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Published in: BMC Complementary Medicine and Therapies 1/2021

Open Access 01-12-2021 | Osteoarthrosis | Research

The benefit of combining curcumin, bromelain and harpagophytum to reduce inflammation in osteoarthritic synovial cells

Authors: Sybille Brochard, Julien Pontin, Benoit Bernay, Karim Boumediene, Thierry Conrozier, Catherine Baugé

Published in: BMC Complementary Medicine and Therapies | Issue 1/2021

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Abstract

Background

Osteoarthritis (OA) is the most common form of arthritis, affecting millions of people worldwide and characterised by joint pain and inflammation. It is a complex disease involving inflammatory factors and affecting the whole joint, including the synovial membrane. Since drug combination is widely used to treat chronic inflammatory diseases, a similar strategy of designing plant-derived natural products to reduce inflammation in OA joints may be of interest. In this study, we characterised the response of OA synovial cells to lipopolysaccharide (LPS) and investigated the biological action of the combination of curcumin, bromelain and harpagophytum in this original in vitro model of osteoarthritis.

Methods

Firstly, human synovial cells from OA patients were stimulated with LPS and proteomic analysis was performed. Bioinformatics analyses were performed using Cytoscape App and SkeletalVis databases. Additionally, cells were treated with curcumin, bromelain and harpagophytum alone or with the three vegetal compounds together. The gene expression involved in inflammation, pain or catabolism was determined by RT-PCR. The release of the encoded proteins by these genes and of prostaglandin E2 (PGE2) were also assayed by ELISA.

Results

Proteomic analysis demonstrated that LPS induces the expression of numerous proteins involved in the OA process in human OA synovial cells. In particular, it stimulates inflammation through the production of pro-inflammatory cytokines (Interleukin-6, IL-6), catabolism through an increase of metalloproteases (MMP-1, MMP-3, MMP-13), and the production of pain-mediating neurotrophins (Nerve Growth Factor, NGF). These increases were observed in terms of mRNA levels and protein release. LPS also increases the amount of PGE2, another inflammation and pain mediator. At the doses tested, vegetal extracts had little effect: only curcumin slightly counteracted the effects of LPS on NGF and MMP-13 mRNA, and PGE2, IL-6 and MMP-13 release. In contrast, the combination of curcumin with bromelain and harpagophytum reversed lots of effects of LPS in human OA synovial cells. It significantly reduced the gene expression and/or the release of proteins involved in catabolism (MMP-3 and -13), inflammation (IL-6) and pain (PGE2 and NGF).

Conclusion

We have shown that the stimulation of human OA synovial cells with LPS can induce protein changes similar to inflamed OA synovial tissues. In addition, using this model, we demonstrated that the combination of three vegetal compounds, namely curcumin, bromelain and harpagophytum, have anti-inflammatory and anti-catabolic effects in synovial cells and may thus reduce OA progression and related pain.
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Literature
2.
go back to reference Berenbaum F. Osteoarthritis as an inflammatory disease (osteoarthritis is not osteoarthrosis!). Osteoarthr Cartil. 2013;21:16–21.CrossRef Berenbaum F. Osteoarthritis as an inflammatory disease (osteoarthritis is not osteoarthrosis!). Osteoarthr Cartil. 2013;21:16–21.CrossRef
3.
go back to reference Neogi T. The epidemiology and impact of pain in osteoarthritis. Osteoarthr Cartil. 2013;21:1145–53.CrossRef Neogi T. The epidemiology and impact of pain in osteoarthritis. Osteoarthr Cartil. 2013;21:1145–53.CrossRef
4.
go back to reference Robinson WH, Lepus CM, Wang Q, Raghu H, Mao R, Lindstrom TM, et al. Low-grade inflammation as a key mediator of the pathogenesis of osteoarthritis. Nat Rev Rheumatol. 2016;12:580–92.PubMedPubMedCentralCrossRef Robinson WH, Lepus CM, Wang Q, Raghu H, Mao R, Lindstrom TM, et al. Low-grade inflammation as a key mediator of the pathogenesis of osteoarthritis. Nat Rev Rheumatol. 2016;12:580–92.PubMedPubMedCentralCrossRef
5.
go back to reference Bigoni M, Sacerdote P, Turati M, Franchi S, Gandolla M, Gaddi D, et al. Acute and late changes in intraarticular cytokine levels following anterior cruciate ligament injury. J Orthop Res Off Publ Orthop Res Soc. 2013;31:315–21.CrossRef Bigoni M, Sacerdote P, Turati M, Franchi S, Gandolla M, Gaddi D, et al. Acute and late changes in intraarticular cytokine levels following anterior cruciate ligament injury. J Orthop Res Off Publ Orthop Res Soc. 2013;31:315–21.CrossRef
6.
go back to reference Kapoor M, Martel-Pelletier J, Lajeunesse D, Pelletier J-P, Fahmi H. Role of proinflammatory cytokines in the pathophysiology of osteoarthritis. Nat Rev Rheumatol. 2011;7:33–42.PubMedCrossRef Kapoor M, Martel-Pelletier J, Lajeunesse D, Pelletier J-P, Fahmi H. Role of proinflammatory cytokines in the pathophysiology of osteoarthritis. Nat Rev Rheumatol. 2011;7:33–42.PubMedCrossRef
7.
go back to reference Scotece M, Conde J, Abella V, López V, Francisco V, Ruiz C, et al. Oleocanthal inhibits catabolic and inflammatory mediators in LPS-activated human primary osteoarthritis (OA) chondrocytes through MAPKs/NF-κB pathways. Cell Physiol Biochem Int J Exp Cell Physiol Biochem Pharmacol. 2018;49:2414–26.CrossRef Scotece M, Conde J, Abella V, López V, Francisco V, Ruiz C, et al. Oleocanthal inhibits catabolic and inflammatory mediators in LPS-activated human primary osteoarthritis (OA) chondrocytes through MAPKs/NF-κB pathways. Cell Physiol Biochem Int J Exp Cell Physiol Biochem Pharmacol. 2018;49:2414–26.CrossRef
8.
go back to reference Konttinen YT, Sillat T, Barreto G, Ainola M, Nordström DCE. Osteoarthritis as an autoinflammatory disease caused by chondrocyte-mediated inflammatory responses. Arthritis Rheum. 2012;64:613–6.PubMedCrossRef Konttinen YT, Sillat T, Barreto G, Ainola M, Nordström DCE. Osteoarthritis as an autoinflammatory disease caused by chondrocyte-mediated inflammatory responses. Arthritis Rheum. 2012;64:613–6.PubMedCrossRef
9.
go back to reference Di Paola R, Fusco R, Impellizzeri D, Cordaro M, Britti D, Morittu VM, et al. Adelmidrol, in combination with hyaluronic acid, displays increased anti-inflammatory and analgesic effects against monosodium iodoacetate-induced osteoarthritis in rats. Arthritis Res Ther. 2016;18:291.PubMedPubMedCentralCrossRef Di Paola R, Fusco R, Impellizzeri D, Cordaro M, Britti D, Morittu VM, et al. Adelmidrol, in combination with hyaluronic acid, displays increased anti-inflammatory and analgesic effects against monosodium iodoacetate-induced osteoarthritis in rats. Arthritis Res Ther. 2016;18:291.PubMedPubMedCentralCrossRef
10.
go back to reference Cordaro M, Siracusa R, Impellizzeri D, D’ Amico R, Peritore AF, Crupi R, et al. Safety and efficacy of a new micronized formulation of the ALIAmide palmitoylglucosamine in preclinical models of inflammation and osteoarthritis pain. Arthritis Res Ther. 2019;21:254.PubMedPubMedCentralCrossRef Cordaro M, Siracusa R, Impellizzeri D, D’ Amico R, Peritore AF, Crupi R, et al. Safety and efficacy of a new micronized formulation of the ALIAmide palmitoylglucosamine in preclinical models of inflammation and osteoarthritis pain. Arthritis Res Ther. 2019;21:254.PubMedPubMedCentralCrossRef
11.
go back to reference Fusco R, Siracusa R, Peritore AF, Gugliandolo E, Genovese T, D’Amico R, et al. The Role of Cashew (Anacardium occidentale L.) Nuts on an Experimental Model of Painful Degenerative Joint Disease. Antioxidants. 2020;9:511.PubMedCentralCrossRef Fusco R, Siracusa R, Peritore AF, Gugliandolo E, Genovese T, D’Amico R, et al. The Role of Cashew (Anacardium occidentale L.) Nuts on an Experimental Model of Painful Degenerative Joint Disease. Antioxidants. 2020;9:511.PubMedCentralCrossRef
12.
go back to reference Xiao Y, Ding L, Yin S, Huang Z, Zhang L, Mei W, et al. Relationship between the pyroptosis of fibroblast-like synoviocytes and HMGB1 secretion in knee osteoarthritis. Mol Med Rep. 2021;23:1.CrossRef Xiao Y, Ding L, Yin S, Huang Z, Zhang L, Mei W, et al. Relationship between the pyroptosis of fibroblast-like synoviocytes and HMGB1 secretion in knee osteoarthritis. Mol Med Rep. 2021;23:1.CrossRef
13.
go back to reference Santangelo KS, Nuovo GJ, Bertone AL. In vivo reduction or blockade of interleukin-1β in primary osteoarthritis influences expression of mediators implicated in pathogenesis. Osteoarthr Cartil. 2012;20:1610–8.CrossRef Santangelo KS, Nuovo GJ, Bertone AL. In vivo reduction or blockade of interleukin-1β in primary osteoarthritis influences expression of mediators implicated in pathogenesis. Osteoarthr Cartil. 2012;20:1610–8.CrossRef
14.
go back to reference Griffin TM, Huebner JL, Kraus VB, Yan Z, Guilak F. Induction of osteoarthritis and metabolic inflammation by a very high-fat diet in mice: effects of short-term exercise. Arthritis Rheum. 2012;64:443–53.PubMedPubMedCentralCrossRef Griffin TM, Huebner JL, Kraus VB, Yan Z, Guilak F. Induction of osteoarthritis and metabolic inflammation by a very high-fat diet in mice: effects of short-term exercise. Arthritis Rheum. 2012;64:443–53.PubMedPubMedCentralCrossRef
15.
go back to reference Huang Z, Kraus VB. Does lipopolysaccharide-mediated inflammation have a role in OA? Nat Rev Rheumatol. 2016;12:123–9.PubMedCrossRef Huang Z, Kraus VB. Does lipopolysaccharide-mediated inflammation have a role in OA? Nat Rev Rheumatol. 2016;12:123–9.PubMedCrossRef
16.
go back to reference Li K, Liu A, Zong W, Dai L, Liu Y, Luo R, et al. Moderate exercise ameliorates osteoarthritis by reducing lipopolysaccharides from gut microbiota in mice. Saudi J Biol Sci. 2021;28:40–9.PubMedCrossRef Li K, Liu A, Zong W, Dai L, Liu Y, Luo R, et al. Moderate exercise ameliorates osteoarthritis by reducing lipopolysaccharides from gut microbiota in mice. Saudi J Biol Sci. 2021;28:40–9.PubMedCrossRef
18.
go back to reference Hosseini-Zare MS, Sarhadi M, Zarei M, Thilagavathi R, Selvam C. Synergistic effects of curcumin and its analogs with other bioactive compounds: a comprehensive review. Eur J Med Chem. 2021;210:113072.PubMedCrossRef Hosseini-Zare MS, Sarhadi M, Zarei M, Thilagavathi R, Selvam C. Synergistic effects of curcumin and its analogs with other bioactive compounds: a comprehensive review. Eur J Med Chem. 2021;210:113072.PubMedCrossRef
19.
go back to reference Henrotin Y, Malaise M, Wittoek R, de Vlam K, Brasseur J-P, Luyten FP, et al. Bio-optimized Curcuma longa extract is efficient on knee osteoarthritis pain: a double-blind multicenter randomized placebo controlled three-arm study. Arthritis Res Ther. 2019;21. https://doi.org/10.1186/s13075-019-1960-5. Henrotin Y, Malaise M, Wittoek R, de Vlam K, Brasseur J-P, Luyten FP, et al. Bio-optimized Curcuma longa extract is efficient on knee osteoarthritis pain: a double-blind multicenter randomized placebo controlled three-arm study. Arthritis Res Ther. 2019;21. https://​doi.​org/​10.​1186/​s13075-019-1960-5.
20.
go back to reference Madhu K, Chanda K, Saji MJ. Safety and efficacy of Curcuma longa extract in the treatment of painful knee osteoarthritis: a randomized placebo-controlled trial. Inflammopharmacology. 2013;21:129–36.PubMedCrossRef Madhu K, Chanda K, Saji MJ. Safety and efficacy of Curcuma longa extract in the treatment of painful knee osteoarthritis: a randomized placebo-controlled trial. Inflammopharmacology. 2013;21:129–36.PubMedCrossRef
21.
go back to reference Atabaki M, Shariati-Sarabi Z, Tavakkol-Afshari J, Mohammadi M. Significant immunomodulatory properties of curcumin in patients with osteoarthritis; a successful clinical trial in Iran. Int Immunopharmacol. 2020;85:106607.PubMedCrossRef Atabaki M, Shariati-Sarabi Z, Tavakkol-Afshari J, Mohammadi M. Significant immunomodulatory properties of curcumin in patients with osteoarthritis; a successful clinical trial in Iran. Int Immunopharmacol. 2020;85:106607.PubMedCrossRef
22.
go back to reference Nakagawa Y, Mukai S, Yamada S, Murata S, Yabumoto H, Maeda T, et al. The efficacy and safety of highly-bioavailable Curcumin for treating knee osteoarthritis: a 6-month open-labeled prospective study. Clin Med Insights Arthritis Musculoskelet Disord. 2020;13:1179544120948471.PubMedPubMedCentralCrossRef Nakagawa Y, Mukai S, Yamada S, Murata S, Yabumoto H, Maeda T, et al. The efficacy and safety of highly-bioavailable Curcumin for treating knee osteoarthritis: a 6-month open-labeled prospective study. Clin Med Insights Arthritis Musculoskelet Disord. 2020;13:1179544120948471.PubMedPubMedCentralCrossRef
23.
go back to reference Belcaro G, Cesarone MR, Dugall M, Pellegrini L, Ledda A, Grossi MG, et al. Efficacy and safety of Meriva®, a curcumin-phosphatidylcholine complex, during extended administration in osteoarthritis patients. Altern Med Rev J Clin Ther. 2010;15:337–44. Belcaro G, Cesarone MR, Dugall M, Pellegrini L, Ledda A, Grossi MG, et al. Efficacy and safety of Meriva®, a curcumin-phosphatidylcholine complex, during extended administration in osteoarthritis patients. Altern Med Rev J Clin Ther. 2010;15:337–44.
24.
go back to reference Yeh C-C, Su Y-H, Lin Y-J, Chen P-J, Shi C-S, Chen C-N, et al. Evaluation of the protective effects of curcuminoid (curcumin and bisdemethoxycurcumin)-loaded liposomes against bone turnover in a cell-based model of osteoarthritis. Drug Des Devel Ther. 2015;9:2285–300.PubMedPubMedCentral Yeh C-C, Su Y-H, Lin Y-J, Chen P-J, Shi C-S, Chen C-N, et al. Evaluation of the protective effects of curcuminoid (curcumin and bisdemethoxycurcumin)-loaded liposomes against bone turnover in a cell-based model of osteoarthritis. Drug Des Devel Ther. 2015;9:2285–300.PubMedPubMedCentral
25.
go back to reference Nicoliche T, Maldonado DC, Faber J, da Silva MCP. Evaluation of the articular cartilage in the knees of rats with induced arthritis treated with curcumin. PLoS One. 2020;15:e0230228.PubMedPubMedCentralCrossRef Nicoliche T, Maldonado DC, Faber J, da Silva MCP. Evaluation of the articular cartilage in the knees of rats with induced arthritis treated with curcumin. PLoS One. 2020;15:e0230228.PubMedPubMedCentralCrossRef
26.
go back to reference Jhun J, Min H-K, Na HS, Kwon JY, Ryu J, Cho K-H, et al. Combinatmarion treatment with lactobacillus acidophilus LA-1, vitamin B, and curcumin ameliorates the progression of osteoarthritis by inhibiting the pro-inflammatory mediators. Immunol Lett. 2020;228:112–21.PubMedCrossRef Jhun J, Min H-K, Na HS, Kwon JY, Ryu J, Cho K-H, et al. Combinatmarion treatment with lactobacillus acidophilus LA-1, vitamin B, and curcumin ameliorates the progression of osteoarthritis by inhibiting the pro-inflammatory mediators. Immunol Lett. 2020;228:112–21.PubMedCrossRef
28.
go back to reference Mariano A, Di Sotto A, Leopizzi M, Garzoli S, Di Maio V, Gullì M, et al. Antiarthritic effects of a root extract from Harpagophytum procumbens DC: novel insights into the molecular mechanisms and possible bioactive phytochemicals. Nutrients. 2020;12:2545. Mariano A, Di Sotto A, Leopizzi M, Garzoli S, Di Maio V, Gullì M, et al. Antiarthritic effects of a root extract from Harpagophytum procumbens DC: novel insights into the molecular mechanisms and possible bioactive phytochemicals. Nutrients. 2020;12:2545.
29.
go back to reference Allas L, Brochard S, Rochoux Q, Ribet J, Dujarrier C, Veyssiere A, et al. EZH2 inhibition reduces cartilage loss and functional impairment related to osteoarthritis. Sci Rep. 2020;10:19577.PubMedPubMedCentralCrossRef Allas L, Brochard S, Rochoux Q, Ribet J, Dujarrier C, Veyssiere A, et al. EZH2 inhibition reduces cartilage loss and functional impairment related to osteoarthritis. Sci Rep. 2020;10:19577.PubMedPubMedCentralCrossRef
30.
go back to reference Fischer R, Kessler BM. Gel-aided sample preparation (GASP)—a simplified method for gel-assisted proteomic sample generation from protein extracts and intact cells. Proteomics. 2015;15:1224–9.PubMedPubMedCentralCrossRef Fischer R, Kessler BM. Gel-aided sample preparation (GASP)—a simplified method for gel-assisted proteomic sample generation from protein extracts and intact cells. Proteomics. 2015;15:1224–9.PubMedPubMedCentralCrossRef
31.
go back to reference Meier F, Brunner A-D, Koch S, Koch H, Lubeck M, Krause M, et al. Online parallel accumulation-serial fragmentation (PASEF) with a novel trapped ion mobility mass spectrometer. Mol Cell Proteomics MCP. 2018;17:2534–45.PubMedCrossRef Meier F, Brunner A-D, Koch S, Koch H, Lubeck M, Krause M, et al. Online parallel accumulation-serial fragmentation (PASEF) with a novel trapped ion mobility mass spectrometer. Mol Cell Proteomics MCP. 2018;17:2534–45.PubMedCrossRef
32.
go back to reference Tran NH, Qiao R, Xin L, Chen X, Liu C, Zhang X, et al. Deep learning enables de novo peptide sequencing from data-independent-acquisition mass spectrometry. Nat Methods. 2019;16:63–6.PubMedCrossRef Tran NH, Qiao R, Xin L, Chen X, Liu C, Zhang X, et al. Deep learning enables de novo peptide sequencing from data-independent-acquisition mass spectrometry. Nat Methods. 2019;16:63–6.PubMedCrossRef
33.
go back to reference Soul J, Hardingham TE, Boot-Handford RP, Schwartz J-M. SkeletalVis: an exploration and meta-analysis data portal of cross-species skeletal transcriptomics data. Bioinformatics. 2019;35:2283–90.PubMedCrossRef Soul J, Hardingham TE, Boot-Handford RP, Schwartz J-M. SkeletalVis: an exploration and meta-analysis data portal of cross-species skeletal transcriptomics data. Bioinformatics. 2019;35:2283–90.PubMedCrossRef
34.
go back to reference Soul J, Barter MJ, Little CB, Young DA. OATargets: a knowledge base of genes associated with osteoarthritis joint damage in animals. Ann Rheum Dis. 2021;80:376–83.CrossRef Soul J, Barter MJ, Little CB, Young DA. OATargets: a knowledge base of genes associated with osteoarthritis joint damage in animals. Ann Rheum Dis. 2021;80:376–83.CrossRef
35.
go back to reference Allas L, Rochoux Q, Leclercq S, Boumédiene K, Baugé C. Development of a simple osteoarthritis model useful to predict in vitro the anti-hypertrophic action of drugs. Lab Investig J Tech Methods Pathol. 2020;100:64–71.CrossRef Allas L, Rochoux Q, Leclercq S, Boumédiene K, Baugé C. Development of a simple osteoarthritis model useful to predict in vitro the anti-hypertrophic action of drugs. Lab Investig J Tech Methods Pathol. 2020;100:64–71.CrossRef
36.
go back to reference Aury-Landas J, Bazille C, Allas L, Bouhout S, Chesneau C, Leclercq S, et al. Anti-inflammatory and chondroprotective effects of the S-adenosylhomocysteine hydrolase inhibitor 3-Deazaneplanocin a, in human articular chondrocytes. Sci Rep. 2017;7:6483.PubMedPubMedCentralCrossRef Aury-Landas J, Bazille C, Allas L, Bouhout S, Chesneau C, Leclercq S, et al. Anti-inflammatory and chondroprotective effects of the S-adenosylhomocysteine hydrolase inhibitor 3-Deazaneplanocin a, in human articular chondrocytes. Sci Rep. 2017;7:6483.PubMedPubMedCentralCrossRef
37.
go back to reference Lorenz W, Buhrmann C, Mobasheri A, Lueders C, Shakibaei M. Bacterial lipopolysaccharides form procollagen-endotoxin complexes that trigger cartilage inflammation and degeneration: implications for the development of rheumatoid arthritis. Arthritis Res Ther. 2013;15:R111.PubMedPubMedCentralCrossRef Lorenz W, Buhrmann C, Mobasheri A, Lueders C, Shakibaei M. Bacterial lipopolysaccharides form procollagen-endotoxin complexes that trigger cartilage inflammation and degeneration: implications for the development of rheumatoid arthritis. Arthritis Res Ther. 2013;15:R111.PubMedPubMedCentralCrossRef
38.
go back to reference Caccese RG, Zimmerman JL, Carlson RP. Bacterial lipopolysaccharide potentiates type II collagen-induced arthritis in mice. Mediat Inflamm. 1992;1:273–9.CrossRef Caccese RG, Zimmerman JL, Carlson RP. Bacterial lipopolysaccharide potentiates type II collagen-induced arthritis in mice. Mediat Inflamm. 1992;1:273–9.CrossRef
39.
go back to reference Huang ZY, Stabler T, Pei FX, Kraus VB. Both systemic and local lipopolysaccharide (LPS) burden are associated with knee OA severity and inflammation. Osteoarthr Cartil. 2016;24:1769–75.CrossRef Huang ZY, Stabler T, Pei FX, Kraus VB. Both systemic and local lipopolysaccharide (LPS) burden are associated with knee OA severity and inflammation. Osteoarthr Cartil. 2016;24:1769–75.CrossRef
40.
go back to reference Mendez ME, Sebastian A, Murugesh DK, Hum NR, McCool JL, Hsia AW, et al. LPS-induced inflammation prior to injury exacerbates the development of post-traumatic osteoarthritis in mice. J Bone Miner Res Off J Am Soc Bone Miner Res. 2020;35:2229–41.CrossRef Mendez ME, Sebastian A, Murugesh DK, Hum NR, McCool JL, Hsia AW, et al. LPS-induced inflammation prior to injury exacerbates the development of post-traumatic osteoarthritis in mice. J Bone Miner Res Off J Am Soc Bone Miner Res. 2020;35:2229–41.CrossRef
41.
go back to reference Park S, Lee LR, Seo JH, Kang S. Curcumin and tetrahydrocurcumin both prevent osteoarthritis symptoms and decrease the expressions of pro-inflammatory cytokines in estrogen-deficient rats. Genes Nutr. 2016;11:2.PubMedPubMedCentralCrossRef Park S, Lee LR, Seo JH, Kang S. Curcumin and tetrahydrocurcumin both prevent osteoarthritis symptoms and decrease the expressions of pro-inflammatory cytokines in estrogen-deficient rats. Genes Nutr. 2016;11:2.PubMedPubMedCentralCrossRef
42.
go back to reference Yang Q, Wu S, Mao X, Wang W, Tai H. Inhibition effect of curcumin on TNF-α and MMP-13 expression induced by advanced glycation end products in chondrocytes. Pharmacology. 2013;91:77–85.PubMedCrossRef Yang Q, Wu S, Mao X, Wang W, Tai H. Inhibition effect of curcumin on TNF-α and MMP-13 expression induced by advanced glycation end products in chondrocytes. Pharmacology. 2013;91:77–85.PubMedCrossRef
43.
go back to reference Kumar D, Kumar M, Saravanan C, Singh SK. Curcumin: a potential candidate for matrix metalloproteinase inhibitors. Expert Opin Ther Targets. 2012;16:959–72.PubMedCrossRef Kumar D, Kumar M, Saravanan C, Singh SK. Curcumin: a potential candidate for matrix metalloproteinase inhibitors. Expert Opin Ther Targets. 2012;16:959–72.PubMedCrossRef
44.
go back to reference Zhao P, Cheng J, Geng J, Yang M, Zhang Y, Zhang Q, et al. Curcumin protects rabbit articular chondrocytes against sodium nitroprusside-induced apoptosis in vitro. Eur J Pharmacol. 2018;828:146–53.PubMedCrossRef Zhao P, Cheng J, Geng J, Yang M, Zhang Y, Zhang Q, et al. Curcumin protects rabbit articular chondrocytes against sodium nitroprusside-induced apoptosis in vitro. Eur J Pharmacol. 2018;828:146–53.PubMedCrossRef
45.
go back to reference Dragos D, Gilca M, Gaman L, Vlad A, Iosif L, Stoian I, et al. Phytomedicine in joint disorders. Nutrients. 2017;9. Dragos D, Gilca M, Gaman L, Vlad A, Iosif L, Stoian I, et al. Phytomedicine in joint disorders. Nutrients. 2017;9.
46.
go back to reference Gagnier JJ, Chrubasik S, Manheimer E. Harpgophytum procumbens for osteoarthritis and low back pain: a systematic review. BMC Complement Altern Med. 2004;4:13.PubMedPubMedCentralCrossRef Gagnier JJ, Chrubasik S, Manheimer E. Harpgophytum procumbens for osteoarthritis and low back pain: a systematic review. BMC Complement Altern Med. 2004;4:13.PubMedPubMedCentralCrossRef
47.
go back to reference Lim DW, Kim JG, Han D, Kim YT. Analgesic effect of Harpagophytum procumbens on postoperative and neuropathic pain in rats. Mol Basel Switz. 2014;19:1060–8. Lim DW, Kim JG, Han D, Kim YT. Analgesic effect of Harpagophytum procumbens on postoperative and neuropathic pain in rats. Mol Basel Switz. 2014;19:1060–8.
48.
go back to reference Brien S, Lewith G, Walker A, Hicks SM, Middleton D. Bromelain as a treatment for osteoarthritis: a review of clinical studies. Evid-Based Complement Altern Med ECAM. 2004;1:251–7.CrossRef Brien S, Lewith G, Walker A, Hicks SM, Middleton D. Bromelain as a treatment for osteoarthritis: a review of clinical studies. Evid-Based Complement Altern Med ECAM. 2004;1:251–7.CrossRef
49.
go back to reference Cohen A, Goldman J. Bromelains therapy in rheumatoid arthritis. Pa Med J. 1928;1964(67):27–30. Cohen A, Goldman J. Bromelains therapy in rheumatoid arthritis. Pa Med J. 1928;1964(67):27–30.
50.
go back to reference Kumakura S, Yamashita M, Tsurufuji S. Effect of bromelain on kaolin-induced inflammation in rats. Eur J Pharmacol. 1988;150:295–301.PubMedCrossRef Kumakura S, Yamashita M, Tsurufuji S. Effect of bromelain on kaolin-induced inflammation in rats. Eur J Pharmacol. 1988;150:295–301.PubMedCrossRef
Metadata
Title
The benefit of combining curcumin, bromelain and harpagophytum to reduce inflammation in osteoarthritic synovial cells
Authors
Sybille Brochard
Julien Pontin
Benoit Bernay
Karim Boumediene
Thierry Conrozier
Catherine Baugé
Publication date
01-12-2021
Publisher
BioMed Central
Published in
BMC Complementary Medicine and Therapies / Issue 1/2021
Electronic ISSN: 2662-7671
DOI
https://doi.org/10.1186/s12906-021-03435-7

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