Takahara H, Fujimura M, Taniguchi S, Hayashi N, Nakamura T, Fujimiya M
Department of Second Surgery, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Am J Physiol Gastrointest Liver Physiol. 2001 Sep;281(3):G798-808. doi: 10.1152/ajpgi.2001.281.3.G798.
Few previous studies have discussed the changes in serotonin receptor activity in the small intestine of diabetic animals. Therefore, we examined serotonin content in duodenal tissue and dose-dependent effects of serotonin agonists and antagonists on the motor activity of ex vivo vascularly perfused duodenum of streptozotocin (STZ)-diabetic rats. Serotonin content was significantly increased in enterochromaffin cells but not altered in serotonin-containing neurons in STZ-diabetic rats. Motor activity assessed by frequency, amplitude, and percent motility index per 10 min of pressure waves was reduced in the duodenum of diabetic rats, and this reduction was reversed by insulin treatment. Serotonin dose dependently increased the motor activity in control rat duodenum but only a higher concentration of serotonin increased the motor activity in diabetic rats. The 5-hydroxytryptamine (5-HT) receptor subtype 4 (5-HT(4)) antagonist SB-204070 dose dependently reduced motor activity in both control and diabetic rats, whereas the 5-HT(3) receptor antagonist azasetron, even at a higher concentration, failed to affect motor activity in diabetic rat duodenum but dose dependently reduced motor activity in control rat duodenum. These results suggest that 5-HT(3) receptor activity was impaired but 5-HT(4) receptor activity was intact in STZ-diabetic rat duodenum. Such an impairment of 5-HT(3) receptor activity may induce the motility disturbance in the small intestine of diabetes mellitus.
以往很少有研究探讨糖尿病动物小肠中血清素受体活性的变化。因此,我们检测了十二指肠组织中的血清素含量,以及血清素激动剂和拮抗剂对链脲佐菌素(STZ)诱导的糖尿病大鼠离体血管灌注十二指肠运动活性的剂量依赖性影响。STZ诱导的糖尿病大鼠的肠嗜铬细胞中血清素含量显著增加,但含血清素神经元中的血清素含量未发生改变。通过压力波的频率、振幅和每10分钟的运动指数百分比评估的运动活性在糖尿病大鼠的十二指肠中降低,而胰岛素治疗可逆转这种降低。血清素剂量依赖性地增加对照大鼠十二指肠的运动活性,但只有更高浓度的血清素才能增加糖尿病大鼠的运动活性。5-羟色胺(5-HT)受体亚型4(5-HT(4))拮抗剂SB-204070剂量依赖性地降低对照大鼠和糖尿病大鼠的运动活性,而5-HT(3)受体拮抗剂阿扎司琼即使在较高浓度下也未能影响糖尿病大鼠十二指肠的运动活性,但剂量依赖性地降低对照大鼠十二指肠的运动活性。这些结果表明,STZ诱导的糖尿病大鼠十二指肠中5-HT(3)受体活性受损,但5-HT(4)受体活性完整。5-HT(3)受体活性的这种损害可能会导致糖尿病患者小肠的运动紊乱。