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Effects of endothelin and nitric oxide on cardiac muscle functions in experimental septic shock model

机译:败血性休克模型中内皮素和一氧化氮对心肌功能的影响

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摘要

We aimed to investigate the possible roles of nitric oxide (NO) and endothelin on the changes of cardiac muscle function in both hyper- and hypodynamic septic shock periods. Cecal ligation and puncture was performed in 50 Wistar albino rats to induce septic shock. Changes in atrium and right ventricle papillary muscle contractions, atrium beat rate, adrenergic and cholinergic responses in these tissues were evaluated in vitro. Atrium beat rate increased in hypodynamic period (p < 0.001) that was reversed by bosentan (p < 0.001) and N-G-nitro-l-arginine methylester (l-NAME; p < 0.05). Atrium contractions decreased in both hyper- and hypodynamic periods (p < 0.001) that were partially ameliorated by bosentan in both periods (p < 0.01) and only in hypodynamic period by l-NAME (p < 0.001). l-NAME increased papillary muscle contractions in both periods (p < 0.01), but bosentan increased it only in hyperdynamic period (p < 0.01). Bosentan and l-NAME increased potency of isoproterenol on atrium beat rate in both periods and increased carbachol potency on atrium beat rate and atrium contraction amplitude only in hypodynamic period. Bosentan increased atrium contraction response to isoproterenol in hypodynamic period (p < 0.05). Papillary muscle contraction response to isoproterenol increased in hypodynamic period (p < 0.05). l-NAME increased papillary muscle contraction response to carbachol in both periods (p < 0.01, p < 0.05, respectively). These results show that NO and endothelin may play a role in positive inotropic and negative chronotropic effects for atrium in septic shock. Bosentan and l-NAME may change potency and efficacy of isoproterenol and carbachol via upregulation of adrenergic and cholinergic receptors and/or through post receptor factors.
机译:我们旨在研究一氧化氮(NO)和内皮素在高动力和低动力性败血性休克期对心肌功能变化的可能作用。在50只Wistar白化病大鼠中进行盲肠结扎和穿刺以诱导败血性休克。在体外评估这些组织中心房和右心室乳头肌收缩,心房搏动率,肾上腺素能和胆碱能反应的变化。心房搏动率在低动力期增加(p <0.001),而波生坦(p <0.001)和N-G-硝基-1-精氨酸甲酯(l-NAME; p <0.05)逆转。心房收缩在高动力和低动力期均下降(p <0.001),波生坦在这两个时期(p <0.01)均部分缓解,而在低动力期仅l-NAME(p <0.001)减轻。 l-NAME在两个时期均增加乳头肌收缩(p <0.01),但波生坦仅在高动力时期增加(p <0.01)。 Bosentan和l-NAME在两个时期中均增加了异丙肾上腺素对心房搏动率的效力,而卡巴胆碱对心房搏动率和心房收缩幅度的效力仅在低动力期才增加。波森坦在动力减退期增加了对异丙肾上腺素的心房收缩反应(p <0.05)。低动力期乳头肌对异丙肾上腺素的收缩反应增加(p <0.05)。在两个时期中,l-NAME均增加了对卡巴胆碱的乳头肌收缩反应(分别为p <0.01,p <0.05)。这些结果表明,NO和内皮素可能在败血性休克对心房的正性变力和负性变时作用中起作用。波生坦和l-NAME可能通过上调肾上腺素能和胆碱能受体和/或通过后受体因子改变异丙肾上腺素和卡巴胆碱的效力和功效。

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