Antidepressant, Anxiolytic and Antinociceptive Activities of Constituents from Rosmarinus Officinalis

被引:62
作者
Abdelhalim, Abeer [1 ,2 ]
Karim, Nasiara [3 ]
Chebib, Mary [1 ]
Aburjai, Talal [4 ]
Khan, Imran [3 ]
Johnston, Graham A. R. [5 ]
Hanrahan, Jane R. [1 ]
机构
[1] Univ Sydney, Fac Pharm, Sydney, NSW 2006, Australia
[2] Taibah Univ, Fac Sci, Almadina Almonawara, Saudi Arabia
[3] Univ Malakand, Dept Pharm, Chakdara, Pakistan
[4] Univ Jordan, Fac Pharm, Amman, Jordan
[5] Univ Sydney, Sch Med Sci, Pharmacol, Sydney, NSW 2006, Australia
关键词
GAMMA-AMINOBUTYRIC-ACID; ALZHEIMERS-DISEASE; GABA(A) RECEPTORS; CARNOSIC ACID; MICE; BRAIN; L; HESPERIDIN; SYSTEM; COMPONENT;
D O I
10.18433/J3PW38
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Purpose. Rosmarinus officinalis, traditionally known as rosemary, has been widely used in traditional medicines and has long been known as the herb of remembrance. However, few studies have investigated the effects of non-volatile components of rosemary on central nervous system function. Methods. Fractionation of R. officinalis led to the isolation of salvigenin, rosmanol and cirsimaritin, which were investigated in mouse models of acute toxicity, antinociception (tail immersion and hot plate tests), depression (tail suspension and forced swim tests) and anxiety (elevated plus maze and light/dark box paradigms). Results. Rosmanol, cirsimaritin and salvigenin were not found to exhibit any signs of acute toxicity (50-200 mg/kg), but elicited antinociceptive, antidepressant and anxiolytic activities. Conclusion. Rosmanol, cirsimaritin and salvigenin, all previously shown to have biphasic modulation of GABAA receptors, demonstrated CNS activity in mouse models of antinociception, antidepressant and anxiolysis. The anxiolytic activity of all three compounds was not ameliorated by flumazenil, but was inhibited by pentylenetetrazol, suggesting a mode of action via GABAA receptors at a site other than the high affinity benzodiazepine binding site.
引用
收藏
页码:448 / 459
页数:12
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