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The journal of clinical endocrinology and metabolism, 2013-12, Vol.98 (12), p.4619-4628
2013

Details

Autor(en) / Beteiligte
Titel
The Role of the Parent Compound Vitamin D with Respect to Metabolism and Function: Why Clinical Dose Intervals Can Affect Clinical Outcomes
Ist Teil von
  • The journal of clinical endocrinology and metabolism, 2013-12, Vol.98 (12), p.4619-4628
Ort / Verlag
Bethesda, MD: Endocrine Society
Erscheinungsjahr
2013
Link zum Volltext
Quelle
Oxford Journals 2020 Medicine
Beschreibungen/Notizen
  • Context: There is no doubt that vitamin D must be activated to the hormonal form 1,25-dihydroxyvitamin D to achieve full biological activity or that many tissues participate in this activation process—be it endocrine or autocrine. We believe that not only is 25-hydroxyvitamin D important to tissue delivery for this activation process, but also that intact vitamin D has a pivotal role in this process. Objective: In this review, evidence on the vitamin D endocrine/autocrine system is presented and discussed in relation to vitamin D-binding protein affinity, circulating half-lives, and enzymatic transformations of vitamin D metabolites, and how these affect biological action in any given tissue. Conclusions: Circulating vitamin D, the parent compound, likely plays an important physiological role with respect to the vitamin D endocrine/autocrine system, as a substrate in many tissues, not originally thought to be important. Based on emerging data from the laboratory, clinical trials, and data on circulating 25-hydroxyvitamin D amassed during many decades, it is likely that for the optimal functioning of these systems, significant vitamin D should be available on a daily basis to ensure stable circulating concentrations, implying that variation in vitamin D dosing schedules could have profound effects on the outcomes of clinical trials because of the short circulating half-life of intact vitamin D.
Sprache
Englisch
Identifikatoren
ISSN: 0021-972X
eISSN: 1945-7197
DOI: 10.1210/jc.2013-2653
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3849670

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