AIM: To evaluate histometrically the effect of low and high caloric value of ethanol on ligature-induced bone loss in female rats. METHODS: Sixty female rats were divided into five groups of 12 animals each: Normal Control (water), Test A (low ethanol), Control A (low iso), Test B (high ethanol) and Control B (high iso). Control Groups A and B received diets with the same amount of calories consumed by Test Groups A and B, respectively, with ethanol replaced by isocaloric amounts of carbohydrate. Four weeks prior to the end of the experimental period, half of the rats in each group were randomly assigned to receive a ligature on mandibular molar, whereas the other half of group was left unligated. At 8 weeks, the animals were sacrificed, and the specimens were processed to obtain decalcified sections. The area of periodontal ligament and/or bone loss in the furcation region of the first molars was histometrically measured in five sections per specimen (mm²). RESULTS: Ethanol intake did not have effect on the alveolar bone loss in unligated teeth (p>0.05). However, in ligature-induced periodontitis, high value of calories associated with ethanol feeding enhanced the area of bone loss (p<0.05). CONCLUSIONS: The results of this study demonstrated that a low-ethanol diet did not affect the periodontium, while a high-ethanol diet may aggravate the progression of periodontitis, as demonstrated by the increased furcation region bone destruction in periodontal disease.

Alcohol consumption is a risk indicator for periodontal disease. The purpose of this study was to morphometrically evaluate the influence of alcohol consumption on alveolar bone level associated with ligature-induced periodontitis in rats. Thirty-six female rats (Wistar, 120 days-old) were randomly divided into three groups that received a daily administration of a water diet (control, n = 12), a 10% alcohol diet (10% ethanol, n = 12) or a 20% alcohol diet (20% ethanol, n = 12). Four weeks after the onset of the experiment, cotton ligatures were placed around the cervix of the upper right second molar in six rats. The other 6 rats in each group remained unligated. The rats were sacrificed four weeks after ligature placement. The maxillary bones were removed and alveolar bone loss was analyzed by measuring the distance between the cementoenamel junction and the alveolar bone crest at 2 buccal and 2 palatal sites on the upper right second molar. Analyses between the ligated and unligated groups showed that the presence of ligature induced alveolar bone loss (p < 0.05). Unligated groups showed no significant differences between each other (p > 0.05). In the ligated groups, rats receiving 20% ethanol showed significantly greater bone loss compared to control rats or rats receiving 10% ethanol. These results demonstrate that alcohol consumption may increase alveolar bone loss in female rats in a dose-dependent manner.

OBJETIVO: O propósito deste estudo foi avaliar o efeito do consumo de álcool sobre o suporte ósseo periodontal (SOP) em periodontite induzida por ligaduras em ratos. MATERIAIS E MÉTODOS: Sessenta e três ratos machos foram divididos em sete grupos: G1 (controle); G2 (álcool a 10%); G3 (controle nutricional de G2); G4 (álcool a 20%); G5 (controle nutricional de G4); G6 (álcool a 30%); G7 (controle nutricional de G6). Os grupos G3, G5 e G7 receberam dietas controladas com a mesma quantidade de calorias consumidas por G2, G4 e G6, respectivamente, com o etanol substituído por sacarose. Após anestesia foram instaladas ligaduras no primeiro molar inferior direito, permanecendo o dente contralateral sem ligadura. Após oito semanas, os ratos foram sacrificados e as mandíbulas radiografadas para medição do SOP na proximal distal. RESULTADOS: A análise intragrupo mostrou que a presença da ligadura foi capaz de induzir periodontite (p<0,05). Os grupos sem ligadura não demonstraram diferenças significativas (p=0,1969) no SOP. Contudo, nos grupos com ligadura os ratos que receberam álcool (G2:48,71%±3,88; G4:47,66%±2,54; G6:47,32%±3,24) e o controle nutricional associado a alta concentração de etanol (G7:47,40%±3,24) apresentaram percentual de SOP estatisticamente inferior aos outros grupos (G1:52,40%±2,75; G3:52,83%±2,41; G5:50,85%±4,14). CONCLUSÕES: Os resultados demonstraram que o consumo de álcool em ratos pode resultar em efeito direto na perda óssea alveolar, aumentando o desenvolvimento da periodontite. Além disso, sugere-se que o consumo calórico pesado de etanol também pode apresentar efeito indireto nos tecidos periodontais, como conseqüência da má nutrição.

OBJECTIVE: The aim of this study was to evaluate the effect of the alcohol consumption on the periodontal bone support (PBS) in experimental periodontitis in rats. MATERIALS AND METHODS: Sixty-three male rats were divided into seven groups: G1 (control); G2 (10% ethanol); G3 (nutritional control of G2); G4 (20% ethanol); G5 (nutritional control of G4); G6 (30% ethanol) and G7 (nutritional control of G6). The groups G3, G5 and G7 received controlled diets with equivalent caloric amounts to those consumed in G2, G4 and G6 respectively, with the ethanol replaced by sucrose. After anesthesia, ligatures were installed around the mandibular first molar, leaving the contralateral teeth unligated. After 8 weeks, the rats were killed and their mandibles were radiographed to measure the percentage of PBS on the distal aspect. RESULTS: The intragroup analyses showed that presence of ligatures induced periodontitis (p<0.05). Unligated groups did not show significant differences among the percentages of PBS (p=0.1969). However, in ligated groups the rats that received alcohol (G2:48.71%±3.88; G4:47.66%±2.54; G6:47.32%±3.24) and the nutritional control group associated with a high concentration of ethanol (G7:47.40%±3.24) presented a significantly lower percentage of PBS than the other groups (G1:52.40%±2.75; G3:52.83%±2.41; G5:50.85%±4.14). CONCLUSIONS: These results demonstrated that alcohol consumption in rats may result in a direct effect on alveolar bone loss and increased development of periodontitis. In addition, they suggest that heavy caloric consumption of ethanol may also present an indirect effect on periodontal tissue as a consequence of malnutrition.