Skip to main content
NCBI home page
The Journal of International Medical Research logoLink to The Journal of International Medical Research
. 2022 Aug 23;50(8):03000605221104764. doi: 10.1177/03000605221104764

Loganin attenuates interleukin-1β-induced chondrocyte inflammation, cartilage degeneration, and rat synovial inflammation by regulating TLR4/MyD88/NF-κB

Haishan Wan 1,*, Chaoyi Li 2,*, Yi Yang 3, Dingzhong Chen 3,✉
PMCID: PMC9421229  PMID: 36000146

Abstract

Objective

Inflammation plays a crucial part in osteoarthritis (OA) development. This work aimed to explore loganin’s role and molecular mechanism in inflammation and clarify its anti-inflammatory effects in OA treatment.

Methods

Chondrocytes were stimulated using interleukin (IL)-1β and loganin at two concentrations (1 μM and 10 μM). Nitric oxide (NO) and prostaglandin E2 (PGE2) expression was assessed. Real-time polymerase chain reaction was used to evaluate inducible NO synthase (iNOS), cyclooxygenase (COX)-2, IL-6, and tumor necrosis factor (TNF)-α mRNA levels. Western blot was used to investigate TLR4, MyD88, p-p65, and IκB-α expression. p65 nuclear translocation, synovial inflammatory response, and cartilage degeneration were also assessed.

Results

Loganin significantly reduced IL-1β-mediated PGE2, NO, iNOS, and COX-2 expression compared with that of the IL-1β stimulation group. The TLR4/MyD88/NF-κB pathway was suppressed by loganin, which decreased inflammatory cytokine (TNF-α and IL-6) levels compared with those of the IL-1β stimulation group. Loganin inhibited IL-1β-mediated NF-κB p65 nuclear translocation compared with that of the IL-1β stimulation group. Loganin partially suppressed cartilage degeneration and the synovial inflammatory response in vivo.

Conclusion

This work demonstrated that loganin inhibited IL-1β-mediated inflammation in rat chondrocytes through TLR4/MyD88/NF-κB pathway regulation, thereby reducing rat cartilage degeneration and the synovial inflammatory response.

Keywords: TLR4/MyD88/NF-κB, loganin, osteoarthritis, inflammation, chondrocyte, interleukin, cytokine, nuclear translocation

Introduction

Osteoarthritis (OA) is a chronic joint disease that affects and disables 1 × 108 people around the world and contributes to a large societal burden. 1 Several studies have revealed the importance of chronic inflammation in OA development. Various inflammatory factors, including tumor necrosis factor (TNF)-α and interleukin (IL)-1, -8, -6, -15, and -33, increase in the cartilage in OA patients’ joints, and these factors mediate cartilage degeneration.2–4 IL-1β has been widely studied in OA pathophysiology to stimulate inflammatory cytokine release and chondrocyte apoptosis. 5 Matrix metalloproteases (MMPs) and a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) are degradation enzymes that can be upregulated by several transcription factors, especially nuclear factor kappa B (NF-κB). 6 The microenvironment of inflammatory cytokines combined with older age and biomechanical stress increase the oxidative stress, contributing to up-regulation of reactive oxygen species (ROS) including nitric oxide (NO), prostaglandins (PGs), and superoxide anion and down-regulation of anti-oxidative enzymes. 7 These changes contribute to joint cartilage destruction and bone metabolism, increasing the generation of chondrocytes, osteoblasts, and their precursors. 7 Therefore, regulation of the inflammatory microenvironment homeostasis contributes to OA development.

Loganin is an iridoid glycoside that is isolated from herbs such as Flos lonicerae and Cornus mas L. It mediates immune function and has anti-inflammatory and anti-oxidative effects through inhibiting NF-κB signaling to decrease the release of IL-6, TNF-α, and other inflammatory factors. Loganin attenuates the intestinal inflammatory reaction and oxidative stress through TLR4/NF-κB modulation. 8 It also had an obvious anti-oxidative stress and anti-inflammatory effect on diabetes mellitus-induced reproductive damage through restoration of glutathione levels and superoxide dismutase activity and reduction of reactive oxygen species. 9 Our previous research showed that loganin caused reduced extracellular matrix (ECM) catabolism and IL-1β-induced apoptosis in rat chondrocytes through the regulation of PI3K/Akt signaling. This suggests that loganin is a potential alternative in OA treatment. 10 To further explore loganin’s protective mechanisms, the present research aimed to clarify whether loganin had anti-inflammatory effects in OA treatment.

Materials and methods

Reagents

Loganin was obtained from Sigma-Aldrich (St. Louis, MO, USA, ≥97.0%, Figure 1a). IL-1β was obtained from R&D Systems (St. Paul, MN, USA). Antibodies were purchased from Cell Signaling Technology (Beverly, MA, USA) and Santa Cruz Biotechnology Inc. (Santa Cruz, CA, USA). All other reagents were obtained from Sigma-Aldrich.

Figure 1.

Figure 1.

Open in a new tab

(a) Loganin chemical structure and (b) Primary chondrocyte morphology.

Chondrocyte culture and drug administration

Chondrocytes were isolated from the knee joint of normal Sprague–Dawley rats. 11 Cartilage was removed, minced, and incubated with collagenase II (2 mg/mL) in a cell incubator for 3 to 6 hours.12,13 The samples were then filtered via a filtration system (70 μm) and the solution was centrifuged (300 × g, 5 minutes, 37°C), washed, and incubated with DMEM/F12 medium containing 10% fetal bovine serum. We evaluated the cell morphology (isogenous and elliptic) from primary chondrocytes (Figure 1b). The medium was changed every 2 days, and chondrocytes were passaged after reaching 70% to 80% confluence. Loganin or IL-1β at 10 ng/mL was added to chondrocytes at P2 for 2 hours. The cells were then collected for subsequent testing. All animal experiments were approved by the Animal Care and Use Committee of Hainan Medical College (2016-35).

Chondrocytes were divided into the following four groups: control, IL-1β, 1 μM loganin, and 10 μM loganin. Among these groups, COX-2, iNOS, IL-6, and TNF-α mRNA expression and TLR4, MyD88, p-p65, and IκB-α were evaluated.

Quantitative real time polymerase chain reaction

COX-2, iNOS, IL-6, and TNF-α mRNA expression was assessed. mRNA was isolated using the TRIzol method. The specimen concentration was measured spectrophotometrically at 260 nm, and cDNA synthesis was performed with 1 μg of RNA using the cDNA Synthesis Kit (Thermo Scientific, Waltham, MA, USA). Quantitative real time polymerase chain reaction (PCR) was conducted using SYBR Premix Ex Taq™ under the following conditions: 10 minutes at 95°C and 40 cycles of 15 s at 95°C and 1 minute at 60°C. iNOS, COX-2, TNF-α, and IL-6 mRNA levels were compared with β-actin.

Western blot

Chondrocytes were lysed via a protease- and phosphatase-containing RIPA buffer. The protein concentration was calculated using the Bio-Rad Laboratories protein reagent (Bio-Rad, Hercules, CA, USA). Cellular lysates (20 ng) were separated using polyacrylamide gel electrophoresis. The protein was then transferred onto poly(vinylidene fluoride) membranes for antibody blotting. Specific antibodies were used (e.g., anti-TLR4, anti-MyD88, anti-p-p65, anti-IκB-α, and anti-β-actin) overnight followed by the appropriate secondary antibodies. An enhanced chemiluminescence system (Amersham Biosciences, Piscataway, NJ, USA) was used to visualize the immunoreactive bands.

NO measurement and enzyme-linked immunosorbent assay

NO production was tested by measuring the levels of the stable NO metabolite nitrite using sodium nitrite resuspended in distilled H2O as a standard. 14 The NO concentration was quantitatively measured using the Griess reaction. 15 NO expression was tested by evaluating the expression of the stable metabolite nitrite of NO. After incubation with loganin for 2 hours, cells were simulated with IL-1β (10 ng/mL) for 1 day. The supernatant was incubated with the Griess solution in a 96-well plate for 10 minutes. The specimen was tested using a spectrophotometer at 540 nm. PGE2, IL-1β, IL-6, and TNF-α expression within the medium and rat synovial fluid were measured using ELISA kits (R&D Systems, Minneapolis, MN, USA) in accordance with the manufacturer’s protocol.

Rat osteoarthritis model

Sprague–Dawley rats (200–250 g) were divided into the following three groups: sham, OA, and OA + loganin. Rats in the OA and OA + loganin groups underwent anterior cruciate ligament (ACL) transection and medial meniscus resection in the right knee. The sham rats underwent the same surgery without ACL or meniscus intervention. After surgery, the rats in the OA + loganin group were administered loganin (20 mg/kg/day subcutaneously) for 8 weeks until they were sacrificed using CO2 inhalation (40% vol/minute for 5 minutes). 16

Hematoxylin and eosin staining and Mankin’s score

Eight weeks after surgery, the tissues were harvested and incubated with 4% (v/v) paraformaldehyde for 1 day followed by de-calcification and paraffin embedding. The specimens were cut into slices (5 μm thick), which were stained with hematoxylin and eosin and observed using a light microscope. The degree of cartilage degeneration was assessed using Mankin’s score (0 to 13), which indicates the degradation level of articular cartilage, with a higher score representing more cartilage degeneration. 17

Immunofluorescence assay

Paraffin sections (5 μm) were deparaffinized and rehydrated, followed by 3% (v/v) H2O2 for 10 minutes. Cells were incubated in 4% (v/v) paraformaldehyde for 30 minutes. The specimens were incubated with 5% (w/v) BSA for 60 minutes and then with primary antibodies (anti-CD68 and anti-P65) for 1 hour with Alexa Fluor 488-conjugated anti-IgG secondary antibody. This was followed by incubation with diamidinophenyl indole for 7 minutes. The images were captured under a Nikon Eclipse Ti microscope (Nikon, Tokyo, Japan).

Statistical analysis

Results are presented as the mean ± standard deviation and analyzed using SPSS version 17.0 software (SPSS Inc., Chicago, IL, USA). A one-way analysis of variance was used to compare three or more groups. Values with P < 0.05 were considered to be statistically significant.

Results

Effect of loganin in IL-1β-mediated inflammatory reactions in chondrocytes

Chondrocytes that were isolated from normal rats and cultured as described above were assessed. The Griess reagent was used to determine the NO concentration in the supernatant after centrifuging the chondrocytes, while an ELISA was used to measure the PGE2 production in the culture medium. As shown in Figure 2a and b, NO and PGE2 secretion was significantly increased after IL-1β exposure compared with that in the control group (P < 0.001), while loganin significantly inhibited the IL-1β-mediated increase in PGE2 and NO compared with that in the IL-1β group (P < 0.05). As shown in Figure 2c and d, IL-1β significantly increased the COX-2 and iNOS expression compared with that in the control group (P < 0.001). Loganin also inhibited IL-1β-mediated increase in COX-2 and iNOS mRNA expression in a dose-dependent manner (P < 0.05). TNF-α and IL-6 levels in the culture medium were quantitatively measured using an ELISA. Figure 2e and f shows that compared with that in the control group, IL-6 and TNF-α mRNA expression was significantly up-regulated by IL-1β in chondrocytes (P < 0.001). However, loganin down-regulated the IL-1β-induced increase in IL-6 and TNF-α mRNA expression in a dose-dependent manner (P < 0.05). ELISA was also used to evaluate the effect of loganin on IL-1β-mediated IL-6 and TNF-α protein production. Figure 2g and h shows that TNF-α and IL-6 protein expression was significantly increased by IL-1β compared with that in the control group (P < 0.001). However, TNF-α and IL-6 expression were significantly decreased after loganin pretreatment compared with that in the IL-1β group (P < 0.05).

Figure 2.

Figure 2.

Open in a new tab

Role of loganin in IL-1β-mediated inflammatory reaction in chondrocytes. (a) PGE2 levels were measured by ELISA. (b) NO production was assayed by measuring the levels of the stable NO metabolite nitrite using sodium nitrite resuspended in distilled H2O as a standard. The Griess reaction was performed to evaluate the nitrite contents within the medium. (c–d) (c) COX-2 and (d) iNOS mRNA expression was detected using PCR. (e–f) (e) TNF-α and (f) IL-6 expression was detected using PCR. (g–h) TNF-α and IL-6 levels were calculated using ELISA. Data are presented as the mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001 compared with controls.

IL, interleukin; PGE2, prostaglandin E2; ELISA, enzyme-linked immunosorbent assay; NO, nitric oxide; COX, cyclooxygenase; iNOS, inducible nitric oxide synthase; PCR, polymerase chain reaction; TNF, tumor necrosis factor; SD, standard deviation.

The role of loganin in IL-1β-mediated activation of TLR4/MyD88/NF-κB pathway in chondrocytes

To investigate loganin’s anti-inflammatory mechanism, its role in activating NF-κB by IL-1β was evaluated using western blot. Figure 3a–d shows that IL-1β significantly increased TLR4 and MyD88 expression and NF-κB p65 phosphorylation of chondrocytes compared with that of the control group (P < 0.01). IL-1β also caused significant IκB-α degradation in chondrocytes compared with that in the control group (P < 0.01) (Figure 3a and e). Loganin dose-independently decreased IL-1β-induced TLR4 and MyD88 expression and NF-κB p65 phosphorylation compared with those of the IL-1β group (P < 0.05), and it also reduced the IL-1β-induced IκB-α degradation in chondrocytes in a dose-dependent manner compared with that in the IL-1β group (P < 0.05) (Figure 3). Chondrocyte immunofluorescence in response to IL-1β-mediated NF-κB activation was measured to explore the role of loganin in NF-κB p65 nuclear translocation. Clear and enhanced nuclear p65 staining was observed in chondrocytes upon IL-1β stimulation, indicating that nuclear NF-κB p65 translocation occurred in these cells. However, loganin reversed NF-κB p65 subunit translocation compared with that in the IL-1β stimulation group (Figure 3f). These findings may indicate that loganin exerts protective effects on IL-1β-mediated chondrocytes via the TLR4/MyD88/NF-κB signaling pathway.

Figure 3.

Figure 3.

Open in a new tab

Roles of loganin in IL-1β-mediated expression of TLR4/NF-κB signaling in chondrocytes. (a–e) Western blotting analysis of TLR4, MyD88, p-p65, and IκB-α in each group. Data are shown as the mean ± SD. *P < 0.05, **P < 0.01 compared with controls and (f) Effects of loganin on IL-1β-activated nuclear translocation of p65 in chondrocytes. Fluorescence immunostaining of p65 (green) and nucleus (blue).

IL, interleukin; NF-κB, nuclear factor kappa B; SD, standard deviation.

Loganin inhibits synovial inflammation in OA rats

To further clarify the anti-inflammatory role of loganin in OA, synovial fluid was isolated from joints in OA model rats, and its response to an inflammatory stimulus and loganin was measured using an ELISA. Figure 4a–c shows that surgery increased IL-1β, IL-6, and TNF-α expression in knee synovial fluid compared with that in the sham group (P < 0.01). However, loganin administration reduced these increases compared with those in the OA group (P < 0.05). Additionally, an immunofluorescent assay showed that loganin decreased the number of CD68-labeled inflammatory cells compared with that in the OA group (Figure 4d). All data suggested that loganin attenuated synovial inflammation in OA rats compared with that caused by OA alone.

Figure 4.

Figure 4.

Open in a new tab

Roles of loganin in the synovial inflammatory response in OA rats. (a–c) Loganin inhibited synovial inflammatory factor expression in OA rats. IL-1β (a), IL-6 (b), and TNF-α (c) protein expression was tested using an ELISA. (d) Representative synovial fluid stained with CD68. Data are presented as the mean ± SD. *P < 0.05, **P < 0.01 compared with the OA group.

OA, osteoarthritis; IL, interleukin; TNF, tumor necrosis factor; ELISA, enzyme-linked immunosorbent assay, SD, standard deviation.

Effects of loganin on OA cartilage histopathology

Hematoxylin and eosin staining showed that compared with the sham group, OA rats had severe articular cartilage destruction. Loganin treatment increased knee articular cartilage thickness and seems to have mitigated cartilage decomposition (Figure 5a). Moreover, the Mankin’s score in the OA group was significantly increased compared with that in the sham group (P < 0.05), and this increase was attenuated by loganin treatment (P < 0.01) (Figure 5b). Thus, loganin showed protective effects and enhanced the recovery of OA cartilage in this rat OA model.

Figure 5.

Figure 5.

Open in a new tab

Articular cartilage histology was measured using hematoxylin and eosin staining (×40), and cartilage damage was assessed using the Mankin’s score in rats. Data are presented as the mean ± SD. ***P < 0.05 compared with the sham group; **P < 0.01 compared with the OA group.

SD, standard deviation.

Discussion

An increasing amount of evidence indicates the importance of IL-1β in cartilage degradation caused by OA.18–20 Chondrocytes stimulated with IL-1β showed increased iNOS and COX-2 levels, which contributed to NO and PGE2 expression. Both NO and PGE2 are catabolic factors that are stimulated by MMP production and ECM synthesis inhibition in chondrocytes from OA rats.21–23 NO produced by iNOS is an inflammatory mediator that can trigger MMP secretion and activation, which can also compromise proteoglycan and collagen-II production in OA pathophysiology. 24 PGE2 is a main mediator of inflammation and pain in OA joints, such as enhancing ECM degradation and suppressing chondrocyte proliferation during OA pathogenesis. 25 Previous work demonstrated that suppressing inflammatory factor secretion including NO and PGE2 attenuates cartilage degeneration. 26 Synovial fibroblasts in OA were shown to be sensitive to local NO donors, which contributed to the increase in oxidative stress. 27 Oxidative stress in OA fibroblasts activates mitogen-activated protein kinase and NF-κB signaling and up-regulates COX-2 and PGE2 levels, leading to degenerative changes. 27

Our previous research showed that loganin administration compromised ECM catabolism and IL-1β-mediated apoptotic activity in chondrocytes via activation of PI3K/Akt signaling, which suggests that loganin is a potential therapeutic drug for treating OA. The significant inhibitory role of loganin in IL-1β-stimulated COX-2 and iNOS expression was revealed by the subsequent PGE2 and NO generation. The results of this study were consistent with previously published studies. Loganin decreased the TNF-α mRNA level and the iNOS and COX-2 levels in β-amyloid protein (Aβ)-treated PC12 cells. 28 Additionally, loganin treatment prevented TNF-α, IL-6, MCP-1, NO, and PGE2 over-production and COX-2 and iNOS expression in the Aβ-stimulated BV-2 cells. 29 These findings show loganin’s anti-inflammatory effects that protect cartilage through suppressing IL-1β-mediated COX-2 and iNOS expression with subsequent PGE2 and NO generation in the OA pathogenic mechanism.

TLR4 was shown to be overexpressed in cartilage in OA, and it was essential in the pathological process of cartilage degeneration. 30 The combination of TLR4 and the relevant ligand MyD88 results in NF‐κB activation and phosphorylated NF‐κB translocation to the nucleus, contributing to inflammatory‐related gene transcription. 31 TLR signaling contributes to NF-κB signaling activation, thereby enhancing inflammatory factor and degradative enzyme production. 31 Lipopolysaccharide (LPS) enhances ECM protein degradation through binding with TLR4 in rheumatoid arthritis. 32 LPS, which is a specific TLR ligand, enhances proteoglycan and aggrecan degradation and collagen II expression via TLR4 signaling activation in murine and human articular chondrocytes. 33 This research revealed the significant role of IL-1β in increasing the TLR4 signaling level in chondrocyte cells. We also showed a significant inhibitory role for loganin in IL-1β-induced TLR4 expression.

TLR4 is a main receptor in the inflammatory response. TLR4 ligation activates NF-κB, a downstream transcription factor and main catabolic signal related to OA progression. TLR4 ligation coupling to NF-κB activation is achieved by the adaptor protein MyD88, which is recruited to activate IκB kinase followed by removal of cytosolic p65 subunit sequestration that triggers nuclear translocation of these proteins. Our results showed that loganin markedly attenuated NF-κB p65 phosphorylation and IκB-α degradation in IL-1β-stimulated chondrocytes, causing a decrease in inflammatory cytokines including IL-6 and TNF-α. The NF-κB pathway is a main catabolic signaling pathway engaged in OA pathogenesis, and it exerts significant effects on regulating OA-related inflammatory mediators and the ROS level. 34 Inactivated NF-κB interacts with the inhibitory protein IκB-α and appears within the cytoplasm in the non-activated state. Stimulation by inflammatory mediators and oxidative stress triggered nuclear translocation of activated NF-κB. This translocation up-regulated multiple inflammation-related genes including iNOS, COX-2, NO, PGE2, MMPs, and ADAMTS, thereby facilitating catabolic factor synthesis, cartilage inflammation, and OA chondrocyte apoptosis. 14 Thus, targeted suppression of NF-κB signaling may be helpful in OA treatment. Previous studies revealed that NF-κB suppression inhibited COX-2, MMP-9, and iNOS levels in chondrocytes exposed to IL-1β chondrocytes. 35 Moreover, NF-κB inhibition decreased TNF-α-triggered chondrocyte expression of MMP-3 and MMP-13. 36

Loganin was reported to prevent chronic neuropathic pain triggered by constriction injury through inhibition of TNF-α/IL-1β-mediated NF-κB activation. 37 Loganin reduces Aβ-induced inflammation in BV-2 microglial cells by regulating the TLR4/TRAF6/NF-κB pathway. 29 Loganin seems to prevent M1 macrophage-mediated inflammation through modulating the Sirt1/NF-κB axis and lowering TNF-α, IL-6, and IL-1β levels to ameliorate dextran sulfate sodium-induced ulcerative colitis. 38 Our work and other previous research indicated that loganin prevented IL-1β-triggered inflammation by suppressing TLR4/MyD88/NF-κB activation. The current research revealed the underlying mechanism through which loganin blocks IL-1β-induced TLR4/MyD88/NF-κB activation in chondrocytes. Additionally, our in vivo experiments showed that loganin partially suppressed the synovial inflammatory response. However, more studies are required to illustrate the mechanism by which loganin regulates chondrocyte inflammation.

In summary, this study shows the anti-inflammatory effects of loganin in IL-1β-treated chondrocytes. The results indicated that loganin suppressed IL-1β-induced levels of NO, PGE2, iNOS, COX-2, IL-6, and TNF-α through suppressing the TLR4/MyD88/NF-κB pathway in IL-1β-activated chondrocytes. Our in vivo experiment revealed that loganin partially suppressed cartilage degeneration and the synovial inflammatory response, indicating the potential role of loganin in OA treatment.

Footnotes

Declaration of conflicting interest: The authors declare that there is no conflict of interest.

Funding: The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The present study was supported by the scientific research projects in the health and family planning industry in Hainan Province (Grant No. 20A200096).

ORCID iD: Dingzhong Chen https://orcid.org/0000-0003-0313-5077

References

  • 1.Glyn-Jones S, Palmer AJ, Agricola R, et al. Osteoarthritis. Lancet 2015; 386: 376–387. [DOI] [PubMed] [Google Scholar]
  • 2.Ahmed U, Thornalley PJ, Rabbani N. Possible role of methylglyoxal and glyoxalase in arthritis. Biochem Soc Trans 2014; 42: 538–542. [DOI] [PubMed] [Google Scholar]
  • 3.Wojdasiewicz P, Poniatowski LA, Szukiewicz D. The role of inflammatory and anti-inflammatory cytokines in the pathogenesis of osteoarthritis. Mediators Inflamm 2014; 2014: 561459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Poulet B, Staines KA. New developments in osteoarthritis and cartilage biology. Curr Opin Pharmacol 2016; 28: 8–13. [DOI] [PubMed] [Google Scholar]
  • 5.Csaki C, Mobasheri A, Shakibaei M. Synergistic chondroprotective effects of curcumin and resveratrol in human articular chondrocytes: inhibition of IL-1beta-induced NF-kappaB-mediated inflammation and apoptosis. Arthritis Res Ther 2009; 11: R165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Jiang L, Xu K, Li J, et al. Nesfatin-1 suppresses interleukin-1beta-induced inflammation, apoptosis, and cartilage matrix destruction in chondrocytes and ameliorates osteoarthritis in rats. Aging (Albany NY) 2020; 12: 1760–1777. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Gavriilidis C, Miwa S, Von Zglinicki T, et al. Mitochondrial dysfunction in osteoarthritis is associated with down-regulation of superoxide dismutase 2. Arthritis Rheum 2013; 65: 378–387. [DOI] [PubMed] [Google Scholar]
  • 8.Wen H, Xing L, Sun K, et al. Loganin attenuates intestinal injury in severely burned rats by regulating the toll-like receptor 4/NF-kappaB signaling pathway. Exp Ther Med 2020; 20: 591–598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Chen Y, Jiao N, Jiang M, et al. Loganin alleviates testicular damage and germ cell apoptosis induced by AGEs upon diabetes mellitus by suppressing the RAGE/p38MAPK/NF-kappaB pathway. J Cell Mol Med 2020; 24: 6083–6095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Yang Y, Gu Y, Zhao H, et al. Loganin attenuates osteoarthritis in rats by inhibiting IL-1beta-induced catabolism and apoptosis in chondrocytes via regulation of phosphatidylinositol 3-kinases (PI3K)/Akt. Med Sci Monit 2019; 25: 4159–4168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Wei Y, Wang Y, Wang Y, et al. Transient receptor potential vanilloid 5 mediates Ca2+ influx and inhibits chondrocyte autophagy in a rat osteoarthritis model. Cell Physiol Biochem 2017; 42: 319–332. [DOI] [PubMed] [Google Scholar]
  • 12.Lee SA, Moon SM, Han SH, et al. Chondroprotective effects of aqueous extract of Anthriscus sylvestris leaves on osteoarthritis in vitro and in vivo through MAPKs and NF-kappaB signaling inhibition. Biomed Pharmacother 2018; 103: 1202–1211. [DOI] [PubMed] [Google Scholar]
  • 13.Zhou S, Shi J, Wen H, et al. A chondroprotective effect of moracin on IL-1beta-induced primary rat chondrocytes and an osteoarthritis rat model through Nrf2/HO-1 and NF-kappaB axes. Food Funct 2020; 11: 7935–7945. [DOI] [PubMed] [Google Scholar]
  • 14.Lepetsos P, Papavassiliou KA, Papavassiliou AG. Redox and NF-kappaB signaling in osteoarthritis. Free Radic Biol Med 2019; 132: 90–100. [DOI] [PubMed] [Google Scholar]
  • 15.Zheng W, Chen C, Zhang C, et al. The protective effect of phloretin in osteoarthritis: an in vitro and in vivo study. Food Funct 2018; 9: 263–278. [DOI] [PubMed] [Google Scholar]
  • 16.Au RY, Al-Talib TK, Au AY, et al. Avocado soybean unsaponifiables (ASU) suppress TNF-alpha, IL-1beta, COX-2, iNOS gene expression, and prostaglandin E2 and nitric oxide production in articular chondrocytes and monocyte/macrophages. Osteoarthritis Cartilage 2007; 15: 1249–1255. [DOI] [PubMed] [Google Scholar]
  • 17.Tseng YT, Chen CS, Jong YJ, et al. Loganin possesses neuroprotective properties, restores SMN protein and activates protein synthesis positive regulator Akt/mTOR in experimental models of spinal muscular atrophy. Pharmacol Res 2016; 111: 58–75. [DOI] [PubMed] [Google Scholar]
  • 18.Luo X, Jiang Y, Bi R, et al. Inhibition of notch signaling pathway temporally postpones the cartilage degradation progress of temporomandibular joint arthritis in mice. J Craniomaxillofac Surg 2018; 46: 1132–1138. [DOI] [PubMed] [Google Scholar]
  • 19.Jenei-Lanzl Z, Meurer A, Zaucke F. Interleukin-1beta signaling in osteoarthritis – chondrocytes in focus. Cell Signal 2019; 53: 212–223. [DOI] [PubMed] [Google Scholar]
  • 20.Zeng YF, Wang R, Bian Y, et al. Catalpol attenuates IL-1beta induced matrix catabolism, apoptosis and inflammation in rat chondrocytes and inhibits cartilage degeneration. Med Sci Monit 2019; 25: 6649–6659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Zhao G, Gu W. Effects of miR-146a-5p on chondrocyte interleukin-1beta-induced inflammation and apoptosis involving thioredoxin interacting protein regulation. J Int Med Res 2020; 48: 300060520969550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Wang P, Guan PP, Guo C, et al. Fluid shear stress-induced osteoarthritis: roles of cyclooxygenase-2 and its metabolic products in inducing the expression of proinflammatory cytokines and matrix metalloproteinases. FASEB J 2013; 27: 4664–4677. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Haversath M, Catelas I, Li X, et al. PGE(2) and BMP-2 in bone and cartilage metabolism: 2 intertwining pathways. Can J Physiol Pharmacol 2012; 90: 1434–1445. [DOI] [PubMed] [Google Scholar]
  • 24.Hashimoto K, Akagi M. The role of oxidation of low-density lipids in pathogenesis of osteoarthritis: A narrative review. J Int Med Res 2020; 48: 300060520931609. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Sasaki K, Hattori T, Fujisawa T, et al. Nitric oxide mediates interleukin-1-induced gene expression of matrix metalloproteinases and basic fibroblast growth factor in cultured rabbit articular chondrocytes. J Biochem 1998; 123: 431–439. [DOI] [PubMed] [Google Scholar]
  • 26.Goggs R, Carter SD, Schulze-Tanzil G, et al. Apoptosis and the loss of chondrocyte survival signals contribute to articular cartilage degradation in osteoarthritis. Vet J 2003; 166: 140–158. [DOI] [PubMed] [Google Scholar]
  • 27.Zhang H, Yan J, Zhuang Y, et al. Anti-inflammatory effects of farrerol on IL-1beta-stimulated human osteoarthritis chondrocytes. Eur J Pharmacol 2015; 764: 443–447. [DOI] [PubMed] [Google Scholar]
  • 28.Jovanovic DV, Mineau F, Notoya K, et al. Nitric oxide induced cell death in human osteoarthritic synoviocytes is mediated by tyrosine kinase activation and hydrogen peroxide and/or superoxide formation. J Rheumatol 2002; 29: 2165–2175. [PubMed] [Google Scholar]
  • 29.Kim H, Youn K, Ahn MR, et al. Neuroprotective effect of loganin against Abeta25-35-induced injury via the NF-kappaB-dependent signaling pathway in PC12 cells. Food Funct 2015; 6: 1108–1116. [DOI] [PubMed] [Google Scholar]
  • 30.Cui Y, Wang Y, Zhao D, et al. Loganin prevents BV-2 microglia cells from Abeta1-42 -induced inflammation via regulating TLR4/TRAF6/NF-kappaB axis. Cell Biol Int 2018; 42: 1632–1642. [DOI] [PubMed] [Google Scholar]
  • 31.Gomez R, Villalvilla A, Largo R, et al. TLR4 signalling in osteoarthritis–finding targets for candidate DMOADs. Nat Rev Rheumatol 2015; 11: 159–170. [DOI] [PubMed] [Google Scholar]
  • 32.Zhang Y, Zeng Y. Curcumin reduces inflammation in knee osteoarthritis rats through blocking TLR4/MyD88/NF-kappaB signal pathway. Drug Dev Res 2019; 80: 353–359. [DOI] [PubMed] [Google Scholar]
  • 33.Lorenz W, Buhrmann C, Mobasheri A, et al. 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. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Bobacz K, Sunk IG, Hofstaetter JG, et al. Toll-like receptors and chondrocytes: the lipopolysaccharide-induced decrease in cartilage matrix synthesis is dependent on the presence of toll-like receptor 4 and antagonized by bone morphogenetic protein 7. Arthritis Rheum 2007; 56: 1880–1893. [DOI] [PubMed] [Google Scholar]
  • 35.Hu SL, Wang K, Shi YF, et al. Downregulating Akt/NF-kappaB signaling and its antioxidant activity with Loureirin A for alleviating the progression of osteoarthritis: In vitro and vivo studies. Int Immunopharmacol 2020; 78: 105953. [DOI] [PubMed] [Google Scholar]
  • 36.Sanchavanakit N, Saengtong W, Manokawinchoke J, et al. TNF-alpha stimulates MMP-3 production via PGE2 signalling through the NF-kB and p38 MAPK pathway in a murine cementoblast cell line. Arch Oral Biol 2015; 60: 1066–1074. [DOI] [PubMed] [Google Scholar]
  • 37.Chu LW, Cheng KI, Chen JY, et al. Loganin prevents chronic constriction injury-provoked neuropathic pain by reducing TNF-alpha/IL-1beta-mediated NF-kappaB activation and Schwann cell demyelination. Phytomedicine 2020; 67: 153166. [DOI] [PubMed] [Google Scholar]
  • 38.Liu S, Shen H, Li J, et al. Loganin inhibits macrophage M1 polarization and modulates sirt1/NF-kappaB signaling pathway to attenuate ulcerative colitis. Bioengineered 2020; 11: 628–639. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of International Medical Research are provided here courtesy of SAGE Publications

RESOURCES