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Blockade of cholinergic transmission elicits somatic signs in nicotine-na?ve adolescent rats

机译:胆碱能传递的阻断引起幼年尼古丁大鼠的体征

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High doses of the nicotinic acetylcholine receptor (nAChR) antagonist mecamylamine can elicit somatic signs resembling those associated with nicotine withdrawal in nicotine-na?ve adult rats. Understanding this phenomenon, and its possible modulation by acute nicotine and age, could inform the use of mecamylamine as both an experimental tool and potential pharmacotherapy for tobacco dependence and other disorders. This study evaluated the ability of high-dose mecamylamine to elicit somatic signs in adolescent rats, and the potential for acute nicotine pretreatment to potentiate this effect as previously reported in adults. Single or repeated injections of mecamylamine (1.5 or 3.0 mg/kg, s.c.) elicited somatic signs in nicotine-na?ve adolescents, but this effect was not influenced by 2 h pretreatment with acute nicotine (0.5 mg/kg, s.c.). In an initial evaluation of the effects of age in this model, mecamylamine (2.25 mg/kg, s.c.) elicited somatic signs in nicotine-na?ve adolescents and adults. This effect was modestly enhanced following acute nicotine injections in adults but not in adolescents, even when a higher nicotine dose (1.0 rather than 0.5 mg/kg, s.c.) was used in adolescents to account for age differences in nicotine pharmacokinetics. These studies are the first to show that mecamylamine elicits somatic signs in nicotine-na?ve adolescent rats, an effect that should be considered when designing and interpreting studies examining effects of high doses of mecamylamine in adolescents. Our findings also provide preliminary evidence that these signs may be differentially modulated by acute nicotine pretreatment in adolescents versus adults.
机译:高剂量的烟碱乙酰胆碱受体(nAChR)拮抗剂美加明可以引起幼稚的成年大鼠体内类似尼古丁戒断的体征。了解这种现象及其可能受到急性尼古丁和年龄的调节,可能会有助于将美加明胺用作烟草依赖和其他疾病的实验工具和潜在药物疗法。这项研究评估了大剂量美加明胺在青春期大鼠体内引起体征的能力,以及急性尼古丁预处理增强这种作用的潜力,如先前在成人中报道的那样。单次或反复注射美加明胺(1.5或3.0 mg / kg,皮下注射)会在未接受烟碱的青少年中引起体征,但急性尼古丁(0.5 mg / kg,皮下注射)预处理2 h不会影响这种效果。在对该模型中年龄影响的初步评估中,美卡敏(2.25 mg / kg,s.c.)在未使用过尼古丁的青少年和成人中引起体征。即使在青少年中使用较高的尼古丁剂量(1.0而不是0.5 mg / kg,皮下注射)来解决尼古丁药代动力学的年龄差异,成人急性尼古丁注射后,这种作用仍会适度增强,而不是在青少年中。这些研究是第一个显示美卡敏在幼年烟碱幼鼠中引起体征的研究,在设计和解释检查高剂量美卡敏在青少年中的作用时应考虑该作用。我们的发现还提供了初步的证据,这些证据表明,青少年与成人相比,急性尼古丁预处理可能会对这些症状有所不同。

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