Morphological and biomechanical study of abdominal aorta of rats submitted to experimental chronic alcoholism

Avaliação morfológica e biomecânica da aorta abdominal de ratos submetidos ao alcoolismo crônico experimental

ORIGINAL ARTICLE

Morphological and biomechanical study of abdominal aorta of rats submitted to experimental chronic alcoholism¹

Avaliação morfológica e biomecânica da aorta abdominal de ratos submetidos ao alcoolismo crônico experimental

Nereide Freire Cerqueira^I; Winston Bonetti Yoshida^II; Sérgio Swain Müller^III; Júlio Lopes Sequeira^IV; Antônio de Castro Rodrigues^V; Carlos Roberto Padovani^VI

^IDoctor of Veterinary Medicine, School of Veterinary Medicine and Animal Science. UNESP São Paulo State University. Botucatu

^IIAssociate Professor, Department of Surgery and Orthopedics. School of Medicine, UNESP São Paulo State University. Botucatu

^IIIAssistant Professor, Dept. of Surgery and Orthopedics, School of Medicine. UNESP Botucatu

^IVAssistante Professor, Dept. of Clinical Veterinary, School of Veterinary Medicine and Animal Science. UNESP - Botucatu

^VAssociate Professor, Dept. of Biological Sciences, School of Odontology. USP. Bauru

^VIChairman, Dept. of Bioestatistics, Institute of Biosciences. UNESP - Botucatu

^{Correspondence}

ABSTRACT

PURPOSE: To assess the influence of experimental chronic alcoholism in the morphology and biomechanics of the aorta, in a rat model.

METHODS: Forty-four Wistar rats were randomly divided into two groups of 22 animals each: in the alcoholism group, the rats received water mixed to increasing concentrations of ethyl alcohol; and control group: the rats received pure water for 180 days. The animals were then killed by an overdose of pentobarbital and the abdominal aortas were excised for histological (hematoxylin-eosin, Masson, Calleja, and Picrosirius red stain), histomorphometrical, and biomechanical analysis.

RESULTS: Histology and histomorphometry did not show differences in aorta morphology of both groups. Biomechanical analysis showed a significantly greater yield point elongation in the alcoholic rat group (p<0.05).

CONCLUSION: Chronic alcoholism did not cause morphological alterations in the aortic wall but increased elongation, without modifying any other mechanical properties.

Key words: Alcoholism. Ethanol. Aorta. Elasticity.

RESUMO

OBJETIVO: avaliar a influência do alcoolismo crônico experimental na morfologia e biomecânica da artéria aorta de ratos.

MÉTODOS:ratos Wistar foram divididos em dois grupos de 22 animais. Grupo alcoolista: os ratos receberam água com concentração crescente de etanol e ração ad libitum durante 6 meses. Grupo controle: os animais receberam água e ração ad libitum pelo mesmo período. Os animais foram sacrificados com overdose de pentobarbital e as aortas abdominais foram excisadas para realização de histologia (hematoxilina-eosina, tricrômio de Masson, Calleja, Picrosirius red), histomorfometria e avaliação biomecânica (carga máxima, alongamento na carga máxima, limite de proporcionalidade, alongamento no limite de proporcionalidade e coeficiente de rigidez).

RESULTADOS: A histologia e a histomorfometria não mostraram diferenças significantes na morfologia da aorta em ambos os grupos. A avaliação biomecânica mostrou aumento do alongamento no limite de proporcionalidade no grupo alcoolista (p<0.05).

CONCLUSÃO: o alcoolismo crônico experimental não provocou alterações morfológicas na parede da aorta, mas causou aumento da sua elasticidade, sem modificar as outras propriedades mecânicas avaliadas.

Descritores: Alcoolismo. Etanol. Aorta. Elasticidade.

Introduction

Alcoholism is a severe and widespread disease all over the world. Approximately 70% of adult Americans drink alcohol occasionally, and alcohol abuse affects 5 to 10% of men and 3 to 5% of women¹. Alcohol has been experienced at least once by 69% of Brazilian people, being 77% men and 60% women². A study of psychiatric morbidity performed in three Brazilian cities (Brasília, São Paulo, and Porto Alegre) showed prevalence of alcohol abuse in 15.4% men and 1.2% women³. In Brazil, alcoholism affects 12 million people, accounting for 90% of drug addiction hospitalizations⁴.

Chronic alcohol abuse is associated with increased morbidity and mortality and may cause morphological alterations in almost all body organs and tissues. Alterations in liver, nervous and cardiovascular systems, gastrointestinal tract, pancreas, skeletal muscle, and blood cell are frequent. Also, incidence of hypertension and certain cancers, as well as accidents and suicides increase with alcoholism^5,6,7. In contrast, epidemiological studies have associated moderate alcohol consumption with a reduced incidence of cardiovascular disease⁸. Alterations in chemical and structural properties of biological membranes are reported after ethanol addiction^9,10. However, clinical significance of the adverse effects of alcohol on the arterial wall remains controversial. Some authors showed morphological changes in the arterial wall^11,12,13, while others did not find any alteration¹⁴. So, the objective of the present study is to evaluate histopathology, histomorphometry, and mechanical properties of the abdominal aorta of rats submitted to chronic alcoholism. To our knowledge, biomechanical properties of blood vessels in alcoholic rats were not previously studied.

Methods

All procedures were performed in strict accordance to the guidelines of the U.S. National Research Council's "Guide for the care and use of laboratory animal" (NRC publication - 1996) and were approved by the local "Ethical Committee for Animal Research". Forty-four adult male Wistar rats weighing 302.9 ± 14.1 g were used. The animals were randomly divided into 2 experimental groups of 22 animals each (control and alcoholic). Food and water were given ad libitum to the control group. The alcoholic animal group was fed with the same food, but received water with increasing concentrations of sugar cane ethanol (Pirassununga 51 Müller Liquor Industry, Ltd. Piracicaba, SP, Brazil) ad libitum. The final ethanol concentrations in drinking water were 10º in the first 7 days, 20º in the following 7 days, and 30º from the 14^th day to the end of the study, with 180 days of ethanol consumption.

The animals were kept in groups up to 5 rats per cage in a dry and airy place at steady and controlled temperature. Food and liquid intakes were recorded daily in each cage. Animal weight was determined weekly, always in morning time. At the end of the observation period, the animals were killed by an overdose of pentobarbital (HYPNOL^Ò 3%, Cristália, São Paulo, SP, Brazil) with the excision of the abdominal portion of aorta and liver.

Liver samples were fixed in 10% formaldehyde and stained with hematoxylin-eosin (HE) and aortic histological examination was performed in 5 animals of each group chosen at random. Aortic samples were fixed in 10% formaldehyde and stained with HE, Masson, Calleja, and Picrosirius red. Aortic slides stained with Calleja were sent for histomorphometrical analysis using a LEICA DMLB microscope. Digital images were processed in an IBM personal computer using IPWIN32 software which was used to calculate the proportion of collagen in the tunica media and adventitia and the width of the media, adventitia, and media + adventitia.

Aortic mechanical properties were studied in the 17 control and 17 alcoholic remaining rats. Before biomechanical testing, the aortas were promptly immersed in saline solution containing 0.25mg/mL of papaverine, to relax the muscle bundles of the arteries, and to standardize the state of muscle tension in all aortic samples¹⁵.

The biomechanical analysis was performed using a EMIC DL 10.000 Universal Machine of Mechanical Assays (Equipments and Testing Systems, Ltd. Curitiba, PR, Brazil). The aortas were immediately fixed with grasping clamps using smooth non-cutting metallic bars fastened with two screws. The stretching speed was 30mm/minute and a 50N load cell was used. Failure load, failure elongation, yield point by Johnson's method, yield point elongation, and stiffness were obtained¹⁶. Failure load may be defined as the highest load tolerated by materials until rupture. Yield point is the maximum tension value below which materials comply with Hooke's law (where tension-deformation function is linear). Beyond the yield point, some degree of lesion may be found and materials already present of plastic deformation, making the return to initial length impossible, even if loading stops. Failure elongation is the difference between length in the failure load region and initial length; yield point elongation is the difference between length in the yield point region and initial length. Stiffness is the linear and constant numeric relation between load and elongation calculated at the yield point (Figure 1)¹⁶.

The Student's t test (two independent samples) was used for the biomechanical results and width of the media and adventitia. The proportion of collagen in these tunicas was compared using the Mann-Withney test. Pearson's and Spearman's coefficient was used for the correlation between weight and biomechanical variables¹⁷. Mean body weight evolution of both groups along the experiment was compared using the profile analysis¹⁸.

Results

Histological analysis of the liver in control animals was normal, and steatosis was observed in the liver of all alcoholic animal's group. Mean weight of all rats increased along the experiment but was significant higher in control rats than that in alcoholic rats (p < 0.01) (Figure 2).

The biomechanical study showed that only the strength at the yield point elongation increased in the alcoholic group (1.94 ± 0.92 vs 2.54 ± 0.79, p < 0.05) (Figure 1, Table 1). No correlation between the biomechanical variables and animal weight was observed in both groups (Table 2). No differences in the thickness of arterial tunicas (Figure 3, Table 3) and proportion of collagen (Table 4) were found. The pathologist observed no histological difference between two groups in any case.

Discussion

Alcoholism is associated with structural and functional alterations of blood vessels. Decreased thickness of the intima and media in the thoracic aorta was reported in histological and ultrastructural studies with rats submitted to chronic alcoholism¹⁹. Another study reported degeneration of the endothelial surface of myocardium capillaries in mice treated with 15% ethanol for 3 months¹³. Sarphie et al.²⁰ showed that alcohol caused structural changes in hepatic sinusoids of rats. Vascular wall edema, perivascular fibrosis, vascular sclerosis, subendothelial humps, and vascular wall inflammation in intramyocardium coronary arteries of alcoholic patients were observed in another morphological study²¹. In the present study, no differences in the thickness of arterial tunicas and proportion of collagen were found, maybe because of variability which would demand for a greater sample size. Anyway, no detectable histological difference was observed between both groups by the pathologist.

Alcohol can exert direct actions on cerebral blood vessels. Altura et al.¹¹ showed that alcohol caused vasospasm in intact cerebral arterioles and venules and in isolated cerebral arteries. The same authors described a canine coronary artery vasospasm in an in vitro study¹². In the same study, they also demonstrated that acetaldehyde, which is the major metabolite of ethanol, produced relaxation in coronary basal tone. However, the bulk of the evidence suggests that ethanol increases coronary blood flow and decreases coronary vascular resistance⁸.

Authors did not find alterations in the anatomy, histology, histochemistry, and electronic microscopy of the arteries, veins, and capillaries of rats receiving liquid diet containing alcohol during one year¹⁴. Phillips²² observed that the endothelial cells of brain blood vessels in rats breathing continuous ethanol vapor during 3 weeks were normal, which is in accordance to the present study, with no histopathological alterations in the endothelium, collagen, and muscle fibers found in comparison to controls. Differences related to animal species, type of artery, and experimental model may explain the discrepancies found in literature. In the present study, the only biomechanical difference observed was related to the increase in yield point elongation in alcoholic group. In these words, the aortas of alcoholic group stretched more than controls, before irreversible changes occurrence. The highest aortic elongation capacity in alcoholic rats might be due to either lower collagen synthesis, increase in collagen lysis, or even higher elastin synthesis, which were not detectable in our microscopic studies. Santi¹⁸ observed an increase of non-oriented collagen fibers in the media, suggesting that alcohol interferes with collagen synthesis, and that the disorganized increase of these fibers triggers a vascular fibrosis process.

Biomechanical parameters in blood vessels are frequently used in the study about aneurism²³, diabetes^24,25, hypertension²⁶, age²⁷, drug action^28,29,30, and exercise training³¹. Tensile testing reflects ultimately the stiffness, distensibility, elasticity and mechanical strength, of collagen and elastin in aortic samples²⁵. The extracellular matrix (ECM) plays a critical role in the development, growth and biomechanical properties of virtually every organ. The wall of a vessel has a complex structure, and elastic properties of the wall are affected mainly by the interrelation of collagen and elastin³⁰. The cross-links stabilize the collagen fibrils and provide distensibility, elasticity and mechanical strength to the blood vessels, but the excessive formation of cross-links leads to the deranged biomechanical properties of vessel tissue²⁵.

Altered degradation of extracellular matrix (ECM) underlies vascular remodeling, a hallmark in the pathogenesis of another cardiovascular diseases including hypertension and aneurismal dilatation³². The molecular structure of collagen and elastin may alter the mecanical properties of the aortic wall and change the aortic susceptibility to hemodynamic injury. A primary increase in the extensibility implies a secondary fibroproliferative response of the aortic wall. The excess deposition or alterations in collagen and elastin lead to increased stiffness at small "stress" values, which in turn may increase the hemodynamic strain. Increased stiffness of the aorta may be of pathogenic significance in atherosclerosis^26,28. It is impossible to rain any extrapolation of increased elongation of aorta predisposing to aneurysm formation or influencing systemic blood pressure levels.

The amount of aortic wall collagen and elastin was not substantially changed by alcohol in the present study, as determined by the histomorphometric study performed.

Further studies are necessary to unify eventual aortic elastin and collagen quality changes after alcohol addiction inducing biomechanical aortic properties alterations.

Conclusion

In conclusion, this study suggests that chronic alcoholism does not promote morphological alterations in rat abdominal aorta wall, but may increase its elongation, without modifying any other mechanical properties. Further analysis involving ultrastructural and biochemical evaluation of aortic wall components are necessary to explain these results.

Received: January 18, 2005

Review: February 21, 2005

Accepted: March 23, 2005

Conflict of interest: none

Financial source: FUNDUNESP

How to cite this article: Cerqueira, NF, Yoshida, WB, Müller, SS, Sequeira, JL, Rodrigues, AC, Padovani, CR. Morphological and biomechanical study of abdominal aorta of rats submitted to experimental chronic alcoholism. Acta Cir Bras. [serial online] 2005 May-June;20(3). Available from URL: http://www.scielo.br/acb

*Color figure available from http://www.scielo.br/acb

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Article from School of Veterinary Medicine and Animal Science. UNESP São Paulo State University. Botucatu.

Publication Dates

• Publication in this collection
  16 June 2005
• Date of issue
  June 2005