Kitamura Kazuo, Ashizuka Shinya, Inatsu Haruhiko, Kita Toshihiro
Department of Internal Medicine, Circulatory and Body Fluid Regulation, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki City, Miyazaki, 889-1692, Japan
Adrenomedullin (AM) was originally isolated from human pheochromocytoma as a biologically active peptide with potent vasodilating action, but it also has a wide range of physiological properties including cardiovascular protection, neovascularization, and the ability to suppress apoptosis. It is constitutively produced by various tissues including the gastrointestinal tract. AM production and secretion can be induced by pro-inflammatory cytokines such as tumor necrosis factor-α and interleukin-1, as well as by lipopolysaccharide. Conversely, AM causes the downregulation of inflammatory cytokines in cultured cells and downregulates inflammatory processes in various models of colitis, including those induced by acetic acid and by dextran sulfate sodium. AM works by exerting anti-inflammatory and antibacterial effects and by stimulating mucosal regeneration and supporting maintenance of the colonic epithelial barrier. The present findings suggest that AM could serve as a novel agent for treating refractory ulcerative colitis.
肾上腺髓质素(AM)最初是从人嗜铬细胞瘤中分离出来的一种具有强大血管舒张作用的生物活性肽,但它也具有广泛的生理特性,包括心血管保护、新血管形成以及抑制细胞凋亡的能力。它由包括胃肠道在内的各种组织组成性产生。AM的产生和分泌可由促炎细胞因子如肿瘤坏死因子-α和白细胞介素-1以及脂多糖诱导。相反,AM可导致培养细胞中炎性细胞因子的下调,并在各种结肠炎模型中下调炎症过程,包括由乙酸和葡聚糖硫酸钠诱导的模型。AM通过发挥抗炎和抗菌作用以及刺激黏膜再生和维持结肠上皮屏障来发挥作用。目前的研究结果表明,AM可作为治疗难治性溃疡性结肠炎的新型药物。