A mixture of curcuminoids (curcumin, 55.2%; demethoxycurcumin, 22.9%; and bisdemethoxycurcumin, 21.8%) was purchased from Tianjin Jian Feng Pharmaceutical Co., Ltd (Tianjin, China). Male Wistar-derived rats (200–250 g body weight, 8–10 weeks old, provided by the Laboratory Animal Center of the Shenyang Pharmaceutical University, Shenyang, China) were housed under controlled temperature (22±2°C), humidity (55±10%) and light (8:00 a.m. to 8:00 p.m.) conditions in a breeding room. Normal food and water were available ad libitum but were withdrawn 24 h prior to administration. Curcuminoids were administered per os as a 30% aqueous 1,2-propylene glycol solution. Urine and feces were collected for 48 h from the animals housed in stainless steel metabolism cages equipped with a urine and feces separator (B6–10, Suhang Technology Equipment Co., Ltd., Suzhou, China). Animal experiments were performed in accordance with the Guide for the Care and Use of Laboratory Animals of the Shenyang Pharmaceutical University (approval date: 08/10/2010, no. 100810; Liaoning, China). Tetrahydrocurcumin, hexahydrocurcumin and octahydrocurcumin (Fig. 1) were isolated from feces and urine of rats over 48 h following oral administration of the curcuminoid mixture, as previously described (26). The purity of tetrahydrocurcumin, hexahydrocurcumin and octahydrocurcumin was determined using high-performance liquid chromatography (HPLC; Waters 600; Waters Corp., Milford, MA, USA) and a ultraviolet detector (Waters 490; Waters Corp.); peak areas were normalized and the purities of the metabolites were 98.2, 98.6 and 98.5%, respectively.

RPMI 1640 medium and fetal bovine serum (FBS) were obtained from Invitrogen Life Technologies (Carlsbad, CA, USA). Mouse tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) ELISA kits as well as a bicinchoninic acid (BCA) protein concentration assay kit were obtained from Yantai Science and Biotechnology Co., Ltd (Shandong, China). Anti-NOS2 antibody (sc-651, rabbit polyclonal IgG, dilution 1:1,000), anti-Cox-2 antibody (sc-1746, goat polyclonal IgG, dilution 1:1,000), anti-IκB-α antibody (sc-371, rabbit polyclonal IgG, dilution 1:1,000), anti-NFκB p65 antibody (sc-372, rabbit polyclonal IgG, dilution 1:1,000) and anti-actin antibody (sc-1616, goat polyclonal IgG, dilution 1:1,000), as well as horseradish peroxidase (HRP)-conjugated secondary antibodies were purchased from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA). Phenylmethylsulfonyl fluoride, dithiothreitol, E. coli, LPS and all other chemicals used in the present study were purchased from Sigma-Aldrich (St. Louis, MO, USA). A 50 mM solution of tested samples was prepared in 100% cell culture grade dimethyl sulfoxide, stored as small aliquots at −20°C, and then diluted to the required concentrations prior to use. Hydrocortisone (H4001; purity, ≥98%; Sigma-Aldrich) was used as the positive control drug for all experiments performed.

Mouse monocyte-macrophage RAW 264.7 cells (TIB-71; American Type Culture Collection, Manassas, VA, USA) were maintained in RPMI 1640 medium supplemented with penicillin (100 U/ml; Yantai Science and Biotechnology Co., Ltd.), streptomycin (100 μg/ml; Yantai Science and Biotechnology Co., Ltd.) and 10% heat-inactivated FBS at 37°C in a humidified incubator with 5% CO₂ and 95% air. Medium was routinely replaced every two days and cells were passaged using 0.25% trypsin (Yantai Science and Biotechnology Co., Ltd.) until they attained confluence.

The amount of nitrite in the cell culture supernatant was determined using a commercial Griess reagent kit (a mixture of Griess reagent A and Griess reagent B, ratio 1:1, A: 1% sulphanilamide in 5% H₃PO₄ and B: 0.1% naphthylethylene diamine dihydrochloride) (Yantai Science and Biotechnology, Co., Ltd.) as previously described (27). RAW 264.7 cells were treated with LPS (1 μg/ml) and curcumin or its respective metabolites (12.5–100 μM) for 24 h. Cell culture supernatant (100 μl) was added to 100 μl Griess reagent and then incubated at room temperature for 10 min. Absorbance was measured at 540 nm (Biotek Synergy HT; BioTek Instruments, Inc., Winooski, VT, USA) and inhibitory rates were calculated using a standard calibration curve of different concentrations of sodium nitrite as previously prepared (28).

RAW 264.7 cells were treated with LPS (1 μg/ml) and curcumin or its respective metabolites (12.5–100 μM) for 6 h. Mouse tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) ELISA kits (Yantai Science and Biotechnology Co., Ltd.) were used according to the manufacturer’s instructions in order to determine the protein expression levels of TNF-α or IL-6 using 100 μl culture supernatant as previously described (29).

Total protein was extracted by using western cell lysis buffer (Yantai Science and Biotechnology Co., Ltd.) in order to determine the protein expression levels of iNOS and COX-2. Cytoplasmic and nuclear proteins were separated using a nuclear and cytoplasmic protein extraction kit according to the manufacturer’s instructions (Yantai Science and Biotechnology Co., Ltd.) for further use for the western blot analysis of IκB-α and nuclear factor kappa B (NF-κB) p65 subunit (30).

Protein concentrations were determined using a BCA protein concentration assay kit (Yantai Science and Biotechnology Co., Ltd.). Each respective protein (30 μg) was boiled in SDS-PAGE loading buffer (Yantai Science and Biotechnology Co., Ltd.), subjected to gel electrophoresis and then electrophoretically transferred onto nitrocellulose membranes (Pall Corporation, Port Washington, NY, USA). The membranes were blocked using 5% nonfat dried milk in Tris-buffered saline with Tween 20 (TBST; 20 mM Tris-HCl, 150 mM NaCl and 0.05% Tween 20) at room temperature for 1 h. Samples were then washed and incubated in their respective primary antibody solution (anti-iNOS, anti-COX-2, anti-IκB-α, anti-p65 or anti-β-actin, dilution 1:1,000) overnight at 4°C. Membranes were then washed with TBST and incubated with HRP-conjugated secondary antibody solution for 1 h at room temperature. Blots were then washed three times in TBST, detected using enhanced chemiluminescence (Beyotime Institute of Biotechnology, Haimen, China) and exposed to photographic films (Kodak, Tokyo, Japan). Images were collected and the corresponding protein bands for iNOS, COX-2, IκB-α, p65 and β-actin were quantified by densitometric analysis using DigDoc100 software (Alpha Innotech Corporation, San Leandro, CA, USA).). β-actin was used as the internal control.

Data were analyzed using SPSS 13.0 (SPSS, Inc., Chicago, IL, USA). Values are expressed as the mean ± standard deviation. Statistical comparisons were conducted using a one-way or two-way analysis of variance followed by a two-way post hoc test. P<0.05 was considered to indicate a statistically significant difference between values.

A preliminary MTT assay showed that curcumin and its metabolites (3.125–100 μM) did not affect the viability of RAW 264.7 cells within 24 h.

RAW 264.7 cells were treated with 1 μg/ml of LPS only or in combination with different concentrations of curcumin and its metabolites or hydrocortisone as the positive control. The concentration of nitrite was determined by detecting NO production levels 24 h following treatment (Fig. 2). LPS induced a significant increase in nitrite concentration compared with that of the untreated group (P<0.01; 34.78±2.54 and 3.96±0.29 μM, respectively). In addition, curcumin and its three metabolites significantly inhibited the LPS-induced NO overproduction in a dose-dependent manner (P<0.01); however, curcumin exhibited a more potent inhibition of nitrate concentrations compared to that of its metabolites.

RAW 264.7 cells were treated with 1 μg/ml LPS only or in combination with different concentrations of curcmin and its metabolites or hydrocortisone as the positive control. Following 6 h of incubation, an ELISA assay was used to determine the levels of TNF-α and IL-6 in the supernatants. As shown in Figs. 3 and 4, compared to the untreated control group, LPS significantly induced the release of proinflammatory cytokines TNF-α (63.57±6.41 and 3389.97±39.11 pg/ml, respectively) and IL-6 (811.95±32.84 and 10536.81±833.99 pg/ml, respectively). Curcumin exerted a significant inhibitory effect on TNF-α as well as IL-6 release compared to that of the LPS-only group; LPS-induced TNF-α and IL-6 release were almost completely inhibited following 100 μM curcumin treatment. In addition, the curcumin metabolite tetrahydrocurcumin significantly inhibited the release of TNF-α and IL-6, whereas hexahydrocurcumin and octahydrocurcumin did not exhibit any marked inhibitory effects on the release of TNF-α and IL-6 at concentrations of 12.5–100 μM.

As demonstrated above, curcumin and its metabolites were able to inhibit LPS-induced NO overproduction (Fig. 2). NO overproduction is associated with the upregulation of iNOS expression; therefore, in the present study, western blot analysis was used to determine the expression levels of iNOS and COX-2 following treatment with LPS in the presence or absence of 50 μM curcumin or its metabolites (Fig. 5A). Densitometric analysis revealed that 50 μM curcumin completely inhibited LPS-induced expression of iNOS and COX-2 (Fig. 5B and C, respectively); in addition, curcumin metabolites significantly inhibited iNOS and COX-2 expression compared to that of the LPS only treatment. Furthermore, the metabolite tertrahydrocurcumin appeared to exhibit a more potent effect on iNOS expression compared to that of the other metabolites; however, statistical analyses were not performed to confirm this observation.

Translocation of NF-κB to the nucleus is the result of IκB-α protein degradation. Western blot analysis was used to determine the effect of curcumin and its metabolites on LPS-induced IκB-α degradation and translocation of NF-κB to the nucleus. As shown in Figs. 6 and 7, treatment with 50 μM curcumin or its metabolites significantly inhibited the LPS-induced decrease in cytoplasmic IκB-α expression as well as the LPS-induced increase in nuclear protein expression of the NF-κB subunit p65. This therefore indicated that curcumin and its metabolites inhibited IκB-α degradation and, as a result, prevented the translocation of NF-κB to the nucleus. Futhermore, the three metabolites of curcumin produced significant results; however, they appeared to have a less potent effect on LPS-induced degradation of IκB-α and p65 expression than that of curcumin.