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首页> 外文期刊>Pulmonary pharmacology & therapeutics >Mechanism of decongestant activity of alpha(2)-adrenoceptor agonists.
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Mechanism of decongestant activity of alpha(2)-adrenoceptor agonists.

机译:α(2)-肾上腺素受体激动剂减充血活性的机制。

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The vascular bed in nasal mucosa of different species, including human, is highly vascularized and an extensive sinusoidal network of large capacitance vessels is present deep within the submucosa. When this network of venous sinusoids is engorged with blood, the swollen mucosa reduces the size of the airway lumen and congestion ensues. Nasal vasculature tone is strongly influenced by the sympathetic nervous system and the only drugs approved specifically to relieve vascular nasal obstruction are alpha-adrenoceptor sympathomimetic agents. Due to their vasoconstrictor action, the sympathomimetic decongestants oppose vasodilation, reducing nasal airway resistance and thus facilitating nose breathing. However, standard decongestants that are non-selective alpha-adrenoceptor agonists are associated with the potential for side-effect liabilities including hypertension, stroke, insomnia and nervousness. We propose than a selective alpha(2)-adrenoceptor agonist, by acting preferentially on nasal venous capacitance vessels, will elicit decongestion with a reduced side-effect liability. In the present study, we evaluated the effects of the selective alpha(2)-adrenoceptor agonist BHT-920 in a real-time tissue contractility assay using isolated pig nasal explants and in an in vivo cat model of congestion. The vasoconstrictor and decongestant effects of BHT-920 were compared to the non-selective alpha-adrenoceptor agonist epinephrine and the standard decongestant oxymetazoline. Our results showed that the alpha(2)-adrenoceptor agonist BHT-920 preferentially contracts venous sinusoids confirming previous observations [Corboz MR, Varty LM, Rivelli MA, Mutter JC, Mingo G, McLeod R, et al. Effects of an alpha(2)-adrenoceptor agonist in nasal mucosa. Arch Physiol Biochem 2003;11: 335-6, Corboz MR, Rivelli MA, Varty LM, Mutter J, Cartwright M, Rizzo CA, et al. Pharmacological characterization of postjunctional alpha-adrenoceptor in human nasal mucosa. Am J Rhinol 2005;19: 495-502] and displays decongestion without affecting blood pressure. Therefore, an alpha(2)-adrenoceptor agonist, by causing constriction in the capacitance vessels of nasal mucosa, can produce nasal decongestion without the effects on blood pressure observed with the standard selective alpha(1)-adrenoceptor and non-selective alpha-adrenoceptor sympathomimetic decongestants.
机译:包括人类在内的不同物种的鼻粘膜中的血管床高度血管化,并且在粘膜下层深处存在大电容血管的广泛正弦网络。当静脉血窦的网络充血时,黏膜肿胀会缩小气道内腔的大小,继而出现充血。鼻脉管张力受交感神经系统的强烈影响,唯一被批准用于缓解鼻腔阻塞的药物是α-肾上腺素受体拟交感神经药。由于拟交感神经减充血药具有血管收缩作用,因此可以对抗血管舒张作用,从而降低鼻气道阻力,从而有利于鼻呼吸。然而,作为非选择性α-肾上腺素受体激动剂的标准减充血剂与潜在的副作用相关,包括高血压,中风,失眠和神经紧张。我们建议比选择性的alpha(2)-肾上腺素受体激动剂,通过优先作用于鼻腔静脉血管,会引起充血,副作用减少。在本研究中,我们评估了选择性α(2)-肾上腺素受体激动剂BHT-920在使用分离的猪鼻外植体的实时组织收缩性测定中以及在体内猫充血模型中的作用。将BHT-920的血管收缩作用和减充血作用与非选择性α-肾上腺素受体激动剂肾上腺素和标准减充血剂氧甲唑啉进行了比较。我们的研究结果表明,α(2)-肾上腺素受体激动剂BHT-920优先收缩静脉正弦曲线,从而证实了先前的观察[Corboz MR,Varty LM,Rivelli MA,Mutter JC,Mingo G,McLeod R等。 α(2)-肾上腺素受体激动剂在鼻粘膜中的作用。 Arch Physiol Biochem 2003; 11:335-6,Corboz MR,Rivelli MA,Varty LM,Mutter J,Cartwright M,Rizzo CA等。人鼻粘膜中结后α-肾上腺素受体的药理学表征。 Am J Rhinol 2005; 19:495-502]并显示充血而不影响血压。因此,通过引起鼻粘膜电容血管收缩,α(2)-肾上腺素受体激动剂可产生鼻充血,而对标准选择性α(1)-肾上腺素受体和非选择性α-肾上腺素受体所观察到的血压没有影响拟交感神经充血剂。

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