糖尿病药物疗法对胰岛素抵抗大鼠尼古丁、食物和水摄入量的影响

Sebastian Ortegon, Priscilla Giner, Bryan Cruz, Luis M. Carcoba, Benjamin Clapp, Deborah J. Clegg, Laura E. O’Dell
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摘要

我们以雌性和雄性大鼠为研究对象,评估了糖尿病药物与尼古丁摄入量之间的交叉性。简而言之,给大鼠喂食高脂饮食(HFD)或普通饮食(RD)4周。然后,各组分别接受药物或低剂量链脲佐菌素(STZ;25 毫克/千克)。三天后,通过测量注射胰岛素(0.75 U/kg)后 180 分钟的血浆葡萄糖水平来评估胰岛素抵抗。然后给大鼠准备颈静脉导管,让它们在家中的笼子里进行23小时的尼古丁静脉自我给药(IVSA),4天为一个周期,3天强制戒断,在笼子里吃各自的食物。在静脉自我给药期间,记录它们对食物和水的操作反应以及体重变化。在施用药物治疗之前,大鼠可摄入两种剂量的尼古丁(0.015 毫克/千克和 0.03 毫克/千克,其余研究剂量为 0.015 毫克/千克)。然后,每天在暗周期开始时(下午 6 点)按照以下顺序注射药物治疗:1)达帕格列净(3.0 然后 10.0 mg/kg);2)胰岛素(0.75 U/kg,两次);3)溴隐亭(3.0 然后 10.0 mg/kg)。结果表明,HFD+STZ方案诱导了雌性和雄性大鼠的胰岛素抵抗。此外,无论性别如何,HFD喂养大鼠的尼古丁摄入量均高于RD对照组。给予胰岛素,而不是达帕格列净或溴隐亭,可使高密度脂蛋白喂养大鼠的尼古丁摄入量恢复到控制水平。这些结果对胰岛素控制糖尿病患者摄入过多尼古丁的潜在疗效具有临床意义。
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Effectiveness of pharmacotherapies for diabetes on nicotine, food, and water intake in insulin-resistant rats
The intersectionality between diabetes medications and nicotine consumption was assessed in female and male rats. Briefly, the rats were fed a high-fat diet (HFD) or regular diet (RD) for 4 weeks. Then separate groups received vehicle or a low dose of streptozotocin (STZ; 25 mg/kg). Three days later, insulin resistance was assessed by measuring plasma glucose levels for 180 min following an injection of insulin (0.75 U/kg). The rats were then prepared with jugular catheters, and they were given 23 h access to nicotine intravenous self-administration (IVSA) in 4 days cycles with 3 days of forced abstinence in their home cages where they consumed their respective diet. During the IVSA sessions, operant responses for food and water and changes in body weight were recorded. Prior to administration of the pharmacotherapies, the rats were given access to two doses of nicotine (0.015 then 0.03 mg/kg for the remainder of the study). Then, daily injections of the pharmacotherapies were given at the onset of dark cycle (6 p.m.) in the following order: 1) dapagliflozin (3.0 then 10.0 mg/kg), 2) insulin (0.75 U/kg twice), and 3) bromocriptine (3.0 then 10.0 mg/kg). The results suggest that our HFD+STZ regiment induced insulin resistance in female and male rats. Also, the HFD-fed rats displayed higher nicotine intake than RD controls, regardless of sex. Administration of insulin, but not dapagliflozin or bromocriptine, normalized nicotine intake in HFD-fed rats to control levels. These results have clinical implications regarding the potential efficacy of insulin to control excessive nicotine intake in persons with diabetes.
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