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首页> 外文期刊>The Journal of Physiology >Antioxidants prevent depression of the acute hypoxic ventilatory response by subanaesthetic halothane in men.
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Antioxidants prevent depression of the acute hypoxic ventilatory response by subanaesthetic halothane in men.

机译:抗氧化剂可防止男性麻醉后氟烷降低急性低氧通气反应的能力。

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We studied the effect of the antioxidants (AOX) ascorbic acid (2 g, I.V.) and alpha-tocopherol (200 mg, P.O.) on the depressant effect of subanaesthetic doses of halothane (0.11 % end-tidal concentration) on the acute isocapnic hypoxic ventilatory response (AHR), i.e. the ventilatory response upon inhalation of a hypoxic gas mixture for 3 min (leading to a haemoglobin saturation of 82 +/- 1.8 %) in healthy male volunteers. In the first set of protocols, two groups of eight subjects each underwent a control hypoxic study, a halothane hypoxic study and finally a halothane hypoxic study after pretreatment with AOX (study 1) or placebo (study 2). Halothane reduced the AHR by more than 50 %, from 0.79 +/- 0.31 to 0.36 +/- 0.14 l min(-1) %(-1) in study 1 and from 0.79 +/- 0.40 to 0.36 +/- 0.19 l min(-1) %(-1) in study 2, P < 0.01 for both. Pretreatment with AOX prevented this depressant effect of halothane in the subjects of study 1 (AHR returning to 0.77 +/- 0.32 l min(-1) %(-1), n.s. from control), whereasplacebo (study 2) had no effect (AHR remaining depressed at 0.36 +/- 0.27 l min(-1) %(-1), P < 0.01 from control). In a second set of protocols, two separate groups of eight subjects each underwent a control hypoxic study, a sham halothane hypoxic study and finally a sham halothane hypoxic study after pretreatment with AOX (study 3) or placebo (study 4). In studies 3 and 4, sham halothane did not modify the control hypoxic response, nor did AOX (study 3) or placebo (study 4). The 95 % confidence intervals for the ratio of hypoxic sensitivities, (AOX + halothane) : halothane in study 1 and (AOX - sham halothane) : sham halothane in study 3, were [1.7, 2.6] and [1.0, 1.2], respectively. Because the antioxidants prevented the reduction of the acute hypoxic response by halothane, we suggest that this depressant effect may be caused by reactive species produced by a reductive metabolism of halothane during hypoxia or that a change in redox state of carotid body cells by the antioxidants prevented or changed the binding of halothane to its effect site. Our findings may also suggest that reactive species have an inhibiting effect on the acute hypoxic ventilatory response.
机译:我们研究了抗氧化剂(AOX)抗坏血酸(2 g,IV)和α-生育酚(200 mg,PO)对亚麻醉剂量的氟烷(潮气末浓度为0.11%)的麻醉作用对急性等碳酸血症低氧的抑制作用通气反应(AHR),即健康男性志愿者吸入低氧气体混合物3分钟(导致血红蛋白饱和度为82 +/- 1.8%)时的通气反应。在第一组方案中,两组分别由八名受试者组成,分别接受AOX(研究1)或安慰剂(研究2)预处理后的对照低氧研究,氟烷低氧研究,最后进行氟烷低氧研究。氟烷将AHR降低了50%以上,从研究1中的0.79 +/- 0.31降至0.36 +/- 0.14 l min(-1)%(-1),从0.79 +/- 0.40降至0.36 +/- 0.19 l研究2中的min(-1)%(-1),两者均P <0.01。在研究1的受试者中,用AOX进行的预处理预防了氟烷的这种抑制作用(AHR恢复为0.77 +/- 0.32 l min(-1)%(-1),ns来自对照),而安慰剂(研究2)无效( AHR保持压低至0.36 +/- 0.27 l min(-1)%(-1),相对于对照组P <0.01)。在第二组方案中,由八个受试者组成的两组分别进行了对照低氧研究,假氟烷低氧研究,最后接受AOX(研究3)或安慰剂(研究4)预处理的假氟烷低氧研究。在研究3和4中,假氟烷没有改变对照的低氧反应,AOX(研究3)或安慰剂(研究4)也没有改变。研究1中低氧敏感性比(AOX +氟烷):氟烷和研究3(AOX-假氟烷):假氟烷的比率的95%置信区间分别为[1.7,2.6]和[1.0,1.2]。 。因为抗氧化剂阻止了氟烷减少急性低氧反应,所以我们认为这种抑制作用可能是由于低氧状态下氟烷的还原性代谢产生的反应性物种引起的,或者是由于防止了抗氧化剂改变了颈动脉体细胞的氧化还原状态或改变了氟烷与其作用部位的结合。我们的发现还可能表明,反应性物种对急性低氧通气反应具有抑制作用。

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