Lohsiriwat Varut, Scholefield John H, Wilson Vincent G, Dashwood Michael R
Division of Gastrointestinal Surgery, Queen's Medical Centre, University of Nottingham, Nottingham, UK.
School of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, UK.
Br J Pharmacol. 2017 Apr;174(7):569-579. doi: 10.1111/bph.13719. Epub 2017 Feb 16.
Haemorrhoids is a common anorectal condition affecting millions worldwide. We have studied the effect of endothelin-1 (ET-1) and the role of endothelin ET and ET receptors in haemorrhoid tissue.
Protein expression of ET-1, ET and ET receptors were compared between haemorrhoids and normal rectal submucosa using Western blot analysis, with the localization of proteins determined by autoradiography and immunohistochemistry. Effects of ET-1 and sarafotoxin 6a on human colonic and rectal arteries and veins was assessed by wire myography and the involvement of receptor subtypes established by selective antagonists.
Dense binding of [ I]-ET-1 to haemorrhoidal sections was reduced by selective receptor antagonists. A higher density of ET than ET receptors was found in haemorrhoidal, than in control rectal tissue and confirmed by Western blot analysis. ET and ET receptors were localized to smooth muscle of haemorrhoidal arteries and veins, with ET receptors on the endothelium. Human colonic and rectal arteries and veins were similarly sensitive to ET-1 and affected by the ET selective antagonist, but sarafotoxin S6a-induced contractions were more pronounced in veins and antagonized by a selective ET receptor antagonist.
ET and ET receptors are present in human haemorrhoids with ET receptors predominating. ET receptors are activated by ET-1 to mediate a contraction in arteries and veins, but the latter are selectively activated by sarafotoxin S6a - a response that involves ET receptors at low concentrations. Selective ET agonists may have therapeutic potential to reduce congestion of the haemorrhoidal venous sinusoids.
痔疮是一种常见的肛肠疾病,全球数百万人受其影响。我们研究了内皮素 -1(ET -1)的作用以及内皮素(ET)和ET受体在痔组织中的作用。
采用蛋白质印迹分析比较痔疮组织与正常直肠黏膜下层中ET -1、ET及ET受体的蛋白表达,通过放射自显影和免疫组织化学确定蛋白的定位。采用线肌张力描记法评估ET -1和沙拉新6a对人结肠和直肠动静脉的影响,并通过选择性拮抗剂确定受体亚型的参与情况。
选择性受体拮抗剂可降低[I] -ET -1与痔组织切片的紧密结合。通过蛋白质印迹分析证实,痔组织中ET的密度高于ET受体,高于对照直肠组织。ET及ET受体定位于痔动静脉的平滑肌,内皮上有ET受体。人结肠和直肠动静脉对ET -1同样敏感,并受ET选择性拮抗剂的影响,但沙拉新S6a诱导的收缩在静脉中更明显,并被选择性ET受体拮抗剂拮抗。
人痔疮组织中存在ET及ET受体,且ET受体占主导。ET受体被ET -1激活,介导动静脉收缩,但静脉被沙拉新S6a选择性激活——这种反应在低浓度时涉及ET受体。选择性ET激动剂可能具有减少痔静脉窦充血的治疗潜力。