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Additional specific drugs and compounds of interest from which the drug moiety may be derived include, but are not limited to: Central nervous system depressants: general anesthetics (barbiturates, benzodiazepines, steroids, cyclohexanone derivatives, and miscellaneous agents), sedative-hypnotics (benzodiazepines, barbiturates, piperidinediones and triones, quinazoline derivatives, carbamates, aldehydes and derivatives, amides, acyclic ureides, benzazepines and related drugs, phenothiazines, etc.), central voluntary muscle tone modifying drugs (anticonvulsants, such as hydantoins, barbiturates, oxazolidinediones, succinimides, acylureides, glutarimides, benzodiazepines, secondary and tertiary alcohols, dibenzazepine derivatives, valproic acid and derivatives, GABA analogs, etc.), analgesics (morphine and derivatives, oripavine derivatives, morphinan derivatives, phenylpiperidines, 2,6-methane-3-benzazocaine derivatives, diphenylpropylamines and isosteres, salicylates, p-aminophenol derivatives, 5- pyrazolone derivatives, arylacetic acid derivatives, fenamates and isosteres, naltrexone, methylnaltrexone, etc.) and antiemetics (anticholinergics, antihistamines, antidopaminergics, etc.), analgesic agents as disclosed in U

55 Longitudinal clinical study Participants in this longitudinal follow-up study were entirely distinct from those in the above cross-sectional study

However, this feature of astrocytes to modify and thereby inactivate xenobiotics has also to be considered in the context of the application of therapeutic drugs for the treatment of neurological disorders, as GSHdependent removal of such compounds in astrocytes may lower the therapeutic benefit of a given treatment

JAMA 309 , 24732479 (2013)