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一氧化碳诱导羔羊动脉导管舒张:反对鸟苷酸环化酶主要作用的证据

Carbon monoxide-induced relaxation of the ductus arteriosus in the lamb: evidence against the prime role of guanylyl cyclase.

作者信息

Coceani F, Kelsey L, Seidlitz E

机构信息

Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Br J Pharmacol. 1996 Aug;118(7):1689-96. doi: 10.1111/j.1476-5381.1996.tb15593.x.

Abstract
  1. We have previously found that carbon monoxide (CO) potently relaxes the lamb ductus arteriosus and have ascribed this response to inhibition of a cytochrome P450-based mono-oxygenase reaction which sustains contractile tone. Our proposal, however, has been questioned on the evidence of findings in other blood vessels implicating the guanylyl cyclase-based relaxing mechanism as the target for CO. To investigate this issue further, we have carried out experiments in the isolated ductus from near-term foetal lambs and have examined the effect of CO concomitantly on muscle tone and cyclic GMP content, both in the absence and presence of guanylyl inhibitors, or during exposure to monochromatic light at 450 nm. 2. CO (65 microM) reversed completely, or nearly completely, the tone developed by the vessel in the presence of oxygen (30%) and indomethacin (2.8 microM). Cyclic GMP content tended to increase with the relaxation, but the change did not reach significance. Sodium nitroprusside (SNP), a NO donor, mimicked CO in relaxing the ductus. Contrary to CO, however, SNP caused a marked accumulation of cyclic GMP with levels being positively correlated with the relaxation. 3. Methylene blue (10 microM) reduced marginally the CO relaxation, whilst LY-83583 (10 microM) had an obvious, albeit variable, inhibitory effect. Basal cyclic GMP content was lower in tissues treated with either compound and rose upon exposure to CO. However, the levels attained were still within the range of values for tissues prior to any treatment. Furthermore, the elevation in cyclic GMP was not related to the magnitude of the CO relaxation. 4. Illumination of the ductus with monochromatic light at 450 nm reversed the CO relaxation and any concomitant increase in cyclic GMP. In the absence of CO, light by itself had no effect. 5. Ductal preparation with only muscle behaved as the intact preparations in reacting to CO, both in the absence and presence of guanylyl cyclase inhibitors, or during illumination. 6. We conclude that the primary action of CO in the ductus arteriosus is not exerted on the guanylyl cyclase heme and that cyclic GMP may only have an accessory role in the relaxation to this agent. This finding reasserts the importance of a cytochrom P450-based mono-oxygenase reaction for generation of tone and as a target for CO in the ductus.
摘要
  1. 我们之前发现一氧化碳(CO)能有效舒张羔羊动脉导管,并将这种反应归因于对一种基于细胞色素P450的单加氧酶反应的抑制,该反应维持收缩张力。然而,基于其他血管中发现的证据,我们的提议受到了质疑,这些证据表明基于鸟苷酸环化酶的舒张机制是CO的作用靶点。为了进一步研究这个问题,我们对近期胎羊的离体动脉导管进行了实验,并在有无鸟苷酸抑制剂的情况下,或在暴露于450nm单色光期间,研究了CO对肌张力和环磷酸鸟苷(cGMP)含量的影响。2. CO(65微摩尔)完全或几乎完全逆转了在氧气(30%)和吲哚美辛(2.8微摩尔)存在下血管产生的张力。cGMP含量倾向于随着舒张而增加,但变化不显著。一氧化氮供体硝普钠(SNP)在舒张动脉导管方面模拟了CO。然而,与CO相反,SNP导致cGMP显著积累,其水平与舒张呈正相关。3. 亚甲蓝(10微摩尔)对CO舒张作用的减弱作用微乎其微,而LY - 83583(10微摩尔)具有明显的抑制作用,尽管存在变化。用这两种化合物处理的组织中基础cGMP含量较低,暴露于CO后升高。然而,达到的水平仍在任何处理前组织的值范围内。此外,cGMP的升高与CO舒张的幅度无关。4. 用450nm单色光照射动脉导管逆转了CO舒张作用以及cGMP的任何伴随增加。在没有CO的情况下,光本身没有作用。5. 仅含肌肉的导管制剂在有无鸟苷酸环化酶抑制剂的情况下,或在光照期间,对CO的反应与完整制剂相同。6. 我们得出结论,CO在动脉导管中的主要作用不是作用于鸟苷酸环化酶血红素,并且cGMP在对该物质的舒张作用中可能仅起辅助作用。这一发现再次强调了基于细胞色素P450的单加氧酶反应在动脉导管中产生张力以及作为CO作用靶点的重要性。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2579/1909852/da007e207a56/brjpharm00086-0139-a.jpg

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