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Updated: Jun 6, 2026

Preparation of Naringenin Solution for In Vivo Application
Published on: August 10, 2021
Naringenin more effectively inhibits inducible nitric oxide synthase and cyclooxygenase-2 expression in macrophages
Chia-Lun Chao1, Ching-Sung Weng, Nen-Chung Chang
1Division of Cardiology, Department of Internal Medicine, Taoyuan General Hospital, Department of Health, Executive Yuan, 33004 Taoyuan, Taiwan.
Abstract:
Macrophages and microglia are thought to account for initial disease progression in acute myocardial infarction and acute ischemic stroke. Before our study, the inhibitory effects of naringenin, a flavonoid, on lipopolysaccharide (LPS)-induced inflammation in macrophages and microglia have not been fully reported and compared. We hypothesized that naringenin can effectively inhibit LPS-induced inflammation of macrophages and microglia at different concentrations, the range of which is broader, with the lowest concentration more easily achieved in macrophages. In this study, we compared the anti-inflammatory effects of naringenin on LPS-stimulated RAW 274.6 macrophages and BV2 microglia and the suppression effects of naringenin and vitamin C (a well-known anti-inflammatory agent) on LPS-induced nitrite production. The results show that macrophages could maintain cell viability at higher naringenin concentrations and were more easily activated by LPS in comparison to microglia (200 vs 100 μmol/L; 0.1 vs 1 μg/mL). Under LPS (1 μg/mL) stimulation in both cell types, naringenin (up to 200 μmol/L in macrophages and 100 μmol/L in microglia) inhibited nitrite production and inducible nitric oxide synthase and cyclooxygenase-2 expression in a dose-dependent manner. The range of naringenin concentrations for inhibition was broader, and the lowest concentration was more easily achieved in macrophages; the lowest effective concentrations of naringenin to achieve constant suppression effect were 50 μmol/L in macrophages and 100 μmol/L in microglia, respectively. Vitamin C (100 μmol/L), compared with naringenin (100 μmol/L), had less and no suppression effect on LPS (1 μg/mL)-induced nitrite production in macrophages and microglia, respectively. In conclusion, naringenin more effectively inhibits the LPS-induced inflammatory status, including nitrite production and inducible nitric oxide synthase and cyclooxygenase-2 expression, in macrophages than in microglia. The findings of the present study suggest that consumption of naringenin-containing flavonoids might be beneficial to the cardiovascular and cerebrovascular inflammatory process.
Insights
Naringenin, a flavonoid, effectively reduces inflammation in macrophages and microglia, crucial in conditions like heart attack and stroke. It shows greater anti-inflammatory effects in macrophages, suggesting potential benefits for cardiovascular and cerebrovascular health.
Area of Science:
- Biochemistry and Molecular Biology
- Immunology
- Pharmacology
Background:
- Macrophages and microglia are key players in the initial stages of acute myocardial infarction and ischemic stroke.
- The comparative anti-inflammatory effects of naringenin on these cells, particularly in response to lipopolysaccharide (LPS), were not fully elucidated.
- Naringenin, a flavonoid, was investigated for its potential to modulate inflammatory responses in these critical immune cells.
Purpose of the Study:
- To compare the anti-inflammatory efficacy of naringenin on LPS-stimulated macrophages and microglia.
- To determine the dose-dependent inhibitory effects of naringenin on nitrite production and key inflammatory markers.
- To compare the anti-inflammatory potential of naringenin with Vitamin C in these cellular models.
Main Methods:
- Utilized RAW 264.7 macrophages and BV2 microglia cell lines stimulated with lipopolysaccharide (LPS).
- Assessed cell viability, nitrite production, and expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2).
- Compared the effects of varying concentrations of naringenin and a fixed concentration of Vitamin C.
Main Results:
- Naringenin demonstrated dose-dependent inhibition of nitrite production and iNOS/COX-2 expression in both cell types under LPS stimulation.
- Macrophages exhibited higher viability at elevated naringenin concentrations and were more sensitive to LPS activation compared to microglia.
- Naringenin showed a broader effective concentration range and lower effective concentrations in macrophages (50 μmol/L) versus microglia (100 μmol/L).
Conclusions:
- Naringenin is a potent inhibitor of LPS-induced inflammation in macrophages and microglia, with superior efficacy observed in macrophages.
- Vitamin C (100 μmol/L) exhibited less suppression of nitrite production than naringenin (100 μmol/L) in macrophages and microglia.
- Dietary intake of naringenin-rich flavonoids may offer protective benefits against inflammatory processes in cardiovascular and cerebrovascular diseases.
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