Effects of evocalcet on parathyroid calcium‐sensing receptor and vitamin D receptor expression in uremic rats

Author:

Saito Tomohiro1ORCID,Mizobuchi Masahide1ORCID,Sakai Mariko2,Kawata Takehisa3,Kitayama Tetsuya2,Kato Tadashi1,Suzuki Taihei1,Ogata Hiroaki4,Koiwa Fumihiko5,Honda Hirokazu1

Affiliation:

1. Division of Nephrology Department of Medicine Showa University School of Medicine Tokyo Japan

2. Biomedical Science Research Laboratories 1 Research Unit, R&D Division Kyowa Kirin Co., Ltd. Shizuoka Japan

3. Medical Affairs Department Kyowa Kirin Co., Ltd. Tokyo Japan

4. Department of Internal Medicine Showa University Northern Yokohama Hospital Yokohama Japan

5. Division of Nephrology Department of Internal Medicine Showa University Fujigaoka Hospital Yokohama Japan

Abstract

AbstractLittle is known about the effect of the recently developed calcimimetic evocalcet (Evo) on parathyroid calcium‐sensing receptor (CaSR) and vitamin D receptor (VDR) expression. We examined the effects of Evo and cinacalcet (Cina) on CaSR and VDR expression in 5/6 nephrectomized Sprague–Dawley rats fed a high‐phosphorus diet for 4 weeks to develop secondary hyperparathyroidism (SHPT). These uremic rats were divided into 4 groups—baseline control (Nx4W) and groups with additional treatment with either the Vehicle, Evo, or Cina for 2 weeks; normal rats were used as normal controls (NC). Blood parameters and parathyroid tissue were analyzed. CaSR and VDR expression levels were determined using immunohistochemistry. The degree of kidney injury and hyperphosphatemia was similar in the uremic groups (Nx4W, Vehicle, Cina, and Evo). Serum parathyroid hormone levels were significantly higher in the Nx4W and Vehicle groups than in the NC group. This increase was significantly suppressed in the Cina and Evo groups compared with that in the Vehicle group. Serum calcium levels were significantly and equally lower in the Cina and Evo groups relative to those in the Vehicle group. CaSR expression was significantly lower in the Nx4W and Vehicle groups than in the NC group. This downregulation was of an equally lesser magnitude in the Cina and Evo groups. A similar trend was observed for VDR expression. These results indicate that Evo and Cina treatment can increase parathyroid CaSR and VDR expression in uremic rats with SHPT, which could provide better control of mineral and bone disorder markers.

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

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