||
+ | **Bone growth predominates | ||
+ | **Modelling is important | ||
+ | *In adults: | ||
+ | **Formation of bone is balanced by resorption - remodelling | ||
+ | **Continues throughout life under the influence of hormones and mechanical pressure | ||
+ | **Bone resorption may exceed formation in pathological states (hormonal, trauma, nutritional) or in old age and disuse | ||
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+ | |||
+ | |||
+ | <big><center>[[Bones|'''BACK TO BONES''']]</center></big> |
Revision as of 10:23, 18 July 2008
Normal structure
- Damage to periosteum:
- Invokes a hyperplastic reaction of the inner layer
- Is painful
- Exostoses can remodel or remain
- Lifting of periosteum causes new bone formation below
- Circumferential incision (e.g. during fracture)
- Longitudinal bone growth results
- May be only on one side where periosteum is damaged
- Used by surgeons to treat angular limb deformities
- Damage to periosteum:
- Blood vessels
Bone development
- Two main types of bone development:
- Endochondral ossification (cartilage model)
- Long bones mainly - physis and metaphysis
- Mesenchymal cells differentiate into chondroblasts
- Produce scaffold of mineralised cartilage on which osteoblasts deposit bone
- Vascularised
- Developed centres of ossification
- Primary (diaphyseal)
- Secondary (epiphyseal)
- Intramembranous ossification
- Flat bones mainly (e.g. skull), shaft of long bones
- Mesenchymal cells differentiate into osteoblasts
- No cartilage precursor template
- Endochondral ossification (cartilage model)
Physis (Growth plate)
- Originates from the cartilage model that remains only at the junction of the diaphyseal and epiphyseal centres
- Cartilage of metaphyseal growth plate is divided into: (from right to left on the magnified image)
- - Resting (reserve) zone
- - Proliferative zone
- - Hypertrophic zone
- Site of many congenital or nutritional bone diseases in the growing animal
- Open in neonates and growing animals
- Chondrocyte proliferation balances cell maturation and death
- Closes and ossifies at maturity
- Regulated by androgens
- If growth teporarily stops -> layer of bone seals the growth plate -> moves into metaphysis when growth resumes -> forms Harris lines
Bone resorption
- Mediated by two hormones:
- Parathyroid hormone (PTH)
- Produced by chief cells in the parathyroid glands in response to decreased serum calcium
- In response, osteoclasts increase in number and resorb mineralised matrix - increase Ca in blood
- Calcitonin
- Produced by C-cells in the thyroid glands in response to increased serum calcium
- Inhibits osteoclasts
- Parathyroid hormone (PTH)
Bone dynamics
- Bone growth and maintenance of normal structure are directly related to mechanical forces
- Mechanical forces generate bioelectrical potentials (piezoelectricity)
- These potentials strengthen bone
- Inactivity reduces the potentials -> bone loss
- In neonates:
- Bone growth predominates
- Modelling is important
- In adults:
- Formation of bone is balanced by resorption - remodelling
- Continues throughout life under the influence of hormones and mechanical pressure
- Bone resorption may exceed formation in pathological states (hormonal, trauma, nutritional) or in old age and disuse