Osteonecrosis of the femoral head was induced experimentally in chicke
ns after the administration of a high dose of corticosteroids. Lovasta
tin was used to prevent the effects of the steroid on adipogenesis in
cultured cells, and adipogenesis and osteonecrosis in chickens. The in
vitro study, with marrow cells in culture, showed that Lovastatin inh
ibited steroid induced fat specific gene expression and counteracted t
he inhibitory effects of steroids on osteoblastic gene expression, For
the in vivo study, 83 adult chickens were used: 48 received methylpre
dnisolone 3 mg/kg weekly via intramuscular injection (Group A). Fiftee
n received the steroid (as in Group A) plus Lovastatin 20 mg per anima
l per day orally (Group B), Ten chickens received Lovastatin only (Gro
up C), Another 10 received no medication and served as the control gro
up (Group D). Evidence of osteonecrosis was observed in specimens from
Group A, including subchondral bone death and resorption, fat cell pr
oliferation, and new hone formation. Conversely, sections from Group B
showed less adipogenesis and no bone death. It is concluded that the
bipedal chicken is a useful animal model for studies of osteonecrosis
and that lipid clearing agents, such as Lovastatin, may be helpful in
preventing the development of steroid induced osteonecrosis.