• Archives of Pharmacal Research
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• 제27권7호
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• pp.781-789
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• 2004

The effect of 1,8-cineole on cytochrome P450 (CYP) expression was investigated in male Sprague Dawley rats and female BALB/c mice. When rats were treated orally with 200, 400 and 800 mg/kg of 1,8-cineole for 3 consecutive days, the liver microsomal activities of benzy-loxyresorufin- and pentoxyresorufin-D-dealkylases and erythromycin N-demethylase were dose-dependently induced. The Western immunoblotting analyses clearly indicated the induction of CYP 2B1/2 and CYP 3A1/2 proteins by 1,8-cineole. At the doses employed, 1,8-cineole did not cause toxicity, including hepatotoxicity. Subsequently, 1,8-cineole was applied to study the role of metabolic activation in thioacetamide-induced hepatotoxicity and/or immunotoxicity in animal models. To investigate a possible role of metabolic activation by CYP enzymes in thioacetamide-induced hepatotoxicity, rats were pre-treated with 800 mg/kg of 1,8-cineole for 3 days, followed by a single intraperitoneal treatment with 50 and 100 mg/kg of thioacetamide in saline. 24 h later, thioacetamide-induced hepatotoxicity was significantly potentiated by the pretreatment with 1,8-cineole. When female BALB/c mice were pretreated with 800 mg/kg of 1,8-cineole for 3 days, followed by a single intraperitoneal treatment with 100 mg/kg of thioace-tamide, the antibody response to sheep red blood cells was significantly potentiated. In addition, the liver microsomal activities of CYP 2B enzymes were significantly induced by 1,8-cineole as in rats. Taken together, our results indicated that 1,8-cineole might be a useful CYP modulator in investigating the possible role of metabolic activation in chemical-induced hepato-toxicity and immunotoxicity.

• BMB Reports
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• 제45권10호
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• pp.565-570
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• 2012

We recently reported that a water extract of laurel or turmeric, 1,8-cineole enriched fractions, showed hypolipidemic activity in the zebrafish model. Therefore, the present study investigated the cineole's anti-oxidant and anti-inflammatory activities in lipoprotein metabolism in vitro and in vivo. Cineole had inhibitory effects on cupric ion-mediated oxidation of lipoproteins in general, while simultaneously enhancing ferric ion removal ability in high-density lipoprotein (HDL). Hypercholesterolemia was induced in zebrafish using cholesterol-feeding treatment, 4% cholesterol, for 3 weeks. After feeding with or without the addition of cineole, the results revealed that cineole possessed lipid-lowering and anti-inflammatory activities in hypercholesterolemic zebrafish. In addition, serum amyloid A and interleukin-6 levels were lowered and lipid accumulation was decreased in the liver. Conclusively, 1,8-cineole was found to have anti-oxidant activities in lipoprotein metabolism both in vitro and in vivo with simultaneous reduction of lipid accumulation in the liver of zebrafish.

• Natural Product Sciences
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• 제14권1호
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• pp.27-31
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• 2008

We have evaluated the combined antifungal effects of the essential oil from Eucalyptus globulus or its main component 1,8-cineole with ketoconazole. Checkerboard microtiter tests were used to analyze their effects against three Candida and six Trichophyton species. The susceptibility of the Trichophyton species to E. globulus essential oil differed distinctly. The fractional inhibitory concentration indices (FICIs) against the tested Candida species ranged between 0.09 and 0.38 for ketoconazole combined with E. globulus essential oil or 1,8-cineole, indicating significant synergism between ketoconazole and the oil samples. Similar experiments using Trichophyton species resulted in FICIs between 0.28 and 0.63, indicating relatively weaker combined effects than those observed with Candida species. Thus, the data reported here show that the anti-Candida effects of ketoconazole can be significantly improved in the presence of E. globulus essential oil or 1, 8-cineole.

• 대한본초학회지
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• 제22권4호
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• pp.271-277
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• 2007

Objective : The content of essential oils from Ssajuari and Sajabalssuk was analyzed based on storage period. A total of eight samples old Ssajuari (harvested in 2000, 2001, 2002, 2003, and 2004), fresh Ssajuari (harvested in 2004), old Sajabalssuk (harvested in 2002), and fresh Sajabalssuk (harvested in 2004) was analyzed. Methods : The analysis of the content of essential oils from Ssajuari and Sajabalssuk was conducted by GC/MS. Results : The main essential oils of Ssajuari were ${\beta}$-thujone and 1.8-cineole. The ${\alpha},{\beta}$-thujone and 1,8-cineole were increased but the caryophyllene oxide was decreased. in accordance with storage period. The main essential oils of fresh Sajabalssuk were trans-${\beta}$-caryophyllene, terpinen-4-ol. The main essential oils of old Sajabalssuk was ${\beta}$-thujone and 1,8-cineole like Ssajuari. But 1,8-cineole was higher than that of Ssajuari samlpes. Conclusion : All samples had trans-sabinene hydrate, 1,8-cineole, terpinen-4-ol and caryophyllene oxide. According to stored year, ${\beta}$-thujone, ${\alpha}$-thujone were increased but terpinen-4-ol, caryophyllene oxide were decreased.

• 생약학회지
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• 제36권3호통권142호
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• pp.252-256
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• 2005

The in visto inhibitory activities of essential oils of the Rosmarinus officinalis as well as its main constituents were evaluated against antibiotic-susceptible and -resistant strains of Staphylococcus aureus, streptococcus pneumoniae, Salmonella enteritidis and S. typhimurium. The essential oil fraction of R. officinalis and its main components, 1,8-cineole and camphor, exhibited significant inhibitory activities against most of the tested strains in this study, with MICs(minimum inhibitory concentrations) racing from 0.5mg/ml to 16mg/ml. The total oil fraction showed higher activity than its main components, 1,8-cineole and camphor against S. aureus strains. No remarkable differences were evident between MICs of the susceptible and resistant strains of S. aureus. Among the tested strains, S. pneumoniae CCARM 3523, the resistant strain to norfloxacin, oxacillin and erythromycin exhibited significantly lower sensitivity to the tested oils than antibiotic-susceptible strain. The oils revealed mostly higher inhibitory activity against S. typhimurium than against S. enteritidis.

• Applied Biological Chemistry
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• 제45권2호
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• pp.101-107
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• 2002

순비기나무의 잎, 꽃, 줄기 및 열매로부터 수증기 증류법으로 정유를 분리한 다음 GC-MS 및 GC를 이용한 표준품과 머무름 시간의 비교에 의해 76종의 성분을 동정하였다. 동정된 성분은 monoterpene hydrocarbons 16종, oxygenated monoterpenes 30종, sesquiterpene hydrocarbons 10종, oxygenated sesquiterpenes 8종, diterpenes 3종, 기타 성분 9종으로서, 특히 ${\alpha}-pinene$, ${\beta}-pinene$, sabinene, 1,8-cineole, terpinen-4-ol, ${\alpha}-terpineol$등의 monoterpene류가 주요 구성성분들이었다. 부위별 주요 구성성분으로서 잎에서는 ${\alpha}-pinene$ (30.25%) > 1,8-cineole (19.89%) > sabinene (9.56%) > ${\alpha}-ternineol$ (7.94%) > ${\beta}-pinene$ (5.69%) > terpinen-4-ol (2.37%), 꽃에서는 ${\alpha}-pinene$ (25.47%) > 1,8-cineole (7.69%) > manoyl oxide(6.21%) > ${\beta}-pinene$ (4.20%) > ${\alpha}-terpineol$ (3.76%) >sabinene (2.78%), 줄기에서는 ${\alpha}-pinene$ (13.24%)>${\alpha}-terpineol$ (10.64%)>1,8-cineole (4.40%)>manoyl oxide (4.02%) > ${\beta}-pinene$ (2.39%) > terninen-4-ol (2.21%), 그리고 열매에서는 ${\alpha}-pinene$ (20.24%) > 1,8-cineole (11.47%) > ${\beta}-pinene$ (9.79%) > u-terpineol (7.08%) > sabinene (3.68%) limonene (2.77%)의 순서로 조성비율이 높았다. 전반적으로 순비기나무의 잎과 열매에서 분리한 정유에서는 monoterpene류의 조성비율이 높았으나 꽃과 줄기에서는 잎이나 열매에 비해 sesquitepene류, diterpene류 이외에도 구조를 동정하지 못하였으나 diterpene류 일 것으로 예상되는 분자량이 비교적 큰 성분들의 조성비율이 높았다.

• Applied Biological Chemistry
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• 제45권2호
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• pp.108-113
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• 2002

산국과 감국의 정유성분 조성의 차이점을 비교하기 위하여 수증기 증류에 의해 정유를 분리한 다음 GC-MS, GC를 이용한 표준품과 머무름 시간 비교 또는 문헌상의 각 성분의 RI값과 비교에 의해 성분을 동정하였다. 산국에서 분리한 정유에서는 94개 성분을 동정하였으며 그 중 GC peak area를 기준으로 했을 때 주요 구성성분은 camphor (15.40%), cis-chrysanthenol (14.11%), ${\alpha}-thujone$ (13.27%), 1,8-cineole (4.16%), ${\alpha}-pinene$ (3.80%), ${\beta}-caryophyllene$ (3.58%), germacrene D (2.69%), camphene (2.40%), umbellulone (2.24%) 및 ${\beta}-pinene$ (2.00%) 등이었다. 감국에서 분리한 정유에서는 80개 성분을 동정하였으며, 주요 구성성분은 germacrene D (16.50%), camphor (10.04%) 이외에도 ${\alpha}-thujone$ (6.40%), ${\alpha}-pinene$ (4.50%), ${\alpha}-cadinol$ (3.97%), cam-phene (3.82%), ${\beta}-pinene$ (3.67%), zingiberene (3.64%), cis-chrysanthenol (3.45%), piperitone (3.09%), 1,8-cineole (2.61%) 및 chrysanthenone (2.42%) 등이었다. 산국과 감국의 정유성분 조성상의 차이점으로 산국의 정유에서는 감국에 비해 camphor, cis-chrysanthenol, ${\alpha}-thujone$, 1,8-cineole 및 umbellulone의 함유비율이 높은 반면 감국의 정유에서는 germacrene D, ${\beta}-caryophyllene$, ${\alpha}-cadinol$, zingiberene, cis-chrysanthenol 및 piperi-tone의 함유비율이 높은 것이 특징이었다.

• 한국자원식물학회지
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• 제21권4호
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• pp.237-248
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• 2008

자생 상록활엽수의 부위별 재료에서 추출한 주요 정유성분으로 광나무의 꽃에는 hotrienol(9.21%), 돈나무의 잎에는 undecane(32.12%), 붓순나무의 잎에는 1,8-cineole(45.32%), 새덕이나무의 잎에는 ${\gamma}$-terpinene(15.62%), 생달나무의 잎에는 1,8-cineole(14.66%), 차나무의 잎에는 2-acetyl-5-methylfuran(54.51%), 황칠나무의 잎에는 ${\gamma}$-elemene(18.59%) 등의 성분함량이 특히 높음을 알 수 있었다.

• 한국응용곤충학회지
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• 제41권4호
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• pp.285-292
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• 2002

본 연구는 표고원목재배시 골목을 가해하는 털두꺼비하늘소(Moechotypa diphysis) 성충에 대해서 25종 monoterpenoid의 훈증독성, 접촉독성 및 산란기피효과를 조사하였다. 훈증독성은 20(equation omitted)/954 ml (공기)의 농도에서 1, 8-cineole, fenchone, pulegone, (equation omitted)-terpinene이, 10(equation omitted)/954 ml (공기)의 농도에서는 pulegone과 (equation omitted)-terpinene이, 그리고 5(equation omitted)/954 m1 (공기)의 농도에서는 pulegone만이 100%의 살충률을 나타내었다. 접촉독성은 pulegone만이 70%의 살충률을 보인 것 외에 대부분의 monoterpenoid에서 활성이 낮거나 없었다. 후각계를 이용한 기피반응은 1 (equation omitted)에서 bornylacetate, carvacrol, 1, 8-cineole, menthol은 기피반응을 보였고, 반면 citronellol은 유인반응을 보였다. 실내에서 수행한 산란기피효과는 25개의 monoterpenoid중 1,000ppm의 농도에서 carveol, geraniol, perillyl alcohol이 각각 82.1%, 78.3%, 87.5%의 효과를 보였다. 이 3 화합물을 가지고 야외포장 적용시험을 수행한 결과 10,000ppm과 1,000ppm의 농도에서 3일째까지 geraniol이 가장 효과가 좋았으나 잔효성은 없는 것으로 나타났다.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.188.2-189
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• 2003

To develop cytochrome P450 (P450) modulators with low toxicity from natural products, we have evaluated more than 20 compounds in mouse and rat models. Among those, the effects of 1,8-cineole and diallyl sulfide (DAS) were most profound in modulating P450 expression. In this presentation, the effects of 1,8-cineole and diallyl sulfide (DAS) on P450 expression were introduced. (omitted)