Nitric Oxide as a Mediator of Estrogen Effects in Osteocytes
Joshua, J; Kalyanaraman, H; Marathe, N; Pilz, RB
| HERO ID | 2841350 |
|---|---|
| In Press | No |
| Year | 2014 |
| Title | Nitric Oxide as a Mediator of Estrogen Effects in Osteocytes |
| Authors | Joshua, J; Kalyanaraman, H; Marathe, N; Pilz, RB |
| Journal | Nitric Oxide |
| Volume | 96 |
| Page Numbers | 247-263 |
| Abstract | Postmenopausal osteoporosis due to estrogen deficiency is a major health problem, and available therapies rely largely on the inhibition of bone resorption, because estrogen replacement is associated with risks. Estrogen promotes bone health in large part by increasing osteocyte survival, but the molecular mechanisms involved are only partly understood. We showed that estradiol stimulates nitric oxide (NO) production in osteocytes, leading to increased cGMP synthesis and activation of cGMP-dependent protein kinases (PKGs). Moreover, we found that 17 beta-estradiol protects osteocytes against apoptosis via the NO/cGMP signaling pathway: type II PKG mediates estradiol-induced activation of the prosurvival kinases Erk and Akt, whereas type I PKG contributes to prosurvival signaling by directly phosphorylating and inactivating the cell death protein BAD. Preclinical data support an important role of NO in bone biology, and clinical trials suggest that NO donors may prevent bone loss in postmenopausal women. Our data provide novel insights into estrogen signaling through the NO/cGMP/PKG pathway and a rationale for using NO donors and other cGMP-elevating agents for treating postmenopausal osteoporosis. |
| Doi | 10.1016/B978-0-12-800254-4.00010-6 |
| Pmid | 25189390 |
| Wosid | WOS:000341216500010 |
| Is Certified Translation | No |
| Dupe Override | No |
| Is Public | Yes |