Tetracyclines (TCs) have an anticollagenase effect; an action unrelated to their antimicrobial property. Recently, it was shown that TCs also inhibited extracellular osteoblastic collagenase (C'ase) activity. However, apart from this anticollagenase action, TCs have another novel property as potent inhibitors of osteoclast function. Therefore, TCs and a new generation of chemically modified nonantimicrobial analogs (CMTs), have enormous therapeutic potential for the treatment of the human lytic bone diseases. This application has a major focus: to define the mechanisms of action for the therapeutic uses of TCs where bone resorption is clinically significant.
The specific aims i nclude the following in vitro studies with TCs/CMTs: (1) to examine the transcription, synthesis (intracellular pathways), and activity (extracellular) of the matrix metalloproteinases (MMPs), C'ase and gelatinase (G'ase), with osteoblasts (OBs) and osteoclasts (OCs); (2) to examine the transcription, synthesis, and activity of the TIMPs (tissue inhibitors of the MMPs) with OBs and OCs; (3) to characterize OC reactive oxygen species (ROS); and to investigate the potential of TCs/CMTs to block the extracellular activation of proMMPs from OBs and OCs with or without ROS; (4) to assess the potential inhibitory potency of the new generation CMTs on parameters of OC function; and (5) to determine whether TCs interact with the OC calcium """"""""receptor"""""""". cDNA probes to C'ase, G'ase, TIMPs 1 and 2, and the lysosomal enzymes (cathepsin L and TRAP) will measure steady state mRNA levels (transcription). Antibodies will measure synthesis of MMPs and TIMPs. Functional assays will assess the inhibitory action of TCs/CMTs on extracellular MMPs, TIMPs, and lysosomal enzymes. The resorption pit assay will determine the extent of bone resorption with or without TCs/CMTs. ROS will be assayed in OCs with established techniques. To determine whether TCs interact with the OC calcium """"""""receptor"""""""", studies will include immunocytochemistry, cytosolic calcium measurements, autoradiography, and morphometry. The proposed studies should provide additional insights into the mechanisms underlying the lytic bone diseases, including periodontitis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
2R01DE009576-04
Application #
2130633
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Project Start
1990-07-01
Project End
1997-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
4
Fiscal Year
1994
Total Cost
Indirect Cost
Name
New York University
Department
Other Basic Sciences
Type
Schools of Dentistry
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
Ramamurthy, Nungavarum S; Rifkin, Barry R; Greenwald, Robert A et al. (2002) Inhibition of matrix metalloproteinase-mediated periodontal bone loss in rats: a comparison of 6 chemically modified tetracyclines. J Periodontol 73:726-34
Llavaneras, A; Golub, L M; Rifkin, B R et al. (1999) CMT-8/clodronate combination therapy synergistically inhibits alveolar bone loss in LPS-induced periodontitis. Ann N Y Acad Sci 878:671-4
Sorsa, T; Ramamurthy, N S; Vernillo, A T et al. (1998) Functional sites of chemically modified tetracyclines: inhibition of the oxidative activation of human neutrophil and chicken osteoclast pro-matrix metalloproteinases. J Rheumatol 25:975-82
Vernillo, A T; Rifkin, B R (1998) Effects of tetracyclines on bone metabolism. Adv Dent Res 12:56-62
Zaidi, M; Shankar, V S; Adebanjo, O A et al. (1996) Regulation of extracellular calcium sensing in rat osteoclasts by femtomolar calcitonin concentrations. Am J Physiol 271:F637-44
Debari, K; Sasaki, T; Udagawa, N et al. (1995) An ultrastructural evaluation of the effects of cysteine-proteinase inhibitors on osteoclastic resorptive functions. Calcif Tissue Int 56:566-70
Zaidi, M; Shankar, V S; Tunwell, R et al. (1995) A ryanodine receptor-like molecule expressed in the osteoclast plasma membrane functions in extracellular Ca2+ sensing. J Clin Invest 96:1582-90
Kremer, M; Judd, J; Rifkin, B et al. (1995) Estrogen modulation of osteoclast lysosomal enzyme secretion. J Cell Biochem 57:271-9
Ramamurthy, N; Greenwald, R; Moak, S et al. (1994) CMT/Tenidap treatment inhibits temporomandibular joint destruction in adjuvant arthritic rats. Ann N Y Acad Sci 732:427-30
Vernillo, A T; Ramamurthy, N S; Golub, L M et al. (1994) The nonantimicrobial properties of tetracycline for the treatment of periodontal disease. Curr Opin Periodontol :111-8

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