首页> 外文期刊>European Journal of Pharmacology: An International Journal >Ranbezolid, a novel oxazolidinone antibacterial: in vivo characterisation of monoamine oxidase inhibitory potential in conscious rats.
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Ranbezolid, a novel oxazolidinone antibacterial: in vivo characterisation of monoamine oxidase inhibitory potential in conscious rats.

机译:Ranbezolid,一种新型的恶唑烷酮抗菌药物:清醒大鼠体内单胺氧化酶抑制潜能的体内表征。

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摘要

Ranbezolid, a novel oxazolidinone antibacterial, competitively inhibits monoamine oxidase-A (MAO-A), in vitro. The consequences of MAO-A inhibition was evaluated in vivo, by testing interaction of Ranbezolid with tyramine (in solution or mixed with feed), and amine containing cold remedies on pressor response in conscious rats. Single and repeat doses of Ranbezolid (50 mg/kg, p.o.) did not affect pressor response to tyramine (5 or 15 mg/kg), but potentiated the same after a single dose of 100 mg/kg. Co-administration of Ranbezolid with tyramine in feed or with cold remedies also did not potentiate the respective pressor responses. These results suggest that Ranbezolid exhibits minimal cardiovascular liability associated with MAO-A inhibition.
机译:Ranbezolid,一种新型的恶唑烷酮抗菌剂,在体外竞争性抑制单胺氧化酶-A(MAO-A)。通过测试兰伯唑利德与酪胺(在溶液中或与饲料混合)和含胺的感冒药对有意识大鼠的升压反应的相互作用,在体内评估了MAO-A抑制的后果。兰伯唑利的单次和重复剂量(50 mg / kg,p.o.)不会影响对酪胺的升压反应(5或15 mg / kg),但是在单次剂量100 mg / kg后会增强升压反应。饲料中的兰伯唑利德与酪胺或感冒药的共同给药也未增强各自的升压反应。这些结果表明,兰贝唑胺显示出与MAO-A抑制有关的最小心血管作用。

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