Circadian rhythm of activin A and related parameters of mineral metabolism in normal and uremic rats

• DOI: 10.1007/s00424-019-02291-2
• Publication Date: 2019-06-24T22:13:35Z
• Authors: Anders Nordholm; Søren Egstrand; Eva Gravesen; Maria L. Mace; Marya Morevati; Klaus Olgaard; Ewa Lewin
• Keywords: Male; 0301 basic medicine; Metabolic/blood; Wistar; 610; 630; Phosphates; Glucuronidase/blood; 03 medical and health sciences; Phosphates/blood; Molecular and Cellular Mechanisms of Disease; Uremia/blood; Animals; Renal Insufficiency; Rats, Wistar; Renal Insufficiency, Chronic; Activins/blood; Bone Diseases, Metabolic/blood; Klotho Proteins; Glucuronidase; Uremia; Fibroblast Growth Factors/blood; Activins; Circadian Rhythm; Rats; Fibroblast Growth Factors; Bone Diseases, Metabolic; Chronic/blood; Parathyroid Hormone; Parathyroid Hormone/blood; Renal Insufficiency, Chronic/blood; Bone Diseases

Activin A is a new fascinating player in chronic kidney disease-mineral and bone disorder (CKD-MBD), which is implicated in progressive renal disease, vascular calcification, and osteodystrophy. Plasma activin A rises early in the progression of renal disease. Disruption of circadian rhythms is related to increased risk of several diseases and circadian rhythms are observed in mineral homeostasis, bone parameters, and plasma levels of phosphate and PTH. Therefore, we examined the circadian rhythm of activin A and CKD-MBD-related parameters (phosphate, PTH, FGF23, and klotho) in healthy controls and CKD rats (5/6 nephrectomy) on high-, standard- and low-dietary phosphate contents as well as during fasting conditions. Plasma activin A exhibited circadian rhythmicity in healthy control rats with fourfold higher values at acrophase compared with nadir. The rhythm was obliterated in CKD. Activin A was higher in CKD rats compared with controls when measured at daytime but not significantly when measured at evening/nighttime, stressing the importance of time-specific reference intervals when interpreting plasma values. Plasma phosphate, PTH, and FGF23 all showed circadian rhythms in control rats, which were abolished or disrupted in CKD. Plasma klotho did not show circadian rhythm. Thus, the present investigation shows, for the first time, circadian rhythm of plasma activin A. The rhythmicity is severely disturbed by CKD and is associated with disturbed rhythms of phosphate and phosphate-regulating hormones PTH and FGF23, indicating that disturbed circadian rhythmicity is an important feature of CKD-MBD.