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Experimental research

Effect of feeding a high-fat diet independently of caloric intake on reproductive function in diet-induced obese female rats

Mona A. Hussain
,
Noha M. Abogresha
,
Ranya Hassan
,
Dalia A. Tamany
,
Mariam Lotfy

Arch Med Sci 2016; 12, 4: 906–914
Online publish date: 2016/05/11
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Introduction

The prevalence of overweight and obesity is increasing globally, predisposing females to health hazards including compromised reproductive capacity. Formerly considered a problem of developed countries, this epidemic is now dramatically on the rise in low- and middle-income countries [1]. Anovulation, ir­regular menses, subfertility, miscarriage, and adverse pregnancy outcomes, with lasting effects for children, are reproductive sequelae of obesity among women of reproductive age. On the other hand, not all obese women experience poor reproductive health. Because of this, it is important to recognize factors other than obesity that affect reproductive function in obese women. Nutrition is one of them [2].
A handful of studies have previously reported altered reproductive functions in diet-induced obese animal models [3], and several studies have addressed the effects of dietary restriction using standard rodent diets on reproductive function of female rats [4–6]. Currently, dietary restriction using a high-fat diet (HFD) is more relevant to dietary status in most world countries [7].
Leptin is an adipocyte hormone that functions as an afferent signal in a negative feedback loop regulating body weight. Since its discovery in 1995, several studies have suggested a pivotal role of leptin in reproductive function [8–10].
Programmed cell death or apoptosis is attributed to the exhaustion of the oocyte reserve through germ cell death and follicular atresia, so apoptosis is an essential component of normal reproductive function and it has been proposed to be the major mechanism that determines female reproductive life span [11].
The corpus luteum is primarily responsible for the synthesis and release of progesterone, a hormone essential for the establishment and maintenance of pregnancy in mammals. In the absence of pregnancy, the corpus luteum will cease to synthesize progesterone, and the bulk of the luteal tissue will decrease in mass. This process is termed luteolysis [12]. The luteolytic process is typically subdivided, whereby the decline in progesterone is described as functional luteolysis and the structural involution is described as structural luteolysis [13]. Luteolysis, at least in part, is mediated by apoptosis in essentially all mammalian species. It has become evident that apoptosis is triggered by the activation of cysteine aspartate-specific proteases (caspases). A cascade of proteolysis beginning with the activation of caspase-8 leads to activation of caspase-3, which is the principal downstream effector enzyme of cell death, and activation of caspase-3 is considered by many as a final executioner of the apoptotic cell death program [12, 14].
To our knowledge, no studies have been carried out to investigate the effect of HFD feeding independently from caloric intake on reproductive function in obese female rats. So our objective was to investigate the effect of ad libitum, isocalorically restricted and hypocalorically restricted HFD feeding on reproductive function in diet-induced obese female rats.

Material and methods

This study was performed at the Physiology and Clinical Pathology departments, Faculty of Medicine, Suez Canal University, Ismailia, Egypt. All experimental protocols were approved by the Institutional Animal Care and Use Committee at Suez Canal University. All efforts were made to minimize animal suffering and to reduce the number of animals used. The “Principles of laboratory animal care” were followed, as well as specific national laws where applicable.

Animals and nutritional management

Twenty female albino Sprague Dawley rats (7–9 weeks of age, weighing 137–176 g at the beginning of the experiment) purchased from the center for experimental animals, Faculty of Veterinarian Medicine, Zagazig University, were used in the study. All rats were left to acclimatize for one week prior to the experiment and were housed in plastic cages maintained at controlled room temperature (22–24°C), 60% humidity with 12-hour day/night cycle with free access to a standard pellet animal diet (purchased from El Gomhorya company, Ismailia, Egypt) containing 67% carbohydrates, 10% fat, and 23% protein as the energy sources (overall calories: 3.6 kcal/g) and tap water. After weight matching, 5 rats were kept on a standard pellet animal diet to serve as a control group (group A) and 15 rats were fed a HFD consisting of 88% of standard pellet animal diet, 10% lard and 2% cholesterol for 9 weeks to induce obesity. The HFD was composed of the following energy sources: 52% carbohydrates, 30% fat, and 18% protein (overall calories: 4.8 kcal/g). The amount of calories in each gram was calculated in the Nutrition and Food Science Department, Faculty of Education, Suez Canal University. The major composition of the diets used in this study is presented in Table I [15, 16]. Next the HFD fed animals were equally divided into three weight-matched groups: the ad libitum HFD group (group B), which was freely maintained on the same composition of HFD for another 4 weeks; the isocaloric restricted HFD group (group C), which was fed 75% of their average food intake before restriction (overall calories: 3.6 kcal/g) for another 4 weeks; and the hypocaloric restricted HFD group (group D), which was fed 50% of their average food intake before restriction (overall calories: 2.4 kcal/g) for another 4 weeks. Food intake was measured per cage to avoid the stress of individual housing [16]. Food intake was measured daily for 1 week before the start of food restriction, and the average amount was calculated [17].

Methods

All animals were weekly weighed from the first week of study onwards. Estrous cyclicity was daily examined (5 days per week) for all animals from the start of HFD restriction until the end of the study. Estrous cyclicity monitoring was done by vaginal smear between 9 and 11 a.m. The vaginal smears were examined by standard light microscope to observe proportions of cells to determine the phase of rat estrous cycle. The rat estrous cycle takes 4–5 days and consists of four phases: diestrus, proestrus, estrus and metestrus. The diestrus phase is characterized by predominance of leucocytes, the proestrus phase is characterized by appearance of predominant nucleated epithelial cells, the estrus phase is characterized by appearance of clustered large cornified epithelial cells, and the metestrus phase is characterized by appearance of equal proportions of these cells [18, 19]. Irregular estrous cycles were characterized by keeping in the same phase during 4–5 days or when the alternation among the phases did not follow the sequence of proestrus, estrus, metestrus and diestrus [18].
At the end of the study the following procedures were done for all animals:
1) Measuring the body weight and length. Body mass index (BMI) was calculated according to the formula: BMI = body weight (g)/length2 (cm2). The Lee index was calculated according to the formula: Lee index = cubic root of body weight in grams divided by length in centimeters [20]. Corrected ovarian weight was calculated as % of ovarian weight/body weight [19].
2) After 5 h of food withdrawal [21], blood samples were taken from the retro-bulbar venous plexus from anesthetized rats to measure the concentrations of serum glucose, cholesterol, triglycerides, free fatty acids, follicle-stimulating hormone (FSH), luteinizing hormone (LH), estradiol, progesterone and leptin.
3) Assay of fasting serum concentrations of glucose, cholesterol, triglycerides and free fatty acids: glucose, cholesterol and triglyceride measurements were performed with commercial kits on the Cobas c311 analyzer (Roche Diagnostics, Germany). The free fatty acid assay was performed with BioVision’s Free Fatty Acid Quantification Colorimetric Kit.
4) Assay of FSH, LH, estradiol, progesterone and leptin: The serum was obtained by centrifugation (2400 rpm, for 20 min at 4°C) and the concentrations of estradiol, LH, progesterone and FSH were determined by (Vidas, BioMerieux). Assays of serum leptin concentrations were performed using ELISA kits (R&D Systems) according to the manufacturer’s manual. The sensitivity of the assay is 22 pg/ml with an interassay coefficient of variation 5%.
5) Anesthetized rats were sacrificed and dissected for collection of both ovaries, which were weighed then processed for subsequent histopathological studies.
6) Histopathological studies:
a) Hematoxylin and eosin study: ovaries were stored in 10% neutral buffered formalin, embedded in paraffin blocks, and sectioned (5 µm). Ovarian sections were stained with hematoxylin and eosin. Histological analysis of the ovarian sections was done by a professional pathologist. The follicles and corpora lutea were counted. Graafian follicles were characterized by the presence of a confluent antral space filled with fluid with a diameter greater than 350 µm [3].
b) Caspase-3 immunohistochemistry: the detection of caspase-3 protein expression in the ovarian sections relied on immunohistochemistry, which was based on a streptavidin biotin peroxidase method (Biogenex, San Ramon, CA, USA). Ovarian paraffin sections and polyclonal antibody to caspase-3 (Santa Cruz, USA, at dilution 1 : 150) were incubated for 1 h at room temperature. Diaminobenzidine (Sigma Fast 3,3’-diaminobenzidine tablets, D-4293; Sigma, St. Louis, MO, USA) was used as the chromogen. Cytoplasmic staining for caspase-3 was considered positive. The integral optical density (IOD) of immunohistochemical intensity was then calculated using Image-Pro plus 6.0 software. Each value represents IOD counted at a high-power view (400×) by a microscope. The mean value represents the average number derived from the 5 high-power fields of each case [22].

Statistical analysis

All the data were expressed as mean ± standard error of mean (SEM) and analyzed using the program Statistical Package for the Social Sciences (SPSS) (IBM SPSS Statistics, Version 20). All the comparisons among groups were carried out using one-way analysis of variance (ANOVA) followed by the Bonferroni post hoc test to test the significance difference among group means. Data were considered statistically significant at p ≤ 0.05.

Results

Characteristics of the animals

Ad libitum HFD feeding for 13 weeks significantly increased the body weight and BMI in group B vs. groups A, C and D and significantly increased the Lee index in group B vs. groups A and D. Isocalorically restricted HFD for 4 weeks significantly reduced the ovarian weight in group C vs. groups A and B and significantly reduced the corrected ovarian weight in group C vs. group A. Hypocalorically restricted HFD for 4 weeks significantly reduced the body and ovarian weights in group D vs. group A (Table II).

Serum concentrations of glucose, cholesterol, triglycerides and free fatty acids

Ad libitum HFD for 13 weeks caused no significant changes in the fasting serum levels of glucose, triglycerides, cholesterol or free fatty acids. Isocalorically restricted HFD for 4 weeks significantly increased the fasting serum cholesterol level in group C vs. groups A and B. Hypocaloric restricted HFD for 4 weeks caused no significant changes in fasting serum levels of glucose, triglycerides, cholesterol or free fatty acids (Table III).

Estrous cyclicity results

In group A, 80% of female rats had regular estrous cycles with mean duration of 4–5 days and with the sequence of proestrus, estrus, metestrus and diestrus. The HFD feeding independently of caloric intake in groups B, C and D significantly reduced this percentage. Most of the irregular cycles were characterized by prolonged diestrus. During the last week before the sacrifice of rats, 20% of rats in groups C and D and 0% of rats in group B had regular cycles. Most of the irregular cycles were characterized by persistent diestrus (Figure 1).

Serum FSH, LH, estradiol, progesterone and leptin results

Ad libitum HFD for 13 weeks caused no significant changes in serum levels of FSH, LH, estradiol, or progesterone in group B. Isocalorically restricted HFD for 4 weeks significantly increased the serum LH level in group C vs. groups A and B, and significantly reduced the serum progesterone level in group C vs. groups A and B. Hypocalorically restricted HFD for 4 weeks significantly reduced the serum progesterone level in group D vs. group A. There was no significant change in serum leptin among the study groups (Table IV).

Histopathological results

There was no significant difference between the study groups in the count of ovarian follicles or corpora lutea (Figure 2 A). The ovaries of rats in group B showed a significant increase in immunoreactivity for caspase-3 versus groups A, C and D. The ovaries of rats in group C showed a significant increase in immunoreactivity for caspase-3 versus groups A and D (Figures 2 B, 3).

Discussion

“The reproductive function in women is impaired by a negative and positive nutritional status” [6]. In the current study, ad libitum HFD for 13 weeks significantly increased the body weight, BMI and Lee index. Isocaloric HFD restriction caused the body weight of obese rats to decrease to a mean value that did not significantly differ from that of the control group. Hypocaloric HFD restriction significantly reduced the body weight of obese rats. These results are in agreement with the results of Park et al.; they found that rats gradually developed obesity when placed on a HFD, and when rats were subjected to 40% restricted HFD treatment, they had a significant reduction in body weights [23].
In the current study, ovarian weight of restricted HFD fed rats was significantly decreased. A similar result was obtained by other studies that subjected rats to different protocols of dietary restriction using standard rodents’ diets [5, 9, 19]. Concerning corrected ovarian weight, we found a significant decrease in corrected ovarian weight of the rats that were subjected to isocaloric HFD restriction only. This finding may be due to the fact that the body weights of these rats were not significantly different from control rats, and at the same time they had a significant decrease in ovarian weight. Hypocaloric HFD restriction caused a proportional significant decrease in both rats’ body weights and ovarian weights, and this resulted in no significant change in corrected ovarian weight in rats treated with hypocaloric HFD restriction. This result is in agreement with Dos Santos et al., as they found that ovarian weight when corrected to the body weight did not differ in dietary restricted rats [19].
In the current study we found that ad libitum HFD caused no significant change in fasting concentrations of blood glucose, cholesterol, triglycerides, or free fatty acids when compared to standard diet fed rats. This result was also found in lean mice under a HFD [24]. Restricted HFD had no effect on blood glucose triglycerides and free fatty acids. Similar results were obtained by Meidenbauer et al., as they found that mice, when treated with a lard-based HFD in restricted amounts, exhibited decreased glucose levels and a normolipidemic profile [25]. On the other hand, we found that serum cholesterol level was significantly increased with isocaloric HFD restriction. This effect may be explained by the fact that we used lard- based diets which are rich in saturated fatty acids and poor in polyunsaturated fatty acids [26]. Saturated fatty acids have a strong cholesterol-raising effect when isocalorically replacing carbohydrates in the diet [27].
In the current study, there was no significant difference in the ovarian follicles count among the studied groups. A similar result was obtained by Akamine et al., who found that HFD for 120 days did not promote a significant change in ovarian morphology [21]. In the present study, ad libitum HFD feeding interfered with the normal estrous cycle, significantly increased luteal cell apoptosis, and caused no significant effect on the serum levels of FSH, LH, estradiol or progesterone. Akamine et al. found that HFD extended the estrous cycle in rats, caused no significant effect on serum FSH or estradiol, significantly changed serum progesterone after HFD for 120 and 180 days, and changed serum LH after HFD for 120 days only. The difference between our results and those results may be due to the difference in duration of HFD treatment: 90 days in the present study versus 120 and 180 days in the Akamine et al. study [21].
The seeming discrepancy between enhanced apoptosis in luteal cells which signifies ageing of the corpus luteum in female rats [11] and absence of any significant effect on progesterone concentrations in ad libitum HFD treatment may be explained by the fact that steroidogenic cells of the corpus luteum which produce progesterone lose their capacity via mechanisms independent of those responsible for executing apoptosis and that structural and functional luteolysis might be separately regulated [12, 28].
In the current study, we observed that isocaloric HFD restriction partially but significantly ameliorated the enhanced ovarian apoptosis, and hypocaloric HFD restriction completely ameliorated this effect. On the other hand, isocaloric HFD restriction interfered with the normal estrous cycle and caused a significant decrease in serum progesterone and a significant increase in serum LH. The significant increase in LH concentrations in isocaloric HFD restriction may be explained by withdrawal of progesterone’s negative feedback effect on LH secretion [29]. Also hypocaloric HFD restriction interfered with the normal estrous cycle and caused a significant decrease in serum progesterone only. This finding may be attributed to the presence of two antagonizing factors that controlled LH secretion in hypocalorically restricted HFD fed rats. The first one is withdrawal of progesterone’s negative feedback effect, and this factor tends to increase LH secretion. The second factor is energy restriction, which tends to reduce LH secretion [30–32], so our hypothesis is that both effects blunted each other and resulted in no significant change in LH concentrations in hypocalorically restricted HFD fed rats.
In the present study we found a tendency of serum leptin to increase with ad libitum HFD, but this increase failed to reach a significant level. The results of leptin concentration changes with a HFD are conflicting. Some studies have found that leptin concentrations significantly increased with a HFD due to increased adiposity [3, 23]. In contrast, Ainslie et al. found that leptin level significantly decreased after a HFD protocol for 4 weeks, and they found no change in leptin concentrations after a HFD protocol for 14 weeks. The authors suggested that the decrease in leptin concentrations is the cause of weight gain occurring with the HFD [33]. The duration of the HFD protocol may be responsible for this different result, as Soulis et al. found that with longer HFD protocols in female rats, leptin levels were decreased [34]. In the current study we found no significant effect on leptin levels in HFD restriction. Shi et al. also found the same result in female mice with moderate food restriction [35]. On the other hand, some studies have found a significant decrease in serum leptin concentrations [7, 36]. In the present study, animal feeding and sampling were done in the morning. Schlitt and Schulz suggested that detection of the effects of feeding restriction on leptin concentrations is strongly dependent on the timing of both feeding and sampling and their interaction and that the circadian rhythms of leptin release result in a decline in leptin concentrations in the morning, leading to an inability to detect differences between the ad libitum and restricted groups during the morning [36]. According to the present results concerning leptin concentrations, it is difficult to relate serum leptin concentrations to reproductive effects of ad libitum and restricted HFD, and more work is needed to elucidate this relation.
In the current study, the HFD contained an increased ratio of saturated fatty acids and a decreased ratio of polyunsaturated fatty acids. This change in the composition of the dietary fats may be responsible for the observed reproductive effects, as many previous studies have reported [37–39].
Obesity has a constantly growing prevalence worldwide, and it represents one of the most important health risks of our time [40–42], so it is recommended that studies that deal with obesity effects on different aspects of health must be continued.
Our results suggest that HFD feeding determinately affects female rats’ reproductive function independently of caloric intake. Further studies are required to address the role of leptin, increased saturated fatty acid and decreased polyunsaturated fatty acid concentrations to clarify the mechanism of the caloric-independent effect of HFD on reproductive function.
In conclusion, the ad libitum HFD interfered with the normal estrous cycle and caused enhanced apoptosis of luteal cells in obese female rats. The HFD restriction interfered with the normal estrous cycle and caused functional insufficiency of the corpus luteum in obese female rats. These results suggest that HFD feeding determinately affects female reproductive function independently of caloric intake.

Acknowledgments

We thank Dr. Rasha Farghaly (School of Medicine, Suez Canal University, Egypt) for helping in statistical analyses. This work did not receive funds from any organizations.

Conflict of interest

The authors declare no conflict of interests.

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