氟硝西泮在大鼠体内对酒精抑制作用的增效作用:皮层电图、呼吸和心电图研究

Luiz Freitas, Anthony Amaral, Raína Conceição, Gabriela Barbosa, Maria Klara Hamoy, Anara Barbosa, Clarissa Paz, Murilo Santos, Akira Hamoy, Allane Paz, Dielly Favacho-Lopes, Vanessa Mello, Moisés Hamoy
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摘要

酒精是一种广泛商业化的精神药物,苯二氮卓类药物氟硝西泮是一种抗焦虑药,被广泛用于治疗焦虑和失眠问题。这两种药物的滥用和联用是一些国家的公共卫生问题,由于其协同作用会增强不良反应,可能会造成瞬间、长期甚至致命的神经生理问题。本研究观察了这两种药物对 Wistar 大鼠大脑、心脏和呼吸频率的电生理反应的影响。共确定了 8 个实验组:对照组、1 个酒精组(20%,剂量为 1 毫升/100 克 VO)、3 个氟硝西泮组(剂量分别为 0.1、0.2 和 0.3 毫克/千克)和 3 个酒精-氟硝西泮组(20%,剂量为 1 毫升/100 克 VO 的酒精,分别与 0.1、0.2 和 0.3 毫克/千克的氟硝西泮)。结果显示,酒精-氟硝西泮组的α波和θ波功率下降更明显,β波振荡功率下降,镇静作用更强。在酒精-氟硝西泮联合用药组中,随着氟硝西泮剂量的增加,呼吸频率逐渐降低。观察到高剂量氟硝西泮会改变心率和 Q-T 间期。因此,我们得出结论,酒精-氟硝西泮联合用药会随着苯二氮卓剂量的增加而加深抑制协同效应,这可能会导致患者的低频脑振荡、呼吸和血液动力学发生变化。
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Potentiation of the depressant effect of alcohol by flunitrazepam in rats: an electrocorticographic, respiratory and electrocardiographic study

Alcohol, a widely commercialized psychotropic drug, and the benzodiazepine Flunitrazepam, an anxiolytic widely prescribed for patients with anxiety and insomnia problems, are well known drugs and both act on the central nervous system. The misuse and the association of these two drugs are public health concerns in several countries and could cause momentary, long-lasting and even lethal neurophysiological problems due to the potentiation of their adverse effects in synergy. The present study observed the result of the association of these drugs on electrophysiological responses in the brain, heart, and respiratory rate in Wistar rats. 8 experimental groups were determined: control, one alcohol group (20% at a dose of 1 ml/100 g VO), three Flunitrazepam groups (doses 0.1; 0.2 and 0.3 mg/kg) and three alcohol-Flunitrazepam groups (20% at a dose of 1 ml/100 g VO of alcohol, combined with 0.1; 0.2 and 0.3 mg/kg of Flunitrazepam, respectively). The results showed that there was a more pronounced reduction in alpha and theta wave power in the alcohol-Flunitrazepam groups, a decrease in the power of beta oscillations and greater sedation. There was a progressive decrease in respiratory rate linked to the increase of Flunitrazepam dose in the alcohol-Flunitrazepam associated administration. It was observed alteration in heart rate and Q-T interval in high doses of Flunitrazepam. Therefore, we conclude that the association alcohol-Flunitrazepam presented deepening of depressant synergistic effects according to the increase in the dose of the benzodiazepine, and this could cause alterations in low frequency brain oscillations, breathing, and hemodynamics of the patient.

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