Okada Yoshinori, Matsumura Yuji, Shimada Kazuyoshi, Sado Tetsu, Oyaizu Takeshi, Sugawara Takafumi, Matsuda Yasushi, Hoshikawa Yasushi, Takahashi Hiroto, Sato Masami, Kondo Takashi
Department of Thoracic Surgery, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.
J Heart Lung Transplant. 2004 Dec;23(12):1392-5. doi: 10.1016/j.healun.2003.09.020.
Tranilast is an anti-allergic agent known to inhibit the release of histamine, interleukin-1beta, transforming growth factor beta1, and platelet-derived growth factor from various cells and currently is used to treat allergic diseases, keloids, and hypertrophic scars. We evaluated the ability of tranilast to inhibit the development of obliterative airway disease (OAD) in a rat model of heterotopic tracheal transplantation.
We transplanted tracheal segments from donor rats (Brown Norway) into subcutaneous pouches in major histocompatibility complex-incompatible recipient rats (Lewis). At Days 21 and 28 after transplantation, we histologically assessed the harvested allografts scored the degree of OAD, on a scale from zero to 4 as previously described, caused by fibroproliferative tissue.
Recipient animals treated orally with 400 mg/kg/day tranilast throughout the experiment showed significantly decreased OAD compared with control animals, with a histologic score of 1.1 +/- 0.4 vs 3.0 +/- 1.3, respectively (mean +/- SD, p=0.007), at Day 21 after transplantation and 2.0 +/- 1.4 vs 3.9 +/- 0.4, respectively (mean +/- SD, p=0.017), at Day 28 after transplantation.
These results showed that treatment with tranilast significantly decreased fibroproliferative airway changes associated with allograft rejection in a rat model of tracheal transplantation, suggesting that tranilast may be useful in preventing bronchiolitis obliterans after lung transplantation.
曲尼司特是一种抗过敏药物,已知可抑制组胺、白细胞介素-1β、转化生长因子β1和血小板衍生生长因子从各种细胞中释放,目前用于治疗过敏性疾病、瘢痕疙瘩和增生性瘢痕。我们在大鼠异位气管移植模型中评估了曲尼司特抑制闭塞性气道疾病(OAD)发展的能力。
我们将供体大鼠(棕色挪威大鼠)的气管段移植到主要组织相容性复合体不匹配的受体大鼠(刘易斯大鼠)的皮下袋中。在移植后第21天和第28天,我们对收获的同种异体移植物进行组织学评估,对由纤维增生性组织引起的OAD程度进行评分,评分范围为0至4分,如前所述。
在整个实验过程中口服400mg/kg/天曲尼司特的受体动物与对照动物相比,OAD明显减轻,移植后第21天组织学评分为1.1±0.4 vs 3.0±1.3(平均值±标准差,p = 0.007),移植后第28天分别为2.0±1.4 vs 3.9±0.4(平均值±标准差,p = 0.017)。
这些结果表明,在大鼠气管移植模型中,曲尼司特治疗可显著减少与同种异体移植排斥相关的纤维增生性气道变化,提示曲尼司特可能有助于预防肺移植后的闭塞性细支气管炎。