HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Low-dose combination of alendronate and atorvastatin reduces ligature-induced alveolar bone loss in rats.

AbstractBACKGROUND AND OBJECTIVE:
Atorvastatin (ATV) has bone anabolic properties, and alendronate (ALD) is an important antiresorptive drug. This study aimed to evaluate the effects of the combination of ALD and ATV on ligature-induced alveolar bone loss in rats.
MATERIAL AND METHODS:
Periodontitis was induced by ligature in 78 Wistar rats. Groups of six rats prophylactically received 0.9% saline (SAL), ALD (0.01 or 0.25 mg/kg subcutaneously) or ATV (0.3 or 27 mg/kg by gavage). Then, groups of six rats received the combination of ALD+ATV (0.25 mg/kg + 27 mg/kg, 0.01 mg/kg + 0.3 mg/kg, 0.25 mg/kg + 0.3 mg/kg or 0.01 mg/kg + 27 mg/kg) prophylactically. An extra group of six rats received therapeutic SAL or a lower-dose combination of ALD+ATV (0.01 mg/kg + 0.3 mg/kg, respectively) therapeutically. Three extra groups of six rats each received SAL or a lower-dose combination of ALD+ATV (0.01 mg/kg + 0.3 mg/kg, respectively) prophylactically or therapeutically for histometric and immunohistochemical analyses. The rats were killed on day 11 after ligature placement, and the maxillae were removed and processed for macroscopic, histomorphometric and TRAP immunohistochemical analyses. Gingival samples were collected to evaluate myeloperoxidase (MPO) activity. Blood samples were collected to measure serum bone-specific alkaline phosphatase (BALP) and transaminase levels and for hematological studies. Rats were weighed daily.
RESULTS:
All combined therapies prevented alveolar bone loss when compared with SAL or low doses of monotherapy (ALD or ATV) (p < 0.05). The lower-dose combination of ALD+ATV (0.01 mg/kg + 0.3 mg/kg, respectively), administered either prophylactically (39.0%) or therapeutically (53.5%), prevented alveolar bone loss. Decreases in bone and cementum resorption, in leukocyte infiltration and in immunostaining for TRAP and MPO activity corroborated the morphometric findings. The lower-dose combination of ALD+ATV (0.01 mg/kg + 0.3 mg/kg, respectively) prevented BALP reduction (p < 0.05) and did not alter the level of serum transaminases. Moreover, the lower-dose combination of ALD+ATV (0.01 mg/kg + 0.3 mg/kg, respectively) also reduced neutrophilia and lymphomonocytosis and did not cause weight loss when compared with administration of SAL.
CONCLUSION:
The lower-dose combination of ALD+ATV (0.01 mg/kg + 0.3 mg/kg, respectively) demonstrated a protective effect on alveolar bone loss.
AuthorsP Goes, I M Melo, L M C M Silva, N M B Benevides, N M N Alencar, R A Ribeiro, V Lima
JournalJournal of periodontal research (J Periodontal Res) Vol. 49 Issue 1 Pg. 45-54 (Feb 2014) ISSN: 1600-0765 [Electronic] United States
PMID23742139 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Chemical References
  • Bone Density Conservation Agents
  • Heptanoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Isoenzymes
  • Pyrroles
  • Atorvastatin
  • Peroxidase
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Alkaline Phosphatase
  • Acid Phosphatase
  • Tartrate-Resistant Acid Phosphatase
  • Alendronate
Topics
  • Acid Phosphatase (analysis)
  • Alanine Transaminase (blood)
  • Alendronate (administration & dosage)
  • Alkaline Phosphatase (blood)
  • Alveolar Bone Loss (prevention & control)
  • Animals
  • Aspartate Aminotransferases (blood)
  • Atorvastatin
  • Body Weight
  • Bone Density Conservation Agents (administration & dosage)
  • Dental Cementum (drug effects)
  • Gingiva (enzymology)
  • Heptanoic Acids (administration & dosage)
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors (administration & dosage)
  • Infusions, Parenteral
  • Injections, Subcutaneous
  • Isoenzymes (analysis)
  • Leukocyte Disorders (prevention & control)
  • Leukocytes (drug effects)
  • Leukocytosis (prevention & control)
  • Male
  • Monocytes (drug effects)
  • Neutrophils (drug effects)
  • Peroxidase (analysis)
  • Pyrroles (administration & dosage)
  • Rats, Wistar
  • Root Resorption (prevention & control)
  • Tartrate-Resistant Acid Phosphatase

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: