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使用新型β-肾上腺素能受体阻断药物替他洛尔对正常血压和高血压大鼠肾脏中突触前β-肾上腺素能受体的研究。

Study of prejunctional beta-adrenoceptors in kidneys of normotensive and hypertensive rats using the new beta-adrenoceptor blocking drug tertatolol.

作者信息

Verbeuren T J, Herman A G

出版信息

Am J Nephrol. 1986;6 Suppl 2:30-5. doi: 10.1159/000167330.

Abstract

The prejunctional beta-adrenoceptors present in the isolated perfused kidney of normotensive rats (NR) and spontaneously hypertensive rats (SHR) were compared and the effects of tertatolol on these receptors were investigated. Kidneys of NR (Wistar + Wistar-Kyoto [WKY]) and SHR, were continuously perfused with Tyrode solution at constant flow and the changes in perfusion pressure were monitored. The constrictor responses to norepinephrine (2-8 X 10(-10) moles) were slightly but significantly decreased by isoproterenol (2 X 10(-7) M) to a similar degree in NR and SHR. Tertatolol (3 X 10(-7) M) did not alter the constriction caused by norepinephrine, but abolished the dilator response to isoproterenol. Electrical stimulation of renal nerves (8 Hz) evoked constrictions in both NR and SHR; these constrictor responses were augmented in the presence of isoproterenol (2 X 10(-7) M) to a similar extent in NR and SHR. In kidneys of NR and SHR, previously incubated with 3H norepinephrine, renal nerve electrical stimulation (6 Hz) evoked an overflow of the 3H transmitter. This overflow was enhanced by isoproterenol (2 X 10(-6) M) to a similar degree in NR and SHR. Both the augmented constrictor response and the augmented overflow of 3H norepinephrine caused by electrical stimulation in the presence of isoproterenol, were inhibited by tertatolol (3 X 10(-7) M). Our results show that the beta-receptor agonist isoproterenol evokes comparable effects at prejunctional beta-adrenoceptors in kidneys of NR and SHR; they also show that tertatolol is an inhibitor of pre- and postjunctional beta-adrenoceptors in the renal circulation of the rat.

摘要

比较了正常血压大鼠(NR)和自发性高血压大鼠(SHR)离体灌注肾脏中存在的节前β-肾上腺素能受体,并研究了替他洛尔对这些受体的影响。将NR(Wistar + Wistar-Kyoto [WKY])和SHR的肾脏以恒定流量用台氏液连续灌注,并监测灌注压力的变化。在NR和SHR中,异丙肾上腺素(2×10⁻⁷ M)使对去甲肾上腺素(2 - 8×10⁻¹⁰摩尔)的收缩反应略有但显著降低,降低程度相似。替他洛尔(3×10⁻⁷ M)未改变去甲肾上腺素引起的收缩,但消除了对异丙肾上腺素的舒张反应。肾神经电刺激(8 Hz)在NR和SHR中均引起收缩;在异丙肾上腺素(2×10⁻⁷ M)存在下,这些收缩反应在NR和SHR中增强程度相似。在预先用³H去甲肾上腺素孵育的NR和SHR肾脏中,肾神经电刺激(6 Hz)引起³H递质溢出。在NR和SHR中,异丙肾上腺素(2×10⁻⁶ M)使这种溢出增强程度相似。在异丙肾上腺素存在下,电刺激引起的增强的收缩反应和³H去甲肾上腺素的增强的溢出,均被替他洛尔(3×10⁻⁷ M)抑制。我们的结果表明,β受体激动剂异丙肾上腺素在NR和SHR肾脏的节前β-肾上腺素能受体上引起类似的效应;它们还表明,替他洛尔是大鼠肾循环中节前和节后β-肾上腺素能受体的抑制剂。

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