Inhibitory effects of the fragrance inhalation of essential oil from Acorus gramineus on central nervous system

被引:1
|
作者
Koo, BS
Park, KS
Ha, JH
Park, JH
Lim, JC
Lee, DU [1 ]
机构
[1] Dongguk Univ, Coll Nat Sci, Dept Biochem, Gyeongju 780714, South Korea
[2] Pusan Natl Univ, Coll Pharm, Pusan 609735, South Korea
[3] Yeungnam Univ, Coll Med, Dept Pharmacol, Taegu 705717, South Korea
[4] Dongguk Univ, Coll Oriental Med, Dept Oriental Neuropsychiat, Seoul 135010, South Korea
关键词
Acorus gramineus; essential oil; anticonvulsive effect; sedative effect; aroma therapy;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study was designed to evaluate central inhibitory effects of the essential oil from Acori graminei Rhizoma (AGR), the dry rhizomes of Acorus gramineus SOLANDER (Araceae) upon fragrance inhalation (aroma therapy). Preinhalation of the oil markedly delayed the appearance of pentylenetetrazole-induced convulsion. Furthermore, inhalation impressively inhibited the activity of gamma-aminobutyric acid (GABA) transaminase, a degrading enzyme for GABA as the inhalation period was lengthened. The GABA level was significantly increased and glutamate content was significantly decreased in mouse brain by preinhalation of the essential oil. The above results suggest that the anticonvulsive effect of this AGR oil is originated by the enhancement of GABA level in the mouse brain, because convulsion depends partially on GABA concentration which can be properly preserved by inhibiting GABA transaminase. Moreover, fragrance inhalation progressively prolonged the pentobarbital-induced sleeping time as inhalation time was lengthened. Ten hour inhalation corresponded almost to the effect (145% increase) of oral administration (60 mg/kg). This sedative effect after inhalation or oral administration of AGR essential oil suggests that this oil may act on the CNS via the GABAergic system. The inhibitory activity of preinhalation of the essential oil on lipid peroxidation, to which the anticonvulsive action is attributed, also supported the above results, confirming and amplifying our previous reports on the CNS inhibitory effects of AGR.
引用
收藏
页码:978 / 982
页数:5
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