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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Combined effects of diethylpropion and alcohol on locomotor activity of mice: participation of the dopaminergic and opioid systems
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Combined effects of diethylpropion and alcohol on locomotor activity of mice: participation of the dopaminergic and opioid systems

机译:二乙基丙酸和乙醇对小鼠运动功能的联合影响:多巴胺能和阿片样物质系统的参与

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The widespread consumption of anorectics and combined anorectic + alcohol misuse are problems in Brazil. In order to better understand the interactive effects of ethanol (EtOH) and diethylpropion (DEP) we examined the locomotion-activating effects of these drugs given alone or in combination in mice. We also determined whether this response was affected by dopamine (DA) or opioid receptor antagonists. A total of 160 male Swiss mice weighing approximately 30 g were divided into groups of 8 animals per group. The animals were treated daily for 7 consecutive days with combined EtOH + DEP (1.2 g/kg and 5.0 mg/kg, ip), EtOH (1.2 g/kg, ip), DEP (5.0 mg/kg, ip) or the control solution coadministered with the DA antagonist haloperidol (HAL, 0.075 mg/kg, ip), the opioid antagonist naloxone (NAL, 1.0 mg/kg, ip), or vehicle. On days 1, 7 and 10 after the injections, mice were assessed in activity cages at different times (15, 30, 45 and 60 min) for 5 min. The acute combination of EtOH plus DEP induced a significantly higher increase in locomotor activity (day 1: 369.5 ± 34.41) when compared to either drug alone (day 1: EtOH = 232.5 ± 23.79 and DEP = 276.0 ± 12.85) and to control solution (day 1: 153.12 ± 7.64). However, the repeated administration of EtOH (day 7: 314.63 ± 26.79 and day 10: 257.62 ± 29.91) or DEP (day 7: 309.5 ± 31.65 and day 10: 321.12 ± 39.24) alone or in combination (day 7: 459.75 ± 41.28 and day 10: 427.87 ± 33.0) failed to induce a progressive increase in the locomotor response. These data demonstrate greater locomotion-activating effects of the EtOH + DEP combination, probably involving DA and/or opioid receptor stimulation, since the daily pretreatment with HAL (day 1: EtOH + DEP = 395.62 ± 11.92 and EtOH + DEP + HAL = 371.5 ± 6.76; day 7: EtOH + DEP = 502.5 ± 42.27 and EtOH + DEP + HAL = 281.12 ± 16.08; day 10: EtOH + DEP = 445.75 ± 16.64 and EtOH + DEP + HAL = 376.75 ± 16.4) and NAL (day 1: EtOH + DEP = 553.62 ± 38.15 and EtOH + DEP + NAL = 445.12 ± 55.67; day 7: EtOH + DEP = 617.5 ± 38.89 and EtOH + DEP + NAL = 418.25 ± 61.18; day 10: EtOH + DEP = 541.37 ± 32.86 and EtOH + DEP + NAL = 427.12 ± 51.6) reduced the locomotor response induced by combined administration of EtOH + DEP. These findings also suggest that a major determinant of combined anorectic-alcohol misuse may be the increased stimulating effects produced by the combination.
机译:在巴西,厌食药的广泛消费以及厌食药和酒精的混合滥用是一个问题。为了更好地了解乙醇(EtOH)和二乙基丙酸(DEP)的相互作用,我们研究了这些药物在小鼠中单独或联合给予时的运动激活作用。我们还确定了该反应是否受到多巴胺(DA)或阿片受体拮抗剂的影响。将总共​​160只重约30g的瑞士雄性小鼠分成每组8只动物的组。每天用连续的EtOH + DEP(1.2 g / kg和5.0 mg / kg,ip),EtOH(1.2 g / kg,ip),DEP(5.0 mg / kg,ip)或对照组治疗动物,连续7天与DA拮抗剂氟哌啶醇(HAL,0.075 mg / kg,ip),阿片样物质拮抗剂纳洛酮(NAL,1.0 mg / kg,ip)或溶媒共同给药的溶液。在注射后的第1、7和10天,在不同时间(15、30、45和60分钟)的活动笼中评估小鼠5分钟。与单独使用任何一种药物(第1天:EtOH = 232.5±23.79和DEP = 276.0±12.85)和对照溶液相比,EtOH和DEP的急性结合诱导的运动活动明显增加(第1天:369.5±34.41)。第1天:153.12±7.64)。但是,单独或组合(第7天:459.75±41.28)重复施用EtOH(第7天:314.63±26.79和第10天:257.62±29.91)或DEP(第7天:309.5±31.65和第10天:321.12±39.24)和第10天:427.87±33.0)未能引起运动反应的逐步增强。这些数据表明,自从每天进行HAL预处理以来,EtOH + DEP组合可能具有DA和/或阿片样物质受体刺激作用,具有更大的运动激活作用(第1天:EtOH + DEP = 395.62±11.92,EtOH + DEP + HAL = 371.5 ±6.76;第7天:EtOH + DEP = 502.5±42.27和EtOH + DEP + HAL = 281.12±16.08;第10天:EtOH + DEP = 445.75±16.64和EtOH + DEP + HAL = 376.75±16.4)和NAL(第1天) :EtOH + DEP = 553.62±38.15和EtOH + DEP + NAL = 445.12±55.67;第7天:EtOH + DEP = 617.5±38.89和EtOH + DEP + NAL = 418.25±61.18;第10天:EtOH + DEP = 541.37±32.86 (EtOH + DEP + NAL = 427.12±51.6)降低了EtOH + DEP联合给药引起的运动反应。这些发现还表明,厌食药联合滥用的一个主要决定因素可能是该组合产生的刺激作用增加。

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