Department of Physiology, Royal College of Surgeons in Ireland, 123 St. Stephen's Green, Dublin 2, Ireland.
Department of Physiology, Royal College of Surgeons in Ireland, 123 St. Stephen's Green, Dublin 2, Ireland.
Eur J Pharmacol. 2015 Jul 5;758:142-6. doi: 10.1016/j.ejphar.2015.03.079. Epub 2015 Apr 8.
The stimulants cathinone (from Khat leaves) and methylenedioxymeth-amphetamine (MDMA) produce adrenoceptor mediated tachycardia and vasopressor actions that may be the result of direct receptor stimulation, actions on the noradrenaline transporter, and/or displacement of noradrenaline from nerve terminals. Effects of cathinone or MDMA were compared with those of the indirect sympathomimetic tyramine. Male Wistar rats were anaesthetized with pentobarbitone for blood pressure and heart rate recording. Some rats were sympathectomised by treatment with 6-hydroxydopamine. In the anaesthetised rat, cathinone, MDMA and tyramine (all 0.001-1 mg/kg) produced marked tachycardia, tyramine produced marked pressor responses and MDMA produced small pressor responses. The tachycardia to cathinone and MDMA was almost abolished by propranolol (1mg/kg). Pretreatment with cocaine (1mg/kg) did not significantly affect the tachycardia to cathinone or MDMA, but reduced the response to tyramine. However, in sympathectomised rats, the tachycardia to cathinone or MDMA was markedly attenuated, but the tachycardia to tyramine was only partially reduced. Blood pressure effects of tyramine and MDMA were also markedly attenuated by sympathectomy. The results demonstrate firstly that cocaine may not be the most suitable agent for assessing direct versus indirect agonism in cardiovascular studies. Secondly, the use of chemical sympathectomy achieved the desired goal of demonstrating that cardiac β-adrenoceptor mediated actions of cathinone and MDMA are probably largely indirect.
刺激剂卡西酮(来自阿拉伯茶)和 3,4-亚甲基二氧甲基苯丙胺(MDMA)产生肾上腺素能受体介导的心动过速和血管加压作用,这可能是直接受体刺激、对去甲肾上腺素转运体的作用以及/或从神经末梢置换去甲肾上腺素的结果。比较了卡西酮或 MDMA 的作用与间接拟交感胺酪胺的作用。雄性 Wistar 大鼠用戊巴比妥钠麻醉以记录血压和心率。一些大鼠用 6-羟多巴胺处理进行交感神经切除术。在麻醉大鼠中,卡西酮、MDMA 和酪胺(均为 0.001-1mg/kg)产生明显的心动过速,酪胺产生明显的升压反应,而 MDMA 产生较小的升压反应。普萘洛尔(1mg/kg)几乎完全消除了卡西酮和 MDMA 的心动过速。可卡因(1mg/kg)预处理对卡西酮或 MDMA 的心动过速没有显著影响,但降低了对酪胺的反应。然而,在交感神经切除大鼠中,卡西酮或 MDMA 的心动过速明显减弱,但酪胺的心动过速仅部分减少。交感神经切除术也显著减弱了酪胺和 MDMA 的血压效应。结果表明,首先,可卡因可能不是评估心血管研究中直接与间接激动作用的最合适药物。其次,化学交感神经切除术达到了预期的目标,即证明了卡西酮和 MDMA 的心脏β-肾上腺素能受体介导作用可能主要是间接的。