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50 ANTI-AGEING


Skin Hydration Using Corneometer


Measurement Schedule


T (1hr) T (2hr) T (4hr) T (8hr) T (24hr) T (48hr)


Skin Hydration - Regression Using Corneometer


Skin Hydration - Regression Using Corneometer


Treatment Schedule


Wash with Non- Moisturizing Soap: 2X/Day


Volar Forearm


T(-2)


Wash with Non- Moisturizing Soap: 2X/Day


Volar Forearm


T(-1)


Final Volar Forearm Wash with Non- Moisturizing Soap: Morning


T(0)


1x Product Application Figure 12: Schematic outline of extended skin hydration protocol.


Many of these threats are directed to the skin cells’ mitochondrial functions and cause an increased expression of free radicals. These errant and damaging molecules cause the circulating NLR proteins to assemble into a unique, flower- like structure, called an Inflammasome Complex, that contains ASC elements that attract inert Pro-Caspase-1 (Fig 15).13


Upon


binding to the ASC portion of the NLRP Inflammasome Complex, the Pro-Caspase-1 is cleaved and active Caspase-1 is released. In 2017, O’Brien et al., reported on a bioluminescence-based assay that allows for direct detection of active Caspase-1 released via the activated NLRP Inflammasome Complex.14


We employed


this new assay to examine the effects of various potential activators to cause increased expression of active Caspase-1 in skin cells. Our work with UVB radiation confirmed Faustin’s earlier work, demonstrating in this testing model, that UVB radiation is a potent activator of the NLRP inflammasomes as measured by active Caspase-1 release.3 The term “inflammaging” has been


n StrataPhixTM


350 300 250 200 150 100 50 0


p≤0.001 p≤0.28


p≤0.009 p≤0.0009 p≤0.008


p≤0.0009 p≤0.006


p≤0.0003 p≤0.02


coined to describe the effects of errant or chronic inflammation in the body’s ageing processes.14-16


Essentially, it is suggested


that while it is essential for the body to respond to exogenous threats with inflammation, continuous or repeated upregulation of the inflammation response leads to accelerated ageing, including ageing of the skin. In the work reported by Mejias et al., they were able to examine fibroblasts isolated from the same individual at ages 49, 52 and 64 years.11


known as autophagy.17 As skin cells age, The


studies demonstrated that: 1) ageing cells accumulate markers of inflammasome activation including ACS protein and active Caspase-1 and 2) reduction of these markers via treatments with a known Caspase-1 inhibitor, Ac-YVAD-CMK, after oxidative stress demonstrated that “inhibition of the inflammasome in the aging process has the potential to treat the cellular damage associated with oxidative stress”. This study directly links the ageing process with inflammasome activation in human fibroblasts. Inflammasome activation is intimately associated as well with the cellular protein recycling mechanisms


POLY (3%) n Placebo nWashed Control


2.5 2.0 1.5 1.0 0.5 0


T1 (1 hr) T2 (2 hr) T3 (4 hr) T4 (8 hr) T5 (24 hr) T6 (48 hr)


Figure 13: Results of extended skin hydration study on n=10 volunteers applying formulations to the inner volar forearm. Asterisks indicate statistical significance (p≤0.05).


PERSONAL CARE EUROPE


p=0.004 p=0.5


they begin to produce more abnormal proteins due to excessive mitochondrial release of Reactive Oxygen Species (ROS). As the cells make more damaged proteins, this leads to activation of the NLRP Inflammasome inflammation processes which leads, ultimately, to more inflammaging. Of even more interest is the work by Furman et al., who noted that expression of inflammasomes can stratify individuals into groupings based on their ageing phenotypes.18


This study links the cellular


activity of inflammasomes to people’s actual physical appearance and health. In the studies described here, it has been found that UV energy and ATP were very effective at activating NHEKs to express NLRP-activated Caspase-1 release as measured using a newly developed bioluminescent assay. Further studies have demonstrated three powerful blends, collectively called StrataPhix Technology Series, each has the ability, in vitro, to modulate the expression of active Caspase- 1 in inflammasome-activated NHEKs. Further examination of one important blend


n StrataPhixTM


p=0.0002 p=0.000004


POLY (3%) n Placebo nWashed Control


p=0.0002 p=0.000005


p=0.003 p=0.003


p=0.03 p=0.4


p=0.0002 p=0.2


T1 (1 hr)


T2 (2 hr)


T3 (4 hr)


T4 (8 hr)


T5 (24 hr) T6 (48 hr)


Figure 14: Skin hydration data comparing a commercial moisturiser that contains glycerin and sodium hyaluronate versus the same formulation containing 3% StrataPhix™ POLY on n=6 volunteers. Asterisks indicate statistical significance (p≤0.05).


April 2020


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