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Abstract Title:

Inhaled essential oil from Chamaecyparis obtuse ameliorates the impairments of cognitive function induced by injection ofβ-amyloid in rats.

Abstract Source:

Pharm Biol. 2012 Jul ;50(7):900-10. Epub 2012 Apr 3. PMID: 22468783

Abstract Author(s):

Donghyuck Bae, Heejin Seol, Ho-Geun Yoon, Ju-Ryun Na, Kyonyeo Oh, Chul Yung Choi, Dong-wook Lee, Woojin Jun, Kwang Youl Lee, Jeongmin Lee, Kwontack Hwang, Yoo-Hyun Lee, Sunoh Kim

Article Affiliation:

Donghyuck Bae

Abstract:

CONTEXT: Chamaecyparis obtusa Sieb.&Zucc., Endlicher (Cupressaceae) forest bathing or aromatherapy has been shown in various studies to have biological functions such as anticancer, antiallergies, antiinflammatory, and antioxidant activity. However, no reports exist on the pharmacological or biological activities of the essential oil of C. obtusa (EOCO) or its effects on central nervous system.

OBJECTIVE: The aggregation and formation ofβ-amyloid peptides (Aβ) into fibrils are central events in the pathogenesis of Alzheimer's disease (AD), and overproduction and aggregation of Aβ into oligomers have been known to trigger neurotoxicity. In this study, we investigated the effects of inhaled EOCO on cognitive function and neuronalapoptosis in rats intrahippocampally injected with Aβ.

MATERIALS AND METHODS: To model AD, 4μg of aggregated Aβ was injected into the hippocampus. To test the effects of EOCO, behavioral performance in the Morris water maze was tested 4 days after injection. After behavioral testing, brain sections were prepared for TTC staining and TUNEL assay.

RESULTS: Inhaled EOCO protected spatial learning and memory from the impairments induced by Aβ(1-40) injection. In addition, the behavioral deficits accompanying Aβ(1-40)-induced AD were attenuated by inhalation of EOCO. Furthermore, acetylcholinesterase (AChE) activity and neuronal apoptosis were significantly inhibited in rats treated with Aβ(1-40) and EOCO compared to rats treated only with Aβ(1-40).

DISCUSSION AND CONCLUSION: EOCO suppressed both AD-related neuronal cell apoptosis and AD-related dysfunction of the memory system. Thus, the results of this study support EOCO as a candidate drug for the treatment of AD.

Study Type : Animal Study

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Sayer Ji
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