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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Kacso A, Goia-Socol M, Hazi G, Tomoaia G, Kacso IM, Georgescu CE
Effect of Experimental Dysglycemia on Under-Carboxylated Osteocalcin Production in Human Primary Osteoblast-Like Cell Cultures
Acta Endo (Buc) 2018, 14 (1): 11-15doi: 10.4183/aeb.2018.11
Context. The undercarboxylated form of
osteocalcin (ucOC) and osteoprotegerin (OPG) are bonederived
molecules involved in the endocrine crosstalk
governing the bone, the adipose tissue and the pancreas.
In addition, glucocorticoids are major determinants of both
insulin resistance and osteoporosis.
Objective. We aimed to investigate the response
of ucOC and OPG to dysglycemia and/or dexamethasone
(DXM) in primary human osteoblastic cell (HOC) cultures.
Design and methods. Third-passage sub-confluent
primary HOC cultures were treated with glucose: 2.8 mmol/L,
5.6 mmol/L, 11.1 mmol/L and 28 mmol/L, respectively.
Alternatively, HOC cultures were subjected to DXM 1
μmol/L. In more complex experiments, HOC cultures were
pre-treated with glucose (5.6 mmol/L) with/without insulin
(1 pmol/L) followed by DXM (1 μmol/L). 24-hours posttreatment,
culture medium ucOC and OPG were measured
by ELISA.
Results. ucOC production differed significantly
(p<0.05) between cell groups, decreasing in a dosedependent
manner as glucose concentration in the medium
increased. Insulin prevented this effect. OPG levels appeared
not to be significantly influenced by the hyperglycemic
culture medium and were not related to ucOC concentration
(p>0.05). Addition of DXM resulted in significantly lower
ucOC concentrations compared to vehicle-treated cells
(p<0.05). However, the effect of insulin co-treatment on
ucOC was not counteracted by DXM (p<0.05).
Conclusions. An obvious alteration of OC
production/metabolism was observed as glucose levels
changed in the bone microenvironment, to potentially be
involved in diabetes-related osteopenia. DXM suppressed
ucOC levels however not in insulin-rich environment.
Keywords: human osteoblasts, undercarboxylated osteocalcin, osteoprotegerin, insulin, dexamethasone, osteopenia, diabetes mellitus.
Correspondence: Carmen Emanuela Georgescu MD PHD, “Iuliu Hatieganu” University of Medicine and Pharmacy Cluj-Napoca, Discipline
of Endocrinology, 6th Medical Specialties Dept, 44F Eugen Ionesco St, Cluj-Napoca, 400496, Romania, E-mail: c_e_georgescu@yahoo.com