J Nutr Health.  2015 Feb;48(1):1-8. 10.4163/jnh.2015.48.1.1.

Effects of an aqueous extract of purple sweet potato on nonalcoholic fatty liver in high fat/cholesterol-fed mice

Affiliations
  • 1Department of Nutritional Science and Food Management, Ewha Womans University, Seoul 120-750, Korea. orank@ewha.ac.kr
  • 2Department of Nutritional Science and Food Management, Soongeui Women's College, Seoul 100-751, Korea.

Abstract

PURPOSE
Anthocyanins from purple sweet potato (PSP) have been investigated in vitro and in animals and found to have a protective effect against oxidative hepatic damage. In this study, we investigated that aqueous extract of PSP can ameliorate the dysfunction of lipid metabolism in mice fed a high fat/cholesterol diet.
METHODS
Forty C57BL/6J mice were randomly divided into 5 groups (n = 8) and fed one of the following diets for 8 weeks; normal fat (NF) diet; high fat/cholesterol (HFC) diet; HFC with 1.25% PSP (HFPL) diet; HFC with 2.5% PSP (HFPM) diet; HFC with 5% PSP (HFPH) diet.
RESULTS
Non-alcoholic fatty liver was manifested in the HFC group by showing increased levels in plasma alanine aminotransferase (ALT) activity, total cholesterol (TC) and low density lipoprotein cholesterol (LDL-C), increased level of TC and presence of many large lipid droplets in the liver, and increased fat cell size in the HFC group compared with the NF group. However, administration of HFC induced a significant decrease in food intake, resulting in decrease in fat mass. Coadministration of PSP did not lead to reversal of body weight changes, ALT activity, and lipid levels in plasma and the liver, but suppressed excess enlargement of the fat cell size through increasing carnitine palmitoyltransferase-1 (CPT-1) gene expression in the liver. Accordingly, the number of fat droplets in the liver was reduced in PSP administered groups.
CONCLUSION
Taken together, these results suggest that PSP may have a protective effect on the dysfunction of lipid metabolism. Conduct of further studies on the coordinated regulation of PSP for lipid metabolic homeostasis at the liver-adipose tissue axis is needed.

Keyword

purple sweet potato; aqueous extract; high fat/cholesterol diet; non-alcoholic fatty liver

MeSH Terms

Adipocytes
Alanine Transaminase
Animals
Anthocyanins
Axis, Cervical Vertebra
Body Weight Changes
Carnitine
Cholesterol
Cholesterol, LDL
Diet
Eating
Fatty Liver*
Gene Expression
Homeostasis
Ipomoea batatas*
Lipid Metabolism
Liver
Mice*
Plasma
Alanine Transaminase
Anthocyanins
Carnitine
Cholesterol
Cholesterol, LDL

Figure

  • Fig. 1. Effects of purple sweet potato extract on food intake and body weight in high fat/cholesterol diet-fed C57BL/6 mice: (A) food intake, (B) energy intake, (C) total body weight gain and (D) body weight changes by week. NF, normal fat control; HFC, high fat control; HFPL, HFC + PSP 1.25%; HFPM; HFC + PSP 2.5%; HFPH, HFC + PSP 5%. Values are expressed as Mean ± SE (n = 8 for each group). Means with different letters on the bar are significantly different from each other at p < 0.05 by Duncan's multiple range test.

  • Fig. 2. Effects of purple sweet potato extract on liver enzymes in plasma and liver histology in high fat/cholesterol-fed C57BL/6 mice: (A) AST, (B) ALT and (C) liver histology. NF, normal fat control; HFC, high fat control; HFPL, HFC + PSP 1.25%; HFPM; HFC + PSP 2.5%; HFPH, HFC + PSP 5%. Values are expressed as Mean ± SE (n = 8 for each group). Means with different letters on the bar are significantly different from each other at p < 0.05 by Duncan's multiple range test. Histology bar represents 50 μm.

  • Fig. 3. Effects of purple sweet potato extract on plasma lipid levels in high fat/cholesterol-fed C57BL/6 mice: (A) TG, (B) TC, and (C) LDL-C. NF, normal fat control; HFC, high fat control; HFPL, HFC + PSP 1.25%; HFPM; HFC + PSP 2.5%; HFPH, HFC + PSP 5%. Values are expressed as Mean ± SE (n = 8 for each group). Means with different letters on the bar are significantly different from each other at p < 0.05 by Duncan's multiple range test.

  • Fig. 4. Effects of purple sweet potato extract on lipid and mRNA levels in the liver of high fat/cholesterol-fed C57BL/6 mice: (A) TC, (B) TG, and (C) mRNA levels. NF, normal fat control; HFC, high fat control; HFPL, HFC + PSP 1.25%; HFPM; HFC + PSP 2.5%; HFPH, HFC + PSP 5%; SREBP-1c, sterol regulatory element-binding protein-1c; FAS, fatty acid synthase; CPT-1, carnitine palmitoyltransferase-1. Values are expressed as Mean ± SE (n = 8 for each group). Means with different letters on the bar are significantly different from each other at p < 0.05 by Duncan's multiple range test.

  • Fig. 5. Effects of purple sweet potato extract on fat mass and epididymal fat tissue histology in high fat/cholesterol-fed mice: (A) adipose tissue weight and (B) adipose tissue histology. NF, normal fat control; HFC, high fat control; HFPL, HFC + PSP 1.25%; HFPM; HFC + PSP 2.5%; HFPH, HFC + PSP 5%. Values are expressed as Mean ± SE (n = 8 for each group). Means with different letters on the bar are significantly different from each other at p < 0.05 by Duncan's multiple range test. Histology bar represents 50 μm.


Reference

1.Samuel VT., Liu ZX., Qu X., Elder BD., Bilz S., Befroy D., Romanelli AJ., Shulman GI. Mechanism of hepatic insulin resistance in nonalcoholic fatty liver disease. J Biol Chem. 2004. 279(31):32345–32353.
Article
2.Lee E., Kim WJ., Lee YJ., Lee MK., Kim PG., Park YJ., Kim SK. Effects of natural complex food on specific enzymes of serum and liver and liver microstructure of rats fed a high fat diet. J Korean Soc Food Sci Nutr. 2003. 32(2):256–262.
3.Ministry of Food and Drug Safety. Influence of dietary intake on nonalcoholic fatty liver disease in Korean. Cheongwon: Ministry of Food and Drug Safety;2012.
4.Hna KH., Lee JC., Kim JH., Lee JS. Manufacture and physiological functionality of Korean traditional liquor by using purple-fleshed sweet potato. Korean J Food Sci Technol. 2002. 34(4):673–677.
5.Rossi A., Serraino I., Dugo P., Di Paola R., Mondello L., Genovese T., Morabito D., Dugo G., Sautebin L., Caputi AP., Cuzzocrea S. Protective effects of anthocyanins from blackberry in a rat model of acute lung inflammation. Free Radic Res. 2003. 37(8):891–900.
Article
6.Hwang YP., Choi JH., Han EH., Kim HG., Wee JH., Jung KO., Jung KH., Kwon KI., Jeong TC., Chung YC., Jeong HG. Purple sweet potato anthocyanins attenuate hepatic lipid accumulation through activating adenosine monophosphate-activated protein kinase in human HepG2 cells and obese mice. Nutr Res. 2011. 31(12):896–906.
Article
7.Ramirez-Tortosa C., Andersen ØM., Cabrita L., Gardner PT., Morrice PC., Wood SG., Duthie SJ., Collins AR., Duthie GG. Anthocyanin-rich extract decreases indices of lipid peroxidation and DNA damage in vitamin E-depleted rats. Free Radic Biol Med. 2001. 31(9):1033–1037.
Article
8.Hwang YP., Choi JH., Yun HJ., Han EH., Kim HG., Kim JY., Park BH., Khanal T., Choi JM., Chung YC., Jeong HG. Anthocyanins from purple sweet potato attenuate dimethylnitrosamine-induced liver injury in rats by inducing Nrf2-mediated antioxidant enzymes and reducing COX-2 and iNOS expression. Food Chem Toxicol. 2011. 49(1):93–99.
Article
9.Han KH., Matsumoto A., Shimada K., Sekikawa M., Fukushima M. Effects of anthocyanin-rich purple potato flakes on antioxidant status in F344 rats fed a cholesterol-rich diet. Br J Nutr. 2007. 98(5):914–921.
Article
10.Sakatani M., Suda I., Oki T., Kobayashi S., Kobayashi S., Takahashi M. Effects of purple sweet potato anthocyanins on development and intracellular redox status of bovine preimplantation embryos exposed to heat shock. J Reprod Dev. 2007. 53(3):605–614.
Article
11.Hwang YP., Choi JH., Choi JM., Chung YC., Jeong HG. Protective mechanisms of anthocyanins from purple sweet potato against tert-butyl hydroperoxide-induced hepatotoxicity. Food Chem Toxicol. 2011. 49(9):2081–2089.
Article
12.Friedewald WT., Levy RI., Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972. 18(6):499–502.
Article
13.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(1):497–509.
Article
14.Lovejoy JC. The influence of dietary fat on insulin resistance. Curr Diab Rep. 2002. 2(5):435–440.
Article
15.Wildman RP. Healthy obesity. Curr Opin Clin Nutr Metab Care. 2009. 12(4):438–443.
16.Siriwardhana N., Kalupahana NS., Cekanova M., LeMieux M., Greer B., Moustaid-Moussa N. Modulation of adipose tissue inflammation by bioactive food compounds. J Nutr Biochem. 2013. 24(4):613–623.
Article
17.Posey KA., Clegg DJ., Printz RL., Byun J., Morton GJ., Vivekanan-dan-Giri A., Pennathur S., Baskin DG., Heinecke JW., Woods SC., Schwartz MW., Niswender KD. Hypothalamic proinflammatory lipid accumulation, inflammation, and insulin resistance in rats fed a high-fat diet. Am J Physiol Endocrinol Metab. 2009. 296(5):E1003–E1012.
Article
18.Nam KS., Kim J., Noh SK., Park JH., Sung EG. Effect of sweet persimmon wine on alcoholic fatty livers in rats. J Korean Soc Food Sci Nutr. 2011. 40(11):1548–1555.
Article
19.Yun TS., Min AK., Kim NK., Kim MK., Cho HC., Kim HS., Hwang JS., Ryu SY., Park KG., Lee IK. Effects of alpha-lipoic acid on SREBP-1c expression in HepG2 cells. J Korean Endocr Soc. 2008. 23(1):27–34.
Article
20.Marceau P., Biron S., Hould FS., Marceau S., Simard S., Thung SN., Kral JG. Liver pathology and the metabolic syndrome X in severe obesity. J Clin Endocrinol Metab. 1999. 84(5):1513–1517.
Article
21.Bruce CR., Hoy AJ., Turner N., Watt MJ., Allen TL., Carpenter K., Cooney GJ., Febbraio MA., Kraegen EW. Overexpression of carnitine palmitoyltransferase-1 in skeletal muscle is sufficient to enhance fatty acid oxidation and improve high-fat diet-induced insulin resistance. Diabetes. 2009. 58(3):550–558.
Article
Full Text Links
  • JNH
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr