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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Repeated exposure of adolescent rats to oral methylphenidate does not induce behavioral sensitization or cross-sensitization to nicotine
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Repeated exposure of adolescent rats to oral methylphenidate does not induce behavioral sensitization or cross-sensitization to nicotine

机译:青春期大鼠反复接触口服哌醋甲酯不会引起对尼古丁的行为敏化或交叉敏化

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Several lines of evidence indicate that the use of stimulant drugs, including methylphenidate (MPD), increases tobacco smoking. This has raised concerns that MPD use during adolescence could facilitate nicotine abuse. Preclinical studies have shown that repeated treatment with an addictive drug produces sensitization to that drug and usually cross-sensitization to other drugs. Behavioral sensitization has been implicated in the development of drug addiction. We examined whether repeated oral MPD administration during adolescence could induce behavioral sensitization to MPD and long-lasting cross-sensitization to nicotine. Adolescent male Wistar rats were treated orally with 10 mg/kg MPD or saline (SAL) from postnatal day (PND) 27 to 33. To evaluate behavioral sensitization to MPD in adolescent rats (PND 39), the SAL pretreated group was subdivided into two groups that received intragastric SAL (1.0 mL/kg) or MPD (10 mg/kg); MPD pretreated rats received MPD (10 mg/kg). Cross-sensitization was evaluated on PND 39 or PND 70 (adulthood). To this end, SAL- and MPD-pretreated groups received subcutaneous injections of SAL (1.0 mL/kg) or nicotine (0.4 mg/kg). All groups had 8 animals. Immediately after injections, locomotor activity was determined. The locomotor response to MPD challenge of MPD-pretreated rats was not significantly different from that of the SAL-pretreated group. Moreover, the locomotor response of MPD-pretreated rats to nicotine challenge was not significantly different from that of the SAL-pretreated group. This lack of sensitization and cross-sensitization suggests that MPD treatment during adolescence does not induce short- or long-term neuroadaptation in rats that could increase sensitivity to MPD or nicotine.
机译:有几条证据表明,使用兴奋剂,包括哌醋甲酯(MPD),可增加吸烟。这引起了人们的担忧,即在青春期使用MPD可能会促进尼古丁滥用。临床前研究表明,用成瘾性药物反复治疗会引起对该药物的致敏,并通常对其他药物产生交叉致敏。行为致敏作用与药物成瘾的发展有关。我们检查了青春期反复口服MPD是否可以引起对MPD的行为致敏和对尼古丁的长期交叉致敏。从出生后第27天到第33天,口服10 mg / kg MPD或生理盐水(SAL)治疗青春期雄性Wistar大鼠。为评估青春期大鼠(PND 39)对MPD的行为敏感性,将SAL预处理组分为两类接受胃内SAL(1.0 mL / kg)或MPD(10 mg / kg)的组;经MPD预处理的大鼠接受MPD(10 mg / kg)。在PND 39或PND 70(成人)上评估交叉敏化。为此,SAL和MPD预处理组接受皮下注射SAL(1.0 mL / kg)或尼古丁(0.4 mg / kg)。所有组有8只动物。注射后立即确定运动活性。 MPD预处理的大鼠对MPD攻击的运动反应与SAL预处理的组无明显差异。此外,MPD预处理的大鼠对尼古丁攻击的运动反应与SAL预处理的组没有显着差异。这种缺乏致敏性和交叉致敏性的现象表明,青春期进行MPD治疗不会引起大鼠短期或长期的神经适应,而这可能会增加对MPD或尼古丁的敏感性。

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