• Applied Microscopy
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• 제40권4호
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• pp.201-209
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• 2010

한방에서 사용되는 약재 중 가자와 지모, 단삼은 면역조절 및 항암효과, 항염증효과가 있다고 알려졌다. 그러나 비만세포와 관련된 아나필락스를 이해할 수 있는 세포학적 기전에 대한 가자와 지모, 단삼의 효과에 대해서는 알려진 바 없다. 본 연구에서는 가자와 지모, 단삼의 메탄올 추출물이 아나필락시스 반응에 대해 어떠한 영향을 끼치는지를 조사하였다. 시험관내 실험과 생체 실험을 통하여, 가자와 지모, 단삼의 메탄올 추출물이 compound 48/80에 의한 아나필락시스와 비만세포 활성화 및 IgE에 의한 피부반응을 관찰하였다. 실험결과는 다음과 같다. 1) 가자와 지모, 단삼의 메탄올 추출물은 compound 48/80에 의한 전신성 아나필락시스와 귀부종 반응, IgE에 의한 피부반응을 억제하였다. 2) Compound 48/80에 의한 비만세포 탈과립과 흰쥐 복강 비만세포로부터 히스타민 유리가 가자와 지모, 단삼의 메탄올 추출물 전처리에 의해 억제되었다. 3) Compound 48/80에 의한 흰쥐 복강 비만세포내로의 칼슘 유입이 가자와 지모, 단삼의 메탄올 추출물 전처리에 의해 현저하게 억제되었다. 이상의 결과로 가자와 지모, 단삼의 메탄올 추출물은 비만세포 탈과립과 비만세포로부터 히스타민 유리, 비만세포내로 칼슘유입을 억제함으로써 compound 48/80에 의한 아나필락시스와 IgE에 의한 피부반응을 억제한다는 것을 알 수 있었다. 이로써 가자와 지모, 단삼은 알레르기 질환에 대한 효과적인 치료제로 이용될 수 있을 것으로 생각된다.

• 대한한방내과학회지
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• 제26권1호
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• pp.119-128
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• 2005

모든 알레르기 반응의 중심축이 되는 비만세포는 주로 피부, 위장관 및 호흡기관의 점막에 분포하고 있다. 활성화된 비만세포는 즉각형 알레르기 반응을 일으키는 여러 인자들을 방출시키게 된다. 方藥合編(방약합편)에 따르면 蔘蘇飮(삼소음)은 알레르기 鼻炎(비염), 發熱(발열), 風寒(풍한), 頭痛(두통), 기침에 效能(효능)이 있는 處方(처방)이다. 본 硏究(연구)는 蔘蘇飮(삼소음)의 肥滿細胞(비만세포) 의존성 아나필락시 반응(anaphylactic reaction)에 대한 藥理(약리) 效果(효과)를 조사하기 위한 것이다. 蔘蘇飮(삼소음)은 compound 48/80으로 유발되는 전신성 아나필락시 쇼크(systemic anaphylactic shock)와 耳介(이개) 浮腫(부종) 反應(반응)(ear swelling response)을 농도 의존적으로 억제하였다. 蔘蘇飮(삼소음)을 0.1, 1 mg/ml로 전처리 하였을 때, 흰쥐 복강 肥滿細胞(비만세포)(rat peritoneal mast cells, RPMCs)에서 compound 40/80에 의해 유발되는 히스타민 분비는 감소하는 것으로 나타났다. 또한 蔘蘇飮(삼소음)은 anti-dinitrophenyl IgE에 의해 활성화 된 수동 피부 아나필락시(passive cutaneous anaphylaxis, PCA)를 농도 의존적으로 抑制(억제)하였다. 결론적으로 蔘蘇飮(삼소음)은 肥滿細胞(비만세포) 의존성 즉각형 알레르기 反應(반응)을 抑制(억제)하여, 항 아나필락시 활성(anti-anaphylactic activity)을 가지는 것으로 보여 진다.

• Archives of Pharmacal Research
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• 제24권3호
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• pp.249-255
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• 2001

We studied the effect of aqueous extract of Magnolia officinalis bark (Magnoliaceae) (MOAE) on the immediate hypersensitivity reaction. MOAE (0.01 to 1g/kg) dose-dependently inhibited compound 48/80 induced systemic anaphylaxis in rats. MOAE (0.1 and 1g/kg) also significantly inhibited local immunoglobulin E (lgE)-mediated passive cutaneous anaphylactic reaction. When MOAE was pretreated at concentrations ranging from 0.01 to 1g/kg, the levels of plasma histamine were reduced in a dose-dependent manner. MOAE (0.001 to 1 mg/ml) dose-dependently inhibited the histamine release from rat peritoneal mast cells (RPMC) activated by compound 48/80 or anti-dinitrophenyl (DNP) Igl. The level of cyclic AMP (CAMP) in RPMC, when MOAE was added, significantly increased compared with that of the normal control. Moreover, MOAE (0.01 to 1 mg/ml) had a significant inhibitory effect on anti-DNP Igl-induced tumor necrosis factor-$\alpha$ production from RPMC. These results indicate that MOAE inhibits immediate hypersensitivity reaction in vivo and in vitro.

• 동의생리병리학회지
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• 제16권2호
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• pp.239-244
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• 2002

Okbyungpoongsan-Gami (OG) has been used for the treatment of excessive sweating with general weakness and allergic rhinitis recently. Anal therapy is another way of taking Oriental medicine. It is an important pathway but not available in common clinical situation. This experiment was performed in order to study the inhibitory effect of immediate-type allergic reaction of OG by anal therapy. In addition, the experiment was practised by 1 H-NMR spectroscopy to examine molecular structure of OG. The results were obtained as follows : OG concentration-dependently inhibited compound 48/80- induced immediate type systemic allergic reaction with concentrations of 0.01-1.0g/kg by anal administration 1 h before injection of compound 48/80. OG also concentration-dependently inhibited compound 48/80- induced ear swelling response with concentrations of 0.01-1g/kg by anal administration 1h before injection of compound 48/80. OG also inhibited the passive cutaneous anaphylaxis activated by anti-dinitrophenyl (DNP) IgE antibody concentration- dependently at concentrations ranging from 0.01 to 1g/kg. When OG was pretreated at concentrations ranging from 0.01 to 1g/ℓ, the histamine release from the rat peritoneal mast cells induced by compound 48/80 was reduced in a concentration-dependent manner. OG (0.1-1g/ℓ) had a significant inhibitory effect on histamine release from IgE-induced activated mast cells. OG is seen to be a biochemical compound certainly by 1 H-NMR spectroscopy According to above results, anal therapy of OG may be beneficial in the treatment of systemic and local immediate-type allergic reactions by inhibition of histamine release from mast cells.

• 대한한방소아과학회지
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• 제18권2호
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• pp.61-76
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• 2004

Objective : To demonstrate of regulatory effect of atopic allergic regulation by Chungsangbangpoong-Tang(CBT), This experiment was studied. Methods : The author investigated a possible effect of CBT on cytokines production using human T cell line (MOLT-4) or human mast cell line (HMC-1). In addition, the author investigated whether CBT has inhitory effects on compound 48/80- induced histamine release from rat peritoneal mast cells (RPMC) and compound 48/80-induced ear swelling in ICR mice. Results : CBT (0.01 mg/ml)-containing medium in stimulated culture supernatants significantly increased IL-2 secretion compared with untreated MOLT-4, whereas CBT (0.01-1.0 mg/ml)-containing medium in stimulated culture supernatants significantly decreased IL-4 secretion compared with untreated MOLT-4. Significant reduced levels of IL -6 and $TNF-{\alpha}$ were observed in the HMC-l with CBT (P<0.05). CBT did not inhibit the histamine release from the RPMC but inhibit ear swelling response. Conclusion : These results suggest that CBT contributes to the treatment of atopic allergic reactions, such as atopic dermatitis and that its action may be due to regulation of cytokine production.

• 한국식품영양과학회지
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• 제36권2호
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• pp.155-162
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• 2007

본 연구에서는 녹차(Camellia sinensis)잎 추출물, 구아바(Psidium guajava)잎 추출물 그리고 장미(Rosa hybrida)꽃잎 추출물로 이루어진 식물추출 복합물(PEM381)에 대하여 제I형 알레르기 반응 억제 효능 및 생화학적 기전을 밝히기 위하여 COX 억제 활성, LO 억제 활성, compound 48/80에 의한 랫드 복강 비만세포의 탈과립과 히스타민 유리에 미치는 영향 그리고 수동피부아나필락시스 반응 억제효능을 측정하였다. 그 결과 PEM381은 5-LO $IC_{50}$ 값이 $14.11{\pm}0.51ppm$으로 나타났고, COX-1에 비해 COX-2를 선택적으로 억제하는 것으로 나타났다. 또한 PEM381은 compound 48/80에 의한 비만세포의 탈과립과 히스타민 유리를 농도 의존적으로 억제할 뿐만 아니라 수동피부아나필락시스 반응도 억제하였다. 이상의 결과로 PEM381은 알레르기성 비염, 아토피 피부염 및 기관지천식 같은 제I형 알레르기 질환에 대하여 예방 및 치료에 유용하게 사용될 수 있을 것으로 생각된다.

• 한국식품영양과학회지
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• 제43권11호
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• pp.1635-1641
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• 2014

본 연구는 고욤잎 유래 EA 분획물의 항산화 및 항가려움 활성을 조사하였다. EA 분획물은 DPPH 라디칼 소거 활성이 수용성 및 MeOH 추출물보다 매우 우수하였을 뿐만 아니라 합성 항산화제인 BHT보다 현저히 높았다. 또한 ABTS 라디칼 소거 활성도 수용성과 MeOH 추출물뿐만 아니라 Trolox보다 현저히 높았다. 본 연구에 사용된 EA 분획물과 수용성 및 MeOH 추출물은 세포에 대한 독성이 없었다. 또한 EA 분획물은 농도에 의존적으로 활성화된 비만세포로부터 히스타민 방출 억제와 TNF-${\alpha}$ 생성 억제 효과가 있었으며, 같은 농도에서 수용성 및 MeOH 추출물보다 억제 효과가 우수하였다. 더욱이 EA 분획물은 농도 의존적으로 compound 48/80으로 유도된 가려움증을 효과적으로 억제하는 활성이 있었고, 같은 농도에서 항가려움 약제로 알려진 azelastine보다는 그 효과가 낮았지만 수용성 및 MeOH 추출물뿐만 아니라 methysergide보다 우수한 항가려움 효과를 발휘하였다. 앞으로 이러한 항가려움 효과에 대한 EA분획물의 분자적 작용기전을 규명해야 할 필요가 있으며, 고욤잎 유래 EA 분획물은 강력한 항산화 및 항가려움 활성을 지닌 우수한 소재라 사료된다.

• Advances in Traditional Medicine
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• 제7권3호
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• pp.235-243
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• 2007

Anemarrhenae Rhizoma (AR) is used in traditional oriental medicine for various medicinal purposes. However, the exact mechanism that accounts for the anti-allergy and anti-inflammatory effects of the AR is still not fully understood. The aim of The present study is to elucidate whether and how AR modulates the allergic reactions in vivo, and inflammatory reaction in vitro. In this study, we showed that AR significantly decreased compound 48/80-induced systemic anaphylaxis, paw oedema, and histamine release from preparation of rat peritoneal mast cells. Also, AR inhibited the expression of inflammatory cytokine in PMA plus A23187-stimulated human mast cells (HMC-1). In addition, we showed that anti-inflammatory mechanism of AR is through suppression of nuclear factor-${\kappa}B$ activation $I{\kappa}B-{\alpha}$degradation. These results provided new insight into the pharmacological actions of AR as a potential molecule for therapy of inflammatory allergic diseases.

• Advances in Traditional Medicine
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• 제9권2호
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• pp.115-127
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• 2009

Samsoeum (SSE) is used in traditional oriental medicine for various medicinal purposes. However, the exact mechanism that accounts for the anti-allergy and anti-inflammatory effects of the SSE is still not fully understood. The aim of the present study is to elucidate whether and how SSE modulates the allergic reactions in vivo, and inflammatory reaction in vitro. In this study, we showed that SSE significantly decreased compound 48/80-induced systemic anaphylaxis, ear-swelling response, histamine release from preparation of rat peritoneal mast cells and anti-dinitropheny IgE-induced passive cutaneous reaction. Also, SSE inhibited the expression of inflammatory cytokine and cyclooxygenase-2 in PMA plus A23187-stimulated human mast cells (HMC-1). In addition, we showed that anti-inflammatory mechanism of SSE is through suppression of nuclear factor-${\kappa}B$ activation and $I{\kappa}B-{\alpha}$ phosphorylation/degradation in HMC-1. These results provided new insight into the pharmacological actions of SSE as a potential molecule for therapy of inflammatory allergic diseases.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1994년도 춘계학술대회 and 제3회 신약개발 연구발표회
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• pp.176-176
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• 1994

Moraceae comprise a large family of sixty genera and neary 1,400 specieses, including important groups such as Artocarpus, Morus, and Ficus. In particular, Morus(mulberry) is a small genus of tree and shrubs found in temperate and subtropical regions of the Northern hemishere and has been widely cultivated in China and Korea, In addition, the root bark of mulberry tree have been used as an antiphlogic, diuretic, and expectorant in white medicine, and the crude drug is known as "Sangbaikpi" in Korea. Recently, some papers have been published reporting the hypotensive effect, antiviral effect, antifungal effect, inhibitory effect of cAMP-phosphodiesterase, and anticancer effect of this extract. Little is known about that Cortex mori could have been an antiallergic effect. The purpose of this study was the development of an antiallergic agent with an antiallergic effect from Cortex mori. For this, several in vivo and in vitro experimental models were used. Results are 1) Cortex mori inhibited the compound 48/80-induced degranu-lation, histamine release and calcium uptake of rat peritoneal mast cells, 2) compound 48/80-induced anaphylactic shock and cutaneous reaction were significantly inhibited by pretreatment of Cortex mori, and 3) Cortex mori inhibited the ovalbumin-induced late astmatic reaction. From the above results it is suggested that Cortex mori has some substances with an antiallergic activity. Our final purpose of this study is to develope the new drug with an antiallergic activity from Cortex mori