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Somatostatin analogs for idiopathic pulmonary fibrosis therapy.

机译:生长抑素类似物用于特发性肺纤维化治疗。

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BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a potentially lethal disease characterized by diffuse multifocal fibrosis. SOM230 (also known as pasireotide), a somatostatin analog, is a potential antifibrotic therapy in early evaluative phase. OBJECTIVE: Evaluation of data on the role of somatostatin receptors in pulmonary fibrosis and of in vivo and in vitro SOM230 antifibrotic activities. METHODS/RESULTS: This study assessed somatostatin receptor expression in human normal and IPF lungs, and in animal lungs with bleomycin-induced fibrosis, as well as the effects of SOM230. The overall overexpression of somatostatin receptor subtype 2 and the anti-inflammatory/antifibrotic activities of SOM230 were demonstrated. CONCLUSION: These results are promising for further preclinical and clinical testing of SOM230 as an antifibrotic therapy.
机译:背景:特发性肺纤维化(IPF)是一种潜在的致死性疾病,其特征是弥漫性多灶性纤维化。 SOM230(也称为帕瑞肽)是一种生长抑素类似物,在早期评估阶段是一种潜在的抗纤维化疗法。目的:评估生长抑素受体在肺纤维化中的作用以及体内外SOM230抗纤维化活性的数据。方法/结果:本研究评估了生长抑素受体在人正常肺和IPF肺以及博来霉素诱导的纤维化的动物肺中的表达以及SOM230的作用。证实了生长抑素受体亚型2的总体过表达和SOM230的抗炎/抗纤维化活性。结论:这些结果有望作为抗纤维化疗法对SOM230进行进一步的临床前和临床测试。

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