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Psychoneuroendocrinology. 2013 Oct;38(10):2343-53. doi: 10.1016/j.psyneuen.2013.05.005. Epub 2013 Jun 12.
2
Sex differences in escalation of methamphetamine self-administration: cognitive and motivational consequences in rats.性别的差异在冰毒自我给药的升级中:大鼠的认知和动机后果。
Psychopharmacology (Berl). 2012 Oct;223(4):371-80. doi: 10.1007/s00213-012-2727-8. Epub 2012 May 17.
3
Human sex differences in d-amphetamine self-administration.人类在自我给药中对安非他命的性别差异。
Addiction. 2010 Apr;105(4):727-31. doi: 10.1111/j.1360-0443.2009.02858.x. Epub 2010 Feb 9.
4
Impact of repeated methamphetamine pretreatment on intravenous self-administration of the drug in males and estrogenized or non- estrogenized ovariectomized female rats.重复给予甲基苯丙胺预处理对雄性大鼠以及去卵巢后雌激素化或未雌激素化的雌性大鼠静脉注射该药物进行自我给药行为的影响。
Neuro Endocrinol Lett. 2009;30(5):663-70.
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Sex differences in (+)-amphetamine- and (+)-methamphetamine-induced behavioral response in male and female Sprague-Dawley rats.雄性和雌性斯普拉格-道利大鼠中,(+)-苯丙胺和(+)-甲基苯丙胺诱导的行为反应的性别差异。
Pharmacol Biochem Behav. 2007 Jan;86(1):140-9. doi: 10.1016/j.pbb.2006.12.018. Epub 2007 Jan 9.
6
Methamphetamine blood concentrations in human abusers: application to pharmacokinetic modeling.人体滥用者的甲基苯丙胺血药浓度:在药代动力学建模中的应用。
Synapse. 2007 Apr;61(4):216-20. doi: 10.1002/syn.20365.
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Menstrual cycle phase and responses to drugs of abuse in humans.月经周期阶段与人类对滥用药物的反应。
Drug Alcohol Depend. 2006 Sep 1;84(1):1-13. doi: 10.1016/j.drugalcdep.2005.12.007. Epub 2006 Jan 18.
8
Sex- and dose-dependency in the pharmacokinetics and pharmacodynamics of (+)-methamphetamine and its metabolite (+)-amphetamine in rats.大鼠体内(+)-甲基苯丙胺及其代谢产物(+)-苯丙胺药代动力学和药效学的性别及剂量依赖性
Toxicol Appl Pharmacol. 2005 Dec 15;209(3):203-13. doi: 10.1016/j.taap.2005.04.007.
9
Development of a liquid chromatography-tandem mass spectrometric method for the determination of methamphetamine and amphetamine using small volumes of rat serum.建立一种使用少量大鼠血清测定甲基苯丙胺和苯丙胺的液相色谱-串联质谱法。
J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Jul 5;806(2):81-7. doi: 10.1016/j.jchromb.2004.03.038.
10
Effects of murine-derived anti-methamphetamine monoclonal antibodies on (+)-methamphetamine self-administration in the rat.鼠源抗甲基苯丙胺单克隆抗体对大鼠(+)-甲基苯丙胺自身给药的影响。
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甲基苯丙胺在雄性和雌性大鼠体内自我给药的药代动力学。

The pharmacokinetics of methamphetamine self-administration in male and female rats.

作者信息

Milesi-Hallé Alessandra, Hambuchen Michael D, McMillan Donald E, Michael Owens S

机构信息

Department of Pharmacology and Toxicology, College of Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham, Little Rock, AR 72205, USA.

出版信息

Drug Alcohol Depend. 2015 May 1;150:164-9. doi: 10.1016/j.drugalcdep.2015.02.032. Epub 2015 Mar 9.

DOI:10.1016/j.drugalcdep.2015.02.032
PMID:25796510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4387073/
Abstract

BACKGROUND

Because methamphetamine (METH) pharmacokinetics after single iv doses show significant differences between male and female rats, we hypothesized that pharmacokinetic differences in METH disposition could be a contributing factor to the patterns of METH self-administration behaviors in rats.

METHODS

For the studies, we used a passive (non-contingent) METH dosing schedule consisting of 27 METH iv bolus injections (0.048mg/kg) over 2h derived from a previous active (contingent) METH self-administration behavioral study in male rats. After METH dosing of male and female Sprague-Dawley rats (n=5/group), METH and amphetamine serum concentrations were determined by LC-MS/MS. Pharmacokinetic analysis, including predictive mathematical simulations of the data, was then conducted.

RESULTS

Male and female rats achieved relatively stable METH serum concentrations within 20min, which remained constant from 20 to 120min. While not statistically different, METH clearance and volume of distribution values for females were 25% and 33% lower (respectively) than males. Linear regression analysis of predicted METH concentrations from pharmacokinetic simulations versus observed concentrations showed a substantially better correlation with male data than female data (r(2)=0.71 vs. 0.56; slope=0.95 vs. 0.45, respectively). At 120min, the time of predicted peak METH serum concentrations, female values were 42% higher than expected, while male values were within 3%.

CONCLUSIONS

Unlike METH male pharmacokinetic data, the female data was less predictable during multiple METH administrations and produced overall higher than expected METH concentrations. These findings demonstrate that METH pharmacokinetics could contribute to differences in METH self-administration behaviors in rats.

摘要

背景

由于单次静脉注射剂量的甲基苯丙胺(METH)在雄性和雌性大鼠中的药代动力学表现出显著差异,我们推测METH处置的药代动力学差异可能是导致大鼠METH自我给药行为模式的一个因素。

方法

在这些研究中,我们采用了一种被动(非条件性)METH给药方案,该方案由27次静脉推注METH(0.048mg/kg)组成,在2小时内完成,此方案源自先前一项针对雄性大鼠的主动(条件性)METH自我给药行为研究。对雄性和雌性斯普拉格-道利大鼠(每组n = 5)进行METH给药后,通过液相色谱-串联质谱法(LC-MS/MS)测定METH和苯丙胺的血清浓度。然后进行药代动力学分析,包括对数据的预测性数学模拟。

结果

雄性和雌性大鼠在20分钟内达到了相对稳定的METH血清浓度,在20至120分钟内保持恒定。虽然无统计学差异,但雌性的METH清除率和分布容积值分别比雄性低25%和33%。药代动力学模拟预测的METH浓度与观察到的浓度的线性回归分析显示,与雄性数据的相关性明显优于雌性数据(r²分别为0.71和0.56;斜率分别为0.95和0.45)。在120分钟时,即预测的METH血清浓度峰值时间,雌性的值比预期高42%,而雄性的值在3%以内。

结论

与雄性METH药代动力学数据不同,雌性数据在多次METH给药期间较难预测,并且产生的METH浓度总体高于预期。这些发现表明,METH药代动力学可能导致大鼠METH自我给药行为的差异。