Allium hookeri root extract restores streptozotocin-induced pancreatic β-cells dysfunction in a type 1 diabetic rat model

  • Hyun Ju Kim Kimchi Functionality Research Group, World Institute of Kimchi, Gwangju, Republic of Korea
  • Seong-Soo Roh ollege of Korean Medicine, Daegue Haany University, Daegu, Republic of Korea
  • Sung-Hyen Lee Functional Food Division, Department of Agro-food resources, National Institute of Agricultural Sciences, Rural Development Administration, Wanju, Jeonbuk, Republic of Korea
  • Miran Kang Kimchi Industry Promotion Division, World Institute of Kimchi, Gwangju, Republic of Korea
  • Jong-Sik Jin Department of Pharmacy, Jeonbuk National University, Iksan, Republic of Korea;; DLED-Agri-bio Fusion Technology Research Center, Jeonbuk National University, Iksan, Republic of Korea
Keywords: Allium hookeri root, diabetes, oxidative stress, apoptosis, β-cell regeneration

Abstract

Background: Allium hookeri (AH), a traditional herb in Southeast Asia, has been documented for its significant health benefits in metabolic diseases. This study was to explore the effects of AH root extract (AHRE) on pancreatic β-cell regeneration in streptozotocin (STZ)-induced diabetic rats.

Methods: AHRE (100 mg/kg body weight) was administered daily to STZ-induced diabetic rats for 2 weeks. Serum glucose and insulin levels, total-cholesterol, hemoglobin A1c, alanine transaminase, aspartate transaminase, and pancreatic peroxynitrite and thiobarbituric acid reactive substances were measured. Protein expression associated with pancreatic β-cell apoptosis and regeneration was analyzed through Western blotting.

Results: Diabetic rats exhibited hyperglycemia, insulin deficiency, increased levels of oxidative stress markers, and pancreatic β-cell apoptosis and impairment. AHRE treatment reduced hyperglycemia, insulin insufficiency, and oxidative stress, implying a reduction in pancreatic β-cell apoptosis and restoration of pancreatic β-cell regeneration-associated protein expression.

Conclusions: AHRE can facilitate β-cell regeneration in the impaired pancreatic islets through STZ by reducing oxidative stress markers and apoptosis in pancreatic tissue. Owing to pancreatic β-cells are susceptible to oxidative stress, the protective and enhancing effects of AHRE on the apoptosis and regeneration of these cells may be a significant mechanism for its hypoglycemic effect.

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References


1.
Cho NH, Shaw JE, Karuranga S, Huang Y, da Rocha Fernandes JD, Ohlrogge AW, et al. IDF diabetes atlas: global estimates of diabetes prevalence for 2017 and projections for 2045. Diabetes Res Clin Pract 2018; 138: 271–81. doi: 10.1016/j.diabres.2018.02.023

2.
Turner RC, Holman RR, Matthews D, Hockaday TDR, Peto J. Insulin deficiency and insulin resistance interaction in diabetes: estimation of their relative contribution by feedback analysis from basal plasma insulin and glucose concentrations. Metabolism 1979; 28: 1086–96. doi: 10.1016/0026-0495(79)90146-x

3.
Volpe CMO, Villar-Delfino PH, Dos Anjos PMF, Nogueira-Machado JA. Cellular death, reactive oxygen species (ROS) and diabetic complications. Cell Death Dis 2018; 9: 119–27. doi: 10.1038/s41419-017-0135-z

4.
Poitout V, Robertson RP. Glucolipotoxicity: fuel excess and β-cell dysfunction. Endocr Rev 2008; 29: 351–66. doi: 10.1210/er.2007-0023

5.
Bensellam M, Laybutt DR, Jonas JC. The molecular mechanisms of pancreatic beta-cell glucotoxicity: recent findings and future research direction. Mol Cell Endocrinol 2012; 364: 1–27. doi: 10.1016/j.mce.2012.08.003

6.
Nukatsuka M, Yoshimura Y, Nishida M, Kawada J. Importance of the concentration of ATP in rat pancreatic beta cells in the mechanism of streptozotocin-induced cytotoxicity. J Endocrinol 1990; 127: 161–5. doi: 10.1677/joe.0.1270161

7.
Szkudelski T. The mechanism of alloxan and streptozotocin action in B cells of the rat pancreas. Physiol Res 2001; 50: 537–46. doi: 10.1007/s00125-007-0886-7

8.
Wu J, Yan LJ. Streptozotocin-induced type 1 diabetes in rodents as a model for studying mitochondrial mechanisms of diabetic β-cell glucotoxicity. Diabetes Metab Syndr Obes 2015; 8: 181–8. doi: 10.2147/DMSO.S82272

9.
Hui H, Dotta F, Di Mario U, Perfetti R. Role of caspases in the regulation of apoptotic pancreatic islet beta-cells death. J Cell Physiol 2004; 200: 177–200. doi: 10.1002/jcp.20021

10.
Brissova M, Blaha M, Spear C, Nicholson W, Radhika A, Shiota M, et al. Reduced PDX-1 expression impairs islet response to insulin resistance and worsens glucose homeostasis. Am J Physiol Endocrinol Metab 2005; 288: E707–14. doi: 10.1152/ajpendo.00252.2004

11.
Yang BT, Dayeh TA, Volkov PA, Kirkpatrick CL, Malmgren S, Jing X, et al. Increased DNA methylation and decreased expression of PDX-1 in pancreatic islets from patients with type 2 diabetes. Mol Endocrinol 2012; 26: 1203–12. doi: 10.1210/me.2012-1004

12.
Miettinen PJ, Ustinov J, Ormio P, Gao R, Palgi J, Hakonen E, et al. Downregulation of EGF receptor signaling in pancreatic islets causes diabetes due to impaired postnatal beta-cell growth. Diabetes 2006; 55: 3299–308. doi: 10.2337/db06-0413

13.
Song Z, Fusco J, Zimmerman R, Fischbach S, Chen C, Ricks DM, et al. Epidermal growth factor receptor signaling regulates β-cell proliferation in adult mice. J Biol Chem 2016; 291: 22630–7. doi: 10.1074/jbc.M116.747840

14.
Sharma G, Gohil RN, Kaul V. Cytological status of Allium hookeri Thwaites (2n = 22). Genet Resour Crop Evol 2011; 58: 1041–50. doi: 10.1007/s10722-010-9641-x

15.
Rhyu DY, Park SH. Characterization of alkyl thiosulfinate in Allium hookeri root using HPLC-ESI-MS. J Korean Soc Appl Biol Chem 2013; 56: 457–9. doi: 10.1007/s13765-013-3069-x

16.
Ayam VS. Allium hookeri, Thw. Enum. A lesser known terrestrial perennial herb used as food and its ethnobotanical relevance in Manipur. Afric J Food Agric Nutr Develop 2011; 11: 5389–412. doi: 10.18697/ajfand.47.9330

17.
Hwang JS, Lee BH, An X, Jeong HR, Kim YE, Lee I, et al. Total phenolics, total flavonoids, and antioxidant capacity in the leaves, bulbs, and roots of Allium hookeri. Korean J Food Sci Technol 2015; 47: 261–6. doi: 10.9721/KJFST.2015.47.2.261

18.
Lee EB, Kim JH, Yang JH, Kim YS, Jun HI, Kim BH, et al. Antioxidant and longevity properties of the root of Allium hookeri in Caenorhabditis elegans. Kor J Pharmacogn 2015; 46: 234–42.

19.
Kim S, Kim DB, Lee S, Park J, Shin D, Yoo M. Profiling of organosulphur compounds using HPLC-PDA and GC/MS system and antioxidant activities in hooker chive (Allium hookeri), Nat Prod Res 2016; 30: 2798–804. doi: 10.1080/14786419.2016.1164700.

20.
Li R, Wang YF, Sun Q, Hu HB. Chemical composition and antimicrobial activity of the essential oil from Allium hookeri consumed in Xishuangbanna, southwest China. Nat Prod Commun 2014; 9: 863–4. doi: 10.1177/1934578X1400900636

21.
Singh KD, Chetia D, Gogoi N, Gogoi B, Rudrapal M. In vivo and in silico based evaluation of antidiabetic potential of an isolated flavonoid from Allium hookeri in type 2 diabetic rat model. Chem Biodiversity 2024; 21: e202301299. doi: 10.1002/cbdv.202301299.

22.
Roh SS, Kwon OJ, Yang JH, Kim YS, Lee SH, Jin JS, et al. Allium hookeri root protects oxidative stress-induced inflammatory response and β-cell damage in pancreas of streptozotocin-induced diabetic rats. BMC Complement Altern Med 2016; 16: 63–72. doi: 10.1186/s12906-016-1032-1

23.
Yang HS, Choi YJ, Jin HY, Lee SC, Huh CK. Effects of Allium hookeri root water extracts on inhibition of adipogenesis and GLUT-4 expression in 3T3-L1 adipocytes. Food Sci Biotechnol 2016; 25: 615–21. doi: 10.1007/s10068-016-0086-7

24.
Park S, No K, Lee J. Anti-obesity effect of Allium hookeri leaf extract in high-fat diet-fed mice. J Med Food 2018; 21: 254–60. doi: 10.1089/jmf.2017.3962

25.
Kim HJ, Lee MJ, Jang JY, Lee SH. Allium hookeri root extract inhibits adipogenesis by promoting lipolysis in high fat diet-induced obese mice. Nutrients 2019; 11: 2262–77. doi: 10.3390/nu11102262

26.
Rho SH, You S, Kim GH, Park HJ. Neuroprotective effect of Allium hookeri against H2O2-induced PC12 cell cytotoxicity by reducing oxidative stress. Food Sci Biotechnol 2020; 29: 1519–30. doi: 10.1007/s10068-020-00805-8

27.
Choi JH, Lee EB, Jang HH, Cha YS, Park YS, Lee SH. Allium hookeri extracts improve Scopolamine-induced cognitive impairment via activation of the cholinergic system and anti-neuroinflammation in mice. Nutrients 2021; 13: 2890. doi: 10.3390/nu13082890

28.
Jang JY, Lee MJ, You BR, Jin JS, Lee SH, Yun YR, et al. Allium hookeri root extract exerts anti-inflammatory effects by nuclear factor-κB down-regulation in lipopolysaccharide-induced RAW264.7 cells. BMC Complement Altern Med 2017; 17: 126–34. doi: 10.1186/s12906-017-1633-3

29.
Park H, Jeong J, Hyun H, Kim J, Kim H, Oh HI, et al. Effects of a hot-water extract of Allium hookeri roots on bone formation in human osteoblast-like MG-63 cells in vitro and in rats in vivo. Planta Med 2016; 82: 1410–5. doi: 10.1055/s-0042-108733

30.
Lee HA, Hong S, Yoo JH, Chung Y, Kim O. Anti-Helicobacter pylori activity and inhibition of gastritis by Allium hookeri extract. Lab Anim Res 2018; 34: 75–9. doi: 10.5625/lar.2018.34.2.75

31.
Lee YS, Lee SH, Gadde UD, Oh ST, Lee SJ, Lillehoj HS. Allium hookeri supplementation improves intestinal immune response against necrotic enteritis in young broiler chickens. Poult Sci 2018; 97: 1899–908. doi: 10.3382/ps/pey031

32.
Jeong UY, Jung J, Lee EB, Choi JH, Kim JS, Jang HH, et al. Antioxidant and immune stimulating effects of Allium hookeri extracts in the RAW264.7 cells and immune-depressed C57BL/6 mice. Antioxidants 2022; 11: 1927. doi: 10.3390/antiox11101927

33.
Park SH, Bae UJ, Choi EK, Jung SJ, Lee SH, Yang JH, et al. A randomized, double-blind, placebo-controlled crossover clinical trial to evaluate the anti-diabetic effects of Allium hookeri extract in the subjects with prediabetes. BMC Complement Med Ther 2020; 20: 211. doi: 10.1186/s12906-020-03005-3

34.
Kim JS, Kim HJ, Lee EB, Choi JH, Jung J, Jang HH, et al. Supplementary effects of Allium hookeri extract on glucose tolerance in prediabetic subjects and C57BL/KsJ-db/db mice. Pharmaceuticals 2023; 16: 1364. doi: 10.3390/ph16101364

35.
Choi JH, Kim SH, Lee EB, Kim JS, Jung JE, Jeong UY, et al. Anti-diabetic effects of Allium hookeri extracts prepared by different methods in type 2 C57BL/J-db/db mice. Pharmaceuticals 2022; 15: 486. doi: 10.3390/ph15040486

36.
Kolb-Bachofen V, Epstein S, Kiesel U, Kolb H. Low-dose streptozotocin-induced diabetes in mice: electron microscopy reveals single-cell insulitis before diabetes onset. Diabetes 1988; 37: 21–7. doi: 10.2337/diab.37.1.21

37.
Higgins GM, Anderson RM. Experimental pathology of the liver. Arch Pathol Lab Med 1931; 12: 186–202.

38.
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: 412–9. doi: 10.1007/BF00280883

39.
Kooy NW, Royall JA, Ischiropoulos H, Beckman JS. Peroxynitrite-mediated oxidation of dihydrorhodamine 123. Free Radic Biol Med 1994; 16: 149–56. doi: 10.1016/0891-5849(94)90138-4

40.
Buege JA, Aust SD. Microsomal lipid peroxidation. Methods Enzymol 1978; 52: 302–10. doi: 10.1016/s0076-6879(78)52032-6

41.
Itzhaki RF, Gill DM. A micro-biuret method for estimating proteins. Anal Biochem 1964; 9: 401–10. doi: 10.1016/0003-2697(64)90200-3

42.
Robertson RP, Harmon J, Tran PO, Tanaka Y, Takahashi H. Glucose toxicity in b-cells: type 2 diabetes, good radicals gone bad, and the glutathione connection. Diabetes 2003; 52: 581–7. doi: 10.2337/diabetes.52.3.581

43.
Tangvarasittichai S. Oxidative stress, insulin resistance, dyslipidemia and type 2 diabetes mellitus. World J Diabetes 2015; 6: 456–80. doi: 10.4239/wjd.v6.i3.456

44.
Pacher P, Szabo C. Role of peroxynitrite in the pathogenesis of cardiovascular complications of diabetes. Curr Opin Pharmacol 2006; 6: 136–41. doi: 10.1016/j.coph.2006.01.001

45.
Robertson RP. Chronic oxidative stress as a central mechanism for glucose toxicity in pancreatic islet beta cells in diabetes. J Biol Chem 2004; 279: 42351–4. doi: 10.1074/jbc.R400019200

46.
Kumari K, Augusti KT. Lipid lowering effect of S-methyl cysteine sulfoxide from Allium cepa Linn in high cholesterol diet fed rats. J Ethnopharmacol 2007; 109: 367–71. doi: 10.1016/j.jep.2006.07.045

47.
Qian R, Chen H, Lin H, Jiang Y, He P, Ding Y, et al. The protective roles of allicin on type 1 diabetes mellitus through AMPK/mTOR mediated autophagy pathway. Front Pharmacol 2023; 14: 1108730. doi: 10.3389/fphar.2023.1108730

48.
Li L, Song Q, Zhang X, Yan Y, Wang X. Allicin alleviates diabetes mellitus by inhibiting the formation of advanced glycation end products. Molecules 2022; 27: 8793. doi: 10.3390/molecules27248793

49.
Yang MH, Kim NH, Heo JD, Rho JR, Ock KJ, Shin EC, et al. Comparative evaluation of sulfur compounds contents and antiobesity properties of Allium hookeri prepared by different drying methods. Evid Based Complement Alternat Med 2017; 2017: 2436927. doi: 10.1155/2017/2436927

50.
Al-Adsani AM, Al-Otaibi AN, Barhoush SA, Al-Qattan KK, Al-Bustan SA. Expression profiling of Pdx1, Ngn3, and MafA in the liver and pancreas of recovering streptozotocin-induced diabetic rats. Genes 2022; 13: 1625. doi: 10.3390/genes13091625

51.
Park CH, Lee JY, Kim MY, Shin SH, Roh SS, Choi JS, et al. Oligonol, a low-molecular-weight polyphenol derived from lychee fruit, protects the pancreas from apoptosis and proliferation via oxidative stress in streptozotocin-induced diabetic rats. Food Funct 2016; 7: 3056–63. doi: 10.1039/c6fo00088f

52.
Okura T, Nakamura R, Ito Y, Kitao S, Anno M, Endo S, et al. Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes. BMJ Open Diabetes Res Care 2022; 10: e002908. doi: 10.1136/bmjdrc-2022-002908

53.
Samaha MM, Said E, Salem HA. Nilotinib enhances β-islets integrity and secretory functions in a rat model of STZ-induced diabetes mellitus. Eur J Pharmacol 2019; 860: 172569. doi: 10.1016/j.ejphar.2019.172569

54.
El-Huneidi W, Anjum S, Saleh MA, Bustanji Y, Abu-Gharbieh E, Taneera J. Carnosic acid protects INS-1 β-cells against streptozotocin-induced damage by inhibiting apoptosis and improving insulin secretion and glucose uptake. Molecules 2022; 27: 2102. doi: 10.3390/molecules27072102

55.
Herbst RS. Review of epidermal growth factor receptor biology. Int J Rad Oncol Biol Phys 2004; 59: 21–6. doi: 10.1016/j.ijrobp.2003.11.041

56.
Kulkarni RN, Mizrachi EB, Ocana AG, Stewart AF. Human beta-cell proliferation and intracellular signaling: driving in the dark without a road map. Diabetes 2012; 61: 2205–13. doi: 10.2337/db13-1146

57.
Chen J, Chen JK, Harris RC. EGF receptor deletion in podocytes attenuates diabetic nephropathy. J Am Soc Nephrol 2015; 26: 1115–25. doi: 10.1681/ASN.2014020192

58.
Li Z, Li Y, Overstreet JM, Chung S, Niu A, Fan X, et al. Inhibition of epidermal growth factor receptor activation is associated with improved diabetic nephropathy and insulin resistance in type 2 diabetes. Diabetes 2018; 67: 1847–57. doi: 10.2337/db17-1513

59.
Nurse P. A long twentieth century of the cell cycle and beyond. Cell 2000; 100: 71–8. doi: 10.1016/s0092-8674(00)81684-0
Published
2025-10-13
How to Cite
Kim , H. J., Roh , S.-S., Lee , S.-H., Kang , M., & Jin , J.-S. (2025). Allium hookeri root extract restores streptozotocin-induced pancreatic β-cells dysfunction in a type 1 diabetic rat model. Food & Nutrition Research, 69. https://doi.org/10.29219/fnr.v69.12104
Section
Original Articles