Silveri M M, Spear L P
Department of Psychology and Center for Developmental Psychobiology, Binghamton University, NY 13902-6000, USA.
Alcohol Clin Exp Res. 1999 Jul;23(7):1180-4.
Alcohol use typically begins during adolescence. Little is known regarding the antecedents and impact of this early alcohol use, although age-related changes in the neural systems modulating alcohol sensitivity could contribute to the propensity of adolescents to consume alcohol. We have previously observed a marked ontogenetic decline in acute tolerance to ethanol (EtOH), with preweanling pups exhibiting the most acute tolerance (Silveri and Spear, 1998). The objective of this study was to assess whether rapid tolerance shows a similar ontogenetic profile.
In Experiment I of the present study, female and male Sprague-Dawley preweanling rats at postnatal day (P) 16 or young adults at P56 were examined. On Day 1, preweanlings were pretreated with saline, 1.5, 3.5, or 5.0 g/kg EtOH and adults were pretreated with saline or 3.5 g/kg EtOH. This was followed by challenge with 3.5 g/kg EtOH and assessment of ethanol-induced sleep time on Day 2. In Experiment II, adolescents at P36 were pretreated with saline, 3.5, or 5.0 g/kg EtOH on Day 1 before Day 2 assessment of sleep time after 3.5 g/kg EtOH. Upon awakening, animals were killed and whole brains removed and analyzed for brain alcohol levels (BrALs).
Rapid tolerance was observed in P36 and P56 animals, with EtOH-pretreated animals exhibiting significantly shorter sleep times than age-matched animals treated with saline. In contrast, no evidence for rapid tolerance was seen after any pretreatment dose at P16. Interestingly, although EtOH-pretreated adults woke at higher BrALs than saline-treated adults, this pattern was not evident in the adolescents, which suggests that at this age, metabolic tolerance may play a prominent role in the expression of rapid tolerance. Thus, it seems as though the ability to develop rapid tolerance to EtOH hypnosis emerges during adolescence and continues into adulthood.
Together with previous findings that adolescent animals also display substantial acute tolerance to alcohol (Silveri and Spear, 1998), the propensity of adolescents for developing these two forms of tolerance may have important implications for the increased voluntary consumption of alcohol at this age relative to other ages.
饮酒行为通常始于青春期。尽管调节酒精敏感性的神经系统中与年龄相关的变化可能促使青少年饮酒,但对于这种早期饮酒行为的前因后果及影响却知之甚少。我们之前观察到,幼崽对乙醇(EtOH)的急性耐受性在个体发育过程中显著下降,断奶前的幼崽表现出最强的急性耐受性(西尔维里和斯皮尔,1998年)。本研究的目的是评估快速耐受性是否呈现出类似的个体发育特征。
在本研究的实验一中,对出生后第16天(P16)的雌性和雄性斯普拉格-道利断奶前大鼠或P56的成年大鼠进行了检测。第1天,给断奶前大鼠分别用生理盐水、1.5、3.5或5.0 g/kg乙醇预处理,给成年大鼠用生理盐水或3.5 g/kg乙醇预处理。随后在第2天用3.5 g/kg乙醇进行激发,并评估乙醇诱导的睡眠时间。在实验二中,在第2天评估3.5 g/kg乙醇后的睡眠时间之前,于第1天给P36的青少年大鼠用生理盐水、3.5或5.0 g/kg乙醇预处理。动物苏醒后处死,取出全脑并分析脑酒精水平(BrALs)。
在P36和P56的动物中观察到了快速耐受性,用乙醇预处理的动物的睡眠时间明显短于用生理盐水处理的同龄动物。相比之下,在P16的任何预处理剂量后均未观察到快速耐受性的证据。有趣的是,尽管用乙醇预处理的成年大鼠比用生理盐水处理的成年大鼠在更高的脑酒精水平时苏醒,但这种模式在青少年中并不明显,这表明在这个年龄,代谢耐受性可能在快速耐受性的表现中起主要作用。因此,似乎对乙醇催眠产生快速耐受性的能力在青春期出现并持续到成年期。
与之前的研究结果一致,即青少年动物对酒精也表现出显著的急性耐受性(西尔维里和斯皮尔,1998年),青少年形成这两种耐受性的倾向可能对该年龄段相对于其他年龄段自愿饮酒量增加具有重要意义。