Dick A L W, Simpson A, Qama A, Andrews Z, Lawrence A J, Duncan J R
Division of Behavioural Neuroscience, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, Vic., Australia.
Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich, Germany.
Br J Pharmacol. 2015 Nov;172(21):5174-87. doi: 10.1111/bph.13284. Epub 2015 Oct 22.
Abuse of toluene-containing inhalants is an increasing public health problem, especially among adolescents. Abuse during adolescence is associated with emaciation, while industrial exposure leads to altered glycaemic control suggesting metabolic instability. However, the relationship between adolescent inhalant abuse and metabolic dysfunction remains unknown.
To model human abuse patterns, we exposed male adolescent Wistar rats [postnatal day (PND) 27] to chronic intermittent inhaled toluene (CIT, 10,000 ppm) or air (control) for 1 h·day(-1) , three times a week for 4 weeks. Feeding and body composition were monitored. After 4 weeks, circulating metabolic hormone concentrations and responses to a glucose tolerance test (GTT) were measured. Dietary preference was measured by giving animals access to either a 'western diet' plus standard chow (WC + SC) or standard chow alone during 4 weeks of abstinence. Metabolic hormones and GTT were subsequently measured.
Adolescent CIT exposure significantly retarded weight gain, altered body composition, circulating metabolic hormones and responses to a GTT. While reduced body weight persisted, responses to a GTT and circulating hormones appeared to normalize for animals on standard chow following abstinence. In CIT-exposed WC + SC rats, we observed impaired glucose tolerance associated with altered metabolic hormones. Analysis of hypothalamic genes revealed differential expression profiles in CIT-exposed rats following both the exposure period and abstinence, suggesting a central contribution to inhalant-induced metabolic dysfunction.
CIT exposure during adolescence has long-term effects on metabolic function, which may increase the risk of disorders related to energy balance and glycaemic control.
含甲苯吸入剂的滥用是一个日益严重的公共卫生问题,尤其是在青少年中。青少年滥用与消瘦有关,而职业暴露会导致血糖控制改变,提示代谢不稳定。然而,青少年吸入剂滥用与代谢功能障碍之间的关系尚不清楚。
为模拟人类滥用模式,我们将雄性青春期Wistar大鼠[出生后第(PND)27天]暴露于慢性间歇性吸入甲苯(CIT,10,000 ppm)或空气(对照)中,每天1小时,每周3次,持续4周。监测进食和身体组成。4周后,测量循环代谢激素浓度和对葡萄糖耐量试验(GTT)的反应。通过在4周禁欲期内让动物选择“西方饮食”加标准饲料(WC + SC)或仅选择标准饲料来测量饮食偏好。随后测量代谢激素和GTT。
青春期CIT暴露显著延缓体重增加,改变身体组成、循环代谢激素以及对GTT的反应。虽然体重减轻持续存在,但禁欲后食用标准饲料的动物对GTT的反应和循环激素似乎恢复正常。在暴露于CIT的WC + SC大鼠中,我们观察到与代谢激素改变相关的葡萄糖耐量受损。下丘脑基因分析显示,暴露期和禁欲后,CIT暴露大鼠的基因表达谱存在差异,提示中枢神经系统对吸入剂诱导的代谢功能障碍有影响。
青春期CIT暴露对代谢功能有长期影响,这可能增加与能量平衡和血糖控制相关疾病的风险。