Nutr Res Pract.  2013 Dec;7(6):446-452.

Chamnamul [Pimpinella brachycarpa (Kom.) Nakai] ameliorates hyperglycemia and improves antioxidant status in mice fed a high-fat, high-sucrose diet

Affiliations
  • 1Department of Smart Foods and Drugs, School of Food and Life Science, Inje University, 607 Obang-dong, Gimhae, Gyungnam 621-749, Korea. fdsnkiji@inje.ac.kr
  • 2Department of Food and Nutrition, Inha University, Incheon 402-751, Korea.
  • 3Department of Food Science and Technology, Chung-Ang University, Ansung, Kyunggi 456-756, Korea.

Abstract

Chronic consumption of a high-fat, high-sucrose (HFHS) diet increases insulin resistance and results in type 2 diabetes mellitus in C57BL/6J mice. Hyperglycemia in diabetics increases oxidative stress, which is associated with a high risk of diabetic complications. The purpose of this study was to examine the hypoglycemic and antioxidant effects of chamnamul [Pimpinella brachycarpa (Kom.) Nakai] in an animal model of type 2 diabetes. The alpha-glucosidase inhibitory activity of a 70% ethanol extract of chamnamul was measured in vitro. Five-week-old male C57BL/6J mice were fed a basal or HFHS diet with or without a 70% ethanol extract of chamnamul at a 0.5% level of the diet for 12 weeks after 1 week of adaptation. After sacrifice, serum glucose, insulin, adiponectin, and lipid profiles, and lipid peroxidation of the liver were determined. Homeostasis model assessment for insulin resistance (HOMA-IR) was determined. Chamnamul extract inhibited alpha-glucosidase by 26.7%, which was 78.3% the strength of inhibition by acarbose at a concentration of 0.5 mg/mL. Serum glucose, insulin, and cholesterol levels, as well as HOMA-IR values, were significantly lower in the chamnamul group than in the HFHS group. Chamnamul extract significantly decreased the level of thiobarbituric acid reactive substances and increased the activities of superoxide dismutase, catalase, and glutathione peroxidase in the liver compared with the HFHS group. These findings suggest that chamnamul may be useful in prevention of hyperglycemia and reduction of oxidative stress in mice fed a HFHS diet.

Keyword

Chamnamul [Pimpinella brachycarpa (Kom.) Nakai]; glucose; insulin; cholesterol; antioxidant effect

MeSH Terms

Acarbose
Adiponectin
alpha-Glucosidases
Animals
Antioxidants
Blood Glucose
Catalase
Cholesterol
Diabetes Complications
Diabetes Mellitus, Type 2
Diet*
Ethanol
Glucose
Glutathione Peroxidase
Homeostasis
Humans
Hyperglycemia*
Insulin
Insulin Resistance
Lipid Peroxidation
Liver
Male
Mice*
Models, Animal
Oxidative Stress
Superoxide Dismutase
Thiobarbiturates
Thiobarbituric Acid Reactive Substances
Acarbose
Adiponectin
Antioxidants
Catalase
Cholesterol
Ethanol
Glucose
Glutathione Peroxidase
Insulin
Superoxide Dismutase
Thiobarbiturates
Thiobarbituric Acid Reactive Substances
alpha-Glucosidases

Figure

  • Fig. 1 Inhibitory activities of chamnamul against yeast α-glucosidase. The inhibitory activities of the 70% ethanol extracts of chamnamul and acarbose were measured at a concentration of 0.5 mg/mL. Values represent means ± SEM of triplicate measurements.

  • Fig. 2 Lipid peroxide levels and activities of antioixdative enzymes of the liver in the mice fed the experimental diets. (A) TBARS, (B) SOD activity, (C) CAT activity and (D) GSH-Px activity. Groups are the same as in Table 2. Values are presented as mean ± SEM (n = 7). Significantly different at P < 0.05 (*) and P < 0.01 (**).


Reference

1. Danaei G, Finucane MM, Lu Y, Singh GM, Cowan MJ, Paciorek CJ, Lin JK, Farzadfar F, Khang YH, Stevens GA, Rao M, Ali MK, Riley LM, Robinson CA, Ezzati M. Global Burden of Metabolic Risk Factors of Chronic Diseases Collaborating Group (Blood Glucose). National, regional, and global trends in fasting plasma glucose and diabetes prevalence since 1980: systematic analysis of health examination surveys and epidemiological studies with 370 country-years and 2.7 million participants. Lancet. 2011; 378:31–40.
Article
2. King H, Aubert RE, Herman WH. Global burden of diabetes, 1995-2025: prevalence, numerical estimates, and projections. Diabetes Care. 1998; 21:1414–1431.
Article
3. American Diabetes Association (ADA). Summary of revisions for the 2008 clinical practice recommendations. Diabetes Care. 2008; 31:S3–S4.
4. UK Prospective Diabetes Study (UKPDS) Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet. 1998; 352:837–853.
5. Standl E, Baumgartl HJ, Füchtenbusch M, Stemplinger J. Effect of acarbose on additional insulin therapy in type 2 diabetic patients with late failure of sulphonylurea therapy. Diabetes Obes Metab. 1999; 1:215–220.
Article
6. Bressler R, Johnson D. New pharmacological approaches to therapy of NIDDM. Diabetes Care. 1992; 15:792–805.
Article
7. Joo HJ, Kang MJ, Seo TJ, Kim HA, Yoo SJ, Lee SK, Lim HJ, Byun BH, Kim JI. The hypoglycemic effect of Saururus chinensis Baill in animal models of diabetes mellitus. Food Sci Biotechnol. 2006; 15:413–417.
8. Shim YJ, Doo HK, Ahn SY, Kim YS, Seong JK, Park IS, Min BH. Inhibitory effect of aqueous extract from the gall of Rhus Chinensis on alpha-glucosidase activity and postprandial blood glucose. J Ethnopharmacol. 2003; 85:283–287.
Article
9. Wang H, Du YJ, Song HC. α-Glucosidase and α-amylase inhibitory activities of guava leaves. Food Chem. 2010; 123:6–13.
Article
10. Ministry of Food and Drug Safety (KR). Functional Food [Internet]. Cheongwon: Ministry of Food and Drug Safety;2013. cited 2013 Mar 31. Available from: http://www.foodnara.go.kr/hfoodi/.
11. Maritim AC, Sanders RA, Watkins JB 3rd. Diabetes, oxidative stress, and antioxidants: a review. J Biochem Mol Toxicol. 2003; 17:24–38.
Article
12. Kaneto H, Nakatani Y, Kawamori D, Miyatsuka T, Matsuoka TA, Matsuhisa M, Yamasaki Y. Role of oxidative stress, endoplasmic reticulum stress, and c-Jun N-terminal kinase in pancreatic β-cell dysfunction and insulin resistance. Int J Biochem Cell Biol. 2005; 37:1595–1608.
Article
13. Sinclair AJ, Girling AJ, Gray L, Lunec J, Barnett AH. An investigation of the relationship between free radical activity and vitamin C metabolism in elderly diabetic subjects with retinopathy. Gerontology. 1992; 38:268–274.
Article
14. Lean ME, Noroozi M, Kelly I, Burns J, Talwar D, Sattar N, Crozier A. Dietary flavonols protect diabetic human lymphocytes against oxidative damage to DNA. Diabetes. 1999; 48:176–181.
Article
15. Sun GR, Diao SQ, Yao DD. GC-MS analysis of essential oil from Spuriopimpinella brachycarpa. J Northeast For Univ. 2009; 37:102–103.
16. Na H, Kim KW, Kwack Y, Kim SK, Chun C. Comparative anatomy of embryogenic and non-embryogenic calli from Pimpinella brachycarpa. J Plant Biol. 2007; 50:344–350.
Article
17. Kim SJ, Min SC, Shin HJ, Lee YJ, Cho AR, Kim SY, Han J. Evaluation of the antioxidant activities and nutritional properties of ten edible plant extracts and their application to fresh ground beef. Meat Sci. 2013; 93:715–722.
Article
18. Lu J, Qian W, Xu L, Huang G, Cong W, Wang Z, Deng X, Wang D, Guan S. Phytochemical composition and toxicity of an antioxidant extract from Pimpinella brachycarpa (Kom.) Nakai. Environ Toxicol Pharmacol. 2012; 34:409–415.
Article
19. Surwit RS, Kuhn CM, Cochrane C, McCubbin JA, Feinglos MN. Diet-induced type II diabetes in C57BL/6J mice. Diabetes. 1988; 37:1163–1167.
Article
20. Surwit RS, Seldin MF, Kuhn CM, Cochrane C, Feinglos MN. Control of expression of insulin resistance and hyperglycemia by different genetic factors in diabetic C57BL/6J mice. Diabetes. 1991; 40:82–87.
Article
21. Schreyer SA, Vick C, Lystig TC, Mystkowski P, LeBoeuf RC. LDL receptor but not apolipoprotein E deficiency increases diet-induced obesity and diabetes in mice. Am J Physiol Endocrinol Metab. 2002; 282:E207–E214.
22. Watanabe J, Kawabata J, Kurihara H, Niki R. Isolation and identification of α-glucosidase inhibitors from Tochu-cha (Eucommia ulmoides). Biosci Biotechnol Biochem. 1997; 61:177–178.
Article
23. Raabo E, Terkildsen TC. On the enzymatic determination of blood glucose. Scand J Clin Lab Invest. 1960; 12:402–407.
Article
24. Grossman SH, Mollo E, Ertingshausen G. Simplified, totally enzymatic method for determination of serum triglycerides with a centrifugal analyzer. Clin Chem. 1976; 22:1310–1313.
Article
25. Kattermann R, Jaworek D, Möller G, Assmann G, Björkhem I, Svensson L, Borner K, Boerma G, Leijnse B, Desager JP, Harwengt C, Kupke I, Trinder P. Multicentre study of a new enzymatic method of cholesterol determination. J Clin Chem Clin Biochem. 1984; 22:245–251.
Article
26. Haffner SM, Miettinen H, Stern MP. The homeostasis model in the San Antonio Heart Study. Diabetes Care. 1997; 20:1087–1092.
Article
27. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95:351–358.
Article
28. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976; 72:248–254.
Article
29. Aebi H. Catalase. In : Bergmeyer HU, Gawehn K, editors. Methods of Enzymatic Analysis. New York (NY): Academic Press;1974. p. 673–684.
30. Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem. 1974; 47:469–474.
Article
31. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967; 70:158–169.
32. Yang ZH, Miyahara H, Takeo J, Katayama M. Diet high in fat and sucrose induces rapid onset of obesity-related metabolic syndrome partly through rapid response of genes involved in lipogenesis, insulin signalling and inflammation in mice. Diabetol Metab Syndr. 2012; 4:32.
Article
33. Fernandes-Santos C, Carneiro RE, de Souza Mendonca L, Aguila MB, Mandarim-de-Lacerda CA. Pan-PPAR agonist beneficial effects in overweight mice fed a high-fat high-sucrose diet. Nutrition. 2009; 25:818–827.
Article
34. Muniyappa R, Lee S, Chen H, Quon MJ. Current approaches for assessing insulin sensitivity and resistance in vivo: advantages, limitations, and appropriate usage. Am J Physiol Endocrinol Metab. 2008; 294:E15–E26.
Article
35. Lebovitz HE. α-Glucosidase inhibitors as agents in the treatment of diabetes. Diabetes Rev. 1998; 6:132–145.
36. Lee JJ, Choo MH, Lee MY. Effect of Pimpinella brachycarpa extract on lipid metabolism in rats fed high cholesterol diet. J Korean Soc Food Sci Nutr. 2006; 35:1151–1158.
Article
37. Stamler J, Vaccaro O, Neaton JD, Wentworth D. Diabetes, other risk factors, and 12-yr cardiovascular mortality for men screened in the Multiple Risk Factor Intervention Trial. Diabetes Care. 1993; 16:434–444.
Article
38. Rahimi R, Nikfar S, Larijani B, Abdollahi M. A review on the role of antioxidants in the management of diabetes and its complications. Biomed Pharmacother. 2005; 59:365–373.
Article
39. Witztum JL, Steinberg D. The oxidative modification hypothesis of atherosclerosis: does it hold for humans? Trends Cardiovasc Med. 2001; 11:93–102.
Article
40. Du X, Edelstein D, Obici S, Higham N, Zou MH, Brownlee M. Insulin resistance reduces arterial prostacyclin synthase and eNOS activities by increasing endothelial fatty acid oxidation. J Clin Invest. 2006; 116:1071–1080.
Article
41. Harman D. The aging process: major risk factor for disease and death. Proc Natl Acad Sci U S A. 1991; 88:5360–5363.
Article
42. Dröge W. Free radicals in the physiological control of cell function. Physiol Rev. 2002; 82:47–95.
Article
Full Text Links
  • NRP
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