Modulatory effects of rutin and vitamin A on hyperglycemia induced glycation, oxidative stress and inflammation in high-fat-fructose diet animal model.
Aqsa IqbalSairah Hafeez KamranFarhan SiddiqueSaiqa IshtiaqMisbah HameedMobina ManzoorPublished in: PloS one (2024)
In the current study we investigated the impact of combination of rutin and vitamin A on glycated products, the glyoxalase system, oxidative markers, and inflammation in animals fed a high-fat high-fructose (HFFD) diet. Thirty rats were randomly divided into six groups (n = 5). The treatments, metformin (120 mg/kg), rutin (100 mg/kg), vitamin A (43 IU/kg), and a combination of rutin (100 mg/kg) and vitamin A (43 IU/kg) were given to relevant groups of rats along with high-fructose high-fat diet for 42 days. HbA1c, D-lactate, Glyoxylase-1, Hexokinase 2, malondialdehyde (MDA), glutathione peroxidase (GPx), catalase (CAT), nuclear transcription factor-B (NF-κB), interleukin-6 (IL-6), interleukin-8 (IL-8) and histological examinations were performed after 42 days. The docking simulations were conducted using Auto Dock package. The combined effects of rutin and vitamin A in treated rats significantly (p < 0.001) reduced HbA1c, hexokinase 2, and D-lactate levels while preventing cellular damage. The combination dramatically (p < 0.001) decreased MDA, CAT, and GPx in treated rats and decreased the expression of inflammatory cytokines such as IL-6 andIL-8, as well as the transcription factor NF-κB. The molecular docking investigations revealed that rutin had a strong affinity for several important biomolecules, including as NF-κB, Catalase, MDA, IL-6, hexokinase 2, and GPx. The results propose beneficial impact of rutin and vitamin A as a convincing treatment strategy to treat AGE-related disorders, such as diabetes, autism, alzheimer's, atherosclerosis.
Keyphrases
- oxidative stress
- diabetic rats
- high fat diet
- transcription factor
- molecular docking
- signaling pathway
- physical activity
- breast cancer cells
- lps induced
- cardiovascular disease
- type diabetes
- dna damage
- pi k akt
- molecular dynamics
- molecular dynamics simulations
- nuclear factor
- insulin resistance
- ischemia reperfusion injury
- poor prognosis
- induced apoptosis
- weight loss
- hydrogen peroxide
- nitric oxide
- cell cycle arrest
- high glucose
- endothelial cells
- small molecule
- single cell
- newly diagnosed
- cell death
- intellectual disability
- cell proliferation
- smoking cessation
- genome wide identification
- endoplasmic reticulum stress
- mild cognitive impairment