Effects of long-term consumption of high fructose corn syrup containing peach nectar on body weight gain in sprague dawley rats

Abstract

High fructose corn syrup (HFCS) is one of the most used sweeteners in the food industry. Health concerns regarding the consumption of HFCS-containing foods have developed in parallel with the increasing amount of people who become overweight. This study was conducted to investigate whether HFCS-containing peach nectar (pn-HFCS) consumption has more detrimental effects on anthropometrical and biochemical parameters compared with sucrose-containing peach nectar (pn-sucrose). Fifty-day-old Sprague Dawley rats were divided into three groups and were fed (A) pn-HFCS + ad libitum chow, (B) pn-sucrose + ad libitum chow and (C) only ad libitum chow for 7 months. The percentage change in body weight (PCBW), body mass index (BMI), and Lee index were calculated, and serum triglyceride, glucose, insulin and leptin concentrations were measured. The PCBW, BMI, Lee index, serum triglyceride, glucose, insulin and leptin concentrations were insignificant among the three groups. We can suggest that peach nectar consumption resulted in more energy intake than the control and since pn-HFCS group consumed more chow than the pn-sucrose group. The results show that long term daily HFCS or sucrose consumption in peach nectar is not associated with weight gain and does not stimulate metabolic changes in Sprague Dawley rats.

Keywords:
HFCS; weight gain; insulin; leptin; BMI; peach nectar

1 Introduction

High fructose corn syrup (HFCS) is a corn-based sweetener that is used in various food and beverages. Compared with other sugars, the lower price and easier handling of HFCS has made it the first choice for food and beverage companies which produce beverages, baked goods, canned products, jams and jellies, confectioneries and dairy products (Hanover & White, 1993; Park & Yetley, 1993). HFCS is also extremely resistant to microbial spoilage and requires less storage space compared to an equivalent amount of solid sweeteners (Hanover & White, 1993).

A sufficient consumption of fruit and vegetable is recommended for human diet (Slavin & Lloyd, 2012). USDA’s Food Guide Pyramid (United States Department of Agriculture, 2005) recommends 2-4 servings of fruit and 3-5 servings of vegetables daily. Optimizing the use of fruits and vegetables in different product formats, such as processed juice, provides more options to the consumers. Consumption of fruit juice, which is cheap and easy to access throughout the year, helps to fulfill the recommended amount of fruits and vegetables. Fruit juices, as well as fruits, contain many essential nutrients, such as vitamins, minerals, carotenoids, flavonoids and dietary fiber, which are important and integral part of a healthy diet and are highly recommended for their nutritional content, their phytochemical value and the presence of health-promoting compounds (Khandpur & Gogate, 2015).

Obesity is a health problem worldwide, including in Turkey. According to a National Statistical Institute Health Survey (National Statistical Institute, 2012), more than one third of Turkish adults (34.8%) were defined as overweight, and 17.2% were considered to be obese. Many studies have reported an incremental increase in energy intake over the past several decades, which is believed to be one of the most important underlying reasons of obesity (Nielsen & Popkin, 2004; Harnack et al., 2000; Gibson & Shirreffs, 2013). High consumption of sugar-sweetened beverages is considered to contribute to increased weight gain, increased energy intake and development of diabetes mellitus (Hernández-Cordero et al., 2015). Some authors have noted that excess sugar intake from soft drinks is the main problem (Melanson et al., 2008), and furthermore some others have reported a connection between HFCS intake and obesity (Bray et al., 2004; Elliott et al., 2002). It was suggested that diet containing high-fructose cause hypertriglyceridemia, hyperinsulinemia, insulin resistance, impair glucose tolerance and increased body weight (BW) (Stanhope et al., 2015; Voznesenskaya & Tordoff, 2015; Johnson et al., 2007). There is a hypothesis that fructose consumption could promote weight gain because it does not stimulate insulin secretion or leptin production which may result in disturbances of satiety (Havel, 2005; Bocarsly et al., 2010).

According to the Dietary Guidelines for Americans, the calorie allowance from added sugars and sweeteners should not exceed 10% of the total caloric intake; however, American’s actual consumption was around 11 to 17% at different ages (United States Department of Agriculture, 2015) and sweetened soft drinks constitute 7% of the total energy intake (Gibson & Shirreffs, 2013; Kit et al., 2013). Several short-term in vivo studies (Light et al., 2009; Bocarsly et al., 2010, Babacanoğlu et al., 2013) investigated the effect of HFCS solution consumption (8-20%) on obesity related parameters, and those yielded conflicting results. Since HFCS is common in several food products other than beverages, people are faced with chronic fructose consumption; so further studies are needed to inquire about any long-term consequences of HFCS intake on health. Accordingly, this study was conducted to examine long-term (7 months) peach nectar containing HFCS (pn-HFCS) and peach nectar containing sucrose (pn-sucrose) consumption on weight gain and related anthropometrical and biochemical parameters in Sprague-Dawley rats.

2 Materials and methods

2.1 Materials

For this study, fifty-day-old male Sprague–Dawley rats were provided from the Experimental Animals Breeding and Research Center, Uludag University, Medical Faculty, Bursa, Turkey. Rats were housed individually in conventional cages in a temperature- and humidity-controlled room (21 ± 2 °C, 50 ± 5%) under a 12-h light/dark cycle with free access to chow, peach nectar and water. The animals were cared for in accordance with the “Guide to the Care and Use of Experimental Animals” and all procedures were approved by the Local Ethics Committee for Animal Experiments, Uludag University (2011-05/11).

2.2 Experimental model

Male rats (55-150 g, n = 41 / group) were fed either (A) peach nectar containing HFCS (pn-HFCS) and chow, (B) peach nectar containing sucrose (pn-sucrose) and chow or (C) chow only for 7 months. Rats were sampled to groups systematically. The peach nectar and chow were provided to the rats ad libitum for 24 hours. Peach nectar consumption was measured daily, and chow consumption was measured weekly at the same time period (09:00 to 10:00 a.m.). In this study, HFCS-55 was chosen because of its common and suitable usage in the food industry. HFCS-55 was obtained from a private ingredient provider company and its specifications were 76.5-77.5% dry solids, 3.5-4.5 pH and 55% min. fructose. According to Turkish Juice Industry Association (Meyve Suyu Endüstrisi Derneği, 2011) peach nectar is the most preferred fruit nectar in Turkey. According to consumer’s choice, peach nectar was preferred as a material and formulations were determined based on preliminary tests in this study. The peach nectar was produced in a commercial fruit juice company in Bursa. Peach nectars, which aseptically filled 1L water-soluble dry matter (Association of Analytical Communities, 1980), fat (International Organization for Standardization, 2009), carbohydrate (Food and Agriculture Organization of the United Nations, 1998) and protein (Association of Analytical Communities, 2000b) contents, titratable acidity (Association of Analytical Communities, 2000a), ascorbic acid level (Association of Analytical Communities, 1991), fructose content (Association of Analytical Communities, 1979), total phenolic matter (Zhang & Hamauzu, 2004) and antioxidant activity (2,2-diphenyl-1-picrylhydrazyl - DPPH) (Zhang & Hamauzu, 2004) were analyzed and energy (Food and Agriculture Organization of the United Nations, 2003) values of nectars were calculated. Standard rodent chow (2800 kcal/kg) and tap water were provided to all groups. Body weight (BW) changes were also measured weekly.

2.3 Anthropometrical and biochemical parameters

The abdominal circumference (AC) (anterior to the hindfoot), thoracic circumference (under the foreleg), and body length (BL) (nose-to-anus) were measured in all rats at the end of 7 months. All measurements and surgical procedures were performed under 2.5-3.5% sevoflurane (Abbott Lab., IL, USA) inhaled anesthesia.

The BW and BL were used to determine the body mass index (BMI) and Lee index, which are anthropometrical parameters for the evaluation of obesity. The parameters were calculated as follows:

Body mass index (BMI) = body weight (g) / length² (cm²); and

Lee index = cube root of body weight (g) / nose-to-anus length (cm) (Bernardis, 1970).

Blood samples were collected by cardiocentesis into serum tubes. The samples were centrifuged at 4000 rpm for 5 min. Serum samples were frozen and stored at −80 °C until analyses were performed.

Serum glucose and triglyceride concentrations were measured (n = 10) using an autoanalyzer (Aeroset System Abbott, Abbott Laboratories, Diagnostic Division, IL, USA). Serum insulin and leptin concentrations were measured (n = 10) with a commercially available ELISA kit (Merck Millipore Corporation, Billerica, MA, USA), following the manufacturer’s protocol. Systematic sampling was used to identify 10 rats in each group to assess the biochemical parameters.

Unilateral body fat pads were collected from the hepatic, abdominal and gonadal regions after cardiocentesis and weighed individually.

2.4 Statistical analysis

The Shapiro-Wilk test was used to assess the normality of the variables. The Kruskal-Wallis test was used for comparing more than two groups for the continuous variables. The Mann-Whitney U-test was used for comparing two groups after the Kruskal Wallis test was performed, in cases in which significances was determined. The Mann-Whitney U-test was used for comparing the continuous variables not meeting normality assumption. Continuous variables were presented as the median (of the minimum and maximum values). Correlations between the variables were examined with Pearson, Spearman and partial correlation coefficients. The significance level was set to α = 0.05. Statistical analyses were performed with IBM SPSS Statistics version 21.0 (IBM Corp., NY, USA).

3 Results and discussion

3.1 Composition of peach nectar, consumption of peach nectar and chow and PCBW

The results of physicochemical analyses of the peach nectars were presented as the mean value ± standard deviation in Table 1. Since the fructose content of the pn-HFCS (4.58 ± 0.06%) was higher than the pn-sucrose (3.94 ± 0.03%), fructose intake of the pn-HFCS group was higher (p < 0.05) than the pn-sucrose group (Figure 1) during the study.

Table 1
Results of the physicochemical analysis of the peach nectar.

Analysis	pn-HFCS	pn-sucrose
Water soluble dry matter (g/100 g)	11.0 ± 0.05	13.0 ± 0.00
Energy (Kcal/100 mL)	38 ± 0.00	53 ± 0.00
Fat (%)	0 ± 0.00	0 ± 0.00
Carbohydrate (%)	8.10 ± 0.00	11.9 ± 0.00
Protein (%)	1.34 ± 0.04	1.33 ± 0.04
Fructose (%)	4.58 ± 0.06	3.94 ± 0.03
Titratable acidity* (g/100 mL)	0.29 ± 0.01	0.30 ± 0.00
Ascorbic acid (mg/100 mL)	11.87 ± 4.88	12.07 ± 4.10
Total phenolic matter (mg GAE**/100 mL)	280.48 ± 23.54	315.61 ± 8.80
Antioxidant activity (μmol trolox/mL sample)	9.02 ± 0.35	8.65 ± 0.51

• Values were presented as median ± standard deviation.
• ^*
  citric acid;
• ^**
  gallic acid equivalent.

Figure 1
HFCS amount in peach nectars over the 7 months (p < 0.05). Values were presented as median.

There were significant differences in total chow consumption (Figure 2) and total caloric (chow + peach nectar) intake (Table 2) among the study groups. When the groups were compared pairwise in terms of total caloric intake (chow + peach nectar), significant differences were observed between the control and pn-HFCS groups and the control and pn-sucrose groups (Table 2). Light et al. (2009) investigated the effects of drinking different caloric beverages sweetened with 13% (w/v) glucose, sucrose, fructose, and HFCS-55 on the development of adiposity and metabolic disorders in female rats over a period of 8 weeks. Similar with our results, Light et al. (2009) found significant difference in total energy intake in control group versus study groups, but there were no significant differences in total energy intake among the sucrose, HFCS-55 and fructose consuming study groups during 8 weeks.

Figure 2
Cumulative chow consumption over the 7 months (p < 0.05). Values were presented as median.

Table 2
Total calories with pairwise comparison of three groups.

	Control	pn-HFCS	pn-sucrose	p- value
Total calorie of chow and peach nectar*	15617 (13362-18924)	17081 (14102-19977)	17440 (14254-20081)	<0.001
Percentage of chow calorie in total calorie	100	82.58 (78-85)	75.78 (71-80)	<0.001
Pairwise comparison of chow consumption
	Control-HFCS	Control-sucrose	HFCS-sucrose
1st month	<0.001	<0.001	0.058
2nd month	<0.001	<0.001	0.013
3rd month	<0.001	<0.001	0.012
4th month	<0.001	<0.001	0.021
5th month	<0.001	<0.001	0.020
6th month	<0.001	<0.001	0.026
7th month	<0.001	<0.001	0.033
Total calorie of chow and peach nectar*	0.002	<0.001	0.183

• ^*
  Total calorie intake at the end of 7 months.

The control group, which was fed with chow, showed the largest amount of chow consumption, followed by the pn-HFCS group and the pn-sucrose group (Figure 2). Similar to our results, Light et al. (2009) reported that rats in the control group obtained the most calories from solid food compared with HFCS and sucrose groups. According to these data, we can assume that rats consuming caloric sweetener reduce caloric intake from solid food.

There was no overall difference in peach nectar consumption between the rats fed pn-HFCS and pn-sucrose (Figure 3). Related to higher energy content of pn-sucrose (Table 1), rats fed pn-sucrose obtained higher energy than did the pn-HFCS group from peach nectar. In line with our results, Light et al. (2009) found that rats consuming sucrose (13% w/v) obtained more calories compared with those that consumed HFCS-55 or fructose solutions.

Figure 3
Cumulative peach nectar consumption over 7 months (p > 0.05). Values were presented as median.

In the present study, there were significant differences among the groups in pairwise comparison of total chow consumption for all measurements performed throughout the 7 months, except for the first month data of the pn-HFCS and pn-sucrose groups (Table 2). Pn-HFCS and pn-sucrose groups obtained most of their energy (82.58% and 75.78%, respectively) from chow, but as mentioned above, they consumed significantly less chow than the control group. Taking total energy intake into consideration, we can assume that peach nectar consumption resulted in more energy intake than the control group. This increment in energy intake might be related to the palatable sweet taste of peach nectar or its effects on metabolism or satiety. However, it is not clear why pn-HFCS group consumed more chow than the pn-sucrose group; it is possible that fructose consumption had more stimulating effect on appetite compared with the sucrose.

Although the peach nectar-consuming groups of the present study obtained higher energy than did the control group, there were no significant differences in the PCBW among the groups during and at the end of 7 months (Figure 4). Babacanoğlu et al. (2013) investigated the effects of 10% HFCS and 20% HFCS-containing solution consumption in rats over a period of 12 weeks and in another study Lowndes et al. (2014) compared the consumption of sucrose or HFCS-sweetened (10% and 20%) low-fat milk at the recommended daily caloric intake for 10 weeks. Similar to our results, both of those authors reported that the consumption of solutions or milk had no effect on the PCBW among the groups compared to control. In another study, Light et al. (2009) investigated the effects of drinking different caloric beverages sweetened with 13% (w/v) glucose, sucrose, fructose, and HFCS-55 on the development of adiposity and metabolic disorders in female rats over a period of 8 weeks. The HFCS-55 group showed a higher final BW compared with the glucose and control groups (p = 0.02), but there were no significant differences observed among the HFCS-55, sucrose and fructose groups. The results of Light et al. (2009) are partly comparable to our findings. However, Bocarsly et al. (2010) reported an increased BW in the rats consuming HFCS solution (8% v/v) compared with the sucrose (10% v/v) consuming rats both in 8 weeks and 6 months studies.

Figure 4
Cumulative percentage changes of body weight (PCBW) from baseline over the 7 months (p > 0.05). Values were presented as median.

3.2 Biochemical parameters

In this study, the concentrations of triglycerides, glucose, insulin and leptin did not differ among the three groups at the end of 7^th month (Table 3). Similar to our study, several authors did not find any difference in blood glucose, triglyceride and insulin levels or abdominal adiposity between the groups in their studies (Light et al., 2009; Bocarsly et al., 2010; Iida et al., 2013; Lowndes et al., 2014).

Table 3
Biochemical measurements in serum at the end of 7^th month.

	Control	pn-HFCS	pn-sucrose	p-value
Triglyceride (mg/dL)	34.5 (29-39)	34.5 (30-53)	34.5 (30-51)	0.937
Glucose (mg/dL)	126 (100-169)	115 (99-168)	128.5 (105-159)	0.502
Insulin (ng/mL)	0.45 (0.26-2.61)	0.89 (0.46-2.64)	2.50 (1.41-3.74)	0.070
Leptin (ng/mL)	1.1 (0.73-3.72)	2.2 (0.53-4.86)	2.44 (0.28-6.44)	0.637

• Values were presented as median (minimum value -maximum value).

Babacanoğlu et al. (2013) found that plasma glucose, insulin and triglyceride concentrations increased following the consumption of 10% and 20% HFCS-containing solutions for a period of 12 weeks. Alzamendi et al. (2009) reported that the consumption of 10% fructose-containing feeding caused increases in plasma leptin level and abdominal adipose tissue in male rats compared with the control group. Shapiro et al. (2008) observed that chronic fructose consumption in the form of 60% fructose contained diet caused leptin resistance prior to increases in BW, adiposity, serum leptin in male rats.

In a study conducted on human subjects, researchers compared the metabolic effects of HFCS and sucrose on the twenty-fourth hour after the consumption of an 11% w/w (weight/weight) sugar solution mixed with carbonated water. In that study, the glucose, insulin and leptin concentrations did not significantly differ between the individuals who consumed fructose or sucrose-sweetened beverages with meals (Stanhope et al., 2008). In another study, the consumption of high fructose containing beverages (30%) with meals had lead to a reduction in insulin and leptin in women at the end of a twenty-four hour period, compared to the consumption of the same amount of glucose-containing beverages with meals (Teff et al., 2004).

3.3 Anthropometrical parameters

Body weight gain alone is not sufficient to define obesity. For this reason, criteria, such as the BMI, Lee index, TC and AC are used. In this study, there were no significant differences among the study groups in terms of the BMI and Lee index (Table 4). Novelli et al. (2007) fed male Wistar rats with a sucrose solution, high-carbohydrate diet or control diet for 30 days and compared Lee index and BMI among the groups. They found no difference in Lee index, which ranged from 0.29 to 0.33, among the study groups. In another study, Engelbregt et al. (2001) investigated the body composition of pubertal male rats and reported the BMI of a normal rat as 0.53 g/cm². Novelli et al. (2007) stated that the BMI of normal adult rats ranges from 0.45 to 0.68 g/cm². According to assumption of Novelli et al. (2007), the rats in our study with the BMI of 0.68 g/cm² were accepted as borderline for obesity (Table 4). The differences between BMI and Lee index were not significant among the groups. The HFCS group showed a significantly larger AC than the control group. There were no significant differences in TC or BL among the groups. The ratio of AC to TC was higher in both the HFCS and sucrose groups compared with the control group (Table 4). However, Novelli et al. (2007) found a higher AC to TC ratio in the sucrose group compared with the HFCS and control groups.

Table 4
Anthropometrical parameters and pairwise comparison of three groups.

	Control	pn-HFCS	pn-sucrose	p- value
BMI	0.68 (0.60-0.82)	0.67 (0.60-0.82)	0.68 (0.57-0.80)	0.594
Lee Index	0.30 (0.29-0.32)	0.30 (0.29-0.32)	0.30 (0.28-0.31)	0.205
AC (cm)	16.95 (13-20)	17.80 (13-23)	17.50 (14-23)	0.015
TC (cm)	14.50 (12-16)	14.30 (12-18)	14.40 (12-18)	0.786
BL (cm)	24.50 (23-27)	25 (22-27)	24.80 (23-27)	0.243
AC/TC	1.18 (1.03-1.35)	1.23 (1.05-1.42)	1.24 (1.05-1.39)	<0.001
Hepatic fat (g)	10.73 (6.60-12.56)	10.74 (7.42-13.92)	10.09 (8.21-15.74)	0.991
Abdominal fat (g)	2.69 (0.96-7.43)	3.36 (0.83-7.29)	4.79 (0.89-13.38)	0.725
Gonadal fat (g)	1.55 (0.21-2.15)	1.81 (0.57-5.27)	2.80 (0.52-7.80)	0.523
	Pairwise Comparison
	Control-HFCS	Control-sucrose	HFCS-sucrose
AC	0.003	0.061	0.575
AC/TC	<0.001	0.033	0.153

• Values were presented as median (minimum value -maximum value).

Also in our study, leptin concentration and Lee index were found to be correlated in the control (p = 0.028) and pn-HFCS groups (p = 0.016), but there was no correlation found between leptin concentration and BMI. Maffei et al. (1995) have reported a strong correlation between the plasma leptin concentration and BMI in rodents and humans. Heden et al. (2014) found that daily consumption of 355 mL HFCS-sweetened regular soda did not significantly alter BW, insulin secretion, glucose, lipid, or cholesterol responses in either normal weight or obese individuals.

There were no significant differences in the weights of the hepatic, abdominal and gonadal fat pads among the groups (Table 4). Iida et al. (2013) investigated the tissue accumulation of fat in rats fed corn starch, HFCS or rare sugar syrups (RSS) which contain D-psicose and D-allose. They found that the weight of mesenteric, perirenal and epididymal fat did not differ between the starch and HFCS groups, but they observed significant difference between the HFCS and RSS groups. Bravo et al. (2013) investigated the effect that adding the most often consumed fructose- and glucose-containing sugars to a daily diet had on liver fat content and intramuscular adipose tissue. Sixty-four individuals, men and women, aged 20 to 60, consumed low-fat milk sweetened (8%, 18% and 30%) with either high-fructose corn syrup (HFCS) or sucrose for 10 weeks. Computed tomography imaging was used for fat content determination of the liver and magnetic resonance imaging was used to find the fat content of muscle. There were no significant differences identified in the fat content of the liver, vastus lateralis muscle or gluteus maximus muscle between the study groups. These results showed that fructose consumption as a part of daily diet did not promote fat storage either in the liver or in muscles.

4 Conclusion

The chronic consumption of pn-HFCS or pn-sucrose did not cause significant differences in PCBW or anthropometrical parameters except AC and AC/TC in both of the peach nectar-consuming groups. The concentrations of glucose, insulin, leptin and triglycerides did not significantly change after the consumption of both peach nectars.

The results of the present study suggest that long term daily HFCS or sucrose consumption in peach nectar is not associated with weight gain and does not stimulate metabolic changes (PCBW, BMI, Lee index, serum triglyceride, glucose, insulin and leptin concentrations) in Sprague Dawley rats.

Acknowledgements

This research was supported by Uludag University Scientific Research Project No: UAP(Z)2011/65. All authors critically reviewed the content and have approved the final version of manuscript. The authors had no conflicts of interest.

• Practical Application: This paper shows the effects of peach nectar containing high fructose corn syrup consumption on obesity parameters in Sprague Dawley rats.

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Publication Dates

• Publication in this collection
  29 May 2017
• Date of issue
  Apr-Jun 2017

History

• Received
  23 Sept 2016
• Accepted
  23 Oct 2016