Nutr Res Pract.  2024 Feb;18(1):88-97. 10.4162/nrp.2024.18.1.88.

Daraesoon (shoot of hardy kiwi) mitigates hyperglycemia in db/db mice by alleviating insulin resistance and inflammation

Affiliations
  • 1Department of Food and Nutrition, Changwon National University, Changwon 51140, Korea
  • 2Institute of Digital Anti-Aging Healthcare, Inje University, Gimhae 50834, Korea

Abstract

BACKGROUND/OBJECTIVES
Mitigating insulin resistance and hyperglycemia is associated with a decreased risk of diabetic complications. The effect of Daraesoon (shoot of hardy kiwi, Actinidia arguta) on hyperglycemia was investigated using a type 2 diabetes animal model.
MATERIALS/METHODS
Seven-week-old db/db mice were fed either an AIN-93G diet or a diet containing 0.4% of a 70% ethanol extract of Daraesoon, whereas db/+ mice were fed the AIN-93G diet for 7 weeks.
RESULTS
Consumption of Daraesoon significantly reduced serum glucose and blood glycated hemoglobin levels, along with homeostasis model assessment for insulin resistance in db/db mice. Conversely, Daraesoon elevated the serum adiponectin levels compared to the db/db control group. Furthermore, Daraesoon significantly decreased both serum and hepatic triglyceride levels, as well as serum total cholesterol levels. Additionally, consumption of Daraesoon resulted in decreased hepatic tumor necrosis factor-α and monocyte chemoattractant protein-1 expression.
CONCLUSIONS
These results suggest that hypoglycemic effect of Daraesoon is mediated through the improvement of insulin resistance and the downregulation of pro-inflammatory cytokine expression in db/db mice

Keyword

Actinidia arguta; insulin resistance; adiponectin; inflammation; db/db mice

Figure

  • Fig. 1 Protein expression of MCP-1 (A) and TNF-α (B) of the liver in db/db mice.Seven-week-old db/db mice were fed an AIN-93G diet or a diet containing 0.4% Daraesoon extract, whereas lean control group was offered the AIN-93G diet ad libitum for 7 weeks. Values represent mean ± SEM (n = 7).MCP-1, monocyte chemoattractant protein 1; TNF-α, tumor necrosis factor α; SEM, standard error of the mean.a,b,cEach bar that do not share a common letter are significantly different at P < 0.05.


Reference

1. International Diabetes Federation. IDF diabetes atlas. 10th ed [Internet]. Brussels: International Diabetes Federation;2021. cited 2023 September 10. Available from: https://diabetesatlas.org/.
2. Ormazabal V, Nair S, Elfeky O, Aguayo C, Salomon C, Zuñiga FA. Association between insulin resistance and the development of cardiovascular disease. Cardiovasc Diabetol. 2018; 17:122. PMID: 30170598.
3. Merz KE, Thurmond DC. Role of skeletal muscle in insulin resistance and glucose uptake. Compr Physiol. 2020; 10:785–809. PMID: 32940941.
4. Makki K, Froguel P, Wolowczuk I. Adipose tissue in obesity-related inflammation and insulin resistance: cells, cytokines, and chemokines. ISRN Inflamm. 2013; 2013:139239. PMID: 24455420.
5. Tilg H, Moschen AR. Inflammatory mechanisms in the regulation of insulin resistance. Mol Med. 2008; 14:222–231. PMID: 18235842.
6. Matsuzawa Y. Adiponectin: a key player in obesity related disorders. Curr Pharm Des. 2010; 16:1896–1901. PMID: 20370675.
7. Davies MJ, D’Alessio DA, Fradkin J, Kernan WN, Mathieu C, Mingrone G, Rossing P, Tsapas A, Wexler DJ, Buse JB. Management of hyperglycemia in type 2 diabetes, 2018. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care. 2018; 41:2669–2701. PMID: 30291106.
8. Giacco F, Brownlee M. Oxidative stress and diabetic complications. Circ Res. 2010; 107:1058–1070. PMID: 21030723.
9. Katakami N. Mechanism of development of atherosclerosis and cardiovascular disease in diabetes mellitus. J Atheroscler Thromb. 2018; 25:27–39. PMID: 28966336.
10. Campos C. Chronic hyperglycemia and glucose toxicity: pathology and clinical sequelae. Postgrad Med. 2012; 124:90–97. PMID: 23322142.
11. Hirano T. Pathophysiology of diabetic dyslipidemia. J Atheroscler Thromb. 2018; 25:771–782. PMID: 29998913.
12. Matsuzaka T, Shimano H. New perspective on type 2 diabetes, dyslipidemia and non-alcoholic fatty liver disease. J Diabetes Investig. 2020; 11:532–534.
13. Patel TP, Rawal K, Bagchi AK, Akolkar G, Bernardes N, Dias DD, Gupta S, Singal PK. Insulin resistance: an additional risk factor in the pathogenesis of cardiovascular disease in type 2 diabetes. Heart Fail Rev. 2016; 21:11–23. PMID: 26542377.
14. Alexandraki KI, Piperi C, Ziakas PD, Apostolopoulos NV, Makrilakis K, Syriou V, Diamanti-Kandarakis E, Kaltsas G, Kalofoutis A. Cytokine secretion in long-standing diabetes mellitus type 1 and 2: associations with low-grade systemic inflammation. J Clin Immunol. 2008; 28:314–321. PMID: 18224429.
15. Nedosugova LV, Markina YV, Bochkareva LA, Kuzina IA, Petunina NA, Yudina IY, Kirichenko TV. Inflammatory mechanisms of diabetes and its vascular complications. Biomedicines. 2022; 10:1168. PMID: 35625904.
16. Ahn JH, Park Y, Yeon SW, Jo YH, Han YK, Turk A, Ryu SH, Hwang BY, Lee KY, Lee MK. Phenylpropanoid-conjugated triterpenoids from the leaves of Actinidia arguta and their inhibitory activity on α-glucosidase. J Nat Prod. 2020; 83:1416–1423. PMID: 32315181.
17. Pinto D, Delerue-Matos C, Rodrigues F. Bioactivity, phytochemical profile and pro-healthy properties of Actinidia arguta: a review. Food Res Int. 2020; 136:109449. PMID: 32846546.
18. Lee AY, Kang MJ, Choe E, Kim JI. Hypoglycemic and antioxidant effects of Daraesoon (Actinidia arguta shoot) in animal models of diabetes mellitus. Nutr Res Pract. 2015; 9:262–267. PMID: 26060538.
19. Kwon D, Kim GD, Kang W, Park JE, Kim SH, Choe E, Kim JI, Auh JH. Pinoresinol diglucoside is screened as a putative α-glucosidase inhibiting compound in Actinidia arguta leaves. J Korean Soc Appl Bio Chem. 2014; 57:473–479.
20. Kwak CS, Lee JH. In vitro antioxidant and anti-inflammatory effects of ethanol extracts from sprout of evening primrose (Oenothera laciniata) and gooseberry (Actinidia arguta). J Korean Soc Food Sci Nutr. 2014; 43:207–215.
21. Kim GD, Lee JY, Auh JH. Metabolomic screening of anti-inflammatory compounds from the leaves of Actinidia arguta (hardy kiwi). Foods. 2019; 8:47. PMID: 30717099.
22. Bogdanov P, Corraliza L, Villena JA, Carvalho AR, Garcia-Arumí J, Ramos D, Ruberte J, Simó R, Hernández C. The db/db mouse: a useful model for the study of diabetic retinal neurodegeneration. PLoS One. 2014; 9:e97302. PMID: 24837086.
23. Piattini F, Le Foll C, Kisielow J, Rosenwald E, Nielsen P, Lutz T, Schneider C, Kopf M. A spontaneous leptin receptor point mutation causes obesity and differentially affects leptin signaling in hypothalamic nuclei resulting in metabolic dysfunctions distinct from db/db mice. Mol Metab. 2019; 25:131–141. PMID: 31076350.
24. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985; 28:412–419. PMID: 3899825.
25. 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. PMID: 13428781.
26. Wilding JP. The importance of weight management in type 2 diabetes mellitus. Int J Clin Pract. 2014; 68:682–691. PMID: 24548654.
27. Wikul A, Damsud T, Kataoka K, Phuwapraisirisan P. (+)-Pinoresinol is a putative hypoglycemic agent in defatted sesame (Sesamum indicum) seeds though inhibiting α-glucosidase. Bioorg Med Chem Lett. 2012; 22:5215–5217. PMID: 22818971.
28. Ahlstrom P, Rai E, Chakma S, Cho HH, Rengasamy P, Sweeney G. Adiponectin improves insulin sensitivity via activation of autophagic flux. J Mol Endocrinol. 2017; 59:339–350. PMID: 28954814.
29. Ruan H, Dong LQ. Adiponectin signaling and function in insulin target tissues. J Mol Cell Biol. 2016; 8:101–109. PMID: 26993044.
30. Tamura Y, Yano M, Kawao N, Okumoto K, Ueshima S, Kaji H, Matsuo O. Enzamin ameliorates adipose tissue inflammation with impaired adipocytokine expression and insulin resistance in db/db mice. J Nutr Sci. 2013; 2:e37. PMID: 25191587.
31. Yan F, Dai G, Zheng X. Mulberry anthocyanin extract ameliorates insulin resistance by regulating PI3K/AKT pathway in HepG2 cells and db/db mice. J Nutr Biochem. 2016; 36:68–80. PMID: 27580020.
32. Einarson TR, Acs A, Ludwig C, Panton UH. Prevalence of cardiovascular disease in type 2 diabetes: a systematic literature review of scientific evidence from across the world in 2007-2017. Cardiovasc Diabetol. 2018; 17:83. PMID: 29884191.
33. Bayram HM, Majoo FM, Ozturkcan A. Polyphenols in the prevention and treatment of non-alcoholic fatty liver disease: an update of preclinical and clinical studies. Clin Nutr ESPEN. 2021; 44:1–14. PMID: 34330452.
34. Rodriguez-Ramiro I, Vauzour D, Minihane AM. Polyphenols and non-alcoholic fatty liver disease: impact and mechanisms. Proc Nutr Soc. 2016; 75:47–60. PMID: 26592314.
35. Almeida D, Pinto D, Santos J, Vinha AF, Palmeira J, Ferreira HN, Rodrigues F, Oliveira MB. Hardy kiwifruit leaves (Actinidia arguta): an extraordinary source of value-added compounds for food industry. Food Chem. 2018; 259:113–121. PMID: 29680033.
36. Armandi A, Rosso C, Caviglia GP, Bugianesi E. Insulin resistance across the spectrum of nonalcoholic fatty liver disease. Metabolites. 2021; 11:155. PMID: 33800465.
37. Frankowski R, Kobierecki M, Wittczak A, Różycka-Kosmalska M, Pietras T, Sipowicz K, Kosmalski M. Type 2 diabetes mellitus, non-alcoholic fatty liver disease, and metabolic repercussions: the vicious cycle and its interplay with inflammation. Int J Mol Sci. 2023; 24:9677. PMID: 37298632.
38. Polyzos SA, Kountouras J, Zavos C. Nonalcoholic fatty liver disease: the pathogenetic roles of insulin resistance and adipocytokines. Curr Mol Med. 2009; 9:299–314. PMID: 19355912.
39. Liu Y, Song H, Wang L, Xu H, Shu X, Zhang L, Li Y, Li D, Ji G. Hepatoprotective and antioxidant activities of extracts from Salvia-Nelumbinis naturalis against nonalcoholic steatohepatitis induced by methionine- and choline-deficient diet in mice. J Transl Med. 2014; 12:315. PMID: 25406833.
40. Ni Y, Zhuge F, Nagashimada M, Ota T. Novel action of carotenoids on non-alcoholic fatty liver disease: macrophage polarization and liver homeostasis. Nutrients. 2016; 8:391. PMID: 27347998.
41. Zhong L, Huang L, Xue Q, Liu C, Xu K, Shen W, Deng L. Cell-specific elevation of Runx2 promotes hepatic infiltration of macrophages by upregulating MCP-1 in high-fat diet-induced mice NAFLD. J Cell Biochem. 2019; 120:11761–11774. PMID: 30746746.
42. Rull A, Rodríguez F, Aragonès G, Marsillach J, Beltrán R, Alonso-Villaverde C, Camps J, Joven J. Hepatic monocyte chemoattractant protein-1 is upregulated by dietary cholesterol and contributes to liver steatosis. Cytokine. 2009; 48:273–279. PMID: 19748796.
43. Haukeland JW, Damås JK, Konopski Z, Løberg EM, Haaland T, Goverud I, Torjesen PA, Birkeland K, Bjøro K, Aukrust P. Systemic inflammation in nonalcoholic fatty liver disease is characterized by elevated levels of CCL2. J Hepatol. 2006; 44:1167–1174. PMID: 16618517.
44. Ravipati AS, Zhang L, Koyyalamudi SR, Jeong SC, Reddy N, Bartlett J, Smith PT, Shanmugam K, Münch G, Wu MJ, et al. Antioxidant and anti-inflammatory activities of selected Chinese medicinal plants and their relation with antioxidant content. BMC Complement Altern Med. 2012; 12:173. PMID: 23038995.
45. Silva-Boghossian CM, Dezonne RS. What are the clinical and systemic results of periodontitis treatment in obese individuals? Curr Oral Health Rep. 2021; 8:48–65. PMID: 34367878.
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