首页> 美国卫生研究院文献>Springer Open Choice >Motor vehicle collisions caused by the ‘super-strength’ synthetic cannabinoids MAM-2201 5F-PB-22 5F-AB-PINACA 5F-AMB and 5F-ADB in Japan experienced from 2012 to 2014
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Motor vehicle collisions caused by the ‘super-strength’ synthetic cannabinoids MAM-2201 5F-PB-22 5F-AB-PINACA 5F-AMB and 5F-ADB in Japan experienced from 2012 to 2014

机译:在2012年至2014年间日本的超强合成大麻素MAM-2201、5F-PB-22、5F-AB-PINACA5F-AMB和5F-ADB造成了汽车碰撞

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摘要

From 2012 to 2014 in Japan, 214 cases of motor vehicle collisions were attributed to the use of illegal drugs. In 93 out of 96 investigated cases, the causative agents were a variety of synthetic cannabinoids (SCs). These SCs can be classified into three groups according to the lineage of the chemical structures: (1) naphthoyl indoles, such as MAM-2201, (2) quinolinyl ester indoles, such as 5F-PB-22, and (3) indazole carboxamides, such as 5F-AB-PINACA, 5F-AMB, and 5F-ADB. These SCs became available sequentially with increasing cannabinoid CB1 agonist potencies and reached a nationwide outbreak in the summer of 2014. They caused acute intoxication with impaired consciousness, anterograde amnesia (impaired memory), catalepsy with muscle rigidity, tachycardia, and vomiting or drooling soon after smoking. Drivers who had abused one of these SCs might unexpectedly experience the acute intoxication that caused uncontrolled driving. These SCs were generally difficult to detect from body fluid samples. It is thought that the highly lipophilic SCs disappear from the blood via rapid degradation by liver enzymes and selective accumulation into adipose tissues. Thus, much effort should be directed to the development of fast and sensitive chemical detection of the drug usage.
机译:从2012年到2014年,日本有214起机动车违法事件归因于使用非法毒品。在调查的96个案例中,有93个的病因是各种合成大麻素(SC)。根据化学结构的谱系,这些SC可以分为三类:(1)萘甲吲哚,例如MAM-2201;(2)喹啉基吲哚,例如5F-PB-22;以及(3)吲唑羧酰胺,例如5F-AB-PINACA,5F-AMB和5F-ADB。这些SCs随大麻素CB1激动剂效力的增加而逐渐出现,并于2014年夏季在全国范围内爆发。它们引起急性中毒,意识障碍,顺行性健忘症(记忆力减退),僵直的僵直性僵直,心动过速以及不久后呕吐或流口水抽烟。滥用其中一种SC的驾驶员可能会意外地遭受急性中毒,从而导致无法控制的驾驶。这些SC通常很难从体液样本中检测出来。据认为,高度亲脂性的SC通过肝脏酶的快速降解和选择性地积累到脂肪组织中而从血液中消失。因此,应致力于开发快速,灵敏的药物使用化学检测方法。

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