Acta Scientific Microbiology (ASMI) (ISSN: 2581-3226)

Review Article Volume 3 Issue 6

Analysis of the Protective Effect of NutriSim© and the Inflammatory Response in a Model of LPS-Induced Shock from E. coli Serotype 0111:B4

Daniela L Delgado-Lara1, José J Hernández-Cruz1,2, Luís A Romero- Tirado2, Rolando Roméro-Dávalos2, José J Hernández-Andalón2, Irma E Velázquez-Brizue1 and Genaro Gabriel Ortiz1*

1Department of Philosophical and Methodological Disciplines, University Center of Health Sciences, University of Guadalajara, Guadalajara, Mexico
2Laboratories BioSim©; Scientific Research and Development Area, MXCD, Mexico

*Corresponding Author: Genaro Gabriel Ortiz, Department of Philosophical and Methodological Disciplines, University Center of Health Sciences, University of Guadalajara, Guadalajara, Mexico.

Received: April 15, 2020; Published: May 21, 2020

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Abstract

  The term septic shock or septicemia were considered analogous to endotoxic shock or endotoxicosis and used to designate the state of acute metabolic-circulatory dysfunction, which is trigger after the release into the body of bacterial endotoxins, secondary to an initial septic process, or subsequent to experimental administration of isolated endotoxins, respectively. Despite the extensive use of the term "septic shock" in clinical and preclinical studies to refer to this pathological state, we will now refer to this state only as sepsis or LPS-induced sepsis as appropriate. Experimental animal models treated with isolated bacterial endotoxins replicates many of the hematologic, hemodynamic, and metabolic abnormalities characteristic of patients with bacterial infections that trigger shock. Endotoxins are macromolecular complexes made up of lipopolysaccharides (LPS) and proteins located on the outer membrane of Gram-negative bacteria. The main pro-inflammatory cytokines are tumor necrosis factor-alpha, interleukin 1, interleukin 6 and interleukin 8. The expression of these cytokines is responsible for many of the clinical effects and lesions observed in LPS-induced sepsis. LPS is a potent "stimulator" of the immune response, inducing cytokine production in macrophages and B-cells. The present work aimed to study the effect of Nutrisim© on inflammation in an in vivo model of sepsis-induced by Escherichia coli 0111: B4 lipopolysaccharide. We found that the nutritive supplement NutriSim has shown a decrease in pro-inflammatory cytokines and even a protective effect against LPS. Further clinical research has to be made.

Keywords: NutriSim©; Lipopolysaccharides; Inflammation; Endotoxic Shock

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References

  1. Jean-Louis V., et al. “Circulatory Shock”. New England Journal of Medicine18 (2013): 1726-1734.
  2. Mervyn S., et al. “The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3)”. Journal of the American Medical Association8 (2016): 801-810.
  3. Snigdha J. “Sepsis: An Update on Current Practices in Diagnosis and Management”. American Journal of the Medical Sciences 3 (2018): 277-286.
  4. Jeffrey G., et al. “Sepsis: Pathophysiology and Clinical Management”. British Medical Journal 353 (2016): 1-20.
  5. Jean-Louis V., et al. “Frequency and Mortality of Septic Shock in Europe and North America: A Systematic Review and Meta-Analysis”. Critical Care1 (2019): 1-11.
  6. Manu SH., et al. “Developing a New definition and Assessing New clinical Criteria for Septic Shock: For the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3)”. Journal of the American Medical Association8 (2016): 775-787.
  7. Chris G., et al. “Synthetic and Natural Escherichia Coli Free Lipid A Express Identical Endotoxic Activities”. European Journal of Biochemistry1 (1985):1-5.
  8. Steven O., et al. “Systemic Host Responses in Severe Sepsis Analyzed by Causative Microorganism and Treatment Effects of Drotrecogin Alfa (Activated)”. Clinical Infectious Diseases 1 (2003):50-58.
  9. Tim R., et al. “Cross-Specificity of Protective Human Antibodies against Klebsiella Pneumoniae LPS O-Antigen”. Nature Immunology 6 (2018): 617-624.
  10. James M., et al. “T CELL-INDEPENDENT”. Annual Review of Immunology 13 (1995): 655-692.
  11. Christian R et al. “Lipopolysaccharide Endotoxins”. Annual Review of Biochemistry 1 2002): 635-700.
  12. Yuriy K., et al. “Bacterial Lipopolysaccharides”. Springer (2011): 41-115.
  13. Tony C., et al. “A Gene Coding for 3-Deoxy-D-Manno-Octulosonic-Acid Transferase in Escherichia Coli: Identification, Mapping, Cloning, and Sequencing”. Journal of Biological Chemistry 15 (1991): 9687-9696.
  14. Russell O., et al. “Antibacterial Agents That Inhibit Lipid a Biosynthesis”. Science 5289 (1996): 980-982.
  15. Ernst R., et al. “Bacterial Endotoxin: Molecular Relationships of Structure to Activity and Function”. The FASEB Journal 2 (1994): 217-225.
  16. Christian A., et al. “Invited Review: Bacterial Lipopolysaccharides and Innate Immunity”. Journal of Endotoxin Research 3 (2001): 167-202.
  17. Girish R. “Gram-Positive and Gram-Negative Bacterial Toxins in Sepsis: A Brief Review”. Virulence1 (2014): 213-218.
  18. Jianjin S., et al. “Inflammatory Caspases Are Innate Immune Receptors for Intracellular LPS”. Nature 7521 (2014): 187-192.
  19. Marina F., et al. “Interaction of Lipopolysaccharides and Lipid A with Complement in Rats and Its Relation to Endotoxicity”. Infection and Immunity3 (1978): 875-882.
  20. Kitchens R. “Role of CD 1 4 in Cellular Recognition of Bacterial Lipopolysaccharides”. Chemical Immunology 74 (2000): 61-82.
  21. Beom SP., et al. “The Structural Basis of Lipopolysaccharide Recognition by the TLR4-MD-2 Complex”. Nature7242 (2009): 1191-1195.
  22. Peter T., et al. “Lipopolysaccharide Binding Protein-Mediated Complexation of Lipopolysaccharide with Soluble CD14”. Journal of Biological Chemistry18 (1995): 10482-10488.
  23. Haziot A., et al. “The Monocyte Differentiation Antigen, CD14, Is Anchored to the Cell Membrane by a Phosphatidylinositol Linkage”. The Journal of Immunology2 (1988): 547-552.
  24. Maikel P., et al. “Lipopolysaccharide Regulates Macrophage Fluid Phase Pinocytosis via CD14-Dependent and CD14-Independent Pathways”. Blood11 (1999): 4011-4018.
  25. Alan A., et al. “Toll-like Receptors in the Induction of the Innate Immune Response”. Nature 6797 (2000): 782-787.
  26. Vix K. “Targeting Macrophage Immunometabolism: Dawn in the Darkness of Sepsis”. International Immunopharmacology 58 (2018): 173-185.
  27. Kayle D., et al. “Inflammatory Response to Different Toxins in Experimental Sepsis Models”. International Journal of Molecular Sciences18 (2019): 1-13.
  28. Anthony L., et al. “Biology and Metabolism of Sepsis: Innate Immunity, Bioenergetics, and Autophagy”. Surgical Infections 3 (2016): 286-293.
  29. Jean-Marc C., “Exotoxins and Endotoxins: Inducers of Inflammatory Cytokines”. Toxicon 149 (2018): 45-53.
  30. Min H., et al. “The Pathogenesis of Sepsis and Potential Therapeutic Targets”. International Journal of Molecular Sciences21 (2019): 1-31.
  31. Andrew R., et al. “Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016”. Critical Care Medicine 3 (2017): 486-552.
  32. Jordi R., et al. “Sepsis: A Review of Advances in Management”. Advances in Therapy 11 (2017): 2393-2411.
  33. Danyang L., et al. “Liberal versus Conservative Fluid Therapy in Adults and Children with Sepsis or Septic Shock”. Cochrane Database of Systematic Reviews 12 (2018): 1-38.
  34. Benjamin C., et al. “Cytokine Storm and Sepsis Disease Pathogenesis”. Seminars in Immunopathology 5 (2017): 517-528.
  35. Tom VP., et al. “The Immunopathology of Sepsis and Potential Therapeutic Targets”. Nature Reviews Immunology7 (2017): 407-420.
  36. Yvette L., et al. “Arginine Infusion in Patients with Septic Shock Increases Nitric Oxide Production without Haemodynamic Instability”. Clinical Science1 (2015): 57-67.
  37. Richard B., et al. “Early Enteral Supplementation with Key Pharmaconutrients Improves Sequential Organ Failure Assessment Score in Critically Ill Patients with Sepsis: Outcome of a Randomized, Controlled, Double-Blind Trial*”. Read Online: Critical Care Medicine | Society of Critical Care Medicine 36.1 (2008): 131-144.
  38. Rolando DR., et al. “NutriSim© protects against hippocampal neuronal damage induced by ischemia-reperfusion in Mongolian gerbils (Meriones unguiculatus): Morphological and biochemical approach”. Journal of Neuroscience and Behavioural Health1(2010): 7-11.
  39. Irma VB., et al. “Effect of NutriSim © and the Interactive Response of Pro-inflammatory and Anti-inflammatory Cytokines in a Model of Septic Shock Induced by E coli Serotype 0111 : B4”. American Journal of Biochemistry 1 (2014): 6-13.
  40. Erika GR., et al. “Effect of Nutrisim© on Endotoxic Shock Induced by Lipopolysaccharide from Escherichia coli: 0111:B4 in Rats: Structural Study of Liver, Kidney and Lung”. Journal of Clinical and Experimental Pathology 1 (2013): 1-6.
  41. Erandis TS., et al. “Beneficial effect of NutriSim© against LPS-induced liver injury: Oxidative stress markers and mitochondrial ATP-ase activity”. International Journal of Biological Chemistry 1 (2013): 38-46.
  42. Oscar BQ., et al. “NutriSim© Diminishes Lipopolysaccharide-Stimulated Anti-inflammatory IL-4 and IL-10 Cytokines and Nitric Oxide”. International Journal of Medical Sciences and Health Care8 (2013): 8-12.
  43. Erika GR., et al. “NutriSim© Diminishes an Endotoxin-stimulated Proinflammatory Cytokine Production”. American Journal of Biochemistry6 (2012): 94-97.
  44. Peng L., et al. “Amino acids and immune function”. British Journal of Nutrition2 (2007): 237-252.
  45. Ewa S., et al. “Oxidative changes in the liver, brain and lens of lipopolysaccharide-treated rats”. Archives of Medical Research 26 (1995): 109-115.
  46. Eugui EM., et al. “Some antioxidants inhibit, in a co-ordinate fashion, the production of tumor necrosis factor-alpha, IL-beta, and IL-6 by human peripheral blood mononuclear cells”. International Immunology3 (1994): 409-22.
  47. Barbara L., et al. “L-Arginine reduces lipid peroxidation in patients with diabetes mellitus”. Free Radical Biology and Medicine1 (1997): 355-7.
  48. Guoyao W., et al. “Arginine nutrition in development, health and disease”. Current Opinion in Clinical Nutrition and Metabolic Care 1 (2000): 59-66.
  49. Thomas R., et al. “Antinociceptive and anti-inflammatory effects of choline in a mouse model of postoperative pain”. British Journal of Anaesthesia2 (2010):201-207.
  50. Luis FG., et al. “Compuestos nitrogenados de interés en nutrición clínica”. Nutrición Hospitalaria2 (2006):15-29.
  51. Hui H., et al. “Effects of dietary lysine restriction on inflammatory responses in piglets”. Scientific Reports1 (2018):1-8.
  52. Kohsuke H., et al. “Safety assessment of l-lysine oral intake: a systematic review”. Amino Acids4 (2019):647-659.
  53. Heikki M., et al. “Dietary calcium and magnesium supplements in spontaneously hypertensive rats and isolated arterial reactivity”. British Journal of Pharmacology8 (1995): 1455-1462.
  54. Alyssa M., et al. “Biochemistry, Nutrients”. Stat Pearls (2020).
  55. Juan O., et al. “Effects of L-Arginine on the Proliferation of T Lymphocyte Subpopulations”. Journal of Parenteral and Enteral Nutrition1 (2001): 23-29.
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Citation

Citation: Genaro Gabriel Ortiz., et al. “Analysis of the Protective Effect of NutriSim© and the Inflammatory Response in a Model of LPS-Induced Shock from E. coli Serotype 0111:B4". Acta Scientific Microbiology 3.6 (2020): 90-99.




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