Kapraali M, Söderman C, Marín L, Johansson O, Theodorsson E, Uribe A
Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Sweden.
Digestion. 1997;58(3):249-57. doi: 10.1159/000201451.
Groups of Sprague-Dawley rats were given placebo or prostaglandin E2 (PGE2) at 25 or 5,000 micrograms/kg or 15,R,15-methyl-PGE2 (MePGE2) at 5 or 50 micrograms/kg, twice daily, orally, for 1 month. Histological sections from the proximal duodenum were processed for immunohistochemistry and the volume density of immunoreactive endocrine cells was determined using point-counting grids. The surface density of the villous lining was estimated by using a cycloid test system. Thereafter, the total volumes of endocrine cells and the total surface area of the villous lining were calculated after estimating the mucosal volume. The volume density of serotonin-immunoreactive cells was increased in the duodenum of rats given 25 or 5,000 micrograms/kg PGE2 (p < 0.05). The total volume of these cells increased in the animals given 25 micrograms/kg PGE2 (p < 0.05). The total volume of gastrin/CCK-immunoreactive cells was higher in rats given 25 micrograms/kg PGE2 or 50 micrograms/kg MePGE2 than in controls (p < 0.05). The volume density of somatostatin-immunoreactive cells increased in rats given 5 micrograms/kg MePGE2, but the total volumes were not different between the groups. The area of somatostatin-immunoreactive cell profiles was enlarged in the animals given 5,000 micrograms/kg PGE2 (p < 0.05). The mucosal volume was enlarged by prostaglandins. The epithelial thickness increased in rats given the highest doses of PGE2 (p < 0.05). The concentration of motilin-like immunoreactivity increased in the duodenum of rats given 5 micrograms/kg MePGE2 (p < 0.05). We conclude that oral administration of PGE2 for 1 month increased the total volumes of serotonin- and gastrin-CCK-immunoreactive cells and the tissue concentration of motilin-like immunoreactivity, which indicates that prostaglandins modulate endocrine cells in a stable steady-state condition.
将斯普拉格-道利大鼠分组,分别给予安慰剂、25或5000微克/千克的前列腺素E2(PGE2),或5或50微克/千克的15,R,15-甲基前列腺素E2(MePGE2),每日口服两次,持续1个月。对十二指肠近端的组织切片进行免疫组织化学处理,并使用点计数网格测定免疫反应性内分泌细胞的体积密度。使用摆线测试系统估计绒毛内衬的表面密度。此后,在估计粘膜体积后计算内分泌细胞的总体积和绒毛内衬的总表面积。给予25或5000微克/千克PGE2的大鼠十二指肠中,血清素免疫反应性细胞的体积密度增加(p<0.05)。给予25微克/千克PGE2的动物中,这些细胞的总体积增加(p<0.05)。给予25微克/千克PGE2或50微克/千克MePGE2的大鼠中,胃泌素/CCK免疫反应性细胞的总体积高于对照组(p<0.05)。给予5微克/千克MePGE2的大鼠中,生长抑素免疫反应性细胞的体积密度增加,但各组之间的总体积没有差异。给予5000微克/千克PGE2的动物中,生长抑素免疫反应性细胞轮廓的面积增大(p<0.05)。前列腺素使粘膜体积增大。给予最高剂量PGE2的大鼠上皮厚度增加(p<0.05)。给予5微克/千克MePGE2的大鼠十二指肠中,胃动素样免疫反应性的浓度增加(p<0.05)。我们得出结论,口服PGE2 1个月可增加血清素和胃泌素-CCK免疫反应性细胞的总体积以及胃动素样免疫反应性的组织浓度,这表明前列腺素在稳定的稳态条件下调节内分泌细胞。