Jin Ziqi, Cao Yingying, Zou Huiqiong, Hao Peipei, Xue Yongzhi
Institute of Pharmacokinetics and Liver Molecular Pharmacology, Department of Pharmacology, Baotou Medical College, Baotou, Inner Mongolia, China.
Iran J Pharm Res. 2022 Sep 10;21(1):e129483. doi: 10.5812/ijpr-129483. eCollection 2022 Dec.
The use of police breath alcohol detectors in rat breath alcohol detection experiments has always been a challenge because of the small lung capacity and inability of rats to actively inhale. However, the method of using gas chromatography to detect blood alcohol concentration is time-consuming, complex, relatively expensive, and cannot achieve on-site detection and multi-point unlimited non-invasive detection.
In this study, a laboratory method was validated for rat breath ethanol concentration (BrAC) measurement to estimate blood ethanol concentration (BAC) in rats.
The rats were placed in a gas collection bottle, the breath sample was drawn out with a syringe, and injected into the mouthpiece of the breath alcohol detector through a rubber tube. The results were immediately detected and automatically converted to BAC. Male rats were randomly divided into three groups. The control group received an intraperitoneal injection of normal saline, the liver injury group received an intraperitoneal injection of 50% Carbon tetrachloride (CCL4 1 mL.kg), and the induction group received an intraperitoneal injection of phenobarbital sodium (75 mg.kg). Western blot analysis was used to detect the protein expression of CYP2E1. Similar grouping and experimental methods were used for female rats.
This method was reproducible. The metabolic activity of CYP2E1 was downregulated in the injury group and upregulated in the induction group, which was consistent with the results obtained for CYP2E1 protein expression.
Our results confirmed that the rat gas cylinder breath alcohol assay can be used for multiple detections with immediate and non-invasive determination of alcohol metabolizing capacity. This is important for studies that require repeated assessment of blood alcohol levels.
由于大鼠肺容量小且无法主动吸气,在大鼠呼气酒精检测实验中使用警用呼气酒精探测器一直是一项挑战。然而,使用气相色谱法检测血液酒精浓度的方法耗时、复杂、相对昂贵,且无法实现现场检测和多点无限制非侵入性检测。
本研究验证了一种用于测量大鼠呼气乙醇浓度(BrAC)以估计大鼠血液乙醇浓度(BAC)的实验室方法。
将大鼠置于集气瓶中,用注射器抽出呼气样本,并通过橡胶管注入呼气酒精探测器的吹嘴中。结果立即被检测到并自动转换为BAC。雄性大鼠随机分为三组。对照组腹腔注射生理盐水,肝损伤组腹腔注射50%四氯化碳(CCL4 1 mL·kg),诱导组腹腔注射苯巴比妥钠(75 mg·kg)。采用蛋白质免疫印迹分析检测CYP2E1的蛋白表达。雌性大鼠采用类似的分组和实验方法。
该方法具有可重复性。损伤组中CYP2E1的代谢活性下调,诱导组中上调,这与CYP2E1蛋白表达的结果一致。
我们的结果证实,大鼠气瓶呼气酒精检测可用于多次检测,即时且非侵入性地测定酒精代谢能力。这对于需要反复评估血液酒精水平的研究很重要。