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fixtures.py
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fixtures.py
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MAIN_HTML_PARAGRAPHS = {
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"text": '<!--version=html--> <p align="right"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><b>RESEARCH ARTICLE</b></font></p> ',
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"text": '<p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="4"><b><a name="top"></a>Antioxidant and anti hyperglycemic role of wine grape powder in rats fed with a high fructose diet</b></font></p> ',
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"text": '<p> </p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Romina Hernández-Salinas<sup>I</sup>; Valerie Decap<sup>I</sup>; Alberto Leguina<sup>I</sup>; Patricio Cáceres<sup>I</sup>; Druso Perez<sup>II</sup>; Ines Urquiaga<sup>II</sup>; Rodrigo Iturriaga<sup>I</sup><sup>, </sup><sup>II</sup>; Victoria Velarde<sup>I, II, <a href="#back">*</a></sup></b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><sup>I</sup>Departamento de Fisiología, Facultad de Ciencias Biológicas, Pontifícia Universidad Católica de Chile, Santiago, Chile <br> <sup>II</sup>Center for Molecular Nutrition and Chronic Diseases, Pontifícia Universidad Católica de Chile, Santiago, Chile</font></p> <p> </p> <p> </p> <hr noshade size="1"> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>ABSTRACT</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>BACKGROUND</b>: Metabolic syndrome is a growing worldwide health problem. We evaluated the effects of wine grape powder (WGP), rich in antioxidants and fiber, in a rat model of metabolic syndrome induced by a high fructose diet. We tested whether WGP supplementation may prevent glucose intolerance and decrease oxidative stress in rats fed with a high fructose diet. <br> <b>METHODS</b>: Male Sprague-Dawley rats weighing 180 g were divided into four groups according to their feeding protocols. Rats were fed with control diet (C), control plus 20 % WGP (C + WGP), 50 % high fructose (HF) or 50 % fructose plus 20 % WGP (HF + WGP) for 16 weeks. Blood glucose, insulin and triglycerides, weight, and arterial blood pressure were measured. Homeostasis model assessment (HOMA) index was calculated using insulin and glucose values. A glucose tolerance test was performed 2 days before the end of the experiment. As an index of oxidative stress, thio-barbituric acid reactive substances (TBARS) level was measured in plasma and kidney, and superoxide dismutase was measured in the kidney. <br> <b>RESULTS</b>: Thiobarbituric acid reactive substances in plasma and renal tissue were significantly higher when compared to the control group. In addition, the area under the curve of the glucose tolerance test was higher in HF fed animals. Furthermore, fasting blood glucose, plasma insulin levels, and the HOMA index, were also increased. WGP supplementation prevented these alterations in rats fed with the HF diet. We did not find any significant difference in body weight or systolic blood pressure in any of the groups. <br> <b>CONCLUSIONS</b>: Our results show that WGP supplementation prevented hyperglycemia, insulin resistance and reduced oxidative stress in rats fed with HF diet. We propose that WGP may be used as a supplement in human food as well.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Keywords</b>: Insulin resistance, Oxidative stress, Metabolic syndrome, Wine grape powder</font></p> <hr noshade size="1"> <p> </p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Background</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The development of industrialized countries together with technological advances has produced strong social changes that directly affect the human lifestyle. Changes in diet and a sedentary lifestyle characterized by the lack of exercise in daily life advance in parallel with a growing number of metabolic diseases, resulting in high cardiovascular risk and increased morbidity and mortality rate. The association of a collection of risk factors including hypertension, high triglycerides, low HDL cholesterol, and high fasting glucose, which are linked to type 2 diabetes, cardiovascular disease and stroke, created a condition called metabolic syndrome (MS). The World Health Organization defines MS as a prothrombotic state, with dyslipidemia, alteration in the metabolism of glucose, a sustained rise in blood pressure, abdominal obesity and a systemic pro-inflammatory state [1]. The metabolic syndrome has high prevalence, estimated between 20 and 30 % of adult worldwide population [2, 3]. Abdominal obesity, one of the MS features, produces oxidative stress. Accordingly, it has been found that an increased oxidative stress in abdominal adipocytes may increase various pro-inflammatory cytokines and fatty acids, which exacerbate other MS factors such as insulin resistance, hypertriglyceridemia, and hypertension [4]. In addition, it has been demonstrated that the activity of several antioxidant enzymes decreases in humans with MS [5]. One of the transcription factors responsible for the initiation of the antioxidant response is the nuclear factor E2-related factor-2 (Nrf2), which controls the expression of cellular phase-2 detoxifying and anti-oxidant enzymes [6, 7]. Nrf2 induces the expression of several antioxidant enzymes [8-11] such as superoxide dismutase (SOD) to restore the imbalance of oxidative stress [12, 13].</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Because MS involves several different factors, no unique pharmaceutical treatment exists to prevent or treat it. The best solution seems to be to adjust lifestyle factors like diet and exercise. It is known that grape anti-oxidants play a role in the reduction of the metabolic syndrome risk factors. Grapes contain numerous antioxidants such as polyphenols, anthocyanins, flavonols and resveratrol. A simple way to make grape polyphenols part of the diet is to consume grape products. Wine grape pomace is an underused residue of the wine making process. This grape by-product contains pressed skins, seeds and stems and accounts for about 20 % of the weight of the grapes used to make wine. In addition, grape pomace is a rich source of polyphenols including monomeric and oligomeric proanthocyanidins and a diversity of anthocyanin glycosides [14]. Due to the abundance of antioxidants found in this by-product, grape pomace is increasingly being used to obtain functional food ingredients and as a dietary supplement [15]. Flavonoids that are present in grape pomace are a large group of polyphenolic antioxidants present in a variety of foods. Most naturally occurring flavonoids can induce chelation of transition metals, the scavenging of free radicals, and inhibition of radical producing enzymes [16]. In addition, it has been postulated that a flavonoid-rich diet can prevent several degenerative age-related diseases [17] and several kinds of cancer [18]. It can also reduce the incidence of coronary heart disease [15], and chronic renal disease [19]. As mentioned before, it is well accepted that diets rich in polyphenols have health benefits, but the mechanisms of action of these molecules in the human body are not fully understood [20-22]. Wine grape powder (WGP) made from dried wine grape pomace, is rich in fiber and polyphenols. However, little is known about the potential effects of WGP in the oxidative state or metabolic markers of MS. Therefore, the present study was conducted to investigate the antioxidant and anti-insulin-resistance effect of WGP in an established rat model of MS induced by high fructose diet [23-26].</font></p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Methods</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Wine grape powder</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Wine grape pomace, a waste product from wine production was obtained from a single production lot of red grapes (Cabernet Sauvignon, vintage 2011, Maipo Valley, Chile) from Concha y Toro Winery, and stored at -20 °C until used, for approximately 3 months. The frozen wine grape pomace was thawed at room temperature and dried in a forced air dryer at 60 °C until moisture reached less than 12 %. The dried pomace was grinded with a hammer mill to obtain a wine grape pomace powder (WGP), which was packaged in double plastic bags of 20 kg. WGP has a high content of dietary fiber (48 %) determined by AOAC 991.43. The content of polyphenolic compounds was 41.11 ± 3.01 mg galic acid equivalent/g, determined by the Folin-Ciocalteu procedure [27]. WGP with a high antioxidant capacity of 362.9 ± 24.4 </font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">mol TE/g, measured by the oxygen radical absorbance capacity assay [28].</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Rats, diets, and treatment with WGP</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The experimental protocols were approved by the Bio-ethical Committee of the Faculty of Biological Sciences of the Pontificia Universidad Católica de Chile and were in accordance with the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85-23, revised 1996). Male Sprague-Dawley rats (6 week old, 180 g) were obtained from the Faculty of Biological Sciences Animal Care Facility. Rats were randomly divided into 4 groups according to their feeding treatments: control diet-fed rats (C; n = 8), control diet-fed rats supplemented with WGP (C + WGP; 20 % of WGP; n = 8); high-fructose diet-fed rats (HF; 50 % fructose, n = 7) and high-fructose diet-fed rats supplemented with WGP (HF + WGP, n = 6).</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Mixtures for each of the diets were prepared on an industrial mixer at the Molino La Estampa, Chile, using the proportions for each of the ingredients shown in <a href="#t1">Table 1</a>. Food pellets for each of the animal diets were prepared daily by adding the same amount of water to a fraction of each of the powder mixtures.</font></p> <p align="center"><a name="t1"></a></p> <p align="center"> </p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Table 1 Composition and energy provide by the experimental diets</b></font></p> <p align="center"><img src="/fbpe/img/bres/v48/53t01.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><i>C</i> control diet, <i>C</i> + <i>WGP</i> control diet plus 20 % wine grape powder, <i>HF</i> high fructose diet, <i>HF</i> + <i>WGP</i> high fructose diet plus 20 % wine grape powder</font></p> <p align="center"> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The proximate analysis of the WGP is shown in <a href="#t2">Table 2</a>, and the composition and energy provided by proteins, carbohydrates and fat in experimental diets is shown in <a href="#t1">Table 1</a>. Animals were fed with 36 g (dry mixture) of their respective diets daily for 16 weeks. Rats were individually housed under controlled temperature, 12-h-light/dark cycles, consumed water ad libitum, <i>and were </i>under veterinarian supervision.</font></p> <p align="center"><a name="t2"></a></p> <p align="center"> </p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Table 2 Proximate analysis of wine grape flour</b></font></p> <p align="center"><img src="/fbpe/img/bres/v48/53t02.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Total dietary fiber corresponds to the sum of soluble and insoluble fractions <br> </font><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><sup>a</sup> Nitrogen free extract minus dietary fiber</font></p> <p align="center"> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>P</b><b>hysiological and metabolic variables</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">All rats were continuously monitored for body weight, food and water intake. Blood glucose and triglycerides were measured using a commercial enzymatic kit and strips (Code Free, SD Biosensor Inc, Korea). Oral glucose tolerance test (GTT) was performed 2 days before the end of the experiment, on rats that have been food-deprived for 12 h. Each animal received 2 g/kg of glucose diluted in 2 mL of water by gavage. Rats were anesthetized with isofluorane 2 % in O<sub>2</sub>, and blood samples were obtained from the tail vein at 0 min (before glucose administration) 30, 60 and 120 min. A glucose tolerance curve was obtained and the trapezoidal rule was used to determine the area under the curve (AUC).</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Arterial blood pressure measurements</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Measurements of systolic arterial blood pressure was performed with a non-invasive method in conscious rats, in a room at 25 °C, with noise and light control. These measurements were done using a Power Lab coupled to a NIBP system with pulse transducer/cuff for rat by tail cuff (ADInstruments, Australia). Rats were trained at least for 1 month before the experimental measurements. In separate experimental series, three rats were anesthetized with isofluorane 2 % in O<sub>2</sub> and were implanted with radio-telemetric transmitters (TA11PA, DSI, USA) in one femoral artery. After surgery, rats received Ketoprofen 0.2 mg/ kg (Rhodia Merieux) and Enrofloxacin 20 mg/kg (Bayer) i.m. Rats were allowed to recover for 7 days prior to the surgery and then were fed with control, high fructose and high fructose + WGP diets for 120 days. Arterial blood pressure was averaged from 30 min recordings, performed between 9 and 10 AM every 3 days in the initial 90 days, and then every 10 days during the last 30 days.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Blood and tissue samples</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">At the end of the experiment, blood samples were taken, and then animals were sacrificed under anesthesia (Xyla-sine/Ketamine, 10 mg/90 mg per kg). Kidneys were immediately removed, frozen in liquid nitrogen and stored at -80 °C for later determinations. Plasma insulin level was determined using a rat insulin ELISA kit (EMD Millipore Corporation, USA), calculating the homeosta-sis model assessment of insulin resistance (HOMA-IR), based on the following formula:</font></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2">HOMA - IR = serum glucose (mg/dL) x plasma insulin (</font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">U/ml)/405.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Oxidative stress measurement</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Levels of thiobarbituric acid reactive substances (TBARS) in the plasma and kidneys were estimated using a previously described method [29] with slight modifications. 100 </font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">L of plasma or supernatant from tissue homoge-nate were mixed with 50 </font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">L sodium dodecyl sulphate (8 %w/v), 375 </font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">L thiobarbituric acid (0.8 % w/v), and 375 </font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">L acetic acid (20 %v/v); and then heated for 60 min at 90 °C. The precipitated material was removed by cen-trifugation, and the absorbance of the supernatant was determined at 532 nm. Levels of TBARS were expressed as malondialdehyde (MDA).</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Electrophoresis and Western blot analysis</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">To determine relative levels of Nrf-2 (1:500; Santa Cruz Biotechnology) and mSOD (1:2000, Millipore), kidney homogenates were lysed in RIPA with protease inhibitors (1 mg/mL aminocaproic acid, 1 mg/mL benzamidine, 0.2 mg/mL SBTI and 3 mmol/L PMSF) and phosphatase inhibitors (12 </font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">g/mL sodium orthovanadate, 4.46 mg/mL sodium pyrophosphate, and 4.2 mg/mL sodium fluoride). Lysates were centrifuged and supernatants were collected for Western blot analysis. Protein concentrations were determined by the method of Lowry [30]. Protein samples (100 </font><font size="2">μ</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">g) from homogenates under different treatments were separated by electrophoresis in 10 % SDS-poly-acrylamide gel (SDS-PAGE). Proteins were transferred to a 0.45 </font><font size="2">μηι</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> PVDF membrane, which was blocked at room temperature with Tris pH 7.6/5 % skim milk (w/v)/BSA 1 % (w/v). Then, the PVDF membrane was incubated overnight at 4 °C with primary antibody, followed by incubation with rabbit secondary antibody conjugated to peroxidase (1:2000) for 2 h. Immunoreactive bands were visualized using a chemiluminescent reagent (Western Lightning, Perkin Elmer) according to the procedure described by the supplier and Kodak films X-LS. The bands detected were digitized and subjected to densitometric analysis using the program Image J (NIH, Washington DC, USA).</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Statistical analysis</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Data obtained from different groups of rats were compared with each other by one-way analysis of variance (ANOVA) followed by a Bonferroni\'s post hoc test. The analyses were performed with GraphPad Prism 5 software for Windows (GraphPad Software). Results are expressed as mean ± standard error of the mean (SEM). Differences were considered significant if p <u><</u> 0.05.</font></p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Results</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Effects of the high fructose diet on the physiological parameters measured in rats</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">High fructose diet increased glucose, triglycerides and insulin levels in plasma measured after 12 h of food deprivation, but did not induce changes in systolic arterial pressure, body or heart weight (<a href="#t3">Table 3</a>). Supplementation with WGP to the HF diet reduced the increase in glucose, triglycerides and insulin levels in plasma. In a separate experimental series, we recorded systolic and diastolic arterial pressure with radiotelemetry in three rats fed with control, high fructose and high fructose plus WGP. Arterial blood pressure slightly increased during the experiment in all groups. However a similar trend in the increase of arterial blood pressure was observed in all three rats (<a href="#f1">Fig. 1</a>).</font></p> <p align="center"><a name="t3"></a></p> <p align="center"> </p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Table 3 Physiological parameters of rats fed experimental diets</b></font></p> <p align="center"><a href="/fbpe/img/bres/v48/53t03.jpg"><img src="/fbpe/img/bres/v48/53t03thumb.jpg" border="0"></a></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2">n = 6-8 in each group <br> </font><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><i>C</i> control diet, <i>C</i> + <i>WGP</i> control diet plus wine grape powder, <i>HF</i> high fructose diet, <i>HF</i> + <i>WGP</i> high fructose diet plus wine grape powder <br> </font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">* P < 0.05 Bonferroni after one way ANOVA</font></p> <p align="center"> </p> <p align="center"><a name="f1"></a></p> <p align="center"> </p> <p align="center"><img src="/fbpe/img/bres/v48/53f01.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Fig. 1</b> Arterial blood pressure measured by radiotelemetry in three conscious rats fed with control (C <i>filled circle</i>), high fructose (HF <i>filled square</i>) and high fructose + WGP (HF + WGP <i>unfilled square</i>) diets. Systolic and diastolic arterial blood pressure of the rats was displayed in the <i>upper</i> and <i>lower</i> part of the figure, respectively. Telemeters were implanted into the femoral artery and the recordings started 7 days after the surgery. <i>Arrow</i> indicate the beginning of the diet treatments</font></p> <p align="center"> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>WGP prevented the rise of glucose and the area under the curve on the glucose tolerance test in fructose-fed rats</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Rats treated with a high fructose diet had the highest fasting level of blood glucose, before beginning the GTT (<a href="#f2">Fig. 2a</a>). The GTT showed that the largest increase in blood glucose measured at 30 min and 2 h following glucose administration was observed in the HF group. In addition, it is worth to note that glucose levels in the HF + WGP group were slightly lower than the one on the control group, while the lowest curve was from the C + WGP group. To quantify these differences, we measured the area under curve (AUC) of the glucose tolerance test (<a href="#f2">Fig. 2b</a>). We found a significant increase in the area under the curve in the HF fed group, whereas WGP prevented the increased AUC in the WGP + HF treated rats.</font></p> <p align="center"><a name="f2"></a></p> <p align="center"> </p> <p align="center"><img src="/fbpe/img/bres/v48/53f02.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Fig. 2</b> WGP prevents the increase in the area under the curve for the glucose tolerance test. <b>a</b> Glucose tolerance test curves are shown for control (C <i>filled circle</i>), control + WGP (C + WGP <i>unfilled circle</i>) high fructose (HF <i>filled square</i>) and high fructose + WGP (HF + WGP <i>unfilled square</i>) fed animals. Each <i>curve</i> represents mean ± SEM for at least six animals. <b>b</b> Area under the curve was calculated for the curve of each animal. <i>Bars</i> represent mean ± SEM for n = 6-8 rats in each group. *P < 0.05 HF vs. other groups. Bonferroni after one way ANOVA</font></p> <p align="center"> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>WGP prevented the induction of insulin resistance in fructose-fed rats</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">To evaluate whether the increase in the AUC correlates with the insulin concentration, we measured insulin in the blood obtained after 12 h of starvation. Under these conditions, we found that rats from the HF fed group presented the highest levels of insulin, and its increase was prevented by the supplementation with WGP in the diet, as observed from the HF + WGP fed group (<a href="#f3">Fig. 3a</a>). In addition, glucose levels were measured in these same blood samples and the homeostasis model assessment-estimated IR (HOMA-IR) index was evaluated for each group. HF fed rats presented a significantly higher HOMA-IR index compared to control rats. In addition, this increase was prevented in HF + WGP fed rats (<a href="#f3">Fig. 3b</a>).</font></p> <p align="center"><a name="f3"></a></p> <p align="center"> </p> <p align="center"><img src="/fbpe/img/bres/v48/53f03.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Fig. 3</b> WGP prevents insulin resistance in HF fed rats. a Insulin was measured using a radioimmunoassay in control (C), control + WGP (C + WGP) high fructose (HF) and high fructose + WGP (HF + WGP) fed animals. b HOMA was calculated from insulin values shown in this figure and glucose values obtained at the same time points. <i>Bars</i> represent mean ± SEM for n = 6-8 rats in each group. *P < 0.05 HF vs. other groups. Bonferroni after one way ANOVA</font></p> <p align="center"> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>WGP prevented the rise of TBARS in plasma from fructose-fed rats</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">High fructose diet produced a significant threefold increase in plasma TBARS levels measured at the end of 16 weeks of treatment (<a href="#f4">Fig. 4</a>). WGP effectively prevented this increase in TBARS levels in high fructose-fed rats. When compared to control, TBARS levels in HF + WGP were not significantly different from those of control rats.</font></p> <p align="center"><a name="f4"></a></p> <p align="center"> </p> <p align="center"><img src="/fbpe/img/bres/v48/53f04.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Fig. 4</b> WGP reduces oxidative stress in HF fed rats. TBARS were measured in plasma from control (C), control + WGP (C + WGP) high fructose (HF) and high fructose + WGP (HF + WGP) diets. <i>Bars</i> represent mean ± SEM for n = 6-8 rats in each group. *P < 0.05 HF vs. other groups. Bonferroni after one way ANOVA</font></p> <p align="center"> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>WGP prevented the reduction of SOD protein levels in kidneys from fructose-fed rats</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Nrf-2 is considered a key transcription factor in the cellular response to oxidative stress [31]. This transcription factor regulates the expression of several antioxidant enzymes that participate in the defense against reactive oxygen species such as superoxide dismutase (SOD). Therefore, we evaluated the effect of HF treatment on Nrf-2 levels in renal tissue and found no significant changes after 16 weeks of treatment in this transcription factor. Although Nrf-2 protein levels were not significantly modified by the diet, we speculated that its activity could be modified. For this reason, we measured mSOD protein concentration, one of the proteins regulated by Nrf-2. We found a significant reduction in renal mSOD levels. Consistent with the previous observations, this decrease was not observed in HF rats fed with WGP (<a href="#f5">Fig. 5</a>).</font></p> <p align="center"><a name="f5"></a></p> <p align="center"> </p> <p align="center"><img src="/fbpe/img/bres/v48/53f05.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Fig. 5</b> WGP prevents the reduction in renal mSOD protein levels. Protein extracts from kidneys from control (C), control + WGP (C + WGP) high fructose (HF) and high fructose + WGP (HF + WGP) fed animals were used to evaluate mSOD protein levels. <i>Bars</i> represent mean ± SEM for n = 4 animals in each group. Bars represent mean ± SEM for n = 4, *p < 0.05 HF vs. other groups. Bonferroni after one way ANOVA. Representative blots for mSOD and </font><font size="2">β</font><font face="Verdana, Arial, Helvetica, sans-serif" size="2">-actin used as loading control are shown under the graph</font></p> <p align="center"> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>WGP prevents the rise of TBARS in kidneys from fructose-fed rats</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">To determine whether the changes in mSOD proteins levels correlated with the oxidative state found in the kidney, we measured TBARS in renal tissue. We found a significant increase in TBARS in the HF group, whereas this increase was prevented in the HF + WGP fed group (<a href="#f6">Fig. 6</a>).</font></p> <p align="center"><a name="f6"></a></p> <p align="center"> </p> <p align="center"><img src="/fbpe/img/bres/v48/53f06.jpg"></p> <p align="center"><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Fig. 6</b> WGP prevented oxidative stress in renal tissue. Extracts from kidneys from control (C), control + WGP (C + WGP) high fructose (HF) and high fructose + WGP (HF + WGP) fed animals were used to determine TBARS. <i>Bars</i> represent mean ± SEM for n = 6-8 rats in each group, *P < 0.05 HF vs. other groups. Bonferroni after one way ANOVA</font></p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Discussion</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The main finding of the current study is that 16 weeks of supplementation with WGP protects against fructose-induced oxidative stress and glucose intolerance in a rat model of metabolic syndrome. The metabolic syndrome is a growing health problem and it is important to find a treatment to prevent its development. However, it is difficult to find a single treatment, because of the multiple factors that participate in this syndrome. The use of food supplements is one of the possible approaches to prevent the progression of this syndrome. The presented results show that WGP supplement prevents the evolution of the metabolic syndrome in rats.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Despite that arterial blood pressure did not change, we found that the high-fructose diet produced metabolic alterations similar to those found by others [23-26, 32]. Some studies have reported an increase in body weight [23] and arterial blood pressure [24] in rats treated with a high fructose diet, but other studies failed to find changes in these variables in Sprague-Dawley rats [25, 26]. The difference with other studies may reflect a differential response to stress of different strain rats, or the methods to measure arterial blood pressure. However, we measured arterial blood pressure in conscious rats using both radiotelemetry and the tail cuff methods. Several studies have demonstrated the ability of a high fructose diet to induce insulin resistance, reproducing the features of the metabolic syndrome in laboratory rats [23-26, 32]. Similarly to other studies, we found an increase of the area under curve of the glucose tolerance test, fasting blood glucose, plasma insulin, the HOMA index, and TBARS in plasma and renal tissue of HF-fed rats [23-26, 32].</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">It has been observed that high fructose fed rats develop metabolic syndrome without requiring an increased energy intake, because fructose is metabolized different than glucose ultimately producing uric acid. Uric acid is an antioxidant in the extracellular environment, but when enters the cells it induces an oxidative burst, mediated by the NADPH oxidase. This burst can induce increases in arterial blood pressure when affecting endothelial cells and in body weight. One explanation to the absence of effect on body weight and arterial pressure in our model is that in rats, uricase is expressed in high amounts so there is an efficient degradation of uric acid. Nevertheless, it has been reported that fructose induces insulin resistance even with high levels of uricase [33], and although we did not measure uricase, we did observe insulin resistance in our experimental group.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Oxidative stress is a feature of several metabolic disorders. Kunde et al. [34] evaluated the oxidative stress in the liver of mice exposed to 30 % fructose diet, and found an increase in TBARS, which did not reach significance. Similarly, Yin et al. [35] found that TBARS increased in the hippocampus and cerebral cortex in Wistar rats treated with 10 % fructose from 16 weeks. Moreover, they demonstrated that these changes were prevented by the administration of Pioglitazone, an antihyperglycemic drug. We found an increase in renal TBARS that correlates with the decrease in the levels of mSOD. The ability of WGP to prevent the increases in TBARS and the decreases in mSOD levels, suggests that WGP may be as effective as some pharmacological drugs in preventing the alterations induced by fructose.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The effects of WGP on oxidative stress and glucose intolerance found in this study could be attributed to its high content in polyphenols. These compounds are found in all plant species. They are important in plants for reproduction, growth, pigmentation and protection against pathogens [36]. Polyphenols are abundant in the mediterranean diet that is rich in fruits and wine. Grapes contain a great variety of polyphenols, including resveratrol, flavonoids, flavonols, flavones and anthocya-nines. Polyphenols can exert several effects. It has been postulated that polyphenols from green tea, may reduce cholesterol and fatty acid absorption [37]. In addition, it was shown that a lyophilized grape powder reduced the overall metabolism of lipoproteins [38]. Patel et al. [39] showed that dietary polyphenols may attenuate the inflammation through modulation of the activities of NF-kB and Nrf-2.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">When evaluating one particular polyphenol, it has been reported that resveratrol, extracted from grape skins, increases the activity of SIRT1 [40] and AMPK [41], and inhibits the mitochondrial ATP synthase [42]. On the other hand, EGCG has been used to inhibit several receptor tyrosine kinase activities such as the ones from vascular endothelial growth factor receptor [43] and insulin like growth factor receptor [44]. All together these results suggest that one or the combination of the different polyphenols found in WGP may produce the beneficial effects observed in the rats treated with HF and WGP on this study.</font></p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>Conclusions</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">In summary, the present results show that WGP supplementation prevents glucose intolerance and reduces oxidative stress in rats fed with high fructose diet. Accordingly, WGP could be used as a food supplement for the prevention of the metabolic syndrome in human. Nevertheless, further studies are needed to validate the use of this flour in humans.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Abbreviations</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">WGP: wine grape powder; HF: high fructose; HOMA: homeostasis model assessment; TBARS: thiobarbituric acid reactive substances; HDL: high density lipoproteins; MS: metabolic syndrome; Nrf2: nuclear factor E2-related factor-2; mSOD: mitochondrial superoxide dismutase; GTT: oral glucose tolerance tests; AUC: area under the curve; MDA: malondialdehyde; SBTI: soy bean trypsin inhibitor; PMSF: phenylmethylsulfonyl fluoride; BSA: bovine serum albumin; PVDF: polyvinylidene difluoride.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Authors\' contributions</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">VV, RI, and IU designed research. RH, VD, DP, and PC conducted research. VV, RI, and RH analyzed data. VV, RI, RH, and AL wrote paper. VV had primary responsibility for final content. All authors read and approved the final manuscript.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Financial support</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">This work was supported by project Fondef AF 10i1014 from CONICYT, Chile and project Puente #20/2013, PUC.</font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Compliance with ethical guidelines</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Competing interests</b></font></p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">The authors declare that they have no competing interests.</font></p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>References</b></font></p> ',
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"text": '<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Received: 13 June 2015 <br> Accepted: 22 September 2015 <br> Published online: 30 September 2015</font></p> <p> </p> <p> </p> <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><a name="back"></a><a href="#top">*</a> Correspondence: <a href="mailto:vvelarde@bio.puc.cl">vvelarde@bio.puc.cl</a></font></p> </div></div>',
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