Division of Endocrinology and Metabolism, Department of Medicine, University of California San Diego.
Division of Endocrinology and Metabolism, Department of Medicine, University of California San Diego;
J Vis Exp. 2021 Jun 8(172). doi: 10.3791/62775.
Preclinical studies in mice often rely on invasive protocols, such as injections or oral gavage, to deliver drugs. These stressful routes of administration have significant effects on important metabolic parameters including food intake and body weight. Although an attractive option to circumvent this is to compound the drug in rodent food or dissolve it in water, these approaches also have limitations as they are affected by drug stability at room temperature for extended periods of time, the drug's solubility in water, and that the dosing is highly dependent on timing of food or water intake. The constant availability of the drug also limits translational relevance on how drugs are administered to patients. To overcome these limitations, drugs can be mixed with highly palatable food, such as peanut butter, allowing mice to self-administer compounds. Mice reliably and reproducibly consume the drug/peanut butter pellet in a short time frame. This approach facilitates a delivery approach with minimal stress compared with an injection or gavage. This protocol demonstrates the approach of drug preparation, animal acclimatization to placebo delivery, and drug delivery. The implications of this approach are discussed in studies related to timing of drug administration and the circadian rhythm.
在小鼠的临床前研究中,通常依赖于注射或口服灌胃等侵入性方案来给药。这些有压力的给药途径对包括食物摄入和体重在内的重要代谢参数有显著影响。虽然将药物复合在啮齿动物食物中或溶解在水中是一种有吸引力的选择,但这些方法也存在局限性,因为它们受到药物在室温下长时间稳定性、药物在水中的溶解度以及给药高度依赖于食物或水摄入时间的影响。药物的持续供应也限制了药物在患者中的给药方式的转化相关性。为了克服这些限制,可以将药物与非常美味的食物(如花生酱)混合,让老鼠自行服用化合物。老鼠在短时间内可靠且可重复地消耗药物/花生酱丸。与注射或灌胃相比,这种方法提供了一种应激最小的给药方式。该方案展示了药物制备、动物对安慰剂给药的适应以及药物给药的方法。该方法的意义在与药物给药时间和昼夜节律相关的研究中进行了讨论。