Rosenberg H C
Pharmacol Biochem Behav. 1980 Sep;13(3):415-20. doi: 10.1016/0091-3057(80)90248-8.
Toxic actions of flurazepam (FZP) were studied in cats, mice and rats. High doses caused an apparent central excitation, most clearly seen as clonic convulsions, superimposed on general depression. Following a lethal dose, death was always associated with convulsions. Comparing the relative sensitivity to central depression and excitation revealed that rats were least likely to have convulsions at doses that did not first cause loss of consciousness, while cats most clearly showed marked central excitatory actions. Signs of FZP toxocity in cats included excessive salivation, extreme apprehensive behavior, retching, muscle tremors and convulsions. An interaction between FZP and pentylenetetrazol (PTZ) was shown by pretreating mice with FZP before PTZ challenge. As a function of dose, FZP first protected against convulsions and death. At higher doses, however, convulsions again emerged. These doses of FZP were lower than those that would alone cause convulsions. These results may be relevant to the use of FZP in clinical situations in which there is increased neural excitability, such as epilepsy or sedative-hypnotic drug withdrawal.
在猫、小鼠和大鼠身上研究了氟西泮(FZP)的毒性作用。高剂量会引起明显的中枢兴奋,最明显的表现为阵挛性惊厥,叠加在全身抑制之上。给予致死剂量后,死亡总是与惊厥相关。比较对中枢抑制和兴奋的相对敏感性发现,在未首先导致意识丧失的剂量下,大鼠最不容易发生惊厥,而猫最明显地表现出明显的中枢兴奋作用。猫的FZP毒性迹象包括流涎过多、极度焦虑行为、干呕、肌肉震颤和惊厥。在戊四氮(PTZ)激发前用FZP预处理小鼠,显示出FZP与PTZ之间存在相互作用。作为剂量的函数,FZP首先预防惊厥和死亡。然而,在更高剂量下,惊厥再次出现。这些FZP剂量低于单独会引起惊厥的剂量。这些结果可能与FZP在神经兴奋性增加的临床情况中的使用有关,例如癫痫或镇静催眠药戒断。