Development of experimental chronic kidney disease and vascular calcification alters diurnal variation of phosphate and its hormonal regulators
| Autor: | Emilie Ward, Kimberly Laverty, Michael A. Adams, Bruno Svajger, Justin L. H. Riddoch, Cynthia M. Pruss, Rachel M. Holden |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
Fibroblast growth factor 23
Male medicine.medical_specialty Physiology chemistry.chemical_element Renal function 030204 cardiovascular system & hematology Calcium urologic and male genital diseases lcsh:Physiology Phosphates Rats Sprague-Dawley 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Physiology (medical) Internal medicine medicine CKD Animals Circadian rhythm diurnal Renal Insufficiency Chronic FGF‐23 Original Research phosphate lcsh:QP1-981 business.industry Diurnal temperature variation Phosphate medicine.disease Circadian Rhythm Rats Fibroblast Growth Factors Endocrinology chemistry vascular calcification business 030217 neurology & neurosurgery Kidney disease Hormone |
| Zdroj: | Physiological Reports Physiological Reports, Vol 8, Iss 21, Pp n/a-n/a (2020) |
| ISSN: | 2051-817X |
| Popis: | The mineral‐bone axis is tightly regulated and dependent on renal function. In chronic kidney disease (CKD) progressive loss of renal capacity disrupts this axis over‐time, with marked changes in circulating calcium, phosphate, PTH, and fibroblast growth factor‐23 (FGF‐23). These changes contribute to the development of cardiovascular disease, like vascular calcification (VC), which worsens morbidity and mortality in CKD. Although the chronic changes in these circulating factors and their relationships are well known, no experimental studies have examined how the progressive development of CKD and VC alter the circadian rhythms of these factors. An adenine‐induced experimental model of CKD in rats was used to establish (i) general circulating trends, (ii) if renal dysfunction affects these observed trends, and (iii) identify potential changes in these trends caused by VC. This study clearly discerned patterns of daily variations in circulating minerals and hormones, finding that both phosphate and PTH follow modelable diurnal variations whereas calcium and FGF‐23 maintain relative stability over 24‐hr. Surprisingly, the development of CKD was not sufficient to disrupt these patterns of diurnal variation and only altered the magnitude of change; however, it was found that the diurnal rhythms of circulating phosphate and daily stability of calcium were only significantly altered in the setting of CKD with established VC. In this article, we experimentally and progressively generated CKD in rats using an adenine‐based diet. We examined the effect of worsening CKD and the development of vascular calcification on the daily variations in circulating minerals (phosphate, calcium) and mineral‐regulating hormones (PTH, FGF‐23). It was found that CKD did not alter the daily patterns of circulating minerals and hormones, but the occurrence of VC in CKD did. |
| Databáze: | OpenAIRE |
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