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34 ANTI-AGEING A


■ Control ■ Placebo ■ 2% Sunflower sprout active 200


150 100 50 0 *p<0.05 versus stressed control and placebo


Figure 3: Rejuvenation study on skin explants: sunflower sprout active enhances mitochondrial function and collagen density To evaluate the response to DNA damage


To evaluate the effect of the sunflower


the levels of the DNA damage response marker γH2AX were assessed via immunofluorescence analysis. Ageing stress induced a substantial increase in DNA damage. Co-treatment with sunflower sprout extract significantly reduced this damage compared to the stressed condition, indicating that sunflower sprout extract improves the DNA repair mechanism (Figure 2B).


Rejuvenation study on skin explants Replenished NAD+


levels are recognized for their


potential to slow down and even reverse the ageing process. Consequently, the rejuvenation potential of sunflower sprouts was further investigated. To assess this, skin explants were initially


exposed to UV-A radiation to induce ageing stress and subsequently treated with either a cream containing 2% sunflower sprout active or a corresponding placebo.


A 1 0.5 0 -0.5 -1 *p<0.05 versus initial conditions and p<0.01 versus placebo Figure 4: Clinical rejuvenation study: sunflower sprout active induces a lifting effect and visibly improves signs of skin ageing PERSONAL CARE May 2024 www.personalcaremagazine.com


sprout active on mitochondrial function and proteostasis, mitochondrial protein carbonylation, a marker of mitochondrial protein damage, was analyzed by immunoblotting. UV-A radiation induced an increase in mitochondrial protein carbonylation in the skin explants. The application of sunflower sprout active


significantly reduced the mitochondrial damage compared to the stressed condition as well as the placebo, returning it to levels similar to the ones of the unstressed control (Figure 3A). The obtained rejuvenation results


demonstrate that sunflower sprout active can support mitochondrial function as well as cellular metabolism, and thus potentially slow down the ageing process of skin. Exposure to UV-A radiation plays a


significant role in photoageing due to its ability to penetrate deeply into the dermis, leading to the degradation of collagen fibres.


■ Placebo ■ 2% Sunflower sprout active * B Before After 42 days * UV-A stress + placebo 2% Sunflower sprout active UV-A stress + B Control UV-A stress


K index


Given these effects, the impact of sunflower


sprout active on collagen density was investigated within the rejuvenation model. UV-A radiation was observed to significantly reduce the collagen density in skin explants. However, the application of sunflower


sprout active led to a substantial increase in collagen density when compared to the UV-A exposed control (Figure 3B). A higher K index corresponds to an increased density of collagen fibres.


The representative images of collagen


density, obtained through XPolar® technology, illustrate the more uniform and denser distribution of collagen fibres after the use of 2% sunflower sprout active. This is evidenced by the more evenly distributed blue-green areas and a reduction in black, low-density zones, indicative of strengthened skin connective tissue.


These findings suggest that sunflower sprout active can effectively counteract


Improvement in reshaping compared to initial conditions in %


Mitochondtial protein carbonylation compared to control in %


UV-A stress


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