Fenoterol did not enhance glucocorticoid-induced skeletal changes in male rats

Acta Biochim Pol. 2011;58(3):313-9. Epub 2011 Aug 31.

Abstract

Glucocorticoids and β(2)-adrenergic receptor agonists are the most commonly used drugs in the treatment of asthma. Both therapies are potentially dangerous to the skeletal system. The aim of the present study was to investigate the effects of fenoterol, a β(2)-receptor agonist, on the development of bone changes induced by glucocorticoid (prednisolone) administration in mature male rats. The experiments were carried out on 24-week-old male Wistar rats. The effects of prednisolone 21-hemisuccinate sodium salt (7 mg/kg s.c. daily) or/and fenoterol hydrobromide (1.4 mg/kg i.p. daily), administered for 4 weeks, on the skeletal system were studied. Bone turnover markers, geometric parameters, mass, mass of bone mineral in the tibia, femur and L-4 vertebra, bone histomorphometric parameters and mechanical properties of tibial metaphysis, femoral diaphysis and femoral neck were determined. Both prednisolone and fenoterol had damaging effects on the skeletal system of mature male rats. However, concurrent administration of fenoterol and prednisolone did not result in the intensification of the deleterious skeletal effect of either drug administered separately.

MeSH terms

  • Acid Phosphatase / blood
  • Adrenergic beta-2 Receptor Agonists / pharmacology*
  • Animals
  • Body Weight / drug effects
  • Bone and Bones / drug effects*
  • Calcification, Physiologic / drug effects
  • Diaphyses / drug effects
  • Drug Interactions
  • Femur / drug effects
  • Fenoterol / adverse effects*
  • Fenoterol / pharmacology*
  • Glucocorticoids / pharmacology*
  • Isoenzymes / blood
  • Male
  • Prednisolone / pharmacology
  • Rats
  • Rats, Wistar
  • Tartrate-Resistant Acid Phosphatase
  • Tibia / drug effects

Substances

  • Adrenergic beta-2 Receptor Agonists
  • Glucocorticoids
  • Isoenzymes
  • Fenoterol
  • Prednisolone
  • Acid Phosphatase
  • Tartrate-Resistant Acid Phosphatase