Bergman Jack, Delatte Marcus S, Paronis Carol A, Vemuri Kiran, Thakur Ganesh A, Makriyannis Alex
McLean Hospital-Harvard Medical School. Belmont MA USA.
Physiol Behav. 2008 Mar 18;93(4-5):666-70. doi: 10.1016/j.physbeh.2007.11.007. Epub 2007 Nov 12.
The CB1 inverse agonist/antagonist SR141716A recently has been introduced for the management of obesity (rimonabant; Acomplia) and appears to have beneficial effects. However, its utility may be hampered in some individuals by adverse effects including nausea or emesis or by mood depression. The recent development of biochemically 'neutral' antagonists such as AM4113 (Sink et al., 2007) has allowed an initial evaluation of the proposition that adverse effects of SR141716A are associated with its inverse agonist activity. Thus far, data comparing SR141716A and AM4113 across several species indicate that both drugs produce dose-related direct effects on operant behavior within the same range of doses that serve to antagonize the behavioral and hypothermic effects of a CB1 agonist. However, initial observations suggest that AM4113 may not produce preclinical indications of nausea or emesis. Further studies with AM4113 and other novel CB1 antagonists differing in efficacy should amplify our understanding of the relationship between the pharmacological activity of CB1 antagonists and their behavioral effects.
CB1反向激动剂/拮抗剂SR141716A(利莫那班;Acomplia)最近已被用于治疗肥胖症,且似乎具有有益效果。然而,在一些个体中,其效用可能会受到包括恶心或呕吐等不良反应或情绪低落的阻碍。最近开发的生化“中性”拮抗剂,如AM4113(Sink等人,2007年),使得对SR141716A的不良反应与其反向激动剂活性相关这一命题进行初步评估成为可能。到目前为止,在多个物种中比较SR141716A和AM4113的数据表明,两种药物在相同剂量范围内对操作性行为产生剂量相关的直接影响,这些剂量可拮抗CB1激动剂的行为和体温过低效应。然而,初步观察表明,AM4113可能不会产生恶心或呕吐的临床前指征。对AM4113和其他功效不同的新型CB1拮抗剂进行进一步研究,应能加深我们对CB1拮抗剂的药理活性与其行为效应之间关系的理解。