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神经肽Y与交感神经系统在人体血管控制中的相互作用。

Interaction of neuropeptide Y and the sympathetic nervous system in vascular control in man.

作者信息

Clarke J, Benjamin N, Larkin S, Webb D, Maseri A, Davies G

机构信息

Department of Cardiovascular Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.

出版信息

Circulation. 1991 Mar;83(3):774-7. doi: 10.1161/01.cir.83.3.774.

DOI:10.1161/01.cir.83.3.774
PMID:1999028
Abstract

BACKGROUND

There is increasing evidence that neuropeptide Y (NPY) contributes to the autonomic control of the circulation. NPY coexists with noradrenaline in perivascular nerve terminals, may be released during sympathetic stimulation, and is a potent constrictor of the human coronary circulation and other vascular beds. In vitro studies show that NPY can act either directly on vascular smooth muscle or indirectly by modulation of the presynaptic release or the postsynaptic actions of noradrenaline. It is unclear to what extent these mechanisms operate in vivo.

METHODS AND RESULTS

The effect on forearm blood flow of intra-arterial NPY was studied in six volunteers during coinfusion of noradrenaline and during reflex sympathetic stimulation induced by lower-body negative pressure. NPY alone induced a dose-dependent reduction of forearm blood flow in all subjects studied, to a maximum of 49 +/- 6.1%. The reduction of flow during infusion of noradrenaline alone was 42 +/- 8%. The response to noradrenaline was unaffected by coinfusion of a threshold constrictor dose of NPY (50 pmol/min). Furthermore, the reflex sympathetic vasoconstrictor response to 20 cm H2O of lower-body negative pressure was similar in both the infused and control arms during the infusion of 50 pmol/min NPY. The response to noradrenaline was abolished by alpha-blockade with phentolamine, but the flow reduction induced by NPY was unaffected by alpha-blockade.

CONCLUSIONS

NPY is a potent constrictor of human forearm resistance vessels and has a direct effect independent of alpha-receptors. NPY has no detectable modulating effect in vivo on the action of endogenous or infused noradrenaline.

摘要

背景

越来越多的证据表明神经肽Y(NPY)参与了循环系统的自主控制。NPY与去甲肾上腺素共存于血管周围神经末梢,可能在交感神经刺激时释放,并且是人类冠状动脉循环和其他血管床的强效收缩剂。体外研究表明,NPY可直接作用于血管平滑肌,或通过调节去甲肾上腺素的突触前释放或突触后作用间接发挥作用。目前尚不清楚这些机制在体内的作用程度。

方法与结果

在6名志愿者中,研究了在去甲肾上腺素联合输注期间以及下体负压诱导的反射性交感神经刺激期间,动脉内注射NPY对前臂血流量的影响。单独注射NPY可使所有研究对象的前臂血流量呈剂量依赖性减少,最大减少幅度为49±6.1%。单独输注去甲肾上腺素期间血流量的减少幅度为42±8%。联合输注阈剂量的收缩剂NPY(50 pmol/min)对去甲肾上腺素的反应无影响。此外,在输注50 pmol/min NPY期间,输注侧和对照侧对20 cm H2O下体负压的反射性交感缩血管反应相似。酚妥拉明α受体阻滞可消除对去甲肾上腺素的反应,但NPY诱导的血流量减少不受α受体阻滞的影响。

结论

NPY是人类前臂阻力血管的强效收缩剂,具有独立于α受体的直接作用。NPY在体内对内源性或输注的去甲肾上腺素的作用没有可检测到的调节作用。

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