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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Effect of the anti-anginal agent, perhexiline, on neutrophil, valvular and vascular superoxide formation.
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Effect of the anti-anginal agent, perhexiline, on neutrophil, valvular and vascular superoxide formation.

机译:抗心绞痛药物perhexiline对中性粒细胞,瓣膜和血管超氧化物形成的影响。

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摘要

The prophylactic anti-anginal agent, perhexiline, may also be effective in acute coronary syndromes and advanced aortic valvular stenosis, conditions associated with enhanced inflammation. Its potential effects on superoxide formation via NADPH oxidase were measured by lucigenin-mediated chemiluminescence. Perhexiline inhibited superoxide formation in intact neutrophils stimulated with formyl Met Leu Phe (fMLP) 4 muM or with phorbol myristate acetate (PMA) 162 nM - IC50 2.3 microM (1.5-3.6), n=4. Sub-unit assembly of NADPH oxidase by PMA was unaffected by pretreatment with perhexiline 2 microM, a concentration which reduced superoxide formation by 44+/-5% (n=4) in intact neutrophils. Perhexiline inhibited preassembled neutrophil NADPH oxidase and that in membranes of pig valve interstitial cells, human umbilical vein endothelial cells (HUVECs) and cardiac fibroblasts, but not that in rat aorta (rings or membrane preparations). These data imply that perhexiline inhibits the phagocytic NADPH oxidase directly, and that pig aortic valvular interstitial cells possess a similar enzyme, a conclusion supported by immunohistochemical localisation of the gp91phox subunit in these cells. However further study is required to clarify the effect of perhexiline on different NADPH oxidase isoforms particularly in the vasculature.
机译:预防性抗心绞痛药,perhexiline,也可能在急性冠状动脉综合征和晚期主动脉瓣狭窄(与炎症增强相关的疾病)中有效。通过光泽精蛋白介导的化学发光测定了其对通过NADPH氧化酶形成超氧化物的潜在影响。哌克昔林抑制了完整的嗜中性粒细胞中过氧化物的形成,其中所述完整嗜中性粒细胞是用4μM甲酰蛋氨酸二苯丙氨酸(fMLP)或肉豆蔻酸佛波醇酯(PMA)162 nM刺激的-IC50为2.3 microM(1.5-3.6),n = 4。用Phehexiline 2 microM预处理不会影响PMA对NADPH氧化酶的亚单位组装,该浓度可在完整的嗜中性粒细胞中将超氧化物形成减少44 +/- 5%(n = 4)。 Perhexiline抑制预组装的中性粒细胞NADPH氧化酶,以及猪瓣膜间质细胞,人脐静脉内皮细胞(HUVEC)和心脏成纤维细胞的膜中的抑制作用,但不抑制大鼠主动脉(环或膜制剂)的杀伤作用。这些数据表明,perhexiline直接抑制吞噬NADPH氧化酶,并且猪主动脉瓣膜间质细胞具有类似的酶,这一结论得到了gp91phox亚基在这些细胞中的免疫组织化学定位的支持。然而,需要进一步的研究来阐明哌克昔林对不同NADPH氧化酶同工型的影响,尤其是在脉管系统中。

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