Bone
Bone is living mineralized tissue, constantly remodeled by osteoblasts (building) and osteoclasts (resorbing) under mechanical load and hormonal control. Collagen forms about 30% of bone mass, with calcium and other minerals making up most of the rest.
Thyroid drives renewal, not just resorption
[edit]Ray Peat argued that adequate thyroid hormone supports bone renewal, and that the bone-breakdown markers that rise with active thyroid function reflect healthy turnover rather than pathological loss:[1]
T3 increases the formation of bone.
The thyroid hormone supports bone renewal, and increases indicators of bone breakdown in the blood.
Calcium itself has effects beyond structural mineral supply: Peat described it as lowering the same stress-adjacent signals (adrenaline, parathyroid hormone, prolactin) that drive bone loss:
Calcium activates mitochondrial respiration, and lowers adrenaline, parathyroid hormone, and prolactin.
Vitamin K2 specifically stimulates production of osteocalcin and osteonectin, two of the key non-collagen bone proteins, while progesterone and estrogen act oppositely on the carbonic-anhydrase pathway involved in bone remodeling.[1]
Practice
[edit]Calcium, vitamin K2, vitamin D, adequate protein, and progesterone/estrogen balance all matter; weight-bearing movement helps when the body is adequately fueled to use it.
See also
[edit]References
[edit]- ↑ 1.0 1.1 Ray Peat, "Osteoporosis, aging, tissue renewal, and product science," raypeat.com.
- ↑ Osteoporosis, aging, tissue renewal, and product science, Ray Peat newsletter
- ↑ Osteoporosis, aging, tissue renewal, and product science, Ray Peat newsletter
- ↑ Osteoporosis, aging, tissue renewal, and product science, Ray Peat newsletter