Solanum nigrum Line inhibits osteoclast differentiation and suppresses bone mineral density reduction in the ovariectomy‑induced osteoporosis model.

Bone homeostasis is maintained by osteoclasts that absorb bone and osteoblasts that form bone tissue. Menopausal osteoporosis is a disease associated with aging and hormonal changes due to menopause causing abnormal activation of osteoclasts, resulting in a decrease in bone density. Existing treatments for osteoporosis have been reported to have serious side effects, such as jawbone necrosis and breast and uterine cancer; therefore, their use by patients is decreasing, whilst studies focusing on alternative treatments are increasingly popular. Solanum nigrum Line (SL) has been used as a medicinal plant that possesses several pharmacological effects, such as anti‑inflammatory and hepatotoxic protective effects. To the best of our knowledge, however, its effects on osteoporosis and osteoclasts have not been demonstrated previously. In the present study, the anti‑osteoporotic effect of SL was investigated using a postmenopausal model of osteoporosis in which Sprague‑Dawley rat ovaries were extracted. In addition, the inhibitory effects on osteoclast differentiation and function of SL was confirmed using an osteoclast model treated with receptor activator of NF‑κB ligand (RANKL) on murine RAW 264.7 macrophages. In vivo experiments showed that SL reduced the decrease in bone mineral density and improved changes in the morphological index of bone microstructure, such as trabecular number and separation. In addition, the number of tartrate resistant acid phosphatase‑positive cells in the femur and the expression levels of nuclear factor of activated T‑cells cytoplasmic 1 (NFATc1) and cathepsin K protein were inhibited. In vitro, SL suppressed RANKL‑induced osteoclast differentiation and bone resorption ability; this was mediated by NFATc1/c‑Fos, a key transcription factor involved in osteoclast differentiation, ultimately inhibiting expression of various osteoclast‑associated genes. These experimental results show that SL may be an alternative treatment for osteoporosis caused by abnormal activation of osteoclasts in the future.

Introduction

<pan class="Chemical">span class="Disease">Osteopn>orosisn>an> is a <sppan>an class="Disease">systemic skeletal disease <span class="Disease">characterized by a decrease in bone density (1). Bone homeostasis is maintained by osteoclasts, which absorb bone, and osteoblasts, which form bone (2). This homeostasis can be unbalanced by various causes, such as menopause, aging and steroidal side effects (3). Among these, hormonal changes due to menopause are the cause of abnormal osteoclast activity. Various drugs, such as bisphosphonates, parathyroid hormone, denosumab and selective estrogen receptor modulator, have been used to treat osteoporosis (4), but these drugs are not suitable for long-term treatment due to serious side effects, including mandibular necrosis and cardiovascular disease (5). Therefore, research and development of a natural-based treatment for osteoporosis with fewer and less severe side effects is required.

<pan class="Chemical">span class="Species">Solanum nigrum Ln>an>ine (<sppan>an class="Disease">SL) has been used as a medicinal plant in East Asian countries, such as Korea, Japan and China. <span class="Disease">SL is the above-ground part of Solanum nigrum Linné (Solanaceae) and has traditionally been used to treat conditions associated with inflammatory disease, such as boils, cancer and chronic bronchitis (6). A previous study reported that SL methanol extract inhibits osteoclast differentiation (7). To the best of our knowledge, however, the effects of ethanol extract, mechanism of osteoclast inhibition and effects of SL in osteoporosis have not been identified. In addition, inflammatory conditions and aging are known to increase the risk of developing osteoporosis (8,9). Various natural herbs showing anti-inflammatory effects have been shown to be effective in treating osteoporosis (10,11). In previous studies, SL has been shown to have anti-inflammatory effects (12,13). Therefore, SL may serve as a potential treatment for postmenopausal osteoporosis by suppressing abnormal osteoclast activity.

Osteoclasts are multinucleated giant cells derived from hematopoietic progenitors (14). Receptor a<pan class="Chemical">span class="Gene">ctpan>ivator of NF-κB ligand (<sppan>an class="Gene">RANKL) is a member of the <span class="Disease">tumor necrosis factor (TNF) superfamily and is a cytokine that serves an important role in osteoclast differentiation and mature osteoclast activity (15). When RANKL binds to RANK, TNF receptor-associated factor 6 expression is upregulated, leading to activation of downstream signaling molecules, such as MAPK and NF-κB. Thereafter, c-Fos and nuclear factor of activated T-cells, cytoplasmic 1 (NFATc1), which are key transcription factors involved in osteoclast differentiation, are sequentially expressed (2). Finally, these factors induce expression of factors associated with osteoclast differentiation and bone resorption, such as tartrate-resistant acid phosphatase (TRAP), cathepsin K (CTsK), matrix metallopeptidase-9 (MMP-9) and carbonic anhydrase 2 (CA2) (16).

In the present study, the anti-<pan class="Chemical">span class="Disease">osteoporoticpan> effe<sppan>an class="Gene">cts of <span class="Disease">SL were investigated using an ovariectomy (OVX)-induced osteoporosis model, which is the most commonly used model of postmenopausal osteoporosis (11,17–19). In addition, to confirm the effects of SL on osteoclast differentiation, its ability to inhibit osteoclast differentiation and the underlying mechanism were assessed using a RANKL-induced osteoclast model.

Materials and methods

Reagents

<pan class="Chemical">span class="Disease">SLn>an> was pur<sppan>an class="Disease">chased from Omniherb (Dongwoodang Pharmacy Co., Ltd.); 17β-estradiol (E2), <span class="Gene">TRAP staining kit, chlorogenic and caffeic acid, quercetin and protease and phosphatase inhibitor cocktail were purchased from Sigma-Aldrich (Merck KGaA). Minimum Essential Medium Eagle, α-Modification (α-MEM), FBS, penicillin/streptomycin (P/S) and Dulbecco's PBS (DPBS) were obtained from Gibco (Thermo Fisher Scientific, Inc.). DMEM was purchased from Welgene, Inc. RANKL was obtained from PeproTech, Inc. Anti-NFATc1 (cat. no. 556602) was purchased from BD Pharmingen (BD Biosciences; used for western blotting) and anti-c-Fos (cat. no. sc-447), anti-CTsK (cat. no. sc-48353), anti-NFATc1 (cat. no. sc-7294; used for immunohistochemistry), anti-β-actin (cat. no. sc-8432) and ECL solution were obtained from Santa Cruz Biotechnology, Inc. The SuperScript® IV reverse transcriptase (RT) kit and SYBR Green were purchased from Invitrogen (Thermo Fisher Scientific, Inc.) and Taq polymerase was purchased from MGmed. PCR primers were obtained from GenoTech Corp. All reagents used in cell experiments were analytical grade.

Preparation of SL

<pan class="Chemical">span class="Disease">SLn>an> was verified by Professor Yungmin Bu at the Herbology Labo<sppan>an class="Species">ratory, College of Korean Medicine, Kyunghee University (Seoul, South Korea). The plant specimens were stored in the plant storage cabinet of the Anatomy Laboratory, College of Korean Medicine, Kyunghee University. SL was extracted by immersion in 80% ethanol (Et-OH) for 2 weeks at 4°C. Bottles containing SL and Et-OH was shaken at the same time every day. Et-OH in the solution was removed using a concentrator, and the extracts were lyophilized at −20°C for 48 h to obtain a powder (yield, 13.88%). The extracts were stored in a cryogenic refrigerator at −80°C until required and diluted in DMSO (100 mg/ml) for use in experiments.

Animals and OVX-induced osteoporosis in Sprague Dawley (SD) rats

The in vivo experiments were approved by the Kyunghee University Institutional Animal Care and Use Committee [approval no. KHUApan class="Chemical">SP(SE)-17-052]. A total of 40 12-week-old female SD <span class="Species">rats (weight, 230–250 g) were pur<spn>n>an>an class="Disease">chased from Koatech. The animals were housed at 22±2°C with 55±10% humidity and a 12-h light/dark cycle. Rats were provided ad libitum access to food and water and allowed to acclimatize for 1 week. Body weight was measured weekly. Humane end points were as follows: i) weight loss ≥20% compared with other rats of the same age; ii) difficultly ingesting food or water due to uncomfortable walking; iii) difficulty maintaining a normal posture due to low energy; iv) unconsciousness or lack of reaction to external stimuli; and v) severe infection, laceration and bleeding at the surgical site.

In order to induce <pan class="Chemical">span class="Disease">osteoporosispan>, 32 SD <sppan>an class="Species">rats were deeply anesthetized using O2 diluted with 5% <span class="Chemical">isoflurane. After removing the hair from the surgical site, the epidermis and muscles were incised and both ovaries were removed. Additionally, eight SD rats underwent the same procedure but the ovaries were not removed (sham operation). During surgery, the concentration of isoflurane was maintained at 2–3%. No rats died during surgery. In order to prevent infection following surgery, gentamycin (4 mg/kg) was given intraperitoneally for 3 days. After 1 week stabilization, administration of distilled water (DW), SL and E2 (positive control) was initiated. Experimental groups were as follows: i) Sham, mock surgery then daily oral administration of DW; ii) OVX, OVX surgery then daily oral administration of DW; iii) E2, OVX surgery then daily oral administration of 100 µg/kg E2; iv) SL-low, OVX surgery then daily oral administration of 50 mg/kg SL; and v) SL-high, OVX surgery then daily oral administration of 100 mg/kg SL. The dosage of SL was calculated based on the following criteria: In Korean medicine, an adult human dose of 60 kg is a daily dose of SL of 8 g. Given that the SL used in the present experiment was lyophilized powder, and the yield was 13.88%, 18.5 mg/kg was equivalent to the recommended adult dose. In addition, rats generally metabolize drugs faster than humans (20). SL-low group were administered ~2 times the calculated amount and the SL-high group was administered ~5 times the calculated amount. After the 8-week dosing period, SD rats were sacrificed via cervical dislocation after collecting 10 ml blood via cardiac puncture under deep anesthesia with O2 diluted with 5% isoflurane. In order to determine the success of OVX surgery, the ovaries were collected and weighed and the right femur was extracted for micro-computed tomography (CT) analysis and histological examination.

Micro-CT analysis

In order to confirm the anti-<pan class="Chemical">span class="Disease">osteopn>oroticn>an> effe<sppan>an class="Gene">cts of <span class="Disease">SL, changes in bone microstructure of the femoral head of the right femur were scanned using a high-resolution cone beam micro-CT system (SkyScan1176; Bruker Corporation) with an aluminum filter of 0.5 mm, source set at 50 kV/200 µA and 8.9 µm isotropic resolution. Starting with the growth plate of the femoral head, 200 slides were taken and visualized using Data Viewer software (Skyscan version 1.6.10.1; Bruker Corporation). Bone microstructure indexes, such as bone mineral density (BMD), bone volume fraction (BV/TV), trabecular number (Tb.N) and trabecular separation (Tb.Sp) were measured using Skyscan.

Serum analysis

Blood extra<pan class="Chemical">span class="Gene">ctn>an>ed at the time of sacrifice was stored at room tempe<sppan>an class="Species">rature for 30 min. Then, the serum was separated by centrifugation at 14,310 × g for 20 min at 4°C. In order to measure TRAP activity in the serum, 50 µl serum and 50 µl TRAP solution (4.93 mg para-nitrophenyl phosphate + 850 µl 0.5 M acetate solution + 150 µl tartrate solution) were reacted at 37°C for 1 h. The reaction was terminated with 50 µl 0.5 M NaOH and TRAP activity was measured at an absorbance of 405 nm using an ELISA reader (Versamax; Molecular Devices, LLC).

Histological examination

The femur was fixed for 2 days using 10% (v/v) neutral buffered <pan class="Chemical">span class="Chemical">formalinn>an> at room tempe<sppan>an class="Species">rature. The tissue was demineralized for 8 weeks using a solution of <span class="Chemical">EDTA-2Na at room temperature. The demineralized tissue was dehydrated using Et-OH (at gradient concentration of 70, 80, 90 and 100% for 5 min per concentration), cleared with xylene and embedded in paraffin. The embedded tissue was sectioned to a thickness of 5 µm using a rotary microtome. Histomorphological changes were assessed by 7% hematoxylin and 1% eosin (H&E) staining at room temperature. Moreover, to measure the number of osteoclasts in the femur, a TRAP staining kit was used according to the manufacturer's protocol. For immunohistochemical (IHC) staining, tissue antigens were retrieved with proteinase K (Thermo Fisher Scientific, Inc.) at 37°C for 1 h. Endogenous peroxidase was blocked using 3% H2O2 diluted in methanol at room temperature for 30 min. Normal serum (Gibco; Thermo Fisher Scientific, Inc.) was added at room temperature for 1 h to block the binding of non-specific proteins. Antibodies were diluted in tris-buffered saline containing 0.5% bovine serum albumin and reacted at 4°C overnight with anti-NFATc1 (1:100; cat. no. sc-7294) and anti-CTsK (1:100; cat. no. sc-48353). Subsequently, the secondary antibody (1:100; rabbit; cat. no. BA-1000) was added at room temperature for 1 h, and then VECTASTAIN Elite ABC kit (cat. no. PK-6100; both Vector Laboratories, Inc.; Maravai LifeSciences) was used according to the manufacturer's instructions. The tissue was reacted with 3,3′-diaminobenzidine (Vector Laboratories, Inc.; Maravai LifeSciences) at room temperature for 5 min and counterstained with 7% hematoxylin for 30 sec at room temperature. Dyed tissues were observed using a light microscope (magnification, ×100) and imaged using a DP73 camera (Olympus Corporation). The trabecular area and positive cells for each indicator were assessed using ImageJ software (version 1.51j8; National Institutes of Health).

Cell culture and viability assay

<pan class="Chemical">span class="CellLine">RAW 264.7n>an> cells were pur<sppan>an class="Disease">chased from the Korean Cell Line Bank (cat no. 40071; lot no. 41484). <span class="CellLine">RAW 264.7 cells were cultured in DMEM containing 10% FBS and 1% P/S and sub-cultured every 2 days. MC3T3-E1 Subclone 4 cells were purchased from the American Type Culture Collection (cat no. CRL-2593). MC3T3-E1 cells were cultured in α-MEM without ascorbic acid containing 10% FBS and 1% P/S, and sub-cultured every 3 days. Both cell lines were maintained in a humidified incubator at 37°C, 95% humidity and 5% CO2. In order to measure the cytotoxicity of SL, RAW 264.7 cells were seeded in 96-well plates at a density of 5×103 cells/well and stabilized for 1 day. In addition, in order to investigate the toxicity of SL to osteoclasts, RAW 264.7 cells were stimulated for 5 days using 100 ng/ml RANKL and 5, 10, 20 or 40 µg/ml SL in a humidified incubator at 37°C. To determine the effect of SL on cell viability, cells were treated with SL for 24 h and 20 µl Cell Counting Kit-8 (Dojindo Molecular Technologies, Inc.) solution was subsequently added for 2 h. The absorbance in each well was measured at a wavelength of 450 nm using a microplate reader. SL was considered to be toxic when cell survival rate was ≤90% compared with untreated cells. In order to measure the effect of SL on cell necrosis, RAW 264.7 cells were seeded in 96-well plates at a density of 5×103 cells/well and stabilized for 1 day. Thereafter, cells were treated with 5, 10, 20 or 40 µg/ml SL for 24 h in a humidified incubator at 37°C, and cell necrosis rate was measured using a lactate dehydrogenase (LDH) assay kit (Dojindo Molecular Technologies, Inc.) (21), according to the manufacturer's protocol. LDH is released from cells upon cell death, thus LDH levels in the culture medium were used as an indicator of cell death (21).

TRAP staining and pit formation assays

<pan class="Chemical">span class="Gene">TRAPn>an> is an osteoclast-sppan>ecific marker and is used to determine whether osteoclasts are differentiated (22). In order to induce osteoclast differentiation, <span class="CellLine">RAW 264.7 cells were cultured in α-MEM containing 10% FBS and 1% P/S (5×103 cells/well) in a humidified incubator at 37°C with 5% <span class="Chemical">CO2 and stabilized for 1 day. Subsequently, the cells were exposed to 100 ng/ml <span class="Gene">RANKL and 5, 10, 20 or 40 µg/ml SL for 5 days. The medium was replaced with fresh medium every 2 days. After osteoclast differentiation was completed, cells were fixed with 10% formalin solution at room temperature for 10 min and stained using the TRAP staining kit as aforementioned. In order to test the effects of SL on osteoclast ability to absorb bone, RAW 264.7 cells were cultured in hydroxyapatite-coated plates (Corning, Inc.) with 5, 10, 20 or 40 µg/ml SL in a humidified incubator at 37°C for 5 days. The medium was replaced with fresh medium every 2 days. Thereafter, the cells were lysed with 4% NaClO, washed three times with DPBS and dried completely. Plates were imaged using a light microscope at ×100 magnification in five random fields of view per well. The absorbed area is expressed as a percentage of the total area.

Actin ring formation assay

In order to measure filamentous (F-)a<pan class="Chemical">span class="Gene">ctpan>in ring formation, <sppan>an class="CellLine">RAW 264.7 cells were cultured in α-MEM containing 10% FBS and 1% P/S (5×103 cells/well) and stabilized for 1 day. Subsequently, the cells were exposed to 100 ng/ml <span class="Gene">RANKL and medium containing 5, 10, 20 or 40 µg/ml SL for 5 days. The differentiated cells were fixed with 4% paraformaldehyde at room temperature for 20 min and permeabilized with PBS containing 0.1% Triton X-100 at room temperature for 5 min. Subsequently, the cells were stained with 200 µl 100 nM Acti-Stain™ Fluorescent Phalloidins for 30 min at room temperature (cat. no. PHDG1; Cytoskeleton, Inc.) and the nuclei were counterstained with 200 µl 100 nM DAPI in PBS for 30 sec at room temperature (Sigma-Aldrich; Merck KGaA). The F-actin formation was imaged using an immunofluorescence microscope at ×100 magnification (Celena; Logos Biosystems).

Western blotting

In order to determine protein expression following <pan class="Chemical">span class="Disease">SLpan> treatment, <sppan>an class="CellLine">RAW 264.7 cells were seeded in a 60-mm dish at a density of 5×105 cells/well and stabilized for 1 day. The cells were treated with 100 ng/ml <span class="Gene">RANKL and 5, 10, 20 or 40 µg/ml SL in a humidified incubator at 37°C for 1 day. In order to extract total and nuclear protein, the cells were washed three times using DPBS, and lysed using RIPA buffer and NE-PER™ nuclear and cytoplasmic extraction reagents (Thermo Fisher Scientific, Inc.). The lysates were maintained on ice for 30 min and centrifuged at 58,440 × g for 20 min at 4°C. Protein concentration was quantified using a bicinchoninic acid assay kit (Sigma-Aldrich; Merck KGaA). Equal quantities (30 µg) of protein were loaded on a 10% SDS-gel, and resolved using SDS-PAGE at 100 V for 1.5 h. The resolved proteins were transferred to nitrocellulose membranes (Whatman plc; Cytiva) at 100 V for 1 h. Non-specific proteins in the membrane were blocked using TBST (0.5% Tween-20) and 5% skimmed milk for 1 h at room temperature. The membrane was reacted with primary antibodies against NFATc1 (1:1,000; cat. no. 556602), c-Fos (1:200; cat. no. sc-447) and β-actin (1:500; cat. no. sc-8432) at 4°C overnight. Subsequently, the membranes were incubated with a horseradish peroxidase-conjugated secondary antibody for 1 h at room temperature (1:10,000; mouse; cat. no. 115-035-062; Jackson ImmunoResearch Laboratories, Inc.), and the expression of each indicator was visualized using ECL solution. The expression of each indicator was measured using ImageJ version 1.51j8 (National Institutes of Health) and normalized to β-actin.

RT-semi-quantitative PCR

In order to measure mRNA expression following <pan class="Chemical">span class="Disease">SLn>an> treatment, <sppan>an class="CellLine">RAW 264.7 cells were seeded in 6-well-plates at a density 2×104 cells/well and stabilized for 1 day. The cells were exposed to 100 ng/ml <span class="Gene">RANKL and 5, 10, 20 or 40 µg/ml SL in a humidified incubator at 37°C for 4 days. Thereafter, the cells were washed 3 times using DPBS and were lysed using TRIzol® reagent (Takara Bio, Inc.). The extracted mRNA was quantified using NanoDrop (Thermo Fisher Scientific, Inc.), and 2 µg RNA was reverse transcribed into cDNA using the SuperScript® IV RT kit according to the manufacturer's protocol. cDNA was amplified using Taq polymerase and target primers in a C1000 Touch™ Thermal Cycler (Bio-Rad Laboratories, Inc.). The following thermocycling conditions were used for qPCR: 22–40 cycles of 30 sec at 94°C (denaturation); 30 sec at 53–58°C (annealing); and 30 sec at 72°C (extension). The target primer sequence and annealing temperature are listed in Table I. The PCR reactants were electrophoresed on SYBR-Green-dyed 2% agarose gels diluted in 1% Tris acetate-EDTA buffer. The expression of each mRNA was measured using ImageJ software (version 1.51j8; National Institutes of Health) with β-actin as the loading control.

Table I.

Primers used for reverse transcription-quantitative PCR.

Gene	Sequence, 5′-3′	Accession number	Tm, °C	Base pair
NFATc1	Forward: TGC TCC TCC TCC TGC TGC TC	NM_198429.2	58	480
(Nfatc1)	Reverse: CGT CTT CCA CCT CCA CGT CG
c-Fos	Forward: ATG GGC TCT CCT GTC AAC AC	NM_010234.3	55	480
(Fos)	Reverse: GGC TGC CAA AAT AAA CTC CA
TRAP	Forward: ACT TCC CCA GCC CTT ACT ACC G	NM_007388.3	58	381
(Acp5)	Reverse: TCA GCA CAT AGC CCA CAC CG
RANK	Forward: AAA CCT TGG ACC AAC TGC AC	NM_009399.3	53	377
(Tnfrsf11a)	Reverse: ACC ATC TTC TCC TCC CHA GT
CTsK	Forward: AGG CGG CTA TAT GAC CAC TG	NM_007802.4	58	403
(Ctsk)	Reverse: CCG AGC CAA GAG AGC ATA TC
CA2	Forward: CTC TCA GGA CAA TGC AGT GCT GA	NM_001357334.1	58	411
(Ca2)	Reverse: ATC CAG GTC ACA CAT TCC AGC A
MMP-9	Forward: CGA CTT TTG TGG TCT TCC CC	NM_013599.4	58	258
(Mmp9)	Reverse: TGA AGG TTT GGA ATC GAC CC
ATP6v0d2	Forward: ATG GGG CCT TGC AAA AGA AAT CTG	NM_175406.3	58	504
(Atp6v0d2)	Reverse: CGA CAG CGT CAA ACA AAG GCT TGT A
OSCAR	Forward: CTG CTG GTA ACG GAT CAG CTC CCC AGA	NM_001290377.1	53	310
(Oscar)	Reverse: CCA AGG AGC CAG AAC CTT CGA AAC T
Actin	Forward: TTC TAC AAT GAG CTG CGT GT	NM_007393	58	456
(Actb)	Reverse: CTC ATA GCT CTT CTC CAG GG

NFATc1, nuclear factor of activated T cells c1; TRAP, tartrate-resistant acid phosphatase; RANK, receptor activator of NF-κB; CTsK, cathepsin K; CA2, carbonic anhydrase II; OSCAR, osteoclast-associated immunoglobulin-like receptor; ATP6v0d2, ATPase H+ transporting V0 subunit d2.

Alizarin red S staining

In order to induce osteoblast differentiation, <pan class="Chemical">span class="CellLine">MC3T3-E1pan> cells were cultured in α-MEM without <sppan>an class="Chemical">ascorbic acid containing 10% FBS and 1% P/S (1.5×104 cells/24-well plate) in a humidified incubator at 37°C and stabilized for 1 day. Subsequently, the cells were exposed to 25 µg/ml <span class="Chemical">ascorbic acid, 10 mM β-glycerophosphate and medium containing SL (5, 10, 20 µg/ml) in a humidified incubator at 37°C for 14 days. The medium was replaced with fresh culture medium every 3 days. After osteoblast differentiation was completed, calcified nodules in the plate were fixed with 80% Et-OH at 4°C for 1 h and stained using 0.1% alizarin red S solution (Duksan Pharmaceutical Co., Ltd.) at room temperature for 5 min. The nodules were imaged using a camera and light microscope (magnification, ×100). The stained dye was extracted using 10 mM sodium phosphate (pH 7.0) diluted in 10% cetylpyridinium chloride and measured at absorbance at 405 nm.

High-performance liquid chromatography (HPLC) analysis

<pan class="Chemical">span class="Chemical">Chlorogenic acidn>an>, <sppan>an class="Chemical">caffeic acid and <span class="Chemical">quercetin are active ingredients of SL (23,24). In order to analyze the SL extracts, HPLC was performed. Absorbance was measured using a UV detector (2996 Waters 2695). Xbridge C18 (250.0×4.6 mm, 5 µm) was used as the column and proceeded at 30°C for 50 min at a flow rate of 1 ml/min. Samples were injected in a volume of 10 µl. As the mobile phase, (A) acetonitrile and (B) H2O diluted with 1% acetic acid were used (ratio, 9:1). Ingredients were detected at an absorbance of 280 nm.

Statistical analysis

Data are presented as the mean ± SEM (n≥3) and were analyzed using GraphPad prism software (version 5.01; GraphPad Software Inc.). Comparisons between groups were performed using one-way ANOVA with post hoc Tukey's test. P<0.05 was considered to indicate a statistically significant difference.

Results

SL decreases loss of bone density and changes in bone microstructure caused by OVX

In order to investigate the effe<pan class="Chemical">span class="Gene">ctpan>s of <sppan>an class="Disease">SL on menopausal <span class="Disease">osteoporosis, SL was administered following removal of both ovaries. Changes in bone density of the femoral head were measured using micro-CT (Fig. 1A). The density of trabecular bone in the femoral head was lower in the OVX group than in the sham group. The positive control group E2 exhibited a reduced decrease in bone density; the SL-low and -high groups also exhibited a suppressed decrease in bone density. As a result of analyzing the microstructure of the femur images using CT analyzer software, BMD and BV/TV were decreased due to OVX, and E2, SL-low and SL-high groups suppressed this reduction. The difference between the E2 and SL-high group was significant (Fig. 1B and C). In addition, Tb.N and Tb.Sp of the femur were decreased and increased by OVX, respectively. For Tb.N, E2, SL-low and SL-high groups were significantly different from the sham group; for Tb.Sp, E2 and SL-high were significantly different. These results indicated that the effect of SL on bone density recovery was comparable with that of the positive control group (E2 treatment). Analyzing the TRAP activity in serum revealed that OVX did not significantly affect the expression of TRAP, but the SL-low and SL-high groups showed a notable ability to inhibit TRAP activity (Fig. 1F). The OVX group exhibited increased body weight and decreased uterine weight compared with the sham group. In addition, administration of E2 significantly suppressed this change and the SL-low and SL-high groups exhibited no effect on changes in weekly body and uterine weight (Fig. 1G and H).

Figure 1.

Effect of SL on bone density in an OVX-induced osteoporosis model. Osteoporosis was induced in Sprague Dawley rats (12-weeks-old) via OVX. Rats were then treated with SL or E2 for 8 weeks. (A) Changes in the bone microstructure in the femoral tissue induced by OVX were imaged using micro-CT (scale bar, 2 mm). (B) BMD, (C) BV/TV, (D) Tb.N and (E) Tb.Sp was analyzed using micro-CT. (F) Body weight was measured weekly. (G) Uterine weight was measured after sacrifice. (H) TRAP activity in serum was measured using ELISA. The results are expressed as the mean ± SEM (n=8). #P<0.05 and ##P<0.01 vs. sham; *P<0.05 and **P<0.01 vs. OVX. OVX, ovariectomy; SL, Solanum nigrum Line; E2, 17β-estradiol; CT, computed tomography; BMD, bone mineral density; BV/TV, bone volume/total volume; Tb.N, trabecular number; Tb.Sp, trabecular separation; TRAP, tartrate-resistant acid phosphatase; OD, optical density; BW, body weight.

SL inhibits trabecular bone loss, osteoclast formation and expression of NFATc1 and CTsK in femoral tissue

H&E, <pan class="Chemical">span class="Gene">TRAPn>an> and IHC staining were performed to observe histological and histochemical <sppan>an class="Disease">changes in the femoral head. The trabecular area of the femoral head was decreased following OVX; this was suppressed by administ<span class="Species">ration of E2 and SL-high (Fig. 2A and E). Measuring the area revealed a significant difference between the E2 and SL-high and OVX group. Consistent with the H&E staining results, the number of osteoclasts in the femoral head was increased following OVX and decreased following treatment with E2, SL-low and SL-high (Fig. 2B and F). IHC staining was performed to measure the protein expression of NFATc1 and CTsK in the femoral head. Expression of NFATc1 in the femoral head was increased in the OVX group compared with the sham group (Fig. 2C and G). Treatment with E2 inhibited this expression. In particular, the SL-high group notably inhibited expression of NFATc1 compared with the OVX group. Consistent with the NFATc1 staining results, the expression of CTsK in the femoral head was induced following OVX and decreased by E2 and SL (Fig. 2D and H).

Figure 2.

Effect of SL on histological changes in femoral tissue. (A) Decrease in the density of trabecular bone in the femoral tissue induced by OVX was analyzed by H&E staining. (B) Number of osteoclasts in the femoral head was detected using a TRAP staining kit. TRAP-positive cells are marked with black arrows. (C) NFATc1 (green) and (D) CTsK (red) protein expression in the tissue was detected via IHC. All images were captured using a phase-contrast microscope. Magnification, ×100; scale bar, 200 µm. (E) Trabecular area was measured using ImageJ. Number of (F) TRAP-, (G) NFATc1- and (H) CTsK-positive cells were counted. The results are expressed as the mean ± SEM (n=8). ##P<0.01 vs. sham; *P<0.05, **P<0.01 vs. OVX. OVX, ovariectomy; SL, Solanum nigrum Line; E2, 17β-estradiol; H&E, hematoxylin and eosin; TRAP, tartrate-resistant acid phosphatase; IHC, immunohistochemistry; NFATc1, nuclear factor-activated T cells c1; CTsK, cathepsin K.

SL inhibits osteoclast differentiation and bone absorption capacity

After confirming the positive effe<pan class="Chemical">span class="Gene">ctn>an>s of <sppan>an class="Disease">SL in the <span class="Disease">osteoporotic in vivo model, the effects of SL in the osteoclast model were confirmed using a RANKL-induced in vitro model. RAW 264.7 cells were cultured for 5 days in a medium containing RANKL (Fig. 3A). Differentiated osteoclasts were stained using the TRAP staining kit and multinucleated red giant cells were observed. SL decreased the area and number of TRAP-positive cells in a dose-dependent manner. In the pit formation assay, the absorbed area of the plate was used to measure the activity of osteoclasts. The absorbed area induced by RANKL treatment was decreased in cells treated with SL. Consistent with this, measuring the number of osteoclasts and TRAP activity in the medium demonstrated that SL inhibited osteoclast differentiation and activity (Fig. 3B and C). In addition, measuring the pit area formed by osteoclasts showed that SL also suppressed the absorbed area in a concentration-dependent manner (Fig. 3D). At 40 µg/ml, SL decreased viability of RAW 264.7 cells and osteoclasts (Fig. 3E and F). Therefore, 40 µg/ml was considered toxic and subsequent cell experiments were performed using 0–20 µg/ml SL. In addition, LDH was slightly increased following 40 µg/ml SL treatment but was not detected at 0–20 µg/ml SL, indicating that 0–20 µg/ml SL did not induce necrosis (Fig. 3G).

Figure 3.

Effect of SL on osteoclast differentiation and bone absorption capacity. (A) Osteoclasts differentiated by RANKL stimulation were stained using TRAP. Osteoclast calcium absorption ability was measured using a pit formation plate. Images were captured using an optical microscope. Magnification, ×100; scale bar, 200 µm. (B) TRAP-positive cells were counted. (C) Activity of TRAP in the medium was measured using the para-nitrophenyl phosphate method. (D) Absorbed area was measured using ImageJ. Cytotoxicity of SL on (E) RAW 264.7 cells and (F) osteclasts was verified via Cell Counting Kit-8. (G) Effect of SL on necrosis of RAW 264.7 cell was measured via LDH assay. The results are expressed as the mean ± SEM (n=3). ##P<0.01 vs. untreated; **P<0.01 vs. RANKL-alone. SL, Solanum nigrum Line; RANKL, receptor activator of nuclear factor-κB ligand; TRAP, tartrate-resistant acid phosphatase; LDH, lactate dehydrogenase.

SL suppresses formation of actin rings

The formation of an a<pan class="Chemical">span class="Gene">ctpan>in ring is an important target to measure bone absorption capacity via pit formation assay (25). The a<sppan>an class="Gene">ctin ring formation of osteoclasts treated with <span class="Gene">RANKL was observed via immunofluorescence analysis (Fig. 4). F-actin was observed in RANKL-treated RAW 264.7 cells, and the number of nuclei stained through DAPI decreased as cells fused during differentiation. SL treatment significantly decreased formation of F-actin in a concentration-dependent manner, which was consistent with the results of TRAP staining and pit formation assay.

Figure 4.

Effect of SL on formation of actin rings. (A) Formation of filamentous actin was detected with fluorescent phalloidin. (B) Formed actin rings were counted using an immunofluorescence microscope. Magnification, ×100; scale bar, 200 µm. Results are expressed as the mean ± SEM (n=3). ##P<0.01 vs. untreated; *P<0.05, **P<0.01 vs. RANKL-alone. SL, Solanum nigrum Line; RANKL, receptor activator of nuclear factor-κB ligand.

SL inhibits expression of NFATc1 and c-Fos

Western blotting and RT-qPCR were used confirm protein and gene expression of <pan class="Chemical">span class="Gene">NFATc1n>an> and <sppan>an class="Gene">c-Fos, which are important transcription factors for osteoclast differentiation (2). Following incubation for 24 h with RANKL and SL, proteins were extracted to confirm the effect of SL on expression of NFATc1 and c-Fos (Fig. 5A). These indicators were significantly inhibited when treated with 20 µg/ml SL (Fig. 5B). mRNA expression was observed 4 days after RANKL and SL treatment (Fig. 5C). RANKL treatment upregulated expression of both indicators. SL showed inhibitory effects on NFATc1 expression levels at concentrations of 10 and 20 µg/ml. In addition, Fos expression was inhibited at all concentrations of SL (Fig. 5D). Given the differences in sampling times between western blotting and RT-qPCR experiments, it was hypothesized that the inhibitor effect of SL on osteoclasts was exerted in the late, rather than the early, stage of differentiation.

Figure 5.

Effect of SL on expression of NFATc1 and c-Fos. (A) Protein expression of NFATc1 and c-Fos was verified by western blotting and (B) normalized to actin. (C) mRNA expression of NFATc1 and c-Fos was analyzed by reverse transcription-quantitative PCR and (D) normalized to actin. Data are expressed as the mean ± SEM (n=3). #P<0.05, ##P<0.01 vs. untreated cells; *P<0.05, **P<0.01 vs. RANKL-alone. SL, Solanum nigrum Line; RANKL, receptor activator of NF-κB ligand; NFATc1, nuclear factor-activated T cells c1.

SL suppresses expression of osteoclast-associated genes

The effe<pan class="Chemical">span class="Gene">ctn>an>s of <sppan>an class="Disease">SL on osteoclast-associated genes was demonst<span class="Species">rated using RT-qPCR. Osteoclast-associated genes, such as Acp5 (TRAP), Tnfrsf11a (RANK), Ctsk, Mmp9, osteoclast-associated immunoglobulin-like receptor (OSCAR, Oscar), ATPase H+ transporting V0 subunit d2 (ATP6v0d2, Atp6v0d2) and Ca2 were increased by RANKL treatment; SL treatment decreased the expression of these genes (Fig. 6A). Normalized to Actb, Acp5, Ctsk and Atp6v0d2 were significantly suppressed following treatment with 20 µg/ml SL compared with the RANKL-alone group. In addition, Tnfrsf11a, Ca2, Mmp9 and Oscar were significantly decreased when treated with 10 and 20 µg/ml SL (Fig. 6B).

Figure 6.

Effect of SL on expression of osteoclast-associated genes. (A) Inhibitory effects of SL on expression of osteoclast-associated mRNA was verified by reverse transcription-quantitative PCR and (B) normalized to Actb. The results are expressed as the mean ± SEM (n=3). #P<0.05, ##P<0.01 vs. untreated; *P<0.05 and **P<0.01 vs. RANKL-alone. SL, Solanum nigrum Line; RANKL, receptor activator of NF-κB ligand; NFATc1, nuclear factor-activated T cells c1; Tnfrsf11a, receptor activator of NF-κB; Acp5, tartrate-resistant acid phosphatase; Ctsfk, cathepsin K; Mmp9, matrix metallopeptidase 9; Oscar, osteoclast-associated immunoglobulin-like receptor; Atp6v0ds, ATPase H+ transporting V0 subunit d2; Ca2, carbonic anhydrase II; Actb, β-actin.

SL does not significantly affect osteoblast differentiation

After demonst<pan class="Chemical">span class="Species">ratpan>ing the inhibitory effe<sppan>an class="Gene">cts of <span class="Disease">SL in an osteoclastogenesis in vitro model, the effects of SL in an osteoblast model were confirmed using a MC3T3-E1 cell model. SL did not significantly affect osteoblast differentiation and formation of calcified nodules. These results indicate that SL specifically acted on osteoclasts rather than osteoblasts (Fig. 7A and B). The concentration of SL did not affect the viability of MC3T3-E1 cells (Fig. 7C and D).

Figure 7.

Effect of SL on osteoblast differentiation and calcified nodules. (A) Deposited calcified nodules were stained using alizarin red S. The differentiated osteoblasts were photographed with a camera and an optical microscope. Magnification, ×100; scale bar, 200 µm. (B) Stained dye was extracted and measured at an absorbance of 405 nm. Cytotoxicity of SL on MC3T3-E1 cell was verified via Cell Counting Kit-8 at (C) 24 and (D) 72 h. The results are expressed as the mean ± SEM (n=3). ##P<0.01 vs. untreated. SL, Solanum nigrum Line; A.A, ascorbic acid; B.G.P, β-glycerophosphate.

Quantitative analysis of SL

<pan class="Chemical">span class="Chemical">Chlorogenic acidn>an>, <sppan>an class="Chemical">caffeic acid and <span class="Chemical">quercetin are well-known active ingredients of SL (23,24). The chromatography peak of ingredient standard is shown in Fig. 8A. In the SL Et-OH extract, peaks were observed from 0 to 50 min and each peak was detected at the same retention time (chlorogenic acid, 9.420; caffeic acid, 10.836; quercetin, 23.722 min) as the ingredient standard (Fig. 8B).

Figure 8.

High-performance liquid chromatography analysis of SL and its ingredients. (A) Standard peaks of chlorogenic acid, caffeic acid and quercetin were detected at 280 nm. Retention time, 9.439, 10.867 and 23.862 min, respectively. (B) Ingredients were detected in SL. Retention time, 9.420, 10.836 and 23.722 min, respectively. SL, Solanum nigrum Line.

Discussion

In vivo, <pan class="Chemical">span class="Disease">SLn>an> inhibited expression of <sppan>an class="Gene">NFATc1 and <span class="Gene">CTsK in the femoral head and significantly decreased bone density and osteoclast differentiation. In vitro, SL inhibited the expression of NFATc1/c-Fos during early and late osteoclast differentiation and suppressed expression of genes associated with differentiation and bone resorption. As a result, SL inhibited osteoclast differentiation, bone resorption activity and formation of actin rings.

<pan class="Chemical">span class="Disease">Osteopn>orosisn>an> is <sppan>an class="Disease">chara<span class="Gene">cterized by a decrease in bone density and fragility. However, previous studies have shown that measuring bone volume and BMD is insufficient to determine improvement in osteoporosis, and that structural changes of trabecular bone must also be assessed (26,27). In the present study, the administration of SL in the OVX osteoporosis model not only increased BMD and bone volume, but also improved the trabecular bone microstructure. These results indicated that SL suppressed a decrease in bone density, which is a phenotype of osteoporosis, and improved bone quality via improved bone microstructure. The OVX-induced osteoporosis model shows the phenotype of postmenopausal osteoporosis and is used to research osteoporosis treatments (28,29). Following OVX, an increase in body weight and a decrease in uterine weight due to hormonal changes are considered to indicate successful surgery (17). In the present study, the E2 group exhibited suppressed changes in body and uterine weight, whereas the SL group exhibited no effect. These results indicated that OVX surgery was successful and SL did not exert a hormone-associated effect similar to that of E2 (30).

<pan class="Chemical">span class="CellLine">RAW 264.7pan> cells are monocyte/macrophages extra<sppan>an class="Gene">cted from male BALB/c <span class="Species">mice and are used as a cell model for various pathological diseases, such as inflammation, antioxidant and osteoclast differentiation (31–34). When RAW 264.7 cells are treated with RANKL, which is a member of the TNF superfamily and a type of cytokine, the monocytes induce differentiation, fusion, function and maturation of osteoclasts (35). Osteoclasts express various phenotypic markers, the most representative of which is TRAP, as its concentration in serum is used as a biochemical indicator of osteoclast activity and bone resorption (36). In the present study, SL decreased serum levels and activity of TRAP and the number of TRAP-positive cells in the femur of OVX-induced osteoporotic rats and inhibited the differentiation of RANKL-induced TRAP-positive cells. These results suggested that the anti-osteoporotic effect of SL is mediated by suppression of osteoclast differentiation.

Osteoclast differentiation involves essential transcription fa<pan class="Chemical">span class="Gene">ctpan>ors such as <sppan>an class="Gene">NFATc1 (37). The importance of <span class="Gene">NFATc1 in osteoclast differentiation has been demonstrated in transgenic mice and cell models. Aliprantis et al (38) found that cells of NFATc1-deficient mice do not differentiate into osteoclasts, leading to osteopetrosis. The embryonic stem cells from which NFATc1 was removed from did not differentiate into osteoclasts, even following stimulation with RANKL, whereas embryonic stem cells overexpressing NFATc1 differentiate into osteoclasts without the need for stimulation with RANKL (39). In the present study, SL significantly inhibited the expression of NFATc1 in femoral tissue and RANKL-induced RAW 264.7 cells. These results indicated that the inhibitory effect of SL on osteoclast differentiation is mediated by NFATc1. In addition, NFATc1 regulates expression of various osteoclast differentiation and bone resorption factors, such as CTsK, MMP-9, OSCAR and ATP6v0d2 (40). CTsK and MMP-9 are expressed in mature osteoclasts attached to the bone surface and degrade the bone. According to Saftig et al (41), osteoclasts extracted from CTsK-knockout mice impair bone resorption. In the present study, SL suppressed expression of CTsK in femoral tissue and cell models of osteoclast differentiation. These results indicated that SL served an important role not only in inhibiting osteoclast differentiation, but also in suppressing its ability to absorb bone. OSCAR is expressed in preosteoclasts and mature osteoclasts and is an etiological factor in osteoporosis and rheumatoid arthritis (42). ATP6v0d2 serves an important role in cell-cell fusion and actin ring formation (10,43). The actin ring is associated with the ‘sealing zone’ that is formed when osteoclasts attach to bone, which is a structural factor essential for osteoclast bone absorption (44). In the present study, SL inhibited the formation of actin rings and expression of ATP6v0d2, suggesting that SL controlled cell fusion during the early stages of osteoclast differentiation, as well as formation of the skeletal structure of the mature osteoclast.

<pan class="Chemical">span class="Gene">c-Fospan> is a representative osteoclast transcription fa<sppan>an class="Gene">ctor that controls expression of <span class="Gene">NFATc1 (40). c-Fos recruits the NFATc1 promoter in the early stages of osteoclast differentiation (45,46). In addition, c-Fos-deficient cells cause disorders in NFATc1 expression and osteoclast differentiation via induction of RANKL, which is improved by overexpression of NFATc1 (46). c-Fos also controls expression of CA2, which serves an important role in osteoclast bone absorption function (47). CA2 acidifies the bone surface prior to osteoclast-mediated bone absorption, creating an environment in which various enzymes can function (48,49). In the present study, SL inhibited both c-Fos and CA2 expression. These results showed that the inhibitory effect of SL on NFATc1 expression was mediated by regulation of c-Fos. In conclusion, it was confirmed that SL inhibited osteoclast differentiation and function by suppressing the expression of NFATc1/c-Fos, and thus, significantly suppressing OVX-induced decreases in bone density. These results highlight the possibility of SL as a therapeutic agent for management of osteoporosis.

The present study had certain limitations. The a<pan class="Chemical">span class="Gene">ctn>an>ivity of osteoclasts was investigated via stimulation of <sppan>an class="Gene">RANKL. Various factors, such as inflammation, steroids and aging, cause osteoporosis (50–52). However, the effect of SL on these factors was not investigated in the present study. Research on treatment of osteoporosis research has focused on patients with postmenopausal osteoporosis (53). However, with an increase in the elderly population, male and senile osteoporosis is becoming increasingly important (54). Additionally, treatment with steroids results in potential social implications for patients due to adverse side effects (50). Therefore, studying the effect of SL on other osteoporosis-causing factors such as inflammation, steroids and aging may highlight more generalizable targets and mechanisms. Previous studies have shown that the fruit of SL contains solanine, which is known to be toxic (55–57). However, a previous study demonstrated that it displays hepatoprotective effects (58). Additional studies on the administration method and toxic concentration of SL are required. Expression of NFATc1 is controlled by MAPK, NF-κB and c-Fos (2). However, only c-Fos expression was investigated in the present study. In order to confirm the anti-osteoporotic and inhibitory effects of SL on osteoclast differentiation, the effects of SL on phosphorylation of MAPK, ERK, JNK and p38 and expression of NF-κB induced by RANKL should be studied. The present study demonstrated the effect of SL on osteoclast differentiation but did not investigate the active ingredients in SL. In previous studies, SL has been shown to contain several active ingredients (24,55), some of which have an effect on osteoclasts and osteoporosis. For example, diosgenin and ferulic acid inhibit differentiation of osteoclasts via NF-κB (59,60). According to Wu et al (61), protocatechuic acid inhibits osteoclast differentiation via apoptosis of osteoclasts. In addition, Rutin inhibits osteoclast differentiation via its antioxidant effect (62). However, most of the components of SL have not been studied yet. Therefore, analysis of the structure and anti-osteoclastogenic effect of each component will be helpful in understanding the anti-osteoporosis mechanism of SL. It is necessary to verify the inhibitory effect of active ingredients in SL on osteoclasts in future.