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阿扑吗啡和培高利特对大鼠后肢神经源性血管收缩的抑制作用。

Inhibitory effects of apomorphine and pergolide on neurogenic vasoconstriction in the hindquarters of the rat.

作者信息

Dupont A G, Lefebvre R A, Bogaert M G

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 Apr;329(2):146-51. doi: 10.1007/BF00501204.

Abstract

The effects of locally administered apomorphine and pergolide were studied in the isolated autoperfused hindquarters of the rat, in an attempt to assess the possible role of presynaptic dopamine receptors at that level in the hypotensive effect of these dopamine agonists. Local infusion of apomorphine (1 micrograms . kg-1 . min-1 for 5 min) or pergolide (1 micrograms . kg-1 . min-1 for 5 min) [into the hindquarters] did not alter perfusion pressure per se, but reduced the pressor response to electrical stimulation of the lumbar sympathetic chains for the whole frequency range used during a cumulative frequency-response curve (0.25-16 Hz, 1 ms, supramaximal voltage). Apomorphine and pergolide reduced the pressor response elicited by 4 Hz electrical stimulation (applied until maximum response was reached) to 54.8 +/- 7.1% and 53.9 +/- 1.7% respectively, but they did not modify similar increases of perfusion pressure produced by locally administered noradrenaline. The inhibition by apomorphine and pergolide of the 4 Hz stimulation-evoked pressor response was completely antagonized by local administration of the dopamine antagonist haloperidol (1 microgram . kg-1), but was not influenced by the alpha 2-antagonist rauwolscine (100 micrograms . kg-1). This dose of rauwolscine antagonized the inhibitory effect of the alpha 2-agonist UK-14,304, which was not influenced by haloperidol. Local administration of rauwolscine increased the pressor response to stimulation at 4 Hz by 37.4-46.2%. In contrast, local administration of haloperidol did not influence the 4 Hz stimulation-evoked pressor response.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了局部给予阿扑吗啡和培高利特对大鼠离体自灌注后肢的影响,旨在评估该水平的突触前多巴胺受体在这些多巴胺激动剂降压作用中可能发挥的作用。局部输注阿扑吗啡(1微克·千克⁻¹·分钟⁻¹,持续5分钟)或培高利特(1微克·千克⁻¹·分钟⁻¹,持续5分钟)[至后肢]本身并未改变灌注压,但在累积频率-反应曲线(0.25 - 16赫兹,1毫秒,超最大电压)所用的整个频率范围内,降低了对腰交感链电刺激的升压反应。阿扑吗啡和培高利特分别将4赫兹电刺激(施加直至达到最大反应)引起的升压反应降低至54.8±7.1%和53.9±1.7%,但它们并未改变局部给予去甲肾上腺素所产生的类似灌注压升高。局部给予多巴胺拮抗剂氟哌啶醇(1微克·千克⁻¹)可完全拮抗阿扑吗啡和培高利特对4赫兹刺激诱发的升压反应的抑制作用,但不受α₂拮抗剂萝芙木碱(100微克·千克⁻¹)的影响。该剂量的萝芙木碱可拮抗α₂激动剂UK - 14,304的抑制作用,而UK - 14,304不受氟哌啶醇的影响。局部给予萝芙木碱可使4赫兹刺激诱发的升压反应增加37.4 - 46.2%。相比之下,局部给予氟哌啶醇并未影响4赫兹刺激诱发的升压反应。(摘要截短至250字)

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