The effect of Phaseolus vulgaris pods extract on cytokines profile in the condition of alkali burn esophagus 2 degree
- Department of Biochemistry, Educational and Scientific Center” Institute of Biology and Medicine” of Taras Shevchenko National University of Kyiv, Ukraine
Abstract
Introduction: As a result of alkaline substances entering the esophagus wall, necrosis occurs, as well as destruction of the mucous, submucosal and muscular layers of the esophagus. The cellular immune system plays an important role in regulating the various phases of the wound healing process, during which, depending on the time and through specific adhesion interactions, polymorphonuclear leukocytes, macrophages, and lymphocytes penetrate the site of the trauma and lead to an intensive proliferation of fibroblasts, endothelial cells, and keratinocytes. The substances of natural origins based on polyphenolic compounds are possible as a remedy for the normalization of physiological and biochemical parameters in a condition of various pathologies. Phaseolus vulgaris pods extract (PVPE) are an example of a rich source of bioactive compounds with proven human health benefits. Our results revealed imbalance of pro-inflammatory and anti-inflammatory cytokines in esophageal homogenates in rats with alkali burn of esophagus II degree, which can indicate a prolonged inflammation in the burned area. In the groups of animals with the alkaline burn of the esophagus, that were injected extract there can be traced a change of the indicators in the direction of normalization, indicating about the therapeutic effect of aqueous extract of pods of Phaseolus vulgaris.
Objective: The cellular immune system plays an important role in regulating the various phases of the wound healing process, and can be used as a marker of pathological post-burn wound healing, Phaseolus vulgaris pods extract (PVPE) are an example of a rich source of bioactive compounds with proven human health benefits. The aim of the study was to investigate changes in cytokines levels in rat esophageal supernatants in the condition of alkali burn esophagus second degree (AEB 2) and treatment with Phaseolus vulgaris pods extract.
Material and Methods: The animals were experimentally simulated with the alkali esophageal burn with 20% (grade II) solvent of NaOH. Levels of cytokines in esophageal tissue homogenates were done by ELISA.
Results: In the present study, we investigate the imbalance of pro-inflammatory and anti-inflammatory cytokines in esophageal homogenates in rats with AEB 2, which can indicate a prolonged inflammation in the burned area. In the groups of animals with the AEB 2, that were injected extract there can be traced a change of the indicators in the direction of normalization.
Conclusion: The administration of the extract, in conditions of alkaline burn of the esophagus, contributes change of the indicators in the direction of normalization indicating the therapeutic effect of aqueous extract of pods of Phaseolus vulgaris.
Introduction
In the modern world, cases of poisoning with chemical agents are increasingly occurring. Chemical burns are the most common pathology of the esophagus in children1. Alkaline solutions are often bottled, or placed to wrappers similar to sweets, so children can swallow the alkaline. As a result of alkaline substances entering the esophagus wall, necrosis occurs, as well as destruction of the mucous, submucosal and muscular layers of the esophagus2,3. Despite the wide range of drugs used to treat the effects of chemical burns of the esophagus, there is a lack of information in the literature about their effectiveness4.
The process of wound healing consists of three phases that overlap with each other: inflammation, proliferation, and remodeling. An alkaline burn of the esophagus induces an inflammatory response that is characterized by the release of pro-inflammatory and anti-inflammatory cytokines5. Inflammation is needed to successful burn wound healing. Inflammatory mediators such as cytokines, kinins, lipids, and others provide immune signals to recruit leukocytes and macrophages that initiate the proliferative phase6. Inflammation phase is controlled by the balance between pro- and anti-inflammatory mediators in a complex cytokine network. Cytokine balance is essential for cell adhesion control, movement, proliferation, and synthesis of extracellular matrix proteins within the healing wound7. Prolonged inflammation is harmful and may impend the progress of normal burn wound healing by affecting other stages of wound healing8. Prolonged inflammation has also been associated with excessive scarring9. According to modern concepts of burn disease development, one of the major burn complications is the occurrence of inflammation10.
Wound healing in rodents is very similar to humans, and rodents model are a well-characterized model of human wound healing11. There are many difficulties in treating chemical burns of the esophagus1. The effect of therapeutic approaches is reduced due to a decrease in the immune balance, and this is due to pathogenic microflora. As a consequence, the complication of regeneration and other abnormalities in patients. The recovery of functional immunity is a very important step in the complex therapy of chemical-induced esophageal burns.
Analysis of recent data from the literature suggests that substances of natural origins based on polyphenolic compounds are possible as a remedy for the normalization of physiological and biochemical parameters in a condition of various pathologies. pods extract (PVPE) are an example of a rich source of bioactive compounds with proven human health benefits12. However, this study was designed to explore the anti-inflammatory activity of pods extract by measuring their effects on pro-inflammatory and anti-inflammatory cytokines secretion in post-burn esophageal tissue homogenates.
Methods
Preparation of plant extract
Plant material was harvested and collected in Kyiv region of Ukraine. The aqueous extract was prepared by the next method: 132 g of dried pods ofwas poured into 1.0 liter of water at 100°C. The mixture was held in a boiling water bath for 20 minutes, then allowed to cool for overnight and filtered. The obtained extract was centrifuged at 1000 g for 10 min, for removing plant debris, and the supernatant was dried using The Telstar LyoQuess freeze dryer (Spain). Dry extract (8 g) was stored at -20ºC until the time of use. When needed, the residual extract was suspended in distilled water and used in the study12.
Experimental animals
White non-linear male rats, each in the weight range of 100-120g, were obtained from the Animal house of Taras Shevchenko National University of Kyiv, Ukraine. The animals were kept on a standard vivarium diet. The protocol of the experiments in this study have been examined and approved by the Bioethics Commission of Educational and scientific center "Institute of biology and medicine" of Taras Shevchenko National University of Kyiv, Ukraine (protocol №3 from 15.08.2018) and have been performed in accordance with the standards of the Helsinki declaration (International medical assemble), European Convention for the protection of vertebrate animals that used for experimental and other scientific purposes, and other international agreements and national legislation in this field.
Experimental design
A total of 160 rats were divided into 4 groups in equal amount (40 rats in each group): group 1 (G1)– intact control rats (saline injection), group 2 (G2)- control rats, which was injected with PVPE start from 2 day of the experiment at a dose of 200mg/kg b.w. per day 12 for 21 days, group 3 (G3)- AEB 2 with saline injection, group 4 (G4)-AEB of 2 grade, which was injected with PVPE start from the 2 day of the experiment at a dose of 200mg/kg b.w. per day for 31 days. Before modeling of esophageal burn, each rat was anesthetized with 50 mg/kg ketamine HCl intramuscular. The animals were experimentally simulated with the alkali esophageal burn with 20% (grade II) solvent of NaOH1. After 7, 14, 21 and 31 days, the animals were killed by cervical dislocation.
Analytical methods
Histopathological examination for all the groups was done to confirm the tissue damage and stage of alkali burn of esophagus. Levels of cytokines in homogenates were done by ELISA immune assays with primary and secondary antibodies from Santa Cruz Biotechnology, CA, USA. ELISA plates were coated overnight at 4°C with samples of esophageal homogenate previously diluted with Tris-HCl buffer, pH 7.4 to the obtained concentration of proteins 10 µg/mL. After being washed, plates were blocked with 5% nonfat dry milk for 1 h at 37ºC and washed again. After that plates were incubated for 1 h at 37ºC with specific primary antibodies against the cytokines. Plates were washed and incubated for 1 h at 37ºC with corresponding secondary antibodies conjugated to horseradish peroxidase. After washing, the substrate (OPD and hydrogen peroxide) was added. The reaction was stopped by addition of 2.5 N HSO. Plates were read at 492 nm by a microplate reader (µQuantTM, BioTek Instruments, Inc)13.
Statistical analysis
The data of biochemical estimations were reported as mean ± SE for ten animals in each group (after 7, 14, 21, and 31 days after burn). Statistical analyses were performed using one-way analysis of variance (ANOVA). To determine the reliability of the differences between the two samples we used the Student test (t). Whereby differences P˂ 0.05 were deemed reliable. All statistical analyses were performed with statistically available software (SPSS 16 for WINDOWS).
IL-1β levels (st.u.) in esophageal tissue homogenates obtained from the rats
| IL-1β (st.u.) | 7 days | 14 days | 21 days | 31 days |
|---|---|---|---|---|
| G1 | 29.75±1.3 | 29.3±1.3 | 33.2±2.4 | 29.92±2.3 |
| G2 | 31.6±1.4 | 30.15±2.3 | 32.94±2.3 | 31.54±2.5 |
| G3 | 48.89±3.2* | 42.05±3.9* | 46±2.2* | 31.97±2.4 |
| G4 | 41.88±3.1*# | 37.72±3.8* | 40.26±2.1*# | 31.82±2.7 |
IL-6 levels (st.u.) in esophageal tissue homogenates obtained from the rats
| IL-6 (st.u.) | 7 days | 14 days | 21 days | 31 days |
|---|---|---|---|---|
| G1 | 28.42±1.2 | 28.36±2.1 | 28.95±2.1 | 29.35±2.1 |
| G2 | 30.25±1.5 | 29.34±2.2 | 29.79±2.4 | 30.78±2.6 |
| G3 | 42.97±4.1* | 35.96±2.9* | 33.7±2.3* | 31.26±2.8 |
| G4 | 39.54±3.6* | 32.94±3.2 | 31.97±2.2 | 30.72±2.3 |
Results
We investigated the changes in levels of pro-inflammatory cytokines (IL-1β, IL-6, IL-12β, IFN-γ, TNF-α). The levels of pro-inflammatory cytokines in esophageal supernatants of rats with AEB 2 was significantly increased (except TNF-α) over time in groups G3 and G4. Peak levels of pro-inflammatory cytokines were detected on the 7 day and some cytokines levels were constantly and significantly higher up to the 31 day.
IL-12β levels (st.u.) inesophageal tissue homogenates obtained from the rats
| IL-12β (st.u.) | 7 days | 14 days | 21 days | 31 days |
|---|---|---|---|---|
| G1 | 27.67±1.2 | 27.31±2.0 | 26.78±1.4 | 27.67±1.9 |
| G2 | 27.97±1.1 | 28.64±2.1 | 25.34±1.1 | 27.99±2.1 |
| G3 | 40.71±4.0 | 38.7±3.5* | 29.16±2.7 | 28.96±2.2 |
| G4 | 38.31±3.8 | 35.51±2.4* | 29.07±2.1 | 28.74±2.1 |
The level of IL-1β in group G3 increased by 64.3%, 43.5%, 38.6%, and 6.8% after 7, 14, 21 and 31 days post-burn (
TNF-α levels (st.u.) in esophageal tissue homogenates obtained from the rats
| TNF-α (st.u.) | 7 days | 14 days | 21 days | 31 days |
|---|---|---|---|---|
| G1 | 26.7±1 | 26.71±1.8 | 26.88±1.0 | 26.41±1.4 |
| G2 | 27.24±1 | 27.53±1.6 | 26.95±1.1 | 26.89±2.7 |
| G3 | 35.31±4.4* | 21.54±1.4* | 22.9±1.9* | 24.07±2.4 |
| G4 | 34.53±3.8* | 21.99±1.6* | 22.59±2.1* | 22.99±1.9* |
IFN-γ levels (st.u.) in esophageal tissue homogenates obtained from the rats
| IFN-γ (st.u.) | 7 days | 14 days | 21 days | 31 days |
|---|---|---|---|---|
| G1 | 31.63±1.2 | 31.14±2.1 | 33.75±1.3 | 33.04±1.7 |
| G2 | 32.42±1.4 | 31.52±2.2 | 33.96±2.6 | 33.76±1.3 |
| G3 | 38.63±3.7* | 36.47±2.3* | 35.75±2.4 | 35.04±1.4 |
| G4 | 38.45±2.5* | 35.29±2.7 | 35.44±2.8 | 34.99±1.4 |
We investigated the changes in levels of anti-inflammatory cytokines (IL-4, IL-10). The results indicated a significant decrease in the levels of anti-inflammatory cytokines within 21 days after burning. The level of IL-4 (
IL-4 levels (st.u.) in esophageal tissue homogenates obtained from the rats
| IL-4 (st.u.) | 7 days | 14 days | 21 days | 31 days |
|---|---|---|---|---|
| G1 | 38.01±2.5 | 36.47±2.4 | 38.2±1.5 | 35.83±1.4 |
| G2 | 35.95±2.4 | 35.68±2.6 | 39.2±1.5 | 36.8±1.4 |
| G3 | 29.52±1.9* | 30.26±1.9* | 36.31±1.4 | 33.76±1.3 |
| G4 | 32.74±1.8* | 32.41±1.4* | 36.52±1.4 | 35.4±1.4 |
IL-10 levels (st.u.) in esophageal tissue homogenates obtained from the rats
| IL-10 (st.u.) | 7 days | 14 days | 21 days | 31 days |
|---|---|---|---|---|
| G1 | 47±2.9 | 46.53±1.8 | 45.85±1.8 | 44.48±1.7 |
| G2 | 48.11±2.8 | 46.85±0.6 | 45.63±1.8 | 44.69±1.7 |
| G3 | 32.25±2.4* | 28.13±1.2* | 36.87±1.4* | 45.92±1.8 |
| G4 | 35.71±2.7* | 38.4±1.5*# | 38.13±1.5* | 46.2±1.8 |
Discussion
In the condition of esophageal chemical burns, the organism is capable of expression of non-specific inflammatory reactions, leading to cytokine synthesis in the burned area10. The cellular immune system plays an important role in regulating the various phases of the wound healing process, during which, depending on the time and through specific adhesion interactions, polymorphonuclear leukocytes, macrophages, and lymphocytes penetrate the site of the trauma and lead to an intensive proliferation of fibroblasts, endothelial cells, and keratinocytes14. Pro-inflammatory cytokines play a key role in the progression of inflammatory trauma both at the local and systemic levels. In strong inflammatory conditions, cytokines can enter the bloodstream, eliciting acute responses from various tissue organs.
The imbalance in the release of pro-inflammatory and anti-inflammatory cytokines may contribute to immunological dysfunction and systemic inflammation, resulting in tissue damage, multiple organ failure, or death from the burn15. The burn wound healing process characterized by a prolonged inflammatory phase, and that is one of the main complications caused by chemical burns. Due to violations of the skin barrier, sepsis occurs and the immune system weakens10.
Acute inflammatory response is initiated due to the activation of tissue macrophages and the secretion of inflammatory cytokines, in particular, interleukin (IL-1), tumor necrosis factor (TNF-α), IL-6, which cause many local and systemic changes detected during the development of an acute inflammatory response16. IL-1 launches a complex of local defense reactions involving almost all types of inflammatory effector cells in the elimination of the pathogen and the restoration of the integrity of the damaged tissue17. This local cytokine production has multiple local and systemic consequences, such as inflammatory cell migration, activation of immune response and changes in the processes of proliferation and differentiation of keratinocytes and of fibroblasts10,17.
We investigated changes in levels of pro-inflammatory cytokines (such as IL-1β, IL-12β, IFN-γ, IL-6, TNF-α) which can enhance the proliferation of T- and B- lymphocytes, antibody synthesis, production of adhesion molecules, and synthesis of acute phase proteins. Also, they are involved in processes of specific and non-specific immunity. IL-1β is one of the key cytokines in wound defense and regulation. The data obtained for IL-1β levels in esophageal homogenate supernatants show that IL-1β increases in the condition of AEB 2 during all period of the experiment (
Plants, including herbs, contain polyphenols, which are a potential source of natural antioxidants. Herbal extracts and their products prevent or reduce oxidative stress. The reported in literature anti-inflammatory mechanisms included reduction of some pro-inflammatory cytokines, and increasing anti-inflammatory IL-10 secretion, reduction of cyclooxygenase-2 (COX-2) and nitric oxide synthase expression20. In our experiment, we showed some normalization of inflammatory indicators due to the introduction of the extract, which may be a sign of the positive effect of the extract on the healing of alkaline burn of the esophagus.
Conclusions
Our results revealed imbalance of pro-inflammatory and anti-inflammatory cytokines in esophageal homogenates in rats with alkali burn of esophagus second degree, which can indicate a prolonged inflammation in the burned area. In the groups of animals with the alkaline burn of the esophagus, that were injected extract there can be traced a change of the indicators in the direction of normalization, indicating about the obvious therapeutic effect of aqueous extract of pods of .
Abbreviations
AEB 2: Alkali esophageal burn of second degree
ANOVA: Analysis of variance
COX-2: Cyclooxygenase-2
ELISA: The enzyme-linked immunosorbent assay
PVPE: pods extract
Competing Interests
None of the authors of this article have conflicting interests.
Authors' Contributions
Ya. B. Raetska - the experiment planning, article planning and writing; V.V Dmytryk - measurement of the indicators presented in the article; N.M. Chornenka - measurement of the indicators presented in the article; O.M Savchuk - the experiment planning, article planning and writing; T. I Halenova - the experiment planning, extract of pods of preparation; N. G. Raksha -measurement of the indicators presented in the article; T. Vovk- the experiment planning, extract of pods of preparation; L.I. Ostapchenko - the experiment planning. All authors reviewed and commented on final draft.