Sirolimus and Aging Skin
Sirolimus and Aging Skin
By Sarah Taylor, PharmD
As the
average age of the world population increases, there has been growing demand
for anti-aging products. Recent estimates put the size of the global anti-aging
marketplace at about 50 billion Dollars (USD).1 Compounding
pharmacies often get requests from doctors for products that comprise
anti-wrinkle or skin tightening creams. The pathophysiology of aging is
multi-modal, and though of course aging is inevitable, it can be accelerated by
a variety of factors. Such factors include, but are not limited to: hormonal
changes, metabolic processes, and external factors such as UV light, smoking,
and air pollution. The reversal of photoaging is
often targeted as the main culprit in early wrinkles and skin degeneration.2
A variety of Active Pharmaceutical Ingredients
(APIs) are often used for aging skin, including niacinamide, tretinoin,
retinol, and ascorbic acid (among others). Described in more detail below,
sirolimus is one emerging API with a unique mechanism of action for the
management of aging skin.
Sirolimus
is commercially available in oral, intravenous, and (as of April 2022) a
topical gel form. The topical form is indicated for facial angiofibroma. Sirolimus is typically indicated
for suppression of the immune system and utilized to help manage patients who
have undergone organ transplant.3 Though it shares a name to
calcineurin inhibitors such as tacrolimus or pimecrolimus, it has a separate
mechanism of action involving mammalian target of rapamycin (mTOR) inhibition. MTOR is a protein kinase that is involved in
the control of cell growth, proliferation, and survival.4 In addition to this mechanism of action, recent studies have demonstrated
that topical sirolimus can reduce the expression of the p16INK4A
protein resulting in a reduction of cellular aging processes.5 It’s been found that increased
expression the p16INK4A protein present in the skin, is correlated
with markers of aging such as skin elasticity and formation of wrinkles.5
One placebo-controlled randomized exploratory study had patients apply 0.5ml of
10uM (equivalent to approximately 0.001%) sirolimus cream to one hand, and a
placebo product to the other and monitored patients at 2,4,5, and 8 months
after initiation of treatment .5 Clinical
improvement in skin photoaging, including a decrease in fine wrinkles, a
decrease in dermal volume, and a brighter and more even skin tone was noted for
the sirolimus treated skin. No treatment related adverse effects were noted in
this study and no blood samples from patients noted detectable levels of
sirolimus.5 In addition to this evidence to support the use of
topical sirolimus, multiple studies in mouse models have reported that systemic
sirolimus treatment resulted in increased life span, with one study concluding
that the treatment “can robustly delay aging” in their studied mouse models.6,7
A review of studies of sirolimus in mice concluded with a recommendation to move to human preclinical
trials for certain related conditions.6,7
Though
more literature is needed, current information regarding low dose topical
sirolimus as a potential treatment option for photoaged skin is promising. Click
here for more
information on formulation of sirolimus into topical dosage forms.
Sources:
1.
“Value
of the global anti-aging market 2018-2023,”
Statista, March 18, 2022,.
https://www.statista.com/statistics/509679/value-of-the-global-anti-aging-market/.
2.
Mukherjee S, Date A, Patravale V,
Korting H, Roeder A, Weindl G, “.
Retinoids in the treatment of skin aging: an overview of clinical
efficacy and safety,”.
Clin Interv Aging. 2006; 1(4): 327-348.
3.
Rapamune – sirolimus solution. [Package
Insert]. Wyeth Pharmaceuticals LLC. Philadelphia, PA. 2021.
4.
Ballou LM, Lin RZ, “.
Rapamycin and mTOR kinase inhibitors.,”
J Chem Biol. 2008 Nov;1(1-4):27-36,.
doi: 10.1007/s12154-008-0003-5,.
Epub 2008 May 15,.
PMID: 19568796; PMCID: PMC2698317.
5.
Lee Chung C, Lawrence I, Hoffman M,.
“Topical rapamycin reduces markers of senescence
and aging in human skin: an exploratory, prospective, randomized trial,”.
GeroScience . 2019;
41: 861-869.
6.
Selvarani, R., Mohammed, S. &
Richardson, A,. “Effect
of rapamycin on aging and age-related diseases—past and future,”.
GeroScience 43, 1135–1158 (2021).
7.
Bitto A, Ito TK, Pineda VV, LeTexier
NJ, Huang HZ, Sutlief E, Tung H, Vizzini N, Chen B, Smith K, Meza D, Yajima M,
Beyer RP, Kerr KF, Davis DJ, Gillespie CH, Snyder JM, Treuting PM, Kaeberlein M,.
“Transient rapamycin treatment can
increase lifespan and healthspan in middle-aged mice,”.
Elife,. 2016
Aug 23;5:e16351, . doi:
10.7554/eLife.16351.
Comments
Post a Comment