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多种阿片受体介导芬太尼类药物对大鼠的呼吸抑制作用。

Multiple opioid receptors mediate the respiratory depressant effects of fentanyl-like drugs in the rat.

作者信息

Yeadon M, Kitchen I

机构信息

Department of Biochemistry, University of Surrey, Guildford, England.

出版信息

Gen Pharmacol. 1990;21(5):655-64. doi: 10.1016/0306-3623(90)91013-h.

Abstract
  1. Respiratory depressant effects of five drugs of the fentanyl series have been studied in anaesthetised rats. 2. The potency ratios of the fentanyl drugs to produce apnea and depress minute volume were dissimilar. Further, in vivo naloxone pA2 values were identical for blockade of apnea for the fentanyl drugs but different for antagonism of minute volume. 3. Differences in agonist potency and in naloxone pA2 values were also seen in vagotomised rats where only depression of minute volume is observed. 4. The data suggests that multiple receptor interactions are involved in the respiratory depressant effects of these drugs; the apnea response is primarily mediated through peripheral mu receptors but minute volume depression involves both mu receptors and non-mu sites.
摘要
  1. 研究了芬太尼系列五种药物对麻醉大鼠的呼吸抑制作用。2. 芬太尼类药物产生呼吸暂停和降低分钟通气量的效价比不同。此外,体内纳洛酮pA2值在芬太尼类药物阻断呼吸暂停方面相同,但在拮抗分钟通气量方面不同。3. 在迷走神经切断的大鼠中也观察到激动剂效价和纳洛酮pA2值的差异,在这些大鼠中仅观察到分钟通气量降低。4. 数据表明,这些药物的呼吸抑制作用涉及多种受体相互作用;呼吸暂停反应主要通过外周μ受体介导,但分钟通气量降低涉及μ受体和非μ位点。

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