Figures
Abstract
Insulin resistance and hepatic steatosis are the most common complications of obesity. Pitaya is an important source of phytochemicals such as polyphenols, flavonoid and vitamin C which are related to its antioxidant activity. The present study was conducted to evaluate the influence of white pitaya juice (WPJ) on obesity-related metabolic disorders (e.g. insulin resistance and hepatic steatosis) in high-fat diet-fed mice. Forty-eight male C57BL/6J mice were assigned into four groups and fed low-fat diet with free access to water or WPJ, or fed high-fat diet with free access to water or WPJ for 14 weeks. Our results showed that administration of WPJ improved high-fat diet-induced insulin resistance, hepatic steatosis and adipose hypertrophy, but it exerted no influence on body weight gain in mice. Hepatic gene expression analysis indicated that WPJ supplement not only changed the expression profile of genes involved in lipid and cholesterol metabolism (Srebp1, HMGCoR, Cpt1b, HL, Insig1 and Insig2) but also significantly increased the expression levels of FGF21-related genes (Klb, FGFR2, Egr1 and cFos). In conclusion, WPJ protected from diet-induced hepatic steatosis and insulin resistance, which was associated with the improved FGF21 resistance and lipid metabolism.
Citation: Song H, Zheng Z, Wu J, Lai J, Chu Q, Zheng X (2016) White Pitaya (Hylocereus undatus) Juice Attenuates Insulin Resistance and Hepatic Steatosis in Diet-Induced Obese Mice. PLoS ONE 11(2): e0149670. https://doi.org/10.1371/journal.pone.0149670
Editor: Jonathan Peterson, East Tennessee State University, UNITED STATES
Received: September 18, 2015; Accepted: February 1, 2016; Published: February 25, 2016
Copyright: © 2016 Song et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by National Key Technology R&D Program of China (Grant No.2012BAD33B08, http://program.most.gov.cn/, received by XDZ), Zhejiang Provincial Natural Science Foundation of China (Grant No. Z14C200006, http://www.zjnsf.gov.cn/, received by XDZ) and the Foundation of Fuli Institute of Food Science, Zhejiang University (Grant No. KY201301, http://fifs.zju.edu.cn/content/detail.php?sid=3&cid=642, received by XDZ). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Type 2 diabetes and non-alcoholic fatty liver disease (NAFLD) are common consequences of a combination of metabolic disorders such as dyslipidemia, hepatic steatosis, glucose intolerance and insulin resistance [1]. Mounting evidence suggests that insulin resistance and hepatic steatosis, the most common complications of obesity, are characterized by impaired energy metabolism and attributed by complex interactions between genetic background and environmental impacts such as dietary and sedentary habits[2–6]. Moreover, insulin resistance is often accompanied by hepatic steatosis [7]. Traditional pharmacotherapies for type 2 diabetes and NAFLD are often accompanied by side effects. Recently, growing evidence has suggested that natural bioactive compounds in food exerts many beneficial effects on obesity and its metabolic consequences [8–10].
Pitaya, also known as dragon fruit, is among the most important commercial tropical fruits around the world, and three varieties have been classified as Hylocereu polyrhizus (red pitaya), Hylocereus undatus (white pitaya) and Hylocereus megalanthus (Yellow pitaya) [11]. Pitaya is an important source of phytochemicals such as polyphenols, flavonoid and vitamin C which are related to its antioxidant activity [12, 13]. Especially the red and white pitaya have recently drawn growing attention worldwide not only because of their economic values but also their health benefits [14]. Red pitaya consumption was reported to decrease total cholesterol (TC), triglyceride (TG) and low-density lipoprotein cholesterol (LDL-C) levels while increasing the high-density lipoprotein cholesterol (HDL-C) levels in type 2 diabetic subjects. The similar lipid-improving effect of its menthol extract was found in high-fat diet-fed rats [15, 16]. In addition, the antidiabetic effect of red pitaya has also recently been demonstrated. For instance, red pitaya significantly improved insulin resistance in rats and 600 g amount of red pitaya fruit consumption every day decreased the blood glucose level in type II diabetic subjects [15, 17]. Ramli et al. also reported that supplementation of red pitaya juice could induce a trend of glucose and uric acid normalization associated with reduced ALP and ALT but increased AST levels in high-carbohydrate and high-fat diet-fed rats [18].Though both red and white pitaya are reported to be rich, natural and cost-effective source of bioactive nutrients, few studies focused on the beneficial effects of white pitaya on diabetes and NAFLD.
The objective of the present study was to investigate the influence of white pitaya juice (WPJ) on obesity-related hepatic steatosis and insulin resistance in high-fat diet-induced obese mice and explore the underlying mechanism by which pitaya juice exerted its beneficial effects. To the best of our knowledge, this is the first study to evaluate the effect of white pitaya on type II diabetes and NAFLD.
Materials and Methods
Chemical reagents and juice preparation
The solvents and reagents were obtained from Aladdin (Shanghai, China). Fresh white pitayas (Hylocereus undulatus) were purchased from agricultural and sideline products wholesale center which is located in 183 Yisheng Road, Yuhangtang District, Hangzhou. The peels were removed and the juice was squeezed out of the fruits using a juice maker. The extracted juice was then centrifuged at 10,000 g for 40 min at 4°C. After that, the supernatant was filtered, collected and stored at -80°C. The content of bioactive compounds (e.g. total polyphenol and total flavonoids) in pitaya juice were determined using the methods described previously [19, 20].
Animals and diets
All the protocols in this study were approved by the Committee on the Ethics of Animal Experiments of Zhejiang University (Permission Number: ZJU201550501) and the experimental procedures were performed according to the National Institutes of Health regulations for the care and use of animals in research. Moreover, all efforts were made to minimize suffering. Four-week-old C57BL/6J mice (male, n = 48) were supplied by the National Breeder Center of Rodents (Shanghai, China) and housed in a 12-hour light/dark cycle environment with free access to water and food and the temperature was kept at 23±3°C with a relative humidity of 50%±10%. After one week of acclimation, the mice were randomly assigned to the following four groups (n = 12): LFD, mice fed low-fat diet with free access to water, LFDJ, mice fed low-fat diet with free accesses to WPJ; HFD, mice fed high-fat diet with free access to water and HFDJ, mice fed high-fat diet with free access to WPJ. The ingredients and energy densities of the low-fat and high-fat diets are listed in the S1 Table. Juice and water were replaced every other day and the volumes consumed were recorded. The monitoring for body weight and food consumption started in the first week and continued through the entire experiment. Food consumption of each dietary group was determined by weighing the total amount of food given on Monday and then subtracting by the amount of food remaining on Wednesday. The average food intake of each mouse was obtained by dividing the total number of the mice in the group. The low-fat diet (LFD) contained 3.85 kcal in each gram of food, and high-fat diet (HFD) contained 4.73 kcal in each gram of food. Based on the energy density and the amount of daily consumed food, the daily calorie intake was calculated. After 14 weeks of treatment, the mice were fasted overnight and sacrificed by decapitation. Blood samples were collected for serum preparation by centrifugation at 2000g for 15 minutes. The livers, hearts, kidneys, spleens, epididymal and perirenal fat and interscapular brown fat were collected, weighted and stored at -80°C prior to use.
Biochemical analysis
Serum concentrations of glucose, TG, TC, ALT, AST, HDL-C and LDL-C were measured using an automatic biochemistry analyzer (ACCUTE TBA-40FR, Japan) according to the manufacturer’s instructions. The commercial ELISA assay kits were used to determine the serum levels of leptin (Cat#: MOB00), insulin (Cat#: E-EL-M2614c), adiponectin (Cat#: MRP300), LPS (Cat#: E-EL-0025c), FGF21 (Cat#: MF2100) and NPY (Cat#: E-EL-M0820c).
HOMA-IR and HOMA-IS analysis
The homeostasis model assessment (HOMA) was applied to calculate the insulin resistance (HOMA-IR) and insulin sensitive index (HOMA-IS) in accordance with the following formulas:
Hepatic lipid profile analysis
Liver total lipids were extracted using the Folch method with minor modifications [21]. Briefly, the liver tissues were homogenized with chloroform/methanol mixture to a final volume 15 times the volume of the sample (0.2 g in 3 ml of solvent mixture). After dispersion, the mixture was agitated for 20 min. Then the homogenate was centrifuged to recover the liquid phase. After that, the solvent was washed with 0.2 volume (0.2 ml for 1 ml) of 0.9% NaCl solution. After vortexing for some seconds, the mixture was centrifuged at 2000 rpm/min to separate the two phases. After centrifugation and removing of the upper phase, the lower chloroform phase containing total lipids was evaporated under a nitrogen stream and the lipids were resuspended using 1% Triton X-100 in chloroform. The extracting contents of TG and TC in livers were determined using commercially available kits (Elabscience, Cat#: E-EL-M2603c and E-EL-M2608c) according to the manufacturer's instructions.
Histological analysis
Specimens of liver, epididymal and perirenal white adipose and interscapular brown adipose were cut and fixed in 10% buffered formalin. For oil red O staining, the liver tissues were embedded in Optimal Cutting Temperature gel and the air-dried 6μm thick sections were dipped in formalin and washed with 0.5% oil red O solution. For H&E staining, the liver and adipose tissues were embedded in paraffin, sliced at 6μm and stained with hematoxylin and eosin (H&E). The images were captured by Olympus CX41 camera (Japan). To evaluate hepatic steatosis and the adipocyte size, the morphometric analysis was performed on 3 randomly selected sections at different depths for each mouse, and the representative sections were from six mice of each individual dietary group. The two softwares ImageJ and Photoshop were used for cell counting and the quantification of adipocyte size. Initial assessment of adipocyte size was performed under lower magnification (40×, containing> 300 cells) and confirmed under higher magnification (100×, containing> 300 cells; or 400×, containing>50 cells). The liver steatosis was scored as follows: 0, steatosis involving <5% of fatty hepatocytes; 1, steatosis involving 5–33% of fatty hepatocytes; 2, steatosis involving 34–66% of fatty hepatocytes; 3, steatosis involving >66% of fatty hepatocytes [22].
RNA extraction and quantitative Real-Time PCR Analysis
Total RNA was extracted from the liver with Trizol (Invitrogen Technologies, USA) according to the manufacturer’s instructions. Then the total RNA concentrations were measured by NanoDrop 2000 (Thermo Scientific, Wilmington, USA). 1μg total RNA was converted to cDNA using a reverse transcription kit (Takara, Cat# RR047A). 3 pooled RNA samples were from the n = 12 total samples in which 4 mice were pooled to generate one individual sample in each dietary group. The 20μl PCR reaction mixtures consisted of 1μl cDNA, paired-primers (300nM) and 10μl SYBR® Green QPCR Master Mix (Roche). The amplification program performed on Applied Biosystems 7500 system was as follows: 3 min at 50°C, 10 min at 95°C, then 31 cycles of 15 s at 95°C and then 60s at 60°C followed by melting curve for 60s at 95°C, then gradual decrease to 50°C, 20 s at 50°C, then gradually increase to 95°C, and last 20 s.
The primers are presented in the S2 Table. The relative expression of mRNA was normalized using the geometric mean of 5 housekeeping genes, including β-actin, RPS18, B2M, TBP and ARBP and the relative fold change was calculated using the 2-△△Ct method.
Statistical analysis
Values were expressed as means ± SEM. The statistical analyses were performed using SPSS 19.0 statistical software and the differences among multiple groups were assessed by one-way analysis of variance (ANOVA) followed by Duncan’s post-hoc test. p< 0.05 was considered statistically significant.
Results
Characterization of white pitaya juice
The bioactive compounds contained in WPJ were listed in Table 1.
Effect of WPJ on body weight gain, tissue weights, food intake, liquid intake and serum lipid profile
As depicted in Table 2, high-fat diet feeding induced a great body weight gain in mice, but no significant differences in either final body weight or the cumulative weight gain were observed between the HFDJ and HFD group. The similar results were found between LFD and LFDJ group.
In addition, mice in LFD and LFDJ group consumed more food than those in HFD and HFDJ group, and mice in LFDJ and HFDJ group intake more liquid than those in LFD and HFD group. But there were no differences in the calorie intake among all the dietary groups. In addition, according to the FDA ratio of conversion, the human-equivalent dose for pitaya juice based on body surface area is approximately 440ml for a 60Kg human. High-fat diet-induced a decrease in the relative weight of heart, liver and kidney but a significant increase in the relative weight of perirenal and epididymal white adipose and no influence on spleen and interscapular brown adipose compared to mice fed low-fat diet (Table 2). No difference in the organ weights existed between the LFD and LFDJ group. The same results were also found between the HFD and HFDJ group, except a decrease in the weight of epididymal white adipose in HFDJ group. Moreover, the serum levels of TG, TC, HDL-C, LDL-C, ALT and AST were significantly increased in mice fed high-fat diet compared to those fed low-fat diet, while administration of WPJ significantly reduced the levels of TG, TC, LDL-C, ALT and AST but not HDL-C. In addition, WPJ also tended to decrease TG and ALT in mice fed low-fat diet (Table 2).
Effect of WPJ on serum cytokines
WPJ supplementation significantly reduced high-fat diet feeding-induced increase of serum levels of FGF21 and LPS and also tend to decrease the leptin level, although not significant (Fig 1B, 1C and 1D). Though there is not a significant increase in the serum level of adiponectin in LFDJ group compared to that in LFD group, the level of serum adiponectin in the HFDJ group was significantly higher than that in the HFD group (Fig 1A). In addition, neither high-fat diet feeding nor WPJ administration influenced the serum levels of and NPY (Fig 1E).
The fasting serum levels of adiponectin (A) and leptin (B). (C) Circulating levels of FGF21. The fasting serum levels of LPS (D) and NPY (E). FGF21, fibroblast growth factor 21; NPY, neuropeptide Y; LFD, mice fed low-fat diet; LFDJ, mice fed low-fat diet with supplementation of WPJ; HFD, mice fed high-fat diet; HFDJ, mice fed high-fat diet with supplementation of WPJ. n = 10 (A, B, C and D). Values are presented as means ± SEM. Data not sharing a common superscript differ significantly among groups (p<0.05, ANOVA).
WPJ alleviates obesity-related hepatic steatosis and adipose tissue hypertrophy
H&E and Oil red O staining of livers revealed an obvious hepatic lipid droplets accumulation in mice fed high-fat diet and the mice developed high degree of hepatic steatosis with swelling of hepatocytes and severe cytoplasmic vacuoles, while the supplementation of WPJ significantly alleviated lipid accumulation in livers and greatly improved liver steatosis (Fig 2A and 2B). The liver steatosis grades were significantly lower in the HFDJ group than that in the HFD group (Fig 2F). Consistent with these results, WPJ supplementation also significantly decreased high-fat diet-induced elevation in the hepatic TG and TC levels (Fig 2G and 2H).
H&E staining (A) and oil red O staining (B) of liver tissues. H&E staining of epididymal white adipose (C), perirenal white adipose (D) and interscapular brown adipose (E). (F) Hepatic steatosis grade. (G) Hepatic triglycerides levels. (H) Hepatic cholesterol levels. eWAT, epididymal white adipose; pWAT, perirenal white adipose; iBAT, interscapular brown adipose; LFD, mice fed low-fat diet; LFDJ, mice fed low-fat diet with supplementation of WPJ; HFD, mice fed high-fat diet; HFDJ, mice fed high-fat diet with supplementation of WPJ. n = 6 (F), n = 10 (G and H). Values are presented as means ± SEM. Data not sharing a common superscript differ significantly among groups (p<0.05, ANOVA).
Histological analysis also showed that WPJ reduced the cell size of white adipocyte tissue (WAT) (Fig 2C, 2D and 2I) and brown adipocyte tissue (BAT) (Fig 2E). No significant abnormalities were observed in the LFD and LFDJ group.
WPJ improves diet-induced insulin resistance
High-fat diet induced an increase in the fasting serum levels of glucose and insulin, accompanied by an increase of HOMA-IR and decrease of HOMA-IS index, while the mice in HFDJ group revealed a significant decrease in the fasting serum glucose and insulin levels and HOMA-IR index but a distinct increase of HOMA-IS index compared to mice in HFD group (Fig 3), suggesting that WPJ significantly improved high-fat diet-induced hyperglycemia and insulin resistance in mice. No significant differences were observed between the LFD and LFDJ group.
(A) The fasting serum levels of glucose. (B) The fasting serum levels of insulin. (C) HOMA-IR index. (D) HOMA-IS index. LFD, mice fed low-fat diet; LFDJ, mice fed low-fat diet with supplementation of WPJ; HFD, mice fed high-fat diet; HFDJ, mice fed high-fat diet with supplementation of WPJ. n = 10 (A), n = 10 (B, C and D). Values are presented as means ± SEM. Data not sharing a common superscript differ significantly among groups (p<0.05, ANOVA).
WPJ alters the hepatic gene expression profiles
For genes involved in fatty acid metabolism, WPJ supplementation significantly increased the expression levels of Cpt1b (Carnitine palmitoyltransferase 1b) and HL (Hepatic lipase) (Fig 4A). Similarly, the expression levels of genes involved in cholesterol biosynthesis, including insulin-induced gene 1, 2 (Insig1 and Insig2) were reduced by high-fat diet feeding but significantly increased by WPJ treatment (Fig 4B). In addition, WPJ treatment suppressed the expression of HMGCoR (Hydroxy-3-Methylglutaryl-Coenzyme A Reductase) and Srebp-1(Sterol regulatory element-binding transcription factor 1), but no significant changes in the expression of Pparα (Peroxisome proliferator-activated receptor alpha), Pparγ (Peroxisome proliferator-activated receptor gamma) and LDFR (The Low-Density Lipoprotein Receptor) were observed (S1 Fig). Moreover, high-fat diet feeding increased the expression level of FGF21 and it suppressed the expression of its receptors, Klb (β-Klotho) and FGFR2 (fibroblast growth factor receptor 2) as well as its target genes, including Egr1 and cFos. However, WPJ treatment decreased the expression level of fibroblast growth factor 21 (FGF21), but it significantly increased the expression levels of Klb, FGFR2, Egr1 and cFos (Fig 4C).
(A) The relative expression levels of genes involved in lipid metabolism and in cholesterol biosynthesis in livers. (B) The relative expression levels of fibroblast growth factor 21-related genes in livers. Cpt1b, carnitine palmitoyltransferase 1b; HL, hepatic lipase; Insig1, insulin-induced gene 1; Insig2, insulin-induced gene 2; FGF21, fibroblast growth factor 21; Klb, β-klotho; FGFR2, fibroblast growth factor receptor 2; LFD, mice fed low-fat diet; LFDJ, mice fed low-fat diet with supplementation of WPJ; HFD, mice fed high-fat diet; HFDJ, mice fed high-fat diet with supplementation of WPJ. Values are presented as means ±SEM. Data not sharing a common superscript differ significantly among groups (p<0.05, ANOVA).
Discussion
Increasing evidence indicates that the consumption of vegetables and fruits is inversely related to many metabolic disorders, thus decreasing the risk of type II diabetes, NAFLD and obesity, and the beneficial health effects of these plant foods are due to their high content of polyphenols, flavonoids, vitamins, dietary fibers and minerals [23–26]. Pitaya, which are mainly cultivated in East and Southeast Asia, Central and South America and northern Australia, is reported to be a natural source of bioactive nutrients, but few studies focused on its beneficial effects on metabolic syndromes. The present study was conducted to investigate the effects of WPJ on type-2 diabetes and NAFLD in high-fat diet-induced obese mice. Our results clearly demonstrated that WPJ supplementation significantly attenuated diet-induced hepatic steatosis as revealed by reduced hepatic lipid accumulation, and the beneficial effect was accompanied by the improved insulin resistance and insulin sensitivity, as revealed by lower fasting serum glucose and insulin levels and a lower HOMA-IR index but higher HOMA-IS index. Moreover, WPJ administration did not affect the body weight gain and the calorie intake of mice, but it decreased the relative weight of epididymal white adipose and attenuated high-fat diet-induced adipose hypertrophy, as revealed by the downsized white and brown adipocyte.
Human and animal studies have proved the lipid-improving and antidiabetic effect of red pitaya [15–17]. Considering the difference of constituents in white and red pitaya, especially the absence of betacyanins in white pitaya, the beneficial effect of white pitaya needs to be clarified. And consistent with the studies focused on red pitaya, our results indicated that WPJ supplementation significantly decreased the serum levels of TG, TC and LDL-C in high-fat diet fed mice, suggesting the lipid -reducing effect of WPJ. In addition, we observed that WPJ supplementation did not induce a weight loss in high-fat diet-fed mice, which was consistent with the previous results, and we postulated that this condition might be due to the high content of sugar and fat in WPJ that counteracted the weight-loss effect. Despite of no influence on body weight gain, WPJ administration significantly reduced the size of white and brown adipocytes, as revealed by histological analysis of adipose, suggesting that WPJ could attenuate high-fat diet-induced adipose tissue hypertrophy, which has not been reported previously. In addition, there was no difference in the daily calorie intake among all the dietary groups. Consistent with these results, the serum levels of NPY, which could regulate food intake and storage of energy [27], were not affected by HFD feeding or WPJ intervention, suggesting that WPJ exerted its beneficial effects on lipid metabolism without affecting the energy intake of mice.
Leptin plays an important role in regulating energy homeostasis and lipid metabolism, and most of obese animals exhibit a leptin-resistant status [28]. Consistently, the leptin level of HFD-fed mice has been elevated and WPJ treatment induced a clear decrease, although not significant, in the serum level of leptin, implying that WPJ administration might improve HFD-induced leptin-resistance, directly or indirectly. Furthermore, we also identified elevated serum levels of adiponectin in the WPJ-treated HFD mice. Adiponectin has been proved to regulate the metabolism of lipids and glucose [29]. These findings implied that the beneficial effects of WPJ on these metabolic syndromes might be associated with the improved lipid metabolism.
Hepatic lipid accumulation is a biomarker of liver steatosis, which in combination with oxidative stress and inflammation can lead to NAFLD [30]. Few studies have been conducted to assess the effect of pitayas intake on the obesity-related NAFLD. In this study, H&E staining of livers revealed that WPJ supplementation reduced the hepatic lipid accumulation, alleviated the swelling of hepatocytes and prevented the formation of liver steatosis in high-fat diet-fed mice. Consistently, WPJ administration also decreased the hepatic TG and TC levels as well as the serum ALT and AST levels. To the best of our knowledge, this was the first study reported that pitaya possessed anti-hepatosetatosis effect.
Hepatic gene expression analysis indicated that WPJ treatment changed the expression profile of the genes (Cpt1b, LPL and Srepb1) involved in fatty acid metabolism and the genes (Insig1, Insig2 and HMGCoR) involved in cholesterol biosynthesis. These genes have been fully elucidated to play crucial roles in the modulation of cholesterol biosynthesis, fatty acid biosynthesis or beta-oxidation [31–35]. Lipopolysaccharides (LPS), also known as lipoglycans and endotoxins. High-fat diet has been proved to induce elevated levels of serum LPS, a condition referred to as endotoxemia. The elevated levels of serum LPS triggers several inflammatory markers which are a precursor to the progression towards metabolic syndrome, resulting in significant inflammation, body weight gain, insulin resistance, and ultimately type-2 diabetes [36, 37]. Accordingly, the bioactivity of white pitaya juice to blunt circulating LPS levels may be accounted for the reduced lipid accumulation in livers and the protection from NAFLD and insulin resistance in high-fat diet-fed mice. Regarding these considerations, we decided to examine the serum levels of LPS. Consistent with the previous studies, 14 weeks of HFD feeding induced a significant increase in circulating LPS level, which was fully prevented by WPJ supplementation. This finding was associated with the reduced serum and hepatic TG levels by WPJ treatment.
Obesity and hepatic steatosis are usually accompanied by insulin resistance, therefore increasing the risk of type II diabetes [7, 38], and insulin resistance in obese diabetic II subjects is worse than that in non-obese diabetic subjects [39]. The blood glucose-controlling and hyperinsulinemia-improving effects of red pitaya have been reported respectively in diabetic patients and rats [15, 17]. However, Ramli et al. recently reported that red pitaya juice exert no influence on blood glucose levels in high-carbohydrate and high-fat diet-fed rats [18]. So the anti-diabetic effect of red pitaya seems controversial. In this study, we found that WPJ administration not only significantly decreased the serum levels of glucose and insulin but also decreased the HOMA-IR index, suggesting that WPJ improved high-fat diet-induced insulin resistance in mice. Moreover, the increased HOMA-IS index in WPJ-treated mice also implied the insulin-sensitizing effect of WPJ. These results indicated a strong anti-diabetic activity of white pitaya.
FGF21, as a novel member of the FGFs family, is mainly expressed in liver [40]. A growing body of literatures show that exogenous FGF21 administration improve glucose and lipid homeostasis, insulin sensitivity and hepatic steatosis [41, 42]. However, mounting studies also support that plasma FGF21 levels are markedly increased in obesity, insulin-resistant, hypertriglyceridemia, hepatosteatosis and liver injury states [43, 44], suggesting that FGF21 did not exert its beneficial effects on lipid and glucose homeostasis. The failure of endogenous FGF21 to improve these metabolic syndromes implied a FGF21-resistant state due to impaired FGF21 action. Consistent with the previous findings, our results showed that high-fat diet feeding induced an increase of serum level of FGF21, which implied that obese state could result in a compensatory overproduction of FGF21. Numerous studies have proven that FGF21 activity depends on binding to its cofactor, β-Klotho, (Klb) and its receptors (FGFRs) [45]. Our results showed that high-fat diet feeding increased the hepatic expression level of FGF21, but it significantly suppressed the expression of FGFR2 and Klb. High-fat diet also significantly resulted in the impaired induction of Egr1 and cFos which are the target genes of FGF21. Though WPJ treatment decreased the expression FGF21, it significantly increased the expression levels of Klb, FGFR2, Egr1 and cFos. These data suggested that WPJ could improve the expression profile of FGF21 receptor and cofactor, thus attenuating FGF21 resistance. So one potential action site for WPJ to exert its anti-diabetic and anti-hepatosteatosis effect might be restoring the function of FGF21.
In summary, our results demonstrated that WPJ administration improved diet-induced insulin resistance and hepatic steatosis in mice. The beneficial effects of WPJ on these metabolic syndromes were associated with the improved FGF21 resistance and lipid metabolism. These findings suggest a dietary choice in the management of type II diabetes and NAFLD.
Supporting Information
S1 Fig. The influence of white pitaya juice (WPJ) on the expression profiles of Pparα, Pparγ, LDLR, HMGCoR and Srebp-1.
HMGCoR, hydroxy-3-Methylglutaryl-Coenzyme A Reductase); Srebp-1, sterol regulatory element-binding transcription factor 1; Pparα, peroxisome proliferator-activated receptor alpha; Pparγ, peroxisome proliferator-activated receptor gamma; LDFR, low-Density Lipoprotein Receptor; LFD, mice fed low-fat diet; LFDJ, mice fed low-fat diet with supplementation of WPJ; HFD, mice fed high-fat diet; HFDJ, mice fed high-fat diet with supplementation of WPJ. Values are presented as means ±SEM. Data not sharing a common superscript differ significantly among groups (p<0.05, ANOVA).
https://doi.org/10.1371/journal.pone.0149670.s001
(TIF)
S2 Table. Primers used for real-time quantitative PCR.
https://doi.org/10.1371/journal.pone.0149670.s005
(DOCX)
Author Contributions
Conceived and designed the experiments: HZS XDZ. Performed the experiments: HZS ZHZ. Analyzed the data: JNW. Contributed reagents/materials/analysis tools: JL QC. Wrote the paper: HZS XDZ.
References
- 1. Balkau B, Eschwege E. The metabolic syndrome. Lancet. 2005;366(9501):1921–. pmid:WOS:000233777900013.
- 2. Beaton MD. Current treatment options for nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Can J Gastroenterol. 2012;26(6):353–7. pmid:WOS:000306217200009.
- 3. Doria A, Patti ME, Kahn CR. The emerging genetic architecture of type 2 diabetes. Cell Metab. 2008;8(3):186–200. pmid:WOS:000258939500007.
- 4. Walley AJ, Asher JE, Froguel P. The genetic contribution to non-syndromic human obesity. Nat Rev Genet. 2009;10(7):431–42. pmid:WOS:000267142100011.
- 5. Leclercq IA, Morais ADS, Schroyen B, Van Hul N, Geerts A. Insulin resistance in hepatocytes and sinusoidal liver cells: Mechanisms and consequences. J Hepatol. 2007;47(1):142–56. pmid:WOS:000247706700021.
- 6. Hossain P, Kawar B, Nahas ME. Obesity and diabetes in the developing world—A growing challenge. New Engl J Med. 2007;356(3):213–5. pmid:WOS:000243488100003.
- 7. Bugianesi E, Gastaldelli A, Vanni E, Gambino R, Cassader M, Baldi S, et al. Insulin resistance in non-diabetic patients with non-alcoholic fatty liver disease: sites and mechanisms. Diabetologia. 2005;48(4):634–42. pmid:WOS:000228515900007.
- 8. Dembinska-Kiec A, Mykkanen O, Kiec-Wilk B, Mykkanen H. Antioxidant phytochemicals against type 2 diabetes. Brit J Nutr. 2008;99:Es109–Es17. pmid:WOS:000208467500006.
- 9. Liu RH. Health benefits of fruit and vegetables are from additive and synergistic combinations of phytochemicals. Am J Clin Nutr. 2003;78(3):517s–20s. pmid:WOS:000184985500005.
- 10. Espin JC, Garcia-Conesa MT, Tomas-Barberan FA. Nutraceuticals: facts and fiction. Phytochemistry. 2007;68(22–24):2986–3008. pmid:17976666.
- 11. Suh DH, Lee S, Heo DY, Kim YS, Cho SK, Lee S, et al. Metabolite Profiling of Red and White Pitayas (Hylocereus polyrhizus and Hylocereus undatus) for Comparing Betalain Biosynthesis and Antioxidant Activity. J Agr Food Chem. 2014;62(34):8764–71. pmid:WOS:000340992100029.
- 12. Esquivel P, Stintzing FC, Carle R. Phenolic compound profiles and their corresponding antioxidant capacity of purple pitaya (Hylocereus sp.) genotypes. Z Naturforsch C. 2007;62(9–10):636–44. pmid:WOS:000251331700003.
- 13.
Ruzlan N, Kamarudin KR, Idid SO, Idid SZ, Mohamed Rehan A, Koya MS. Antioxidant study of pulp and peel of dragon fruits: A comparative study. 2008.
- 14. Wybraniec S, Mizrahi Y. Fruit flesh betacyanin pigments in Hylocereus cacti. J Agr Food Chem. 2002;50(21):6086–9. pmid:WOS:000178501300048.
- 15. Abd Hadi N, Mohamad M, Rohin MAK, Mohd Yusof R. EFFECTS OF RED PITAYA FRUIT (HYLOCEREUS POLYRHIZUS) CONSUMPTION ON BLOOD GLUCOSE LEVEL AND LIPID PROFILE IN TYPE 2 DIABETIC SUBJECTS. Borneo Science Journal. 2012;31(2):113–29.
- 16. Yusof RM, Akhiruddin MA. Hypocholesterolemic Effect of Fermented Red Pitaya (Hylocereus Polyrhizus) Juice in Diet-Induced Hypercholesterolemic Rats. Ann Nutr Metab. 2009;55:92–. pmid:WOS:000270827200344.
- 17. Omidizadeh A, Yusof RM, Roohinejad S, Ismail A, Abu Bakar MZ, Bekhit AEA. Anti-diabetic activity of red pitaya (Hylocereus polyrhizus) fruit. Rsc Adv. 2014;4(108):62978–86. pmid:WOS:000345701500023.
- 18. Ramli NS, Brown L, Ismail P, Rahmat A. Effects of red pitaya juice supplementation on cardiovascular and hepatic changes in high-carbohydrate, high-fat diet-induced metabolic syndrome rats. Bmc Complem Altern M. 2014;14. Artn 189 10.1186/1472-6882-14-189. pmid:WOS:000338162800001.
- 19. Singleton VL, Orthofer R, Lamuela-Raventos RM. Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin-Ciocalteu reagent. Methods Enzymol. 1999;299:152–78. pmid:WOS:000079431900014.
- 20. Meda A, Lamien CE, Romito M, Millogo J, Nacoulma OG. Determination of the total phenolic, flavonoid and proline contents in Burkina Fasan honey, as well as their radical scavenging activity. Food Chem. 2005;91(3):571–7. pmid:WOS:000226920500024.
- 21. Folch J, Lees M, Sloane Stanley GH. A simple method for the isolation and purification of total lipides from animal tissues. The Journal of biological chemistry. 1957;226(1):497–509. pmid:13428781.
- 22. Kleiner DE, Brunt EM, Van Natta M, Behling C, Contos MJ, Cummings OW, et al. Design and validation of a histological scoring system for nonalcoholic fatty liver disease. Hepatology. 2005;41(6):1313–21. pmid:15915461.
- 23. Seymour EM, Singer AAM, Kirakosyan A, Urcuyo-Llanes DE, Kaufman PB, Bolling SF. Altered hyperlipidemia, hepatic steatosis, and hepatic peroxisome proliferator-activated receptors in rats with intake of tart cherry. J Med Food. 2008;11(2):252–9. pmid:WOS:000257633800008.
- 24. He JA, Giusti MM. Anthocyanins: Natural Colorants with Health-Promoting Properties. Annu Rev Food Sci T. 2010;1:163–87. pmid:WOS:000278069300008.
- 25. Munir KM, Chandrasekaran S, Gao F, Quon MJ. Mechanisms for food polyphenols to ameliorate insulin resistance and endothelial dysfunction: therapeutic implications for diabetes and its cardiovascular complications. Am J Physiol-Endoc M. 2013;305(6):E679–E86. pmid:WOS:000324751900001.
- 26. Timmers S, Hesselink MKC, Schrauwen P. Therapeutic potential of resveratrol in obesity and type 2 diabetes: new avenues for health benefits? Ann Ny Acad Sci. 2013;1290:83–9. pmid:WOS:000326091100010.
- 27. Brennan AM, Mantzoros CS. Drug Insight: the role of leptin in human physiology and pathophysiology—emerging clinical applications. Nature clinical practice Endocrinology & metabolism. 2006;2(6):318–27. pmid:16932309.
- 28. Haslam DW, James WP. Obesity. Lancet. 2005;366(9492):1197–209. pmid:16198769.
- 29. Diez JJ, Iglesias P. The role of the novel adipocyte-derived hormone adiponectin in human disease. European journal of endocrinology/European Federation of Endocrine Societies. 2003;148(3):293–300. pmid:12611609.
- 30. Charlton M. Nonalcoholic Fatty Liver Disease: A Review of Current Understanding and Future Impact. Clin Gastroenterol H. 2004;2(12):1048–58. pmid:WOS:000208072400003.
- 31. Baumann CA, Ribon V, Kanzaki M, Thurmond DC, Mora S, Shigematsu S, et al. CAP defines a second signalling pathway required for insulin-stimulated glucose transport. Nature. 2000;407(6801):202–7. pmid:WOS:000089241000052.
- 32. Auinger A, Rubin D, Sabandal M, Helwig U, Ruther A, Schreiber S, et al. A common haplotype of carnitine palmitoyltransferase 1b is associated with the metabolic syndrome. Brit J Nutr. 2013;109(5):810–5. pmid:WOS:000315456700005.
- 33. Yang T, Espenshade PJ, Wright ME, Yabe D, Gong Y, Aebersold R, et al. Crucial step in cholesterol homeostasis: Sterols promote binding of SCAP to INSIG-1, a membrane protein that facilitates retention of SREBPs in ER. Cell. 2002;110(4):489–500. pmid:WOS:000177653200010.
- 34. Mead JR, Irvine SA, Ramji DP. Lipoprotein lipase: structure, function, regulation, and role in disease. J Mol Med-Jmm. 2002;80(12):753–69. pmid:WOS:000180587300004.
- 35. Chang J-J, Hsu M-J, Huang H-P, Chung D-J, Chang Y-C, Wang C-J. Mulberry anthocyanins inhibit oleic acid induced lipid accumulation by reduction of lipogenesis and promotion of hepatic lipid clearance. J Agr Food Chem. 2013;61(25):6069–76.
- 36. Cani PD, Neyrinck AM, Fava F, Knauf C, Burcelin RG, Tuohy KM, et al. Selective increases of bifidobacteria in gut microflora improve high-fat-diet-induced diabetes in mice through a mechanism associated with endotoxaemia. Diabetologia. 2007;50(11):2374–83. pmid:17823788.
- 37. Cani PD, Amar J, Iglesias MA, Poggi M, Knauf C, Bastelica D, et al. Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes. 2007;56(7):1761–72. pmid:17456850.
- 38. Kruszynska YT, Olefsky JM. Cellular and molecular mechanisms of non-insulin dependent diabetes mellitus. J Invest Med. 1996;44(8):413–28. pmid:WOS:A1996VR07100003.
- 39. Defronzo RA, Ferrannini E. Insulin Resistance—a Multifaceted Syndrome Responsible for Niddm, Obesity, Hypertension, Dyslipidemia, and Atherosclerotic Cardiovascular-Disease. Diabetes Care. 1991;14(3):173–94. pmid:WOS:A1991EZ64800001.
- 40. Nishimura T, Nakatake Y, Konishi M, Itoh N. Identification of a novel FGF, FGF-21, preferentially expressed in the liver. Bba-Gene Struct Expr. 2000;1492(1):203–6. pmid:WOS:000087924000024.
- 41. Kharitonenkov A, Shiyanova TL, Koester A, Ford AM, Micanovic R, Galbreath EJ, et al. FGF-21 as a novel metabolic regulator. J Clin Invest. 2005;115(6):1627–35. pmid:WOS:000229592300037.
- 42. Xu J, Lloyd DJ, Hale C, Stanislaus S, Chen M, Sivits G, et al. Fibroblast Growth Factor 21 Reverses Hepatic Steatosis, Increases Energy Expenditure, and Improves Insulin Sensitivity in Diet-Induced Obese Mice. Diabetes. 2009;58(1):250–9. pmid:WOS:000262187100037.
- 43. Chavez AO, Molina-Carrion M, Abdul-Ghani MA, Folli F, DeFronzo RA, Tripathy D. Circulating Fibroblast Growth Factor-21 Is Elevated in Impaired Glucose Tolerance and Type 2 Diabetes and Correlates With Muscle and Hepatic Insulin Resistance. Diabetes Care. 2009;32(8):1542–6. pmid:WOS:000268687800037.
- 44. Zhang X, Yeung DCY, Karpisek M, Stejskal D, Zhou ZG, Liu F, et al. Serum FGF21 levels are increased in obesity and are independently associated with the metabolic syndrome in humans. Diabetes. 2008;57(5):1246–53. pmid:WOS:000255628700014.
- 45. Cuevas-Ramos D, Aguilar-Salinas CA, Gomez-Perez FJ. Metabolic actions of fibroblast growth factor 21. Curr Opin Pediatr. 2012;24(4):523–9. pmid:WOS:000306372200015.