LPS (from Escherichia coli 055:B5) and 3-[4,5-dimethyl-2-thiazolyl]-2,5-diphenyltetrazolium bromide (MTT) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Fetal bovine serum (FBS), Dulbecco’s modified Eagle’s medium (DMEM), penicillin, streptomycin, 0.05% (w/v) trypsin/EDTA, and phosphate-buffered saline (PBS) were obtained from Gibco-BRL (Gaithersburg, MD, USA). Cytokine (IL-6, TNF-α and IL-1β) ELISA kits were purchased from R&D Systems (Minneapolis, MN, USA). Antibodies for western blot analysis included: i) TLR4 antibody (rodent-specific) rabbit polyclonal antibody; ii) MyD88 (D80F5) rabbit mAb; iii) inhibitor of κBα (IκBα) (L35A5) mouse mAb (amino-terminal antigen); iv) phospho-IκBα (Ser32/36) (5A5) mouse mAb; v) anti-β-actin (8H10D10) mouse mAb; vi) horseradish peroxidase (HRP)-conjugated secondary antibodies (all from Cell Signaling Technology, Beverly, MA, USA). The antibody for immunofluorescence was NF-κB p65 (F-6) (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA).

Medicinal plants were supplied by Guo Yi Tang Chinese Herbal Medicine Store (Fujian, China) for the preparation of the GLGZD water extract. The preparation was a mixture of six crude plant extract ingredients soaked in (5-fold of the plant) double distilled water (DDW) for 30 min. The mixture was heated to 100°C for 1 h, and the decoction was filtrated. The filtrates obtained from two cycles of the procedures were mixed, then filtered and concentrated using a rotary evaporator (Model RE-2000; Yarong Biochemistry Instrument Co., Shanghai, China). The extract of GLGZD was obtained by a spraying desiccation method using a spray dryer (Model B-290; Büchi Labortechnik AG, Flawil, Switzerland). The stock and working concentrations of GLGZD were prepared by dissolving the extract in culture media to a concentration of 50 mg/ml and 50, 100, 200 μg/ml.

A murine BV-2 microglial cell line [purchased from the American Type Culture Collection, Manassas, VA, USA] was maintained in DMEM supplemented with FBS (10%), 100 U/ml penicillin and 100 μg/ml streptomycin. Cells were incubated in culture medium at 37°C in a 95% atmospheric air and 5% CO₂ humidified atmosphere. Briefly, the numbers of viable cells were evaluated by counting trypan blue-excluding cells that were then plated at a density of 1×10⁵ cells/well in 96-well trays, 2×10⁵ cells/well in 24-well trays, or plated at a density of 5×10⁵ cells/well in 6-well trays (for remaining experiments), incubated at 37°C for 24 h, and given a fresh change of medium. Cells were then incubated with or without LPS (1 μg/ml) in the presence of various concentrations of GLGZD (50, 100, 200 or 500 μg/ml) at 37°C for an additional 24 h, and in all experiments, cells were serum starved for 4 h prior to the treatment. The cultured cells were treated with LPS with or without GLGZD for 24 h (for ELISA), or for 12 h (for RT-PCR), or for 1 h for NF-κB translocation activity and western blotting for relative protein expression.

Microglial BV-2 cells were grown in 96-well plates and then incubated with or without LPS (1 μg/ml) in the presence of GLGZD at various concentrations for 24 h. MTT assay was used to measure the viability of the cells. MTT is a pale yellow substrate that produces a dark blue formazan product when incubated with living cells; an MTT ring is cleaved in active mitochondria, which occurs only in living cells. After the supernatants were removed for nitrite determination, cells were incubated at 37°C with MTT (0.05 mg/ml) for 4 h. The resulting color was assayed at 570 nm using a microplate absorbance reader (EXL 8008, Germany).

Inducible NO synthase (iNOS)-derived NO release is one of the major contributing factors during the inflammatory process in cerebral ischemic injury (14,15). Nitrite production was assessed by the Griess reaction (16). In brief, each 50 μl aliquot of the above-mentioned culture supernatants was collected and mixed with an equal volume of Griess reagent [0.1% N-(1-naphthyl)-ethylenediamine, 1% sulfanilamide in 5% phosphoric acid] and incubated at room temperature (RT) for 10 min. Absorbance at 540 nm was measured in a microplate absorbance reader. Nitrite concentration was determined from a sodium nitrite standard curve.

BV-2 cells were plated in a 24-well cell culture plate and incubated with GLGZD water extract (50, 100 and 200 μg/ml) in the presence or absence of LPS (1 μg/ml) for 24 h. Following the manufacturer’s instructions, a volume of 1 ml of culture-medium supernatant was collected for measurement of the concentration levels of IL-6, TNF-α and IL-1β by the relevant ELISA kit.

Total RNA was extracted from cultured microglial cells by using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) and following the standard protocol. Purity and integrity of the RNA were assessed using a NanoDrop reader. Subsequently, first-strand cDNA synthesis was performed with 2 μg total RNA using RevertAid™ H Minus First Strand cDNA Synthesis Kit (Fermentas, St. Leon-Rot, Germany) according to the manufacturer’s instructions. The obtained cDNA was used to determine the mRNA levels of TNF-α, IL-6, IL-1β and iNOS by a PCR kit (Fermentas). β-actin was used as an internal control.

BV-2 cells were plated overnight in 6 culture flasks and were then further incubated in serum-free medium for at least 4 h before treatments. After washing with cold PBS for three times, cells were lysed in RIPA buffer containing protease inhibitor PMSF (Roche Diagnostics, Mannheim, Germany). The content of the cells was pooled and centrifuged for 10 min at 12,000 × g and stored at −80°C. The protein concentration of the lysates was measured using BCA quantification assay (Pierce, Rockford, IL, USA). Proteins (50 μg) were separated using 12% (10% for TLR4 analysis) SDS-PAGE and transferred to PVDF membranes with a 0.45-μm pore size (IPVH00010; Millipore, Billerica, MA, USA). The membranes were incubated with primary antibodies overnight at 4°C: rabbit TLR4 monoclonal Ab, rabbit myd88, mouse IκBα, phospho-IκBα, β-actin monoclonal Ab (1:1,000) diluted in immunoblot buffer (TBS containing 0.05% Tween-20 and 5% non-fat dry milk). Following washing with TBST three times, membranes were incubated with the secondary antibody HRP-conjugated anti-mouse (or rabbit) IgG (1:1,000) for 1 h at RT. After washing, the blots were detected with Chemiluminescence (ECL)-Plus (RPN2132; GE Healthcare Life Sciences, Pittsburgh, PA, USA) for 1 min using a camera along with the VersaDoc System (Bio-Rad, Hercules, CA, USA). The pixel intensities of the immunoreactive bands were quantified using the percentage adjusted volume feature of Quantity One 5.4.1 software (Bio-Rad). Data are expressed as a ratio of the intensity of the band of the protein of interest over the intensity of the band of the loading control protein (β-actin).

For the detection of intracellular location of NF-κB p65, BV-2 cells were cultured on sterile glass coverslips and treated with GLGZD and LPS as described above. Following the various treatments, BV-2 cells were fixed with 4% paraformaldehyde in PBS for 30 min. After rinsing with PBS for three times, the cell membrane was permeabilized with 0.1% Triton X-100 for 2 min, and the coverslips with adherent cells were submitted to the double-immunofluorescence labeling assay. BV-2 cells were incubated with Hoechst (dilution 1:50,000; Sigma-Aldrich) plus NF-κB p65 (sc-8008, dilution 1:50; Santa Cruz Biotechnology, Inc.). The fluorescence signals were detected and analyzed using laser scan confocal microscopy (LSM 700; Carl Zeiss, Göttingen, Germany).

Data are expressed as means ± SD. One-way ANOVA was used when comparing the data obtained from the different experimental conditions. In vitro experiments were conducted in triplicates; representative results are shown. A P-value of <0.05 was considered to indicate a statistically significant result.

We first evaluated the effect of GLGZD on LPS-induced inflammation in BV-2 cells by measuring the production of NO and secretion levels of pro-inflammatory cytokines (TNF-α, IL-6 and IL-1β). As shown in Fig. 1, LPS stimulation for 24 h significantly induced the release of NO, TNF-α, IL-6 and IL-1β, indicating an inflammatory response in BV-2 cells. However, the LPS-induced inflammation was significantly inhibited by GLGZD treatment in a dose-dependent manner. To further verify these observations, we determined the effect of GLGZD on the mRNA expression of the pro-inflammatory factors. As shown in Fig. 2, LPS stimulation profoundly increased the mRNA expression of iNOS, TNF-α, IL-6 and IL-1β in BV-2 cells, which was dose-dependently and significantly suppressed by GLGZD treatment.

We next performed an MTT assay to evaluate the effect of GLGZD on cell viability. As shown in Fig. 3, treatment with various concentrations of GLGZD and/or LPS had no effect on the viability of the BV-2 cells, suggesting that inhibition of the LPS-induced inflammatory response in BV-2 cells did not result from the cytotoxic action of GLGZD.

TLR4/NF-κB signaling is one of the major pathways mediating immune and inflammation responses, which are involved in the expression of inflammatory mediators. The process of NF-κB activation includes several key links such as TLR4 activation, the presence of MyD88, phosphorylation/degradation of IκB, and subsequent nuclear translocation of NF-κB. To elucidate the mechanism of the anti-inflammatory activity of GLGZD, we examined its effect on the TLR4/NF-κB signaling pathway in microglial cells. As shown in Fig. 4, upon LPS stimulation, the expression of TLR4 and MyD88 as well as the phosphorylation level of IκB were significantly increased. However, GLGZD significantly neutralized the effect of LPS stimulation, dose-dependently reducing TLR4 and MyD88 protein expression and IκB phosphorylation levels in BV-2 cells. To further verify these results, we evaluated the effect of GLGZD on the nuclear translocation of NF-κB which is a critical step for NF-κB activation. The NF-κB p65 subunit was visualized by immunofluorescence staining. The cells were counterstained with DAPI, and NF-κB nuclear translocation was recognized by the co-localization of the p65 subunit with DAPI. As shown in Fig. 5, LPS stimulation caused the nuclear translocation of the NF-κB p65 subunit, which was not observed in unstimulated cells. However, GLGZD treatment significantly blocked LPS-induced NF-κB nuclear translocation in the BV-2 cells, in a dose-dependent manner. Collectively, these data suggest that the anti-inflammatory effect of GLGZD is mediated by suppression of TLR4/NF-κB signaling in microglial BV-2 cells.