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Bones are living tissues that undergo constant remodelling. In a healthy bone that has finished growing, the breakdown of old bone (by osteoclasts) and the formation of new bone (by osteoblasts) is a carefully regulated process.
When osteoporosis occurs or when cancer affects the bones, the proportion of osteoclasts and osteoblasts becomes unbalanced and more bone is broken down than is replaced. This can cause the bones to weaken and become more prone to fracture, even on minor trauma or injury.
Bisphosphonates reduce the number and action of the osteoclasts, slowing the process of bone breakdown. Bisphosphonates cannot replace lost bone but can strengthen existing bone and reduce the damage that is caused by the disease process.
Bisphosphonate molecules adhere to calcium and since the largest store of calcium in the human body is found in bones, high levels of bisphosphonates accumulate. The osteoclasts ingest the bound bisphosphonates and are eventually destroyed.
Bisphosphonates can be divided into two classes, which include:
The two types of bisphosphonates differ in their mechanism of action for killing osteoclast cells. The non-nitrogenous bisphosphonates are taken up by the osteoclasts, which then die. Nitrogenous bisphosphonates bind and block the enzyme farnesyl diphosphate synthase in the HMG-CoA reductase pathway (also known as the mevalonate pathway). This prevents formation of farnesol and geranylgeraniol, metabolites that are important for connecting some small proteins to the cell membrane. This phenomenon is known as prenylation. Prenylation is an important part of bone health and remodelling.
Some examples of the benefits bisphosphonate therapy provides include: