Compared to normal, diabetic skin is characterized by great sensitivity. Oxidative stress is directly involved, contributing to accelerated skin aging, xerodermia and poor wound healing. In the last 10 years, cigarette smoke (CS) exposure has been associated with several skin and dermatological conditions and is directly related to the oxidative stress affecting the skin. However, limited data exist concerning the effect of CS on diabetic skin. Some of the effects of cigarette smoke exposure on the skin of hairless diabetic mice were hereby studied and the potential skin protection by topical applications of Pinus halepensis bark extract was investigated. Female hairless SKH-2 diabetic mice were exposed for 8 days to tobacco smoke and topical applications were performed twice daily. Biophysical parameters such as transepidermal water loss (TEWL), skin elasticity and erythema were measured. In addition, the oxidative stress was evaluated. The results show that diabetes and CS have a synergistic negative action on skin condition, with the development of xerosis and high ROS levels whilst topical applications of Pinus halepensis bark extract protect efficiently the toxic effect of CS on skin, by decreasing skin dryness, oxidative stress and blood glucose levels.
Tobacco was responsible for more than 100 million deaths worldwide in the 20th Century. The World Health Organization has estimated that, if current trends continue, tobacco could cause a billion deaths in the 21st Century [
The skin constitutes the first barrier against environmental aggression and is in direct contact with CS. CS is the result of sidestream and mainstream CS released into ambient air by the actively smoking individuals and contains over 4600 compounds both in gaseous and particulate state that are able to induce oxidative stress to cells. There is considerable evidence showing that reactive oxygen species (ROS) are key contributors to the de- leterious effects of CS on skin by increasing oxidant free radicals activity. Tobacco smoke toxins are also known to have a detrimental effect on collagen and elastin integrity and to decrease the microcirculation [
In the last 10 years, CS exposure has been associated with several skin and dermatological conditions, such as premature skin aging, psoriasis, atopic dermatitis, melanoma, poor wound healing, acne, as well as with the yellowing of fingers and nails [
Diabetes mellitus is a metabolic disorder characterized by hyperglycemia and insufficiency of secretion or action of endogenous insulin that can lead to several complications, including dermatological ones. Cutaneous disorders reported include xerosis, acceleration of skin aging, poor wound healing, cutaneous infections and several skin diseases associated with diabetes, such as scleroderma-like changes of the hand, necrobiosis lipoidica, and diabetic dermopathy [
The genus Pinus belongs to the family Pinaceae and comprises about 250 species. The medicinal and aromatic properties of the chemical compounds (e.g., turpentine, resins and essential oil…) of pine make it one of the most popular plants. In the Northern Mediterranean basin, Pinus halepensis is a pioneer and expansionist species that colonizes abandoned agricultural lands characterized by high biodiversity.
Essential oils from Pinus species have been reported to have various therapeutic properties. They are also used as fragrances in cosmetics, flavoring additives for food and beverages, scenting agents in a variety of household products and intermediates in the synthesis of perfume chemicals [
Some previous research suggested that CS was associated with an increased incidence of diabetic skin lesions [
Hairless female mice type SKH-2 (23 - 32 g) were obtained from the breading stock of the small animal laboratory of the School of Pharmacy of the University of Athens and housed into 4 cages in temperature and humidity controlled chambers (12 h light/12 h dark cycle) with free access to tap water and standard chow diet (Keramaris, Greece). All mice were allowed to acclimate for 20 days prior to the treatment. The housing and treatments of animals were in accordance with our national and institutional guidelines from where specific license was obtained.
Diabetes was induced to all mice by a single intraperitoneal injection of streptozocin (150 mg/kg) solution in sodium citrate buffer (0.1 M, pH 3.5 - 4.5). Blood was collected from the tail for blood glucose determination levels 5 and 8 days after the STZ injection using a glucose monitoring system with electrochemical detector and strips (ABBOTT Precision Xtra Plus, USA). The mice were considered as diabetic when the glucose levels were above 180 mg/dl and in the presence of polydipsia and polyuria symptoms.
The experiment lasts 10 days and was divided into two main phases: phase I before CS exposure (days 0 - 2) and phase II after the start of CS exposure (days 2 - 9). Topical applications were performed during phase I and II.
Mice were divided into the following 3 groups: Seven air-exposed diabetic mice in the first group received a topical application of CMC gel and served as a control. Seven diabetic mice in the second group received a topical application of CMC gel and were exposed to CS. Seven diabetic mice in the third group received a topical treatment of Pinus halepensis bark extract and were exposed to CS.
Pinus halepensis bark was collected from Kaisariani Forest which is asuburb close to Athens, in Greece. An extract of it (12.6% w/w) was prepared after 48 hours contact of fine pieces of bark with water solution containing 2% v/v of ethyl alcohol and paper filtration.
The gels were made adding 4% w/w of Carboxymethyl Cellulose (CMC) to the hydro-alcoholic solution containing or not the pine bark extract.
Mice from groups 1 and 2 were topically treated with the hydro alcoholic gel of Carboxymethyl Cellulose (CMC), twice daily, during 10 days. Mice from group 3 were treated with the hydro alcoholic CMC gel containing the Pinus halepensis bark extract. The topical applications were performed twice daily (morning and evening) with cotton swabs for three days (phase I). Before each application, mice dorsal skin was wiped lightly with cotton to clean the area. After 72 hours (6 applications), CS exposure started for groups 2 and 3 (phase II).
Whole body exposure of mice to CS was achieved by using a smoking device (Ismatec SA, model CH8152, type MCF, Glattbrugg, Zurich) placed in a custom-made chamber (
combination of sidestream (89%) and mainstream smoke (11%). CS exposure was generated by burning a cigarette produced in Greece (ASSOS Papastratos; Xanthi, Greece) having a declared content of 10 mg tar, 0.7 mg nicotine and 6 mg CO each. The experiments described above used the standard Federal Trade Commission conditions (puff volume, 35 ml; puff duration, 3 s; puff frequency, 1/min). Mice from groups 2 and 3 were exposed to 8 cigarettes for the first day (day 3 of the experiment) and to 4 cigarettes daily for the rest of the experiment. The cigarettes were kept under standardized conditions (4˚C). The animals were maintained in cages within the chamber for continuous exposure and the chamber was ventilated 10 min twice a day after the topical applications. The mice were exposed to CS 1 hour after the topical applications.
Measures were taken on day 0 (start of the topical application), on day 5 (the 4th day after the start of exposure to CS) and on day 8 (7th day after the start of CS exposure).The following parameters were measured: 1) blood glucose levels (ABBOTT Precision Xtra Plus, USA), 2) erythema levels by use of a Mexameter MX 18 (Courage and Khazaka, Koln, Germany), 3) transepidermal water loss (TEWL) using a Tewameter TM 210 (Courage and Khazaka, Koln, Germany), 4) skin elasticity by making a skin fold and measuring its restoration time, 5) body weight (Kern Balance 440 45), 6) overall health of the animals was monitored daily and appropriate pictures were obtained with a digital camera (Sony DSC-W210 Cybershot, 12.1 MPixels, Japan).
After the sacrifice of mice on day 9 (10th day of experiment), oxidative stress was estimated in skin.
ROS levels were measured using a fluorescent probe chloro methyl derivative of dichlorodihydrofluorescein (CM-H2DCFDA). After treatment and incubation of skin homogenized sample, fluorescence was evaluated using Fluostar Galaxy spectrometer, fluorescence and chemiluminescence meter (BMG, Germany) with excitation filter at 485 nm and emission at 520 nm.
Results were expressed as means +/− SD. Statistical differences were estimated using analysis of variance (ANOVA) single factor test and considered significant when p < 0.05.
Diabetic smoked mice showed faster and more advanced skin aging signs than diabetic control mice. Xerodermia was observed on day 8 on diabetic smoked mice, whereas in control group, no skin dryness was observable after the same period of time. Among diabetic smoked mice, the group treated with Pinus halepensis bark extract showed less intense aging signs compared to non treated animals. No xerodermia was observed and skin condition was improved compared to the diabetic smoked micenon treated with antioxidant extract (
Macroscopic observation of the skin of diabetic smoked mice showed a yellowish coloration and a decreased vascularisation. It was thinner compared with the skin of diabetic smoked mice treated with the antioxidant extract.
A significant decrease in blood glucose levels was observed for the group of diabetic mice exposed to CS and treated with Pinus halepensis extract on day 8 in comparison with the beginning of the experiment (p = 0.033 < 0.05). On day 8, blood glucose levels of this same group of mice were significantly lower compared with diabetic controls (p = 0.039 < 0.05) whereas this difference was not significant at the beginning of the experiment (
Within the group of diabetic smoked mice with antioxidant protection, a significant decrease of skin redness
levels was observed between day 5 and day 8 (p =< 0.05). No important changes were noticed between the other groups of diabetic mice (
No statistic difference was noticed between diabetic smoked mice and diabetic control.
Among diabetic mice exposed to CS, TEWL levels measured on day 8 were notably lower for group treated with the Pinus halepensis bark extract compared with the non treated animals (p = 0.00043 < 0.05) (
No statistic difference was noticed between diabetic smoked mice and diabetic control mice.
Among diabetic smoked mice, a significant increase of skin elasticity was observed on pine bark treated mice
compared with the untreated group (day 5: p = 0.024 < 0.05; day 8: p = 0.0039 < 0.05) (
No statistical differences were observed between the mice groups (
A significant increase in skin oxidative stress of CS exposed mice was observed in comparison with diabetic controls (p = 0.0045 < 0.05).
Among CS exposed diabetic mice, a significant reduction of skin oxidative stress was noticed for the group treated with pine extract compared with the non-treated one (p = 0.047 < 0.05) (
The present study results show that exposure of diabetic mice to CS caused xerodermia and shedding (figure 2). In addition, the skin of these mice took a yellowish coloration, was thinner, had decreased vascularization and elasticity compared to this of the control diabetic mice. These results are in agreement with previous studies which suggest that tobacco smoke alters skin integrity due to impairment of collagen production and increase of tropoelastin and matrix metalloproteinases (MMP) production which leads to elastic fibers and proteoglycans degradation [
Diabetic animal skin exposed to CS presented increased TEWL compared to the corresponding control animal (figure 5). That was also observed by Pavlou et al. [
that this phenomenon should also be attributed to the diabetic profile of animals. Previous studies have shown that diabetes induces many pathphysiological changes in the skin such as reduced mechanical properties (main- ly anomalies regarding elastin fibers) and delayed wound healing. Skin dryness has been reported as one of the earliest and most common manifestations of the disease. These cutaneous changes have been reported in both experimental and clinical studies and include a reduced hydration state of the stratum corneum, decreased sebaceous gland activity, impaired desquamation process and decreased triglyceride stratum corneum content [
No xerodermia and shedding was noticed and the overall appearance of the skin was improved in the group of treated with Pinus halepensis mice that was thicker and more vascularized compared to nontreated ones (figure 2). Also, an important and significant reduction of TEWL levels was noticed in this same group of treated mice while TEWL remained merely stable in the two other animal groups (figure 5). Skin elasticity was also statis- tically improved in the group of treated mice compared with the non treated group of diabetic mice submitted to tobacco smoke, on days 5 and 8 (figure 6). The above observations indicate that the local administration of Pi- nus halepensis bark extract helps to maintain a significant degree of hydration in the skin of CS exposed diabetic mice. Another parameter measured was skin erythema that was significantly decreased in the group of treated mice, in contrast to the two other groups of animals in which results were not significant (figure 4). The improvement of erythema levels, TEWL levels and skin elasticity as well as overall clinical conditions suggest that the topical administration of Pinus halepensis bark extract can effectively protect the skin from CS. This could be due to the potent antioxidant activity of Pinus halepensis bark extract. Previous studies have shown that bark extracts from pinus could protect skin from ROS generated from UV light, chemicals and smoke [
Within the group of diabetic mice exposed to CS and treated with Pinus halepensis bark extract, blood glucose reduction was statistically significant on day 8 compared with day 0 but was also significant compared with the diabetic control group. On the contrary, in the two other groups of animals, blood glucose remained generally stable during the experiment. Thus, it can be concluded that the topically administered antioxidant compounds crossed the disrupted skin barrier and had a hypoglycemia action. So, topical application of Pinus halepensis bark extract could be a candidate to improve glucose levels in diabetes.
The results show that diabetes and CS have a synergistic negative action on skin condition. There is strong evidence that Pinus halepensis bark extract could improve oxidative stress induced from environmental factors especially for patients with diabetes. For this reason, some more studies on the synergestic action of UV light and diabetes as well as on the protection of skin by Pinus halepensis bark extract are pending.
Authors would like to thank Abbott pharmaceutical company for providing strips and apparatus for measuring glucose levels, IFET, the National Institute of Pharmaceutical Research and Technology for providing Streptozotocin and Verisfield Company for their financial support.