Skip to main content

Advertisement

Log in

Protective and therapeutic effects of two novel strains of Lactobacilli on diabetes-associated disorders induced by a high level of fructose

  • Original Article
  • Published:
Molecular Biology Reports Aims and scope Submit manuscript

Abstract

Diabetes is a metabolic disorder described as insufficient secretion of insulin in the pancreas or the inability of the existing insulin to function properly. It poses a greater risk on human health as it is considered the base of several diseases. Thus, this study was designed to evaluate two novel strains of Lactobacillus in handling pancreas disorders. 50 BALB/c male mice were divided into five groups; (a) feeding on normal diet only as control group, (b) given 21% fructose in drinking water as diabetes group, (c) feeding on Lactobacillus rhamnosus strain Pro2 (MT505335.1) plus 21% fructose as LR group, (d) feeding on Lactobacillus plantarum strain Pro1 (MT505334.1) plus 21% fructose as LP group and (e) mixture of two strains plus 21% fructose as Mix group. The serum content of glucose, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) was determined. Pancreases histopathology was examined. Expression of GH, IGF1, and GLP-1 genes was measured in the liver and pancreas by RT-qPCR. Serum content of glucose, ALT, and AST significantly increased in diabetes group, and significantly reduced in (LP) and (Mix) groups compared with control. Pathological changes occurred in the exocrine and endocrine components of the diabetes group pancreas. Besides, islet cells are almost entirely disturbed and acinar cells degenerated. However, in (LP) and (Mix) groups, the pathological changes significantly decreased and became related to the control group. Expression of GH, IGF1, and GLP-1 genes was significantly downregulated in the liver and pancreas of mice given fructose compared with control. Expression of these genes was either significantly upregulated in groups (LP and Mix) or identical to the control group. This study shows that the strain Pro1 (MT505334.1) or a combination of two strains is useful in reducing diabetic risk.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Data availability

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

References

  1. Alipour FG, Ashoori MR, Pilehvar-Soltanahmadi Y, Zarghami N (2017) An overview on biological functions and emerging therapeutic roles of apelin in diabetes mellitus. Diabetes Metab Syndr 11:S919–S923. https://doi.org/10.1016/j.dsx.2017.07.016

    Article  PubMed  Google Scholar 

  2. Majdi MA, Mohammadzadeh NA, Lotfi H, Mahmoudi R, Alipour FG, Shool F, Moghanloo MN, Porfaraj S, Zarghami N (2017) Correlation of resistin serum level with fat mass and obesity-associated gene (FTO) rs9939609 polymorphism in obese women with type 2 diabetes. Diabetes Metab Syndr 11(2):S715–S720. https://doi.org/10.1016/j.dsx.2017.05.004

    Article  PubMed  Google Scholar 

  3. Mofarrah M, Ziaee S, Pilehvar-Soltanahmadi Y, Zarghami F, Boroumand M, Zarghami N (2016) Association of KALRN, ADIPOQ, and FTO gene polymorphism in type 2 diabetic patients with coronary artery disease: possible predisposing markers. Coron artery Dis 27(6):490–496. https://doi.org/10.1097/MCA.0000000000000386

    Article  PubMed  Google Scholar 

  4. Mihanfar A, Rahmati-Yamchi M, Mota A, Abediazar S, Pilehvar-Soltanahmadi Y, Zarghami N (2018) Serum levels of vaspin and its correlation with nitric oxide in type 2 diabetic patients with nephropathy. Curr Diabetes Rev 14(2):162–167. https://doi.org/10.2174/1573399813666170530103216

    Article  CAS  PubMed  Google Scholar 

  5. Mohammadzadeh G, Zarghami N (2013) Serum leptin level is reduced in non-obese subjects with type 2 diabetes. Int J Endocrinol Metab 11(1):3–10. https://doi.org/10.5812/ijem.6535

    Article  CAS  PubMed  Google Scholar 

  6. Aguirre GA, De Ita JR, de la Garza RG et al (2016) Insulin-like growth factor-1 deficiency and metabolic syndrome. J Transl Med 14:3. https://doi.org/10.1186/s12967-015-0762-z

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Succurro E, Andreozzi F, Marini MA, Lauro R, Hribal ML, Perticone F et al (2009) Low plasma insulin-like growth factor-1 levels are associated with reduced insulin sensitivity and increased insulin secretion in nondiabetic subjects. Nutr Metab Cardiovasc Dis 19(10):713–719. https://doi.org/10.1016/j.numecd.2008.12.011

    Article  CAS  PubMed  Google Scholar 

  8. Natalie JH, Thomas AS, Connor JM, Stephen BW (2019) The insulin like growth factor and binding protein family: novel therapeutic targets in obesity and diabetes. Mol Metab 19:86–96. https://doi.org/10.1016/j.molmet.2018.10.008

    Article  CAS  Google Scholar 

  9. Gautier JF, Choukem J, Girard J (2008) Physiology of incretins (GIP and GLP-1) and abnormalities in type 2 diabetes. Diabetes Metab 34:65–72. https://doi.org/10.1016/S1262-3636(08)73397-4

    Article  Google Scholar 

  10. Williams JA (2014) GLP-1. Pancreapedia. https://doi.org/10.3998/panc.2014.7

    Article  Google Scholar 

  11. Mann E, Sunni M, Bellin MD (2020) secretion of insulin in response to diet and hormones. Pancreapedia. https://doi.org/10.3998/panc.2020.16

    Article  Google Scholar 

  12. Matthias PL, Signe ST (2017) Glucagon-like peptide 1: a predictor of type 2 diabetes? J Diabetes Res. https://doi.org/10.1155/2017/7583506

    Article  Google Scholar 

  13. Jens JH (2019) The incretin system in healthy humans: the role of GIP and GLP-1. Metabolism 96:46–55. https://doi.org/10.1016/j.metabol.2019.04.014

    Article  CAS  Google Scholar 

  14. Nauck MA, Vardarli I, Deacon CF, Holst JJ, Meier JJ (2011) Secretion of glucagon-like peptide-1 (GLP-1) in type 2 diabetes: what is up, what is down? Diabetologia 54:10–18. https://doi.org/10.1007/s00125-010-1896-4

    Article  CAS  PubMed  Google Scholar 

  15. Shafiei-Irannejad V, Samadi N, Salehi R, Yousefi B, Zarghami N (2017) New insights into antidiabetic drugs: possible applications in cancer treatment. Chem Biol Drug Des 90(6):1056–1066. https://doi.org/10.1111/cbdd.13013

    Article  CAS  PubMed  Google Scholar 

  16. Laleye S, Igbakin A, Akinyanju J (2008) Antidiabetic effect of nono (a Nigerian fermented milk) on alloxan-induced diabetic rats. Am J Food Technol 3:394–398. https://doi.org/10.3923/ajft.2008.394.398

    Article  Google Scholar 

  17. Héctor R, José AC, José ML, Blanca R, Félix LF, Carmen G et al (2008) Metabolism of food phenolic acids by Lactobacillus plantarum CECT 748 T. Food Chem 107(4):1393–1398. https://doi.org/10.1021/jf703779s

    Article  CAS  Google Scholar 

  18. Meng C, Bai C, Brown TD, Hood LE, Tian Q (2018) Human gut microbiota and gastrointestinal cancer. Genom Proteom Bioinform 16(1):33–49. https://doi.org/10.1016/j.gpb.2017.06.002

    Article  Google Scholar 

  19. Sheng J, Shi-Xin P, Cui-Lan H, Fen-Fen M, Na L, Xing-Hui L et al (2015) Cardiac H2S generation is reduced in ageing diabetic mice. Oxid Med Cell Longev 2015:1–14. https://doi.org/10.1155/2015/758358

    Article  Google Scholar 

  20. WHO (2021) diabetes fact sheet. https://www.who.int/news-room/fact-sheets/detail/diabetes. Accessed 13 Apr 2021

  21. Feizollah A, Asghar T, Mohammad RA, Ali A, Nosratollah Z (2017) Investigating the effects of Lactobacilluscasei on some biochemical parameters in diabetic mice. J Endocrinol Metab Diabetes S Afr 22(3):47–50. https://doi.org/10.1080/16089677.2017.1378460

    Article  Google Scholar 

  22. Yadav H, Jain S, Sinha P (2007) Antidiabetic effect of probiotic dahi containing Lactobacillus acidophilus and Lactobacillus casei in high fructose fed rats. Nutrition 23(1):62–68. https://doi.org/10.1016/j.nut.2006.09.002

    Article  PubMed  Google Scholar 

  23. Yadav H, Jain S, Sinha PR (2008) Oral administration of dahi containing probiotic Lactobacillus acidophilus and Lactobacillus casei delayed the progression of streptozotocin-induced diabetes in rats. J Dairy Res 75(2):189–195. https://doi.org/10.1017/S0022029908003129

    Article  CAS  PubMed  Google Scholar 

  24. Bäckhed F, Ding H, Wang T, Hooper LV, Koh GY, Nagy A et al (2004) The gut microbiota as an environmental factor that regulates fat storage. Proc Natl Acad Sci U S A 101(44):15718–15723. https://doi.org/10.1073/pnas.0407076101

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Liu Y, Lou X (2020) Type 2 diabetes mellitus-related environmental factors and the gut microbiota: emerging evidence and challenges. Clinics. https://doi.org/10.6061/clinics/2020/e1277

    Article  PubMed  PubMed Central  Google Scholar 

  26. Lye HS, Kuan CY, Ewe JA, Fung WY, Liong MT (2009) The improvement of hypertension by probiotics: effects on cholesterol, diabetes, renin, and phytoestrogens. Int J Mol Sci 10(9):3755–3775. https://doi.org/10.3390/ijms10093755

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Baggio LL, Drucker DJ (2007) Biology of incretins: GLP-1 and GIP. Gastroenterology 132:2131–2157. https://doi.org/10.1053/j.gastro.2007.03.054

    Article  CAS  PubMed  Google Scholar 

  28. Gallwitz B (2016) Glucagon-like peptide-1 and gastric inhibitory polypeptide: new advances. Curr Opin Endocrinol Diabetes Obes 23:23–27. https://doi.org/10.1097/MED.0000000000000217

    Article  CAS  PubMed  Google Scholar 

  29. Holst JJ (2010) Glucagon and glucagon-like peptides 1 and 2. Results Probl Cell Differ 50:121–135. https://doi.org/10.1007/400_2009_35

    Article  CAS  PubMed  Google Scholar 

  30. Gilor C, Gilor S, Graves TK, Borst LB, Labelle P, Ridge TK et al (2013) Distribution of K and L cells in the feline intestinal tract. Domest Anim Endocrinol 45:49–54. https://doi.org/10.1016/j.domaniend.2013.04.004

    Article  CAS  PubMed  Google Scholar 

  31. Halban PA, Polonsky KS, Bowden DW, Hawkins MA, Ling C, Mather KJ et al (2014) β-cell failure in type 2 diabetes: postulated mechanisms and prospects for prevention and treatment. Diabetes Care 37:1751–1758. https://doi.org/10.2337/dc14-0396

    Article  PubMed  PubMed Central  Google Scholar 

  32. Lugari L, Dell’Anna C, Ugolotti D, Gnudi A (2000) Effect of nutrient ingestion on glucagon-like peptide-1-induced insulin secretion in human type 1 and type 2 diabetes. Horm Metab Res 32:424–448. https://doi.org/10.1055/s-2007-978665

    Article  CAS  PubMed  Google Scholar 

  33. Rajkumar K, Krsek M, Dheen ST, Murphy LJ (1996) Impaired glucose homeostasis in insulin-like growth factor binding protein-1 transgenic mice. J Clin Invest 98:1818–1825. https://doi.org/10.1172/JCI118982

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Hong H, Cui ZZ, Zhu L, Fu SP, Rossi M, Cui YH, Zhu BM (2017) Central IGF1 improves glucose tolerance and insulin sensitivity in mice. Nutr Diabetes 7(12):2. https://doi.org/10.1038/s41387-017-0002-0

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Martinez CS, Piazza VG, Ratner LD, Matos MN, Gonzalez L, Rulli SB et al (2013) Growth hormone STAT5-mediated signaling and its modulation in mice liver during the growth period. Growth Horm IGF Res 23:19–28. https://doi.org/10.1016/j.ghir.2012.11.002

    Article  CAS  PubMed  Google Scholar 

  36. Kjems LL, Holst JJ, Vølund A, Madsbad S (2003) The influence of GLP-1 on glucose-stimulated insulin secretion. Effects on β-cell sensitivity in type 2 and nondiabetic subjects. Diabetes 52:380–386. https://doi.org/10.2337/diabetes.52.2.380

    Article  CAS  PubMed  Google Scholar 

  37. Tabuchi M, Ozaki M, Tamura A, Yamada N, Ishida T, Hosoda M et al (2003) Antidiabetic effect of Lactobacillus GG in streptozotocin-induced diabetic rats. Biosci Biotechnol Biochem 67(6):1421–1424. https://doi.org/10.1271/bbb.67.1421

    Article  CAS  PubMed  Google Scholar 

  38. Sheikh HS, Gol A, Khaleghi M (2019) The effects of the Lactobacillus acidophilus ATCC 4356 on the oxidative stress of reproductive system in diabetic male rats. Int J Reprod Biomed. 17(7):493–502. https://doi.org/10.18502/ijrm.v17i7.4861

    Article  CAS  Google Scholar 

Download references

Funding

Funding

None funding received.

Author information

Authors and Affiliations

Authors

Contributions

This study was done in collaboration with all authors. A.K. and A.D. designed this study. N.A., A.D. and A.K. participated in the conduct of the study. N.A. and A.D. analyzed the data. A.D. and A.K. drafted the manuscript. A.D. and N.A. critically revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Ahmed M. Darwish.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

The experimental protocol used in the study was approved by the Animal Care and Use Committee of National Research Centre, Egypt. The laboratory experiments and protocols were handled in accordance with the guidelines described by National Research Centre and AlQunfudah, Umm Al-Qura University.

Informed consent

The authors declare that they consent to participate to this study.

Consent for publication

The authors declare that they consent for publication of this study.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

ALSuhaymi, N., Darwish, A.M. & Khattab, A.EN. Protective and therapeutic effects of two novel strains of Lactobacilli on diabetes-associated disorders induced by a high level of fructose. Mol Biol Rep 48, 4333–4340 (2021). https://doi.org/10.1007/s11033-021-06448-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11033-021-06448-0

Keywords

Navigation