- Research article
- Open Access
Effects of habitual exercise and dietary restriction on intrahepatic and periepididymal fat accumulation in Zucker fatty rats
BMC Research Notes volume 8, Article number: 121 (2015)
Habitual exercise and dietary restriction are commonly recommended to prevent or ameliorate obesity and lifestyle-related diseases, including fatty liver. This study investigated the effects of habitual exercise and dietary restriction on hepatic triglyceride (TG) levels, serum leptin levels, and histological adipocyte size in periepididymal adipose tissue from Zucker fatty (ZF) rats.
Six-week-old male ZF rats were randomly assigned to one of three groups: sedentary (Sed), sedentary and dietary restriction (Sed + DR), and training and dietary restriction (Tr + DR). Male Zucker lean (L) rats were used as control animals. All rats had access to water and the allowed quantity of food ad libitum. The rats in the Sed + DR and Tr + DR groups were fed a 30% restricted diet, while those in the Tr + DR group exercised voluntarily on a wheel ergometer. After 12 weeks, the rats were sacrificed for a histological examination of their liver and periepididymal adipose tissue. Hepatic and serum TG, serum total cholesterol, glutamic-oxaloacetic transaminase, glutamic-pyruvic transaminase, free fatty acid, and leptin levels were also measured.
The hepatic TG levels were significantly higher in the Sed + DR group than in the L (P < 0.001) and Sed (P < 0.05) groups. By contrast, the hepatic TG levels in the Tr + DR group were significantly lower than those in the Sed (P < 0.05) and Sed + DR (P < 0.001) groups, but not significantly different from the L group values. The periepididymal adipocytes were significantly larger in the Sed, Sed + DR, and Tr + DR groups than in the L group (P < 0.001) and were significantly smaller in the Tr + DR group compared to the Sed and Sed + DR groups (P < 0.001).
Our results suggest a relationship between lipid metabolism and the size of adipose cells in ZF rats. Exercising plays an important role in decreasing hepatic TG levels, serum leptin levels, and the size of adipose cells.
Although obesity increases the risk of fatty liver disease, hepatic fat accumulation can also develop in non-obese individuals [1,2]. Furthermore, the conditions associated with severe malnutrition (e.g., kwashiorkor) can cause fatty liver disease . These observations suggest that excessive food intake and poor nutrition contribute to fat accumulation in the liver. In general, habitual exercise and dietary modification have an inhibitory effect on obesity [4,5]. Previous large-scale cohort studies found that physical fitness as assessed by muscle strength and endurance, body mass index (BMI), and fat percentage influenced the health profile of individuals [6-8]. Moreover, studies suggest that exercise has an effect on morbidity and mortality from lifestyle-related diseases. For instance, individuals with elevated BMI values who engage in habitual exercise have been found to have a lower mortality rate than those with a normal BMI who do not exercise regularly [6-8]. Furthermore, a lack of habitual exercise is equivalent to smoking as a risk for noncommunicable disease .
Both habitual exercise and dietary restriction contribute to weight loss. However, few reports have examined these effects simultaneously. We recently characterized the effects of habitual exercise and/or diet restriction on hepatic fat accumulation in Zucker fatty (ZF) rats . Histologically, the intrahepatic accumulation of triglycerides (TGs) was suppressed by habitual exercise, but not by dietary restriction alone . ZF rats have a mutation in the leptin receptor gene that causes increased appetite and weight gain; thus, they are used as an animal model of obesity .
We used ZF rats to examine the effects of habitual exercise and dietary restriction on hepatic TG levels, serum leptin levels, and histological adipocyte size in periepididymal adipose tissue.
Our study was approved by the Biological and Epidemiologic Research Committee for Animal Use of Wayo Women’s University (Ichikawa, Japan). All procedures were performed in accordance with the Declaration of Helsinki. Male Zucker lean (L) rats and male ZF rats were purchased at 5 weeks of age (87.0–100.9 and 118.4–138.0 g each, respectively) from Charles River Laboratories Japan, Inc. (Yokohama, Japan). All animals were housed in individual cages in a temperature-controlled (21.8 ± 0.6°C) animal room with a 12-h light (08:00–20:00)/dark (20:00–08:00) cycle. Following a 1-week acclimation period, the ZF rats, aged 6 weeks, were allocated to one of three groups using computer-generated randomization: sedentary (Sed), sedentary + dietary restriction (Sed + DR), or training + dietary restriction (Tr + DR). All animals received standard rodent chow (NMF; Oriental Yeast Co., Ltd., Tokyo, Japan) and were allowed ad libitum access to water and the allowed quantity of food. Body weight and food consumption were monitored daily throughout the study period. The animals in the Sed + DR group received 70% of the mean volume of food consumed by the animals in the Sed group. The animals in the Tr + DR group were subjected to a dietary restriction but were allowed unrestricted access to a running wheel. Running distance was measured by an ergometer; the mean distance was 2,533 m/24 h. Furthermore, the quantity of food was regulated to allow equivalent weight gain in the Tr + DR and Sed + DR groups. L rats, a non-hyperphagic strain used as a control, were maintained under sedentary conditions.
At 12 weeks of age, all animals were fasted overnight to exclude the influence of diet up until the day before and the Tr + DR running wheels were locked. The rats were anesthetized with isoflurane, and blood samples were collected into serum gel separator tubes (VENOJECT II plastic vacuum tube; Terumo, Tokyo, Japan) and centrifuged to separate the serum for blood chemistry tests. The liver and periepididymal adipose tissue were rapidly resected from the anesthetized rats. Samples of adipose tissue and hepatic tissue were placed in 10% formalin, and the remaining tissues were frozen in liquid nitrogen and stored at −80°C until analysis. The rats were then sacrificed by fatal exsanguination.
Serum levels of free fatty acids (FFA), leptin, TG, total cholesterol (T-CHO), high-density lipoprotein cholesterol (HDL-C), glutamic-oxaloacetic transaminase (GOT), and glutamic-pyruvic transaminase (GPT) were measured using commercially available kits according to the manufacturer’s instructions (FFA: NEFA E-test, Wako Pure Chemical Industries Ltd., Osaka, Japan; leptin: YK050 Rat Leptin ELISA Kit, Yanaihara Institute, Shizuoka, Japan; TG: TG E-test, Wako Pure Chemical Industries Ltd.; T-CHO, HDL-C, GOT, and GPT: Dri-Chem 4000, Fujifilm, Tokyo, Japan).
Liver tissue preparation for TG analysis
To extract lipids, the resected liver was homogenized with a 2:1 chloroform-methanol mixture (vol/vol) . Hepatic TG levels were determined using a kit (TG E-Test, Wako Pure Chemical Industries Ltd.).
Resected hepatic and periepididymal adipose tissues were fixed in 10% formalin. Hematoxylin and eosin (H&E) staining was outsourced to SRL (Tokyo, Japan). Photomicrographs of the sections were made for digital storage. Adipocyte size was determined by measuring the cross-point intervals as described previously [13,14]. Briefly, more than 2,000 parallel lines were superimposed onto the tissue sections of three animals using ImageJ software (version 1.46, http://rsb.info.nih.gov/ij/; National Institutes of Health, Bethesda, MD, USA). Then, the distances between the intersections of the lines and the cell membranes were measured. All ambiguous structures (e.g., vascular structures and the parallel lines touching the edges of the image fields) were excluded from analysis.
A one-way analysis of variance was performed for each outcome measure. Significant main effects were followed up using Fisher least-significant difference post hoc comparisons. All values are expressed as means ± standard error of the mean (SEM); P-values < 0.05 were deemed to indicate statistical significance.
At 12 weeks of age, the rats in the Sed (P < 0.001), Sed + DR (P < 0.05), and Tr + DR (P < 0.05) groups weighed significantly more than the animals in the L group. The rats in the Sed group also weighed significantly more than those in the Sed + DR and Tr + DR groups (both, P < 0.001); however, body weight was not significantly different between the Sed + DR and Tr + DR groups. Mean daily food intake was significantly greater in the Sed, Sed + DR, and Tr + DR groups than in the L group (P < 0.001) and significantly less in the Sed + DR and Tr + DR groups than in the Sed group (P < 0.001); however, mean daily food intake did not differ between the Sed + DR and Tr + DR groups. The wet weight of the liver was significantly greater in the Sed (P < 0.001) and Sed + DR (P < 0.05) rats compared to the L group and significantly less in the Tr + DR than in the Sed group (P < 0.01). Moreover, the weight of the soleus muscle was significantly lower in the Sed, Sed + DR, and Tr + DR groups than in the L group (P < 0.001), but significantly higher in the Tr + DR than in the Sed and Sed + DR groups (P < 0.001; Table 1).
Hepatic fat levels
Hepatic TG levels were significantly higher in the Sed + DR group than in the L (P < 0.001) and Sed (P < 0.05) groups. In contrast, the hepatic TG levels in the Tr + DR group were significantly lower than those in the Sed (P < 0.05) and Sed + DR (P < 0.001) groups, but not significantly different from the L group values (Figure 1). Representative photomicrographs of H&E-stained hepatic tissue samples are shown in Figure 2.
The results of serum chemical analyses are shown in Table 2 and Figure 3. The serum FFA levels were significantly higher in the Sed and Sed + DR groups than in the L group (P < 0.001), and the Sed + DR group levels were higher than those in the Tr + DR group (P < 0.05; Figure 3). The serum leptin levels were higher in the Sed, Sed + DR, and Tr + DR groups than in the L group (P < 0.001), and the serum leptin levels in the Sed and Sed + DR groups were higher than those in the Tr + DR group (P < 0.001; Figure 3). The serum TG levels were significantly higher in the Sed (P < 0.001) and Sed + DR (P < 0.01) groups than in the L group (Table 2). Serum T-CHO was significantly higher in the Sed and Sed + DR groups than in the L group (P < 0.001), and higher in the Sed (P < 0.05) and Sed + DR (P < 0.001) groups than in the Tr + DR group (Table 2). Serum HDL-C was significantly higher in the Sed + DR group than in the L (P < 0.001), Sed + DR (P < 0.05), and Tr + DR (P < 0.001) groups (Table 2). Moreover, the serum HDL-C levels were significantly higher in the Sed than in the L (P < 0.001) and Tr + DR (P < 0.05) groups (Table 2). Serum GOT was significantly higher in the Sed + DR than in the L group (P < 0.05), and serum GPT levels were significantly higher in the Sed + DR than in the L and Tr + DR groups (both, P < 0.05; Table 2).
Periepididymal adipose tissue
Representative photomicrographs of H&E-stained periepididymal adipose tissue, adipocyte size distribution, and periepididymal fat pad weight and adipocyte sizes are shown in Figures 4, 5 and 6, respectively. The mean periepididymal fat pad weight was significantly higher in the Sed, Sed + DR, and Tr + DR groups than in the L group (P < 0.001); however, the weight was not significantly different among the Sed, Sed + DR, and Tr + DR groups (Figure 6). The periepididymal adipocyte size was significantly larger in the Sed, Sed + DR, and Tr + DR groups than in the L group and larger in the Sed and Sed + DR groups than in the Tr + DR group (all, P < 0.001; Figure 6).
To our knowledge, this is the first study to examine the effects of habitual exercise and dietary restriction on adipocyte size in periepididymal adipose tissue. The original goal of this study was to make a direct comparison of the effect on fatty liver disease between the restricted diet group and the restricted diet plus exercise group.
We found no significant difference in food consumption (i.e., consumed calories) between the Sed + DR and Tr + DR groups. Moreover, body weight and periepididymal fat weight were similar between these groups after 12 weeks. However, the hepatic TG levels and periepididymal adipocyte size were significantly lower in the Tr + DR than in the Sed + DR group. These data indicate positive effects of exercise on hepatic TG levels and adipocyte size in the epididymis.
In this study, despite the fact that body weight gain was suppressed by dietary restriction as expected, hepatic fat accumulation was greatly facilitated. On this point, we considered the possibility that the metabolic state of the animals in the Sed + DR group was similar to that during starvation. ZF rats are affected by overeating, and the reported level of overeating is great . Therefore, we considered that the metabolic state of the ZF rats was probably close to the starvation state.
From the hepatic fat accumulation data, we speculated that the suppression of serum FFA with exercise induced the suppression of hepatic fat accumulation mediated by a decrease in fatty acid uptake into hepatocytes. In addition, regarding the increase in serum FFA caused by dietary restriction only, we speculated that lipolysis, which occurs in fat cells during severe starvation, occurred in the Sed + DR group. We also postulated that the result of the increased hepatic fat accumulation in the Sed + DR group was induced by increased fatty acid uptake into hepatocytes, which was caused by the increased serum level of FFA. Indeed, previous studies suggested that high levels of FFA are secreted from large size of fat cell [16,17].
Hoffstedt et al.  compared obese patients with a few large adipocytes (adipose hypertrophy) and those with many small adipocytes (adipose hyperplasia) and found that patients with many small adipocytes had healthier blood glucose, insulin, and lipid level profiles than did patients with large adipocytes. We found that the serum T-CHO, HDL-C, FFA, GOT, and GPT levels were lower in the Tr + DR group than in the Sed + DR group. Our results also suggest a relationship between lipid metabolism and adipocyte size. In general, the conditions that cause excessive fat accumulation (i.e., fatty liver) are related to the development of insulin resistance and various internal organ dysfunctions . The suppression of adipocyte hypertrophy is said to be an important factor in maintaining healthy lipid metabolism.
In a study of Wistar rats subjected to exercise, Miyazaki et al.  found that exercise reduced leptin mRNA expression and the size of adipocytes in adipose tissue, and they concluded that the exercise-induced change in leptin levels was dependent on a reduction in adipocyte size. Similar changes were observed in morbidly obese ZF rats. Noto et al.  reported a decrease in both serum leptin levels and the size of adipose cells after the intake of conjugated linoleic acid. Our findings indicate a significant decrease in serum leptin levels and adipocyte size in the Tr + DR but not in the Sed + DR group (Figures 3 and 6), consistent with these previous findings [20,21], and suggest an association between leptin levels and adipocyte size in the exercise group. If changes in adipocyte size can induce hepatic fat accumulation, then adipocytes maintained in good condition could prevent hepatic fat accumulation with habitual exercise.
Our results suggest that a relationship exists between lipid metabolism and the size of adipose cells in ZF rats. Exercise plays an important role in decreasing hepatic TG levels, serum leptin levels, and the size of adipose cells.
Body mass index
- Sed + DR:
Sedentary + dietary restriction
- Tr + DR:
Training + dietary restriction
Free fatty acid
High-density lipoprotein cholesterol
Hematoxylin and eosin
Standard error of the mean
Das K, Das K, Mukherjee PS, Ghosh A, Ghosh S, Mridha AR, et al. Nonobese population in a developing country has a high prevalence of nonalcoholic fatty liver and significant liver disease. Hepatology. 2010;51:1593–602.
Azuma K, Kadowaki T, Cetinel C, Kadota A, El-Saed A, Kadowaki S, et al. Higher liver fat content among Japanese in Japan compared with non-Hispanic whites in the United States. Metabolism. 2009;58:1200–7.
Lewis B, Hansen JD, Wittman W, Krut LH, Stewart F. Plasma free fatty acids in kwashiorkor and the pathogenesis of the fatty liver. Am J Clin Nutr. 1964;15:161–8.
Kimura M, Shinozaki T, Tateishi N, Yoda E, Yamauchi H, Suzuki M, et al. Adiponectin is regulated differently by chronic exercise than by weight-matched food restriction in hyperphagic and obese OLETF rats. Life Sci. 2006;79:2105–11.
Suzuki M, Shindo D, Kimura M, Waki H. Effects of exercise, diet, and their combination on metabolic-syndrome-related parameters in OLETF rats. Int J Sport Nutr Exerc Metab. 2011;21:222–32.
Blair SN, Kohl 3rd HW, Paffenbarger Jr RS, Clark DG, Cooper KH, Gibbons LW. Physical fitness and all-cause mortality. A prospective study of healthy men and women. JAMA. 1989;262:2395–401.
Lee CD, Blair SN, Jackson AS. Cardiorespiratory fitness, body composition, and all-cause and cardiovascular disease mortality in men. Am J Clin Nutr. 1999;69:373–80.
Lee DC, Sui X, Artero EG, Lee IM, Church TS, McAuley PA, et al. Long-term effects of changes in cardiorespiratory fitness and body mass index on all-cause and cardiovascular disease mortality in men: the Aerobics Center Longitudinal Study. Circulation. 2011;124:2483–90.
Lee IM, Shiroma EJ, Lobelo F, Puska P, Blair SN, Katzmarzyk PT. Effect of physical inactivity on major non-communicable diseases worldwide: an analysis of burden of disease and life expectancy. Lancet. 2012;380:219–29.
Kurosaka Y, Kitamura H, Yamauchi H, Shiroya Y, Minato K. Effects of habitual exercise and diet restriction on the hepatic fat accumulation in Zucker fatty rats. Tairyoku Kagaku Japanese J Phys Fit Sports Med. 2014;63:223–9.
Wang T, Hartzell DL, Flatt WP, Martin RJ, Baile CA. Responses of lean and obese Zucker rats to centrally administered leptin. Physiol Behav. 1998;65:333–41.
Folch J, Lees M, Sloane Stanley GH. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957;226:497–509.
Knudsen L, Weibel ER, Gundersen HJ, Weinstein FV, Ochs M. Assessment of air space size characteristics by intercept (chord) measurement: an accurate and efficient stereological approach. J Appl Physiol. 2010;108:412–21.
Simon DM, Tsai LW, Ingenito EP, Starcher BC, Mariani TJ. PPARgamma deficiency results in reduced lung elastic recoil and abnormalities in airspace distribution. Respir Res. 2010;11:69.
AleixandredeArtinano A, Miguel Castro M. Experimental rat models to study the metabolic syndrome. Br J Nutr. 2009;102:1246–53.
Laurencikiene J, Skurk T, Kulyte A, Heden P, Astrom G, Sjolin E, et al. Regulation of lipolysis in small and large fat cells of the same subject. J Clin Endocrinol Metab. 2011;96:E2045–9.
Jacobsson B, Smith U. Effect of cell size on lipolysis and antilipolytic action of insulin in human fat cells. J Lipid Res. 1972;13:651–6.
Hoffstedt J, Arner E, Wahrenberg H, Andersson DP, Qvisth V, Lofgren P, et al. Regional impact of adipose tissue morphology on the metabolic profile in morbid obesity. Diabetologia. 2010;53:2496–503.
Slawik M, Vidal-Puig AJ. Adipose tissue expandability and the metabolic syndrome. Genes Nutr. 2007;2:41–5.
Miyazaki S, Izawa T, Ogasawara JE, Sakurai T, Nomura S, Kizaki T, et al. Effect of exercise training on adipocyte-size-dependent expression of leptin and adiponectin. Life Sci. 2010;86:691–8.
Noto A, Zahradka P, Yurkova N, Xie X, Truong H, Nitschmann E, et al. Dietary conjugated linoleic acid decreases adipocyte size and favorably modifies adipokine status and insulin sensitivity in obese, insulin-resistant rats. Metabolism. 2007;56:1601–11.
This study was supported by Grants-in-aid for Scientific Research (KAKENHI; nos. 26860774 and 26870553) and by a grant from the Meiji Yasuda Life Foundation of Health and Welfare.
KS reports receiving research grants from Janssen Pharmaceutical, Dainippon Sumitomo Pharma, Astellas Pharma, Taiho Pharmaceutical, and POLA-Pharma. The other authors declare that they have no potentially competing interests.
YK conceptualized this study, integrated the data, and wrote the manuscript as a major contributor; YS and HY were associated with the conception and design of the study, the acquisition of data, analysis, interpretation of the data, and in drafting part of the manuscript. TS and YO produced some of the adipocyte images and were involved in the statistical analysis. TK helped revise the manuscript and provided helpful discussions. KM helped design the study, acquire the data, supervise the study, and draft the manuscript. All authors contributed towards the conceptualization, writing, reading, and approval of the final manuscript.
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Kurosaka, Y., Shiroya, Y., Yamauchi, H. et al. Effects of habitual exercise and dietary restriction on intrahepatic and periepididymal fat accumulation in Zucker fatty rats. BMC Res Notes 8, 121 (2015). https://doi.org/10.1186/s13104-015-1063-6
- Fatty liver
- Dietary restriction