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糖尿病药物疗法对胰岛素抵抗大鼠尼古丁、食物及水摄入量的影响。

Effectiveness of pharmacotherapies for diabetes on nicotine, food, and water intake in insulin-resistant rats.

作者信息

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

机构信息

Department of Psychology, The University of Texas at El Paso, El Paso, TX, United States.

Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, United States.

出版信息

Adv Drug Alcohol Res. 2024 Jan 4;3:11812. doi: 10.3389/adar.2023.11812. eCollection 2023.

Abstract

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.

摘要

在雌性和雄性大鼠中评估了糖尿病药物与尼古丁摄入之间的交叉关系。简要来说,将大鼠分为高脂饮食(HFD)组或正常饮食(RD)组,喂养4周。然后,不同组分别给予赋形剂或低剂量链脲佐菌素(STZ;25mg/kg)。三天后,通过在注射胰岛素(0.75U/kg)后180分钟测量血浆葡萄糖水平来评估胰岛素抵抗。随后给大鼠植入颈静脉导管,让它们在4天的周期内有23小时可进行尼古丁静脉自我给药(IVSA),期间有3天在其饲养笼中强制戒断,在此期间它们食用各自的饮食。在IVSA期间,记录对食物和水的操作性反应以及体重变化。在给予药物治疗之前,给大鼠使用两剂尼古丁(在研究的剩余时间里,先给予0.015mg/kg,然后是0.03mg/kg)。然后,在黑暗周期开始时(下午6点)按以下顺序每日注射药物治疗:1)达格列净(先给予3.0mg/kg,然后是10.0mg/kg),2)胰岛素(0.75U/kg,注射两次),3)溴隐亭(先给予3.0mg/kg,然后是10.0mg/kg)。结果表明,我们的HFD+STZ方案在雌性和雄性大鼠中诱导了胰岛素抵抗。此外,无论性别如何,高脂饮食喂养的大鼠比正常饮食对照组显示出更高的尼古丁摄入量。给予胰岛素可使高脂饮食喂养的大鼠的尼古丁摄入量恢复到对照水平,而达格列净或溴隐亭则不能。这些结果对于胰岛素控制糖尿病患者过量尼古丁摄入的潜在疗效具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49f1/10880793/ea4842135e97/adar-03-11812-g001.jpg

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