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尽管成年自发性高血压大鼠体内AT2受体的表达增强,但其血管紧张素II介导的血管舒张作用仍减弱。

Angiotensin II-mediated vasodilation is reduced in adult spontaneously hypertensive rats despite enhanced expression of AT2 receptors.

作者信息

Ognibene D T, Oliveira P R B, Marins de Carvalho L C R, Costa C A, Espinoza L A, Criddle D N, Tano T, Soares de Moura R, Resende A C

机构信息

Department of Pharmacology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Clin Exp Pharmacol Physiol. 2009 Jan;36(1):12-9. doi: 10.1111/j.1440-1681.2008.05054.x. Epub 2008 Sep 26.

DOI:10.1111/j.1440-1681.2008.05054.x
PMID:18986337
Abstract
  1. The vasodilator action of angiotensin (Ang) II has not yet been demonstrated in spontaneously hypertensive rats (SHR), nor have any possible changes in this response during the development of hypertension. 2. In the present study, the vasodilator effect of AngII was evaluated in the rat isolated, preconstricted mesenteric arterial bed (MAB) from 6- (young) and 24-week-old (adult) SHR and compared with effects on MAB from age-matched normotensive rats (control). 3. Angiotensin II (10-300 nmol) induced vasodilation in noradrenaline (NA)-preconstricted MAB that was greater in vessels from young compared with adult rats in both the control and SHR groups. Angiotensin II-induced vasodilation was reduced by the angiotensin AT(2) receptor antagonist PD 123319 (10 micromol/L), the angiotensin-(1-7) receptor antagonist A779 (1 micromol/L) and the bradykinin B(2) receptor antagonist HOE-140 (0.01 micromol/L), but not by the AT(1) receptor antagonist losartan (30 micromol/L). Expression of AT(2) receptors was weak in vessels from adult control rats compared with that in young control rats, whereas in young SHR AT(2) receptor expression was increased compared with that in young control rats. This increased expression of AT(2) receptors was maintained in adult SHR and there was no significant difference in AT(2) receptor expression between young and old SHR. 4. The findings of the present suggest that AngII induces an AT(2) receptor-mediated vasodilator effect in the MAB via activation of angiotensin-(1-7) and bradykinin receptors, an action that is reduced in adult control rats and adult SHR. In adult control rats, the attenuated response of AngII is probably due to endothelial dysfunction and reduced expression of AT(2) receptors, whereas in adult SHR it is associated with endothelial dysfunction alone. Increased expression of AT(2) receptors in SHR may represent a counteracting response for modulating blood pressure.
摘要
  1. 血管紧张素(Ang)II的血管舒张作用尚未在自发性高血压大鼠(SHR)中得到证实,在高血压发展过程中这种反应也未出现任何可能的变化。2. 在本研究中,评估了AngII对6周龄(幼年)和24周龄(成年)SHR分离的、预先收缩的肠系膜动脉床(MAB)的血管舒张作用,并与年龄匹配的正常血压大鼠(对照)的MAB的作用进行比较。3. 血管紧张素II(10 - 300 nmol)在去甲肾上腺素(NA)预先收缩的MAB中诱导血管舒张,在对照组和SHR组中,幼年大鼠血管的舒张作用均大于成年大鼠。血管紧张素II诱导的血管舒张被血管紧张素AT(2)受体拮抗剂PD 123319(10 μmol/L)、血管紧张素-(1 - 7)受体拮抗剂A779(1 μmol/L)和缓激肽B(2)受体拮抗剂HOE - 140(0.01 μmol/L)减弱,但不被AT(1)受体拮抗剂氯沙坦(30 μmol/L)减弱。与幼年对照大鼠相比,成年对照大鼠血管中AT(2)受体的表达较弱,而与幼年对照大鼠相比,幼年SHR中AT(2)受体的表达增加。成年SHR中AT(2)受体的这种增加表达得以维持,幼年和成年SHR之间AT(2)受体表达无显著差异。4. 本研究结果表明,AngII通过激活血管紧张素-(1 - 7)和缓激肽受体在MAB中诱导AT(2)受体介导的血管舒张作用,这种作用在成年对照大鼠和成年SHR中减弱。在成年对照大鼠中,AngII反应减弱可能是由于内皮功能障碍和AT(2)受体表达降低,而在成年SHR中,它仅与内皮功能障碍有关。SHR中AT(2)受体表达增加可能代表一种调节血压的抵消反应。

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