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The l-Ser analog #290 promotes bone recovery in OP and RA mice.
- Source :
-
Pharmacological research [Pharmacol Res] 2011 Sep; Vol. 64 (3), pp. 203-9. Date of Electronic Publication: 2011 May 13. - Publication Year :
- 2011
-
Abstract
- We previously characterized the l-Ser analog #290, H(tBut)-l-Ser-O-Methyl·HCl, as a novel inhibitor of osteoclastogenesis which functions in both mouse and human cells. Here, we assessed the activity of #290 in animal models of osteoporosis and rheumatoid arthritis. Treatment of animals with #290 both prevented bone loss and led to the recovery of lost bone in osteoporotic mice. When inflammatory arthritis was induced in SKG mice, #290 treatment suppressed arthritis scores and significantly prevented the destruction of calcaneous bones. Additionally, #290 reciprocally modulated the mammalian target of rapamycin (mTOR) pathway in osteoclasts and osteoblasts in vitro, suggesting a dual effect on bone homeostasis. Our results demonstrate that #290 is a potential novel therapeutic tool for the treatment and/or study of diseases associated with bone destruction.<br /> (2011 Elsevier Ltd. All rights reserved.)
- Subjects :
- 3T3 Cells
Animals
Arthritis, Rheumatoid pathology
Bone Resorption drug therapy
Bone Resorption pathology
Bone and Bones cytology
Bone and Bones drug effects
Bone and Bones pathology
Cell Differentiation drug effects
Cell Line
Female
Humans
Mice
Mice, Inbred C57BL
Osteoblasts cytology
Osteoblasts drug effects
Osteoblasts pathology
Osteoclasts cytology
Osteoclasts drug effects
Osteoclasts pathology
Osteoporosis pathology
Serine chemistry
Serine therapeutic use
TOR Serine-Threonine Kinases metabolism
Arthritis, Rheumatoid drug therapy
Lipids chemistry
Lipids therapeutic use
Osteoporosis drug therapy
Serine analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1096-1186
- Volume :
- 64
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Pharmacological research
- Publication Type :
- Academic Journal
- Accession number :
- 21605676
- Full Text :
- https://doi.org/10.1016/j.phrs.2011.05.004