Healthy
Conditions
Keywords
Oranges, Lycopene, Healthy, Oxidative stress, Inflammation, gene expression
Brief summary
This study aims to evaluate the antioxidant and anti-inflammatory effects of acute and chronic consumption of two sweet orange (Citrus sinensis) varieties-'Rosy Red Valencia', which is rich in carotenoids such as lycopene, phytoene, and phytofluene, and 'Olinda Valencia', which lacks these carotenoids-in healthy adults. In this 4-week, randomized, parallel-arm clinical trial, participants will consume either 'Rosy Red Valencia' or 'Olinda Valencia' oranges daily. The study will assess the effects of sweet orange intake on markers of oxidative stress and inflammation, plasma carotenoid concentrations, gene expression in peripheral blood mononuclear cells, and gut health. Findings from this study may help identify potential health benefits associated with specific carotenoid profiles in sweet oranges and provide insights into their role in modulating inflammation and oxidative stress.
Detailed description
The health benefits of orange consumption have been described; however, the specific bioactive compounds responsible for these effects, as well as the underlying mechanisms of action, are not fully understood. There are several varieties of sweet oranges, each with a unique phytochemical profile and potentially distinct health-promoting properties. The 'Rosy Red Valencia' sweet orange is enriched in carotenoids such as lycopene, phytoene, and phytofluene, whereas the commonly consumed 'Olinda Valencia' contains negligible levels of these compounds. This randomized, parallel-arm clinical trial aims to evaluate and compare the antioxidant and anti-inflammatory effects of 'Rosy Red Valencia' and 'Olinda Valencia' sweet orange consumption in healthy men and women. Participants will be randomized to consume one of the two orange varieties twice daily for four weeks. The study includes both an acute phase (1-day consumption) and a chronic phase (4-week daily consumption). Blood samples will be collected at baseline, after 1 day, and after 4 weeks of consumption to assess changes in plasma carotenoid concentrations, markers of oxidative stress and inflammation, and gene expression profiles in peripheral blood mononuclear cells. Fecal samples will be collected at baseline and after 4 weeks to assess the effects on gut microbiota composition. By evaluating and comparing the biological effects of these two orange varieties, the study aims to elucidate the role of specific carotenoids in mediating the health benefits of sweet orange consumption.
Interventions
OTHER'Rosy Red Valencia' sweet orange
The participants consume 2 'Rosy Red Valencia' sweet oranges daily for 4 weeks
OTHER'Olinda Valencia' sweet oranges
The participants consume 2 'Olinda Valencia' sweet oranges daily for 4 weeks
Sponsors
University of California, Davis
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
25 Years to 40 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy men and women * Age Range: 25-40 years * Body mass index (BMI) with values between 21 and 29.9 kg\^m2 * Willingness to accept randomization, undergo the testing and intervention procedures, and deliver blood and stool samples * Willingness to refrain from consuming foods rich in lycopene, phytoene, and phytofluene and limit the intake of some polyphenol-rich foods * Willingness to discontinue the use of antioxidant supplements (such as carotenoid, polyphenol supplements), prebiotics and/or probiotics
Exclusion criteria
* Pregnancy/lactation * History of cardiovascular diseases, diabetes, uncontrolled hypertension, heart failure, stroke, liver, gallbladder, kidney, thyroid disease, gastrointestinal, autoimmune disorder, or cancer. * Psychiatric disease that interferes with the understanding and implementation of the intervention * History of eating disorders (such as bulimia nervosa and anorexia nervosa) in the last 5 years * Current smokers * Vegan, vegetarian, or other special diets (e.g., keto, paleo) * Use of antibiotics or laxatives in the previous month * History of substance abuse or alcohol abuse * involvement in a weight loss intervention program within the past month or weight change \> 10% * Self-report of allergic reactions to study products or their phytochemicals.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Levels of lycopene and noncolored carotenoids | 0, 1 day, 4 weeks | Levels in plasma |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Oxidative stress | 0, 1 day, 4 weeks | Oxidative stress marker DNA/RNA oxidative damage assessed in blood samples from participants by a commercial kit |
| Inflammation | 0, 1 day, 4 weeks | Levels of inflammatory marker CRP assessed in blood samples from participants using commercial assay kits. |
| Gene expression | 0, 1 day, 4 weeks | Gene expression in Peripheral Blood Mononuclear Cells (PBMCs) |
| Microbiota composition | 0, 4 weeks | From stool samples |
| Lipid/metabolic profile | 0, 4 weeks | Measured in blood samples |
| Systolic and diastolic blood pressure | 0, 4 weeks | Measured by automated sphygmomanometer |
Countries
United States
Contacts
STUDY_DIRECTORGerardo G Macknezie, PhD
Univeristy of California Davis
Outcome results
None listed