Division of Gastroenterology and Hepatology, Department of Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania.
Division of Gastroenterology and Hepatology, Department of Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania
Am J Physiol Gastrointest Liver Physiol. 2014 Sep 15;307(6):G595-601. doi: 10.1152/ajpgi.00159.2014. Epub 2014 Jul 17.
A compromise in the internal anal sphincter (IAS) tone and fibroelastic properties (FEP) plays an important role in rectoanal incontinence. Herein, we examined the effects of heme oxygenase (HO)-1 upregulation on these IAS characteristics in young rats. We determined the effect of HO-1 upregulator hemin on HO-1 mRNA and protein expressions and on basal IAS tone and its FEP before and after HO-1 inhibitor tin protoporphyrin IX. For FEP, we determined the kinetics of the IAS smooth muscle responses, by the velocities of relaxation, and recovery of the IAS tone following 0 Ca(2+) and electrical field stimulation. To characterize the underlying signal transduction for these changes, we determined the effects of hemin on RhoA-associated kinase (RhoA)/Rho kinase (ROCK) II, myosin-binding subunit of myosin light chain phosphatase 1, fibronectin, and elastin expression levels. Hemin increased HO-1 mRNA and protein similar to the increases in the basal tone, and in the FEP of the IAS. Underlying mechanisms in the IAS characteristics are associated with increases in the genetic and translational expressions of RhoA/ROCKII, and elastin. Fibronectin expression levels on the other hand were found to be decreased following HO-1 upregulation. The results of our study show that the hemin/HO-1 system regulates the tone and FEP of IAS. The hemin/HO-1 system thus provides a potential target for the development of new interventions aimed at treatment of gastrointestinal motility disorders, specifically the age-related IAS dysfunction.
在直肠肛门失禁中,内肛门括约肌(IAS)张力和纤维弹性特性(FEP)的折衷起着重要作用。在此,我们研究了血红素加氧酶(HO)-1上调对年轻大鼠这些 IAS 特征的影响。我们测定了 HO-1 上调剂血红素对 HO-1 mRNA 和蛋白表达以及 HO-1 抑制剂锡原卟啉 IX 前后 IAS 基础张力及其 FEP 的影响。对于 FEP,我们通过 IAS 平滑肌反应的动力学,即 IAS 张力在 0 Ca(2+)和电场刺激后的松弛和恢复速度来确定。为了描述这些变化的潜在信号转导,我们测定了血红素对 RhoA 相关激酶(RhoA)/Rho 激酶(ROCK)II、肌球蛋白轻链磷酸酶 1 的肌球蛋白结合亚基、纤维连接蛋白和弹性蛋白表达水平的影响。血红素增加了 HO-1 mRNA 和蛋白的表达,类似于基础张力和 IAS 的 FEP 的增加。IAS 特征的潜在机制与 RhoA/ROCKII 和弹性蛋白的遗传和翻译表达增加有关。另一方面,HO-1 上调后发现纤维连接蛋白的表达水平降低。我们的研究结果表明,血红素/HO-1 系统调节 IAS 的张力和 FEP。血红素/HO-1 系统因此为开发旨在治疗胃肠道动力障碍的新干预措施提供了一个潜在的靶点,特别是与年龄相关的 IAS 功能障碍。