bixin and Inflammation

bixin has been researched along with Inflammation* in 4 studies

Other Studies

4 other study(ies) available for bixin and Inflammation

ArticleYear
Bixin Attenuates High-Fat Diet-Caused Liver Steatosis and Inflammatory Injury through Nrf2/PPAR
    Oxidative medicine and cellular longevity, 2021, Volume: 2021

    Nonalcoholic fatty liver disease is the most common liver disease worldwide. Hepatic steatosis and oxidative stress are the main characteristics of NAFLD (nonalcoholic fatty liver disease), which also affect its prognosis. Bixin acts as novel Nrf2 (NF-E2 p45-related factor 2) activator with the cytoprotection against oxidative stress and inflammation; this study mainly focused on the mechanism of Nrf2 activation by bixin and explored its potential feasibilities in long-term high-fat diet- (HFD-) caused hepatic steatosis and inflammatory response

    Topics: Animals; Carotenoids; Cell Line; Cysteine; Cytoprotection; Diet, High-Fat; Fatty Liver; Feeding Behavior; Humans; Inflammation; Kelch-Like ECH-Associated Protein 1; Lipid Metabolism; Liver; Mice, Knockout; NF-E2-Related Factor 2; PPAR alpha; Protein Stability; Signal Transduction; Ubiquitination; Up-Regulation

2021
Antinociceptive and Anti-Inflammatory Effects of Bixin, a Carotenoid Extracted from the Seeds of Bixa orellana.
    Planta medica, 2019, Volume: 85, Issue:16

    Topics: Acetic Acid; Analgesics; Animals; Anti-Inflammatory Agents; Bixaceae; Carotenoids; Carrageenan; Disease Models, Animal; Edema; Inflammation; Male; Mice; Pain Measurement; Rats; Rats, Wistar

2019
Annatto carotenoids attenuate oxidative stress and inflammatory response after high-calorie meal in healthy subjects.
    Food research international (Ottawa, Ont.), 2017, Volume: 100, Issue:Pt 1

    The aim of this study was to evaluate the effect of annatto carotenoids intake associated to a single high-calorie meal (high fat and high carbohydrate) in postprandial biochemical, inflammatory and oxidative stress markers. Twelve healthy subjects (6 men, 6 women) were included in this randomised, controlled crossover study. Baseline blood samples were collected from fasting subjects that immediately received high-calorie meal without carotenoid (placebo) or containing 1.2mg/kg bixin (BIX) or 0.06mg/kg norbixin (NBIX). Blood samples were taken 60, 120 and 240min after meal intake. NBIX intake did not affect biochemical blood markers but reduced the postprandial levels of inflammatory cytokines (IL-1, IL-6 and TNF-α) and lipid oxidation 60-120min after meal. BIX only partially prevented postprandial-induced lipid oxidation. Results indicate that the intake of NBIX may be an alternative to reduce the postprandial inflammatory and oxidative stress responses to high-calorie meals.

    Topics: Adult; Bixaceae; Blood Glucose; Blood Pressure; Carotenoids; Cytokines; Diet; Female; Humans; Inflammation; Male; Oxidative Stress; Plant Extracts; Postprandial Period; Young Adult

2017
Bixin ameliorates high fat diet-induced cardiac injury in mice through inflammation and oxidative stress suppression.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2017, Volume: 89

    Diabetic cardiomyopathy is known as an essential complication of diabetes, a main reason leading to mortality for diabetic patients, and novel therapeutic strategies for treatment are urgently required. Bixin (BX), isolated from the seeds of Bixa orellana, is a carotenoid, possessing anti-inflammatory, anti-tumor and anti-oxidant activities. In our study, we attempted to calculate the role of bixin in cardiac injury progression, and reveal the possible molecular mechanism. Bixin treatment ameliorated cardiac dysfunction through inhibiting fibrosis, inflammation and reactive oxygen species (ROS) generation. It reduced fibrosis levels via collagen deposition down-regulation. Inflammatory response was attenuated by reducing pro-inflammatory cytokines secretion via Toll-like receptor 4/nuclear factor kappa B (TLR4/NF-κB) signaling pathway inactivation in mice induced by high fat diet. Also, in in vitro studies, lipopolysaccharide (LPS)-treated cardiac muscle cells exhibits pro-inflammatory cytokines over-expression, which was reduced by bixin through blocking TLR4/NF-κB pathway. Additionally, oxidative stress triggered by high fat in vivo and LPS in vitro was down-regulated for bixin administration via nuclear factor-E2-related factor 2 (Nrf2) signaling pathway activation. Our study suggested that bixin might be a novel and protective agent with therapeutic activity against cardiac injury by suppressing fibrosis, inflammation and oxidative stress.

    Topics: Animals; Carotenoids; Cell Line; Dietary Fats; Dose-Response Relationship, Drug; Heart Diseases; Humans; Inflammation; Male; Mice; Mice, Inbred C57BL; Oxidative Stress

2017