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大鼠外周多巴胺受体的刺激:新型抗高血压药物的一种机制。

Stimulation of peripheral dopamine receptors in rats: a mechanism for novel antihypertensive agents.

作者信息

Lefèvre-Borg F, Cavero I

出版信息

Clin Sci (Lond). 1980 Dec;59 Suppl 6:291s-294s. doi: 10.1042/cs059291s.

Abstract
  1. The aim of this investigation was to provide support for the hypothesis that stimulation of peripheral dopamine receptors reduces sympathetic vasomotor tone and thus may be a mechanism for novel antihypertensive agents. 2. NN-Di-n-propyldopamine (DPDA: 0.03-0.1 mg min-1 kg-1 intra-arterially) produced sustained decreases in blood pressure measured from the cannulated tail artery in conscious spontaneously hypertensive rats. 3. This antihypertensive action of DPDA was antagonized by sulpiride but not by atropine, promethazine, propranolol or indomethacin. 4. DPDA failed to lower blood pressure in spontaneously hypertensive rats in which peripheral stores of catecholamines had been previously depleted with syrosingopine. 5. In the pithed atropine-pretreated spontaneously hypertensive rats in which the low blood pressure was elevated by electrical stimulation of the spinal cord, DPDA produced hypotensive effects which were antagonized by sulpiride. However, DPDA, in contrast to phentolamine, did not modify the blood pressure raised by an infusion of adrenaline. 6. In conclusion, the blood pressure-lowering action of DPDA is due to stimulation of dopamine receptors which decreases noradrenaline release and consequently sympathetic vasomotor tone. These receptors may be located on sympathetic ganglia or sympathetic endings innervating resistance vessels.
摘要
  1. 本研究的目的是为以下假说提供支持:刺激外周多巴胺受体可降低交感缩血管紧张性,因此可能是新型抗高血压药物的作用机制。2. NN-二正丙基多巴胺(DPDA:0.03 - 0.1毫克·分钟⁻¹·千克⁻¹,动脉内给药)使清醒的自发性高血压大鼠经插管的尾动脉测量的血压持续下降。3. DPDA的这种抗高血压作用被舒必利拮抗,但不受阿托品、异丙嗪、普萘洛尔或吲哚美辛的影响。4. 在先前已用利血平耗竭儿茶酚胺外周储备的自发性高血压大鼠中,DPDA未能降低血压。5. 在预先用阿托品处理的脊髓横断的自发性高血压大鼠中,通过电刺激脊髓使低血压升高,DPDA产生的降压作用被舒必利拮抗。然而,与酚妥拉明不同,DPDA不改变肾上腺素输注引起的血压升高。6. 总之,DPDA的降压作用是由于刺激多巴胺受体,减少去甲肾上腺素释放,从而降低交感缩血管紧张性。这些受体可能位于交感神经节或支配阻力血管的交感神经末梢上。

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