Rump L C, Majewski H
J Cardiovasc Pharmacol. 1987 Apr;9(4):500-7. doi: 10.1097/00005344-198704000-00016.
The aim of this study was to investigate alpha-adrenoceptor modulation of norepinephrine (NE) release from sympathetic nerves in rat isolated perfused kidney. After preincubation with [3H]NE, the renal nerves were stimulated. The stimulation-induced (S-I) outflow of radioactivity was used as an index of NE release. Clonidine (0.1 mumol/L) decreased the S-I outflow of radioactivity. This effect was abolished by the alpha 1-adrenoceptor antagonist idazoxan (0.1 mumol/L) but not by the alpha 2-adrenoceptor antagonist prazosin (0.1 mumol/L). Methoxamine (10 mumol/L) also had an inhibitory effect; this was abolished by prazosin (0.1 mumol/L), but not by idazoxan. Individually, these alpha-blocking drugs and the alpha 1-adrenoceptor antagonist corynanthine (0.3 mumol/L) enhanced S-I outflow of radioactivity. In the presence of indomethacin (10 mumol/L), the inhibitory effect of methoxamine was abolished but clonidine still inhibited S-I outflow of radioactivity. The facilitatory effect of prazosin was also unaltered by indomethacin. These results suggest the existence of inhibitory prejunctional alpha 1- and alpha 2-adrenoceptors in the kidney. The inhibitory effect of methoxamine seems to be mediated through prostaglandin inhibition of NE release. However, the evidence for inhibitory prejunctional alpha 1-adrenoceptors rests solely on the facilitatory effects of prazosin and corynanthine.
本研究的目的是探讨大鼠离体灌注肾中去甲肾上腺素(NE)从交感神经释放的α-肾上腺素能受体调节。用[³H]NE预孵育后,刺激肾神经。刺激诱导的放射性流出用作NE释放的指标。可乐定(0.1μmol/L)降低了刺激诱导的放射性流出。这种作用被α₁-肾上腺素能受体拮抗剂咪唑克生(0.1μmol/L)消除,但未被α₂-肾上腺素能受体拮抗剂哌唑嗪(0.1μmol/L)消除。甲氧明(10μmol/L)也有抑制作用;这被哌唑嗪(0.1μmol/L)消除,但未被咪唑克生消除。单独使用这些α-阻断药物和α₁-肾上腺素能受体拮抗剂育亨宾(0.3μmol/L)可增强放射性的刺激诱导流出。在吲哚美辛(10μmol/L)存在下,甲氧明的抑制作用被消除,但可乐定仍抑制放射性的刺激诱导流出。吲哚美辛对哌唑嗪的促进作用也无改变。这些结果表明肾中存在抑制性节前α₁和α₂-肾上腺素能受体。甲氧明的抑制作用似乎是通过前列腺素对NE释放的抑制介导的。然而,抑制性节前α₁-肾上腺素能受体的证据仅基于哌唑嗪和育亨宾的促进作用。