|Year : 2019 | Volume
| Issue : 3 | Page : 93-97
Amlodipine improves skin flap viability in rats exposed to nicotine
Fatih Irmak1, Isil Akgun Demir1, Selami Serhat Sirvan1, Soysal Bas1, Semra Karsidag1, Aysim Ozagari2
1 Department of Plastic, Reconstructive, and Aesthetic Surgery, Sisli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey
2 Department of Pathology, University of Health Sciences, Sisli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey
|Date of Web Publication||4-Jul-2019|
Dr. Isil Akgun Demir
Sisli Hamidiye Etfal Egitim Ve Arastirma Hastanesi Kat: 7 Plastik, Rekonstruktif Ve Estetik Cerrahi Klinigi 34373 Sisli, Istanbul
Source of Support: None, Conflict of Interest: None
Background: A recent series of experimental and clinical studies have demonstrated the negative effects of nicotine such as ischemia and necrosis of skin flaps. In order to overcome the negative effects of nicotine numerous studies have been conducted with various agents and methods. In this study, we investigated the effects of amlodipine (AML) on flap survival in nicotinized rats. Materials and Methods: Thirty Sprague Dawley rats were randomly divided into three groups: Group A nicotine; Group B nicotine + AML; Group C control group. The rats in Group A and B have received nicotine for 4 weeks before the surgical intervention. At the end of the 4th week, MacFarlane flaps were elevated and adapted back by suturing in all groups. In Group B, AML has been administered to the rats after the surgery and continued for 10 days. All the flaps were visualized with fluorescein angiography and underwent histopathological assessment. The necrotic areas of the flaps were measured as well. Results: The necrosis rate in Group A was found to be significantly higher compared to Group B (P< 0.001). The perfusion rates in Group B were found to be significantly higher when compared to Group A (P < 0.05). Vascular proliferation was found to be significantly higher in Group B compared to Group A and C (P < 0.05). Vasodilation rates were significantly higher in Group B and C (P < 0.05). Conclusions: AML was found to be useful to enhance flap survival in nicotinized subjects. Its clinical use might be promoted in the future with the help of further studies supporting our findings.
Keywords: Amlodipine, flap survival, nicotine
|How to cite this article:|
Irmak F, Demir IA, Sirvan SS, Bas S, Karsidag S, Ozagari A. Amlodipine improves skin flap viability in rats exposed to nicotine. Turk J Plast Surg 2019;27:93-7
|How to cite this URL:|
Irmak F, Demir IA, Sirvan SS, Bas S, Karsidag S, Ozagari A. Amlodipine improves skin flap viability in rats exposed to nicotine. Turk J Plast Surg [serial online] 2019 [cited 2019 Aug 18];27:93-7. Available from: http://www.turkjplastsurg.org/text.asp?2019/27/3/93/250622
| Introduction|| |
Cigarette smoking is a worldwide problem. The WHO guesses that there are now nearly 1.3 billion smokers in the world, and 84% of them live in the developing world. Cigarette smoke contains more than 250 components, among which the adrenergic activator and vasoconstrictive substance nicotine is the best known., A recent series of experimental and clinical studies have demonstrated the negative effects of nicotine such as ischemia and necrosis of skin flaps.,,,,,, Even side-stream smoking has been found to affect random-pattern skin flap survival in rats. In order to overcome the negative effects of nicotine, studies with hyperbaric oxygen therapy, sildenafil citrate, phosphodiesterase-5 inhibition, angiotensin 1–7, TENS (transcutaneous electrical nerve stimulation), buflomedil, pentoxifylline, and calcium channel blockers (CCBs) (mainly verapamil and nifedipine) have been reported in the literature.,,,,,,, Amlodipine (AML) is a widely used CCB to treat patients with hypertension. It dilates vessels by blocking the calcium uptake through voltage-gated calcium channels which leads to a decrease in the vascular tone. AML has also been shown to stimulate local nitric oxide release and have some antioxidant features.,, In this study, we hypothesized that amlodipine enhances flap survival in nicotinized rats by providing sufficient vasodilation and angiogenesis.
| Materials and Methods|| |
This study has been conducted with the approval of the Local Ethics Committee at Uskudar University Experimental Research Unit. Thirty Sprague Dawley rats weighing between 200–400 g were used. The rats were randomly divided into three groups as follows: Group A nicotine; Group B nicotine + AML; and Group C control group. The rats in Group A and B have received nicotine (Sigma-Aldrich®) (2 mg/kg, twice a day, per oral) for 4 weeks before the surgical intervention. On the day of surgery, ketamine hydrochloride (50 mg/kg) and xylazine (10 mg/kg) were administered intraperitoneally for anesthesia. MacFarlane flaps (9 × 3 cm) were elevated and adapted back by suturing in all groups [Figure 1]. In Group B, after the adaptation of the flaps, AML (2.5 mg/kg/day) has been administered to the rats through oral gavage and continued for 10 days. On the 10th day, all the flaps were visualized with SPY Intraoperative Perfusion Assessment System (Lifecell Corp., Branchburg, NJ, USA). Once the femoral vein was dissected, 0.5 mg/kg indocyanine green (ICG) was administered as a bolus to each rat. The digital images showing the perfusion rates in both necrotic and healthy areas of the flaps were recorded to be compared. After imaging with ICG was completed, all the rats were euthanized, and flaps were excised for histopathologic assessment. The necrotic areas of the flaps were measured by projecting them on transparency paper. The specimens were fixed with 10% neutrally buffered formalin. After fixation, they were processed routinely and embedded in paraffin. 5 mm sections were obtained from the tissue blocks, which were obtained from the transitional area between healthy and necrotic zones, and stained with hematoxylin and eosin and CD105 (endoglin). Immunohistochemical staining for CD105 antibody (clone SN6 h, 1:10, DAKO North America, CA) was used to determine the newly formed vascular structures. Histopathological assessment was performed under a light microscope in terms of neutrophil infiltration, chronic inflammation, vascular proliferation, and vasodilation. The quantitative analysis of the findings was done by the pathologist as follows: (1) low, (2) intermediate, and (3) high. The pathologist was also blinded to the study groups to prevent tendentiousness.
|Figure 1: (a) Elevation of the MacFarlane flaps and (b) The appearance after the flaps was sutured back|
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Statistical analyses were perusing the SPSS for Windows version 15.0 program. The data for ordinal variables were reported as mean, Standard Deviation and median. For groups having more than two ordinal variables, Kruskal Wallis test was performed. Subgroup analyses were performed with Mann–Whitney-U test and interpreted with Bonferroni correction. The categorical variables were analyzed with Chi-square test with Monte Carlo simulation. Differences at P < 0.05 were considered to be statistically significant.
| Results|| |
Comparison of macroscopic data
In all rats, the necrotic areas of the flaps were measured by projecting them on transparency paper. The necrosis rate in Group A was found to be significantly higher compared to Group B (P < 0.001) [Figure 2] and [Table 1].
The data provided by the SPY system showed that the distal segments of the flaps in Group A had decreased perfusion (mean perfusion index: 18.6% [3.1%–24.8%]), whereas the same areas in Group B and C demonstrated better perfusion rates (mean perfusion index: 58.9% [40.2%–94.8%]) [Figure 3]. The perfusion rates in Group B were found to be significantly higher when compared to Group A (P < 0.05).
|Figure 3: Macroscopic appearances of the necrotic areas in all three groups on the postoperative 10th day. The necrosis rate in Group A was significantly higher compared to Group B|
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Comparison of microscopic data
The microscopic data were compared in all three groups in terms of neutrophil infiltration, vascular proliferation, and vasodilation [Figure 4]. Neutrophil infiltration was found to be higher in Group A compared to Group B and C (P < 0.05). Vasodilation rates were significantly higher in Group B and C (P < 0.05) [Table 2] and [Figure 5]. Staining with CD105 showed that vascular proliferation was significantly higher in Group B compared to Group A and C (P < 0.05) [Figure 6].
|Figure 4: Evaluation of the perfusion rates through the SPY system. The perfusion rates of Group B were significantly higher at the distal segments of the flaps than those of Group A|
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|Table 2: Microscopic data with mean and median values according to the scoring system*|
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|Figure 5: Microscopic evaluation of the groups. There was a marked vasodilation of vessels in Group B. Hematoxylin-eosin stain, (×40)|
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|Figure 6: CD105 (endoglin) staining shows increased vascular proliferation. Lacunes with terracotta color indicate new vessel formation (×20)|
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| Discussion|| |
Numerous clinical and experimental studies demonstrated the detrimental effects of smoking and nicotine on flap survival.,,,,, Nicotine has been shown to cause vasoconstriction and intravascular thrombosis mainly through changing the levels of vasoactive substances such as catecholamine, prostaglandin, and thromboxane A2 levels., It also reduces the proliferation of red blood cells, fibroblasts, and macrophages. Hence, smoking causes hypoxia in tissues while interfering with wound healing.
It is well-known that the most distal part of a flap is more prone to ischemic injury because of its distant localization to the pedicle. Random flaps are composed of three parts according to their localizations to the pedicle: distal, proximal, and critical zone. The prevention of ischemia in the critical zone is crucial to prevent flap necrosis. Taking into account the vasoconstrictor effects of nicotine, an ischemic injury in a random flap in a nicotinized subject is much more likely to occur. In their study, Forrest et al. showed that nicotine affects the viability of random flaps in rats by impairing capillary blood flow. It has also been shown that smokers are more likely to develop necrotic damage after surgery.
Numerous vasodilator agents were examined to overcome vasoconstriction such as phosphodiesterase inhibitors, papaverin, pentoxifylline, amrinone, lidocaine, magnesium sulfate, sodium nitroprusside, prostaglandine E1, hydralazine, phentolamine, chlorpromazine, and CCBs, nifedipine, and verapamil in particular.
Various studies have been conducted to improve flap survival in nicotinized subjects. Mauad et al. studied the effects of buflomedil and pentoxifylline on flap survival in rats. Both buflomedil and pentoxifylline were found to increase flap survival, but none of them was superior to the other. Aker et al. also recommended pentoxifylline use in patients who cannot quit smoking to reduce skin flap necrosis. In their study, Baykan et al. showed that sildenafil citrate enhanced skin flap survival without a significant effect on blood flow. In another study, the same author concluded that angiotensin,,,,,, is beneficial to improve flap survival by promoting angiogenesis. Electrical stimulation has been found to increase flap survival in ischemic flaps.
Acting on voltage-gated CCBs decrease intracellular calcium concentration and thus provide vasodilation. Consequently, relaxed vasculature provides increased blood flow to the tissues. Nicardipine, verapamil, and nifedipine are the most commonly used CCBs for experimental purposes.,
Nifedipine is a strong vasodilator, however, its effect on flap survival is controversial. As with nifedipine, verapamil is also an effective vasodilator with additional effects, the most important being prevention of the free radical damage.
Kilinc et al. reported that verapamil administered flaps showed better survival, whereas nifedipine administered flaps showed no effect. They suggested that the beneficial effect of verapamil on flap survival may be attributed to verapamil's effect on free oxygen radical-mediated injury. Besides verapamil also was shown to cause less reperfusion injury. Rinker et al. concluded that the use of nifedipine and verapamil may provide a means of reducing the perioperative risk in active smokers who require skin flap surgery. Qin et al. applied azithromycin-AML-heparin gel to the infected random ischemic flaps transdermally in rats and they asserted that gels without azithromycin have no effect on the survival of infected ischemic flaps.
In the present study, we preferred to use amlodipine to provide vasodilation to enhance flap survival in nicotinized rats. AML is a dihydropyridine CCB and has been extensively used in various cardiovascular and non-cardiac conditions. Apart from treating hypertension, it also attenuates LDL-induced endothelial dysfunction and has protective effects on ischemia-perfusion induced heart injury, and AML can also inhibit angiotensin-converting enzyme to some extent while enhancing nitric oxide release. In their study, they also concluded that AML promotes ischemia-induced neovascularization by activating endothelial progenitor cell mobilization from bone marrow in diabetic rats. AML is also known for its antioxidant features and Dogan et al. suggested that AML has protective effects on ischemia/reperfusion injury in rat testis torsion model by decreasing free radicals and increasing antioxidants.
The SPY system is a fluorescence imaging system utilizing ICG. It shows flap perfusion via sensitive topographic evaluation. ICG binds to the globulins in the bloodstream, alfa-1 lipoproteins in particular. Perfusion is demonstrated 1–2 s after intravenous injection of ICG. The SPY system provides objective data with numeric values.
In our study on the 10th day, before the rats were euthanized, ICG was administered to all of the rats and the data regarding perfusion rates were collected via the SPY system. The analysis of the data revealed that the perfusion rate in Group B was significantly higher than that in Group A (P < 0.05). The rate of necrosis in Group A was higher compared to Group B, and this was statistically significant. The images obtained with the SPY system support our findings. Our results also showed that the vasodilator effect of AML was sufficient to enhance flap survival in nicotinized subjects compared to those did not receive AML. The microscopic evaluation revealed that the vasodilation rates were higher in Group B compared to Group A.
Vascular proliferation was expected to increase in all groups since ischemia promotes angiogenesis. However, the data showed that there was a significant increase in vascular proliferation in Group B. We believe that AML may have promoted angiogenesis by means of enhancing NO release as Sun et al. suggested.
Since smokers are more likely to have cardiovascular problems including hypertension, AML may be utilized both to treat hypertension and to improve skin flap survival in case of a surgical intervention in such patients if suitable. However, this assertion should be supported with further experimental and clinical studies.
| Conclusions|| |
AML was found to be useful to enhance flap survival in nicotinized subjects. Its clinical use might be promoted in the future with the help of further studies supporting our findings.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
[Table 1], [Table 2]