In Vivo Acute Toxicity and Immunomodulation Assessment of a Novel Nutraceutical in Mice.
Tatiana OniseiBianca-Maria TihauanGeorgiana DoleteMădălina Axinie BucosManuela RăscolGheorghița IsvoranuPublished in: Pharmaceutics (2023)
Achieving and maintaining a well-balanced immune system has righteously become an insightful task for the general population and an even more fundamental goal for those affected by immune-related diseases. Since our immune functions are indispensable in defending the body against pathogens, diseases and other external attacks, while playing a vital role in maintaining health and modulating the immune response, we require an on-point grasp of their shortcoming as a foundation for the development of functional foods and novel nutraceuticals. Seeing that immunoceuticals are considered effective in improving immune functions and reducing the incidence of immunological disorders, the main focus of this study was to assess the immunomodulatory properties and possible acute toxicity of a novel nutraceutical with active substances of natural origin on C57BL/6 mice for 21 days. We evaluated the potential hazards (microbial contamination and heavy metals) of the novel nutraceutical and addressed the acute toxicity according to OECD guidelines of a 2000 mg/kg dose on mice for 21 days. The immunomodulatory effect was assessed at three concentrations (50 mg/kg, 100 mg/kg and 200 mg/kg) by determining body and organ indexes through a leukocyte analysis; flow cytometry immunophenotyping of lymphocytes populations and their subpopulations (T lymphocytes (LyCD3+), cytotoxic suppressor T lymphocytes (CD3+CD8+), helper T lymphocytes (CD3+CD4+), B lymphocytes (CD3-CD19+) and NK cells (CD3-NK1.1.+); and the expression of the CD69 activation marker. The results obtained for the novel nutraceutical referred to as ImunoBoost indicated no acute toxicity, an increased number of lymphocytes and the stimulation of lymphocyte activation and proliferation, demonstrating its immunomodulatory effect. The safe human consumption dose was established at 30 mg/day.
Keyphrases
- liver failure
- nk cells
- respiratory failure
- peripheral blood
- flow cytometry
- immune response
- drug induced
- aortic dissection
- oxidative stress
- high fat diet induced
- heavy metals
- signaling pathway
- healthcare
- hepatitis b virus
- dendritic cells
- extracorporeal membrane oxygenation
- insulin resistance
- intensive care unit
- oxide nanoparticles
- climate change
- clinical practice
- type diabetes
- mental health
- inflammatory response
- anaerobic digestion