On-line version ISSN 1678-2674
Acta Cir. Bras. vol.27 no.3 São Paulo Mar. 2012
6 - ORIGINAL ARTICLE
Intestinal healing in rats submitted to ethanol ingestion1
Cicatrização intestinal em ratos submetidos à ingestão de etanol
Rodrigo Severo de Camargo PereiraI; Cláudia Nishida HasimotoII; Leonardo PelafskyIII; Juan Carlos LlanosIV; Daniele Cristina CataneoV; César Tadeu SpadellaVI; José Guilherme MinossiVII
IPhD, Surgeon, Division of Gastroenterology Surgery, Surgery and Orthopedics Department, Botucatu School of Medicine, UNESP, Brazil. Involved with technical procedures, manuscript writing
IIMaster, Surgeon, Division of Gastroenterology Surgery, Surgery and Orthopedics Department, Botucatu School of Medicine, UNESP, Brazil. Involved with technical procedures, animals care and biochemical analysis
IIIMD, Surgeon, Division of Gastroenterology Surgery, Surgery and Orthopedics Department, Botucatu School of Medicine, UNESP, Brazil. Involved with technical procedures and animals care
IVPhD, Associate Professor, Division of Gastroenterology Surgery, Surgery and Orthopedics Department, Botucatu School of Medicine, UNESP, Brazil. Critical review
VPhD, Associate Professor, Division of Thoracic Surgery, Surgery and Orthopedics Department, Botucatu School of Medicine, UNESP, Brazil. Critical review and responsible for English language
VIPhD, Chairman, Division of the Gastroenterology Surgery, Surgery and Orthopedics Department, Botucatu School of Medicine, UNESP, Brazil. Critical review
VIIPhD, Associate Professor, Division of Gastroenterology Surgery, Surgery and Orthopedics Department, Botucatu School of Medicine, UNESP, Brazil. Mentor, designed the protocol and critical review
PURPOSE: To study the effect of alcoholism on intestinal healing and postoperative complications in rats
METHODS: One hundred and sixty rats were divided into two groups: control and treated. The control group received water and the treated group 30% ethanol. After 180 days, colotomy with anastomosis were performed. After, the groups were divided into four subgroups: 20 rats for study at the following moments: 4th, 7th, 14th and 21st postoperative. The analyzed parameters were: weight gain, breaking strength, tissue hydroxyproline, postoperative complications and histopathological study
RESULTS: Weight gain was greater in the control group (p<0.05). When all the subgroups were clustered, breaking strength was significantly greater in the control (p<0.05). Histopathology and hydroxyproline dosage did not show differences. There were five surgical site infections in the treated group while the control group showed two (p>0.05). Nine fistulas occurred in the treated group whereas the control group two (p<0.05). There were three deaths in the control group and seven in the treated group (p>0.05).
CONCLUSIONS: Treated group undergo a malnutrition process that is revealed by lower weight gain. Impaired intestinal healing as indicated by smaller breaking strength. There were a larger number of postoperative complications in the treated animals.
Key words: Wound Healing. Alcoholism. Ethanol. Tensile Strenght. Hydroxyproline. Rats.
OBJETIVO: Estudar o efeito do alcoolismo no processo de cicatrização intestinal e suas complicações pós-operatórias em ratos.
MÉTODOS: Cento e sessenta ratos foram divididos em dois grupos: tratado e controle. O controle recebeu água, enquanto o tratado etanol a 30%. Após 180 dias foram realizadas colotomia, seguida de anastomose. Após os animais foram divididos em quatro subgrupos de 20 ratos para estudo nos seguintes momentos: 4º, 7º, 14º e 21º pós-operatório. Os parâmetros analisados foram: ganho de peso, força de ruptura, hidroxiprolina tecidual, complicações pós-operatórias e estudo histopatológico.
RESULTADOS: O ganho de peso foi superior no grupo controle (p<0,05). Após agrupamento dos momentos a força de ruptura foi superior no controle (p<0,05). Não houve diferença quanto à histopatologia e hidroxiprolina. Houve cinco infecções de incisão no grupo tratado, enquanto no controle ocorreram duas (p>0,05). Houve nove fístulas no grupo tratado, enquanto no controle duas (p<0,05). Ocorreram sete mortes no grupo tratado e apenas três no controle (p>0,05).
CONCLUSÕES: No grupo tratado ocorreu um processo de subnutrição evidenciado pelo menor ganho de peso. Piora na cicatrização intestinal, indicada pela menor força de ruptura. Ocorreu um maior número de complicações pós-operatórias no grupo tratado.
Descritores: Cicatrização. Alcoolismo. Etanol. Resistência à Tração. Hidroxiprolina. Ratos.
Abusive alcohol consumption is considered to be a serious public health problem, and it is responsible for 3.2% of mortality worldwide1. In Brazil, an emerging country, the scenario is even worse. A Brazilian multicenter study on 107 cities with more than 200 thousand inhabitants showed prevalence of alcoholism in 11.2% of the studied population2.
Due to easy access, alcohol consumption in adolescence has progressively increased. Several studies report that 60 to 90% of students at the end of high school have already ingested some type of alcoholic beverage3-5, and the date of first ingestion between 14 and 15 years old6. This fact makes this issue even more serious, since it has been found that approximately 14% of the individuals who began consumption when they were younger than 14 years old became addicted, whereas only 2% of individuals whose first ingestion occurred when they were older than 19 years old became addicted7.
In the United States, of all car accidents associated with alcohol consumption, 4% resulted in death, and 42% in some lesion type, whereas in car crashes that were unrelated to the ingestion of alcoholic beverages, 0.6% resulted in death, and 31% in some type of injury8. Alcohol abuse is present in 53% of fatal traffic accidents victims9. In a General Hospital, 56% of the patients with head trauma by aggressions were drunk10 and a recent research found frequent binge drinking to be the strongest predictor of both intoxicated rape and other forms of rape, with an odds ratio of 7.83 and 2.82, respectively11.
Abusive and indiscriminate use of alcoholic beverages is responsible for more than 60 health aggravations, such as esophageal, stomach and liver cancer, cardiovascular diseases, hepatic cirrhosis, chronic pancreatitis and peptic ulcers in addition to traumas of all types12-14, with an estimate that the abuse of alcoholic beverages reduces the life expectancy in five years15. In many of such pathologies, interventions on the digestive tract may be required.
The gastrointestinal tract is the first body segment to come into contact with ethanol, and it is exposed to concentrations that are often larger than in other tissues16. The chronic ingestion of ethanol changes intestinal histology, resulting in reduced villi, increased microvascular permeability17and cellular regeneration processes, with the possibility of carcinogenesis18.
Our research group has studied intestinal healing in clinical conditions considered to be deleterious to its development, such as malnutrition, peritoneal infection, use of non-hormonal anti-inflammatory agents and diabetes, which show healing delay with increased risk for dehiscence in the postoperative period19.
Despite the recent advancements in surgical techniques, intensive care and antibiotic therapy, anastomotic fistulas still concern surgeons and patients. In the world, a lot of thousands digestive-system surgeries occurred every year, with an estimate of 10 to 20% of anastomotic fistulas20,21.
Intestinal healing comprises a series of consecutive events that are carefully regulated in order to re-establish the immune barrier and heal the injured tissue. Failure or delay in one of such events may lead to anastomotic dehiscence.
The probable mechanisms involved in healing retardation would be related to reduced synthesis and/or increased collagenic lysis, in addition to delayed cellular regeneration. Collagen is responsible for all tissues resistance and by the strength and integrity of regeneration sites. Healing depends on the type and quantity of collagen fibers22.
As regards the abovementioned alcoholism problem, there is a series of alterations that may affect anastomosis in the intestinal tract, such as: malnutrition and hepatic lesions, in addition to the direct effect of ethanol on the mucosa in the digestive system, thus hindering its healing. For these reasons, the present study aims at analyzing the behavior of intestinal healing in rats submitted to ethanol ingestion.
The experimental protocol was conducted according to the Guide for the Care and Use of Laboratory Animals, published by the U.S. National Institute of Health. It was also approved by the Ethics and Animal Experimentation Committee of the Botucatu School of Medicine, Sao Paulo State University - UNESP. One hundred and sixty adult Wistar rats weighing approximately 180 to 200 grams were used. The animals were kept in polyurethane cages, each containing five rats. They were fed commercial chow and allowed to have free access to water. The diet was interrupted 12 hours prior to the surgical procedure. After a seven-day adaptation period in the Surgical Technique and Experimental Surgery, they were randomly distributed, according to the random number table23, into two groups as follows:
Control Group: consisted of 80 animals that were fed commercial chow and allowed to have free access to water for 180 days and then submitted to distal-colon anastomosis. This group was divided into four sub-groups of 20 rats each, and necropsy was performed 4, 7, 14 and 21 days after the surgical procedure.
Treated Group: consisted of 80 animals that received 30% ethanol and commercial chow for 180 days and then submitted to distal-colon anastomosis. This group was divided into four subgroups of 20 rats each, and necropsy was performed 4, 7, 14 and 21 days after the surgical procedure.
Twenty animals from each group, five from each subgroup were allocated for histopathological study while the remaining 60 were allocated for study of the following variables: breaking strength, hydroxyproline, postoperative complications and weight. These parameters were analyzed in 15 animals at each moment. The animals that died before the surgery were replaced. Ethanol dilution was performed by using Gay-Lussac alcoholmeter.
The animals were weighed on a Mark 8000 scale with capacity for 8,000 grams when admitted at the animal colony and immediately prior to the surgical procedure.
After the preconized period, the animals were anesthetized with sodium pentobarbital, 30 miligrams/kilogram, intraperitoneally. After anesthesia, the animals were weighed, which was followed by abdominal trichotomy, disinfection with 2% iodinated alcohol and a 5 centimeters median incision in the lower abdominal area. Next, total colotomy was performed five centimeters above the peritoneal deflection (Figure 1A). Then, end to end, colon-colonic anastomosis was carried out on a single plane, using separate total stitches with 6-0 polypropylene suture (Figure 1B). Wall closure was performed by the synthesis of the peritoneum, musculature and aponeurosis, with a single suture and separate stitches using 4-0 Nylon. The skin was sutured by using 4-0 Nylon suture and separate stitches. After the procedure, the rats were randomly selected for the moments according to the random number table23.
After the standardized period, 15 rats from each moment were again anesthetized and submitted to a new laparotomy for removal of a 3 centimeters colonic segment containing the anastomosis. The fragments were soaked in a mixture of saline solution and papaverine hydrochloride (250 miligram/liters) for 30 minutes at 370C. The segments were then submitted to breaking strength evaluation. The rats were then sacrificed by using an intramuscular anesthetic overdose of sodium pentobarbital.
In order to evaluate longitudinal breaking strength, the Mechanic Assay Universal Testing Machine EMIC DL10-000 was used.
Morphological analysis was performed in the Department of Pathology of the Botucatu School of Medicine, Sao Paulo State University - UNESP. After the standardized period, five rats remaining from each moment were again anesthetized for removal of a 3 centimeters colonic segment with the anastomosis in its center. Three cuts were performed perpendicularly to the anastomosis region, and slides were prepared and respectively stained with Hematoxylin-eosin and Masson's Trichrome. The criteria adopted for the histopathological evaluation of the healing process were: mucosal regeneration, inflammatory reaction, granulation tissue and collagenogenesis.
The biochemical analyses were performed at the Internal Medicine Experimental Laboratory of the Botucatu School of Medicine, UNESP. After application of breaking strength, the tissues were cut, and the segments consisting of both anastomotic borders were removed. Tissue hydroxyproline was dosed according to the method described by Switzer24. The variables used to evaluate surgical complication were: deaths, anastomotic dehiscence and surgical site infection.
For statistical analysis, Tukey's method was used for variables breaking strength and tissue hydroxyproline dosage. In each group and at each moment, 15 animals were used, and the means and standard deviations were calculated as indicators for central tendency and variability, respectively. The level of significance used was of 5%. Surgical complications, deaths, infections and fistulas were analyzed by the Z test. The level of significance used was of 5%. The rats' weight gain was analyzed by the chi-square test. The level of significance used was of 5%.
Weight gain in the group submitted to ethanol ingestion until the date of surgery varied from 108.0 to 321.0 grams, with a mean and standard deviation of 218.7±49.4 grams whereas, in the control group, it ranged from 211.0 to 513.0 grams, with a mean and standard deviation of 303.5±57.6 grams. Significant difference was found between the groups (p<0.05). The mean and standard deviation of the animals' weight on the day of surgery in each group and at each moment as well as the general mean of each group and the statistical interpretation are shown in Table 1.
The means and standard deviations for the breaking strengths were respectively of 225.1±76.8 gramsforce on the 4th postoperative day; 282.3±76.2 gramsforce on the 7th day; 476.5±94.8 gramsforce on the 14th day and 535.2±133.3 gramsforce no 21st day in the treated group. In the control group, such values were 257.0±46.7 gramsforce on the 4th postoperative day; 340.9±64.7 gramsforce on the 7th day; 535.2±113.2 gramsforce on the 14th day and 602.6±96.2 gramsforce on the 21st day. Although the breaking strength means were higher in control group, there were no statistically significant differences between the groups at each moment, this is shown by a significant interaction group * moment was not significant (P> 0.05). There was a difference between the overall mean of the control group in contrast to the treated group (TG<GC) and also showed differences between the overall averages of the moments, being M1=M2<M3=M4 (Figure 2).
In the treated group, the mean/standard deviation for the tissue hydroxyproline dosage was 4.98±2.20micrograms/deciliter on the 4th postoperative day; 7.82±1.50 micrograms/deciliter on the 7th postoperative day; 11.02±3.00 micrograms/deciliter on the 14th postoperative day and 16.64±6.90 micrograms/deciliter on the 21st postoperative day. In the control group, the values were respectively 6.31±2.10µg/ml on the 4th postoperative day; 9.08±1.50µg/ml on the 7th postoperative day; 12.11±1.30 micrograms/deciliter on the 14th postoperative day and 14.33±2.60 micrograms/deciliter on the 21st postoperative day. The hydroxyproline dosage did not show differences between the groups at each studied moment, but a significant difference was only found between the moments, with the smallest value at moment M1 and the largest at moment M4 (Figure 3).
The histopathological analysis did not show significant alterations between the control group and the treated group. No delay was observed for the intestinal healing phases in the group submitted to ethanol ingestion as compared to the animals in the control group. On the first postoperative days, partial mucosal regeneration occurred with development to complete healing in four of the five samples on the 21st day in both groups. At first, inflammatory reaction was incipient on the 4th day after the procedure, with slight neutrophilic exudate, a process that showed a major increase on the 7th day after the procedure. On the 21st day, there was virtually no inflammatory process in both groups. As regards the formation of granulation tissue and collagenogenesis, the presence of a few neoformed vessels was observed on the 4th day. They were perpendicular to the anastomosis and showed a small number of fibroblasts and collagen fibers. Increased vascular formation occurred over time, with a larger number of fibroblasts and collagen. Collagen density increased progressively during the experiment. On the 21st postoperative day, more structurally organized fibers were observed.
As regards complications, five surgery site infections occurred in the group submitted to ethanol ingestion whereas there was only one in the control group. The control group showed two anastomotic fistulas, and the treated group showed nine. Seven deaths occurred in the group submitted to ethanol ingestion whereas only three took place in the control group (Table 2).
Intestinal healing can be evaluated by means of the anastomosis breaking strength or collagen quantification22. Mechanically, the tissue repair process can be measured by both the longitudinal breaking strength used in our study and the radial bursting strength25. Longitudinal breaking strength is the measure of the intestinal wall resistance to forces applied on its longitudinal direction26 while radial breaking strength, also known as bursting pressure, measures the resistance of the intestinal wall to increased intraluminal pressure27. Longitudinal strength is determined by the quality and quantity of collagen fibers and, on the first three days, reflects primarily the resistance of suture materials28. On the first two days of healing, the breaking strength of suture, in either of the abovementioned methods, is low due to the action of collagenase25 which degrades part of the collagen existing in the lesioned tissue. Therefore, during this period, anastomosis resistance depends on the suture material and/or on the metal clamps used. As days go by, tissue resistance progressively increases, and it is proportional to collagen production by the tissue. Decrease in rupture strength, both longitudinal and radial during the first days after suturing is not consensual in the literature. A study that experimentally evaluated anastomoses in rats did not find any reduction in radial breaking strength on the first days of the healing process, but rather a progressive increase in such strength which was directly proportional to the increase in the number of neutrophils in the repair site26. The criticism in the literature as regards the sensitivity of the longitudinal breaking strength on the first three postoperative days is that it does not change in that period, thus remaining constant and progressively increasing from the 4th day26,27. Such event has not been fully understood, and it probably occurs due to the fact that this measure is extremely sensitive to the surgical technique used in producing anastomoses26. In our study, a difference was soon found in breaking strength between the groups on the 4th postoperative day, although without statistical significance. The use of the longitudinal breaking strength is criticized due to the difficulty to apply the same strength on the whole colonic circumference29. Radial breaking pressure is also questioned because of the difficulty to compare the various studies due to the absence of standardization with which the anastomosis is insufflated30 and if such measure must be taken in situ or with the piece out of the cavity31.
A recent meta-analysis has found that the pre-operative intestinal preparation is not related to colonic healing and that it may even increase the risk for fistula occurrence in the postoperative period32. In our study, we chose to not perform colon preparation, and the animals were operated on by only two researchers so as to minimize the bias of surgical technique used.
Alcoholism is one of the major causes of malnutrition in the United States33. A study published in 1998 analyzed 32 alcoholic individuals without signs of hepatic dysfunction or intestinal malabsorption. Lower weight was observed in those patients, especially at the expense of body fat reduction34. Such weight reduction probably occurs due to the fact that the alcoholic individual can replace up to 50% of his daily intake of calories by alcohol35. Our experimental study showed substantially lower weight gain in the group submitted to ethanol ingestion, with statistical significance, thus revealing a correlation with the abovementioned studies.
Intestinal healing can be negatively influenced by several factors such as: surgical technique, suture materials used, malnutrition, anemia, diabetes, irradiation, shock, immunosuppression, infection and pre-operative blood transfusion. As regards the alcohol problem, a retrospective study analyzed 355 patients submitted to colonic and rectal anastomoses for benign and malignant diseases, and it found increased risk for dehiscence in individuals that ingested more than 35 doses of alcoholic beverages a week, considering that a dose contained from 9 to 13 grams of alcohol36. A Danish article published in 2005, including 5.181 patients submitted to coloproctologic surgeries due to neoplasias, confirmed the abovementioned information as it found significant worsening in intestinal healing and an increased rate of anastomotic fistulas37. These data are in agreement with those in our study, which found smaller breaking strength in the anastomoses of individuals to ethanol intake, in addition to a larger number of fistulas, both with statistical significance. The longitudinal breaking strength of anastomoses at the four postoperative moments was larger in the control group, although without statistical significance, which may be due to the small number of animals evaluated at those moments. However, when analyzed by groups, control group showed significantly larger breaking force than treated group. Other studies have also confirmed the negative influence of alcohol abuse, both acute and chronic, on the tissue healing process38-42. There is evidence that not only chronic alcohol abuse delays healing, but its acute ingestion previously to the surgical event also does. An experimental study analyzed the cutaneous healing of rats submitted to moderate doses of ethanol (100 miligrams/deciliter) and concluded that drastic worsening in the proliferative phase of the tissue healing process and decreased collagen synthesis occurred41.
The biochemical measurements of intestinal healing mainly comprise tissue hydroxyproline and the collagen deposition rate25. In our study, it was observed that the amount of hydroxyproline significantly increased over time at all studied moments, but no difference was found for its dosage between the groups, which may be due to the fact that chronic alcohol abuse does not affect the amount of collagen production or change only the quality of collagen produced. Another possibility would be the increase of enzyme collagenase on the anastomotic site, an event that would cause greater collagen degradation, which is not quantified by hydroxyproline dosage, since this method only measures collagen production, but not its degradation. The effect of ethanol probably begins in the inflammatory phase of cicatrization and also influences the later phases of process and tissue repair. An experimental study evaluated cutaneous healing among rats and showed that the production of chemoattractive cytokines by neutrophils had decreased in the group submitted to ethanol ingestion, which had been caused by the decrease in interleucin-1β production in the lesioned tissue43. Deficiency of such interleukin reduces topical inflammation and the expression of adherence molecules in endothelial cells, in addition to hindering cellular infiltration to the target tissue43-45.
In our study, no significant alterations were found between the groups as concerns the histopathological analysis. The absence of difference occurred due to the fact that light microscopy is a "rough" method to study ethanol-mediated alterations in the tissue repair process since such alterations probably occur in the ultra-structural level of collagen and in the biochemistry of intestinal healing. Additionally, hematoxylin-eosin and Masson's trichrome staining, which was used in our study, is not a quantitative method for collagen dosage, and it was utilized only to illustrate the healing process of colonic anastomoses.
A published article which compiling studies conducted from 1967 to 1998 analyzed pre-operative alcoholism and its postoperative morbidity46. The most common complications found by the authors were bleeding, infections and cardiopulmonary insufficiency that required intensive care therapy46. A study published in 2007 analyzed 163.624 patients submitted to surgical procedures and detected 14 independent variables for surgical site infection risk, and one of them was alcoholism47. Our study agrees with previous investigations, as it found a total number of complications in treated group with statistical significance and fivefold more surgery-site infections in the treated group for which no statistical difference was found probably due to the small number of animals.
It is known that ethanol modulates immune response in a complex fashion48, including the increase in the blood levels of certain immunoglobulins49. Despite such increase, alcoholic patients are knowingly immunodeficient, which probably results from a deregulation in antibody production due to cytokine alterations49, suppression of processes involving lymphocyte migration50 and reduction in phagocytosis capacity of monocytes, neutrophils and macrophages51. An article published after a symposium held in the United States which compiled studies on cytokines and alcohol suggests that the acute and moderate intake of ethanol leads to a dual anti-inflammatory effect due to pro-inflammatory inhibition, in addition to an increase in the anti-inflammatory cytokines produced by monocytes46. Despite all these alcohol-dependent immunological alterations, other factors such as malnutrition and smoking are likely to contribute to an alcoholic individual's susceptibility to infections46. An article published in 2004 found decreased levels of cytokines interleucin -1β, interleucin -6 and interleucin -8 at the beginning of infection in alcoholic patients, thus corroborating the other findings for immunosuppression in this group52. A study published in 2002 analyzed 45 patients, 25 of whom were alcoholics, submitted to resections of tumors in the high digestive tract and who required an intensive care regimen in the postoperative period53. A higher infection rate was found for alcoholics, 68% as compared to 30%, in addition to a longer period of mechanical ventilation and the need for an intensive care regimen53. A Danish study has also found a significant increase in postoperative mortality in alcoholic patients submitted to curative resection for lung cancer30. Postoperative mortality was threefold higher in alcoholic patients in a study conducted by Tonnesen and Kehlet46. Our experimental study found 2.33fold more deaths in rats submitted to ethanol intake, a fact that is in agreement with the previously mentioned studies.
The mechanism related to this larger number of complications is multifactor, including the dysfunction of multiple organs and systems, an exaggerated response to surgical stress and the abstinence syndrome46, probably associated with the lack of various nutrients. Additionally, the response to surgical stress contributes to reduced immunity, coagulation deficit and cardiac overload, which together can increase the rates of surgical complications46. It is important to point out a randomized and controlled trial that analyzed 42 alcoholic patients without hepatic diseases who, after one month of abstinence, showed significantly reduced morbidity following the surgical procedure54.
The animals submitted to ethanol intake presented a malnutrition process shown by significantly lower weight gain in relation to the control group. They showed impaired intestinal healing as demonstrated by the significantly smaller longitudinal breaking strength in the treated group. They also displayed a higher rate of postoperative complications characterized by a larger number of lesion infections, fistulas and higher mortality.
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Rodrigo Severo de Camargo Pereira
Faculdade de Medicina de Botucatu-UNESP
Departamento de Cirurgia e Ortopedia
Rubião Junior, SN, Anexo Verde
18618-970 Botucatu - SP Brasil
Tel.: (55 14)3813-9227
Fax: (55 14)38157428
Received: October 11, 2011
Review: December 07, 2011
Accepted: January 10, 2012
Conflict of interest: none
Financial source: none.
1 Research performed at Surgical Technique and Experimental Surgery Laboratory, Botucatu Medical School. Sao Paulo State University (UNESP), Brazil