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NO-cGMP 途径在毒蕈碱对人心房肌细胞 L 型钙电流调节中的作用。

Role of the NO-cGMP pathway in the muscarinic regulation of the L-type Ca2+ current in human atrial myocytes.

作者信息

Vandecasteele G, Eschenhagen T, Fischmeister R

机构信息

Laboratoire de Cardiologie Cellulaire et Moléculaire, INSERM U-446, Université de Paris-Sud, Faculté de Pharmacie, Châtenay-Malabry, France.

出版信息

J Physiol. 1998 Feb 1;506 ( Pt 3)(Pt 3):653-63. doi: 10.1111/j.1469-7793.1998.653bv.x.

Abstract
  1. The whole-cell patch-clamp technique was used to examine the participation of nitric oxide synthase (NOS) and soluble guanylyl cyclase in the muscarinic regulation of the L-type Ca2+ current (ICa) in freshly isolated human atrial myocytes. 2. Acetylcholine (ACh, 1 microM) decreased basal ICa by 39.1 +/- 5.5% (n = 8) under control conditions, and by 38.0 +/- 6.1% (n = 6) in the presence of 1H-[1,2,4]oxadiazolo[4,3-a]-quinoxaline-1-one (ODQ, 10 microM), a potent guanylyl cyclase inhibitor, and NG-monomethyl-L-arginine (L-NMMA, 1 mM), a competitive NOS inhibitor. L-NMMA alone had no effect on ICa, whilst ODQ increased ICa in 50% of the cells. 3. The accentuated antagonism of ACh on ICa, i.e. its ability to antagonize the stimulatory effect of beta-adrenergic agonists and, by extension, of other cAMP-elevating agents, was examined after the current was stimulated by either the beta-adrenergic agonist isoprenaline (Iso) or serotonin (5-HT). ACh (100 nM or 1 microM) completely blocked the stimulatory effects of 10 nM Iso or 10 nM 5-HT on ICa. 4. Extracellular application of Methylene Blue (MBlue, 10 microM), a guanylyl cyclase inhibitor, antagonized the inhibitory effect of 1 microM ACh on Iso- or 5-HT-stimulated ICa. However, this effect was overcome by a 100-fold higher ACh concentration and was not mimicked by an intracellular application of MBlue. 5. Inhibition of NOS and soluble guanylyl cyclase activities by addition of ODQ (10 microM) and L-NMMA (1 mM) to both extracellular and intracellular solutions, or by a 2 h pre-incubation of the cells with these inhibitors, modified neither the Iso (10 nM) response nor the inhibitory effect of ACh (100 nM or 1 microM) on Iso-stimulated ICa. 6. Extracellular application of the NO donor SNAP (S-nitroso-N-acetyl-D,L-penicillamine) at 100 nM produced a stimulatory effect on ICa in control conditions. This stimulatory effect was abolished by intracellular MBlue (20 microM) or by intracellular and extracellular application of ODQ (10 microM) in combination with L-NMMA (1 mM). 7. We conclude that the NO-cGMP pathway does not contribute significantly to the muscarinic regulation of ICa in human atrial myocytes.
摘要
  1. 采用全细胞膜片钳技术,研究一氧化氮合酶(NOS)和可溶性鸟苷酸环化酶在新鲜分离的人心房肌细胞毒蕈碱调节L型钙电流(ICa)中的作用。2. 在对照条件下,乙酰胆碱(ACh,1 μM)使基础ICa降低39.1±5.5%(n = 8),在存在强效鸟苷酸环化酶抑制剂1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ,10 μM)和竞争性NOS抑制剂NG-甲基-L-精氨酸(L-NMMA,1 mM)时,使基础ICa降低38.0±6.1%(n = 6)。单独使用L-NMMA对ICa无影响,而ODQ使50%的细胞ICa增加。3. 在电流由β-肾上腺素能激动剂异丙肾上腺素(Iso)或5-羟色胺(5-HT)刺激后,研究了ACh对ICa的增强拮抗作用,即其拮抗β-肾上腺素能激动剂以及其他cAMP升高剂刺激作用的能力。ACh(100 nM或1 μM)完全阻断了10 nM Iso或10 nM 5-HT对ICa的刺激作用。4. 细胞外应用鸟苷酸环化酶抑制剂亚甲蓝(MBlue,10 μM)可拮抗1 μM ACh对Iso或5-HT刺激的ICa的抑制作用。然而,这种作用可被高100倍的ACh浓度克服,且细胞内应用MBlue不能模拟该作用。5. 通过在细胞外和细胞内溶液中加入ODQ(10 μM)和L-NMMA(1 mM),或用这些抑制剂对细胞进行2小时预孵育来抑制NOS和可溶性鸟苷酸环化酶活性,既不改变Iso(10 nM)反应,也不改变ACh(100 nM或1 μM)对Iso刺激的ICa的抑制作用。6. 在对照条件下,细胞外应用100 nM的NO供体S-亚硝基-N-乙酰-D,L-青霉胺(SNAP)对ICa产生刺激作用。这种刺激作用可被细胞内MBlue(20 μM)或细胞内和细胞外联合应用ODQ(10 μM)与L-NMMA(1 mM)消除。7. 我们得出结论,NO-cGMP途径对人心房肌细胞ICa的毒蕈碱调节作用不显著。

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