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TRPV1, ASICs and P2X2/3 expressed in bone cells simultaneously regulate bone metabolic markers in ovariectomized mice
1Department of Orthopaedic Surgery, Sapporo Medical University School of Medicine, South-1, West-16, Chuo-ku, Sapporo, 060-8543, Japan.
Journal of Musculoskeletal & Neuronal Interactions
|June 11, 2016
Summary
Nociceptors like TRPV1 are found in bone cells and influence bone metabolism. Blocking these nociceptors, including acid-sensing ion channels (ASICs) and P2X2/3 receptors, reduced bone metabolic markers in ovariectomized mice.
Area of Science:
- Bone Biology
- Neuroscience
- Pain Research
Background:
- Nociceptors, involved in pain sensation, are increasingly recognized for roles beyond pain.
- Transient Receptor Potential Vanilloid 1 (TRPV1) is a nociceptor found in bone, impacting skeletal metabolism.
- Ovariectomy (OVX) in mice leads to altered bone metabolism and pain-like behaviors.
Purpose of the Study:
- To investigate the expression of nociceptors (TRPV1, ASICs, P2X2/3) in bone cells.
- To determine the effect of nociceptor antagonists on bone metabolism markers in OVX mice.
Main Methods:
- Examined nociceptor expression in femoral bone and bone marrow cells from OVX and sham-operated mice.
- Assessed the impact of nociceptor antagonists on key bone metabolic markers (Runx2, Osterix, osteocalcin, RANKL).
Main Results:
- TRPV1, ASIC 2/3, and P2X2/3 were expressed in bone and bone marrow cells.
- Expression of ASIC1/2 and P2X2 was elevated in OVX mice compared to sham controls.
- Nociceptor antagonist treatment significantly suppressed the expression of bone metabolic markers in OVX mice.
Conclusions:
- Multiple nociceptors, including TRPV1, ASICs, and P2X2/3, are present in bone cells.
- These nociceptors appear to regulate both skeletal pain and bone turnover, particularly in the context of OVX.
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