Todorović V, Koko V, Varagić J, Lacković V, Vuzevski V, Milin J
Institute for Medical Research, Belgrade, Yugoslavia.
Histol Histopathol. 1993 Apr;8(2):285-96.
The present study describes our observations on optical and ultrastructural features of serotonin-containing cells in the rat antral and upper duodenal mucosa, utilizing optic morphometric measurements in a model of experimental chronic alcoholism of rat in which nutrition was well controlled. Male Wistar rats were given ethanol to provide 23 per cent of the total calories, while starch replaced ethanol isocalorically in controls. Twenty-five per cent of the calories were provided by protein in both groups. Blood levels of serotonin were significantly raised after chronic ethanol feeding (0.059 +/- 0.06 vs. 0.159 +/- 0.012 micrograms/ml, p < 0.01). Decrease in the number of immunohistochemically-detectable serotonin-containing cells was found in the pyloric gland mucosal area specimens of the chronically ethanol-treated rats (68.9 +/- 5.2 vs 43.3 +/- 3.0; p < 0.001). The immunohistologically-evaluated number of the same cells in the duodenal mucosa specimens was significantly decreased by alcohol feeding. Although total villi and crypt count per whole circular section, and the number of crypts per villus were not significantly changed either in control animals or in chronically ethanol-fed rats, decreased number of these cells per whole circular section (289 +/- 21.6 vs. 183 +/- 10.5; p < 0.001) per villus (2.52 +/- 0.14 vs. 1.21 +/- 0.10; p < 0.001) and per crypts (0.97 +/- 0.08 vs. 0.79 +/- 0.04; p < 0.05) were reported after alcohol consumption. In both control and experimental rats the cells were predominantly found in the basal half of the antropyloric mucosa. Alcohol did not lead to any changes in normal distribution of the duodenal serotonin-producing cells. The above quantitative changes in serotonin-producing cells were not accompanied by changes in their subcellular appearance in stomach and duodenal mucosa of alcohol-treated rat.
本研究描述了我们对大鼠胃窦和十二指肠上段黏膜中含5-羟色胺细胞的光学和超微结构特征的观察结果,采用光学形态计量学测量方法,以营养得到良好控制的大鼠实验性慢性酒精中毒模型为研究对象。雄性Wistar大鼠摄入乙醇,使其提供总热量的23%,而对照组则用淀粉等量替代乙醇。两组中25%的热量由蛋白质提供。慢性乙醇喂养后,血清素的血液水平显著升高(0.059±0.06对0.159±0.012微克/毫升,p<0.01)。在慢性乙醇处理大鼠的幽门腺黏膜区域标本中,发现免疫组化可检测到的含5-羟色胺细胞数量减少(68.9±5.2对43.3±3.0;p<0.001)。乙醇喂养使十二指肠黏膜标本中相同细胞的免疫组化评估数量显著减少。尽管在对照动物和慢性乙醇喂养大鼠中,每个完整圆形切片的总绒毛和隐窝数量以及每个绒毛的隐窝数量均无显著变化,但饮酒后报告称,每个完整圆形切片(289±21.6对183±10.5;p<0.001)、每个绒毛(2.52±0.14对1.21±0.10;p<0.001)和每个隐窝(0.97±0.08对0.79±0.04;p<0.05)中这些细胞的数量减少。在对照大鼠和实验大鼠中,这些细胞主要位于胃幽门黏膜的下半部分。乙醇并未导致十二指肠5-羟色胺产生细胞的正常分布发生任何变化。上述5-羟色胺产生细胞的定量变化并未伴随乙醇处理大鼠胃和十二指肠黏膜中其亚细胞外观的变化。