Cathine and cathinone disposition kinetics and neurotransmitter profile in several organs of rats exposed to a single dose of Catha edulis (Vahl) Forssk. ex Endl. extract.

Q2 Pharmacology, Toxicology and Pharmaceutics Drug metabolism and personalized therapy Pub Date : 2023-06-01 DOI:10.1515/dmpt-2022-0154
Ahmad M Alamir, Mohammed A Jeraiby, Hesham M Korashy, Emad Sayed Shaheen, Mohammad A Attafi, Magbool E Oraiby, Ahmed M Hakami, Mohammed Y Albeishy, Ibrahim A Khardali, Ismail A Juraybi, Abeer A Alobaida, Ibraheem M Attafi
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引用次数: 1

Abstract

Objectives: Catha edulis (Vahl) Forssk. ex Endl. (Khat) is a stimulant plant that contains cathine and cathinone, which its abuses induce euphoria, alertness, and motor activity. Since the toxicokinetics of these substances remain unclear, this study was carried out to investigate the disposition kinetics of cathine and cathinone, the neurotransmitter profile, following a single dose of C. edulis extract in rats.

Methods: Twenty-four adult male Wistar albino rats (250-300 g) were randomly selected and divided into six groups of four rats each. All groups received a single oral dose of 2,000 mg/kg body weight, and blood and tissue samples from the brain, lung, heart, liver, and kidney were obtained at intervals of 0.5, 1, 2.5, 5, 12, and 24 h. The cathine and cathinone concentrations were identified and quantified using ion trap ultra-high performance liquid chromatography (HPLC-IT/MS). The neurotransmitter profile was detected using the quadrupole time of flight UPLC-QTOF/MS method.

Results: The lung, liver, and heart tissues attained the highest levels of cathine, while the highest level of cathinone was determined in the heart. Cathine and cathinone concentrations in the blood and heart peaked at 0.5 h. The concentrations peaked in the brain 2.5 h later, indicating that the heart had an immediate effect, whereas the brain had a longer-lasting one. They have longer half-lives (2.68 and 5.07 h, respectively) and may remain in the brain for longer durations (3.31 and 2.31 h, respectively). The neurotransmitters epinephrine, dopamine, norepinephrine, and serotonin were detected in a delayed, prolonged and organ-specific manner.

Conclusions: Cathine and cathinone were deposited in considerable concentrations in all tissues analyzed, with the highest Cmax in the lung and Tmax in the heart tissues but not in the brain. In addition, neurotransmitters such as adrenaline, dopamine, norepinephrine, and serotonin were differentially detected in all tested samples in a organ-specific fashion. More study is needed to identify cathine and cathinone's effects on neurotransmitter profiles. Nevertheless, these findings provided a further basis for experimental, clinical, and forensic investigations.

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暴露于单剂量长春花的大鼠的几个器官中的Cathine和Cathine酮处置动力学和神经递质谱。Endl交货。提取。
目的:Catha edulis (Vahl) Forssk。Endl交货。(阿拉伯茶)是一种兴奋剂植物,含有cathine和cathinone,其滥用会引起欣快感,警觉性和运动活动。由于这些物质的毒性动力学尚不清楚,本研究旨在研究单剂量毛竹提取物对大鼠体内碱和卡西酮(神经递质)的处置动力学。方法:取成年雄性Wistar白化大鼠24只(250 ~ 300 g),随机分为6组,每组4只。所有组均给予单次口服剂量2000 mg/kg体重,每隔0.5、1、2.5、5、12和24 h分别取脑、肺、心、肝和肾的血液和组织样本。采用离子阱超高效液相色谱(HPLC-IT/MS)鉴定和定量cathine和cathinone的浓度。采用四极杆飞行时间UPLC-QTOF/MS法检测神经递质谱。结果:肺、肝、心脏组织中卡西酮含量最高,而心脏组织中卡西酮含量最高。血液和心脏中的凯瑟琳和卡西酮浓度在0.5小时达到峰值,2.5小时后大脑中的浓度达到峰值,这表明心脏有立竿见影的效果,而大脑有更持久的效果。它们的半衰期较长(分别为2.68和5.07小时),并可能在大脑中停留较长时间(分别为3.31和2.31小时)。神经递质肾上腺素、多巴胺、去甲肾上腺素和血清素以延迟、延长和器官特异性的方式检测。结论:所分析的各组织中均有相当浓度的Cathine和cathinone沉积,Cmax在肺组织中最高,Tmax在心脏组织中最高,而在脑组织中最低。此外,神经递质如肾上腺素、多巴胺、去甲肾上腺素和血清素在所有测试样本中以器官特异性的方式被不同地检测到。需要更多的研究来确定cathine和cathinone对神经递质谱的影响。然而,这些发现为实验、临床和法医调查提供了进一步的基础。
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来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
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