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关于不同受体亚型参与血管紧张素II在大鼠交感神经效应器部位的节前和节后作用的证据。

Evidence for the involvement of different receptor subtypes in the pre- and postjunctional actions of angiotensin II at rat sympathetic neuroeffector sites.

作者信息

Cox S L, Ben A, Story D F, Ziogas J

机构信息

Department of Medical Laboratory Science, RMIT, Melbourne, Victoria, Australia.

出版信息

Br J Pharmacol. 1995 Mar;114(5):1057-63. doi: 10.1111/j.1476-5381.1995.tb13313.x.

Abstract
  1. The effects of the nonpeptide angiotensin II receptor (AT) antagonists losartan and PD 123319 on actions of angiotensin II in the rat caudal artery and rat vas deferens preparations were investigated. 2. Angiotensin II (1.0 microM) increased perfusion pressure in isolated segments of the rat caudal artery. This increase in perfusion pressure was prevented by the AT1-antagonist, losartan (0.1 microM) but was not affected by the AT2-antagonist, PD 123319 (0.1 microM). 3. Angiotensin II (0.1-3.0 microM) produced a concentration-dependent enhancement of the stimulation-induced (S-I) efflux of [3H]-noradrenaline from isolated segments of rat caudal artery in which the noradrenergic transmitter stores had been labelled with [3H]-noradrenaline. The maximum enhancement of S-I efflux was approximately 60% with 1.0 microM angiotensin II. 4. Losartan (0.01 and 0.1 microM) reduced the enhancement of S-I efflux produced by 1.0 microM angiotensin II in the caudal artery. 5. PD 123319 (0.01 microM) did not affect the enhancement of S-I efflux produced by angiotensin II (1.0 microM) in the caudal artery. However, in a higher concentration (0.1 microM), PD 123319 reduced the enhancement of S-I efflux produced by 1.0 microM angiotensin II. 6. Angiotensin II produced concentration-dependent enhancement of the purinergic twitch responses (1 pulse/60 s) in the rat vas deferens. 7. Losartan (0.03 microM) and PD 123319 (0.03 microM) each reduced the angiotensin II-induced enhancement of the twitch responses in the rat vas deferens. 8. These findings indicate that the enhancement of sympathetic neuroeffector transmission in both the caudal artery and vas deferens of the rat involves angiotensin receptor subtype(s) sensitive to both losartan and PD 123319. In contrast, the direct vasoconstrictor effect of angiotensin II in the rat caudal artery involves activation of a receptor subtype sensitive only to losartan.
摘要
  1. 研究了非肽类血管紧张素II受体(AT)拮抗剂氯沙坦和PD 123319对大鼠尾动脉和大鼠输精管制剂中血管紧张素II作用的影响。2. 血管紧张素II(1.0微摩尔)可增加大鼠尾动脉离体节段的灌注压。AT1拮抗剂氯沙坦(0.1微摩尔)可阻止灌注压的升高,但AT2拮抗剂PD 123319(0.1微摩尔)对此无影响。3. 血管紧张素II(0.1 - 3.0微摩尔)可使大鼠尾动脉离体节段中[3H] - 去甲肾上腺素的刺激诱导(S - I)流出产生浓度依赖性增强,其中去甲肾上腺素能递质储存已用[3H] - 去甲肾上腺素标记。血管紧张素II浓度为1.0微摩尔时,S - I流出的最大增强约为60%。4. 氯沙坦(0.01和0.1微摩尔)可降低血管紧张素II(1.0微摩尔)在尾动脉中引起的S - I流出增强。5. PD 123319(0.01微摩尔)不影响血管紧张素II(1.0微摩尔)在尾动脉中引起的S - I流出增强。然而,在较高浓度(0.1微摩尔)时,PD 123319可降低血管紧张素II(1.0微摩尔)引起的S - I流出增强。6. 血管紧张素II可使大鼠输精管中嘌呤能抽搐反应(1次脉冲/60秒)产生浓度依赖性增强。7. 氯沙坦(0.03微摩尔)和PD 123319(0.03微摩尔)均可降低血管紧张素II诱导的大鼠输精管抽搐反应增强。8. 这些发现表明,大鼠尾动脉和输精管中交感神经效应器传递的增强涉及对氯沙坦和PD 123319均敏感 的血管紧张素受体亚型。相反,血管紧张素II在大鼠尾动脉中的直接血管收缩作用涉及仅对氯沙坦敏感的受体亚型的激活。

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