1-Methylnicotinamide and nicotinamide: two related anti-inflammatory agents that differentially affect the functions of activated macrophages

Abstract

Introduction:

1-Methylnicotinamide (MNA), a major metabolite of nicotinamide (NA), is known to exert anti-inflammatory effects in vivo. Treatment of inflammatory skin diseases by topical application of MNA provides certain advantages over the use of NA. However, in contrast to NA, the molecular mechanisms of the anti-inflammatory properties of MNA are not well known. In this study the influence of exogenous MNA and NA in vivo on the generation of inflammatory mediators by macrophages (Mϕ) was investigated.

Materials and Methods:

Peritoneal Mϕ of CBA/J mice were activated in vitro with lipopolysaccharide and incubated with MNA or NA. The effect of these compounds on biological functions of Mϕ was measured by evaluation of the production of reactive oxygen species (ROS) by luminol-dependent chemiluminescence, cytokines and prostaglandin E₂ (PGE₂) by ELISA, and nitric oxide (NO) by the Griess method. Moreover, the expressions of inducible NO synthase and cyclooxygenase-2 were measured by Western blotting.

Results:

It was shown that at non-cytotoxic concentrations, NA inhibits the production of a variety of pro-inflammatory agents, such as tumor necrosis factor α, interleukin 6, NO, PGE₂, and the generation of ROS. In contrast to NA, exogenous MNA inhibited only the generation of ROS, while its effect on the synthesis of other mediators was negligible.

Conclusions:

These results indicate that the anti-inflammatory properties of MNA demonstrated previously in vivo do not depend on its capacity to suppress the functions of immune cells, but more likely may be related to its action on vascular endothelium. The authors suggest that the limited permeability for exogenous MNA, in contrast to that for NA, may be responsible for its lack of suppressor activity against Mϕ.

Introduction

1-Methylnicotinamide (MNA), a major metabolite of nicotinamide (NA), has been shown recently to act in vivo as a very efficient anti-inflammatory agent [9]. After topical application of MNA, a remarkable therapeutic effect was observed in such inflammatory skin diseases as rosacea and acne vulgaris as well as in skin burns and wound healing [22, 23]. On the other hand, MNA therapy was not effective in cases with accompanying bacterial infection, which indicates that MNA’s therapeutic effectiveness is related to its anti-inflammatory, but not anti-bacterial, properties [1]. Moreover, it was demonstrated that MNA displays an anti-thrombotic potential [3]. All these observations contradict the common view that MNA is a biologically inactive metabolite of NA [19]. However, in contrast to NA, the mechanism of MNA’s anti-inflammatory activity is still unclear. It remains to be examined whether MNA is able to inhibit the functions of immune cells, especially those involved in an inflammatory response (Fig. 1).

Fig. 1.

Chemical structure of NA and MNA.

NA (niacinamide) is the amide of nicotinic acid (niacin, vitamin PP or B₃) [4]. Over the years, NA has been tried in the treatment of various diseases, such as pellagra, psoriasis, diabetes, and schizophrenia [12, 21, 24]. In the last decade it has been shown that NA exerts a number of anti-inflammatory properties, e.g. inhibition of the synthesis of pro-inflammatory cytokines (tumor necrosis factor (TNF)-α, interleukin (IL)-1, IL-6, IL-8, interferon (IFN)-γ), inhibition of inducible nitric oxide synthase (iNOS), modulation of free radical scavenging, and suppression of the expression of MHC class II and some adhesion molecules on immune cells [10, 11, 13, 14, 16]. It has been suggested that the anti-inflammatory properties of NA are related to the inhibition of NAD-dependent enzymes, such as poly(ADP-ribose) polymerase-1 [16, 20].

In this study we examined the anti-inflammatory potential of both MNA and NA in vitro. We chose macrophages (Mϕ) as representative immune inflammatory cells, potential targets for MNA and NA. In our experimental model, peritoneal murine Mϕ activated in vitro with lipopolysaccharide (LPS) were incubated with MNA and NA and the anti-inflammatory potential of the agents was estimated by their ability to inhibit the production of selected pro- and anti-inflammatory mediators.

Materials and Methods

Animals

Inbred CBA/J mice (8–10 weeks old) from the Department of Immunology (Jagiellonian University Medical College, Kraków, Poland) were used. The animals were kept in a constant-climate environment with respect to the temperature (22±2°C), humidity (50±10%), and daylight cycle (light 6 am–6 pm) and were fed standard laboratory diet with water and food ad libitum. All animal procedures conformed with the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85-23, revised 1996) and the experimental procedures used in the present study were approved by the local Jagiellonian University Ethics Committee on Animal Experiments.

Measurement of MNA/NA concentration

LPS-stimulated Mϕ (5×10⁵) were cultured with MNA or NA used at the non-cytotoxic concentrations of 10 and 4 mM, respectively. After 24 h the supernatant and cells were collected separately. The cells were rapidly washed three times to remove extracellular MNA or NA and frozen until analysis. Fifty percent acetonitrile in water was used for extraction. The protein precipitate was removed by centrifugation and the supernatants were freeze dried and reconstituted with the initial mobile phase of the chromatographic system. Samples were analyzed using a liquid-chromatography mass-spectrometry system previously described elsewhere in detail [18].

Macrophages

Peritoneal mouse Mϕ were induced by an intraperitoneal injection of 1.0 ml of paraffin oil (Marcol 52, Exxon, USA). The cells were collected 72 h later by washing out the peritoneal cavity with 5 ml of phosphate-buffered saline solution (PBS) containing 5 U heparin/ml (Polfa, Poland). The cells were centrifuged and red blood cells were lysed by osmotic shock using distilled water. Osmolarity was restored by addition of twice-concentrated PBS. The presence of Mϕ (85–90%) was judged by cytochemical demonstration of nonspecific esterase-positive mononuclear cells using α-naphtyl acetate (Sigma, USA).

Cell viability

The effect of treatment on cell viability was assessed by measuring lactic dehydrogenase (LDH) activity in the culture supernatants with the use of the LDH Cytotoxity Detection Kit (Takara Biomedicals, Japan) and the CellTiter 96 AQueous One Solution Cell Proliferation Assay (Promega, USA) according to the manufacturers’ instructions. In accordance with statistical analysis (non-linear curve fitting), the nontoxic dose ranges of NA and MNA were determined. A threshold of 90% viable cells was established for testing.

Cell culture: activation of cells for the production of inflammatory mediators

Mϕ stimulated with LPS (100 ng/ml) were incubated with different concentrations of MNA or NA (1–30 mM) to test the possible anti-inflammatory activity of the agents. Mϕ were cultured in 96-well flat-bottom cell culture plates at 1×10⁵ cells/well in RPMI 1640 medium supplemented with 5% fetal calf serum at 37°C in an atmosphere of 5% CO₂. After 24 h of culture the cells and supernatants were collected and frozen at 80°C for further analyses.

Determination of cytokines

Cytokine concentrations in culture supernatants were measured using capture ELISA. For TNF-α, IL-6, IL-10, and IL-12p40 determination, microtiter plates (Corning, USA) were coated overnight with rat mononuclear antibody (mAb) against a mouse cytokine (capture antibody). After blocking the plates with 3% non-fat dried milk (for IL-10: 4% albumin), the standards and tested supernatants were added and incubated overnight. The plates were then coated with biotinylated antibodies against the same cytokine-detecting antibody for 1 h. The ELISA was developed with horseradish peroxidase streptavidin (Vector, USA), followed by o-phenylenediamine and H₂O₂ (both Sigma-Aldrich, Germany) as substrates, incubated for 30 min. The reaction was stopped with 3 M H₂SO₄ and the optical density of each well was measured at 492 nm in a 96-well plate reader. Recombinant murine cytokines were used as standard agents. 0.05% Tween 20 in phosphate buffer was used as a washing solution.

The following reagents were used for the following assays:

• IL-6: rat anti-mouse IL-6 and biotinylated rat anti-mouse IL-6 (both Pharmingen, USA) mAbs were used as capture and detecting antibodies. Recombinant mouse IL-6 (PeproTech, USA) was used as a standard. The detection limit was about 15 pg IL-6/ml;

• IL-10: rat anti-mouse IL-10 and biotinylated rat anti-mouse IL-10 mAbs were used as capture and detecting antibodies. Recombinant mouse IL-10 was used as a standard (all reagents from Pharmingen, USA). The limit of detection was 15 pg IL-10/ml;

• IL-12 p40: rat anti-mouse IL-12 (p40/p70) clone 15.6 (Pharmingen, USA) mAb and biotinylated rat anti-mouse IL-12(p40) clone 17.8 (Endogen, USA) mAb were used as capture and detecting antibodies. Recombinant mouse IL-12 (Genzyme, UK) was used as a standard. The detection limit was about 30 pg IL-12 p40/ml;

• TNF-α: hamster anti-mouse/rat TNF-α and biotinylated rabbit anti-mouse/rat TNF-α (both Pharmingen, USA) mAbs were used as capture and detecting antibodies. Recombinant mouse TNF-α (Sigma, Germany) was used as a standard. The limit of detection was 30 pg TNF-α/ml;

• prostaglandin E₂ (PGE₂) immunoassay: PGE₂ concentration in supernatants was determined using a monoclonal antibody/enzyme immunoassay kit from Cayman Chemical Co. according to the manufacturer’s instructions;

• nitrite determination: nitric oxide (NO), quantified by the accumulation of nitrite as a stable end-product, was determined by a microplate assay [6]. Briefly, 100-µl samples were removed from the supernatants of the Mϕ culture and incubated with an equal volume of Griess reagent [0.35% 4-aminophenyl sulfone (Sigma-Aldrich, Germany), 0.1% N-(1-naphthyl)ethylenediamine dihydrochloride in 1M HCl (POCh, Poland)] at room temperature for 10 min. The absorbance at 550 nm was measured and nitrite concentration was calculated from a sodium nitrite standard curve.

Western blot analysis of iNOS and COX-2 expression

Mϕ were cultured with different concentrations of MNA and NA for 24 h and the expressions of iNOS and cyclooxygenase-2 (COX-2) in cytosol were determined by a Western blot technique. Briefly, after incubation the cells were lysed in a lysis buffer (1% Triton X-100, 0.1% sodium dodecyl sulfate (SDS) in PBS) containing a protease inhibitor cocktail (Sigma-Aldrich, Germany). Protein concentrations of lysates were determined using a bicinchoninic acid protein assay kit (Sigma-Aldrich, Germany). Samples containing equal amounts of total protein were mixed with gel loading buffer [0.125 M Tris, 4% SDS, 20% glycerol, 0.2 M DTT (dithiothreitol), 0.02% bromophenol blue] in a ratio 2:1 (v/v) and boiled (4 min). Then the samples (20 µg of total protein per lane) were separated on 10% SDS-polyacrylamide gels (Mighty Small II, Amersham Biosciences, USA) using a Laemmli buffer system and the proteins were transferred to nitrocellulose membranes (Bio-Rad, USA). Non-specific binding sites were blocked overnight with 3% non-fat dried milk at 4°C and the membranes were incubated for 2 h at room temperature (RT) with rabbit polyclonal antibody to iNOS (1:2000) (Stressgen, Canada) or rabbit polyclonal antibody to COX-2 (1:1000) (Cayman, USA). Bands were detected with alkaline phosphatase-conjugated secondary antibody (1 h at RT, 1:3000, Sigma-Aldrich, Germany) and developed with BCIP/NBT alkaline phosphatase substrate (Sigma-Aldrich, Germany). Additionally, membranes were reprobed with monoclonal anti-β-actin antibody (1 h at RT, 1:3000, Sigma-Aldrich, Germany). Prestained SDS-PAGE Standards, Low Range (Bio-Rad, USA), were used for molecular weight determinations. Protein bands were scanned and analyzed with the freeware Scion Image (Scion Corporation, USA). The data were normalized to the constitutively expressed β-actin protein.

Reactive oxygen species generation: luminol-dependent chemiluminescence assay

Chemiluminescence was tested at 37°C in a temperature-stabilized Lucy 1 luminometer (Anthos, Austria). Mϕ (1×10⁷ cells/ml) in Hank’s balanced salt solution were preincubated (60 min at 37°C in an atmosphere of 5% CO₂) on a 96-well flat-bottom black plate (Nunc, Denmark) with luminol sodium salt (0.4 mg/ml; Sigma, Germany) and with different concentrations of the agents tested (1–30 mM). After incubation, the cells (200 µl/well) were quickly stimulated with opsonized zymosan (0.4 mg/ml) and photon emission over 75 min with 3-min intervals was measured. Each type of experiment was performed in duplicate.

Statistics

The statistical significance of differences between groups was analyzed using a factorial ANOVA (Microsoft Excel) followed by the Student’s t-test, if appropriate. A p-value less than 0.05 was considered statistically significant.

Results

Distribution of exogenous MNA and NA added to the culture of LPS-stimulated Mϕ

To compare the cell-membrane permeability and stability of MNA and NA in vitro, the compounds were added to LPS-activated Mϕ for 24 h. The final intracellular (cell lysates) and extracellular (supernatants) levels of MNA and NA were estimated and compared with the initial concentrations of the compounds. As shown in Table. 1, the concentration of NA in culture medium decreased by about 20% with a concomitant increase in the intracellular level. However, NA was not metabolized to MNA by Mϕ, as the concentration of MNA in the culture was not elevated above the baseline (data not shown). The ratio of the concentration of NA measured in the culture medium to its final concentration in Mϕ was 8.57. Under the same experimental conditions, the concentration of exogenous MNA in culture medium decreased after 24 h also by about 20% of the initial value. However, the ratio of the MNA concentration in the medium to the final concentration in Mϕ was 35.8, which is four times higher than the ratio for NA. This may indicate a limited cell-membrane permeability for MNA compared with NA. Further conversion of exogenous MNA by Mϕ to its metabolites 1-methyl-2-pyridone-5-carboxamide and 1-methyl-4-pyridone-5-carboxamide is unlikely to be significant since these compounds remained below the detection limit of the method (data not shown).

Table. 1.

Distribution of MNA and NA added to the culture of LPS-stimulated macrophages

Exogenous compounds (µM)a	Final concentrationb		The ratio of medium to cytosol concentration
	medium	cytosol
MNA (0.0)	<0.1	<0.5	ND
MNA (10.000)	7991±461	223±32	35.8
NA (0.0)	9±1	47±3	ND
NA (4.000)	3598±87	420±26	8.57

^aMNA or NA was added to the culture of LPS-stimulated Mϕ at the concentrations indicated in brackets. ^bAfter 24 h, supernatant and Mϕ were collected separately and the concentrations of extracellular (medium) and intracellular (cytosol) MNA and NA were measured as described in Materials and Methods. ND — not done.

Effect of MNA and NA on reactive oxygen species generation: scavenging properties of MNA and NA

Luminol-dependent chemiluminescence (LCL) observed during the respiratory burst of Mϕ is commonly attributed to the production of reactive oxygen species (ROS) [17]. Upon addition of opsonized zymosan, macrophage LCL increased light emission 30 times over baseline. When either MNA or NA was added to the reaction mixture, a dose dependent decrease in LCL was observed for both reagents (Fig. 2). NA was more effective than MNA. However, preincubation of the cells with either MNA or NA did not affect LCL; therefore the generation of ROS was not inhibited (data not shown). These results therefore indicate scavenging properties of the agents.

Fig. 2.

Scavenging properties of MNA and NA. Mϕ (1×10⁶ cells/well) in Hank’s solution were preincubated (60 min at 37°C in an atmosphere of 5% CO₂) on 96-well flat-bottom black plate with luminol sodium salt (0.4 mg/ml) and different concentrations of (A) MNA and (B) NA (1–30 mM). After incubation the cells were stimulated with opsonized zymosan (0.4 mg/ml) and photon emission was measured. Results are expressed as the percentage of ROS production by OZ-stimulated Mϕ ±SEM diminished by that of non-stimulated cells. Each bar represents the mean (±SEM) of three individual experiments. *p<0.05.

Effect of MNA and NA on the production of cytokines by LPS-stimulated Mϕ

Stimulation of Mϕ in vitro with LPS resulted in a pronounced release of pro- and anti-inflammatory cytokines. Addition of NA to cultured cells at the time of activation resulted in a dose-dependent inhibition of both pro-inflammatory cytokines (TNF, IL-6). NA at concentrations below 10 mM did not significantly affect the production of IL-12p40 and only slightly inhibited the release of IL-10, an anti-inflammatory cytokine. MNA, in contrast to NA, did not affect the release of any of the cytokines tested (Fig. 3).

Fig. 3.

Effect of MNA and NA on the production of cytokines by LPS-stimulated Mϕ. Cells stimulated with LPS (100 ng/ml) were exposed to MNA and NA in the culture medium for 24 h and then the content of cytokines in the medium was measured by ELISA. A — TNF-α, B — IL-6, C — IL-12p40, D — IL-10. Results are expressed as the percentage of the cytokine production by control Mϕ ±SEM. Data were calculated 5–8 separate experiments. *p<0.05.

Effect of MNA and NA on the production of NO by LPS- and IFN-γ-stimulated Mϕ

In our experimental set-up, exposure of Mϕ to LPS and IFN-γ resulted in the generation of nitrite (∼14 µM), the end product of NO oxidation. As shown in Fig. 4, NA inhibited the release of nitrite in a dose-dependent manner. The highest non-cytotoxic concentration of NA (10 mM) almost completely abrogated the generation of nitrite (Fig. 4A) without affecting the expression of iNOS (Fig. 4B). MNA at non-cytotoxic concentrations did not affect either nitrite release or the expression of iNOS.

Fig. 4.

Effect of MNA and NA on the production of NO and iNOS expression by LPS plus IFN-γ-stimulated Mϕ. Cells stimulated with LPS (100 ng/ml) and IFN-γ (50 U/ml) were exposed to MNA and NA in the culture medium for 24 h and then both the medium and the cells were collected for further assay. A — the release of nitrites (NO⁻₂); the results are expressed as the percentage of the (NO⁻₂) production by control Mϕ ±SEM. Data were calculated from three separate experiments. B — the expression of iNOS; the data are normalized to constitutively expressed β-actin protein ±SEM. Densitometric analysis of bands from two independent experiments. *p<0.05.

Effect of MNA and NA on prostaglandin synthesis by LPS-stimulated Mϕ

As shown in Fig. 5, NA, but not MNA, inhibited the production of PGE₂, a major COX-2-dependent prostaglandin produced by activated Mϕ, in a dose-dependent manner. However, Western blot analyses showed that NA did not reduce the expression of COX-2. On the other hand, a slight increase in COX-2 expression was observed in cells incubated with MNA.

Fig. 5.

Effect of MNA and NA on the production of PGE2 and COX-2 expression by LPS-stimulated macrophages. Cells stimulated with LPS (100 ng/ml) were exposed to MNA and NA in the culture medium for 24 h and then both the medium and the cells were collected for further assays. A — the release of PGE₂; results are expressed as the percentage of the PGE₂ production by control Mϕ ±SEM. Data were calculated from two separate experiments. B — the expression of COX-2; the data are normalized to constitutively expressed β-actin protein ±SEM. Densitometric analysis of bands from two independent experiments. *p<0.05.

Discussion

In the present study we showed that the stimulation of peritoneal Mϕ with LPS results in a massive secretion of a variety of inflammatory mediators, such as TNF-α, IL-6, IL-12p40, IL-10, NO, and PGE₂. Incubation of these cells with NA showed a dose-dependent reduction of the synthesis of all the mediators tested. Especially mediators with pro-inflammatory properties, such as NO, IL-6, TNF-α, and PGE₂ (the major eicosanoid produced by inflammatory phagocytic cells), were suppressed. The production of IL-10, a cytokine with anti-inflammatory potential, was inhibited to a lesser extend, which supports the anti-inflammatory properties of NA. These results are in agreement with previous observations [7, 20]. For example, it has been shown that NA is a potent inhibitor of pro-inflammatory cytokines produced by cells of the innate immune system [20]. Moreover, it has been shown that NA, but not MNA, inhibits cytokine synthesis, especially the synthesis of TNF-α [5, 8, 15]. Collectively, all these observations clearly indicate that the anti-inflammatory properties of NA are related to its ability to down-regulate functions of the cells of the immune system. However, the mechanism of anti-inflammatory activity of NA is still unclear.

MNA, in contrast to NA, as shown in this study, does not affect the functions of Mϕ. Thus it seems to be unlikely that the anti-inflammatory properties of MNA demonstrated in vivo [22, 23] depend on the same mechanisms as those of NA. Examination of the therapeutic potential of MNA in cardiovascular pharmacology provides some evidence and suggestions that a major target for MNA at a site of inflammation seems to be endothelium [3, 9]. Our investigations also support this hypothesis. We recently demonstrated that exogenous, orally administered MNA profoundly attenuates the contact hypersensitivity reaction to oxazolone in mice through endothelial PGI₂-dependent mechanisms [2].

Therefore, the divergent biological activities of MNA and NA in vitro and their similar anti-inflammatory effect in vivo may be explained by the fact that distinct cells seem to be targets for MNA and NA. Nevertheless, the mechanisms of the different effects of exogenous MNA and NA on the functions of Mϕ remain to be explained. The present data show that Mϕ are not able to metabolize exogenous NA to MNA in vitro. This clearly indicates that NA, but not its metabolites, is responsible for the observed effects. Thus it is tempting to speculate that the limited cell-membrane permeability for MNA compared with that for NA may be responsible for the lack of effect of MNA on the synthesis of inflammatory mediators by activated Mϕ. The results of the LCL experiments also support the thesis that MNA acts in the extracellular space, as it does not inhibit ROS generation but acts as a scavenging agent. On the other hand, it was found previously that MNA, but not NA, can be bound to glycosaminoglycans located on the surface of vascular endothelium cells without effective penetration of the tissue, thus increasing its local concentration on the cell surface [9].

All these observations, the lack of effect of MNA on the synthesis of inflammatory mediators in vitro together with the remarkable anti-inflammatory properties of MNA in vivo as demonstrated in the experimental contact hypersensitivity reaction in mice [2] and in the treatment of contact dermatitis in humans [22, 23] suggest that endothelial cells, but not immune cells, are the target for MNA. Thus in our opinion, MNA can be regarded as an effective anti-inflammatory agent, the action of which does not impair the immunity of patients.

Abbreviations:

MNA

1-methylnicotinamide

NA

nicotinamide

Mϕ

macrophages

ROS

reactive oxygen species

PGE₂

prostaglandin E₂

LCL

luminol-dependent chemiluminescence

NO

nitric oxide

iNOS

inducible NO synthase

COX-2

cyclooxygenase-2

TNF-α

tumor necrosis factor α

IFN-γ

interferon γ

IL

interleukin

LPS

lipopolysaccharide

PBS

phosphate-buffered saline solution

LDH

lactic dehydrogenase

SDS

sodium dodecyl sulfate

RT

room temperature