LAQV-REQUIMTE, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Department of Immuno-Physiology and Pharmacology, Institute of Biomedical Sciences Abel Salazar, University of Porto (ICBAS-UP), 4050-313 Porto, Portugal.
Int J Mol Sci. 2022 Oct 31;23(21):13233. doi: 10.3390/ijms232113233.
Diabetes mellitus (DM) is a chronic progressive metabolic disorder associated with several gastrointestinal complications, affecting up to 75% of patients. Knowing that Angiotensin II (AngII) also regulates intestinal contraction, we decided to evaluate changes in ileum and colon histomorphometry and AngII reactivity in a rat model of DM. Streptozotocin (STZ, 55 mg/kg) was administered to induce DM to 24 adult male Wistar rats. Diabetic rats displayed all the characteristic signs of type 1 DM (T1DM) and fecal excretion increased about 4-fold over 14 days, while the excretion of controls remained unaltered. Compared to controls, diabetic ileum and colon presented an increase in both macroscopic (length, perimeter and weight) and microscopic (muscular wall thickness) parameters. Functionally, AngII-induced smooth muscle contraction was lower in diabetic rats, except in the distal colon. These differences in the contractile response to AngII may result from an imbalance between AngII type 1 (antagonized by candesartan, 10 nM) and type 2 receptors activation (antagonized by PD123319, 100 nM). Taken together, these results indicate that an early and refined STZ-induced T1DM rat model already shows structural remodelling of the gut wall and decreased contractile response to AngII, findings that may help to explain diabetic dysmotility.
糖尿病(DM)是一种慢性进行性代谢紊乱,与多种胃肠道并发症有关,影响高达 75%的患者。由于知道血管紧张素 II(AngII)也调节肠道收缩,我们决定在糖尿病大鼠模型中评估回肠和结肠组织形态学和 AngII 反应性的变化。链脲佐菌素(STZ,55mg/kg)用于诱导 24 只成年雄性 Wistar 大鼠发生 DM。糖尿病大鼠表现出 1 型糖尿病(T1DM)的所有典型特征,粪便排泄量在 14 天内增加了约 4 倍,而对照组的排泄量保持不变。与对照组相比,糖尿病回肠和结肠的宏观(长度、周长和重量)和微观(肌壁厚度)参数均增加。在功能上,糖尿病大鼠对 AngII 诱导的平滑肌收缩较低,除了在远端结肠。这种对 AngII 收缩反应的差异可能是由于 AngII 1 型(被坎地沙坦(10nM)拮抗)和 2 型受体激活(被 PD123319(100nM)拮抗)之间的不平衡所致。综上所述,这些结果表明,早期和精细的 STZ 诱导的 T1DM 大鼠模型已经显示出肠道壁的结构重塑和对 AngII 的收缩反应降低,这些发现可能有助于解释糖尿病运动障碍。