Department of Biology & Institute of Biochemistry, Carleton University, Ottawa, Ontario, K1S 5B6, Canada.
Environmental Health Science and Research Bureau, Health Canada, Ottawa, Ontario K1A 0K9, Canada.
Endocrinology. 2021 Jun 1;162(6). doi: 10.1210/endocr/bqab050.
Human studies consistently show an association between exposure to persistent organic pollutants, including 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, aka "dioxin"), and increased diabetes risk. We previously showed that a single high-dose TCDD exposure (20 µg/kg) decreased plasma insulin levels in male and female mice in vivo, but effects on glucose homeostasis were sex-dependent.
The current study assessed whether prolonged exposure to a physiologically relevant low-dose of TCDD impacts glucose homeostasis and/or the islet phenotype in a sex-dependent manner in chow-fed or high-fat diet (HFD)-fed mice.
Male and female mice were exposed to 20 ng/kg/d TCDD 2×/week for 12 weeks and simultaneously fed standard chow or a 45% HFD. Glucose homeostasis was assessed by glucose and insulin tolerance tests, and glucose-induced plasma insulin levels were measured in vivo. Histological analysis was performed on pancreas from male and female mice, and islets were isolated from females for TempO-Seq transcriptomic analysis.
Low-dose TCDD exposure did not lead to adverse metabolic consequences in chow-fed male or female mice, or in HFD-fed males. However, TCDD accelerated the onset of HFD-induced hyperglycemia and impaired glucose-induced plasma insulin levels in females. TCDD caused a modest increase in islet area in males but reduced the percent beta cell area within islets in females. TempO-Seq analysis suggested abnormal changes to endocrine and metabolic pathways in female TCDDHFD islets.
Our data suggest that prolonged low-dose TCDD exposure has minimal effects on glucose homeostasis and islet morphology in chow-fed male and female mice but promotes maladaptive metabolic responses in HFD-fed females.
人体研究一致表明,接触持久性有机污染物(包括 2,3,7,8-四氯二苯并对二恶英(TCDD,又名“二恶英”))与糖尿病风险增加有关。我们之前的研究表明,单次高剂量 TCDD 暴露(20μg/kg)会降低雄性和雌性小鼠体内的血浆胰岛素水平,但对葡萄糖稳态的影响具有性别依赖性。
本研究评估了长期暴露于生理相关低剂量 TCDD 是否会以性别依赖的方式影响食用标准饲料或高脂肪饮食(HFD)的雄性和雌性小鼠的葡萄糖稳态和/或胰岛表型。
雄性和雌性小鼠每周两次接受 20ng/kg/d TCDD 暴露 12 周,并同时喂食标准饲料或 45%HFD。通过葡萄糖和胰岛素耐量试验评估葡萄糖稳态,体内测量葡萄糖诱导的血浆胰岛素水平。对雄性和雌性小鼠的胰腺进行组织学分析,并从雌性小鼠中分离胰岛进行 TempO-Seq 转录组分析。
低剂量 TCDD 暴露不会导致食用标准饲料的雄性或雌性小鼠或 HFD 喂养的雄性小鼠出现不良代谢后果。然而,TCDD 加速了 HFD 诱导的雌性高血糖的发生,并损害了葡萄糖诱导的血浆胰岛素水平。TCDD 导致雄性胰岛面积略有增加,但降低了雌性胰岛内β细胞面积的百分比。TempO-Seq 分析表明,雌性 TCDDHFD 胰岛中内分泌和代谢途径发生了异常变化。
我们的数据表明,长期低剂量 TCDD 暴露对食用标准饲料的雄性和雌性小鼠的葡萄糖稳态和胰岛形态几乎没有影响,但会促进 HFD 喂养的雌性小鼠产生适应性不良的代谢反应。