Omar N M, Abbas A M, Abdel-Malek H, Suddek G M
Mansoura University Department of Medical Physiology, Faculty of Medicine Mansoura Egypt.
Acta Physiol Hung. 2013 Sep;100(3):266-79. doi: 10.1556/APhysiol.100.2013.3.3.
For evaluating the age-related change in noradrenaline (NA)-induced contraction of isolated rat carotid artery (CA), the effect of α and β adrenoreceptor (AR) blockers and the role of nitric oxide (NO) were investigated.
Concentration-response curves to NA (10-10-10-4 M) and α1 agonist phenylephrine (PE; 10-10-10-5 M) were constructed in isolated CA rings from young and middle-aged rats. The effects of nitric oxide synthase (NOS) inhibitor (L-NAME; 100 μM), α1-AR antagonist (prazosin; 0.1 μM), α2-AR antagonist (yohimbine; 0.1 μM) and β-AR antagonist (propranolol; 1 μM) on NA-induced contraction of isolated CA rings were examined. In CA rings preconstricted with NA, the responses to α2-AR agonist (clonidine; 10-7-10-5 M), β-AR agonist (isoprenaline; 10-8-10-5 M),), sodium nitroprusside (SNP; 10-9-10-5 M) were assessed.
The maximum contractile response of CA to NA and to PE was higher in younger than in middle-aged rats. Prazosin reduced the contractile response to NA in both groups, while propranolol, yohimbine and L-NAME did not affect NA-induced contraction in either of them. Clonidine, isoprenaline and SNP produced a dose-dependent vasorelaxation of CA rings, isoprenaline-induced vasodilatation was lower in middle-aged rats, while there was no difference in clonidine or SNP-induced relaxant effect between the two groups.
NA-induced contraction of isolated rat CA rings is decreased in old rats, this is related to α1-AR. β-AR mediated dilatation was compromised in middle-aged rats (endothelium-dependent). α2-AR and SNP-mediated dilator effect seems to be unchanged.
为评估去甲肾上腺素(NA)诱导的离体大鼠颈动脉(CA)收缩的年龄相关变化,研究了α和β肾上腺素能受体(AR)阻滞剂的作用以及一氧化氮(NO)的作用。
构建来自年轻和中年大鼠的离体CA环对NA(10⁻¹⁰ - 10⁻⁴ M)和α1激动剂去氧肾上腺素(PE;10⁻¹⁰ - 10⁻⁵ M)的浓度 - 反应曲线。研究一氧化氮合酶(NOS)抑制剂(L - NAME;100 μM)、α1 - AR拮抗剂(哌唑嗪;0.1 μM)、α2 - AR拮抗剂(育亨宾;0.1 μM)和β - AR拮抗剂(普萘洛尔;1 μM)对NA诱导的离体CA环收缩的影响。在用NA预收缩的CA环中,评估对α2 - AR激动剂(可乐定;10⁻⁷ - 10⁻⁵ M)、β - AR激动剂(异丙肾上腺素;10⁻⁸ - 10⁻⁵ M)、硝普钠(SNP;10⁻⁹ - 10⁻⁵ M)的反应。
CA对NA和PE的最大收缩反应在年轻大鼠中高于中年大鼠。哌唑嗪降低了两组对NA的收缩反应,而普萘洛尔、育亨宾和L - NAME对两组中NA诱导的收缩均无影响。可乐定、异丙肾上腺素和SNP产生了CA环的剂量依赖性血管舒张,异丙肾上腺素诱导的血管舒张在中年大鼠中较低,而两组之间可乐定或SNP诱导的舒张作用无差异。
老年大鼠中NA诱导的离体大鼠CA环收缩降低,这与α1 - AR有关。中年大鼠中β - AR介导的扩张受损(内皮依赖性)。α2 - AR和SNP介导的舒张作用似乎未改变。