• Journal of Yeungnam Medical Science
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• 제16권2호
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• pp.318-325
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• 1999

항콜린에스테라제 약물은 AChE를 억제하여 ACh을 콜린성 수용체에 축적시켜 지속적인 ACh 자극을 유도하는 약물이다. 이러한 특성이 적출한 위장의 운동성에 미치는 영향과 콜린에스테라제 활성화 약물의 영향을 조사하고, 에탄올이 AChE의 활성도를 감소시키는 보고를 바탕으로 항콜린에스테라제와 에탄올의 동시 투여시 나타나는 위장관의 수축운동의 변화를 규명하고자 다음과 같은 실험을 수행하였다. 흰쥐의 위장을 적출하여 $2{\times}10mm$ 환상근 절편을 만들어 적출근편 실험조에 고정하고 등척성 장력측정기를 이용하여 약물 처치에 따른 위장 절편의 수축 변화를 측정하였다. 비가역성 항콜린에스테라제인 fenthion은 ACh 유발 위장 절편의 수축을 증가시켰으며 콜린에스테라제 활성화 약물인 PAM은 이 작용을 길항하였다. 가역성 항콜린에스테라제인 physostigmine은 그 자체로 인해 위장 절편의 수축이 증가하였는데, 이는 비극성을 나타내어 위장 절편 조직으로의 흡수가 빠르기 때문이라고 생각되고, ACh에 의한 반응성 또한 현저히 증가하였다. PAM에 의한 반응성 감소효과도 대조군과 통계적으로 유의한 차이를 보였다. 최근 평활근 이완을 유도한다고 알려진 에탄올은 fenthion 처치에 의한 수축운동 증가를 억제하였고 이러한 결과로 볼 때 항콜린에스테라제와 에탄올의 동시 투여시에는 콜린에스테라제 활성도 감소보다 에탄올에 의한 위장관 운동성 감소가 많이 작용함을 의미하였다. 이상의 결론은 가역성 및 비가역성 항콜린에스테라제에 의해서 위장관 운동성 항진이 나타나고 이는 콜린에스테라제의 활성화 약물로서 길항되었다. 그리고 에탄올과 항콜린에스테라제에 동시에 노출된 경우는 에탄올의 평활근 이완 효과에 의해 위장관 운동성 감소가 나타남을 알 수 있었다.

• 셀메드
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• 제2권2호
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• pp.19.1-19.6
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• 2012

$Capparis$ $zeylanica$ Linn. a 'Rasayana' drug is used for its memory enhancing effects in the traditional Ayurvedic system of medicine. The aim of this study was to evaluate acetylcholinesterase (AChE) inhibitory and memory enhancing activities of $Capparis$ $zeylanica$ Linn. The$in-vitro$ and $ex-vivo$ models of AChE inhibitory activity were used along with Morris water maze test to study the effect on memory in rats. The anticholinesterase effect of methanolic and aqueous extracts of $Capparis$ $zeylanica$ was measured by spectrophotometric Ellman method at 0.1, 0.3, 1.0, 3.0, 10 and 30 mg/ml and brain monoamine oxidase (MAO-A and MAO-B) activity was assessed by Naoi's method. The results $in-vitro$ and $ex-vivo$ AChE assay revealed that methanolic and aqueous extracts of $Capparis$ $zeylanica$ inhibit AChE activity, whereas these extracts did not alter MAO activity at any concentration tested as compared to moclobemide and L-deprenyl. The results indicate that $Capparis$ $zeylanica$ improves scopolamine-induced memory deficits through inhibition of AChE activity, and not by direct MAO inhibition.

• Asian Pacific Journal of Cancer Prevention
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• 제16권7호
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• pp.2763-2769
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• 2015

Background: Cancer is an unnatural type of tissue growth in which the cells exhibit unrestrained division, leading to a progressive increase in the number of dividing cells. It is now the second largest cause of death in the world. The present study concerned antioxidant, anticancer and anticholinesterase activities and protocatechuic, catechin, caffeic acid, syringic acid, p-coumaric acid and o-coumaric concentrations in methanol extracts of flowers, fruits and seeds of Hypericum amblysepalum. Materials and Methods: Antioxidant properties including free radical scavenging activity and reducing power, and amounts of total phenolic compounds were evaluated using different tests. Protocatechuic, catechin, caffeic acid, syringic acid, p-coumaric acid and o-coumaric concentrations in extracts were determined by HPLC. Cytotoxic effects were determined using the MTT test with human cervix cancer (HeLa) and rat kidney epithelium cell (NRK-52E) lines. Acetyl and butyrylcholinesterase inhibitory activities were measured by by Ellman method. Results: Total phenolic content of H. amblysepalum seeds was found to be higher than in fruit and flower extracts. DPPH free radical scavenging activity of the obtained extracts gave satisfactory results versus butylated hydroxyanisole and butylated hydroxytoluene as controls. Reducing power activity was linearly proportional to the studied concentration range: $10-500{\mu}g/mL\;LC_{50}$ values for H. amblysepalum seeds were 11.7 and 2.86 respectively for HeLa and NRK-52E cell lines. Butyryl-cholinesterase inhibitory activity was $76.9{\pm}0.41$ for seed extract and higher than with other extracts. Conclusions: The present results suggested that H. amblysepalum could be a potential candidate anti-cancer drug for the treatment of human cervical cancer, and good source of natural antioxidants.

• Journal of Yeungnam Medical Science
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• 제16권2호
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• pp.326-332
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• 1999

이 연구에서는 유기인제 농약으로 인한 acetylcholinesterase와 pseudolcholinesterase의 활성도 변화와 알콜과 유기인제 농약의 상호 작용시 효소 활성도 변화를 비교하고, 임상적으로 쓰이고 있는 가역성 항콜린에스터라제 약물과도 비교하여 여러 항콜린에스터라제 약물의 효능과 알콜 섭취가 콜린에스터라제 활성도에 미치는 영향을 파악하는 것에 이 실험의 목적을 두었다. 남자 대학생 15명을 무작위 추출하여 상박부 정맥에서 채혈하여 혈액중 적혈구내에 존재하는 acetylcholinesterase와 혈장에 존재하는 acetylcholinesterase를 분리하였고 cholinesterase가 acetylcholine을 acetic acid와 choline으로 가수분해한다는 점을 이용하여 각 효소에 acetylcholine을 기질로서 주입한 후 1시간 후 생성된 acetic acid에 의해 변화된 pH를 pH meter로 측정하여 간접적으로 활성도를 알아내는 electrometric method를 이용하여 활성도 변화를 측정하였다. 위 실험 조건에서 가역성 항콜린에스터라제 약물이 유기인제 농약보다 콜린에스터라제 활성도를 감소시켰고, 유기인제로 인한 acetylcholinesterase와 pseudocholinesterase의 활성도 변화는 에탄올 처치시 더욱 현저하게 감소되는 것으로 나타났으며, 콜린에스터라제 활성제인 oxime은 acetylcholinesterase에 대해서는 효소 활성도를 높이지만 pseudocholinesterase의 효소 활성도에는 영향을 미치지 않는 것으로 나타났다.

• 약학회지
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• 제46권6호
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• pp.452-458
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• 2002

Dehydroevodiamine-HCl (DHED), which is a component separated from Evodia rutaecarpa Bentham, has novel anticholinesterase and antiamnesic activities in a scopolamine-induced amnesia model. Several studies suggest that DHED might be an effective drug for Alzheimer's disease and a vascular type of dementia. DHED was at dose levels of 0, 50, 100 and 200 mg/kg/day administered intraperitoneally to Sprague-Dawley male rats for 60 days before mating and to females from 14 days before mating to 7 days after mating. Effects of the DHED on general symptom and reproductive performance of parent animals and embryonic development were examined. In male parents, whereas no death was observed, reduction in the increase rate of body weight was found at 200 mg/kg. In female parents, both of the mating performance and the fertility of parent animals were decreased at 200 mg/kg, but not significantly. In 200 mg/kg treated group, the fetal death rate was increased but total fetuses showed no changes compared to the control group. There were no malformed F1 fetuses in all groups.

• 약학회지
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• 제46권3호
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• pp.208-212
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• 2002

Dehydroevodiamine HCl (DHED), which is a component separated from Evodia rutaecarpa Bentham, has novel anticholinesterase and antiamnesic activities in the scopolamine-induced amnesia model. Several studies suggest that DHED might be an effective drug for the Alzheimer's disease and the vascular type of dementia. In order to evaluate the mutagenic potential of DHED, Salmonella typhimurium reversion assay, chromosomal aberration test on Chinese hamster lung cells, in vivo micronucleus assay using mouse bone marrow cells, and comet assay were performed. DHED did not increase the number of revertant in the reverse mutation test using Salmonella typhimurium TA1535, TA1537, TA98, TA100. DHED HCl, at concentration of 5 and 10 $\mu\textrm{g}$/mι, increased the number of chromosome aberrated Chinese hamster lung cells with 5 and 10％, respectively. In mouse micronucleus test, no significant increase in the occurrence of micronucleated polychromatic erythrocyte was observed in ICR mice orally administered with DHED. DHED was tested for ability to induce genotoxic effect in L5178Y cells (mouse lymphoma cells) using the single cell gel electrophoresis assay (comet assay). In comet assay, tail moment did not increase in L5178Y cells treated with 10, 100, 300 $\mu$M DHED.

• Biomolecules & Therapeutics
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• 제13권1호
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• pp.26-31
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• 2005

The present study examined effects of a water-soluble fraction from mulberry leaves (ML water fraction) on the circulatory and autonomic nervous systems, which were compared with those of acetylcholine (ACh) used as a reference drug in order to elucidate its mechanism of action. Intravenous administration of ACh or a ML water fraction produced temporary depressor and tachycardiac responses in a dose-dependent manner in unrestrained, conscious Sprague-Dawley rats. The systemic hemodynamic effects of ACh and a ML water fraction were almost completely blocked by pretreatment with atropine, a muscarinic antagonist. The depressor responses to ACh and a ML water fraction were slightly enhanced and prolonged by pretreatment with neostigmine, an anticholinesterase, whereas the tachycardiac responses were remarkably blocked by pretreatment with pentolinium, a ganglionic blocking agent. In vitro experiments using the ileum isolated from rats showed that ACh and a ML water fraction increased ileal contractility in a dose-dependent manner. The increases in ileal contractility were also completely abolished in the presence of atropine. Finally, the specific binding of [$^3H$]quinuclidinyl benzilate, a muscarinic antagonist, to rat cortical synaptic membranes was inhibited by a ML water fraction in a concentration-dependent manner with an IC$_{50}$ value of 9.5 mg/ml. The results suggest that the effects of a ML water fraction are mediated through direct stimulation of muscarinic cholinergic receptors by unknown cholinomimetic substance(s) contained in that fraction.