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首页> 外文期刊>The Korean Journal of Physiology & Pharmacology >The Inhibitory Mechanism of Gentamicin on Electrical Field Stimulation Response in Rat Bladder Smooth Muscle
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The Inhibitory Mechanism of Gentamicin on Electrical Field Stimulation Response in Rat Bladder Smooth Muscle

机译:庆大霉素对大鼠膀胱平滑肌电场刺激反应的抑制机制

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To see the inhibitory mechanism of gentamicin in response to electrical field stimulation (EFS) using the rat bladder smooth muscle, atropine or guanethidine was treated but had no effect. Methylsergide, a non-selective 5-HT1, 5-HT2 receptor antagonist was also treated but had on effect. Kinase inhibitors, such as chelerythrine (PKC inhibitor), ML-9 (MLCK inhibitor), or Y27632 (rho kinase inhibitor) were pretreated before gentamicin treatment, but did not have effect. For U73122, a phospholipase C (PLC) inhibitor however, the inhibitory effect to gentamicin was significantly attenuated in all frequencies given by the EFS. Therefore gentamicin induced inhibitory effect on EFS response in rat bladder smooth muscle was not mediated by the activation of adrenergic, cholinergic, or serotonergic receptor. The inhibition of gentamicin might be mediated through the PLC dependent pathway, but not through the PKC, MLCK or rho kinase dependent pathway.
机译:为了了解庆大霉素对使用大鼠膀胱平滑肌的电场刺激(EFS)的抑制机制,对阿托品或胍乙啶进行了处理,但没有效果。甲基麦角酰胺,一种非选择性的5-HT 1 ,5-HT 2 受体拮抗剂也得到了治疗,但有效果。庆大霉素治疗前对白屈菜红碱(PKC抑制剂),ML-9(MLCK抑制剂)或Y27632(rho激酶抑制剂)等激酶抑制剂进行了预处理,但没有效果。但是,对于U73122(磷脂酶C(PLC)抑制剂),在EFS给予的所有频率下,对庆大霉素的抑制作用都会大大减弱。因此,庆大霉素诱导的对大鼠膀胱平滑肌EFS反应的抑制作用不是由肾上腺素能,胆碱能或血清素能受体的激活介导的。庆大霉素的抑制作用可能是通过PLC依赖性途径介导的,而不是通过PKC,MLCK或rho激酶依赖性途径介导的。

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