Synergistic effect of hyperbaric oxygen preconditioning and hydrogen-rich saline in ameliorating rat flap ischemia/reperfusion injury
1Department of Plastic Surgery, Peking Union Medical College Hospital, Dongcheng 100730, Beijing, China.
2College of Life Science and Bioengineering, Beijing University of Technology, Chaoyang 100124, Beijing, China.
Correspondence Address: Dr. You-Bin Wang, Department of Plastic Surgery, Peking Union Medical College Hospital, Dongcheng 100730, Beijing, China. E-mail:
Aim: This study was conducted to evaluate the synergistic effects of hyperbaric oxygen (HBO) preconditioning and hydrogen-rich saline (HRS) treatment on skin flap survival and apoptosis in a rat ischemia/reperfusion (IR) skin flap model.
Methods: Male Sprague-Dawley rats were randomly divided into five groups: one sham surgery group (sham group) and four surgery groups (IR group, HBO group, HRS group, and HBO + HRS group). An extended epigastric adipocutaneous flap (6 cm × 9 cm) was raised over the abdomen in each animal of all five groups. The last four groups underwent 6 h of IR management and were treated, respectively, with normal saline, HBO, HRS (HRS, 0.8 mmol/L), or a combined approach (HBO and HRS). On the 3rd postoperative day, flap survival rate and perfusion condition, apoptotic index, caspase-3 activity, protein expression of pASK1 and Bcl-2/Bax ratio, and Bcl-2 messenger RNA (mRNA) expression were assessed.
Results: Prior studies have shown the protective effects of HBO and HRS, both of which have been associated with an increase in flap survival. Compared to the IR group, the flaps in the HBO, HRS, and HBO + HRS groups showed better perfusion and a larger survival area with a low number of apoptotic cells, low caspase-3 activity and pASK1 expression, and a high Bcl-2/Bax ratio and Bcl-2 mRNA expression. Of these groups, the HBO + HRS group showed the best flap survival.
Conclusion: Both HBO and HRS treatments increase the rate of flap survival, while the synergistic application of HBO and HRS showed a higher survival rate as compared to individual treatments of each. The potential regulation of apoptosis with the use of these two modalities may improve skin flap survival.
Although the transfer of skin flaps is widely used in wound coverage and reconstruction, soft tissue necrosis remains a challenging problem. In a report by Chen et al.,113 cases (9.9%) out of 1,142 free flap operations had complications. Eighty-two percent of these 113 cases demonstrated some form of circulatory compromise within 24 h after surgery.
Postoperative hyperbaric oxygen (HBO) therapy has been used in plastic surgery in the treatment of random skin flaps, axial skin flaps, and flaps with survival problems with satisfactory results.[2,3] The effect of HBO preconditioning has also been studied in many animal models including stroke and spinal cord injury. In a study using a rat skin flap model, HBO preconditioning was found to improve skin flap survival and depress tumor necrosis factor-α (TNF-α) expression in skin tissue.
In 2007, Ohsawa et al. reported that inhalation of H2 could selectively mitigate •OH (oxhydryl), generating an antioxidant effect in a rat model of middle cerebral artery occlusion without affecting the signaling of other reactive oxygen species (ROS). Subsequently, H2 was shown to have protective effects on ischemic/reperfusion (IR) injury in various organs including the liver, heart, kidneys and small intestine.[8-11] The authors have independently verified this protective effect.
It is widely accepted that IR injury is a critical factor in flap failure while apoptosis is one important feature of the IR process.[13,14] In this study, the synergistic effects of HBO preconditioning and hydrogen-rich saline (HRS) treatment were evaluated for their effects on skin flap survival and apoptosis in a rat IR skin flap model.
All protocols were approved by the Committee on Animal Rights Protection of Peking Union Medical College Hospital and were in accordance with the National Institutes of Health guidelines for the care and use of laboratory animals. Adult male Sprague-Dawley (SD) rats weighing 280-320 g were used in this study. The rats were housed in individual cages under standard conditions with 22-25 °C and 12 h of a light-dark cycle. The rats were fed a normal diet with water provided ad lib pre- and post-operatively.
Epigastric skin flap preparation
An extended epigastric adipocutaneous flap (6 cm × 9 cm) was raised over the abdomen in each animal. The left superficial epigastric artery and vein were ligated, and the right was retained as the pedicle. The pedicle artery and vein were occluded with a microvascular clamp and 6 h of skin flap ischemia was induced. The flap was then resutured with a silicone sheet of 0.1 mm deep to it to prevent neovascularization from the wound bed. The clamp was removed, and the flap was reperfused at the end of the ischemic period. Heparin (50,000 U/L in 0.5 mL saline) was injected into the left epigastric artery to avoid thrombus formation prior to ligation.
Hydrogen-rich saline production
Hydrogen was dissolved in normal saline (20 mL) for 20 min with a speed of 0.2 L/min to a supersaturated level. HRS was freshly prepared prior to each use, ensuring that a concentration of more than 0.8 mmol/L was reached by a needle-type H2 sensor (Unisense, Aarhus, Denmark).
Experimental protocol and groups
Fifty male SD rats were divided randomly into five groups with 10 animals in each group: (1) a sham-operated group (sham: no IR, HBO, HRS or normal saline injection). Rats in the sham group underwent the same surgery as the rats in the other four groups but without the period of ischemia; (2) IR group: 6 h of ischemia was induced by clamping the right pedicle, followed by an injected intraperitoneally of 5 mL/kg normal saline, 10 min prior to reperfusion; (3) HRS-treated group: 6 h of ischemia was induced by clamping the right pedicle, followed by an intraperitoneally injection of 5 mL/kg HRS, 10 min prior to reperfusion; (4) HBO group: 6 h of ischemia was induced by clamping the right pedicle after HBO preconditioning for 4 times; and (5) HBO and HRS group: 6 h of ischemia was induced by clamping the right pedicle after HBO preconditioning for 4 times. 5 mL/kg HRS was administered by an intraperitoneally injection, 10 min prior to reperfusion.
Hyperbaric oxygen preconditioning
Rats in the HBO and HBO + HRS groups were treated with HBO 2 days before surgery. Treatment included HBO exposure 4 times for 60 min every 12 h (total exposure time of 4 h). 2 L/min of 100% oxygen was supplied continuously at 0.25 MPa during the HBO treatment. Compression and decompression were performed at 5 psi/min. The time at which the HBO chamber pressure reached 0.25 MPa and remained stable was recorded. Calcium carbonate crystals were placed in the chamber to prevent CO2 accumulation. Flap surgery began 2 h following the final HBO treatment.
Skip flap survival and perfusion evaluation
Skin flap survival was evaluated 72 h after reperfusion by general observation of survival and necrotic phenomena and subsequently confirmed by laser speckle contrast analysis cameras (Perimed AB, Stockholm, Sweden). The surviving and necrotic areas were measured. The percentage of flap survival was defined as the ratio of the surviving area to the original flap area.
To evaluate skin flap perfusion, the rats were secured onto the operative bed such that the entire flap, including part of the normal abdominal skin, was exposed. The PeriScan PSI system (Perimed AB, Stockholm, Sweden) was positioned above the rats, imaging an area of 11 cm × 7.5 cm. The image acquisition rate was 3 Hz and lasted for 3 min. The ambient temperature was maintained between 22 °C and 25 °C during this process. Perfusion of the necrotic and survival areas was analyzed. Vascular flow was measured using perfusion units (PUs).
Rats were sacrificed on the 3rd postoperative day with overdose anesthesia after skin flap survival and perfusion evaluation. The survival flaps were harvested for sampling.
TdT-mediated dUTP-X nick end labeling staining and apoptotic index evaluation
Tissue samples (1 cm2 in size) were taken from the proximal areas of the harvested flaps. Samples were sectioned into smaller pieces and fixed with 4% paraformaldehyde in 0.1 mol/L phosphate buffer. They were then embedded in paraffin, sectioned and mounted onto slides for TdT-mediated dUTP-X nick end labeling (TUNEL) staining.
TUNEL staining was performed using an in situ cell death detection kit (Roche, Basel, Switzerland). After being heated to 60 °C and dewaxed, the sections were rehydrated and then incubated in a 20 µg/mL proteinase K working solution for 15 min at room temperature. The slides were rinsed (5 min, 3 times) with phosphate-buffered saline (PBS) and then incubated in a TUNEL reaction mixture for 1 h at 37 °C. The slides were rinsed once again and dried. Converter-POD (anti-fluorescein antibody, Fab fragment from sheep, and conjugated with peroxidase (POD)) was added to the samples for 1 h at 37 °C. The sections were rinsed with PBS and stained with 3,3’-N-diaminobenzidine tetrahydrochloride. Five slide fields were randomly examined using a defined rectangular field area under ×40 magnification. Cells were then counted under ×400 magnification. The apoptotic index (AI) was represented as the percentage of TUNEL-positive cells versus the total number of cell nuclei per field.
Caspase-3 activity assay
Caspase-3 activity was detected using a Fluorometric Assay Kit (Biovision Research Products, Mountain View, CA, USA). Briefly, 50 mg of skin flap tissue was homogenized in ×2 reaction buffer and incubated for 1 h at 37 °C with caspase-3 substrate (DEVD-APC, 1 mM). Substrate cleavage was measured with a spectrofluorometer at 400 nm.
ASK1 and Bcl-2/Bax Western blot
Skin flap tissue (100 mg) was sampled from the proximal, middle and distal regions of the harvested flaps. The samples used for detection were randomly selected from all the samples in each rat in each group to avoid any deviation caused by using different parts of the skin flap samples. Ninety micrograms of total protein were extracted and analyzed from each sample. The protein samples were mixed with loading buffer and boiled at 95 °C for 15 min. The protein samples were then electrophoresed in a 10% dodecyl sulfate-polyacrylamide gel (Bio-Rad, USA) and transferred onto nitrocellulose filter membranes for 1 h at 80 V. The samples were incubated overnight at 4 °C with goat polyclonal actin antibody (1:1,000 dilution, Santa Cruz Biotechnology, Inc., USA), pASK1 antibody (1:500 dilution Cell Signaling Technology, Boston, MA, USA), rabbit anti-Bcl-2 polyclonal antibody (1:1,000 dilution, Chemicon International, Inc., USA), and rabbit anti-Bax polyclonal antibody (1:1,000 dilution, Stressgen Bioreagents, Corp., USA). The proteins were then incubated with horseradish peroxidase-conjugated secondary antibodies diluted at 1:2,500 for 1 h at 37 °C. The blots were then treated with a chemiluminescence detection reagent (Pierce, USA) and exposed to autoradiography film. The bands were then quantified by densitometry.
Quantitative real-time polymerase chain reaction for Bcl-2 messenger RNA
Skin flap tissue (30 mg) was sampled from the proximal, middle and distal areas of the harvested flaps from each group. The total RNA was extracted from the samples using an RNeasy Fibrous Tissue Mini Kit (Qiagen, Düsseldorf, Germany). One microgram of total RNA was then reversely transcribed into single-stranded complementary DNA with a ProtoScript M-MuLV First Strand cDNA Synthesis Kit (New England Biolabs, Ipswich, MA, USA), according to the manufacturer’s instructions. The complementary DNA was then used for real-time polymerase chain reaction (PCR). The process of amplification and quantification were performed with a real-time quantitative PCR system (Agilent, Santa Clara, CA, USA). β-actin was used as the internal control. The PCR protocol was as follows: heating for 2 min at 50 °C, initialization at 95 °C for 10 min, followed by 40 cycles of denaturation at 95 °C for 15 s, annealing at 58 °C for 30 s, and extension at 72 °C for 30 s. The primers used in quantitative real-time PCR were Rat Bcl-2 (forward: 5’-AGAACCTTGTGTGACAAATGAGAA-3’ and reverse: 5’-TACCCATTAGACA-TATCCAGCTTGA-3’) and β-actin (forward: 5’-GGCGGCCAAACAGAAAG-3’and reverse: 5’-CTGAGGGCACGGAGGAT-3’).
In this study, all data are reported as the mean ± standard error of the mean (SEM). Significant differences were determined via one-way analysis of variance. Least significant difference t-test was used for between-group comparisons. Statistical significance was set at P < 0.05. All analyses were conducted using SPSS 17.0 (SPSS Inc., Chicago).
Skin flap survival
Seventy-two hours following reperfusion, necrotic skin flaps were observed and presented as gray areas with little elasticity. In contrast, surviving areas maintained normal elasticity and skin color [Figure 1a]. The highest skin flap survival percentage was observed in the HBO + HRS group (47.70% ± 12.05%). There were significant differences between the IR (23.30 ± 6.49%), HRS (36.90% ± 7.46%), HBO (39.00% ± 9.14%) and HBO + HRS (47.70% ± 12.05%) groups (values are the mean ± SEM, IR vs. HRS, P < 0.01; IR vs. HBO, P < 0.001; IR vs. HBO + HRS, P < 0.001). Among the HBO, HRS and HBO + HRS groups there were significant differences between HBO and HBO + HRS (P < 0.05), and HRS and HBO + HRS groups (P < 0.05) [Figure 1b].
Figure 1. The evaluation of the abdominal skin flaps 72 h following ischemia-reperfusion. Black zones represent the necrotic areas. Red, yellow, and the adjacent blue areas represent surviving areas with rich blood perfusion. (a) Representative photographs of abdominal skin flap microcirculation in the five groups are shown; (b) the survival rate of the total flap area. Flap survival rates were markedly higher in the hyperbaric oxygen, hydrogen-rich saline, and hyperbaric oxygen + hydrogen-rich saline groups; (c) the average blood perfusion of total skin flaps. The hyperbaric oxygen + hydrogen-rich saline group has the greatest blood perfusion among the surgery groups. IR: ischemia reperfusion, HBO: postoperative hyperbaric oxygen, HRS: hydrogen-rich saline
Skin flap perfusion evaluation
Seventy-two hours following reperfusion, skin flap perfusion stabilized and was analyzed. Skin flap perfusions were 131.10 PU ± 20.14 PU in the sham group, 26.10 PU ± 8.09 PU in the IR group, 62.40 PU ± 14.10 PU in the HBO group, 56.00 PU ± 25.12 PU in the HRS group and 84.70 PU ± 13.44 PU in the HBO + HRS group.
A significantly higher blood perfusion was measured in the sham, HBO and HBO + HRS groups. There were statistical differences between the following groups: IR vs. HBO, P < 0.001; IR vs. HRS, P < 0.001; IR vs. HBO + HRS, P < 0.001; HRS vs. HBO + HRS, P < 0.01; and HBO vs. HBO + HRS, P < 0.01 [Figure 1c].
Apoptotic index evaluation
Apoptotic cell death was observed with TUNEL staining [Figure 2a]. The number of apoptotic cells increased in the IR group (45.85% ± 6.64%) as compared with the sham group (8.57% ± 4.12%). Apoptotic cell number was reduced with HBO preconditioning, HRS and HRS and HBO preconditioning used cooperatively. HRS and HBO preconditioning used cooperatively were more efficient in reducing cell apoptotic death than that of HBO preconditioning or HRS used independently. The AI in HRS was 32.69% ± 6.80%, in the HBO group was 30.80% ± 7.13%, and in the HBO + HRS group was 20.24% ± 6.90%. There were significant differences between each surgical group, (IR vs. HBO, P < 0.001; IR vs. HRS, P < 0.001; IR vs. HBO + HRS, P < 0.001; HBO vs. HBO + HRS, P < 0.01; and HRS vs. HBO + HRS, P < 0.001) with the exception of HBO versus HRS [Figure 2b].
Figure 2. The results of TdT-mediated dUTP-X nick end labeling staining and the apoptosis index 72 h following ischemia-reperfusion. (a) The evaluation of apoptotic cell death by TdT-mediated dUTP-X nick end labeling staining in all groups. Apoptotic cell number was reduced with hyperbaric oxygen preconditioning, hydrogen-rich saline and hydrogen-rich saline and hyperbaric oxygen preconditioning used cooperatively (brown staining indicates apoptotic cells [red arrow]; ×200); (b) the apoptosis index of all groups. The data shown indicate the percentage of TdT-mediated dUTP-X nick end labeling-positive cells and the total cell nuclei per field. Three different slide fields from different skin tissues were counted. TUNEL: TdT-mediated dUTP-X nick end labeling, IR: ischemia reperfusion, HBO: postoperative hyperbaric oxygen, HRS: hydrogen-rich saline
Compared to the IR group (1.25 ± 0.26), the caspase-3 relative activity was significantly lower in the HBO (0.59 ± 0.12), HRS (0.53 ± 0.15), and HBO + HRS (0.36 ± 0.17) groups IR (P < 0.001). Significant differences between the HBO + HRS group and the HBO and HRS groups were also found (HBO + HRS vs. HRS, P < 0.05; HBO + HRS vs. HBO, P < 0.01). However, there was no statistical difference between the HBO and HRS groups [Figure 3].
Figure 3. Caspase-3 activity in all groups 72 h following ischemia-reperfusion. Compared to the ischemia-reperfusion group, caspase-3 activity was significantly inhibited in the hyperbaric oxygen, hydrogen-rich saline, and hyperbaric oxygen + hydrogen-rich saline groups. IR: ischemia reperfusion, HBO: postoperative hyperbaric oxygen, HRS: hydrogen-rich saline
Western blot for pASK1 and Bcl-2/Bax
The protein expression of pASK1, Bcl-2 and Bax proteins was analyzed by Western blot [Figure 4a]. pASK1 expressed the highest level in the IR group (0.25 ± 0.04) compared with other groups and was significantly decreased in the HBO + HRS group (0.13 ± 0.05) as compared to the IR (0.25 ± 0.04), HRS (0.17 ± 0.04) and HBO (0.18 ± 0.03) groups. Statistical differences were observed in HBO + HRS vs. IR, P < 0.001; HRS vs. IR, P < 0.001; HBOvs. IR, P < 0.001; HBO + HRS vs. HBO, P < 0.05; and HBO + HRS vs. HRS, P < 0.05 [Figure 4b].
Figure 4. The results of Western blot, pASK1 relative value and Bcl-2/Bax ratio in each group 72 h following ischemia-reperfusion. (a) Representative images of Western blots for pASK1, Bcl-2, and Bax; (b) pASK1 relative values in all groups. Compared to the ischemia-reperfusion group, the expression of pASK1 was significantly reduced in the hyperbaric oxygen, hydrogen-rich saline, and hyperbaric oxygen + hydrogen-rich saline groups; (c) the ratio between Bcl-2 and Bax in all groups. Bcl-2/Bax ratio reveals the highest level in hyperbaric oxygen + hydrogen-rich saline group. IR: ischemia reperfusion, HBO: postoperative hyperbaric oxygen, HRS: hydrogen-rich saline
The ratio between the level of Bcl-2 to Bax expression increased in the HBO (2.06 ± 0.49), HRS (2.90 ± 0.65) and HBO + HRS (3.27 ± 0.42) groups. The Bcl-2/Bax ratio in the IR group (0.98 ± 0.40) was the lowest. Statistical differences were observed between HBO + HRS vs. IR, P < 0.001; HBO vs. IR, P < 0.001; HRS vs. IR, P < 0.001; HRS vs. HBO, P < 0.001; and HBO + HRS vs. HBO, P < 0.001. The highest Bcl-2/Bax ratio was in the HBO + HRS group, but there was no significant difference between the HBO + HRS and HRS groups [Figure 4c].
Bcl-2 messenger RNA expression
The messenger RNA (mRNA) levels in each group were determined with real-time PCR. β-actin was used as a reference gene. Among all groups, the IR group (0.03 ± 0.03) showed the lowest level of Bcl-2 mRNA expression with the exception of the sham group. Among surgery groups, there were significant differences between the IR group and other groups (IR vs. HBO, P < 0.01; IR vs. HRS, P < 0.001; IR vs. HBO + HRS, P < 0.001). The expression of Bcl-2 mRNA in the HBO + HRS group (0.15 ± 0.05) was higher than in the HBO group (0.08 ± 0.03) and HRS group (0.11 ± 0.05), with statistically significant differences (HBO + HRS vs. HBO, P < 0.001; HBO + HRS vs. HRS, P < 0.05) [Figure 5].
Figure 5. The relative value of Bcl-2 messenger RNA in all groups 72 h following ischemia-reperfusion. Compared to the ischemia-reperfusion group, the hyperbaric oxygen, hydrogen-rich saline, and hyperbaric oxygen + hydrogen-rich saline groups show higher levels of Bcl-2 messenger RNA expression, especially the hyperbaric oxygen + hydrogen-rich saline group. IR: ischemia reperfusion, HBO: postoperative hyperbaric oxygen, HRS: hydrogen-rich saline
Flap transfer has become a basic albeit challenging technique for all plastic surgeons given the high-risk of flap failure. Even in cases of microsurgical transfer with a stable blood supply, skin flap loss still ranges between 1% and 5% in experienced hands.[12,15] There are many reasons for partial or total flap loss, including IR injury. During the process of IR injury, flap cells may change their biochemical properties with the induction of apoptosis, cell shrinkage, nuclear condensation, and cell death,[18-20] leading to flap loss.
In clinical work, HBO has been widely used in the treatment of challenging wounds and selected neurological diseases. HBO is considered to be a successful adjunctive therapy for wound healing. In the plastic field, postoperative HBO treatment is commonly used following flap transfer with satisfactory improvement. There has also been research into the protective effect of HBO therapy through preconditioning. Cheng found that HBO reduced cyclooxygenase-2 expression and provided brain protection following ischemia. The current authors have also examined the effects of HBO preconditioning in a rat skin flap model and found an improvement in flap survival in IR injuries. The mechanisms responsible for its protective effect may be related to attenuation of the inflammatory response and increased flap perfusion.
Recently, other therapeutic gasses have been studied, in particular, hydrogen. Hydrogen can reach relatively high concentrations quickly, and excessive hydrogen can be eliminated from the body via breathing, leaving no side effects. The protective and therapeutic effects of hydrogen in humans have been reported and include such applications as diabetes mellitus type II, hemodialysis, inflammatory myopathies, radiotherapy for liver cancer, and acute erythematous skin diseases. Animal research in the rat skin flap model has also been performed to test the protective effect of HRS and has shown that HRS increases the surviving areas of rat abdominal skin flaps while decreasing oxidative stress and inflammation.
Based on the above theories, this study focused on the combined application of HBO preconditioning and HRS treatment, demonstrating its synergistic effect in protecting a rat skin flap from IR injury by depressing apoptosis. In this study, an abdominal island skin flap IR model was established by ligating the left superficial epigastric artery to investigate cellular and molecular changes following HBO, HRS, and combined treatments. This model was first established by Kuntscher et al. In his study, an extended (6 cm × 10 cm) epigastric adipocutaneous flap was harvested, and then the flap was sutured back over a silicone sheet. This flap model has been widely used to study IR injury for the following reasons: first, the flap size is large enough for observation of the survival area. In the sham group, the epigastric artery could only sustain 75.40% ± 10.01% of the blood supply to the flap; second, with a large flap size, the survival area in each group can be measured scientifically and easily compared. Second, in this model, the flap was supplied by one epigastric artery while other was ligated. A silicon sheet was also used to prevent revascularization. Thus, the blood supply to the model can be easily controlled and manipulated. In this study, several modifications were made including the use of an ultrathin silicon sheet (0.1 mm) to avoid revascularization and heparinized saline to avoid thrombus formation. Analysis of the results showed that skin flaps with HBO preconditioning and HRS treatment have the highest rate of survival in an IR model.
As a new mechanism of inducing cellular IR injury, a TNF-α-induced inflammation via mitochondrial ROS (mtROS) generation has received much attention. mtROS generated by TNF-α can oxidize the reduced thioredoxin-apoptosis signal-regulating kinase 1 complex (Trx [SH] 2-ASK1), and then activate ASK1 and its downstream stress signaling targets including JNK[28-31] to initiate apoptosis. ASK1 could, therefore, be considered to be a bridge during the apoptotic signaling pathway. One pair of proteins plays a paramount role in regulating apoptosis, specifically the antiapoptotic protein Bcl-2 and the pro-apoptotic protein Bax. The ratio of Bcl-2/Bax determines the cellular direction toward apoptosis. Caspase-3 plays an important role in increasing the rate of apoptosis. Activated caspase-3 cuts poly (ADP-ribose) polymerase and increase the activity of Ca2+/Mg2+-dependant endonuclease to destroy DNA molecules.
In this study, the HBO, HRS and HBO + HRS groups showed low levels of apoptotic. HBO preconditioning and HRS used cooperatively were more efficient in reducing cellular apoptosis than HRS or HBO preconditioning used independently. Caspase-3 could increase the rate of apoptosis. ASK1, as a bridge in the apoptotic process, determines the integrity of the JNK pathway. The caspase-3 activity and pASK1 expression were significantly reduced in the HBO, HRS and HBO + HRS groups. Compared to the HBO and HRS groups, the HBO + HRS group showed the lowest level of caspase-3 activity and pASK1 expression. Bcl-2, a mitochondrial anchoring protein, may prevent apoptosis by acting as an antioxidant. The Bcl-2/Bax ratio and Bcl-2 mRNA expression were increased among the HBO, HRS and HBO + HRS groups. The Bcl-2/Bax ratio and Bcl-2 mRNA expression level were higher in the HBO + HRS group than in the HBO or HRS groups.
This study demonstrates the synergistic effect of HBO preconditioning and HRS treatment. By combining the advantages of HBO and HRS, improved flap survival and ischemia tolerance can be used clinically. IR oxygen is not a rare gas and can be readily accessed. However, the application of hydrogen is challenging secondary to its explosive properties and the difficulty of transportation. HRS avoids such problems and can be used in many clinical scenarios. The mechanism of the synergistic effect of HBO preconditioning and HRS treatment have not yet been fully elucidated, and further studies are required. A limitation of this study was the need for an additional IR group with a placebo treatment which would have allowed the comparison of the effects of HBO treatment. With this group, the study would have been more rigorous.
This study showed that compared to an IR group, the rate of skin flap survival is improved, and cellular apoptosis is attenuated secondary to a synergistic effect of HBO preconditioning and HRS treatment.
In conclusion, the synergistic application of HBO and HRS showed a higher flap survival rate, which could be a combined treatment to improve skin flap survival against IR injury.
Financial support and sponsorship
Project supported by the National Natural Science Foundation of China (No. 81171874) and the Beijing Natural Science Foundation (No. 7132169).
Conflicts of interest
There are no conflicts of interest.
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Cite This Article
Xiao YD, Liu YQ, Zhang MZ, Wang YB, Liu YF, Ma XM. Synergistic effect of hyperbaric oxygen preconditioning and hydrogen-rich saline in ameliorating rat flap ischemia/reperfusion injury. Plast Aesthet Res 2015;2:332-9. http://dx.doi.org/10.4103/2347-9264.169499
Xiao YD, Liu YQ, Zhang MZ, Wang YB, Liu YF, Ma XM. Synergistic effect of hyperbaric oxygen preconditioning and hydrogen-rich saline in ameliorating rat flap ischemia/reperfusion injury. Plastic and Aesthetic Research. 2015; 2: 332-9. http://dx.doi.org/10.4103/2347-9264.169499
Xiao, Yi-Ding, Yun-Qi Liu, Ming-Zi Zhang, You-Bin Wang, Yi-Fang Liu, Xue-Mei Ma. 2015. "Synergistic effect of hyperbaric oxygen preconditioning and hydrogen-rich saline in ameliorating rat flap ischemia/reperfusion injury" Plastic and Aesthetic Research. 2: 332-9. http://dx.doi.org/10.4103/2347-9264.169499
Xiao, Y.D.; Liu Y.Q.; Zhang M.Z.; Wang Y.B.; Liu Y.F.; Ma X.M. Synergistic effect of hyperbaric oxygen preconditioning and hydrogen-rich saline in ameliorating rat flap ischemia/reperfusion injury. Plast. Aesthet. Res. 2015, 2, 332-9. http://dx.doi.org/10.4103/2347-9264.169499
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