Hyperbaric oxygen treatments (HBOT) in healthy aging adults can stop the aging of blood cells and reverse the aging process

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A new study from Tel Aviv University (TAU) and the Shamir Medical Center in Israel indicates that hyperbaric oxygen treatments (HBOT) in healthy aging adults can stop the aging of blood cells and reverse the aging process.

In the biological sense, the adults’ blood cells actually grow younger as the treatments progress.

The researchers found that a unique protocol of treatments with high-pressure oxygen in a pressure chamber can reverse two major processes associated with aging and its illnesses: the shortening of telomeres (protective regions located at both ends of every chromosome) and the accumulation of old and malfunctioning cells in the body.

Focusing on immune cells containing DNA obtained from the participants’ blood, the study discovered a lengthening of up to 38% of the telomeres, as well as a decrease of up to 37% in the presence of senescent cells.

The study was led by Professor Shai Efrati of the Sackler School of Medicine and the Sagol School of Neuroscience at TAU and Founder and Director of the Sagol Center of Hyperbaric Medicine at the Shamir Medical Center; and Dr. Amir Hadanny, chief medical research officer of the Sagol Center for Hyperbaric Medicine and Research at the Shamir Medical Center.

The clinical trial was conducted as part of a comprehensive Israeli research program that targets aging as a reversible condition.

The paper was published in Aging on November 18, 2020.

“For many years, our team has been engaged in hyperbaric research and therapy – treatments based on protocols of exposure to high-pressure oxygen at various concentrations inside a pressure chamber,” Professor Efrati explains.

“Our achievements over the years included the improvement of brain functions damaged by age, stroke or brain injury.

“In the current study, we wished to examine the impact of HBOT on healthy and independent aging adults, and to discover whether such treatments can slow down, stop or even reverse the normal aging process at the cellular level.”

The researchers exposed 35 healthy individuals aged 64 or over to a series of 60 hyperbaric sessions over a period of 90 days. Each participant provided blood samples before, during and at the end of the treatments, as well as some time after the series of treatments concluded.

The researchers then analyzed various immune cells in the blood and compared the results.

The findings indicated that the treatments actually reversed the aging process in two of its major aspects:

  • The telomeres at the ends of the chromosomes grew longer instead of shorter at a rate of 20% to 38% depending on the cell type;
  • the percentage of senescent cells in the overall cell population was reduced significantly—by 11%-37% depending on cell type.

“Today, telomere shortening is considered the ‘holy grail’ of the biology of aging,” Professor Efrati says.

“Researchers around the world are trying to develop pharmacological and environmental interventions that enable telomere elongation.

Our HBOT protocol was able to achieve this, proving that the aging process can in fact be reversed at the basic cellular-molecular level.”

“Until now, interventions such as lifestyle modifications and intense exercise were shown to have some inhibiting effect on telomere shortening,” Dr. Hadanny adds.

“But in our study, only three months of HBOT were able to elongate telomeres at rates far beyond any currently available interventions or lifestyle modifications.



Oxygen, at standard temperature and pressure, is a color- less, odorless, tasteless gas. It can exist in its monatomic state, but its preferred state is diatomic, O2.

It also exists in a triatomic form, or more commonly known as ozone, and is found in the upper limits of the atmosphere [1,2].

Since its discovery, oxygen has been used in treating me- dical conditions. The first recorded use of hyperbaric air therapy was in 1662 by Nathaniel Henshaw to treat chro- nic conditions, but it wasn’t until the 1920s when Hyperbaric Oxygen Therapy (HBOT) really received attention and is widely noticed due to previous reports of oxygen toxicity [1].

The first HBOT chamber made in the United States was in 1861 in New York but the most well known chamber was built in 1921 in Kansas [1].

But due to more reports of concentrated oxygen toxicity, HBO therapy was not fully approved and put into practice until the 1937 by Behnke and Shaw for decompression sickness [2].

After the recorded success of HBOT, its use as treatments for numerous medical conditions grew and researches on this subject widen as the treatment has shown itself to be promising.

At present, HBOT has grown and became more than just a treatment for decompression sickness. Starting from the late 1950s until now, HBO is used to treat gangrene, stroke, post cardiac arrest patients, and carbon monoxide poisoning [1-3].

Uses of oxygen for rejuvenation
Joseph Priestley, one of the first discoverers of oxygen, once said, “Who can tell but that, in time, this pure air may become a fashionable article in luxury.” It seems that as the world is developing and Joseph Priestley’s prediction about air is becoming a reality [4].

As the advancement of industrialization, the supply of fresh air is steadily decreasing, making good quality of air more and more of a luxury. Oxygen bar has become available in some big cities such as Los Angeles and Tokyo to provide people with a supply of pure oxygen for a certain fee.

These places sell oxygen for recreational uses and different aromas are available for customers to choose from. There are many health benefits claims made by those supporters of oxygen bars.

They claimed that the usage could enhance health by strengthening the im- mune system, reduce stress, increase energy, and reduce headaches and sinus problems. However, specific researches on these oxygen bars claimed benefits have not been done.

Due to the reigning desire in today’s society to maintain youthful appearance, development of minimally invasive dermatological procedures is progressing to rejuvenate aging face. Quite a few of these minimally invasive procedures have been effectively developed such as chemical peels, intradermal fillers, and botulinum toxins, but one not yet fully understood is HBOT [5,6].

HBOT as a therapy for aesthetic means is a relatively new use so there have not been a great number of researches done specifically on usage of oxygen therapy on reduction of wrinkles.

However, from the few that has been done, positive outcomes were achieved and the use of oxygen therapy for treatment of wrinkles seems an attractive option [7,8]. Receiving regular treatments of HBOT is thought to increase skin elasticity and stimulate collagen production, leading to reduction of wrinkles and fine lines and improvement in skin texture [9].

Many dermatology clinics and even spas have utilized machines that deliver concentrated oxygen to the patient or client to treat age-related skin problems.

Oxygen is used in skin care because it is thought that delivery of natural oxygen increases cell metabolism. The use of oxygen therapy as a process of skin rejuvenation and reduction of loss of elasticity leading to formation of lines and wrinkles are becoming increasingly widespread in skin care clinics because of increasing successful results of their usage due to developing techno- logies. However, scientific evidences for those claims are waiting to be provided.

Causes of wrinkle formation
Health of skin is related to whole body health because the skin not only acts as a physical barrier against infections from foreign materials, but also controls the immune system, and produces hormones and neurotransmitters [10]. Wrinkles and aesthetic skin problems, like blemishes and acne scars, are caused by many factors such as aging, exposure to the environment, especially an overexposure to the sun, smoking, gender, and poor nutrition. Wrinkles caused through aging are an intrinsic factor-caused aging, or genetically programmed aging, that happens over time.

This genetically programmed aging mainly causes a de- crease production of fibroblast, collagen, and elastin, which results in skin wrinkling and elasticity loss [11]. Smoking causes skin aging and wrinkles because tobacco inhibits production of collagen and increase MMP and elastosis production, which degrades matrix proteins im- portant for skin elasticity [12].

Gender wise, skin of women seems to receive more wrinkles than men due to perhaps the estrogen level in women. Estrogen has been found to increase collagen production and skin thickness so as women age with decrease estrogen production, wrin- kles formation are more prominent in women than men [13].

As for dietary intake, increasing vitamin C and linoleic acid consumption is associated with slower aging skin, while increasing fat and carbohydrates consumption cau- ses faster skin aging [14].
UV radiation causes wrinkles and skin damage, which are symptoms of cutaneous aging or photoaging [15]. Photoag- ing is characterized by epidermal hyperplasia or atrophy, thickening of basement membrane and stratum corneum, loss of dermal papillae, unusual keratinocytes and melanocytes, degradation of extracellular matrix molecules such as damage to collagen fibers, excessive deposition of abnormal elastic fibers, and increase of glycosaminoglycans.

Photoaging is also characterized by dryness, rough texture, abnor- mal pigmentation, thickening of epidermis, deep creases, and visible wrinkles [16]. UV-B induces matrix metallopro- teinases (MMPs), which degrades basement membrane and rearranges the extracellular matrix (ECM), and Type I Collagenase, which digest Type I collagen that is important for supporting the skin, are also causes of wrinkle formation [17].

In addition, it has been found that UV radiation can cause cutaneous angiogenesis, the formation of new blood vessels from pre-existing vessels, that can lead to wrinkles formation by inducing the hypoxia inducible factor (HIF-1) and up-regulation of vascular endothelial growth factor (VEGF) [18,19] (Figure 1).

Angiogenesis has been found to be correlated to wrinkling of the skin and can be caused by not only through UV-B radiation but also through hypoxic conditions. There has been researches done and evidences found of hypoxic conditions leading to wrinkling through angio- genesis by affecting and increasing HIF, which regulates the vascular networks [15]. VEGF is a major angiogen- esis factor and a target gene of HIF protein [20,21].

In studies done, the level of VEGF has been shown to be up regulated in areas with necrosis and areas under hyp- oxic conditions [22-24].

Mechanisms for HBOT skin rejuvenation
HIF-1α
As mentioned above, UV-B radiation can cause angio- genesis through inducing the HIF-1 protein, leading to

Figure 1 Overview of possible mechanism used by HBOT to attenuate wrinkle formation from exposure to UVB radiation. UVB irradiation is shown to upregulate pathways that cause wrinkles such as the HIF-1α, neutrophils, and angiogenesis pathways. Hyperoxic condition is shown to inhibit those pathways activated by UVB, which results in decreased wrinkles formation.

wrinkling of skin. There are two subunits to the HIF-1 protein, α and β. Of these two, the subunit directly in- volved with hypoxic condition responses is the HIF-1α.

The mRNA of HIF-1α is normally made in cells. In some cells, the mRNA level of HIF-1α is increased during hypoxia leading to an increase in transcription of many genes including VEGF.

But in most cells under hypoxic condi- tions, the mRNA level remains the same but the level of HIF-1α protein increases, suggesting that during normal oxygen conditions, the HIF-1α protein usually undergoes proteasomal degradation. The lower oxygen tension stabilizes the HIF-1α subunit and promotes angiogenesis to compensate for the hypoxic condition [21,25].

Since HIF-1α subunits are degraded under normal oxygen levels, this suggests that increasing oxygen tension in the epidermal cells through use of oxygen therapy could increase proteasomal degradation of HIF-1α subunit, which will decrease angiogenesis and slow down wrinkling of skin.

The results obtained from studies done by Kawada et al. (26) showed that mice that went through UV-B radiation but receive HBOT did not have a significant increase in HIF-1α protein level like the mice that received only the UV-B irradiation. This result supports that higher oxygen level increases HIF-1α protein degradation and suggests that increase oxygen tension can attenuate formation of wrinkles due to decrease in angiogenesis.

Even though the level of VEGF which is a downstream of the HIF-1α protein was found to be in- creased in both UVB and UVB + HBO group, there was a lower tendency to increase in the UVB + HBO group. Therefore, it is possible that hyperoxia attenuates wrinkle formation through suppressing the HIF-1α angiogenesis- signaling pathway [26].

MMP-2 & MMP-9
MMP stands for matrix metalloproteinases and these groups of proteins are zinc-dependent proteins involved in remodeling of extracellular matrix and have impor- tant roles in angiogenesis, morphogenesis, and metas- tasis [27].

The protein is made up of several domains, mainly propeptide, catalytic, and hemopexin domains. MMPs are also involved in degradation of collagen, pro- teoglycans, and many glycoprotein [28]. MMPs are secreted as inactive zymogens (pro-MMP) and have to be activated for full functional capacity.

Growth factors and cytokines are molecules that regulate the stimulation or inhibition of pro-MMP synthesis, usually at the tran- scriptional level. The MMPs involved with photoaging that have shown to increase in level during experiments with human fibroblasts after UV-irradiation are MMP-1, 2, 3, and 9 [17,29].

In other studies done on MMPs in epidermis of hairless mouse skin, after long period of UV-irradiation the levels of MMP-1 and MMP-3 did not have a significant increase. However, the levels of active MMP-2 and MMP-9, in addition to increase pro-MMP-2 and pro-MMP-9 levels, were found to be significantly higher in the UVB-irradiated wrinkled mice skin com- pared to the unexposed normal mice skin [30].

MMP-2 and MMP-9, also known as gelatinase A and gelatinase B respectively, functions mainly to digest type IV and VII collagens, which are major components of the base- ment membrane. Also, when a potent synthetic inhibi- tor of MMP-2 and MMP-9, CGS27023A, was applied topically over a period of time, significant inhibition of reduction of collagen by UVB radiation was observed, and there was no significant difference between collagen levels in non-irradiated mice and CGS27023A- treated mice, which implies that MMP-2 and MMP-9 are have major roles in inducing skin wrinkles after UVB exposure [30].

Even though MMP-2 and MMP-9 have been found to play important roles in inducing skin-wrinkles and angiogenesis, the results obtained in a study from putting UVB-irradiated hairless mice through hyperoxic (HO) conditions did not show significant reduction in the levels of the MMPs [26,31].

The MMP-9 level was found to be the same for UVB and UVB + HO group and the MMP-2 level was found to be slightly decreased in both UVB and UVB + HO group. Because the level of MMP-2 in both the UVB and UVB + HO group were found to be reduced, whether hyperoxic conditions affect MMP-2 levels remains to be elucidated [26].

Perhaps different concentrations of oxygen or different lengths of HBOT exposures need to be adjusted to obtain a more affective result. Another study done on retina of mice showed that hypoxic conditions leads to increase MMP-2 level and angiogenesis through p53-affected CTGF/CCN2 gene of the cysteine-rich protein 61/connective tissue growth factor/novel over-expressed (CCN), which are subsets of extracellular matrix proteins.

Suppression of CTGF gene decreased MMP-2 levels and since CTGF gene is induced in hypoxic conditions, hyperoxic con- ditions could potentially decrease MMP-2 levels and wrinkle formation through inhibition of the CTGF gene [32]. Further research could still be done on this sub- ject to find out if and how high oxygen concentration affects MMPs on a molecular level, which could lead to explaining in more details HBO’s role in wrinkles reduction.

Inflammatory cells infiltration
Inflammatory cells, especially neutrophils, have the ca- pability to be destructive and can cause damage to the extracellular matrix [33]. Health conditions such as emphysema, adult respiratory distress syndrome, adult peri- odontitis, rheumatoid arthritis, ulcerative colitis, and blistering skin disorders are mediated by tissue-destructive actions of neutrophils [34-36].

Neutrophils are the most abundant white blood cell and after a certain level of tis- sue damage experienced, they will quickly leave the blood stream and move towards the site of damage. Exposure to certain degree of sunlight, and an erythemogenic, or

erythema-causing, dose of UVB radiation can lead to influx of neutrophils, which cause solar elastosis or break down and loss of elastic tissue [37,38]. The de- structive abilities of neutrophils come from the fact that it is filled with potent proteolytic enzymes capable of degrading collagen and elastic fibers, thus causing damage to the extracellular matrix.

Neutrophils are able to release a group of serine proteases, mainly the neutro- phil elastase, which is a potent proteolytic enzyme [39]. Not much attention has been given to neutrophils re- garding its role in causing wrinkles because of more studies explored the hypothesis of MMPs and HIF1 as main causes and also because rate of neutrophil infiltration can only be examined in skin recently exposed to UV radiation [30,40].

In a study done by Rijken et al., they found evidences that infiltrating neutrophils may be the key players in the release of proteolytic enzymes such as MMPs and neutrophil elastase that causes cutaneous damage and photoaging instead of fibroblasts and keratinocytes being the main molecules releasing the enzymes [41].

It has been shown that neutrophils are able to express a few MMPs such as MMP-8, MMP-9, and MMP-12, and in addition the MMP-1 seems co-localized with neutrophil elastase after sun exposure [42,43]. These evidences show that it is likely that neutrophils are the cause of extracellular matrix damage that can lead to elastosis and formation of wrinkles.

UVB-irradiation can lead to angiogenesis in the skin and these additional blood vessels might possibly be the main cause of the increase in inflammatory cells infiltra- tion, which leads to formation of wrinkles. Using HBOT to treat skin wrinkles may be effective because it might be able to decrease the amount of inflammatory cells infiltration and neutrophils releasing the MMPs.

Direct evidence was found and shown that hyperoxic conditions are able to decrease blood flow in active muscle cells and also slow down active angiogenesis in the skin [26,44].

Hyperoxia can reduce skin angiogenesis through possibly increasing degradation of the HIF1α protein and with that angiogenesis pathway being inhibited, new blood vessels are not being formed and leads to reduction of infiltrating neutrophils, which results in attenuating the release of MMPs in the skin.

However, recent studies have suggested that hyperoxic conditions couldn’t have only affected degradation of HIF1α and cause reduction of wrinkle formation. Evidence was found showing inhi- bition of HIF1α protein alone was insufficient to restrain wrinkles formation by higher dose of UV radiation that led up to the regulation of the activities of MMPs [45]. With conflicting evidences, more research needs to be done to find out the specific conditions and mechan- ism of how hyperoxic condition attenuates skin wrinkle formation.

Thrombospondin-1
Thrombospondin-1 (TSP-1) is a matricellular protein that can inhibit proliferation and migration of endothe- lial cells, but more importantly in this case, can effectively diminish angiogenesis [18]. Its mRNA is produced by the basal epidermal keratinocyte in human skin and the TSP-1 protein is deposited in the basement mem- brane area [46].

According to studies done by Kiichiro et al., the epidermal over-expression of TSP-1 inhibits dermal photo-damage and also elastic fiber and collagen disorganization, which lead to prevention of formation of skin wrinkles. They also showed that TSP-1 has a po- tent ability to inhibit angiogenesis caused by UV-B irradiation by decreasing endothelial cell proliferation and increasing its apoptosis rate [18].

Mice that received chronic UVB-induced skin damage and skin-specific over-expression of TSP-1, compared with mice that only re- ceive chronic UVB-induced skin damage, has greater reduction in skin wrinkling rate associated with the protein’s effective inhibition of angiogenesis.

Recent evidence suggests that the ability of TSP-1 to decrease skin wrinkle not only came from its ability to inhibit angiogenesis, but also its ability to inhibit activa- tion of MMP-2 and MMP-9 by inhibiting conversions of MMPs zymogens to its active form.

In addition to degrading basement membrane and rearranging the extracellular matrix, activation of MMP-2 is associated with increased blood vessel growth, while inhibition of this protein leads to decreased angiogenesis level. TSP-1 inter- acts with MMP-2 by binding to it, which leads to the in- hibition of the activity of MMP-2 [47]. I

t is also thought that MMP-9 has the ability to accelerate wrinkle forma- tion so its interaction with TSP-1 is tested. Results showed that TSP-1 does interact with and inhibits the activity of MMP-9 by binding to it in a similar way that TSP-1 binds to MMP-2 because MMP-2 and MMP-9 has similar struc- tural domains.

This property of TSP-1 to inhibit MMPs contributes to its anti-angiogenic effects and also to its ability to reduce UVB-induced skin damage and wrinkles [18,47]. Although TSP-1 has inhibitory activities that can inhibit angiogenesis and slow down wrinkle formation, and hyperoxia conditions and treatments has inhibitory activity on angiogenesis and MMPs level, a direct link between TSP-1 activity and hyperoxic condition has not been made. Apparently more research needs to be done to investigate whether high oxygen tension can increase the level of TSP-1, leading to attenuation of skin wrinkles.

Conclusion
The use of HBOT in medicine has come a long way since its first main use to treat decompression sickness. In order for the HBOT to be used to its full potential in skin care, the exact mechanisms of how high oxygen con- centration reduce formation of wrinkles and photoaging needs to be investigated.

The direct mechanism of how hyperoxic conditions can attenuate formation of wrinkles has not yet been established due to conflicting evidences and a need for further research on the subject. The level of HIF-1α protein has shown to be reduced under hyper- oxic conditions, which suggests that it is degraded under high oxygen concentration and this can inhibit the expres- sion of VEGF and skin angiogenesis (Figure 1).

However, other evidences were found showing that the suppression of HIF1α-angiogenesis pathway under hyperoxic condi- tions alone is not sufficient to attenuate production of MMPs, angiogenesis, and skin wrinkle formation. Though studies have found HBOT to slow down angiogenesis, others have found HBOT to be capable of promoting an- giogenesis in ulcers and wounds [7,48].

More supporting evidence and research is also needed for exactly how high oxygen concentration affects TSP-1 activity and the level of MMP-2 and MMP-9. This is because a direct link between TSP-1 and hyperoxia has not been found and it is not clear yet whether the MMP levels decrease in hyperoxic conditions.

A wider variety of different testing conditions need to be enforced to figure out the exact mechanisms. Even with these missing links, the use of high oxygen concentration to reduce the visibility of wrinkles have shown to be promising and effective to a certain degree since this treatment is currently being used and is becoming more widespread in spas and der- matology clinics worldwide.

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More information: Yafit Hachmo et al, Hyperbaric oxygen therapy increases telomere length and decreases immunosenescence in isolated blood cells : a prospective trial, Aging (2020). DOI: 10.18632/aging.202188

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