Patent Application
20170035713
The present invention relates to a composition comprising synergistic combinations of polyphenols and carotenoids. More specifically, the present invention provides a composition comprising a synergistic combination of the aforementioned compounds, which may be used inter alia to inhibit the production of various inflammatory mediators.
The inflammatory process, which forms an important part of the non-specific immune system, is characterized by a complex set of chemical and cellular changes that are essential for host defense in the face of microbial agents and other potentially harmful environmental factors. However, in many cases, inflammation may be triggered inappropriately, and/or may persist to a degree which becomes harmful to the host. In such cases, there may be a need to inhibit or prevent the development of one or more aspects of the inflammatory process, in particular, in cases of non-infectious inflammatory diseases.
A very large number of different chemical mediators have been shown to be involved in the development and control of the inflammatory process. Recent studies by a number of different laboratories have implicated nitric oxide (NO) as an important modulator of a variety of acute and chronic inflammatory disorders, including various types of arthritis, gastro-intestinal diseases, inflammatory conditions of the central nervous system and certain forms of asthma. Consequently, it has been proposed that inhibition of NO production could provide a useful therapeutic mechanism for the treatment and/or management of these inflammatory disorders. Furthermore, inhibition of NO synthesis has also been shown to be useful in some conditions or states that are not primarily inflammatory in nature. Thus, for example, inhibition of NO synthesis has been found to reduce glucose uptake into limb tissue in individuals with Type 2 diabetes during exercise.
The in vivo production of NO is mediated by a family of nitric oxide synthase (NOS) enzymes, including inducible-nitric oxide synthase (I-NOS), which is activated by many different immunological stimuli including lipopolysaccharide (LPS), interferon gamma and interleukin 1 (IL-1).
Inhibition of NOS may be achieved both in vitro and in vivo by the use of L-NG-monomethyl Arginine citrate (L-NMMA). In addition, several other compounds, including a number of natural products, have also been shown to inhibit NO production. The latter group includes compounds such as lutein [Rafi M. M. et al. Mol Nutr Food Res. 2007 March; 51(3):333-40; Choi, J. S. Nutrition. 2006 June; 22(6):668-71] and lycopene [Rafi, M. M. et al. J Food Sci. 2007 January; 72(1):S069-74]. However, the efficacy and potency of many of the natural product NO inhibitors have proven to be not particularly high. A need therefore exists for improved NO production-inhibiting compositions of natural origin.
Another highly important inflammatory mediator is the tumor necrosis factor-alpha (TNF-alpha), which is a cytokine produced by a variety of cell types including macrophages, neutrophils and lymphocytes. TNF-alpha occupies a key position in the early stage of the inflammatory process and is responsible for stimulating the production of other factors such as nuclear factor-κB which in turn causes activation of a wide range of pro-inflammatory genes. Thus, in view of its key pro-inflammatory role, TNF-alpha is clearly an important potential therapeutic target for anti-inflammatory agents.
A third key inflammatory mediator is prostaglandin E2 (PGE2), a member of the eicosanoid family of regulatory molecules. Thus, PGE2 is produced in significant amounts at inflammatory sites, where it acts as a vasodilator, and also (together with other mediators such as histamine and bradykinin) causes an increase in vascular permeability, thereby contributing to most of the classical signs of inflammation.
Finally, another pro-inflammatory mediator that is released by inflammatory cells such as macrophages and neutrophils is the superoxide ion. While superoxide ions are highly effective in killing microbial invaders, in other (particularly non-infective) inflammatory conditions, these ions may cause extensive host tissue damage. The production of superoxide ions is therefore a potentially useful therapeutic target when considering new means for controlling inflammatory states.
It is a purpose of the present invention to provide a composition that may be used to inhibit the production of one or more key inflammatory mediators, such as superoxide ions, NO, TNF-alpha and/or PGE2, as a means for treating or managing pathological states and processes in which said mediators are implicated.
It is another purpose of the invention to provide a composition that is able to inhibit the production of the aforesaid inflammatory mediators with greater efficacy and/or potency than the compounds and compositions reported in the prior art.
It has now been unexpectedly found by the present inventors that polyphenol compounds may synergistically interact with carotenoids in the inhibition several pro-inflammatory pathways. In particular, it has now been found that the polyphenol compounds carnosic acid and curcumin each cause synergistic enhancement of the inhibitory effect of certain carotenoids such as lycopene, lutein and beta-carotene on the production of inflammatory mediators such as NO, TNF-alpha and PGE2. Furthermore, while this synergistic effect is seen in binary combinations of carnosic acid or curcumin together with lycopene, beta-carotene or lutein, the synergism is significantly greater when the polyphenol (such as carnosic acid or curcumin) is combined with two of the aforementioned carotenoids. The aforementioned synergistic anti-inflammatory effect is also seen when the carotenoids are present in combination with other polyphenols such as quercetin, resveratrol and gallic acid.
The present invention is therefore primarily directed to a therapeutic composition comprising one or more polyphenols and two or more carotenoids selected from the group consisting of lutein, lycopene and beta-carotene.
In one preferred embodiment, the polyphenols used in the compositions of the present invention are selected from the group consisting of carnosic acid, quercetin, resveratrol, gallic acid, chicoric acid, gingerol and curcumin.
In one particularly preferred embodiment, the compositions of the present invention comprise the polyphenol compound carnosic acid.
In another particularly preferred embodiment, the compositions of the present invention comprise the polyphenol compound quercetin.
In another particularly preferred embodiment, the compositions of the present invention comprise the polyphenol compound resveratrol.
In another particularly preferred embodiment, the compositions of the present invention comprise the polyphenol compound gallic acid.
In another particularly preferred embodiment, the compositions of the present invention comprise the polyphenol compound curcumin.
In one embodiment, the aforementioned therapeutic composition comprises carnosic acid, lycopene and lutein.
In another preferred embodiment, the composition comprises carnosic acid, lutein and beta-carotene.
In a still further preferred embodiment, the composition comprises lycopene, beta carotene and carnosic acid.
In another embodiment, the composition consists essentially of lycopene, lutein and carnosic acid.
In a further preferred embodiment, the composition consists essentially of lutein, beta-carotene and carnosic acid.
In a still further preferred embodiment, the composition consists essentially of lycopene, beta-carotene and carnosic acid.
In another embodiment, the aforementioned therapeutic composition comprises curcumin, lycopene and lutein.
In another preferred embodiment, the composition comprises curcumin and lycopene.
In a still further preferred embodiment, the composition comprises curcumin and lutein.
In another embodiment, the composition consists essentially of lycopene, lutein and curcumin.
In a further preferred embodiment, the composition consists essentially of lutein and curcumin.
In a still further preferred embodiment, the composition consists essentially of lycopene and curcumin.
It is to be noted that the term “consists essentially of”, as used throughout this disclosure and appended claims refers to the situation wherein the composition of the present invention may comprise, in addition to the named elements (i.e. carnosic acid together with lycopene and/or lutein), other compounds, substances and agents which do not materially affect the basic and novel characteristics of the present invention.
In other preferred embodiments, the compositions of the above-disclosed preferred embodiments may further comprise one or more additional carotenoids. In one particularly preferred embodiment, the additional carotenoids are selected from the group consisting of phytoene and phytofluene. Thus, in one preferred embodiment, the composition of the present invention comprises curcumin, lycopene, lutein, phytoene and phytofluene. Similarly, in another preferred embodiment, the composition comprises carnosic acid together with two or more carotenoids selected from the group consisting of lycopene, beta-carotene and lutein, and further comprises phytoene and phytofluene.
The active components of the above-disclosed compositions (i.e. polyphenol(s) and carotenoids) may be purified compounds, synthetic compounds or may be present in mixture with other components, for example in plant extracts such as rosemary extract (in the case of carnosic acid), an extract of turmeric rhizomes (in the case of curcumin), marigold extract (in the case of lutein) or a tomato extract (such as Lycomato—which is commercially available from LycoRed, Be'er Sheva, Israel—in the case of lycopene and other carotenoids).
It is to be noted that the term “curcumin” as used in the present disclosure should be taken to include all forms of this polyphenol compound within its scope. Curcumin is the principal curcuminoid of the well-known spice turmeric, which is a member of the ginger family (Zingiberaceae). Curcumin can exist in at least two tautomeric forms, keto and enol, and either or both of these forms may be used to work the presently-disclosed invention. Furthermore, the term “curcumin” as used herein also includes certain derivatives such as curcumin-PC, which is curcumin preparation having improved miscibility in both aqueous and lipid phases, by virtue of the polyphenol having been bound to a phosphatidyl moiety (usually of soy origin). Curcumin-PC is commercially available from Indena S.p.A. (Milan, Italy), and its properties and preparation are described in published European patent application EP1837030.
It should further be noted that the term “lutein” as used in the present disclosure should be understood to include all lutein esters within its scope. In addition, the term “lutein” may also be taken to include within its scope a mixture of lutein and zeaxanthin, since the last-mentioned carotenoid is often present together with lutein (sometimes constituting 0.1%-15%, and more often 4%-6% of the lutein content).
In another aspect, the present invention provides a method for inhibiting or reducing the production of superoxide ions, NO, TNF-alpha and/or PGE2 in a mammalian subject comprising administering to said subject a therapeutic composition according to any of the embodiments disclosed hereinabove.
Furthermore, the present invention also provides a method of treatment of pathological conditions in which superoxide ions, NO, TNF-alpha and/or PGE2 acts as a modulator or mediator of said condition in a mammalian subject in need of such treatment, wherein said method comprises administering to said subject a therapeutic composition according to any one of the embodiments disclosed hereinabove. In one preferred embodiment of this method, the condition to be treated is selected from the group consisting of acute inflammatory conditions, chronic inflammatory conditions, rheumatoid arthritis, adult respiratory distress syndrome (ARDS), asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis, peritonitis and inflammatory bowel disease, and neurodegenerative diseases, such as for example Alzheimer's disease (AD).
In particularly preferred embodiments of the methods described hereinabove, the mammalian subject is a human subject.
While in the above-disclosed methods, the therapeutic composition may be administered by any convenient means, in one preferred embodiment said composition is administered in a pharmaceutical dosage form. In another preferred embodiment, however, the therapeutic composition is incorporated into a foodstuff or beverage.
In another aspect, the present invention is directed to the use of a combination of one or more polyphenols and one or more carotenoids selected from the group consisting of lycopene, beta-carotene and lutein in the manufacture of a medicament for the treatment of conditions responsive to inhibition of NO, TNF-alpha and/or PGE2 production.
In one preferred embodiment of this aspect of the invention, the one or more polyphenols are selected from the group consisting of carnosic acid, quercetin, resveratrol, gallic acid, chicoric acid, gingerol and curcumin.
In one particularly preferred embodiment of this aspect of the invention, the polyphenol is carnosic acid.
In another particularly preferred embodiment of this aspect of the invention, the polyphenol is quercetin.
In yet another particularly preferred embodiment of this aspect of the invention, the polyphenol is resveratrol.
In yet another particularly preferred embodiment of this aspect of the invention, the polyphenol is gallic acid.
In a further particularly preferred embodiment of this aspect of the invention, the polyphenol is curcumin.
In one preferred embodiment, the condition to be treated is an inflammatory condition.
In one preferred embodiment of the above-disclosed use, the condition to be treated is selected from the group consisting of acute inflammatory conditions, chronic inflammatory conditions, rheumatoid arthritis, adult respiratory distress syndrome (ARDS), asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis, peritonitis and inflammatory bowel disease, and neurodegenerative diseases, such as for example Alzheimer's disease (AD).
In one particularly preferred embodiment of this aspect of the invention, carnosic acid is used in combination with both lycopene and lutein.
In another particularly preferred embodiment of this aspect of the invention, carnosic acid is used in combination with both lycopene and beta-carotene.
In a still further preferred embodiment of this aspect of the invention, carnosic acid is used in combination with both lutein and beta-carotene.
In one particularly preferred embodiment of this aspect of the invention, curcumin is used in combination with both lycopene and lutein.
In another particularly preferred embodiment of this aspect of the invention, curcumin is used in combination with lycopene.
In a still further preferred embodiment of this aspect of the invention, carnosic acid is used in combination with lutein.
All the above and other characteristics and advantages of the present invention will be further understood from the following illustrative and non-limitative examples of preferred embodiments thereof.
As disclosed hereinabove, the present invention provides compositions comprising combinations of one or more polyphenols with one or more carotenoids. In a particularly preferred embodiment of the invention, the compositions comprise carnosic acid as the sole polyphenol and one or more carotenoids selected from the group consisting of lycopene (either purified or contained within a tomato extract), lutein and beta-carotene. In another particularly preferred embodiment of the invention, the compositions comprise curcumin as the sole polyphenol In still other preferred embodiments, the sole polyphenol component is selected from the group consisting of quercetin, resveratrol and gallic acid.
Preferred daily amounts of each of the active agents present in the compositions containing carnosic acid that are administered to subjects in need of such administration are as follows:
More preferably, the daily amount of each of the aforementioned active agents is in the range of 1 to 5 mg.
The amount of each of the various active components may be selected such that the weight ratios therebetween fall within the following broad range:
Lycopene : Lutein : Beta-carotene : Carnosic acid 0.1-5.0 : 0.1-5.0: 0.1-5.0 : 0.1-5.0
In one preferred group of compositions, the active components may be combined in the following weight ratio ranges:
Lycopene : Lutein : Beta-carotene : Carnosic acid 0.1-1.0 : 0.1-1.0: 0.1-1.0 : 0.1-1.0
In one preferred embodiment, the active components may be combined in the following ratio:
Lycopene : Lutein : Beta-carotene : Carnosic acid 1.0 : 1.0 : 1.0 : 0.5
In another preferred embodiment, the active components may be combined in the following ratio:
Lycopene : Lutein : Beta-carotene : Carnosic acid 1.0 : 0.3 : 0.3 : 0.4
In a still further preferred embodiment, the active components may be combined in the following ratio:
Lycopene : Lutein : Beta-carotene : Carnosic acid 1.0 : 1.0 : 1.0 : 1.0
It is to be noted that the compositions prepared in accordance with the preceding examples of preferred weight ratios do not require the obligatory presence of all four components listed. Rather, it is sufficient for the composition to comprise carnosic acid (or another polyphenol) together with at least two of the indicated carotenoids, wherein the relative amount of each of these components is as indicated by the figures provided immediately hereinabove.
In another group of preferred embodiments, the active components may be combined in the following weight ratio ranges:
Lycopene : Lutein : Beta-carotene : Carnosic acid 0.1-1.0 : 0.1-5.0: 0.1-1.0 : 0.1-1.0
More preferably, the active components may be combined in the following weight ratio ranges:
Lycopene : Lutein : Beta-carotene : Carnosic acid 0.1-1.0 : 1.0-4.0: 0.1-1.0 : 0.1-1.0
In specific preferred embodiments, the active components may be combined in the following weight ratios:
Lycopene : Lutein : Carnosic acid 0.1 : 1.73 : 0.13
Lycopene : Lutein : Carnosic acid 0.1 : 1.8 : 0.26
B-carotene : Lutein : Carnosic acid 0.29 : 1.29 : 0.1
B-carotene : Lutein : Carnosic acid 0.39 : 1.29 : 0.1
B-carotene : Lutein : Carnosic acid 0.32 : 3.42 : 0.1
B-carotene : Lutein : Carnosic acid 0.16 : 1.71 : 0.1
B-carotene : Lutein : Carnosic acid 0.29 : 1.29 : 0.1
B-carotene : Lutein : Carnosic acid 0.39 : 1.29 : 0.1
In the case of the compositions that contain curcumin as the sole polyphenol, the preferred daily amounts of each of the active agents that are administered to subjects in need of such administration are as follows:
More preferably, the daily amount of each of the aforementioned active agents is in the range of 1 to 5 mg.
The amount of each of the various active components may be selected such that the weight ratios therebetween fall within the following broad range:
Lycopene : Lutein : Curcumin 0.1-5.0 : 0.1-5.0: 0.1-5.0
In one preferred group of compositions, the active components may be combined in the following weight ratio ranges:
Lycopene : Lutein : Curcumin 0.1-1.5 : 0.1-1.5: 0.1-1.0
In one preferred embodiment, the active components may be combined in the following ratio:
Lycopene : Lutein : Curcumin 0.5 : 0.5 : 0.75
The various active components may be formulated for either system or topical use. In the case of systemic administration, the polyphenol(s) and carotenoid(s) may be incorporated into oral dosage forms such as tablets, caplets, capsules, syrups, elixirs, liquids etc.
In other preferred embodiments, the composition of the present invention may be administered topically, for example on the skin or mucous membranes (e.g. as creams, lotions, ointments etc.). Further details of suitable methods of incorporating the polyphenol and carotenoid-containing compositions of the present invention into the various different dosage forms may be obtained from any standard reference work known to the skilled artisan, including, for example, Remington's Pharmaceutical Sciences, Mack Publishing Co, Easton, Pa., USA (1980).
In other preferred embodiments, the composition of the present invention is prepared as a food additive that is suitable for direct incorporation into a foodstuff or a beverage.
The carnosic acid used to prepare the compositions of the present invention may be obtained commercially from several different suppliers including Alexis Biochemicals, Lausen, Switzerland. The curcumin used to prepare the compositions of the present invention may be obtained commercially from several different suppliers including Indena, Italy. Curcumin-PC may also be obtained from Indena. The carotenoids may be obtained from several different suppliers including LycoRed Ltd., Be'er Sheva, Israel.
In some embodiments of the present invention, some of the components of the composition, such as lycopene may be incorporated into said composition in the form of a lycopene-rich tomato extract. One such tomato extract is commercially available (e.g. in capsule form) from LycoRed Ltd., Beer Sheva, Israel under the trade name “Lyc-O-Mato®”. Suitable processes for preparing this extract and similar extracts are described in U.S. Pat. No. 5,837,311, the specification of which is incorporated herein by reference in its entirety. However, it is to be recognized that many other types of preparatory procedures may be used to obtain the carotenoid-containing composition from a variety of plant sources. In addition, the composition may also be prepared from one or more synthetic carotenoids.
The following examples are provided for illustrative purposes and in order to more particularly explain and describe the present invention. The present invention, however, is not limited to the particular embodiments disclosed in these examples.
Macrophage isolation and cell culture—Peritoneal macrophages were collected from the peritoneal cavity of 6-8 week old male ICR mice (Harlan, Israel) that had been given an intraperitoneal injection of 1.5 ml of thioglycollate broth (4%) 4 days before harvest. Peritoneal macrophages were washed three times with PBS and, if needed, a hypotonic lysis of erythrocytes was performed, yielding 90-95% purity. The macrophages were identified by FACS analysis using FITC-conjugated rat anti-mouse F4/80 (MCA497F) (Serotec, Oxford, England) by flow microfluorimetry on FACS (Becton Dickinson, Mountain View, Calif.). For each sample, 10,000 light scatter-gated viable cells were analyzed. Peritoneal macrophages and murine macrophage cell line RAW264.7 were cultured RPMI 1640 medium containing 10% FCS, 2 mM L-glutamine; 100 U/ml penicillin; 100 μg/ml streptomycin (Beit-Haemek, Israel) in 96-well plates (1×106 cells/well) at 37° C. in 5% CO2 atmosphere. Cells were stimulated with LPS (0.1-1 μg/ml) in the presence or absence of carnosic acid and/or one or more of the following carotenoids: carnosic acid, purified lycopene, lycopene-rich tomato extract (Lyc-O-Mato®; LycoRed Ltd., Be'er Sheva, Israel), lutein and beta-Carotene.
The carnosic acid and the various carotenoids were dissolved in DMSO (to a final concentration of 5 mM). The mixture was vortexed and incubated in a water bath at 37° C. (with shaking) for 10 min and then sonicated in a sonicator bath three times for 15 seconds each time. Using this stock solution the desired concentrations were prepared by the addition of appropriate volumes thereof to warm culture medium.
The concentration of lycopene in the solution was determined after extraction as follows: 0.5 ml isopropanol+1.5 hexane/dichloromethane (1:5 V/V) containing 0.025% BHT were added to 1 ml of lycopene solution freshly prepared at a concentration of 20 uM in preheated medium. The solution was vortexed and the phases were separated by centrifugation 3000 rpm for 10 min.
A spectrum analysis is conducted to measure the content of lycopene (absorption peak at 471 nm.)
Appropriate volumes of DMSO (0.1-0.2%) were added to the controls and the percent inhibition in each test tube was calculated in relation to its control.
NO production assay—NO levels in supernatants of cell cultures were determined by assaying nitrite levels using Griess reagent and sodium nitrite as a standard as described in Green, L. C., Wagner, D. A., Glogowski, J., Skipper, P. L., Wishnok, J. S., and Tannenbaum, S. R. (1982) Anal Biochem. 126: 131-138.
PGE2 measurement—Supernatants of resting and stimulated cells were collected and immediately stored at −70° C. PGE2 levels were determined by utilizing a dextran coated charcoal radio-immunoassay protocol as previously described (Dror N, Tveria L, Meniv I, Ben-Shmuel S, Filipovich T, Fleisher-Berkovich S., Regul Pept. 2008 150: 21-5).
Briefly, 100 μl sample or PGE2 standard (Sigma Israel, Rehovot, Israel) were incubated in the presence of 500 μl anti-PGE2 anti-serum (Sigma Israel, Rehovot, Israel) for 30 min. [3H]PGE2 (Amersham Biosciences, NJ, USA) was added next for 24 h at 4° C. 24 h later, 200 □μl cold dextran coated charcoal suspension was added to each tube and incubated for 10 min on ice. The tubes were centrifuged at 3500 RPM for 15 min at 4° C. 500 μl of supernatants containing [3H]PGE2-anti-PGE2 complexes were counted (Packard Spectrometry 1900CA) and the amount of PGE2 was calculated.
TNF-alpha production assay—Concentrations of TNF-alpha were quantified using ELISA kits (Biolegend Inc., San Diego, Calif.).
Statistical analysis—Data are presented as the mean±SEM. Statistical significance for comparisons between groups was determined using Student's paired two-tailed t test.
Results
Dose Dependent Synergistic Inhibition of NO Production by Combination of Lycopene or Lycomato with Carnosic Acid.
The results obtained using carnosic or individual carotenoids alone are as follows: Lycopene or Lycomato in the range of 1-5 μM caused low level inhibition of NO production. Carnosic acid (1 and 2 μM) caused 12% and 18% inhibition of NO production, respectively.
The addition of carnosic acid to lycopene or Lycomato caused a synergistic inhibition of NO production which was dose dependent.
Combination of Carnosic acid with Lycomato is more effective than with purified lycopene.
The results presented in
a.
Inhibition of NO Production by Combination of Optimal Low Concentrations of Two Components: Lycopene or Lycomato with Carnosic Acid, Lutein and Beta-Carotene.
Combination of 1 μM lycopene or Lycomato with 2 μM Carnosic acid caused significant synergistic inhibition of NO production, which was more effective in the presence of Lycomato compared with lycopene.
Combination of 1 μM lycopene or Lycomato with 1 μM lutein or with 2 μM beta-carotene caused an additive or non significant synergistic inhibition of NO production, respectively.
Combination of lycopene or Lycomato with carnosic acid (i.e. a combination of a carotenoid with a polyphenol) is more effective than the combination of two cartenoids.
b.
Inhibition of NO Production by Combination of Optimal Low Concentrations of Lycopene or Lycomato with Two Other Components.
Combination of lycopene or Lycomato with carnosic acid and lutein or with carnosic acid and beta-Carotene (concentrations the same as used to generate the results shown in
Combination of the four components (i.e. lycopene or Lycomato together with carnosic acid, lutein and beta-carotene did not improve upon the combination of the three components.
Combination of Carnosic Acid and Carotenoids Excluding Lycopene or Lycomato.
Combination of either lutein or beta-Carotene with carnosic acid caused a significant and similar synergistic inhibition of NO production (which is similar to the combination of lycopene and carnosic acid but lower than that seen with the combination of Lycomato and carnosic acid). Combination of lutein and beta-Carotene caused additive (or lower) effect. These results further support that both cartenoid(s) and polyphenol(s) are required in order to obtain the optimal synergistic effect.
The results are the means±SEM of 3 independent experiments, each produced in duplicate.
Upper Graph: Inhibition of TNF-Alpha Production by Different Combinations of Optimal Low Concentrations of Lycopene with Carnosic Acid, Lutein and Beta-Carotene.
TNF-alpha production in the same set of experiments as in
Combinations of lycopene with carnosic acid or with beta-carotene caused a low-level synergistic inhibition of TNF-alpha production: 10% and 8%, respectively.
Similar to the effect on NO production, combinations of lycopene with either carnosic acid and lutein or with carnosic acid and beta-carotene caused a significant and similar synergistic inhibition of TNF-alpha production, which was higher than the synergistic inhibition caused by combination excluding carnosic acid.
Combination of carnosic acid with all three carotenoids did not improve upon the synergistic result obtained with the aforementioned combination of carnosic acid with two carotenoids.
Lower graph: Inhibition of TNF-alpha production by different combinations of optimal low concentrations of Lycomato with carnosic acid, lutein and beta-carotene.
TNF-alpha production was inhibited (10%) in the presence of Lycomato (in contrast to the lack of detectable inhibition in the presence of lycopene). Combinations of Lycomato with each of the other carotenoids caused a synergistic inhibition that was higher in the presence of carnosic acid.
Similar to the effect on NO production, combinations of Lycomato with carnosic acid and lutein or with carnosic acid and beta-Carotene caused a significant and similar synergistic inhibition of TNF-alpha production, while a combination excluding carnosic acid caused a lesser synergistic effect.
As in the case of purified lycopene, a combination of carnosic acid with all three carotenoids did not improve upon the synergistic result obtained with the aforementioned combination of carnosic acid with two carotenoids.
The results are the means±SEM of 3 independent experiments, each performed in duplicate.
It is to be noted that combinations that included Lycomato were more effective in inhibiting TNF-alpha production than those that incorporated purified Lycopene.
Inhibition of PGE2 Production by Different Combination of Optimal Low Concentrations of Lycopene with Carnosic Acid, Lutein and Beta-Carotene.
PGE2 production in the same set of experiments as reported in
A low level synergistic inhibition could be detected with a combination of Lycomato with lutein and carnosic acid only, while a combination with carnosic acid and beta-carotene caused only an additive effect. A combination with lutein and beta-carotene caused an additive inhibition of PGE2 production.
It will also be seen from
Inhibition of PGE2 Production by Different Combinations of Optimal Low Concentrations of Lycopene with Carnosic Acid, Lutein and Beta-Carotene.
As already shown in
A low-level synergistic inhibition could be detected in the case of a combination of lycopene with lutein and carnosic acid only, while a combination with carnosic acid and beta-Carotene caused only an additive effect. A combination containing lutein and beta-carotene caused additive inhibition of PGE2 production. Consequently, lower concentrations were studied (as shown in
A combination of all four active agents (i.e. carnosic acid plus three carotenoids) did not improve the combination of the carnosic acid with two carotenoids.
Synergistic Inhibition of PGE2 Production by Different Combination of Optimal Lower Concentrations of Carnosic Acid, Lutein and Beta-Carotene (Lower Panel).
Neither lutein (0.5 μM) nor beta-Carotene (1 μM) alone affected PGE2 production, while carnosic acid (1 μM) caused 10% inhibition. In these conditions combinations of lycopene 1 mM with lower concentrations of either of two other components caused synergistic inhibition.
The combination of all four active agents did not improve the combination of the three.
Inhibition of PGE2 Production by Different Combinations of Optimal Low Concentrations of Lycomato with Carnosic Acid, Lutein and Beta-Carotene.
The upper panel shows that the effect of Lycomato on inhibition of PGE2 production is similar to that of pure Lycopene and the similar combinations resulted with similar effect as shown for lycopene (
Synergistic Inhibition of PGE2 Production by Different Combination of Optimal Lower Concentrations of Carnosic Acid, Lutein and Beta-Carotene (Lower Panel).
As in
A combination of all four active agents (i.e. carnosic acid plus three carotenoids) did not improve the combination of the carnosic acid with two carotenoids.
Synergistic Inhibition of NO Production by Combinations of Lutein, Beta-Carotene and Carnosic Acid.
The upper two graphs (A and B) illustrate the synergistic interaction between the three components of the tested composition on NO production, wherein the final concentration of beta-carotene was 0.5 μM. Similarly, compositions containing a higher concentration of beta-carotene (1.0 μM; graphs C and D) also caused inhibition of NO production in a synergistic manner.
In each of the graphs presented in
Synergistic Inhibition of TNFα Production by Combinations of Lutein, Beta-Carotene and Carnosic Acid.
The upper two graphs (A and B) illustrate the synergistic interaction between the three components of the tested composition on TNFα production, wherein the final concentration of beta-carotene was 0.5 μM. Similarly, compositions containing a higher concentration of beta-carotene (1.0 μM; graphs C and D) also caused inhibition of TNFα production in a synergistic manner.
In each of the graphs presented in
Methods and Materials:
Macrophage isolation and cell culture—Peritoneal macrophages were collected and cultured as described in Example 1, hereinabove.
Preparation of test agents—Lycopene and Lutein were dissolved in DMSO (the volume of DMSO in the test solution did not exceed 0.04%). The mixture was vortexed and shaken at 37° C. for 10 min and sonicated in a sonicator bath for 15 sec×3 times. From this stock solution the desired concentrations were reached by addition of appropriate volumes to warm culture medium. The concentration in the solution was calculated to 1 ml of the highest final concentration 0.5 ml isopropanol+1.5 ml hexane/dichloromethane (1:5 V/V) containing 0.025% BHT. The solution was vortexed and the phases were separated by centrifugation at 3000 rpm for 10 min. A spectrum analysis was conducted to detect the level of nutrients. Carnosic acid, Resveratrol, Gallic acid or Quercetin were dissolved in ethanol (the volume of ethanol in the test solution did not exceed 0.0025%).
Appropriate volumes of DMSO and/or ethanol were added to the controls and the percent inhibition of each test tube was calculated in relation to its control tube.
NO production assay—NO levels in supernatants of cell cultures were determined by assaying nitrite levels using Griess reagent and sodium nitrite as described hereinabove in Example 1.
Statistical analysis—Data are presented as the mean±SEM. Statistical significance for comparisons between groups was determined using Student's paired two-tailed t test.
Results:
A. Synergistic Inhibition of NO Production by Combinations of Low Concentrations of Lycopene, Lutein and Each of the Different Polyphenols
Macrophages were incubated with 1 μM Lycopene, 1 μM Lutein and either 2 μM Carnosic acid, 2 μM Resveratrol, 2 μM Gallic acid or 2 μM Quercetin and their combinations for 1 h before addition of LPS for 16 h at 37° C. NO production was measured and the % of inhibition was calculated. In each experiment the effect of three different concentrations of LPS is analyzed, as the sensitivity of the cells may change in different experiments.
Combinations of 1 μM Lycopene, 1 μM Lutein and 2 μM of either Carnosic acid Resveratrol, Gallic acid or Quercetin, caused a significant synergistic inhibition of NO production (indicated by the letter “S” in the graph, wherein the horizontal line crossing each of the bars representing the synergistic combinations indicates the results to be expected if the interaction were additive and not synergistic) There were no significant differences between each of these various combinations. As shown in the Figure, the effect of each of the carotenoid or polyphenol tested at the given concentration was very low. As shown by the horizontal line in each graph, the synergistic effect was around three fold higher than that of the additive effect.
B. Synergistic Inhibition of NO Production by Combination of Low Concentrations of Lyc-O-Mato, Lutein and Each of the Different Polyphenols.
Macrophages were treated as in A, but the experiments were conducted using Lyc-O-Mato instead of Lycopene.
Although Lyc-O-Mato by itself caused a similar inhibition of NO production as that caused by Lycopene, combinations with Lyc-O-Mato were more effective and resulted in higher synergism of about four fold compared with the additive effect.
The results shown in
Methods and Materials:
Macrophage Isolation:
Peritoneal macrophages were isolated and treated as described hereinabove in Example 1.
Superoxide production: The production of superoxide anion (O2−) by macrophages was measured as the superoxide dismutase-inhibitable reduction of ferricytochrome c by the microtiter plate technique, as known in the prior art. An aliquot of radiolabelled macrophages (5× 105 cells/well) used for the adherence assay was taken and suspended in 100 μl incubation medium containing ferricytochrome c (150 mM). Stimulation was induced with PMA (50 ng/ml). The reduction of ferricytochrome c was followed by a change of absorbance at 550 nm at 2 min intervals for 30 min on a Thermomax Microplate Reader (Molecular Devices, Melno Park, Calif., USA). The maximal rates of superoxide generation were determined and expressed as nanomoles O2−/106 cells/10 min using the extinction coefficient E550=21 mM−1 cm−1.
Results:
Upper Graph (A): Inhibition of Superoxide Production by Different Combinations of Optimal Low Concentrations of Purified Lycopene with Carnosic Acid, Lutein or Beta-Carotene.
Superoxide production was inhibited in the presence of 2 μM beta-carotene (10%).
Combinations of lycopene with carnosic acid or with beta-carotene caused a low-level inhibition of superoxide production that was not significantly different from the effect of beta-carotene.
Similar to the effect on NO production (see Example 1, hereinabove), combinations of lycopene with either carnosic acid and lutein, or with carnosic acid and beta-carotene caused a significant and similar synergistic inhibition of superoxide production, which was higher than the synergistic inhibition caused by a combination excluding carnosic acid.
Combination of carnosic acid with all three carotenoids did not improve upon the synergistic result obtained with the aforementioned combination of carnosic acid with two carotenoids.
Lower Graph (B): Inhibition of Superoxide Production by Different Combinations of Optimal Low Concentrations of Lyc-O-Mato with Carnosic Acid, Lutein or Beta-Carotene.
Superoxide production was inhibited (7%) in the presence of Lyc-O-Mato (in contrast to the lack of detectable inhibition in the presence of lycopene). Combinations of Lyc-O-Mato with each of the other carotenoids caused a caused a low-level inhibition of superoxide production that was not significantly different from the effect of beta-carotene or Lyc-O-Mato.
Similar to the effect on NO production (see Example 1, hereinabove), combinations of Lyc-O-Mato with carnosic acid and lutein or with carnosic acid and beta-Carotene caused a significant and similar synergistic inhibition of superoxide production, while a combination excluding carnosic acid caused a lesser synergistic effect.
As in the case of purified lycopene, a combination of carnosic acid with all three carotenoids did not improve upon the synergistic result obtained with the aforementioned combination of carnosic acid with two carotenoids.
The results are the means±SEM of 3 independent experiments, each performed in duplicate.
Introduction
Expression of inflammatory cytokines as well enzyme protein expression can be regulated by the activation of the transcription factor nuclear factor-kappa B (NFκB), which is critically involved in several aspects of the pathogenesis chronic inflammatory diseases. NFκB is activated as a consequence of phosphorylation, ubiquitination, and subsequent proteolytic degradation of the IκB protein through activation of IκB kinase (IKK). The liberated NFκB translocates into nuclei and binds to motifs in the promoters of pro-inflammatory genes such as inducible nitric oxide synthase (iNOS) and of cyclooxygenase 2 (COX2) TNF-α, and IL-1β, leading to the induction of their mRNA expression. Most of the anti-inflammatory drugs have been shown to suppress the expression of these genes by inhibiting the NFκB activation pathway. Thus, an NFκB inhibitor may be useful as a potential therapeutic drug in clinical applications for regulating the inflammation associated human diseases.
p65 NFκB RelA can be phosphorylated by PKA on Ser-276 or by a redox-sensitive mechanism on Ser-536. It has been shown that reactive oxygen species (ROS) plays an important role in NF-κB activation and inflammatory gene expression.
The aim of this study was to investigate whether low concentrations of the combinations of Lycopene/Lyc-O-Mato+Lutein+carnosic acid can cause a synergistic inhibition of NFκB activation.
NFκB activation was analyzed by its two phosphorylated forms: PKA dependent Ser-276 and redox-sensitive Ser-536.
Methods
Macrophage isolation: Peritoneal macrophages were isolated and treated as described hereinabove in Example 1. For detection of NF-κB activation the cell were treated with LPS for 10 min.
Preparation of nuclear protein extract—2×106 cells were suspended in 600 μl of ice-cold NP-40 lysis buffer (0.1% NP-40, 10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3 mM MgCl2, 1 mM EDTA, 10 μg/ml leupeptin, 10 μg/ml aprotonin, and 1 mM PMSF). The cells were vortexed for 15 s, kept on ice for 5 min, and centrifuged at 300 g for 10 min at 4° C. The resulting pellets (the nuclei containing fractions) were then immediately solubilized in electrophoresis sample buffer Nuclear integrity was verified directly by light microscopy, which also revealed that intact cells were rarely observed in nuclei-containing fraction (<2%).
Total Cell lysates: were prepared using 1% Triton X-100, 50 mM HEPES (pH 7.5), 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 10% glycerol, 25 mM NaF, 10 μM ZnC12, 1 mM PMSF, and 100 μM leupeptin.
Immunoblot analysis: lysate proteins (35-50 μg) were separated by electrophoresis on 7.5% polyacrylamide SDS gels. The resolved proteins were electrophoretically transferred to nitrocellulose, which was stained with Ponsue red to detect protein banding, and then blocked in 5% milk in TBS (10 mM Tris, 135 mM NaCl, pH 7.4). Immunoblot determination was done as described before (17) using primary antibodies p-P65, COX-2 and iNOS (Cell Signaling Technology, Beverly, Mass.) for overnight incubation at 4° C. and second antibody, peroxidase conjugated goat antirabbit or antimouse (Amersham Biosciences, Buckinghamshire, United Kingdom) for 1 hour at room temperature and developed using the enhanced chemiluminescence (ECL) detection system (Amersham Biosciences).
For immunoblot detection of P-65 the nuclei fractions of 2×106 cells were immediately solubilized in electrophoresis sample buffer and processed for separation on 8% SDS polyacrylamide gel electrophoresis (SDS-PAGE).
Results
As shown in
As shown in the immunoblot, there was no phosphorylation of p65 NFκB on Serine 276.
These results demonstrate that the carotenoid-polyphenol composition tested causes significant synergistic inhibition of NFκB activation mediated by phophorylation Ser-536 that is mediated by a redox-sensitive mechanism.
Under the same conditions, addition of the nutrient combinations (in concentrations detailed above) 1 h prior to addition of LPS for 24 h, caused a significant inhibition of iNOS and of COX2 protein expression in total cell lysates (
The intensity of each protein band (iNOS or COX2) was divided by the intensity of each β-actin band after quantitation by densitometry, and expressed as arbitrary units. Shown are the means±SEM of three independent experiments.
These results demonstrate a synergistic inhibition of the induction of both inflammatory enzymes at levels of around 80% and around 60% for iNOS and COX-2, respectively, and provide both support for the inhibition of NO production and PGE2 release reported hereinabove, as well as a molecular explanation therefor.
Methods and Materials:
Macrophage isolation and cell culture—Peritoneal macrophages were collected from the peritoneal cavity of 6-8 week old male ICR mice (Harlan, Israel) that had been given an intraperitoneal injection of 1.5 ml of thioglycollate broth (4%) 4 days before harvest. Peritoneal macrophages were washed three times with PBS and, if needed, a hypotonic lysis of erythrocytes was performed, yielding 90-95% purity. The macrophages were identified by FACS analysis using FITC-conjugated rat anti-mouse F4/80 (MCA497F) (Serotec, Oxford, England) by flow microfluorimetry on FACS (Becton Dickinson, Mountain View, Calif.). For each sample, 10,000 light scatter-gated viable cells were analyzed. Peritoneal macrophages were cultured in RPMI 1640 medium containing 10% FCS, 2 mM L-glutamine; 100 U/ml penicillin; 100 μg/ml streptomycin (Beit-Haemek, Israel) in 96-well plates (2×105 cells/well) at 37° C. in 5% CO2 atmosphere. LycoMato, Lutein and curcumin-PC (Indena product) and, for comparison, LycoMato, Lutein and pure curcumin and their various combinations were added to the cells. One hour later, LPS (0.2 μg/ml) was added and the macrophages were cultured at 37° C. in a 5% CO2 atmosphere for 24 h.
Curcumin PC (Indena) was dissolved in Diethylene glycol monoethyl ether from Sigma (as recommended by Indena). The volume of solvent was 0.12% for 1 □M curcumin PC. The concentration of curcumin PC was calculated according to its content in the formula (Curcumin PC). Lycomato and Lutein or curcumin were dissolved in DMSO (the volume of DMSO in the test solution was 0.01% for either 1 θ□M Lycomato, Lutein or pure curcumin. The mixture was vortexed and shaken at 37° C. for 10 min and sonicated in a sonicator bath for 15 sec×3 times. From this stock solution the desired concentrations were made by addition of appropriate volumes to warm culture medium. The concentration of lycopene in solution was calculated to 1 ml of the highest final concentration 0.5 ml isopropanol+1.5 ml hexane/dichloromethane (1:5 V/V) containing 0.025% BHT. The solution is vortexed and the phases are separated by centrifugation 3000 rpm for 10 min. A spectrum was done to detect the level of nutrients.
To the controls appropriate volumes of DMSO and/or Diethylene glycol monoethyl ether were added and the percent inhibition of each test tube was calculated in relation to its control tube.
NO production assay—NO levels in supernatants of cell cultures were determined by assaying nitrite levels using Griess reagent and sodium nitrite as a standard.
Statistical Analysis. Data are presented as the mean±SEM. Statistical significance for comparisons between groups was determined using Student's paired two-tailed t test.
Results
Curcumin PC or pure curcumin were added to macrophages in final concentrations in a range of 0-20 μM before addition of LPS. As shown in
Low concentrations 1 μM and 2 μM, that had non-significant inhibitory effect and did not differ between curcumin PC and pure curcumin, were chosen to study the effect of combinations with Lycomato and Lutein.
Different combinations of the three phyto-nutrients in final concentrations of 1 or 2 μM were studied in order to find the optimal concentrations that give the best synergistic inhibitory effect of NO production. The results were calculated in relation to their appropriate control tubes.
Key to
The bars shown in each of the graphs, in order from left to right, represent the following test substances: curcumin-PC, lycopene (in the form of LycoMato), lutein, curcumin-PC+lycopene, curcumin-PC+lycopene+lutein.
Conclusions from
As shown in
The results are the mean±SEM from 3 independent experiments done in triplicates.
Addition of either 2 uM Curcumin-PC, 1 μM Lycomato or 1 μM Lutein, had a low effect in inhibiting LPS stimulated NO production by macrophages (1±0.2%, 1±0.3% and 5±0.9% of inhibition, respectively). The combination of 2 μM Curcumin-PC and 1 μM Lycomato caused a synergistic (S) inhibition of NO production, reaching 14±0.8%, while an additive effect caused only 2% of inhibition. The combination of the three compound composition caused a synergistic (S) inhibition of 29±1.7%, in comparison to the additive inhibition of 7%.
Using these concentrations, there was no significant differences between curcumin PC and pure curcumin in the inhibitory effect of the combinations.
Inhibition of LPS stimulated NO production by macrophages by 2 μM pure Curcumin, 1 μM Lycomato or 1 μM Lutein was 2±0.4%, 1±0.3% and 5±0.9% of inhibition, respectively). The combination of 2 μM pure Curcumin and 1 μM Lycomato caused a synergistic (S) inhibition of NO production, reaching 15±1.2%, while an additive effect caused only 3% of inhibition. The combination of the three compounds caused a synergistic (S) inhibition of 28+1.6%, in comparison to the additive inhibition of 8%.
While specific embodiments of the invention have been described for the purpose of illustration, it will be understood that the invention may be carried out in practice by skilled persons with many modifications, variations and adaptations, without departing from its spirit or exceeding the scope of the claims.
This application is a divisional of U.S. application Ser. No. 13/137,061 filed Jul. 18, 2011, which claims benefit of U.S. Provisional Application No. 61/366,376, filed Jul. 21, 2010, and is a continuation-in-part of International Application No. PCT/IL2010/000045 filed Jan. 19, 2010, which claims benefit of U.S. Provisional Application No. 61/145,593 filed Jan. 19, 2009 and U.S. Provisional Application No. 61/266,517, filed Dec. 4, 2009, the entire contents of each of which are hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61366376 | Jul 2010 | US | |
| 61266517 | Dec 2009 | US | |
| 61145593 | Jan 2009 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13137061 | Jul 2011 | US |
| Child | 15299634 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/IL2010/000045 | Jan 2010 | US |
| Child | 13137061 | US |
