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Published in: Clinical Orthopaedics and Related Research® 5/2008

01-05-2008 | Symposium: Molecular and Surgical Advances in Osteonecrosis

Pitavastatin may Reduce Risk of Steroid-induced Osteonecrosis in Rabbits: A Preliminary Histological Study

Authors: Kenjiro Nishida, MD, Takuaki Yamamoto, MD, PhD, Goro Motomura, MD, PhD, Seiya Jingushi, MD, PhD, Yukihide Iwamoto, MD, PhD

Published in: Clinical Orthopaedics and Related Research® | Issue 5/2008

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Abstract

Several animal and human studies suggest pharmacological approaches may prevent steroid-induced osteonecrosis (ON). We asked whether the newly developed 3-hydroxymethyl-3-glutaryl-CoA (HMG-CoA) reductase inhibitor, pitavastatin, could prevent steroid-induced ON in rabbits. We injected 65 adult male Japanese white rabbits once with 20 mg/kg of methylprednisolone acetate into the right gluteus medius muscle. The rabbits were divided into two groups; one group of 35 rabbits received pitavastatins (PS), and the other group of 30 rabbits received no prophylaxis (CTR). Hematological examinations were performed just before the steroid injection (0 weeks) and at 1 and 2 weeks after steroid injection; both the femora and the humeri were histologically examined 2 weeks postinjection. The incidence of histologic changes consistent with early ON in the PS group (13 of 35; 37%) was lower in comparison to the CTR group (21 of 30; 70%). The size of the bone marrow fat cells in the PS group (56.6 ± 10 μm) was smaller than those in the CTR group (60 ± 4 μm). The data suggest pitavastatin has the potential to lower the incidence of steroid-induced ON in rabbits.
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Metadata
Title
Pitavastatin may Reduce Risk of Steroid-induced Osteonecrosis in Rabbits: A Preliminary Histological Study
Authors
Kenjiro Nishida, MD
Takuaki Yamamoto, MD, PhD
Goro Motomura, MD, PhD
Seiya Jingushi, MD, PhD
Yukihide Iwamoto, MD, PhD
Publication date
01-05-2008
Publisher
Springer-Verlag
Published in
Clinical Orthopaedics and Related Research® / Issue 5/2008
Print ISSN: 0009-921X
Electronic ISSN: 1528-1132
DOI
https://doi.org/10.1007/s11999-008-0189-4

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