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伐地米星通过抑制核因子κB和丝裂原活化蛋白激酶的活性来下调一氧化氮、前列腺素E2和细胞因子的产生。

Valnemulin downregulates nitric oxide, prostaglandin E2, and cytokine production via inhibition of NF-kappaB and MAPK activity.

作者信息

Zhang Xuemei, Li Hongyu, Feng Haihua, Xiong Huanzhang, Zhang Lei, Song Yu, Yu Lu, Deng Xuming

机构信息

Institute of Zoonoses, College of Animal Science and Veterinary Medicine, Jilin University, Changchun, Jilin 130062, China.

出版信息

Int Immunopharmacol. 2009 Jul;9(7-8):810-6. doi: 10.1016/j.intimp.2009.02.018. Epub 2009 Mar 16.

Abstract

Valnemulin is a pleuromutilin antibiotic used in clinics for the treatment of various infections. We studied the in vitro anti-inflammatory effects of valnemulin and associated signal transduction mechanisms in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. We found that valnemulin inhibited nitric oxide (NO), prostaglandin E2 (PGE2), tumour necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6), and increased interleukin-10 (IL-10) production. Inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) protein expression were also inhibited by valnemulin. We further observed that valnemulin prevented the LPS-induced NF-kappaB translocation from the cytoplasm into the nucleus. Valnemulin also blocked phosphorylation of three mitogen-activated protein kinases (MAPKs): extracellular signal receptor-activated kinase (ERK) 1/2, p38, and c-Jun N-terminal kinase (JNK). Our data indicate that valnemulin may have therapeutic anti-inflammatory effects independent of its antibacterial activity.

摘要

伐地那非是一种截短侧耳素类抗生素,在临床上用于治疗各种感染。我们研究了伐地那非在脂多糖(LPS)刺激的RAW 264.7巨噬细胞中的体外抗炎作用及相关信号转导机制。我们发现,伐地那非可抑制一氧化氮(NO)、前列腺素E2(PGE2)、肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的产生,并增加白细胞介素-10(IL-10)的产生。诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的蛋白表达也受到伐地那非的抑制。我们进一步观察到,伐地那非可阻止LPS诱导的NF-κB从细胞质向细胞核的转位。伐地那非还可阻断三种丝裂原活化蛋白激酶(MAPK)的磷酸化:细胞外信号受体激活激酶(ERK)1/2、p38和c-Jun氨基末端激酶(JNK)。我们的数据表明,伐地那非可能具有独立于其抗菌活性的治疗性抗炎作用。

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