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腺苷对猫软脑膜动脉的舒张作用及其被茶碱的抑制作用。

The dilatatory action of adenosine on pial arteries of cats and its inhibition by theophylline.

作者信息

Wahl M, Kuschinsky W

出版信息

Pflugers Arch. 1976 Mar 11;362(1):55-9. doi: 10.1007/BF00588681.

Abstract

The effect of adenosine upon pial resistance vessels was studied using local microapplication from the perivascular side and measurement of vascular diameter. Concentration-response curves revealed a concentration-dependent dilatatory effect of adenosine between 10(-7) and 10(-3) M. The degree of dilatation was independent of initial vessel size (47-260 mu). The dilatations due to adenosine could be reduced by theophylline in a reversible competitive antagonism. Concentration-response curves for theophylline yielded no vascular reaction at concentrations of up to 10(-5) M theophylline. From these data is is concluded that the pial arterial resting tone is not influenced under our experimental conditions by adenosine formed and released by brain tissue. The dilatations measured at high theophylline concentrations are apparently due to a mechanism different from the adenosine antagonism.

摘要

利用从血管周围侧进行局部微量应用和测量血管直径的方法,研究了腺苷对软脑膜阻力血管的影响。浓度-反应曲线显示,腺苷在10(-7)至10(-3)M之间具有浓度依赖性舒张作用。舒张程度与初始血管大小(47 - 260μm)无关。茶碱可通过可逆性竞争性拮抗作用降低腺苷引起的舒张。在茶碱浓度高达10(-5)M时,茶碱的浓度-反应曲线未产生血管反应。从这些数据得出结论,在我们的实验条件下,脑组织形成和释放的腺苷不会影响软脑膜动脉的静息张力。在高茶碱浓度下测得的舒张显然是由于一种不同于腺苷拮抗作用的机制。

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