Recently, it has been shown that intrathecal injection of norepinephrine and the mixed A1/A2 adenosine agonist 5'-N-ethylcarboxamide adenosine (NECA) interact in a supra-additive manner to produce antinociception. The present studies were designed to determine whether alpha 1 or alpha 2 noradrenergic receptors are involved in producing the antinociception induced by NECA and norepinephrine. The results indicated that intrathecal injection of NECA (0.97-4.9 nmol), the alpha 2 noradrenergic agonist clonidine (3.8-375 nmol), or the alpha 1 agonist phenylephrine (4.9-73.4 nmol) produced dose-dependent antinociception in rats. Furthermore, intrathecal injection of subeffective doses of NECA and clonidine interacted supra-additively to produce potent antinociception. In contrast, no supra-additive interaction was observed between NECA and phenylephrine. The supra-additive interaction of NECA and clonidine did not appear to result from alterations in cardiovascular tone because changes in blood pressure and nociceptive thresholds were not correlated in time. These results suggest that the noradrenergic component of the supra-additive interaction between adenosine A2 receptor agonists and noradrenergic agonists is mediated by alpha 2 noradrenergic receptors.

译文

最近,已经显示鞘内注射去甲肾上腺素和混合的A1/A2腺苷激动剂5 '-N-乙基羧酰胺腺苷 (NECA) 以超加成方式相互作用以产生抗伤害感受。本研究旨在确定 α1或 α2去甲肾上腺素能受体是否参与产生NECA和去甲肾上腺素诱导的抗伤害感受。结果表明,鞘内注射NECA (0.97-4.9 nmol),α2去甲肾上腺素能激动剂可乐定 (3.8-375 nmol) 或 α1激动剂去氧肾上腺素 (4.9-73.4 nmol) 在大鼠中产生剂量依赖性的抗伤害感受。此外,鞘内注射有效剂量的NECA和可乐定可相互作用,从而产生有效的抗伤害感受。相反,在NECA和去氧肾上腺素之间未观察到超加成相互作用。NECA和可乐定的超加性相互作用似乎不是由心血管张力的改变引起的,因为血压和伤害性阈值的变化与时间无关。这些结果表明,腺苷A2受体激动剂和去甲肾上腺素能激动剂之间的超加成相互作用的去甲肾上腺素能成分是由 α2去甲肾上腺素能受体介导的。

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