Plasma type 1 collagen cross-linked C-telopeptide: a sensitive marker of acute effects of salmon calcitonin on bone resorption
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články
PubMed
11750275
DOI
10.1016/s0009-8981(01)00731-8
PII: S0009898101007318
Knihovny.cz E-zdroje
- MeSH
- biologické markery krev MeSH
- časové faktory MeSH
- dospělí MeSH
- kalcitonin aplikace a dávkování farmakologie MeSH
- kolagen typu I MeSH
- kolagen krev MeSH
- kostní denzita účinky léků MeSH
- lidé MeSH
- osteokalcin krev MeSH
- parathormon krev MeSH
- peptidové fragmenty krev MeSH
- peptidy krev MeSH
- prokolagen krev MeSH
- resorpce kosti farmakoterapie MeSH
- vápník krev MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- biologické markery MeSH
- collagen type I trimeric cross-linked peptide MeSH Prohlížeč
- kalcitonin MeSH
- kolagen typu I MeSH
- kolagen MeSH
- osteokalcin MeSH
- parathormon MeSH
- peptidové fragmenty MeSH
- peptidy MeSH
- procollagen Type I N-terminal peptide MeSH Prohlížeč
- prokolagen MeSH
- salmon calcitonin MeSH Prohlížeč
- vápník MeSH
BACKGROUND: The aim of the study was to determine the acute effects of salmon calcitonin (sCT) on bone resorption as assessed by plasma type 1 collagen cross-linked C-telopeptide (CTX). In addition, the plasma aminoterminal propeptide of type I procollagen (PINP) and osteocalcin (OC) were evaluated as markers of bone formation. METHODS: In six healthy young women, after overnight fasting, single subcutaneous doses of 2, 10 and 50 IU as well as a nasal dose of 200 IU of sCT were administered consecutively with a 1-week washout period. During the control period, no drug was given. Blood samples were drawn at 0700 a.m. (baseline) and throughout the 9-h fasting period. RESULTS: Both intranasal and subcutaneous sCT resulted in a significant reduction in plasma CTX by 50-60% as early as within 1 h. The plasma CTX showed a dose-dependent decrease over a dosage range of 2, 10 and 50 IU after subcutaneous administration of sCT. No significant difference was observed between the areas under curves (AUC) for plasma CTX following intranasal and subcutaneous administration of 200 and 2 IU of sCT, respectively. Synthesis of types I collagen remained unaffected by the dose of 50 IU of subcutaneously administered sCT when the acute effects were considered. CONCLUSIONS: Plasma CTX is a sensitive marker in detecting acute changes of bone resorption after sCT administration.
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