Regulatory Toxicology Research Division, Bureau of Chemical Safety, Food Directorate, HPFB, Health Canada, Ottawa, ON, Canada.
Departments of Biology and Chemistry, Institute of Biochemistry, Carleton University, Ottawa, ON, Canada.
Cardiovasc Toxicol. 2022 Jun;22(6):558-578. doi: 10.1007/s12012-022-09738-6. Epub 2022 Apr 16.
Obesity, ethanol, and contaminants are known risk factors of cardiovascular and metabolic diseases (CMD). However, their interplay on clinical profiles of these diseases remains unclear, and thus were investigated in this study. Male lean or obese JCR rats were given water or 10% ethanol and orally treated with or without a contaminant mixture (CM) dissolved in corn oil and loaded on two cookies at 0, 1.6, or 16 mg/kg BW/day dose levels for 4 weeks. The CM consisted 22 environmental contaminants found in human blood or serum of Northern populations. Over 60 parameters related to CMD were examined. The results revealed that obesity in JCR rats resembles the clinical profiles of non-alcoholic fatty liver disease in humans. Obesity was also associated with increased serum and organ retention of mercury, one of the chemical components of CM. Exposure to ethanol lightened hyperlipidemia, increased liver retention of mercury, and increased risk for hypertension in the obese rats. CM lessened hyperlipidemia and hyperenzymemia, worsened systemic inflammation and increased the risk for hypertension in the obese rats. CM markedly increased serum ethanol levels with or without ethanol exposure. Tissue total mercury contents significantly correlated with clinical parameters with altered profiles by both ethanol and obesity. These results suggest that obese individuals may be more prone to contaminant accumulation. Ethanol and CM exposure can alter clinical profiles associated with obesity, which may lead to misdiagnosis of CMD associated with obesity. CM can alter endogenous production and/or metabolism of ethanol, further complicating disease progression, diagnosis, and treatment.
肥胖、乙醇和污染物是心血管和代谢疾病 (CMD) 的已知危险因素。然而,它们在这些疾病的临床特征中的相互作用尚不清楚,因此本研究对此进行了调查。雄性瘦或肥胖 JCR 大鼠给予水或 10%乙醇,并口服给予或不给予玉米油溶解的污染物混合物 (CM),剂量为 0、1.6 或 16mg/kgBW/天,持续 4 周。CM 由 22 种在人类血液或北方人群血清中发现的环境污染物组成。检查了 60 多个与 CMD 相关的参数。结果表明,JCR 大鼠的肥胖与人类非酒精性脂肪性肝病的临床特征相似。肥胖还与血清和器官中汞(CM 的一种化学成分)的保留增加有关。暴露于乙醇可减轻高脂血症,增加肥胖大鼠肝脏中汞的保留,并增加高血压的风险。CM 减轻了肥胖大鼠的高脂血症和高酶血症,加重了全身炎症,并增加了高血压的风险。CM 明显增加了血清乙醇水平,无论是否暴露于乙醇。组织总汞含量与临床参数显著相关,这些参数受乙醇和肥胖改变了特征。这些结果表明,肥胖个体可能更容易发生污染物积累。乙醇和 CM 暴露会改变与肥胖相关的临床特征,这可能导致肥胖相关 CMD 的误诊。CM 可以改变内源性乙醇的产生和/或代谢,从而使疾病的进展、诊断和治疗更加复杂。