TY - JOUR
T1 - Inhibition of Necrotic Actions of Nitrogen-Containing Bisphosphonates (NBPs) and Their Elimination From Bone by Etidronate (a Non-NBP)
T2 - A Proposal for Possible Utilization of Etidronate as a Substitution Drug for NBPs
AU - Oizumi, Takefumi
AU - Funayama, Hiromi
AU - Yamaguchi, Kouji
AU - Yokoyama, Masayoshi
AU - Takahashi, Harue
AU - Yamamoto, Miou
AU - Kuroishi, Toshinobu
AU - Kumamoto, Hiroyuki
AU - Sasaki, Keiichi
AU - Kawamura, Hiroshi
AU - Sugawara, Shunji
AU - Endo, Yasuo
N1 - Funding Information:
This work was supported by grants from Novartis Pharma KK -(Tokyo, Japan), Dainippon Sumitomo Pharma Co Ltd (Tokyo, Japan), Tohoku University (Sendai, Japan), and the Japan Society for the Promotion of Science ( 20592318 , 21792101 , and 21390529 ). We are grateful to Dr Yoshifumi Shirakami (Nihon Medi-Physics Co Ltd) for providing helpful information concerning bone scintigraphy, Dr Masanori Takahashi (Novartis Pharma KK) and Dr Takashi Katsumata (Dainippon Sumitomo Pharma Co Ltd) for providing clinical information concerning bisphosphonates, and Dr Robert Timms for editing the manuscript.
Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2010/5
Y1 - 2010/5
N2 - Purpose: Nitrogen-containing bisphosphonates (NBPs) have powerful anti-bone-resorptive effects (ABREs). However, recent clinical applications have disclosed an unexpected side effect, osteonecrosis of the jaw. We previously found in mice that etidronate (a non-NBP), when coadministered with alendronate (an NBP), inhibited the latter's inflammatory effects. However, etidronate also reduced the ABRE of alendronate. The present study examined in mice the modulating effects of etidronate on the inflammatory and necrotic actions of zoledronate (the NBP with the strongest anti-bone-resorptive activity and the highest incidence of osteonecrosis of the jaw) and on ABREs of various NBPs including zoledronate. Materials and Methods: NBPs were subcutaneously injected into ear pinnas of mice and ensuing inflammation and necrosis at the site of the injection were evaluated. ABREs of NBPs were evaluated by analyzing sclerotic bands induced in mouse tibias. Results: Coinjection of etidronate reduced inflammatory and necrotic reactions induced by zoledronate, and also reduced the amount of zoledronate retained within the ear tissue. When both agents were intraperitoneally injected, etidronate reduced the ABRE of zoledronate and those of other NBPs. Notably, etidronate reduced the ABRE of zoledronate even when this non-NBP was injected 16 hours after the injection of zoledronate. Bone scintigram indicated that etidronate reduced the amount of zoledronate that had already bound to bone. Conclusions: These results suggest that etidronate may 1) inhibit the entry of NBPs into cells related to inflammation and/or necrosis, 2) inhibit the binding of NBPs to bone hydroxyapatite, 3) at least partly eliminate (or substitute for) NBPs that have already accumulated within bones, and thus 4) if used as a substitution drug for NBPs, be effective at treating or preventing NBP-associated osteonecrosis of the jaw.
AB - Purpose: Nitrogen-containing bisphosphonates (NBPs) have powerful anti-bone-resorptive effects (ABREs). However, recent clinical applications have disclosed an unexpected side effect, osteonecrosis of the jaw. We previously found in mice that etidronate (a non-NBP), when coadministered with alendronate (an NBP), inhibited the latter's inflammatory effects. However, etidronate also reduced the ABRE of alendronate. The present study examined in mice the modulating effects of etidronate on the inflammatory and necrotic actions of zoledronate (the NBP with the strongest anti-bone-resorptive activity and the highest incidence of osteonecrosis of the jaw) and on ABREs of various NBPs including zoledronate. Materials and Methods: NBPs were subcutaneously injected into ear pinnas of mice and ensuing inflammation and necrosis at the site of the injection were evaluated. ABREs of NBPs were evaluated by analyzing sclerotic bands induced in mouse tibias. Results: Coinjection of etidronate reduced inflammatory and necrotic reactions induced by zoledronate, and also reduced the amount of zoledronate retained within the ear tissue. When both agents were intraperitoneally injected, etidronate reduced the ABRE of zoledronate and those of other NBPs. Notably, etidronate reduced the ABRE of zoledronate even when this non-NBP was injected 16 hours after the injection of zoledronate. Bone scintigram indicated that etidronate reduced the amount of zoledronate that had already bound to bone. Conclusions: These results suggest that etidronate may 1) inhibit the entry of NBPs into cells related to inflammation and/or necrosis, 2) inhibit the binding of NBPs to bone hydroxyapatite, 3) at least partly eliminate (or substitute for) NBPs that have already accumulated within bones, and thus 4) if used as a substitution drug for NBPs, be effective at treating or preventing NBP-associated osteonecrosis of the jaw.
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U2 - 10.1016/j.joms.2009.08.027
DO - 10.1016/j.joms.2009.08.027
M3 - Article
C2 - 20156665
AN - SCOPUS:77950861187
SN - 0278-2391
VL - 68
SP - 1043
EP - 1054
JO - Journal of Oral and Maxillofacial Surgery
JF - Journal of Oral and Maxillofacial Surgery
IS - 5
ER -