DOI QR코드

DOI QR Code

The effects of Allomyrina dichotoma larval extract on palmitate-induced insulin resistance in skeletal muscle cells

장수풍뎅이 유충 추출물이 고지방산 처리 골격근세포의 인슐린 저항성에 미치는 영향

  • Kim, Kyong (Department of Food and Nutrition, Eulji University) ;
  • Sim, Mi-Seong (Department of Food and Nutrition, Eulji University) ;
  • Kwak, Min-Kyu (Department of Food and Nutrition, Eulji University) ;
  • Jang, Se-Eun (Department of Food and Nutrition, Eulji University) ;
  • Oh, Yoon Sin (Department of Food and Nutrition, Eulji University)
  • 김경 (을지대학교 식품영양학과) ;
  • 심미성 (을지대학교 식품영양학과) ;
  • 곽민규 (을지대학교 식품영양학과) ;
  • 장세은 (을지대학교 식품영양학과) ;
  • 오윤신 (을지대학교 식품영양학과)
  • Received : 2022.02.03
  • Accepted : 2022.07.21
  • Published : 2022.08.31

Abstract

Purpose: Allomyrina dichotoma larvae are one of the approved edible insects with nutritional value and various functional and medicinal properties. Previously we have demonstrated that the Allomyrina dichotoma larval extract (ADLE) ameliorates hepatic insulin resistance in high-fat diet (HFD)-induced diabetic mice through the activation of adenosine monophosphate-activated protein kinase (AMPK). This study investigated the effects of ADLE on insulin resistance in the skeletal muscle and explored mechanisms for enhancing the glucose uptake in palmitate (PAL)-treated C2C12 myotubes. Methods: To induce insulin resistance, the differentiated C2C12 myotubes were treated with PAL (0.5 mM) for 24 hours, and then treated with a 0.5 mg/ml concentration of ADLE, and the resultant effects were measured. The expression levels of glucose transporter-4 (GLUT4), AMPK, and the mitochondrial metabolism-related proteins were analyzed by western blotting. The mRNA expression levels of lipogenesis- related genes were determined by quantitative reverse-transcriptase PCR. Results: The exposure of C2C12 myotubes to 0.5 mg/ml of ADLE increased cell viability significantly compared to PAL-treated cells. ADLE upregulated the protein expression of GLUT4 and enhanced glucose uptake in the PAL-treated cells. ADLE increased the phosphorylated AMPK in both the PAL-treated C2C12 myotubes and HFD-treated skeletal muscle. The reduced expression levels of peroxisome-proliferator-activated receptor gamma co-activator-1 alpha (PGC1α) and uncoupling protein 3 (UCP3) due to the PAL and HFD treatment were reversed by the ADLE treatment. The citrate synthase activity was also significantly increased with the PAL and ADLE co-treatment. Moreover, the mRNA and protein expressions of fatty acid synthesis-related factors were reduced in the PAL and HFD-treated muscle cells, and this effect was significantly attenuated by the ADLE treatment. Conclusion: ADLE activates AMPK, which in turn induces mitochondrial metabolism and reduces fatty acid synthesis in C2C12 myotubes. Therefore, ADLE could be useful for preventing or treating insulin resistance of skeletal muscles in diabetes.

본 연구는 팔미트산으로 인슐린 저항성을 유도한 C2C12 근육세포주에서 ADLE의 인슐린 저항성개선효과를조사하고이에대한조절기전을확인하고자하였다. C2C12 근육세포주에 ADLE를 처리 시, AMPK의 활성화를 통해 포도당흡수 (glucose uptake)가 증가되었으며, 이는 미토콘드리아-매개 에너지 생합성 조절단백질인 PGC1α, UCP3, CS 활성을 증가시킴과 동시에 지방산 합성인자인 ACC, FAS, SREBP-1의 발현을 억제함을 알 수 있었다. 세포주에서 확인된 결과들을 고지방식이 유도 당뇨마우스의 근육조직에서 조사한 결과, 고지방식이와 ADLE를 동시에 처리한 그룹에서 AMPK 활성화, GLUT4 발현증가와 미토콘드리아 에너지 대사증가, 지방산 합성 감소효과를 보였다. 이상의 결과들로, ADLE가 근육 내 에너지 대사 관련 경로의 상위유전자인 AMPK를 활성화하여 GLUT4의 세포막 이동을 증진시켜 당대사 조절에 관여하는 것을 관찰하였으며, AMPK의 인산화 증가는 PGC1α의 활성화에 관여하고, 이를 통해 열 발산 대사와 관련된 UCP3의 증가 및 CS 활성을 증가시키고, 지방산 합성 관련 유전자 발현을 억제시킴을 알 수 있었다. 본 결과로부터 ADLE는 대사증후군에서 공통적으로 나타나는 인슐린 저항성을 개선시킬 수 있으며, 이는 근육세포에서의 AMPK의 활성화를 통한 에너지생성기전과 관련이 있음을 알 수 있었다. ADLE는 비만, 당뇨 등의 다양한 부작용을 가진 약제와는 다른 안전성을 보장할 수 있는 이점을 가지고 있어 인슐린 저항성 및 제2형 당뇨병 치료를 위한 기능성 식품 소재로의 활용 가능성도 충분히 가지고 있음을 확인할 수 있었다.

Keywords

Acknowledgement

This study was supported by Basic Science Research Program grant (NRF-2021R1F1A1050949) provided by the National Research Foundation of Korea (NRF), which is funded by the Ministry of Science, ICT and Future Planning.

References

  1. Defronzo RA. Banting lecture. From the triumvirate to the ominous octet: a new paradigm for the treatment of type 2 diabetes mellitus. Diabetes 2009; 58(4): 773-795. https://doi.org/10.2337/db09-9028
  2. Dube JJ, Amati F, Stefanovic-Racic M, Toledo FG, Sauers SE, Goodpaster BH. Exercise-induced alterations in intramyocellular lipids and insulin resistance: the athlete's paradox revisited. Am J Physiol Endocrinol Metab 2008; 294(5): E882-E888. https://doi.org/10.1152/ajpendo.00769.2007
  3. Abbud W, Habinowski S, Zhang JZ, Kendrew J, Elkairi FS, Kemp BE, et al. Stimulation of AMP-activated protein kinase (AMPK) is associated with enhancement of Glut1-mediated glucose transport. Arch Biochem Biophys 2000; 380(2): 347-352. https://doi.org/10.1006/abbi.2000.1935
  4. Zheng D, MacLean PS, Pohnert SC, Knight JB, Olson AL, Winder WW, et al. Regulation of muscle GLUT-4 transcription by AMP-activated protein kinase. J Appl Physiol (1985) 2001; 91(3): 1073-1083. https://doi.org/10.1152/jappl.2001.91.3.1073
  5. Fediuc S, Gaidhu MP, Ceddia RB. Regulation of AMP-activated protein kinase and acetyl-CoA carboxylase phosphorylation by palmitate in skeletal muscle cells. J Lipid Res 2006; 47(2): 412-420. https://doi.org/10.1194/jlr.M500438-JLR200
  6. Winder WW, Hardie DG. AMP-activated protein kinase, a metabolic master switch: possible roles in type 2 diabetes. Am J Physiol 1999; 277(1): E1-E10.
  7. Hardie DG, Sakamoto K. AMPK: a key sensor of fuel and energy status in skeletal muscle. Physiology (Bethesda) 2006; 21(1): 48-60. https://doi.org/10.1152/physiol.00044.2005
  8. Wu H, Ballantyne CM. Skeletal muscle inflammation and insulin resistance in obesity. J Clin Invest 2017; 127(1): 43-54. https://doi.org/10.1172/jci88880
  9. Ghosh S, Lee SM, Jung C, Meyer-Rochow VB. Nutritional composition of five commercial edible insects in South Korea. J Asia Pac Entomol 2017; 20(2): 686-694. https://doi.org/10.1016/j.aspen.2017.04.003
  10. Yoon YI, Chung MY, Hwang JS, Han MS, Goo TW, Yun EY. Allomyrina dichotoma (Arthropoda: Insecta) larvae confer resistance to obesity in mice fed a high-fat diet. Nutrients 2015; 7(3): 1978-1991. https://doi.org/10.3390/nu7031978
  11. Song MH, Han MH, Kwak KW, Lee S, Kim ES, Park KH, et al. Effect of different diets on growth and development of the two-spotted cricket, Gryllus bimaculatus (Orthoptera: Gryllidae). Int J Indust Entomol 2016; 33(2): 59-62. https://doi.org/10.7852/IJIE.2016.33.2.59
  12. Lee JE, Jo DE, Lee AJ, Park HK, Youn K, Yun EY, et al. Hepatoprotective and anticancer activities of Allomyrina dichotoma larvae. J Life Sci 2015; 25(3): 307-316. https://doi.org/10.5352/JLS.2015.25.3.307
  13. Shin CS, Kim DY, Shin WS. Characterization of chitosan extracted from Mealworm Beetle (Tenebrio molitor, Zophobas morio) and Rhinoceros Beetle (Allomyrina dichotoma) and their antibacterial activities. Int J Biol Macromol 2019; 125: 72-77. https://doi.org/10.1016/j.ijbiomac.2018.11.242
  14. Kim M, Youn K, Yun EY, Hwang JS, Ahn MR, Jeong WS, et al. Effects of solvent fractions of Allomyrina dichotoma larvae through the inhibition of in vitro BACE1 and β-amyloid(25-35)-induced toxicity in rat pheochromocytoma PC12 cells. Entomol Res 2014; 44(1): 23-30. https://doi.org/10.1111/1748-5967.12046
  15. Kim K, Bae GD, Lee M, Park EY, Baek DJ, Kim CY, et al. Allomyrina dichotoma larva extract ameliorates the hepatic insulin resistance of high-fat diet-induced diabetic mice. Nutrients 2019; 11(7): 1522.
  16. Kim K, Bae GD, Park EY, Baek DJ, Kim CY, Jang SE, et al. Allomyrina dichotoma larval extract attenuates intestinal barrier disruption by altering inflammatory response and tight junction proteins in lipopolysaccharide-induced Caco-2 cells. Biochem Biophys Res Commun 2020; 532(1): 145-150. https://doi.org/10.1016/j.bbrc.2020.08.034
  17. Kim K, Park EY, Baek DJ, Kim CY, Oh YS. Anti-inflammatory activity of AF-13, an antioxidant compound isolated from the polar fraction of Allomyrina dichotoma larva, in palmitate-induced INS-1 cells. Life (Basel) 2021; 11(6): 470.
  18. Kim K, Kwak MK, Bae GD, Park EY, Baek DJ, Kim CY, et al. Allomyrina dichotoma larva extract attenuates free fatty acid-induced lipotoxicity in pancreatic beta cells. Nutr Res Pract 2021; 15(3): 294-308. https://doi.org/10.4162/nrp.2021.15.3.294
  19. Guo W, Wong S, Xie W, Lei T, Luo Z. Palmitate modulates intracellular signaling, induces endoplasmic reticulum stress, and causes apoptosis in mouse 3T3-L1 and rat primary preadipocytes. Am J Physiol Endocrinol Metab 2007; 293(2): E576-E586. https://doi.org/10.1152/ajpendo.00523.2006
  20. Benoit SC, Kemp CJ, Elias CF, Abplanalp W, Herman JP, Migrenne S, et al. Palmitic acid mediates hypothalamic insulin resistance by altering PKC-theta subcellular localization in rodents. J Clin Invest 2009; 119(9): 2577-2589. https://doi.org/10.1172/JCI36714
  21. Funaki M. Saturated fatty acids and insulin resistance. J Med Invest 2009; 56(3-4): 88-92. https://doi.org/10.2152/jmi.56.88
  22. Hardie DG. Minireview: the AMP-activated protein kinase cascade: the key sensor of cellular energy status. Endocrinology 2003; 144(12): 5179-5183. https://doi.org/10.1210/en.2003-0982
  23. Foretz M, Ancellin N, Andreelli F, Saintillan Y, Grondin P, Kahn A, et al. Short-term overexpression of a constitutively active form of AMP-activated protein kinase in the liver leads to mild hypoglycemia and fatty liver. Diabetes 2005; 54(5): 1331-1339. https://doi.org/10.2337/diabetes.54.5.1331
  24. Shepherd PR, Kahn BB. Glucose transporters and insulin action-Implications for insulin resistance and diabetes mellitus. N Engl J Med 1999; 341(4): 248-257. https://doi.org/10.1056/NEJM199907223410406
  25. Jager S, Handschin C, St-Pierre J, Spiegelman BM. AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1α. Proc Natl Acad Sci U S A 2007; 104(29): 12017-12022. https://doi.org/10.1073/pnas.0705070104
  26. Woods A, Azzout-Marniche D, Foretz M, Stein SC, Lemarchand P, Ferre P, et al. Characterization of the role of AMP-activated protein kinase in the regulation of glucose-activated gene expression using constitutively active and dominant negative forms of the kinase. Mol Cell Biol 2000; 20(18): 6704-6711. https://doi.org/10.1128/MCB.20.18.6704-6711.2000
  27. Foretz M, Carling D, Guichard C, Ferre P, Foufelle F. AMP-activated protein kinase inhibits the glucoseactivated expression of fatty acid synthase gene in rat hepatocytes. J Biol Chem 1998; 273(24): 14767-14771. https://doi.org/10.1074/jbc.273.24.14767
  28. Chang L, Chiang SH, Saltiel AR. Insulin signaling and the regulation of glucose transport. Mol Med 2004; 10(7-12): 65-71. https://doi.org/10.2119/2005-00029.Saltiel
  29. Petersen KF, Shulman GI. Pathogenesis of skeletal muscle insulin resistance in type 2 diabetes mellitus. Am J Cardiol 2002; 90(5A): 11G-18G.
  30. Stoppani J, Hildebrandt AL, Sakamoto K, Cameron-Smith D, Goodyear LJ, Neufer PD. AMP-activated protein kinase activates transcription of the UCP3 and HKII genes in rat skeletal muscle. Am J Physiol Endocrinol Metab 2002; 283(6): E1239-E1248. https://doi.org/10.1152/ajpendo.00278.2002
  31. Zou MH, Kirkpatrick SS, Davis BJ, Nelson JS, Wiles WG 4th, Schlattner U, et al. Activation of the AMP-activated protein kinase by the anti-diabetic drug metformin in vivo. Role of mitochondrial reactive nitrogen species. J Biol Chem 2004; 279(42): 43940-43951. https://doi.org/10.1074/jbc.M404421200
  32. Choi HC. AMP-activated protein kinase activating agent and its implication. Endocrinol Metab (Seoul) 2012; 27(2): 109-115. https://doi.org/10.3803/EnM.2012.27.2.109
  33. Kuo YH, Lin CH, Shih CC. Ergostatrien-3β-ol from Antrodia camphorata inhibits diabetes and hyperlipidemia in high-fat-diet treated mice via regulation of hepatic related genes, glucose transporter 4, and AMP-activated protein kinase phosphorylation. J Agric Food Chem 2015; 63(9): 2479-2489. https://doi.org/10.1021/acs.jafc.5b00073
  34. Ji L, Zhang X, Liu W, Huang Q, Yang W, Fu F, et al. AMPK-regulated and Akt-dependent enhancement of glucose uptake is essential in ischemic preconditioning-alleviated reperfusion injury. PLoS One 2013; 8(7): e69910.
  35. Petersen KF, Befroy D, Dufour S, Dziura J, Ariyan C, Rothman DL, et al. Mitochondrial dysfunction in the elderly: possible role in insulin resistance. Science 2003; 300(5622): 1140-1142. https://doi.org/10.1126/science.1082889
  36. Kim JA, Wei Y, Sowers JR. Role of mitochondrial dysfunction in insulin resistance. Circ Res 2008; 102(4): 401-414. https://doi.org/10.1161/CIRCRESAHA.107.165472
  37. Kelley DE, He J, Menshikova EV, Ritov VB. Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes. Diabetes 2002; 51(10): 2944-2950. https://doi.org/10.2337/diabetes.51.10.2944
  38. Simoneau JA, Veerkamp JH, Turcotte LP, Kelley DE. Markers of capacity to utilize fatty acids in human skeletal muscle: relation to insulin resistance and obesity and effects of weight loss. FASEB J 1999; 13(14): 2051-2060. https://doi.org/10.1096/fasebj.13.14.2051
  39. He J, Watkins S, Kelley DE. Skeletal muscle lipid content and oxidative enzyme activity in relation to muscle fiber type in type 2 diabetes and obesity. Diabetes 2001; 50(4): 817-823. https://doi.org/10.2337/diabetes.50.4.817
  40. Choi CS, Fillmore JJ, Kim JK, Liu ZX, Kim S, Collier EF, et al. Overexpression of uncoupling protein 3 in skeletal muscle protects against fat-induced insulin resistance. J Clin Invest 2007; 117(7): 1995-2003. https://doi.org/10.1172/JCI13579
  41. Lin J, Handschin C, Spiegelman BM. Metabolic control through the PGC-1 family of transcription coactivators. Cell Metab 2005; 1(6): 361-370. https://doi.org/10.1016/j.cmet.2005.05.004
  42. Liang H, Ward WF. PGC-1alpha: a key regulator of energy metabolism. Adv Physiol Educ 2006; 30(4): 145-151. https://doi.org/10.1152/advan.00052.2006
  43. Lagouge M, Argmann C, Gerhart-Hines Z, Meziane H, Lerin C, Daussin F, et al. Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1α. Cell 2006; 127(6): 1109-1122. https://doi.org/10.1016/j.cell.2006.11.013
  44. Ouchi N, Shibata R, Walsh K. AMP-activated protein kinase signaling stimulates VEGF expression and angiogenesis in skeletal muscle. Circ Res 2005; 96(8): 838-846. https://doi.org/10.1161/01.RES.0000163633.10240.3b
  45. Park SH, Gammon SR, Knippers JD, Paulsen SR, Rubink DS, Winder WW. Phosphorylation-activity relationships of AMPK and acetyl-CoA carboxylase in muscle. J Appl Physiol (1985) 2002; 92(6): 2475-2482. https://doi.org/10.1152/japplphysiol.00071.2002
  46. Hardie DG. The AMP-activated protein kinase pathway--new players upstream and downstream. J Cell Sci 2004; 117(Pt 23): 5479-5487. https://doi.org/10.1242/jcs.01540
  47. Colinet D, Cazes D, Belghazi M, Gatti JL, Poirie M. Extracellular superoxide dismutase in insects: characterization, function, and interspecific variation in parasitoid wasp venom. J Biol Chem 2011; 286(46): 40110-40121. https://doi.org/10.1074/jbc.M111.288845
  48. Corona M, Robinson GE. Genes of the antioxidant system of the honey bee: annotation and phylogeny. Insect Mol Biol 2006; 15(5): 687-701. https://doi.org/10.1111/j.1365-2583.2006.00695.x