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FACIAL SAGGING
Waterless botanical extract enhancement of PPAR-ϒ DNA binding
350% 300% 250% 200% 150% 100% 50% 0%
Negative control (untreated)
0.1%
0.3%
Positive control (rosiglitazone)
Figure 2: Stimulation of PPARγ association with adipogenesis relevant gene promoters using the waterless botanical extract. Pre-adipocyte cells were incubated with increasing amounts of the waterless botanical extract after which nuclear protein fractions were harvested from the cell nuclei. These fractions were evaluated using an enzyme-linked immunosorbent assay (ELISA) to measure the PPARγ association with the DNA consensus site. Rosiglitazone was used as a positive control (red bar). Untreated cells were used as a negative control (green bar)
Waterless botanical extract stimulation of pre-adipocyte differentiation and fat production
Figure 1: Signature purple coneflower of Echinacea purpurea
the impact of the waterless botanical extract from Echinacea purpurea on the DNA binding capacity of PPARγ to the promoter sequence for the adipogenesis pathway. A pharmacological stimulator of PPARγ association with the promoter called rosiglitazone was included in the experiment as a positive control to compare against.3,4 Pre-adipocytes were left untreated, treated
with rosiglitazone, or treated with the waterless botanical extract at 0.1 or 0.3%. Post-treatment, the nuclear protein fractions were harvested from the cell nuclei that were individually tested for PPARγ binding to the promoter sequence using an enzyme-linked immunosorbent assay (ELISA). As shown in Figure 2, there was a dose-
dependent increase in the amount of PPARγ binding to DNA in response to incubation with the waterless botanical extract that was closely comparable to rosiglitazone. In vitro testing with monolayers of pre-
adipocyte cells continued with an investigation into the capacity of the waterless botanical extract to stimulate their differentiation into actual adipocytes (fat cells). This time, Oil Red O staining (observed as dark
Untreated 0.03%
red) was utilized to visualize the accumulation of fat content in pre-adipocytes treated with increasing levels of the waterless botanical extract, indicative of the transition into professional fat cells.5,6
The cells were further counterstained
with hematoxylin that binds to cell nuclei as a contrasting colour (pale violet). Microscopic imaging revealed a dose-
0.1% 0.3%
Figure 3: Adipocyte differentiation dose-dependently promoted by the waterless botanical extract. Pre-adipocyte cells were incubated with increasing amounts of the waterless botanical extract and subsequently stained using Oil Red O to observe how many of the cells had differentiated into adipocytes. Untreated cells were used as a negative control
PERSONAL CARE MAGAZINE June 2026
dependent increase in adipocyte differentiation with application of the fatty acid alkylamides that was observed through the Oil Red O staining (Figure 3). These findings were further corroborated by morphometric analyses conducted in a subsequent ex vivo study that saw the waterless botanical extract promote both the maturation of large volume adipocytes with corresponding increases in lipid synthesis (data not shown).
Clinical evidence – seeing is believing Finally, a double-blinded, placebo-controlled clinical study was designed to evaluate the plumping efficacy of 3% E. purpurea waterless
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Level of PPAR-ϒ DNA binding
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