Clitoria ternatea: Perspectives on Its Application in Foods and Potential Health Benefits
Abstract
1. Introduction
2. Consumption, Market, and Processing of Edible Flowers
3. Anthocyanins in C. ternatea
4. C. ternatea: Functional Properties, Health Benefits, and Applications in the Food Industry
4.1. Functional and Health-Related Claims
4.1.1. Antidiabetic Effect
4.1.2. Anticarcinogenic Activity
4.1.3. Hepatoprotective Activity
4.1.4. Anti-Obesity
4.1.5. Antioxidant Activity
4.1.6. Anti-Inflammatory Activity
4.2. Technological Applications of C. ternatea
4.2.1. Natural Colorant
4.2.2. Packaging
4.2.3. Other Applications
5. Conclusions
Author Contributions
Funding
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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| Study/Extraction Method | Main Results | Reference |
|---|---|---|
| Antidiabetic Studies | ||
| Methanolic extract of C. ternatea petals (1:10 w/v leaf: solvent) obtained by maceration for 24 h. | The methanolic extract (3865.6 mg GAE/g) inhibited 24.7% of α-glucosidase activity at 100 μg/mL, suggesting a potential antidiabetic effect of C. ternatea petals. | [30] |
| Aqueous extract (1:25, w/v) obtained by microwave-assisted extraction of fresh petals. | At 100 μg/mL, the inhibition rates were as follows:
| [31] |
| Ethanolic extract prepared by maceration of C. ternatea flowers. | Administration of the extract resulted in significant reductions in body weight, obesity index, and Lee index, demonstrating promising effects in controlling obesity in rats. | [32] |
| Anticarcinogenic Studies | ||
| Ethanolic extract of leaves prepared by Soxhlet extraction. | The ethanolic extract (17.7 mg GAE/g) exhibited potent cytotoxic activity against cancer cells, as indicated by low IC50 values. Treatment also increased mRNA levels of GAX and DIABLO while reducing NAIP1 expression, supporting the involvement of pro-apoptotic pathways in the extract’s action. | [33] |
| Extract of C. ternatea obtained by maceration in ethanol. | The extract exhibited high cytotoxic activity against the T47D breast cancer cell line (IC50 = 5.21 µg/mL). | [34] |
| Hepatoprotective Studies | ||
| Ethanolic extract of flowers obtained by maceration. | The most pronounced effects were observed with the highest extract dose (800 mg/kg). Treatment increased hepatic antioxidant enzyme activities (GSH--Px and GST) and significantly reduced alkaline phosphatase levels, indicating protection of the liver against hyperglycemia- and dyslipidemia-induced damage. Additionally, markers of kidney injury, including blood urea, serum creatinine, and uric acid, were reduced. | [35] |
| Ethanolic extract of flowers obtained by maceration. | Administration of the extract significantly reduced levels of aspartate aminotransferase, alanine aminotransferase, and bilirubin. | [36] |
| Anti-obesity Studies | ||
| Aqueous extract of petals (0.125:25, w/v) obtained under stirring at 40 °C for 30 min. | The extract protected C57BL/6 mice against obesity, oxidative stress, and inflammation induced by a high-fat, high-fructose diet. It also enhanced reverse cholesterol transport by increasing HDL-C and decreasing LDL-C levels. | [37] |
| Aqueous extract of dried flowers (1:20, w/v) obtained by double boiling at 90–95 °C for 4 h. | Acute consumption of a high-fat meal with extract reduced postprandial serum triglycerides and free fatty acids. The extract significantly enhanced plasma antioxidant status, increasing FRAP, thiol levels, and endogenous antioxidant enzyme activity, including glutathione peroxidase. However, it did not attenuate postprandial hyperglycemia or the rise in pro-inflammatory cytokines. | [38] |
| Aqueous flower extract obtained by heating at 60 °C and incorporated into the herbal beverage. | An in vivo study in obese mice showed reduced body weight and improved lipid profile. | [39] |
| Antioxidant Studies | ||
| Aqueous flower extract obtained by maceration for 2 h. | The extract exhibited high antioxidant activity and potential protective effects against bisphenol A-induced oxidative damage on reproductive performance, improving pregnancy rates and litter size. | [40] |
| Aqueous extract of dried flowers (1:20, w/v) obtained by double boiling at 90–95 °C for 4 h. | Significant increases in plasma antioxidant capacity (plasma iron reducing capacity (FRAP), oxygen radical absorbance capacity (ORAC), trolox equivalent antioxidant capacity (TEAC), and protein thiol) and decreases in malondialdehyde (MDA) levels were observed in individuals receiving 1 g and 2 g of C. ternatea flower extract (CTE). Furthermore, CTE consumption protected sucrose-induced reductions in ORAC, TEAC, and MDA. | [41] |
| Anti-inflammatory Studies | ||
| Ethanol extract of the roots obtained using a Soxhlet extractor. | The ethanolic extract of C. ternatea (EECT) demonstrated a significant reduction in the mean paw edema volume in both carrageenan- and histamine-induced inflammation. A considerable decrease in paw diameter was observed in the EECT (200 and 400 mg/kg) and diclofenac (10 mg/kg) treated groups after day 7. Diclofenac (10 mg/kg) and EECT (400 mg/kg) demonstrated a significant reduction in paw diameter from day 14 compared with the CFA control (p < 0.001). | [42] |
| Ethanolic flower extract obtained by ultrasonic extraction at 60% power for 15 min. | The extract demonstrated anti-inflammatory, antimicrobial, and antioxidant activity in silico. The anthocyanin compounds in C. ternatea have anti-inflammatory effects by inhibiting or reducing the activity of pro-inflammatory proteins like TNF-α, NFκB, RANKL-RANK, and IL-6, which can trigger the upregulation of anti-inflammatory proteins such as IL-10. | [43] |
| Methanolic extract of fresh flowers prepared for 3 h. | The results showed significant inhibition of the COX-1 and COX-2 enzymes, with values of 82.74 ± 1.42% and 85.29 ± 1.67%, respectively, at a concentration of 200 µg/mL. | [44] |
| Effect | Type of Study | Compounds Involved | Pathways/Mechanisms | Reference |
|---|---|---|---|---|
| Anticancer | In vitro | Anthocyanins | Apoptosis induction, ROS modulation, NF-κB inhibition | [65] |
| Anticancer | In vitro and In vivo | Flavonoids, anthocyanins | Suppression of fatty acid synthesis via SREBP1 pathway, enhancement of cisplatin efficacy | [66] |
| Anti-obesity | In vivo | Anthocyanins | Modulation of lipid metabolism, activation of AMPK, and reduction in oxidative stress | [37] |
| Anti-inflammatory | In vitro | Ternatin Anthocyanins | Inhibition of NF-κB nuclear translocation, reduction in iNOS expression, and NO production | [67] |
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Maia, N.M.A.; Andressa, I.; Cunha, J.S.; Costa, N.d.A.; de Oliveira, E.B.; Leite Júnior, B.R.d.C.; Vieira, É.N.R. Clitoria ternatea: Perspectives on Its Application in Foods and Potential Health Benefits. Plants 2025, 14, 3322. https://doi.org/10.3390/plants14213322
Maia NMA, Andressa I, Cunha JS, Costa NdA, de Oliveira EB, Leite Júnior BRdC, Vieira ÉNR. Clitoria ternatea: Perspectives on Its Application in Foods and Potential Health Benefits. Plants. 2025; 14(21):3322. https://doi.org/10.3390/plants14213322
Chicago/Turabian StyleMaia, Nicole Marina Almeida, Irene Andressa, Jeferson Silva Cunha, Nataly de Almeida Costa, Eduardo Basílio de Oliveira, Bruno Ricardo de Castro Leite Júnior, and Érica Nascif Rufino Vieira. 2025. "Clitoria ternatea: Perspectives on Its Application in Foods and Potential Health Benefits" Plants 14, no. 21: 3322. https://doi.org/10.3390/plants14213322
APA StyleMaia, N. M. A., Andressa, I., Cunha, J. S., Costa, N. d. A., de Oliveira, E. B., Leite Júnior, B. R. d. C., & Vieira, É. N. R. (2025). Clitoria ternatea: Perspectives on Its Application in Foods and Potential Health Benefits. Plants, 14(21), 3322. https://doi.org/10.3390/plants14213322

