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喹吡罗对大鼠原位自体灌注后肢和肾血管床神经源性血管收缩的影响。

Effect of quinpirole on neurogenic vasoconstriction in the in situ autoperfused hindquarters and renal vascular beds of the rat.

作者信息

Roquebert J, Moran A, Demichel P

机构信息

Laboratoire de Pharmacodynamie, UFR de Pharmacie, Université de Bordeaux II, France.

出版信息

J Auton Pharmacol. 1992 Oct;12(5):291-8. doi: 10.1111/j.1474-8673.1992.tb00378.x.

Abstract
  1. The effects of local administration of quinpirole were studied in the in situ autoperfused hindquarters and renal vascular beds, in order to assess whether presynaptic dopamine receptors in these vascular systems could play a role in the hypotensive effect of this agonist. 2. In both preparations, local injection of quinpirole did not alter perfusion pressure, but reduced the pressor response to electrical stimulation of the sympathetic innervation. Increases in perfusion induced by local administration of noradrenaline were not altered by quinpirole. 3. The inhibitory effect of quinpirole on the stimulation-evoked pressor responses was completely antagonized by intravenous administration of the DA2-receptor antagonist domperidone (0.5 mg kg-1) but not by the DA1-receptor antagonist SCH 23390 (0.3 mg kg-1) or the alpha 2-adrenoceptor antagonist idazoxan (0.3 mg kg-1). 4. The results indicate that quinpirole inhibits neurally induced pressor responses in the autoperfused hindquarters and renal vascular beds of the rat by stimulation of presynaptic dopamine receptors. These receptors may be involved in the hypotensive action of quinpirole in the rat.
摘要
  1. 为评估这些血管系统中的突触前多巴胺受体是否在该激动剂的降压作用中发挥作用,研究了喹吡罗局部给药对原位自体灌注后肢和肾血管床的影响。2. 在这两种制备模型中,局部注射喹吡罗并未改变灌注压,但降低了对交感神经支配进行电刺激时的升压反应。喹吡罗未改变局部给予去甲肾上腺素所诱导的灌注增加。3. 静脉注射DA2受体拮抗剂多潘立酮(0.5 mg kg-1)可完全拮抗喹吡罗对刺激诱发的升压反应的抑制作用,但DA1受体拮抗剂SCH 23390(0.3 mg kg-1)或α2肾上腺素能受体拮抗剂咪唑克生(0.3 mg kg-1)则不能。4. 结果表明,喹吡罗通过刺激突触前多巴胺受体抑制大鼠自体灌注后肢和肾血管床中神经诱导的升压反应。这些受体可能参与了喹吡罗在大鼠中的降压作用。

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