2007
DOI: 10.1016/j.jsbmb.2006.12.035
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Parathyroid hormone stimulation of the renal 25-hydroxyvitamin D-1α-hydroxylase—Effect of age and free radicals

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Cited by 13 publications
(8 citation statements)
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“…Considering the increased total urinary Ca excretion concomitant with elevated serum PTH levels, reabsorption function might become desensitization in response to elevated PTH levels in aged rats. Indeed, similar observations have been reported that the capacity of PTH to increase serum levels of 1,25-dihydroxyvitamin D [1,25(OH) 2 D] declines with age in both rats and humans (Ambrecht et al, 2007). In addition, elevated PTH levels in aged rats might be caused by increased urinary Ca excretion to maintain constantly serum Ca levels through facilitation of Ca mobilization from the bone.…”
Section: Discussionsupporting
confidence: 62%
“…Considering the increased total urinary Ca excretion concomitant with elevated serum PTH levels, reabsorption function might become desensitization in response to elevated PTH levels in aged rats. Indeed, similar observations have been reported that the capacity of PTH to increase serum levels of 1,25-dihydroxyvitamin D [1,25(OH) 2 D] declines with age in both rats and humans (Ambrecht et al, 2007). In addition, elevated PTH levels in aged rats might be caused by increased urinary Ca excretion to maintain constantly serum Ca levels through facilitation of Ca mobilization from the bone.…”
Section: Discussionsupporting
confidence: 62%
“…This is unexpected since the efficiency of the photosynthesis of vitamin D in human skin decreases with age [32]. Nevertheless, other factors may explain this discrepancy: food habits and awareness of the possibility of vitamin D deficiency may be different for different age groups, and there may be a low activity of the renal 1-alfa hydroxylase or a lower stimulatory effect of PTH on this enzyme in old than in young persons [33].…”
Section: Discussionmentioning
confidence: 99%
“…Equal protein loading was determined using a mouse anti-ERK 2 monoclonal antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, CA). For detection of 1α-hydroxylase protein, membranes were probed with rabbit anti-1α-hydroxylase polyclonal antibody (1∶1500 dilution) [51]. Equal protein loading was determined using a rabbit anti-β-actin polyclonal antibody (1∶6500) (Cell Signaling Technology, Danvers, MA).…”
Section: Methodsmentioning
confidence: 99%