Skip to main content
Erschienen in: Osteoporosis International 1/2011

01.01.2011 | Original Article

Green tea polyphenols attenuate deterioration of bone microarchitecture in female rats with systemic chronic inflammation

verfasst von: C.-L. Shen, J. K. Yeh, C. Samathanam, J. J. Cao, B. J. Stoecker, R. Y. Dagda, M.-C. Chyu, D. M. Dunn, J.-S. Wang

Erschienen in: Osteoporosis International | Ausgabe 1/2011

Einloggen, um Zugang zu erhalten

Abstract

Summary

Green tea polyphenols (GTP) are promising agents for preventing bone loss. GTP supplementation sustained microarchitecture and improved bone quality via a decrease in inflammation. Findings suggest a significant role for GTP in skeletal health of patients with chronic inflammation.

Introduction

This study evaluated whether GTP can restore bone microstructure along with a molecular mechanism in rats with chronic inflammation. A 2 [placebo vs. lipopolysaccharide (LPS)]× 2 [no GTP vs. 0.5% GTP (w/v) in drinking water] factorial design was employed.

Methods

Female rats were assigned to four groups: placebo, LPS, placebo + GTP, and LPS + GTP for 12 weeks. Efficacy was evaluated by examining changes in bone microarchitecture using histomorphometric and microcomputed tomographic analyses and by bone strength using the three-point bending test. A possible mechanism was studied by assessing the difference in tumor necrosis factor-α (TNF-α) expression in tibia using immunohistochemistry.

Results

LPS lowered trabecular volume fraction, thickness, and bone formation in proximal tibia while increasing osteoclast number and surface perimeter in proximal tibia and eroded surface in endocortical tibial shafts. GTP increased trabecular volume fraction and number in both femur and tibia and periosteal bone formation rate in tibial shafts while decreasing trabecular separation in proximal tibia and eroded surface in endocortical tibial shafts. There was an interaction between LPS and GTP in trabecular number, separation, bone formation, and osteoclast number in proximal tibia, and trabecular thickness and number in femur. GTP improved the strength of femur, while suppressing TNF-α expression in tibia.

Conclusion

In conclusion, GTP supplementation mitigated deterioration of bone microarchitecture and improved bone integrity in rats with chronic inflammation by suppressing bone erosion and modulating cancellous and endocortical bone compartments, resulting in a larger net bone volume. Such a protective role of GTP may be due to a suppression of TNF-α.
Literatur
1.
Zurück zum Zitat Van Dyke TE, Serhan CN (2003) Resolution of inflammation: a new paradigm for the pathogenesis of periodontal diseases. J Dent Res 82:82–90CrossRefPubMed Van Dyke TE, Serhan CN (2003) Resolution of inflammation: a new paradigm for the pathogenesis of periodontal diseases. J Dent Res 82:82–90CrossRefPubMed
2.
Zurück zum Zitat Mann ST, Stracke H, Lange U, Klor HU, Teichmann J (2003) Alternations of bone mineral density and bone metabolism in patients with various grades of chronic pancreatitis. Metabolism 52:579–585CrossRefPubMed Mann ST, Stracke H, Lange U, Klor HU, Teichmann J (2003) Alternations of bone mineral density and bone metabolism in patients with various grades of chronic pancreatitis. Metabolism 52:579–585CrossRefPubMed
3.
Zurück zum Zitat Bernstein CN, Leslie WD, Taback SP (2003) Bone density in a population-based cohort or premenopausal adult women with early onset inflammatory bowel disease. Am J Gastroenterol 98:1094–1100CrossRefPubMed Bernstein CN, Leslie WD, Taback SP (2003) Bone density in a population-based cohort or premenopausal adult women with early onset inflammatory bowel disease. Am J Gastroenterol 98:1094–1100CrossRefPubMed
4.
Zurück zum Zitat Romas E, Gillespie MT, Martin TJ (2003) Involvement of receptor activator of NF-κB ligand and tumor necrosis factor-alpha in bone destruction in rheumatoid arthritis. Bone 30:340–346CrossRef Romas E, Gillespie MT, Martin TJ (2003) Involvement of receptor activator of NF-κB ligand and tumor necrosis factor-alpha in bone destruction in rheumatoid arthritis. Bone 30:340–346CrossRef
5.
Zurück zum Zitat Uaratanawong S, Deesomchoke U, Lertmaharit S, Uaratanawong S (2003) Bone mineral density in premenopausal women with systemic lupus erythematosus. J Rheumatol 30(11):2365–2368PubMed Uaratanawong S, Deesomchoke U, Lertmaharit S, Uaratanawong S (2003) Bone mineral density in premenopausal women with systemic lupus erythematosus. J Rheumatol 30(11):2365–2368PubMed
6.
Zurück zum Zitat Banfi G, Iorio EL, Corsi MM (2008) Oxidative stress, free radicals and bone remodeling. Clin Chem Lab Med 46(11):1550–1555, ReviewCrossRefPubMed Banfi G, Iorio EL, Corsi MM (2008) Oxidative stress, free radicals and bone remodeling. Clin Chem Lab Med 46(11):1550–1555, ReviewCrossRefPubMed
7.
Zurück zum Zitat Miyaura C, Inada M, Matsumoto C, Ohshiba T, Uozumi N, Shimizu T, Ito A (2003) An essential role of cytosolic phospholipase A2 alpha in prostaglandin E2-mediated bone resorption associated with inflammation. J Exp Med 197(10):1303–1310CrossRefPubMed Miyaura C, Inada M, Matsumoto C, Ohshiba T, Uozumi N, Shimizu T, Ito A (2003) An essential role of cytosolic phospholipase A2 alpha in prostaglandin E2-mediated bone resorption associated with inflammation. J Exp Med 197(10):1303–1310CrossRefPubMed
8.
Zurück zum Zitat Cochran DL (2008) Inflammation and bone loss in periodontal disease. J Periodontol 79(8 Suppl):1569–1576CrossRefPubMed Cochran DL (2008) Inflammation and bone loss in periodontal disease. J Periodontol 79(8 Suppl):1569–1576CrossRefPubMed
9.
Zurück zum Zitat Boulos P, Ioannidis G, Adachi JD (2000) Glucocorticoid-induced osteoporosis. Curr Rheumatol Rep 2(1):53–61CrossRefPubMed Boulos P, Ioannidis G, Adachi JD (2000) Glucocorticoid-induced osteoporosis. Curr Rheumatol Rep 2(1):53–61CrossRefPubMed
10.
Zurück zum Zitat Hofbauer LC, Brueck CC, Shanahan CM, Schoppet M, Dobnig H (2007) Vascular calcification and osteoporosis—from clinical observation towards molecular understanding. Osteoporos Int 18(3):251–259, ReviewCrossRefPubMed Hofbauer LC, Brueck CC, Shanahan CM, Schoppet M, Dobnig H (2007) Vascular calcification and osteoporosis—from clinical observation towards molecular understanding. Osteoporos Int 18(3):251–259, ReviewCrossRefPubMed
11.
Zurück zum Zitat Mody N, Parhami F, Saraflan TA, Demer LL (2001) Oxidative stress modulates osteoblastic differentiation of vascular and bone cells. Free Radic Biol Med 31:509–519CrossRefPubMed Mody N, Parhami F, Saraflan TA, Demer LL (2001) Oxidative stress modulates osteoblastic differentiation of vascular and bone cells. Free Radic Biol Med 31:509–519CrossRefPubMed
12.
Zurück zum Zitat Muthusami S, Ramachandran I, Muthusamy B, Vasudevan G, Prabhu V, Subramaniam V, Jagadeesan A, Narasimhan S (2005) Ovariectomy induces oxidative stress and impairs bone antioxidant system in adult rats. Clin Chim Acta 360(1–2):81–86CrossRefPubMed Muthusami S, Ramachandran I, Muthusamy B, Vasudevan G, Prabhu V, Subramaniam V, Jagadeesan A, Narasimhan S (2005) Ovariectomy induces oxidative stress and impairs bone antioxidant system in adult rats. Clin Chim Acta 360(1–2):81–86CrossRefPubMed
13.
Zurück zum Zitat Manolagas SC (2008) De-fense! De-fense! De-fense: scavenging H2O2 while making cholesterol. Endocrinology 149(7):3264–3266CrossRefPubMed Manolagas SC (2008) De-fense! De-fense! De-fense: scavenging H2O2 while making cholesterol. Endocrinology 149(7):3264–3266CrossRefPubMed
14.
Zurück zum Zitat Garrett JR, Boyce BF, Oreffo RO, Bonewald L, Poser J, Mundy GR (1990) Oxygen-derived free radicals stimulate osteoclastic bone resorption in rodent bone in vitro and in vivo. J Clin Invest 85:632–639CrossRefPubMed Garrett JR, Boyce BF, Oreffo RO, Bonewald L, Poser J, Mundy GR (1990) Oxygen-derived free radicals stimulate osteoclastic bone resorption in rodent bone in vitro and in vivo. J Clin Invest 85:632–639CrossRefPubMed
15.
Zurück zum Zitat Shen CL, Yeh JK, Cao JJ, Tatum OL, Dagda RY, Wang JS (2009) Green tea polyphenols mitigate bone loss of female rats in a chronic inflammation-induced bone loss model. J Nutr Biochem (in press) Shen CL, Yeh JK, Cao JJ, Tatum OL, Dagda RY, Wang JS (2009) Green tea polyphenols mitigate bone loss of female rats in a chronic inflammation-induced bone loss model. J Nutr Biochem (in press)
16.
Zurück zum Zitat Shen CL, Yeh JK, Cao J, Wang J-S (2009) Green tea and bone metabolism. Nutr Res 29(7):437–456, ReviewCrossRefPubMed Shen CL, Yeh JK, Cao J, Wang J-S (2009) Green tea and bone metabolism. Nutr Res 29(7):437–456, ReviewCrossRefPubMed
17.
Zurück zum Zitat Weisburger JH (1999) Tea and health: the underlying mechanisms. Proc Soc Exp Biol Med 220(4):271–275, ReviewCrossRefPubMed Weisburger JH (1999) Tea and health: the underlying mechanisms. Proc Soc Exp Biol Med 220(4):271–275, ReviewCrossRefPubMed
18.
Zurück zum Zitat Shen CL, Yeh JK, Stoecker BJ, Chyu MC, Wang JS (2009) Green tea polyphenols mitigate deterioration of bone microarchitecture in middle-aged female rats. Bone 44(4):684–690CrossRefPubMed Shen CL, Yeh JK, Stoecker BJ, Chyu MC, Wang JS (2009) Green tea polyphenols mitigate deterioration of bone microarchitecture in middle-aged female rats. Bone 44(4):684–690CrossRefPubMed
19.
Zurück zum Zitat Smith BJ, Lerner MR, Bu SY, Lucas EA, Hanas JS, Lightfoot SA, Postier RG, Bronze MS, Brackett DJ (2006) Systemic bone loss and induction of coronary vessel disease in a rat model of chronic inflammation. Bone 38(3):378–386CrossRefPubMed Smith BJ, Lerner MR, Bu SY, Lucas EA, Hanas JS, Lightfoot SA, Postier RG, Bronze MS, Brackett DJ (2006) Systemic bone loss and induction of coronary vessel disease in a rat model of chronic inflammation. Bone 38(3):378–386CrossRefPubMed
20.
Zurück zum Zitat Wang JS, Luo H, Wang P, Tang L, Yu J, Huang T, Cox S, Gao W (2008) Validation of green tea polyphenol biomarkers in a phase II human intervention trial. Food Chem Toxicol 46(1):232–240CrossRefPubMed Wang JS, Luo H, Wang P, Tang L, Yu J, Huang T, Cox S, Gao W (2008) Validation of green tea polyphenol biomarkers in a phase II human intervention trial. Food Chem Toxicol 46(1):232–240CrossRefPubMed
21.
Zurück zum Zitat Shen CL, Wang P, Guerrieri J, Yeh JK, Wang JS (2008) Protective effect of green tea polyphenols on bone loss in middle-aged female rats. Osteoporos Int 19(7):979–990CrossRefPubMed Shen CL, Wang P, Guerrieri J, Yeh JK, Wang JS (2008) Protective effect of green tea polyphenols on bone loss in middle-aged female rats. Osteoporos Int 19(7):979–990CrossRefPubMed
22.
Zurück zum Zitat Villanueva AR, Mehr LA (1977) Modifications of the Goldner and Gomori one-step trichrome stains for plastic-embedded thin sections of bone. Am J Medica Tech 43:536–538 Villanueva AR, Mehr LA (1977) Modifications of the Goldner and Gomori one-step trichrome stains for plastic-embedded thin sections of bone. Am J Medica Tech 43:536–538
23.
Zurück zum Zitat Parfitt AM, Drezner MJ, Glorieux FH, Kanis JA, Malluche H, Meunier PJ (1987) Bone histomorphometry: standardization of nomenclature, symbols and units. Report of the ASBMR Histomorphometry Nomenclature Committee. J Bone Miner Res 2:595–610CrossRefPubMed Parfitt AM, Drezner MJ, Glorieux FH, Kanis JA, Malluche H, Meunier PJ (1987) Bone histomorphometry: standardization of nomenclature, symbols and units. Report of the ASBMR Histomorphometry Nomenclature Committee. J Bone Miner Res 2:595–610CrossRefPubMed
24.
Zurück zum Zitat Nielsen FH (2004) Dietary fat composition modifies the effect of boron on bone characteristics and plasma lipids in rats. BioFactors 20:161–171CrossRefPubMed Nielsen FH (2004) Dietary fat composition modifies the effect of boron on bone characteristics and plasma lipids in rats. BioFactors 20:161–171CrossRefPubMed
25.
Zurück zum Zitat Crenshaw TD, Peo ER, Lewis AJ Jr, Moser BD (1981) Bone strength as a trait for assessing mineralization in swine: a critical review of techniques involved. J Anim Sci 53:827–835 Crenshaw TD, Peo ER, Lewis AJ Jr, Moser BD (1981) Bone strength as a trait for assessing mineralization in swine: a critical review of techniques involved. J Anim Sci 53:827–835
26.
Zurück zum Zitat Nakagawa H, Wachi M, Woo JT, Kato M, Kasai S, Takahashi F, Lee IS, Nagai K (2002) Fenton reaction is primarily involved in a mechanism of (-)-epigallocatechin-3-gallate to induce osteoclastic cell death. Biochem Biophys Res Commun 292(1):94–101CrossRefPubMed Nakagawa H, Wachi M, Woo JT, Kato M, Kasai S, Takahashi F, Lee IS, Nagai K (2002) Fenton reaction is primarily involved in a mechanism of (-)-epigallocatechin-3-gallate to induce osteoclastic cell death. Biochem Biophys Res Commun 292(1):94–101CrossRefPubMed
27.
Zurück zum Zitat Hafeez BB, Ahmed S, Wang N, Gupta S, Zhang A, Haqqi TM (2006) Green tea polyphenols induced apoptosis in human osteosarcoma SAOS-2 cells involves a caspase-dependent mechanism with downregulation of nuclear factor-kappaB. Toxicol Appl Pharmacol 216(1):11–19CrossRefPubMed Hafeez BB, Ahmed S, Wang N, Gupta S, Zhang A, Haqqi TM (2006) Green tea polyphenols induced apoptosis in human osteosarcoma SAOS-2 cells involves a caspase-dependent mechanism with downregulation of nuclear factor-kappaB. Toxicol Appl Pharmacol 216(1):11–19CrossRefPubMed
28.
Zurück zum Zitat Nakagawa H, Hasumi K, Takami M, Aida-Hyugaji S, Woo JT, Nagai K, Ishikawa T, Wachi M (2007) Identification of two biologically crucial hydroxyl groups of (-)-epigallocatechin gallate in osteoclast culture. Biochem Pharmacol 73(1):34–43CrossRefPubMed Nakagawa H, Hasumi K, Takami M, Aida-Hyugaji S, Woo JT, Nagai K, Ishikawa T, Wachi M (2007) Identification of two biologically crucial hydroxyl groups of (-)-epigallocatechin gallate in osteoclast culture. Biochem Pharmacol 73(1):34–43CrossRefPubMed
29.
Zurück zum Zitat Yun JH, Pang EK, Kim CS, Yoo YJ, Cho KS, Chai JK, Kim CK, Choi SH (2009) Inhibitory effects of green tea polyphenol (-)-epigallocatechin gallate on the expression of matrix metalloproteinase-9 and on the formation of osteoclasts. J Periodontal Res 39(5):300–307CrossRef Yun JH, Pang EK, Kim CS, Yoo YJ, Cho KS, Chai JK, Kim CK, Choi SH (2009) Inhibitory effects of green tea polyphenol (-)-epigallocatechin gallate on the expression of matrix metalloproteinase-9 and on the formation of osteoclasts. J Periodontal Res 39(5):300–307CrossRef
30.
Zurück zum Zitat Takayanagi H, Kim S, Taniguchi T (2002) Signaling crosstalk between RANKL and interferons in osteoclast differentiation. Arthritis Res 4(Suppl 3):S227–S232, ReviewCrossRefPubMed Takayanagi H, Kim S, Taniguchi T (2002) Signaling crosstalk between RANKL and interferons in osteoclast differentiation. Arthritis Res 4(Suppl 3):S227–S232, ReviewCrossRefPubMed
31.
Zurück zum Zitat Lee JH, Jin H, Shim HE, Kim HN, Ha H, Lee ZH (2009) Epigallocatechin-3-gallate inhibits osteoclastogenesis by down-regulating c-Fos expression and suppressing the NF-{kappa}B signal. Mol Pharmacol Oct 14 (in press) Lee JH, Jin H, Shim HE, Kim HN, Ha H, Lee ZH (2009) Epigallocatechin-3-gallate inhibits osteoclastogenesis by down-regulating c-Fos expression and suppressing the NF-{kappa}B signal. Mol Pharmacol Oct 14 (in press)
32.
Zurück zum Zitat Matsunaga K, Klein TW, Friedman H, Yamamoto Y (2002) In vitro therapeutic effect of epigallocatechin gallate on nicotine-induced impairment of resistance to Legionella pneumophila infection of established MH-S alveolar macrophages. J Infect Dis 185(2):229–236CrossRefPubMed Matsunaga K, Klein TW, Friedman H, Yamamoto Y (2002) In vitro therapeutic effect of epigallocatechin gallate on nicotine-induced impairment of resistance to Legionella pneumophila infection of established MH-S alveolar macrophages. J Infect Dis 185(2):229–236CrossRefPubMed
33.
Zurück zum Zitat Balga R, Wetterwald A, Portenier J, Dolder S, Mueller C, Hofstetter W (2006) Tumor necrosis factor-alpha: alternative role as an inhibitor of osteoclast formation in vitro. Bone 39(2):325–335CrossRefPubMed Balga R, Wetterwald A, Portenier J, Dolder S, Mueller C, Hofstetter W (2006) Tumor necrosis factor-alpha: alternative role as an inhibitor of osteoclast formation in vitro. Bone 39(2):325–335CrossRefPubMed
34.
Zurück zum Zitat Armour KJ, Armour KE, van’t Hof RJ, Reid DM, Wei XQ, Liew FY, Ralston SH (2001) Activation of the inducible nitric oxide synthase pathway contributes to inflammation-induced osteoporosis by suppressing bone formation and causing osteoblast apoptosis. Arthritis Rheum 44(12):2790–2796CrossRefPubMed Armour KJ, Armour KE, van’t Hof RJ, Reid DM, Wei XQ, Liew FY, Ralston SH (2001) Activation of the inducible nitric oxide synthase pathway contributes to inflammation-induced osteoporosis by suppressing bone formation and causing osteoblast apoptosis. Arthritis Rheum 44(12):2790–2796CrossRefPubMed
35.
Zurück zum Zitat Dumitrescu AL, Abd-El-Aleem S, Morales-Aza B, Donaldson LF (2004) A model of periodontitis in the rat: effect of lipopolysaccharide on bone resorption, osteoclast activity, and local peptidergic innervation. J Clin Periodontol 31(8):596–603CrossRefPubMed Dumitrescu AL, Abd-El-Aleem S, Morales-Aza B, Donaldson LF (2004) A model of periodontitis in the rat: effect of lipopolysaccharide on bone resorption, osteoclast activity, and local peptidergic innervation. J Clin Periodontol 31(8):596–603CrossRefPubMed
36.
Zurück zum Zitat Droke EA, Hager KA, Lerner MR, Lightfoot SA, Stoecker BJ, Brackett DJ, Smith BJ (2007) Soy isoflavones avert chronic inflammation-induced bone loss and vascular disease. J Inflamm (Lond) 4:17CrossRef Droke EA, Hager KA, Lerner MR, Lightfoot SA, Stoecker BJ, Brackett DJ, Smith BJ (2007) Soy isoflavones avert chronic inflammation-induced bone loss and vascular disease. J Inflamm (Lond) 4:17CrossRef
Metadaten
Titel
Green tea polyphenols attenuate deterioration of bone microarchitecture in female rats with systemic chronic inflammation
verfasst von
C.-L. Shen
J. K. Yeh
C. Samathanam
J. J. Cao
B. J. Stoecker
R. Y. Dagda
M.-C. Chyu
D. M. Dunn
J.-S. Wang
Publikationsdatum
01.01.2011
Verlag
Springer-Verlag
Erschienen in
Osteoporosis International / Ausgabe 1/2011
Print ISSN: 0937-941X
Elektronische ISSN: 1433-2965
DOI
https://doi.org/10.1007/s00198-010-1209-2

Weitere Artikel der Ausgabe 1/2011

Osteoporosis International 1/2011 Zur Ausgabe

Arthropedia

Grundlagenwissen der Arthroskopie und Gelenkchirurgie. Erweitert durch Fallbeispiele, Videos und Abbildungen. 
» Jetzt entdecken

Update Orthopädie und Unfallchirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.