首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Peripheral sympatho-inhibitory cardiovascular effects of opioid peptides in anaesthetized rabbits.
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Peripheral sympatho-inhibitory cardiovascular effects of opioid peptides in anaesthetized rabbits.

机译:阿片肽对麻醉兔子的外周交感抑制性心血管作用。

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摘要

1. Opioid agonists influence isolated cardiovascular tissues from rabbits, as well as the cardiovascular system of pithed rabbits, through presynaptic receptors on postganglionic sympathetic nerve fibres. The present experiments were carried out in order to study effects which result from activation of these receptors in anaesthetized rabbits. 2. In pithed rabbits with electrically stimulated sympathetic outflow, infusion of [D-Ala2-D-Leu5]-enkephalin (DADLE) 10 micrograms kg-1 min-1 and dynorphin-(1-13) (dynorphin) 1 microgram kg-1 min-1 decreased the plasma noradrenaline concentration, mean arterial pressure (MAP) and heart rate. The effects of dynorphin and, less completely, those of DADLE were antagonized by the peripherally selective opioid antagonists N-methyl naloxone bromide (NMN) 1.3 mg kg-1 and N-methyl levallorphan methanesulphonate (NML) 1-3 mg kg-1. 3. In pentobarbitone-anaesthetized rabbits, DADLE 3-30 micrograms kg-1 min-1 and dynorphin 0.3-3 micrograms kg-1 min-1 decreased the plasma noradrenaline concentration and MAP. The highest dose of dynorphin also decreased heart rate, whereas DADLE 10 micrograms kg-1 min-1 caused slight cardioacceleration. The effects of DADLE but not those of dynorphin decreased upon repeated administration. 4. The effects of dynorphin 10 micrograms kg-1 min-1 were abolished or greatly attenuated by NMN 1.3 mg kg-1 and NML 3 mg kg-1. In contrast, the antagonists reduced only slightly the blood pressure-lowering effect of DADLE 10 micrograms kg-1 min-1 and did not reduce significantly the effects of DADLE on the plasma noradrenaline level and heart rate.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.阿片类激动剂通过节后交感神经纤维上的突触前受体影响家兔离体的心血管组织以及有髓兔子的心血管系统。进行本实验是为了研究在麻醉的兔子中由这些受体的活化产生的作用。 2.在有电刺激的交感神经流出的皮兔中,输注[D-Ala2-D-Leu5]-脑啡肽(DADLE)10微克kg-1 min-1和强啡肽-(1-13)(强啡肽)1微克kg- 1 min-1降低血浆去甲肾上腺素浓度,平均动脉压(MAP)和心率。外周选择性阿片类药物拮抗剂N-甲基纳洛酮溴化物(NMN)1.3 mg kg-1和N-甲基左苯丙氨酸甲磺酸盐(NML)1-3 mg kg-1拮抗强啡肽和DADLE的作用。 3.在戊巴比妥麻醉的兔子中,DADLE 3-30微克kg-1 min-1和强啡肽0.3-3微克kg-1 min-1降低了血浆去甲肾上腺素浓度和MAP。强啡肽的最高剂量也会降低心率,而DADLE 10微克kg-1 min-1会引起轻微的心脏加速。重复给药后,DADLE的作用减弱,但强啡肽的作用未减弱。 4. NMN 1.3 mg kg-1和NML 3 mg kg-1消除或大大减弱了强啡肽10微克kg-1 min-1的作用。相比之下,拮抗剂仅轻微降低了DADLE 10微克kg-1 min-1的降血压作用,而没有显着降低DADLE对血浆去甲肾上腺素水平和心率的影响。(摘要截断为250字)

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