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去铁胺可阻断氟化物与卡巴胆碱在离体哺乳动物心脏标本中的相互作用。

Deferoxamine blocks interactions of fluoride and carbachol in isolated mammalian cardiac preparations.

作者信息

Neumann J, Scholz H

机构信息

Abteilung Allgemeine Pharmakologie, Universitäts-Krankenhaus Eppendorf, Hamburg, Germany.

出版信息

Eur J Pharmacol. 1998 Jun 5;350(2-3):189-94. doi: 10.1016/s0014-2999(98)00235-0.

Abstract

In papillary muscles, carbachol reduced the positive inotropic effects of isoprenaline (10 nmol/l). The negative inotropic effects of carbachol in isoprenaline-stimulated guinea pig papillary muscles were attenuated by additionally applied sodium fluoride (3 mmol/l). These effects of sodium fluoride were blocked by deferoxamine (200 micromol/l). In guinea pig left atria, sodium fluoride alone greatly reduced force of contraction. These effects in atria were blocked by 200 micromol/l deferoxamine, and positive inotropic effects of sodium fluoride were observed. It is suggested that the cardiac effects of muscarinic M2 receptor agonists in the ventricle involve, at least in part, the activation of phosphatases which are blocked by fluoride and reactivated by deferoxamine.

摘要

在乳头肌中,卡巴胆碱降低了异丙肾上腺素(10纳摩尔/升)的正性肌力作用。在异丙肾上腺素刺激的豚鼠乳头肌中,额外施加氟化钠(3毫摩尔/升)可减弱卡巴胆碱的负性肌力作用。去铁胺(200微摩尔/升)可阻断氟化钠的这些作用。在豚鼠左心房中,单独使用氟化钠可大大降低收缩力。心房中的这些作用可被200微摩尔/升去铁胺阻断,并观察到氟化钠的正性肌力作用。提示毒蕈碱M2受体激动剂在心室中的心脏效应至少部分涉及磷酸酶的激活,而磷酸酶被氟化物阻断并被去铁胺重新激活。

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