Composition For Controlling Weight By Modulating Levels Of Peptides Involved In Fullness And/Or Appetite

Abstract

The present invention provides compositions which comprise an extract with at least 5% in weight of anthocyanins and an extract with at least 15% in weight of phenylpropanoids which are specially indicated for their use in weight reduction periods because they reduce appetite and increase satiety though digestive tract-secreted hormones level modification. In a parallel and complementary way, these compositions act on the lipid metabolism of the adipose tissue cells by activating AMPK sensors and the fat oxidative and elimination pathways. Said composition is obtained by hydro-alcoholic extraction of Rosella flowers and Lemon Verbena leafs, using in the case of Lemon Verbena alcohol concentrations (ethanol, methanol, propanol, isopropanol or butanol) greater than 70 and up to 100% in volume).

Claims

1. A composition for use in an individual's food intake modulation by appetite reduction and/or satiety increase through the individual's adipose tissue or digestive tract-secreted appetite-related peptides levels modification, characterised in that said composition comprises an extract with at least 5% in weight of anthocyanins and an extract with at least 15% in weight of phenylpropanoids, wherein the anthocyanins extract comprises a minimum of 25% weight of Rosella (Hibiscus sabdariffa) extract and wherein the phenylpropanoids extract comprises a minimum of 50% in weight of Lemon Verbena (Lippia citriodora) extract.

2. The composition according to claim 1 wherein the extract with at least 5% in weight of anthocyanins comprises an extract with around 10% in weight of anthocyanins.

3. The composition according to claim 1 wherein the extract with at least 15% in weight of phenylpropanoids comprises an extract with around 30% in weight of phenylpropanoids.

4. The composition according claim 1 comprising around 65% in weight of Lemon Verbena (Lippia citriodora) extract and around 35% weight of Rosella (Hibiscus sabdariffa) extract.

5. The composition according to claim 4 administered in a daily dose of 250 to 1000 milligrams.

6. The composition according to claim 5 administered in a daily dose of 500 milligrams.

7. A composition for use in an individual's weight reduction by lipid metabolism modification mediated by the individual's AMP activated protein kinase energetic (AMPK) sensors which translates into the individual's body fat percentage reduction, characterised in that said composition comprises an extract with at least 5% in weight of anthocyanins and an extract with at least 15% in weight of phenylpropanoids, wherein the anthocyanins extract comprises a minimum of 25% weight of Rosella (Hibiscus sabdariffa) extract and wherein the phenylpropanoids extract comprises a minimum of 50% in weight of Lemon Verbena (Lippia citriodora) extract.

8. The composition according to claim 7 wherein the extract with at least 5% in weight of anthocyanins comprises an extract with around 10% in weight of anthocyanins.

9. The composition according to claim 7 wherein the extract with at least 15% in weight of phenylpropanoids comprises an extract with around 30% in weight of phenylpropanoids.

10. The composition according claim 7 comprising around 65% in weight of Lemon Verbena (Lippia citriodora) extract and around 35% weight of Rosella (Hibiscus sabdariffa) extract.

11. The composition according to claim 10 administered in a daily dose of 250 to 1000 milligrams.

12. The composition according to claim 11 administered in a daily dose of 500 milligrams.

13. A method of production of a composition that comprises an extract with at least 5% in weight of anthocyanins and an extract with at least 15% in weight of phenylpropanoids characterised by comprising a Lemon Verbena (Lippia citriodora) hydroalcoholic extraction and a Rosella (Hibiscus sabdariffa) hydroalcoholic extraction wherein the Lemon Verbena (Lippia citriodora) hydroalcoholic extraction is carried out using a alcohol in water dissolution with an alcohol content greater than 70% and up to 100% in volume during two hours at a temperature between 40 and 80 C.

14. The method according to claim 13 wherein the alcohol content is around 70% in volume.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0050] FIG. 1 is a graphic showing the percentage of triglyceride build-up in insulin-resistant hypertrophic adipocytes.

[0051] FIG. 2 is a graphic showing the AMPK activation percentage in insulin-resistant hypertrophic adipocytes treated with different Rosella and Lemon Verbena extract concentrations.

[0052] FIG. 3 is a graphic showing the AMPK activation percentage in insulin-resistant hypertrophic adipocytes treated with different concentrations of Lemon Verbena and Rosella extracts mixtures, with two different ratios.

[0053] FIG. 4 are graphics showing total cholesterol, LDL cholesterol (bad) and HDL cholesterol (good) levels in blood of high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts in a 65:35 weight ratio, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0054] FIG. 5 is a graphic and table showing food efficiency ratio in high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0055] FIG. 6 is a graphic showing blood glucose levels in high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0056] FIG. 7 is a graphic showing blood leptin levels in high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0057] FIG. 8 is a graphic showing adipose tissue leptin levels in high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0058] FIG. 9 is a graphic showing body fat weight in high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0059] FIGS. 10a, 10b, 10c and 10d are graphics showing abdominal adipose tissue and liver metabolic markers in high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0060] FIG. 11 is a Western Blot analysis graphic carried out to determine protein amount in adipose tissue of high-fat diet fed mice and treated separately with Lemon Verbena and Rosella extract, and treated with two different doses of a mixture of Lemon Verbena and Rosella extracts, respectively, and of non-treated high-fat diet fed mice and of normal diet fed mice.

[0061] FIG. 12 are graphics showing the genes corresponding to metabolic markers of immortalized human adipocytes, non-differentiated (ND) and differentiated (MDI), cultured in-vitro and treated separately with different doses of Lemon Verbena (LV) and Rosella (HS) extracts, and with different doses of a Lemon Verbena and Rosella extracts mixture.

[0062] FIG. 13 are graphics showing the lipid content decrease in hypertrophic adipocytes treated with the composition with Lemon Verbena and Rosella extracts and the parallel increase of the AMPK activation in said adipocytes.

[0063] FIG. 14 is a schematic drawing of the production method of a Lemon Verbena extract.

[0064] FIG. 15 is a schematic drawing of the production method of the composition according to an aspect of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

Example 1. Lemon Verbena and Rosella Extracts Ratio Determination

[0065] 3T3-L1 preadipocytes were cultured in 96-well plates with a complete culture medium (DMEM with low glucose at 1 g/L) and sodium pyruvate, enriched with glutamine and supplemented with bovine serum at 10% and antibiotics (100 g/mL streptomycin and 100 U/mL penicillin).

[0066] The adipocyte differentiation was induced by adding adipogenic agents (0.5 mM IBMX, 1 M DEX and 1 M insulin) to the culture medium during two days. The medium was replaced with fresh medium every 48 hours.

[0067] The phenotypic change in the adipocytes was observed with a microscope. In all experiments, more than 90% of the cells were mature adipocytes after 8-10 days incubation. In order to induce cellular hypertrophy, the adipocytes were exposed to a high glucose medium (25 mM).

[0068] The cell cultures were carried out in sterile conditions using an air laminar flow hood for cell cultures and an incubator at 37 C. with a humidified atmosphere with 5% in CO.sub.2.

[0069] The extracts and the extracts composition effect on the triglycerides build-up and on the cytoplasmic AMPK activation in 3T3-L1 adipocytes was studied. The extracts were added after the adipocytes were differentiated until the plates were analyzed. The extracts were previously prepared with culture medium and filtered with a de 0.2 m filter in order to sterilize them.

[0070] The 29 days differentiated hypertrophic adipocytes were separately exposed to Rosella Extract (10% weight in anthocyanins) and to Lemon Verbena extract (30% weight in phenylpropanoids) and to 50:50 and 65:35 weight ratio mixtures of lemon Verbena to Rosella extracts. The extracts were added the 24.sup.th day after adipocytes differentiation and were incubated at 50, 200 and 500 g/mL during 5 days.

[0071] After these 5 days, the lipid content of the adipocytes was evaluated with the commercial reactant AdipoRed and using a multi-mode microplate reader with cellular image capture Cytation 3 from Biotek with a 485 nm excitation wavelength and a 572 nm emission wavelength. The lack of cytotoxicity was evaluated with the purple crystal method. The results are shown in FIG. 1, with a graphic showing the percentage of triglycerides build-up in hypertrophic insulin-resistant adipocytes. HS represents the adipocytes treated with a 10% anthocyanins Rosella extract, LV represents the adipocytes treated with a 30% phenylpropanoids Lemon Verbena extract, HS-LV (1:1) represents the adipocytes treated with a 1 to 1 weight mixture of Lemon verbena and Rosella extracts and HS-LV (36:65) represents the adipocytes treated with a 35:65 in weight mixture of Rosella and Lemon Verbena extracts, respectively. P values are: *p<0.05, **p<0.01 y ***p<0.001.

[0072] AMPK and phosphorylated (activated) AMPK levels were determined with a quantitative immunofluorescence experiment using AMPK and phosphorylated AMPK antibodies. Moreover, the nuclei were marked with the reactant Hoechst 33342. Once the cells were marked, the AMPK fluorescence was quantified with a 490 nm excitation wavelength and a 520 nm emission wavelength, the phosphorylated AMPK fluorescence was quantified with a 593 nm excitation wavelength and a 614 nm emission wavelength and the nuclei fluorescence with a 350 nm excitation wavelength and with a 461 nm emission wavelength, using a multimodal plate reader.

[0073] The results are shown in FIGS. 2 and 3 which show graphics representing the AMPK activation percentage in hypertrophic insulin-resistant adipocytes treated with different doses of Rosella and Lemon Verbena extracts, separately, and combined in two different weight ratios. It can be seen that the most AMPK activation is produced with the greater dose of the composition which contains both extracts in a 65:35 weight ratio of Rosella extract to Lemon verbena extract, respectively. The p values are: *p<0.05, **p<0.01 y ***p<0.001, which indicate statistically significant differences with the control adipocytes (non-treated adipocytes). The legends have the same meaning as in FIG. 1.

Example 2. Body Fat, Hyperlipidaemia, Hyperglycaemia and Adipogenesis Reduction Evaluation in Obese Mice Treated with a Composition which Contains Lemon Verbena and Rosella Extracts

[0074] In-vivo experiments were carried out with normal mice to which a high fat diet was fed (HFD) during 8 weeks. Total blood cholesterol, as well as HDL cholesterol (good cholesterol or high-density lipoprotein) and LDL cholesterol (bad cholesterol or low-density lipoprotein) were analyzed.

[0075] The results are shown in FIG. 4 wherein C57bl/6-Nr corresponds to normal diet mice, HFD-CTL to high-fat diet mice (HFD), HFD-LV to high-fat diet mice taking a 30% weight phenylpropanoids Lemon Verbena extract, HFD-HS to high-fat diet mice taking a 10% weight anthocyanins Rosella extract, and HFD-MetA to high-fat diet mice taking a Lemon Verbena and Rosella extracts composition with 65:35 weight ratio, respectively.

[0076] The results show that mice taking both extracts composition had lower total cholesterol levels, coinciding with a decrease in LDL and an increase in HDL. These values were lower than with the extracts taken separately (* p<0.05, ** p<0.01 with respect to the control HFD-CTL).

[0077] The food amount taken by mice was analyzed daily, with respect to the animals' weight. This value is known as Food Efficiency Ratio. A lower amount implies a lower food intake with respect to its weight. The results can be seen in FIG. 5. (* p<0.01 with respect to control HFD-CTL)

[0078] The blood glucose level was also analyzed, given that the high-fat diet mice are hyperglycaemic. As it can be seen in FIG. 6 ((* p<0.05 with respect to control HFD-CTL), mice taking the highest concentration of the extracts composition were the only ones with an important blood glucose level reduction, close to the normal diet mice.

[0079] Leptin hormone level was analyzed in mice taking a high fat diet. Specifically, the blood level of such hormones was analyzed, as it can be seen in FIG. 7 (*p<0.05, **p<0.01 with respect to control HFD-CTL).

[0080] Comparing the control with the normal diet (C57bl/6J Nr) with respect to the high fat diet mice (HFD-CTL), it can be seen that leptin has a significantly higher expression in the high-fat diet mice. Leptin induces satiety, however, it is known that the membrane receptors of said hormone have an high resistance in obese individuals, and require high leptin levels in order to be stimulated and therefore to activate the signal cascade to induce satiety. Consequently, detecting high leptin levels in high-fat diet mice, consequently obese, confirms the resistance to this hormone.

[0081] The intake of any of the tested extracts or mixtures (Lemon Verbena, Rosella or mixture thereof) decreases the leptin expression in blood, even though only in the case of the extracts mixture composition we can see similar levels to normal diet mice, i.e., non-obese. Therefore, this mixture composition intake can reverse the leptin overexpression, given that it eliminates the resistance to said hormone, thus allowing that HFD mice have satiety levels similar to normal diet mice.

[0082] These data coincide the FER observed results, wherein mice that took the both extracts composition took less food amounts with respect to their weight.

[0083] A similar result can be seen in FIG. 8 with regards to the leptin expression in adipose tissue, wherein it can be seen that only in mice taking the extracts composition the leptin expression in adipose tissue decreased (*p<0.05 vs HFD-CTL), achieving levels observed in normal diet mice. This is due to a possible leptin receptors sensitization in mice that took the extract composition, such that a lower leptin blood concentration was enough to cause satiety feelings.

[0084] The combined and separate effect of Lemon Verbena and Rosella extracts on the adipose tissue metabolism has been studied. In the first place, the amount of adipose tissue of the mice was determined, isolating and weighting the abdominal, epididymis, kidney and intestinal fat.

[0085] As it can be seen in FIG. 9, only mice that took the extracts composition presented significantly less fat amount in the abdomen, epididymis and intestine (*p<0.05, **p<0.01). These values agree with the previously commented results, i.e., that these mice take less food, by means of satiety regulation, which results in weights loss by means of adipose tissue loss.

[0086] Besides the weight, adipose tissue and liver metabolic markers were studied (in the case of overweight/obesity there is an abnormal build-up of adipose tissue in the liver, known as fatty liver) in relation with the accumulation or regulation of triglycerides and fatty acids. The markers analyzed by means of RT-PCR were PPAR, SREBP1 (ADD1), C/EBP and AMPK.

[0087] PPAR is a nuclear membrane receptor found in adipocytes, as well as in colonic cells and macrophages. In the case of adipose tissue, their function is to activate lipogenesis and lipid catchment. SREBP1c regulates lipids homeostasis, and its activation induces cholesterol synthesis when this is low. C/EBP is a transcription factor that regulates adipogenesis as well as normal adipocytes function, and regulates the PPAR expression. Finally, AMPK (AMP kinase) inhibits lipids catchment, cholesterol synthesis and lipogenesis, among other functions, though in order to carry out its function, the protein must be phosphorylated (p-AMPK).

[0088] As it can be appreciated in the FIGS. 10a to 10d histograms, the PPAR y SREBP1c (ADD1) expression significantly decreases only in mice that took the extracts composition, studied in the liver as well as in the abdominal adipose tissue (*p<0.05). Regarding C/EBP, it is also seen an expression decreasing effect with Lemon Verbena and Rosella, but only in the liver, whereas the extracts composition decreased this factor expression in both analyzed tissues. In these three genes, the resulting expression in mice taking the extracts composition was similar to that obtained in control mice taking a normal diet.

[0089] On another hand, the AMPK transcriptional expression was increased in mice taking the extracts compositions (in the liver, mice taking Rosella also exhibited an expression increase, but not in the adipose tissue).

[0090] This result was also confirmed by means of a Western Blot analysis, which allows the analysis of the protein amount present in the adipose tissue and which results are shown in FIG. 11. The legend is interpreted as: N mice with normal diet, CT non-treated mice with high-fat diet, LV Lemon Verbena extract treated mice with high-fat diet, HS Rosella extract treated mice with high-fat diet, MA1 high-fat diet mice treated 65:35 weight ratio composition of Lemon verbena and Rosella extracts at a 50 mg/kg dose and MA2 high-fat diet mice treated 65:35 weight ratio composition of Lemon verbena and Rosella extracts at a 100 mg/kg dose.

[0091] The active form of AMPK is phosphorylated AMPK (p-AMPK). As it can be seen in the Figure, the adipose tissue of mice taking the extract composition were those which exhibited more p-AMPK concentration in active protein form.

[0092] Therefore, mice taking a high-fat diet for 8 weeks (HFD-CTL) show activation of genes involved in fat accumulation, lipogenesis, triglycerides and cholesterol synthesis, adipogenesis, which results in a greater content in body fat, compared with control mice with a normal diet (C57bl/6J Nr). However, when these mice take the extracts composition, these genes expression is reverted to concentrations similar to the ones observed in non-obese normal diet mice. Moreover, the p-AMPK activation indicates that the fatty acids metabolism is increased, thus decreasing its storage at the same time as its degradation increases.

[0093] These in-vivo results carried out on mice were confirmed with in-vitro studies using a human adipocytes cellular line, wherein several concentrations of the different ingredients were tested and incubated for 10 days. The same genes as the ones studied in mice were analyzed for the fatty acid metabolism. The results are shown in FIG. 12. (ND: non-differentiated cell cultures, MDI: differentiated cell cultures, LV: Lemon Verbena, HB: Rosella, MA: LV and HB extracts composition, 125-1000: ingredients concentrations expressed in g/ml)

[0094] In the case of PPAR, SREBP1c(ADD1), C/EBP, a decrease of their expression is observed in the three studied cases with respect of the differentiated adipocytes (MDI), specifically in the 1 mg/ml concentration of Lemon Verbena and Rosella, and also in the 0.5 as well as in the 1 mg/ml concentration of the extracts composition. Therefore, the extracts composition can be used at lower concentrations to induce a repressing effect of said transcripts, compared with the individual extracts.

[0095] Regarding AMPK, it can be observed an important expression increase in the case of the extracts composition at 0.5 and 1 mg/ml, whereas with the separate extracts, no statistically significant differences can be observed with respect to the differentiated cell culture (MDI).

Example 3. Appetite Reduction and/or Satiety Increase by Means of Changes in Digestive Tract and Adipose Tissue-Secreted Peptide Levels Due to Intake of a Composition that Contains a Lemon Verbena Extract with a 30% Weight Content in Phenylpropanoids and a Rosella Extract with a 10% Weight Content in Anthocyanins, in a 65:35 Weight Ratio

[0096] 54 women aged between 35 to 75 years and with a body mass index between 25 to 35 kg/m.sup.2 were selected. The study is a random double-blind, placebo-controlled assay of 8 weeks carried out at the Miguel Hernandez University of Elche, in Spain. After recruitment, the volunteers were randomly assigned to a placebo control group L2 (n=26) or to an experimental group L1 (n=28).

[0097] L1 group members (mean age 51 years) received a 500 mg daily dose of a composition that contains Lemon Verbena and Rosella extracts.

[0098] L2 group members (mean age 51 years) received a 500 mg daily dose of microcrystalline cellulose.

[0099] The placebo and the satiety effect composition capsules had the same size, color, smell and weight. The volunteers took a capsule 20 to 30 minutes before breakfast every day for two months.

[0100] The volunteers were required to follow a balanced isocaloric diet and to walk at least 30 minutes a day.

[0101] The fulfillment of these requirements was monitored during the clinical visits or by telephonic interviews each week. A total of 3 and 4 participants were excluded from L2 and L1 groups, respectively.

[0102] Several parameters were monitored during the study. Anthropometric measurements were taken at the start of the study, after one months and after two months from the start of the study, and include body weight, height, triceps, biceps and abdominal skinfold measurements and arm and abdominal perimetric measurements. The abdomen perimeter (AC) was measured in two different places: frontally midways between the xiphoid process and the belly button and laterally midways between the thoracic chest end and the iliac crests (AC1) and at the belly button (AC2). The body fat percentage was obtained from the abdominal measurement using the Weltman equation. Moreover, the heart rate at rest and diastolic and systolic tension were measured at the start, and after one and two months of study.

[0103] The validated analogue visual scale test (VAS test) was used to register hunger, satiety, fullness feeling, prospective food intake, desire to eat something fatty, savory, sweet or no sweet and the flavor appreciation of the meals. The VAS test was completed at the start of the study at rest, after 15, 20, 45 and 60 days of study. In a complementary way to the subjective evaluation of their heath state, the volunteers filled a SF-36 questionnaire at the start and at the end of the study. Finally, blood samples were obtained from the forearm vein after overnight fasting at the start, and after 30 and 60 of study. The plasma was immediately processed and the samples were stored at80 Celsius degrees.

[0104] Table 1 shows the anthropometric parameters at the start and during the study. Statistically significant differences between the two groups cannot be seen at the start of the study. Table 1 results indicate a statistically significant improvements of the anthropometric parameters after two months study in the L1 group, which took the Lemons Verbena and Rosella extracts composition, specially improving the body fat percentage, the triceps skinfold, body weight and the hip perimeter (AC2). These differences can be more clearly seen in Table 1a.

TABLE-US-00001 TABLE 1 Changes in the anthropometric parameters during the study expressed in mean values plus/minus standard deviations. The intra-group statistical analysis was determined in each period in comparison with the data at the start of the study. L2 Group L1 Group Start Month 1 Month 2 Start Month 1 Month 2 Anthropometric parameters Body weight (kg) 75.64 12.92 74.20 12.62**** 73.56 12.57**** 75.26 9.06 72.80 9.45**** 71.78 9.06**** Body mass index 29.78 4.19 29.15 4.08**** 28.95 4.01**** 29.60 3.40 28.60 3.52**** 28.26 3.46**** (kg/m2) Arm perimeter (cm) 31.20 3.80 31.23 3.80 30.98 4.10 30.58 1.67 30.47 1.83 30.26 1.76**** AC1 (cm) 94.02 13.03 92.84 12.86*** 92.05 13.16**** 90.96 9.03 88.96 9.18**** 88.01 8.90**** AC2 (cm) 100.7 14.01 100.5 14.21 99.90 14.54** 96.42 7.93 94.84 7.87**** 93.85 7.95**** Hip perimeter (cm) 108.8 8.73 108.15 8.55** 107.5 8.48*** 110.4 7.23 108.2 7.56**** 106.9 7.48**** Triceps skin fold (mm) 43.25 9.28 43.15 9.34 43.10 9.42 41.62 8.18 40.96 8-08** 39.98 7.97**** Biceps skin fold (mm) 41.53 14.46 41.25 14.35* 41.09 14.35* 38.33 10.63 37.61 10.87* 36.87 10.52**** Abdominal skin fold 35.72 11.15 35.39 10.68 34.39 10.68 41.45 12.89 39.72 12.95*** 38.60 13.08*** (mm) % body fat 44.98 2.71 44.69 2.65*** 44.53 2.64**** 44.66 2.04 44.10 2.10**** 43.83 2.06**** Vital signs Heart rate (bpm) 71.41 8.89 71.95 8.85 72.09 9.24 73.32 9.70 70.84 7.54* 68.64 7.07**** Systolic tension 114.5 23.26 115.1 23.55* 115.2 23.13* 117.4 12.13 115.1 12.82** 113.9 12.5**** (mmHg) Diastolic tension 73.73 10.57 74.05 11.50 73.73 10.70 73.40 5.00 71.28 5.89**** 69.48 6.62**** (mmHg) The significance was established at: *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

TABLE-US-00002 TABLE 1a Changes in the anthropometric parameters during the study expressed in mean values plus/minus standard deviations. The intra-group statistical analysis was determined in each period in comparison with the data at the start of the study. Differences after 1 month Differences after 2 months Anthropometric parameters Placebo (L2, n = 22) MetabolAid (L1, n = 25) Placebo (L2, n = 22) MetabolAid (L1, n = 25) Body weight (kg) 1.44 0.27 2.46 0.28* 2.08 0.30 3.48 0.40* Body mass index (kg/m2) 0.63 0.14 1.00 0.15* 0.83 0.12 1.37 0.16* Arm perimeter (cm) 0.03 0.03 0.11 0.06 0.22 0.23 0.32 0.08** AC1 (cm) 1.18 0.29 2.00 0.27* 1.97 0.37 2.95 0.36 AC2 (cm) 0.20 0.54 1.58 0.25** 0.80 0.55 2.57 0.34** Hip perimeter (cm) 0.65 0.23 2.20 0.32*** 1.30 0.28 3.50 0.37**** Triceps skin fold (mm) 0.10 0.16 0.66 0.18* 0.15 0.15 1.64 0.29**** Biceps skin fold (mm) 0.28 0.14 0.62 0.22 0.44 0.19 1.46 0.29** Abdominal skin fold (mm) 0.33 0.36 1.73 0.37* 1.33 0.29 2.84 0.53* % body fat 0.29 0.06 0.56 0.06** 0.45 0.07 0.83 0.08*** Heart rate (bpm) 0.54 0.28 2.48 0.89**** 0.68 0.36 4.68 0.36**** Systolic tension (mmHg) 0.60 0.28 2.30 0.64**** 0.70 0.30 3.50 0.61**** Diastolic tension (mmHg) 0.32 0.43 2.12 0.39**** 0 0.50 3.92 0.63**** The significance was established at: *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

[0105] According the scores shown in Table 2, the Lemon Verbena and Rosella extracts composition consumption decreases the hunger feeling consistently along the two months of study. The mean hunger score decreased from 5.92 in day 15 to 2.58 in day 60 in group L1. Whereas in group L2 it increased from 6.18 in day 15 to 6.41 in day 60 in the placebo group. A similar trend can be observed in the scores to question 4.

[0106] Satiety increased from a 5.04 value in day 15 until a 7.58 value in day 60 in group L1, whereas it decreased from a 4.82 values at day 15 to a 4.22 value at day 60 in placebo group L2. A similar trend was observed in the scores to question 3.

TABLE-US-00003 TABLE 2 Scores of appetite-related feelings in group L1 (extracts composition) and in group L2 (placebo) after 15, 30, 45 and 60 days of study, expressed as mean values plus/minus standard deviation. Data are expresses each question score in comparison with placebo. 15 days 30 days 45 days 60 days Items L1 L2 L1 L2 L1 L2 L1 L2 1. How hungry are you? 5.92 6.18 4.00 6.05 3.29 6.18 2.58 6.41 2.48 2.36 2.34** 1.73 2.37**** 2.11 2.35**** 1.87 2. How satisfied do you feel? 5.04 4.82 5.92 4.32 6.45 4.63 7.58 4.22 2.07 1.89 2.02* 1.95 2.32** 1.50 1.72**** 1.38 3. How full do you feel? 4.65 4.45 5.76 4.30 6.42 3.86 7.46 3.52 1.94 1.76 1.80* 1.90 1.87**** 1.83 1.59**** 1.91 4. How much do you think you can eat? 5.57 7.22 4.14 6.95 2.83 6.82 2.54 7.33 2.83 1.52 1.98**** 1.90 2.20**** 1.74 1.90**** 1.90 5. Would you like to eat something sweet? 2.04 2.45 5.65 2.80 4.83 1.95 6.67 1.82 2.23 2.70 2.55** 2.76 2.73*** 2.13 2.18**** 2.17 6. Would you like to eat something savoury? 5.45 5.09 6.38 2.60 7.57 2.86 7.75 3.09 3.42 3.53 2.73**** 1.79 2.27**** 2.59 2.19**** 2.72 7. Would you like to eat something not sweet? 2.70 4.68 4.96 3.68 6.50 2.90 7.67 2.71 2.25* 2.93 2.51 2.73 2.19**** 2.75 1.40**** 2.47 8. Would you like to eat something fatty? 4.29 8.07 6.87 5.60 8.13 5.18 8.21 5.14 3.58*** 2.52 3.18 3.58 2.71** 3.88 2.47** 3.48 Statistically significant differences were established: *p, 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. The scores range according to the following scheme: 1. 0 Not at all hungry-10 I have never been so hungry. 2. 0 I feel completely empty-10 I cannot take even a bite more 3. 0 I am not at all full-10 I am completely full 4. 0 Nothing at all-10 A huge amount 5. 0 Yes, a lot-10 Not at all 6. 0 Yes, a lot-10- Not at all 7. 0 Yes, a lot-10- Not at all 8. 0 Yes, a lot-10- Not at all

TABLE-US-00004 TABLE 3 Appetite and satiety-related gut-secreted peptide levels in blood determined at the start and at the end of the study (second month), expressed as mean values plus/minus standard deviations. Placebo Composition with extracts (L2, n = 10) (L1, n = 10) START MONTH 2 START MONTH 2 GLP-1 5.66 4.228 5.22 6.82 (pg/mL) 1.27 2.04* 1.43 1.78* GHRELIN 30.64 33.74 32.70 32.89 (pg/mL) 0.64 3.48* 4.82 3.23 LEPTIN 9669 5237 9772 4311 (pg/mL) 6617 4886 4455 2304* PYY 7.84 5.82 9.80 9.81 (pg/mL) 4.15 5.01 0.31 0.24 RESISTIN 15593 10799 18101 12049 (pg/mL) 6718 6624 6274 4022* Significance was established for: *p < 0.05.

[0107] It is necessary to mention that some analyzed peptides (such as GLP-1, PYY and ghrelin) are secreted after food intake. Ghrelin stimulates appetite, whereas GLP-1 and PYY are secreted together to promote the satiety feeling. Given that the blood samples were taken before breakfast in the morning, the particular peptide levels correspond to basal levels. Initially, the basal levels in both groups match and no statistically significant differences between them are observed. The other peptides show statistically significant differences in group L1. In this context, the incretin GLP-1 significantly increased in group L1 whereas it decreased in group L2 and the ghrelin increased in group L2 and was kept constant in group L1. Therefore, group l1 volunteers had less appetite and more fullness feeling than the group L2 volunteers.

[0108] On another hand, leptin, which is synthesized in the adipose tissue and produces satiety feeling, significantly decreased in group L1 whereas no changes were observed in group L2. Resistin decreased significantly in group L1 whereas no changes were observed in group L2. The increased leptin level in the blood samples of group L2 is explained by the resistance in the corresponding receptors to cause satiety in response to leptin secretion, it is like the corresponding receptors were desensitized, whereas in group L1 the normal blood leptin level indicates that the corresponding receptors maintain the same or greater sensitivity to the leptin level.

[0109] Generally, these changes in the hormone (peptides) levels correlate positively with the questionnaire scores about appetite and satiety and with the anthropometric parameters evolution previously shown.

Example 4. Body Weight Reduction by Means of Lipid Metabolism Modification Mediated by an AMP Activated Protein Kinase Energetic Sensors Activation (AMPK)

[0110] Triglycerides accumulation and AMPK activation by the polyphenolic compounds was evaluated by means of immunofluorescence with the 3T3-L1 hypertrophic insulin-resistant adipocyte model. On another hand, a double-blind placebo controlled clinical study with volunteers taking placebo or 500 mg a day of a dietetic supplement with Lemon Verbena and Rosella extracts in 65:35 weight ratio, respectively, was carried out, in which 56 overweight volunteers participated during two months. Anthropometric and biochemical parameters were determined.

[0111] 3T3-L1 preadipocytes were cultured in a low glucose medium (1 g/L) DMEM supplemented with 10% bovine serum (CS), 100 g/mL streptomycin and 100 U/mL penicillin and were incubated at 37 C. in a 5% volume CO.sub.2 and a 95% volume of air humidified atmosphere. Adipocyte differentiation was induced by means of a high glucose (4.5 g/L) medium culture supplemented with 10 fetal bovine serum (FBS), 1 M insulin, 1 dexamethasone (DEX) and 0.5 mM de 3-isobutyl-1-methylxanthine (IBMX) during 48 hours. After 48 hours, the cells were kept in a high glucose medium with FBS and insulin, and the medium was replaced every two days, with which hypertrophic adipocytes were obtained after 20 days incubation. Once the hypertrophic adipocytes were obtained, the cells were treated with Lemon verbena extract (30% weight in phenylpropanoids) and Rosella extract (10% weight in anthocyanins) in a weight ratio 65 to 35, respectively, at different concentrations during 72 hours. The extracts were dissolved in medium and filtered in order to be sterilized.

[0112] The lipid content of the hypertrophic adipocytes was evaluated using the AdipoRed reactant. The cell supernatant was eliminated and these were carefully washed with phosphate buffered saline solution (PBS). Consecutively, AdipoRed was added and the cells were left to incubate during 15 minutes at ambient temperature. Triglyceride accumulation was measured using a microplate reader at 485 nm excitation wavelength and 572 nm emission wavelength.

[0113] For the sturdy of AMPK activation in hypertrophic adipocytes, phosphorylated AMPK in Thr172 was quantified (pAMPK) with an immunofluorescence assay. The cells were fixed with a fixation buffer, permeabilized with 0.3% Triton x-100 (Sigma-Aldrich, Spain) and blocked with 4% goat serum. Once this was done, the cells were incubated overnight at 4 C. with Alpha 1+Alpha 2 mice AMPK monoclonal antibodies (Abcam, Cambridge, UK) and with rabbit Alpha 1 phospho-AMPK (Thr172, Cell Signaling Technology, Danvers, Mass., USA). After the incubation with the primary antibodies, the cells were washed with PBS and incubated during 6 hours at ambient temperature with each corresponding secondary polyclonal antibody, goat anti-rabbit IgG CF 594 and anti-mouse FITC (both from Sigma-Aldrich, St. Louis, Mo., USA). The cell fluorescence measured using a multimodal microplate reader with cell image capture (Cytation 3, Biotek, Spain) at 593 nm excitation wavelength and 614 nm emission wavelength to measure the AMPK levels. The AMPK activation is expressed as the ration between normalized AMPK and total AMPK. The results are shown in FIG. 13. The p values are *p<0.05, and ***p<0.001.

[0114] The randomized, double-blind, placebo-controlled human study lasted 8 weeks. The exclusion criteria were a total cholesterol level lower than 200 mg/dL, the presence of any obesity-related pathology, the use of cholesterol or hypertension medication, the consumption of antioxidant supplements of pharmaceuticals, alcohol addiction and breastfeeding or pregnant women. Based on these criteria, 55 healthy women, aged between 36 and 69 years, with a body mass index between 25 to 34 kg/m.sup.2, which passed a telephonic selection and an interview about their health as well as a biochemical and anthropometric assessment.

[0115] Once enrolled to the study, the volunteer were randomly assigned to the placebo group (n=26) or to the experimental group (n=29). During the study, 9 volunteers quitted, 6 in the placebo group and 3 in the experimental group, and a total of 46 volunteers completed the study. The placebo group (mean age 51 years) received two placebo capsules, each containing 400 mg microcrystalline cellulose and the experimental group (mean age 52 years) received two capsules, each containing 250 mg of the Lemon Verbena and Rosella extracts composition and 150 mg excipients (microcrystalline cellulose). Therefore, the experimental group was taking 500 mg a day of the composition under study. Both capsule types had the same color, smell, and weight. The volunteers took two capsules a day 20 to 30 minutes before breakfast for two months. During the selection visit, demographic and lifestyle (age, diet, physical exercise routines, alcohol and tobacco consumption) information was gathered. A doctor asked the volunteers to follow an isocaloric diet with normal hydration and to walk at least 30 minutes a day. The study requirements fulfillment was confirmed in each visit and telephonically, each week, during the two months of study. The parameter measurements were taken at the start of the study and after 30 and 60 days of study.

[0116] During the study, several parameters were monitored. Anthropometric measurements were taken at the start of the study, after a month and after two months since the start of the study, consisting of body weight, height, skinfold measurements at the triceps, biceps and abdomen and arm and abdomen perimetric measurements. The abdomen perimeter (AC) was measured in two different places: frontally midways between the xiphoid process and the belly button and laterally midways between the thoracic chest end and the iliac crests (AC1) and at the belly button (AC2). The body fat percentage was obtained from the abdominal measurement using the Weltman equation.

[0117] Fasted blood samples were taken in order to measure total glucose, glycosylated hemoglobin and the lipids profile, which includes triglycerides, total cholesterol, good cholesterol (high-density lipoprotein) or HDL and bad cholesterol (low density lipoprotein) or LDL. The blood samples were analyzed to measure security parameters such as hematology, electrolytes, creatinine, urea, uric acid, glutamic-pyruvic transaminase, glutamic-oxaloacetic transaminase and C-reactive protein.

[0118] Moreover, the heart rate at rest and diastolic and systolic tension were measured at the start, and after one and two months of study.

TABLE-US-00005 TABLE 4 Anthropometric measurements, at the start and after one and two months of study. Experimental group (N = 26) Placebo group (N = 20) Start Month 1 Month 2 Start Month 1 Month 2 Anthropometric parameters Body weight (kg) 75.12 13.62 72.76 13.51*** 71.08 13.34*** 75.16 11.34 73.36 11.24*** 73.12 11.47** Body mass index 29.20 4.76 28.26 4.63*** 27.59 4.44*** 30.23 4.41 29.52 4.42*** 29.43 4.58* AC1 (cm) 90.87 10.81 86.59 9.51*** 84.39 9.91*** 90.93 13.12 89.21 12.83*** 88.50 11.65** AC2 (cm) 100.52 9.10 97.10 8.20*** 94.71 8.94*** 102.32 11.59 99.87 11.96** 97.05 10.66*** Triceps skin fold 28.36 7.57 26.08 6.95*** 24.67 7.42*** 30.13 5.24 28.45 4.75** 27.88 4.69*** % body fat 44.36 2.86 43.53 2.73*** 43.04 2.64*** 44.67 2.82 44.18 2.83*** 43.95 2.73*** Vital signs Heart rate (bpm) 79.43 9.84 74.36 9.03*** 71 8.40*** 75.75 8.62 75.15 11.86 75.50 11.61 Systolic tension mm Hg 128.70 12.74 118.43 13.91*** 109.96 9.09*** 126.65 19.06 120.70 17.50 118.05 15.64* Diastolic tension mm Hg 77.62 10.99 72.76 10.54* 67.05 9.30*** 78.30 13.12 76.10 8.16 71.10 11.61* Biochemical parameters Glucose mg/dl 93.33 16.10 90.44 14.11 90.06 13.31 93.95 12.96 94.05 11.14 92.63 14.95 Triglycerides mg/dl 84.83 52.61 76.28 35.22 83.17 39.39 85.63 42.37 78.53 27.95 88.74 39.23 Total cholesterol mg/dl 237.78 26.51 215.22 26.90*** 207.94 25.11*** 229.11 26.13 205.53 24.84*** 207.53 28.62** HDL mg/dl 60.59 7.24 59.23 7.15 58.95 8.52 59.00 7.54 56.95 9.02* 57.11 8.58* LDL mg/dl 158.52 25.17 140.90 23.39*** 127.43 20.83*** 153.68 24.88 132.89 23.18*** 132.95 25.39*** Creatinine mg/dl 0.75 0.11 0.85 0.14 0.81 0.12 0.80 0.14 0.91 0.18 0.82 0.12 Urea mg/dl 33.36 7.96 32.09 8.52 32.32 9.15 32.21 10.54 32.37 7.77 31.58 7.44 Uric acid mg/dl 4.66 1.01 4.29 1.09 4.55 1.18 4.97 1.53 4.29 1.03 4.48 0.96 GPT U/l 22.59 7.39 21.59 9.53 21 8.83 21.21 6.82 21.61 9.62 20.05 8.44 GOT U/l 21.00 5.07 21.59 5.66 21.27 6.85 21.11 4.53 21.11 5.51 20.21 5.02 The intra-group statistical values at the end of the study compared with the initial values are: *p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001. Data are expressed as mean values SD.

[0119] As it is shown in FIG. 13, the composition with Lemon Verbena and Rosella extracts causes a potent increase in the pAMPK/AMPK ratio in a dose-dependent way which is statistically significant in comparison with the increase observed in the control experiment at a 350 g/mL dose, whereas at a dose of 500 g/mL an increase of approximately 1.5 is observed.

[0120] The anthropometric parameters of both groups do not show noticeable differences at the start of the study. The study results show a significant enhancement in the experimental group, particularly in body weight, abdominal perimeter and body fat percentage (see Table 4).

[0121] The experimental group showed a greater body weight reduction tan the placebo group which is statistically significant with a p value <0.01. Both abdominal perimeters AC1 and AC2 were reduced after the two months of study, but only the highest abdominal perimeter showed statistically significant differences with the placebo group after one and two months of study. Consequently with these data, the body fat percentage was reduced in both groups, but in the experimental group it was statistically significant more reduced than in the placebo group after two months of study, p<0.01. Besides, also statistically significant differences were observed in the triceps skinfold measurement (p<0.05) and in the body mass index (p<0.01).

Example 5. Method of Production of a Composition with Lemon Verbena and Rosella Extracts According with an Aspect of the Invention

[0122] The composition with Lemon Verbena and Rosella extracts is a mixture of two extracts with a very specific active compounds composition, i.e. at least 10% in weight of anthocyanins in the Rosella extract and at least 30% in weight of phenylpropanoids in the Lemon Verbena extract, which, once mixed in a weight proportion of 35:65, respectively, exhibit synergic activity, especially for the control of satiety.

[0123] The manufacturing method of the Lemon Verbena extract comprises a hydroalcoholic extraction using alcohol concentrations (ethanol, methanol, propanol, isopropanol or butanol) greater than 70 and up to 100% alcohol in volume in water (FIG. 14).

[0124] The Lemon Verbena (Lippia citriodora) leaves are analyzed in order to determine the amount of verbascoside using high-pressure liquid chromatography (HPLC). Approximately 330 g. of Lemon Verbena leafs are extracted in 4 liters of demineralized water-diluted ethanol (greater than 70 and up to 100% of ethanol in volume) keeping the liquid stirred in the recipient, recirculating the evaporated solvent or percolating it in a nutcha filter at a temperature between 40 a 80 C. during two hours. After the two hours, the solution is filtered to separate the leaves and other particles. The filtered solution is vacuum-distilled at a temperature between 60 a 80 C. in order to obtain a concentrated aqueous solution which contains around 15 to 30% in solids. This concentrated solution is spray-dried at a temperature of 70-90 C. in order to obtain a dry-powder extract that contains no less than 30% in weight of total phenylpropanoids. The yield is from 19 to 21 in weight.

[0125] In order to produce the Rosella extract, the plant flowers are selected and analyzed to obtain their anthocyanin content with high-pressure liquid chromatography (HPLC) and ultraviolet light detection. 320 g. of flowers are extracted with 3.2 liters of demineralized water-diluted ethanol at 50% volume, keeping the liquid under stirring in the reactor, and recirculating the evaporated solvent or percolating it in a nutcha filter at a temperature between 40 y 60 C. during 2 hours. After the two hours extraction, the solution is filtered with a 0.5 micron pore filter to separate the flowers. The filtered solution is vacuum-distilled at a temperature between 50 y 70 C. and the obtained concentrate is diluted until obtaining 620 liters.

[0126] The product is subjected to a chromatographic purification step in a polymeric adsorption/desorption resin suitable for polyphenols. The eluate constitutes the purified extract in liquid form. The purified liquid is concentrates until 30 to 50% in weight of solids. The concentrated dissolution is spray-dried at a temperature between 70 y 80 C. to obtain a dry-powder extract which contains no less than 10% in weight of anthocyanins. The yield is from 5 to 7% in weight.

[0127] After producing the Lemon Verbena and Rosella extracts separately, both are sieved and mixed and passed through a metal-detecting system before being packaged, as it is schematically shown in FIG. 15.