ABSTRACT
This
project work introduced some knowledge about the basics involved in finding the
contents of bone. This project work deals with the principle of qualitative analysis
of cations and anions. Skeletal system plays an integral part of most of the
animals “what is it that makes It to form an integral part?”. The solution to
this question can be understood more succinctly from this project work.
This project indeed would be a revolution
in the world, where there is increasing worry about problems of bone like
osteoporosis and osteomalacia. In this industrial age amount of calcium content
in bone is also reducing; this project work would indeed be a very good
solution.
TABLES
OF CONTENTS
Title
Page
Certification
Dedication
Acknowledgement
Table
of contents
CHAPTER ONE
1.0 INTRODUCTION
1.1 FORMATION OF BONE
1.1.0 INTRAMEMBRANOUS OSSIFICATION
1.1.1 ENDOCHONDRAL
OSSIFICATION
1.1.2 BONE
MARROW
1.1.3 REMODELING
1.1.4 PURPOSE
1.1.5 CALCIUM
BALANCE
1.1.6 REPAIR
1.1.7 PARACRINE
CELL SIGNAL
1.1.8 OSTEOBLAST
STIMULATION
1.1.9 OSTEOCLAST
INHIBITION
1.2 INDIVIDUAL
BONE STRUCTURE
1.2.1 CELLULAR STRUCTURE
1.2.2 MOLECULAR STRUCTURE
1.3 CHARACTERISTIC OF BONE
1.4 TYPES OF BONE
1.5 FUNCTIONS OF BONE
1.6 USES OF BONE
1.7
TERMINOLOGIES
CHAPTER TWO
2.0 MATERIAL REQUIRED
2.1 EXPERIMENTAL ANALYSIS
CHAPTER THREE
3.0 RESULT OF ANALYSIS AND DISCUSSION
3.1 ESTIMATION OF CONTENTS OF COW BONE ASH
3.2 ESTIMATION OF CONTENT OF GOAT BONE
3.3 DISCUSSION
CHAPTER FOUR
4.0 CONCLUSION
4.2 RECOMMENDATION
CHAPTER
ONE
1.0 INTRODUCTION
Bones
are rigid organs from part of the endoskeleton of the vertebrates. They support
and protect the various organs of body production red and white blood cells and
store minerals. Bone tissue is a type of tense connective tissue. Bone comes in
a variety of shapes and has a complex internal and external structure, are light
weight yet strong and hard and serve multiple functions. One of the types of
tissue that makes up bone is the mineralized osseous tissue, also called bone
tissue that gives it rigidity and a coral-like three dimensional internal
structure. Other types of tissue found in bones include marrow endosteum,
periosteum, nerves, blood vessel and cartilage. “At birth, there are over 270
bones in an infant human’s body”. (steele D. Gentry et. al (1998). The Anatomy and
Biology of the Human skeleton, Texas
A&M University
press page 4 ISBN-0-89096-300-2), but many of these bones fused together as the
child grows, leaving a total of 206 separate bones in an adult. “The largest
bone in the human body is the femur and the smallest bones are auditory
ossicles.” (Schmiedder et. al (1934) parent and child. An Introductory Study of
Parent Education page 31).
Bones are also a dynamic tissue that
performs mechanical, biological and chemical functions and it depends on
chemical and physical properties and are affected by age, nutrition, hormonal
status and diseases. (Loveridge 1999), the skeletal system forms the external
structure and appearance of mammalian vertebrate species and has the obvious
functions locomotion, structural support of the body and protection of soft
tissue such as brain, heart, spinal cord and lungs. Bone also serves as metabolic
reservoir of Calcium (Ca), Phosphorus (P) and other minerals. Also, it houses
cells responsible for bone formation and resorption (Decke et. al 1993).
1.1 FORMATION OF BONE
The
formation of bone during the fetal stage of development occurs by two processes:
i.
Intra membranous Ossification
ii.
Endochondral Ossification
1.1.0 INTRAMEMBRANOUS OSSIFICATION
This mainly occurs
during formation of the flat bones of the skull; the bone is formed from
mesenchyme tissue. The steps in intramembranous ossification are:
1. Development
of ossification centre
2. Calcification
3. Formation
of trabeculae
4. Development
of periosteum
1.1.10
ENDOCHONDRAL
OSSIFICATION
Endochondral
ossification on the other hand, occurs in long bones such as limbs; the bone is
formed from cartilage. The steps in endochondral ossification are:
1. Development
of cartilage model
2. Growth
of cartilage model
3. Development
of primary ossification center
4. Development
of secondary center
5. Formation
of articular cartilage and epiphyseal plate.
Endochondral
ossification begins with points in the cartilage called primary ossification
centers” they mostly appear during fetal development, though a few short bones
begin their primary ossification after birth. They are responsible for the
formation of the diaphyses of long bones, short bones and certain parts of
irregular bones.
Secondary ossification
occurs after birth, and forms the epiphyses of long bones and the extrimities
of irregular and flat bones. The diaphysis and both epiphyses and a long bone
are separated by a growing zone of cartilage (the epiphyseal plate). When the
child reaches skeletal maturity (18-25 years of age), all of the cartilage is
replaced by bone, fusing the diaphysis and both epiphyses together (epiphyseal
closure).
1.1.11
BONE
MARROW
Bone marrow can be
found in almost any bone that holds cancellous tissue. In newborns, all such
bones are filled exclusively with red marrow, but as the child ages it is
mostly replaced by yellow of fatty marrow. In adults, red marrow is mostly
found in the marrow bones of the femur, the ribs, the vertebrae and pelvic
bones.
1.1.12
REMODELING
Remodeling or bone
turnover is the process of resorption followed by replacement of bone with
little change in shape and occurs throughout a person’s life. Osteoblasts and
osteoclasts, coupled together via pancrine cell signaling, are referred to as
bone remodeling units. Approximately 10% of the skeletal mass of an adult is
remodeling each year.
1.1.13
PURPOSE
The purpose of
remodeling is to regulate calcium homeostasis, repair micro-damaged bones (from
every day stress) but also to shape and sculpture the skeleton during growth.
1.1.14
CALCIUM
BALANCE
The process of bone
resorption by the osteoclasts releases stored calcium into the systematic
circulation and is an important process in regulating calcium balance. As bone
formation actively fixes circulating calcium in its mineral form, removing it
from the blood stream, resorption actively unfixes it thereby increasing
circulating calcium levels. These processes occur in tandem at site specific
locations.
1.1.15
REPAIR
Repeated stress such as
weight bearing exercise or bone healing result in the bone thickening at the
point of maximum stress (Wolff’s law). It has been hypothesized that this is a
result of bones piezoelectric properties which cause bone to generate small
electrical potential under stress.
1.1.16
PARACRINE
CELL SIGNAL
The action of
osteoclasts and osteoblasts are controlled by a number of chemical factors
which either promote or inhibit the activity of the bone remodeling cells,
controlling the rate at which the bone is made, destroyed or changed in shape.
The cells also use paracrine signaling to control the activity of each other.
1.1.17
OSTEOBLAST
STIMULATION
Osteoblast can be
stimulated to increase bone mass through increased secretion of osteoid and by
inhibiting the ability of osteoclasts to breakdown osseous tissue.
Bone building through
increase secretion of osteoid is stimulated by the secretion growth hormone by
the pituitary, thyroid hormone and the sex hormones (estrogens and androgens).
These hormones also promote increased secretion of osteoprotegerin. Osteoblasts
can also be induced to secrete a number of cytokines to promote reabsorbtion of
bone by stimulating osteoclast activity and differentiation from progenitor
cells. Vitamin D, parathyroid hormone and stimulation from osteocytes induce osteblasts
to increase secretion of RANK ligand and interleukin 6, which cytokines then
stimulate increased reabsorbtion of bone by osteoclasts. These same compounds
also increase secretion of macrophage colony-stimulating factor by osteoblasts,
which promotes the differentiation of progenitor cells into osteoclasts and
decrease secretion of osteoprotegerin.
1.1.18
OSTEOCLAST
INHIBITION
The rate at which
osteoclast reabsorb bone is inhibited by calcitonin and osteoprotegerin.
Calcitonin is produced by parafollicular cells in the thyroid gland and can
bind to receptors on osteoclasts to directly inhibit osteoclast activity.
Osteoprotegerin is secreted by osteoblasts and is able to bind RANK-L,
inhibiting the osteoclast stimulation.
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