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首页> 外文期刊>American Journal of Physiology >Peroxynitrite hyperpolarizes smooth muscle and relaxes internal carotid artery in rabbit via ATP-sensitive K+ channels.
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Peroxynitrite hyperpolarizes smooth muscle and relaxes internal carotid artery in rabbit via ATP-sensitive K+ channels.

机译:过氧亚硝酸盐通过ATP敏感的K +通道使兔的平滑肌超极化并放松颈内动脉。

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The goal of this study was to determine the effects of peroxynitrite (ONOO-) on smooth muscle membrane potential and vasomotor function in rabbit carotid arteries. ONOO- is known to affect vascular tone by several mechanisms, including effects on K+ channels. Xanthine (X, 0.1 mM), xanthine oxidase (XO, 0.01 U/ml), and a low concentration of sodium nitroprusside (SNP, 10 nM) were used to generate ONOO-. In the common carotid artery, X and XO (X/XO) in the presence of SNP tended to increase tension. In contrast, in the internal carotid artery, X/XO in the presence of SNP transiently hyperpolarized the membrane (-8.5 +/- 1.8 mV, mean +/- SE) and decreased tension (by 85 +/- 5.6%). In internal carotid arteries, in the absence of SNP, X/XO did not hyperpolarize the membrane and produced much less relaxation (by 23 +/- 5.6%) than X/XO and SNP. Ebselen (50 microM) inhibited both hyperpolarization and relaxation to X/XO and SNP, and uric acid (100 microM) inhibited relaxation. Glibenclamide (1 microM) abolished hyperpolarization and inhibited relaxation during X/XO and SNP. Charybdotoxin (100 nM) or tetraethylammonium (1 mM) did not affect hyperpolarization or relaxation, respectively. These results suggest that ONOO- hyperpolarizes and relaxes smooth muscle in rabbit internal carotid artery but not in common carotid artery through activation of K(ATP) channels.
机译:这项研究的目的是确定过氧亚硝酸盐(ONOO-)对兔颈动脉平滑肌膜电位和血管舒缩功能的影响。已知ONOO-通过几种机制影响血管张力,包括对K +通道的影响。黄嘌呤(X,0.1 mM),黄嘌呤氧化酶(XO,0.01 U / ml)和低浓度的硝普钠(SNP,10 nM)用于生成ONOO-。在颈总动脉中,存在SNP的X和XO(X / XO)倾向于增加张力。相反,在颈内动脉中,存在SNP的X / XO使膜瞬时超极化(-8.5 +/- 1.8 mV,平均+/- SE),张力降低(下降85 +/- 5.6%)。在颈内动脉中,在不存在SNP的情况下,X / XO不会使膜超极化,与X / XO和SNP相比,其松弛度(降低23 +/- 5.6%)要少得多。 Ebselen(50 microM)抑制X / XO和SNP的超极化和松弛,而尿酸(100 microM)抑制松弛。格列本脲(1 microM)消除了超极化作用,并抑制了X / XO和SNP期间的松弛。炭疽毒素(100 nM)或四乙铵(1 mM)分别不影响超极化或松弛。这些结果表明,ONOO-通过激活K(ATP)通道使兔颈内动脉的平滑肌超极化并使其松弛,而在颈总动脉中则不然。

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