Figures & data
Figure 1. Effect of the extract on viability of primary human skin fibroblasts. Cells were treated with 0.1% ethanol (control group) or the extract at concentrations in range of 0.5 to 50 μg/mL for 24, 48 and 72 h. Results are expressed as percentage of cell viability as compared to untreated cells for which the optical density was adjusted to 100%. Each bar represents mean ± SD of triplicate study.
![Figure 1. Effect of the extract on viability of primary human skin fibroblasts. Cells were treated with 0.1% ethanol (control group) or the extract at concentrations in range of 0.5 to 50 μg/mL for 24, 48 and 72 h. Results are expressed as percentage of cell viability as compared to untreated cells for which the optical density was adjusted to 100%. Each bar represents mean ± SD of triplicate study.](/cms/asset/dc1ffe6e-f731-4a53-9a70-d3e17494edee/iphb_a_1179768_f0001_b.jpg)
Figure 2. Morphology of primary human skin fibroblasts, untreated cells or treated with 50 μg/mL extract for 72 h at magnification of 10×.
![Figure 2. Morphology of primary human skin fibroblasts, untreated cells or treated with 50 μg/mL extract for 72 h at magnification of 10×.](/cms/asset/eae23230-74e8-4c89-a4b1-0a864d0dfe36/iphb_a_1179768_f0002_b.jpg)
Figure 3. Effects of the extract (50 μg/mL) on type I procollagen (A), MMP-1 (B) and MMP-13 (C) productions by UVB-irradiated human skin fibroblasts at 4 and 24 h after irradiation. Each bar represents mean ± SD of triplicate study. *p <0.05 and **p <0.01, when compared between two groups (Student’s t-test).
![Figure 3. Effects of the extract (50 μg/mL) on type I procollagen (A), MMP-1 (B) and MMP-13 (C) productions by UVB-irradiated human skin fibroblasts at 4 and 24 h after irradiation. Each bar represents mean ± SD of triplicate study. *p <0.05 and **p <0.01, when compared between two groups (Student’s t-test).](/cms/asset/71ccd55b-f3be-4982-8359-e3a337ea8508/iphb_a_1179768_f0003_b.jpg)
Figure 4. Viability of primary human skin fibroblasts after UVB irradiation for 4 and 24 h. Results are expressed as percentage of cell viability as compared to non-UVB-irradiated group for which the optical density was adjusted to 100%. Each bar represents mean ± SD of triplicate study.
![Figure 4. Viability of primary human skin fibroblasts after UVB irradiation for 4 and 24 h. Results are expressed as percentage of cell viability as compared to non-UVB-irradiated group for which the optical density was adjusted to 100%. Each bar represents mean ± SD of triplicate study.](/cms/asset/d03ab99b-47dc-46d0-baee-21d054276da7/iphb_a_1179768_f0004_b.jpg)
Figure 5. Epidermal thickness of mice skin tissues at 12 weeks after UVB irradiation. Skin was daily applied deionized water, vehicle for extract solution, 3% w/v vitamin C solution or 5% w/v extract solution at 2 h after UVB irradiation. Each bar represents mean ± SD of triplicate study. *p <0.05, when compared between two groups (Student’s t-test).
![Figure 5. Epidermal thickness of mice skin tissues at 12 weeks after UVB irradiation. Skin was daily applied deionized water, vehicle for extract solution, 3% w/v vitamin C solution or 5% w/v extract solution at 2 h after UVB irradiation. Each bar represents mean ± SD of triplicate study. *p <0.05, when compared between two groups (Student’s t-test).](/cms/asset/6ef920ee-65d7-4312-94f5-27c659d1cc49/iphb_a_1179768_f0005_b.jpg)
Figure 6. Light microscope (magnification 20×) of 12 week-UVB irradiated mice skin tissues stained with haematoxylin–eosin to show the effects of extract and vitamin C on epidermal thickness.
![Figure 6. Light microscope (magnification 20×) of 12 week-UVB irradiated mice skin tissues stained with haematoxylin–eosin to show the effects of extract and vitamin C on epidermal thickness.](/cms/asset/3a5b0d21-6836-4f10-9b21-298347cb314e/iphb_a_1179768_f0006_c.jpg)
Figure 7. Hydroxyproline content in dermal skin tissues of mice after UVB irradiation for 12 weeks. Skin was daily applied deionized water, vehicle for extract solution, 3% w/v vitamin C solution or 5% w/v extract solution at 2 h after UVB irradiation for 12 weeks. Each bar represents mean ± SD of triplicate study. **p <0.01, when compared between two group (Student’s t-test).
![Figure 7. Hydroxyproline content in dermal skin tissues of mice after UVB irradiation for 12 weeks. Skin was daily applied deionized water, vehicle for extract solution, 3% w/v vitamin C solution or 5% w/v extract solution at 2 h after UVB irradiation for 12 weeks. Each bar represents mean ± SD of triplicate study. **p <0.01, when compared between two group (Student’s t-test).](/cms/asset/f3f0bc93-8b87-46df-8ae8-53edd0b1cc8e/iphb_a_1179768_f0007_b.jpg)