In this communication we describe the synthesis of \(1 \alpha, 25\)-dihydroxyvitamin \(\mathrm{D}_{3}\) - \(3 \beta\)-bromoacetate \(\left[1,25(\mathrm{OH})_{2}-\mathrm{BE}\right]\), an analog of \(1 \alpha, 25\)-dihydroxyvitamin \(\mathrm{D}_{3}\left[1,25(\mathrm{OH})_{2} \mathrm{D}_{3}\right]\), a
Nongenomic actions of the steroid hormone 1α25-dihydroxyvitamin D3
✍ Scribed by Daniel T. Baran
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 413 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0730-2312
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✦ Synopsis
Recent studies indicate that the vitamin D hormone, 1 a,25-dihydroxyvitamin D3 exerts rapid effects (seconds to minutes) in a variety of cell types. These rapid nongenomic actions in osteoblasts include effects on membrane voltage-gated calcium channels, phospholipase C activity, and the sodium/hydrogen antiport. Since the rapid effects occur in osteoblasts that lack the nuclear vitamin D receptor, it is postulated that the nongenomic responses to the hormone reflect interaction with a separate, membrane localized signalling system. Preliminary studies demonstrate the presence of a receptor on the membranes of osteoblasts that lack the nuclear vitamin D receptor. This membrane receptor recognizes la,25-dihydroxyvitamin D3 and its inaction 1 P epimer, but not 25-hydroxyvitamin D3.
These rapid nongenomic actions generated by interaction with the membrane receptor modulate the effects of the hormone on gene transcription. Thus, the rapid nongenomic pathway may play a regulatory function in modulating the genomic pathways affected by la,25-dihydroxyvitamin D3.
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