Activation of opioid micro-receptors in medullary raphe depresses sighs.
Activation of opioid micro-receptors in medullary raphe depresses sighs.
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中缝髓质中阿片类微受体的激活可抑制叹息。
DOI：
10.1152/ajpregu.90748.2008
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发表时间：
2009
期刊：
影响因子：
--
通讯作者：
Liang,Xiaomin
中科院分区：
文献类型：
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作者：
Zhang,Zhenxiong;Xu,Fadi;Zhang,Cancan;Liang,Xiaomin
Sighs, a well-known phenomenon in mammals, are substantially augmented by hypoxia and hypercapnia. Because (d-Ala2,N-Me-Phe4,Gly-ol)-enkephalin (DAMGO), a μ-receptor agonist, injected intravenously and locally in the caudal medullary raphe region (cMRR) decreased the ventilatory response to hypoxia and hypercapnia, we hypothesized that these treatments could inhibit sigh responses to these chemical stimuli. The number and amplitude of sighs were recorded during three levels of isocapnic hypoxia (15%, 10%, and 5% O2for 1.5 min) or hypercapnia (3%, 7%, and 10% CO2for 4 min) to test the dependence of sigh responses on the intensity of chemical drive in anesthetized and spontaneously breathing rats. The role of μ-receptors in modulating sigh responses to 10% O2or 7% CO2was subsequently evaluated by comparing the sighs before and after1) intravenous administration of DAMGO (100 μg/kg),2) microinjection of DAMGO (35 ng/100 nl) into the cMRR, and3) intravenous administration of DAMGO after microinjection ofd-Phe-Cys-Tyr-d-Trp-Arg-Thr-Pen-Thr-NH2(CTAP, 100 ng/100 nl), a μ-receptor antagonist, into the cMRR. Hypoxia and hypercapnia increased the number, but not amplitude, of sighs in a concentration-dependent manner, and the responses to hypoxia were significantly greater than those to hypercapnia. Systemic and local injection of DAMGO into the cMRR predominantly decreased the number of sighs, while microinjection into the rostral and middle MRR had no or limited effects. Microinjecting CTAP into the cMRR significantly diminished the systemic DAMGO-induced reduction of the number of sighs in response to hypoxia, but not to hypercapnia. Thus we conclude that hypoxia and hypercapnia elevate the number of sighs in a concentration-dependent manner in anesthetized rats, and this response is significantly depressed by activating systemic μ-receptors, especially those within the cMRR.
