Single garlic oil modulates T cells activation and proinflammatory cytokine in mice with high fat diet.

J Ayurveda Integr Med

Department of Biology, Faculty of Mathematics and Natural Sciences, Brawijaya University, Jalan Veteran, Malang, 65145, East Java, Indonesia; Center of Biosystem Study, Brawijaya University, Malang, 65145, East Java, Indonesia.

Published: August 2020

AI Article Synopsis

  • Hyperlipidemia can lead to atherosclerosis by affecting immune cells, specifically T-cells, which are worsened by high-fat diets (HFD).
  • The study investigated the impact of single garlic oil (SGO) on T-cells and inflammatory markers in mice fed a high-fat diet, using various treatment groups over 45 days.
  • Results showed that SGO treatment increased the number of naive T-cells and positively influenced the expression of proinflammatory cytokines, suggesting SGO's potential as a therapeutic option for chronic inflammation associated with HFD.

Article Abstract

Background: Hyperlipidemia triggers atherosclerosis by involving immune cells, such as T-cells. T-cells plays a role in worsening conditions during a high-fat diet (HFD).

Objective: The research aimed to analyze the role of single garlic oil (SGO) on T-cells activation and its proinflammatory cytokine expression in HFD mice.

Methods: Mice were divided into six groups: ND (normal diet); HFD (high-fat diet without treatment); HFD + Simv (HFD + simvastatin 2.6 mg/kg body weight); and HFD + SGO 1-3 (high-fat diet + single garlic oil in a dose of 12.5, 25, and 50 mg/kg body weight), respectively. Treatments were orally given every day for 45 days. At the end of treatments, lymphocytes were isolated from mice spleen. The relative number of T-cells and proinflammatory cytokines were measured using flow-cytometry and analyzed using one-way ANOVA (p < 0.05).

Result: Our result indicated that HFD mice had lower naive T cells (CD4+CD62L+) than normal mice (p < 0.05). SGO treatment in HFD mice increased the relative number of naïve T cells. HFD treatment increased the expression of TNF-α and IFN-γ through NF-κB expression. Furthermore, SGO treatment improved the expression of TNF-α and IFN-γ.

Conclusion: Our study suggests that SGO could act as a promising prospect for therapy to improve chronic inflammation in a HFD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772498PMC
http://dx.doi.org/10.1016/j.jaim.2020.06.009DOI Listing

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