Mechanisms of combined deer antler polysaccharides and postbiotics supplementation for regulating obesity in mice

  • Lanyue Yin College of Food Science and Nutrition Engineering, Jilin Agricultural Science and Technology University, Jilin, China
  • Jiating Li School of Public health, Jilin Medical University, Jilin, P.R. China
  • Xueyue Tai College of Food Science and Engineering, Changchun University, Changchun, China
  • Guoqi Zhang College of Food Science and Nutrition Engineering, Jilin Agricultural Science and Technology University, Jilin, China; College of Food Science and Engineering, Changchun University, Changchun, China
  • Mingran Luan College of Food Science and Nutrition Engineering, Jilin Agricultural Science and Technology University, Jilin, China
  • Bao Zhong College of Food Science and Nutrition Engineering, Jilin Agricultural Science and Technology University, Jilin, China
  • Fenglin Li College of Food Science and Nutrition Engineering, Jilin Agricultural Science and Technology University, Jilin, China
Keywords: deer antler polysaccharides, postbiotics, lipid metabolism, regulatory effects

Abstract

Objective: This study investigated the mechanisms related to lipid metabolism regulation after combined supplementation with deer antler polysaccharides and postbiotics.

Methods: Thirty-two male mice were divided into high-fat diet, HD + deer antler polysaccharides, HD + Bacillus coagulans postbiotics, and HD + deer antler polysaccharides + B. coagulans postbiotics groups. The diets contained 60% fat. After 9 weeks, the effects of deer antler polysaccharides and postbiotics on lipid metabolism were assessed through blood biochemical, histological tissue staining, and polymerase chain reaction analyses.

Results: Supplementation with deer antler polysaccharides and postbiotics significantly inhibited weight gain in obese mice, reduced serum total cholesterol, triglyceride, and low-density lipoprotein levels and markedly increased the serum high-density lipoprotein level. Additionally, hepatic lipid droplet accumulation and adipocyte hypertrophy improved. The expressions of the lipid synthesis genes, sterol regulatory element-binding protein 1 (i.e. SREBP-1c), and fatty acid synthase (i.e. FAS), significantly decreased, while peroxisome proliferator-activated receptor alpha (i.e. PPAR-α) and acyl-CoA oxidase 1 (i.e. ACOX1) expression significantly increased. The expressions of the inflammation-related genes, tumor necrosis factor-alpha (i.e. TNF-α), interleukin (IL)-6, and IL-1 also significantly decreased.

Conclusion: Thus, combined deer antler polysaccharides and postbiotic supplementation regulated obesity in mice, potentially by modulating lipid synthesis and inflammation-related gene expression.

Downloads

Download data is not yet available.

References


1.
Goossens GH. The metabolic phenotype in obesity: fat mass, body fat distribution, and adipose tissue function. Obes Facts 2017; 10(3): 207–15. doi: 10.1159/000471488


2.
Hruby A, Hu FBJP. The epidemiology of obesity: a big picture. Pharmacoeconomics 2015; 33: 673–89. doi: 10.1007/s40273-014-0243-x


3.
Schwartz MW, Seeley RJ, Zeltser LM, et al. Obesity pathogenesis: an endocrine society scientific statement. Endocrine reviews 2017; 38(4): 267–96. doi: 10.1210/er.2017-00111


4.
Swinburn BA, Sacks G, Hall KD, et al. The global obesity pandemic: shaped by global drivers and local environments. The lancet 2011; 378(9793): 804–14. doi: 10.1016/S0140-6736(11)60813-1


5.
Rosen ED, Spiegelman BMJC. What we talk about when we talk about fat. Cell 2014; 156(1): 20–44. doi: 10.1016/j.cell.2013.12.012


6.
Kim YJ, Park JW, Kim JW, et al. Computerized automated quantification of subcutaneous and visceral adipose tissue from computed tomography scans: development and validation study. JMIR medical informatics 2016; 4(1): e4923. doi: 10.2196/medinform.4923


7.
Mlinar B, Marc J, Janež A, Pfeifer MJCca. Molecular mechanisms of insulin resistance and associated diseases. Clinica chimica acta 2007; 375(1–2): 20–35. doi: 10.1016/j.cca.2006.07.005


8.
Albuquerque D, Stice E, Rodriguez-Lopez R, Manco L, Nobrega C. Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspective. Mol Genet Genomics 2015; 290(4): 1191–221. doi: 10.1007/s00438-015-1015-9


9.
Barbagallo F, Condorelli RA, Mongioi LM, et al. Molecular mechanisms underlying the relationship between obesity and male infertility. Metabolites 2021; 11(12): 840. doi: 10.3390/metabo11120840


10.
Kolehmainen M, Vidal H, Alhava E, Uusitupa MI. Sterol regulatory element binding protein 1c (SREBP-1c) expression in human obesity. Obes Res 2001; 9(11): 706–12. doi: 10.1038/oby.2001.95


11.
Dentin R, Girard J, Postic C. Carbohydrate responsive element binding protein (ChREBP) and sterol regulatory element binding protein-1c (SREBP-1c): two key regulators of glucose metabolism and lipid synthesis in liver. Biochimie 2005; 87(1): 81–6. doi: 10.1016/j.biochi.2004.11.008


12.
Tahri-Joutey M, Andreoletti P, Surapureddi S, Nasser B, Cherkaoui-Malki M, Latruffe N. Mechanisms mediating the regulation of peroxisomal fatty acid beta-oxidation by PPARalpha. Int J Mol Sci 2021; 22(16): 8969. doi: 10.3390/ijms22168969


13.
Huang J, Viswakarma N, Yu S, et al. Progressive endoplasmic reticulum stress contributes to hepatocarcinogenesis in fatty acyl-CoA oxidase 1-deficient mice. Am J Pathol 2011; 179(2): 703–13. doi: 10.1016/j.ajpath.2011.04.030


14.
Mohammad IJ, Kashanian S, Rafipour R, Aljwaid H, Hashemi S. Evaluation of the relationship of cytokines concentrations tumor necrosis factor-alpha, interleukin-6, and C-reactive protein in obese diabetics and obese non-diabetics: a comparative study. Biotechnol Appl Biochem 2024; 71(2): 272–9. doi: 10.1002/bab.2539


15.
Cooke AA, Connaughton RM, Lyons CL, McMorrow AM, Roche HM. Fatty acids and chronic low grade inflammation associated with obesity and the metabolic syndrome. Eur J Pharmacol 2016; 785: 207–14. doi: 10.1016/j.ejphar.2016.04.021


16.
Lee YH, Pratley RE. The evolving role of inflammation in obesity and the metabolic syndrome. Curr Diab Rep 2005; 5(1): 70–5. doi: 10.1007/s11892-005-0071-7


17.
Wing RR, Phelan SJTAjocn. Long-term weight loss maintenance. The American journal of clinical nutrition 2005; 82(1): 222S–5S. doi: 10.1093/ajcn.82.1.222S


18.
Foster-Schubert KE, Cummings DEJEr. Emerging therapeutic strategies for obesity. Endocrine reviews 2006; 27(7): 779–93. doi: 10.1210/er.2006-0041


19.
Chan Y, Ng SW, Tan JZX, et al. Natural products in the management of obesity: fundamental mechanisms and pharmacotherapy. South African Journal of Botany 2021; 143: 176–97. doi: 10.1016/j.sajb.2021.07.026


20.
Park S-J, Sharma A, Lee H-JJIJoMS. Postbiotics against obesity: perception and overview based on pre-clinical and clinical studies. International Journal of Molecular Sciences 2023; 24(7): 6414. doi: 10.3390/ijms24076414


21.
Sun H, Xiao D, Liu W, et al. Well-known polypeptides of deer antler velvet with key actives: modern pharmacological advances. Naunyn Schmiedebergs Arch Pharmacol 2024; 397(1): 15–31. doi: 10.1007/s00210-023-02642-y


22.
Wu F, Li H, Jin L, et al. Deer antler base as a traditional Chinese medicine: a review of its traditional uses, chemistry and pharmacology. Journal of Ethnopharmacology 2013; 145(2): 403–15. doi: 10.1016/j.jep.2012.12.008


23.
Orassay A, Sadvokassova D, Berdigaliyev A, et al. Deer antler extract: pharmacology, rehabilitation and sports medicine applications. Pharmacological Research-Modern Chinese Medicine 2024; 10: 100316. doi: 10.1016/j.prmcm.2023.100316


24.
Sui Z, Zhang L, Huo Y, Zhang Y. Bioactive components of velvet antlers and their pharmacological properties. J Pharm Biomed Anal 2014; 87: 229–40. doi: 10.1016/j.jpba.2013.07.044


25.
Chang J-S, Lin H-J, Deng J-S, et al. Preventive effects of velvet antler (Cervus elaphus) against lipopolysaccharide-induced acute lung injury in mice by inhibiting MAPK/NF-κB activation and inducing AMPK/Nrf2 pathways. Evidence-Based Complementary and Alternative Medicine 2018; 2018(1): 2870503. doi: 10.1155/2018/2870503


26.
Cheng W-J, Yang H-T, Chiang C-C, et al. Deer velvet antler extracts exert anti-inflammatory and anti-arthritic effects on human rheumatoid arthritis fibroblast-like synoviocytes and distinct mouse arthritis. The American Journal of Chinese Medicine 2022; 50(06): 1617–43. doi: 10.1142/S0192415X22500689


27.
Lei Z, Ji B-P, Bo L, et al. Immunomodulatory effects of aqueous extract of velvet antler (Cervus elaphus Linnaeus) and its simulated gastrointestinal digests on immune cells in vitro. Journal of Food and Drug Analysis 2009; 17(4): 1. doi: 10.38212/2224-6614.2595


28.
Cui XS, Kim HI, Cho SKJJoAS, Technology. Effect of the water soluble extracts from velvet antler on lipid metabolism and blood components in rats. Journal of Animal Science and Technology 2008; 50(3): 417–28.


29.
Ding Y, Wang Y, Jeon BT, Moon SH, Lee SH. Enzymatic hydrolysate from velvet antler suppresses adipogenesis in 3T3-L1 cells and attenuates obesity in high-fat diet-fed mice. EXCLI J 2017; 16: 328–39. doi: 10.17179/excli2016-638


30.
Bourebaba Y, Marycz K, Mularczyk M, Bourebaba L. Postbiotics as potential new therapeutic agents for metabolic disorders management. Biomed Pharmacother 2022; 153: 113138. doi: 10.1016/j.biopha.2022.113138


31.
Li HY, Zhou DD, Gan RY, et al. Effects and mechanisms of probiotics, prebiotics, synbiotics, and postbiotics on metabolic diseases targeting gut microbiota: a narrative review. Nutrients 2021; 13(9): 3211[EB/OL]. doi: 10.3390/nu13093211


32.
Napolitano M, Fasulo E, Ungaro F, et al. Gut dysbiosis in irritable bowel syndrome: a narrative review on correlation with disease subtypes and novel therapeutic implications. Microorganisms 2023; 11(10): 2369. doi: 10.3390/microorganisms11102369


33.
Huang J, Jiang R, Wang Y. Effects of the probiotic Bacillus coagulans BC69 on the metabolic and histological alterations induced by a high-sugar and high-fat diet in C57BL/6J mice. Food Funct 2023; 14(14): 6596–609. doi: 10.1039/d3fo01104f


34.
Cutting SM. Bacillus probiotics. Food Microbiol 2011; 28(2): 214–20. doi: 10.1016/j.fm.2010.03.007


35.
Jiang N, Zhang S, Zhu J, Shang J, Gao X. Hypoglycemic, hypolipidemic and antioxidant effects of peptides from red deer antlers in streptozotocin-induced diabetic mice. Tohoku J Exp Med 2015; 236(1): 71–9. doi: 10.1620/tjem.236.71


36.
Cani PD, Bibiloni R, Knauf C, et al. Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet-induced obesity and diabetes in mice. Diabetes 2008; 57(6): 1470–81. doi: 10.2337/db07-1403


37.
Hsieh RH, Chien YJ, Lan WY, et al. Bacillus coagulans TCI711 supplementation improved nonalcoholic fatty liver by modulating gut microbiota: a randomized, placebo-controlled, clinical trial. Curr Dev Nutr 2024; 8(3): 102083. doi: 10.1016/j.cdnut.2024.102083


38.
Chen H, Tan H, Wan J, et al. PPAR-gamma signaling in nonalcoholic fatty liver disease: pathogenesis and therapeutic targets. Pharmacol Ther 2023; 245: 108391. doi:10.1016/j.pharmthera.2023.108391


39.
Puengel T, Liu H, Guillot A, Heymann F, Tacke F, Peiseler M. Nuclear receptors linking metabolism, inflammation, and fibrosis in nonalcoholic fatty liver disease. Int J Mol Sci 2022; 23(5): 2668. doi: 10.3390/ijms23052668


40.
Huo X, Yang S, Sun X, Meng X, Zhao Y. Protective effect of glycyrrhizic acid on alcoholic liver injury in rats by modulating lipid metabolism. Molecules 2018; 23(7): 1623. doi: 10.3390/molecules23071623


41.
Coll T, Rodriguez-Calvo R, Barroso E, et al. Peroxisome proliferator-activated receptor (PPAR) beta/delta: a new potential therapeutic target for the treatment of metabolic syndrome. Curr Mol Pharmacol 2009; 2(1): 46–55. doi: 10.2174/1874467210902010046


42.
Ferre P, Foufelle F. Hepatic steatosis: a role for de novo lipogenesis and the transcription factor SREBP-1c. Diabetes Obes Metab 2010; 12 Suppl 2: 83–92. doi: 10.1111/j.1463-1326.2010.01275.x


43.
Illesca P, Valenzuela R, Espinosa A, et al. Hydroxytyrosol supplementation ameliorates the metabolic disturbances in white adipose tissue from mice fed a high-fat diet through recovery of transcription factors Nrf2, SREBP-1c, PPAR-gamma and NF-kappaB. Biomed Pharmacother 2019; 109: 2472–81. doi: 10.1016/j.biopha.2018.11.120


44.
Ying W, Fu W, Lee YS, Olefsky JM. The role of macrophages in obesity-associated islet inflammation and beta-cell abnormalities. Nat Rev Endocrinol 2020; 16(2): 81–90. doi: 10.1038/s41574-019-0286-3


45.
Miller YI, Shyy JY. Context-dependent role of oxidized lipids and lipoproteins in inflammation. Trends Endocrinol Metab 2017; 28(2): 143–52. doi: 10.1016/j.tem.2016.11.002


46.
Collins KH, Herzog W, MacDonald GZ, et al. Obesity, metabolic syndrome, and musculoskeletal disease: common inflammatory pathways suggest a central role for loss of muscle integrity. Front Physiol 2018; 9: 112. doi: 10.3389/fphys.2018.00112


47.
Varra FN, Varras M, Varra VK, Theodosis-Nobelos P. Molecular and pathophysiological relationship between obesity and chronic inflammation in the manifestation of metabolic dysfunctions and their inflammation‑mediating treatment options (Review). Mol Med Rep 2024; 29(6): 95. doi: 10.3892/mmr.2024.13219


48.
Dali-Youcef N, Mecili M, Ricci R, Andres E. Metabolic inflammation: connecting obesity and insulin resistance. Ann Med 2013; 45(3): 242–53. doi: 10.3109/07853890.2012.705015


49.
Bastard JP, Maachi M, Lagathu C, et al. Recent advances in the relationship between obesity, inflammation, and insulin resistance. Eur Cytokine Netw 2006; 17(1): 4–12.


50.
Yang H, Wang L, Sun H, He X, Zhang J, Liu FJJoFB. Anticancer activity in vitro and biological safety evaluation in vivo of Sika deer antler protein. Journal of Food Biochemistry 2017; 41(6): e12421. doi: 10.1111/jfbc.12421


51.
Ji J, Jin W, Liu SJ, Jiao Z, Li XJM. Probiotics, prebiotics, and postbiotics in health and disease. MedComm 2023; 4(6): e420. doi: 10.1002/mco2.420
Published
2025-01-28
How to Cite
Yin , L., Li , J., Tai , X., Zhang , G., Luan , M., Zhong , B., & Li , F. (2025). Mechanisms of combined deer antler polysaccharides and postbiotics supplementation for regulating obesity in mice. Food & Nutrition Research, 69. https://doi.org/10.29219/fnr.v69.11634
Section
Original Articles