• 대한한의학회지
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• 제19권2호
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• pp.439-449
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• 1998

Anal Therapy is another way of taking medicine. It is a traditional pathway but not available in common situation. Nevertheless, It has many benifect and usefulness, it has not treated so much. Through Anal Therapy, the valid compound of Herb med can be reach to the desination in theory of the organism and loca1 medical action. The former is called Jung-Chei Theory(整體論), which is the one of the most important basements in building traditional Korean medicine. As there are many kinds of Anal therapy, this study use reservation type. Sosihotang(SSHT) is one of the well-known korean medicines for a long time. It is used for the treatment of such dieases as infectious diseases, hepatic diseases and gastroenteritis and so on. In this study, the author investigated the effect of an aqueous extract of SSHT by Anal therapy(Reservative Enema) in anaphylactic shock. The following results were obtained 1. SSHT inhibited anaphylactic shock 100% with a dose of 1.0 g/kg 1 hr before intraperitoneal injection of compound 48/80. SSHT significantly reduced serum histamine contents induced by compound 48/80. 2. SSHT (0.1 g/kg) also inhibited to 30.9% (P<0.05)) local cutaneous anaphylactic reaction activated by anti-dinitrophenyl (DNP) IgE. 3. The validity rate of reservative enema is as much as oral pathway. 4. In addition, SSHT dose-dependently inhibited the histamine release from the peritoneal mast cells by compound 48/80 or anti-DNP IgE. These results provide evidence that Anal Therapy(Reservative enema) of SSHT may be beneficial in the treatment of systemic and local anaphylactic reaction. Moreover, I wish another much sincere study of Anal Therapy (Reservative enema) would be obtained.

• Advances in Traditional Medicine
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• 제10권3호
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• pp.173-183
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• 2010

Perilla frutescens var. acuta Kudo (PF) is a traditional Korean medicinal herb for allergic reaction regulation. In the present study, we investigated the effect of 30% ethanol extract powder of PF (EPPF) and rosmarinic acid (RA), the active compound of EPPF on various allergic reactions using in vivo and in vitro models. EPPF and RA significantly inhibited compound 48/48-induced systemic anaphylactic reaction and histamine release (P < 0.05). In addition, EPPF and RA significantly inhibited passive cutaneous anaphylaxis (PCA) in a dose-dependent manner (P < 0.05). These effects were stronger than those of disodium cromoglycate, the reference drug tested. EPPF and RA also significantly inhibited production of inflammatory cytokines, tumor necrosis factor-a interleukin (IL)-6, and vascular endothelial growth factor on the PCA reaction and phorbol 12-myristate 13-acetate and calcium ionophore A23187-stimulated human mast cell line, HMC-1 cells (P < 0.05). Moreover, EPPF and RA showed an inhibitory effect on lipopolysaccharide (LPS)-induced IL-4 production from whole spleen cells. Finally, EPPF and RA significantly decreased IL-4-dependent IgE production by LPS-stimulated whole spleen cells (P < 0.05). In conclusion, these results indicate that EPPF has potent anti-allergic activities.

• 대한본초학회지
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• 제34권3호
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• pp.9-17
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• 2019

Objectives : This study was performed to compare the effect of two Cudrania tricuspidata cultivars; Sancheong native (CT) and varieties in china(SCT) on immediate hypersensitivity of the anaphylactic type and Ova-induced allergic asthma mouse model by calculating serum cytokines and IgE. Methods : We investigated the free radical scavanging effect and quantify total phenol contents and total flavonoids of two Cudrania tricuspidata cultivars; Sancheong native(CT) and varieties in china(SCT). The sample was extracted by 80% EtOH. To induce the allergic asthma, in the control group and the CT group, mice of each group were sensitized intraperitoneally with ovalbumin (OVA) solution at the 1st, the 7th and the 14th day. After then, sensitization was performed by aerosol allergen challenges with 1% OVA solution intratracheally at the 21th, the 23th, 25th and the 27th day. At the 29th day, the mice were killed and the changes of interferon-${\gamma}$, interleukin-4, 5 and 10, total IgE and OVA-specific IgE in serum were checked. Results : CT inhibited compound 48/80-induced systemic anaphylaxis 90% with a dose of 100 mg/kg body weight at 1 hr before injection of compound 48/80. In the allergic asthma mouse model, IFN-${\gamma}$ was did not increased in the CT and SCT group than that in the control group. IL-4, IL-5, the total IgE and OVA-specific IgE were decreased in the CT group as compared with the control group and these results were statistically significant. Conclusions : Considering the above experimental results, this study showed that Sancheong native cultivar could reduce the allergic reaction.

• 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.

• 셀메드
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• 제8권1호
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• pp.5.1-5.4
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• 2018

Pharmacopuncture, or herbal acupuncture, is a new form of therapy derived from combinations of two traditional therapeutic methods, herbal medicine and acupuncture therapy. To compare the efficacy between loratadine-pharmacopuncture (LP) and loratadine-oral administration (LO), the effect of loratadine was investigated in murine models. Anti-anaphylactic effects of loratadine treatments were investigated in compound 48/80-induced systemic anaphylactic reaction and passive cutaneous anaphylaxis (PCA). LP treatment significantly inhibited the compound 48/80-induced systemic anaphylactic reaction and PCA. The effect between LP and LO were on a similar level. These results indicate that LP can be used as an alternative method for LO in case of emergency.

• Clinical and Experimental Pediatrics
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• 제51권8호
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• pp.868-873
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• 2008

목 적 : 면역치료는 흡입성 알레르겐에 의해 유발되는 천식이나 비결막염, 곤충자상 치료에 매우 효과적이다. 이중 집먼지진드기 항원에 감작된 환아를 1-2일 내에 유지용량에 도달하는 초급속면역치료(ultra-rush immunotherapy)에 대한 안전성과 효과를 알아보고자 본 연구를 계획하였다. 방 법 : 분당차병원 소아 알레르기 클리닉에서 알러지성 비염 또는 기관지 천식으로 진단받은 4세 이상의 소아 중, 피부반응 검사에서 Dermatophagoides 항원에만 양성 반응을 보이고 비강유발검사에서 양성소견을 보인 환자를 대상자로 선정하였다. 고식적면역치료는 11명, 초급속면역치료를 신청한 소아는 12명이었다. 초급속면역치료는 목표 농도의 100:1-1,000:1로 희석한 알레르겐을 30분 간격으로 2-3배 증량하며, 주사 후 15분마다 산소포화도와 심박수, 혈압 및 전신반응 유무를 관찰하였고, 이때 나타난 환아의 증상을 점수화하였다. 면역치료의 효과 판정은 초기치료 3개월이 경과한 후에 비강유발검사를 실시하여 점수 변화로써 확인하였다. 결 과 : 고식적면역치료와 초급속면역치료 받은 소아의 평균나이는 각각 $8.3{\pm}2.3$세, $9.2{\pm}2.8$세였다. 초급속면역치료를 받은 12명중 6명(50%)에게서 전신반응이 관찰되었으며, 아나필락시스와 같은 심각한 부작용은 발현되지 않았다. 고식적면역치료의 경우 11명중 1명(9%)에서만이 전신반응이 관찰되었다. 치료 전후의 비강유발검사 평균 점수는 고식적면역치료 군의 경우 치료 전 $8.2{\pm}1.5$점, 치료 후 $4.6{\pm}2.1$점이었으며(P=0.043). 초급속면역치료에서는 치료 전 $6.2{\pm}2.2$점, 치료 후 $3.7{\pm}2.5$점으로(P=0.017) 두 군 모두 치료 전후 비강유발 검사 결과가 호전된 것을 알 수 있었다. 결 론 : 소아에서 Dermatophagoides를 이용한 초급속면역치료는 3개월 후 비강유발검사상 호전된 것을 확인할 수 있었으나 전신반응이 고식적 면역치료보다 높아 소아를 대상으로 시행함에 있어 면밀한 주의가 요구된다.

• Pediatric Infection and Vaccine
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• 제25권1호
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• pp.35-44
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• 2018

목적: 인플루엔자 유행 예방에 대한 가장 효과적인 방법은 인플루엔자 백신이나 한국의 소아청소년을 대상으로 한 면역원성 및 안전성에 대한 자료가 많지 않다. 이에 본 연구는 국내에서 많이 사용되는 불활성화 3가 백신의 면역원성과 안전성을 확인하고자 하였다. 방법: 2008년 10월부터 12월까지 고려대학교 의료원 안산병원 소아청소년과에 인플루엔자 예방접종을 위해 내원한 건강한 소아청소년 중 임상시험 지원자 65명을 대상으로 하여 접종 전과 접종 후 30일째 혈구응집억제(hemagglutinin inhibition) 항체검사를 시행하고 접종 직후부터 접종 후 7일까지 국소반응과 전신반응을 포함한 이상반응을 관찰하여 기록하도록 하였다. 결과: 분할 인플루엔자 백신의 세 항원(H1N1, H3N2, B) 각각에 대한 접종 후 혈청보호율은 87.7%, 89.2%, 89.2% (${\geq}70%$)였으며 혈청전환율은 44.6%, 73.8%, 63.1% (${\geq}40%$), 혈청전환인자는 3.35, 7.18, 5.13 (>2.5)으로 Committee for Proprietary Medicinal Products (CPMP) 기준을 만족하였다. 전체 피험자 65명 중 48명(73.8%)이 백신 접종 후 이상반응을 보고하였으나 아나필락시스나 경련과 같은 심각한 이상반응은 없었다. 발적(29.2%), 동통(43.1%), 종창(41.5%)과 같은 국소반응을 보고한 피험자는 42명(64.6%)이었고, 권태(23.1%), 근육통(20.0%), 두통(10.8%), 관절통(10.8%), 오한(9.2%), 발열(7.7%) 등과 같은 전신반응을 보고한 피험자는 26명(40.0%)이었다. 결론: 6개월에서 18세까지의 소아청소년을 대상으로 한 불활성화 3가 백신의 면역원성과 안전성에 대한 연구 결과 H1N1, H3N2, B 항원 모두 CPMP 기준에 부합하여 적합한 면역원성이 있는 것으로 나타났으며, 국소반응 및 경미한 전신반응 이외에 심각한 이상반응은 보이지 않아 비교적 안전하다고 판단된다.

• 대한한방내과학회지
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• 제36권3호
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• pp.236-251
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• 2015

Objectives: To investigate the anti-inflammatory, analgesic, anti-pyretic and anti-histamine activities of 20 herbal medicines to test their efficacy in common cold treatment. Methods: For all experiments, the herbal medicines were extracted with 80% ethanol and freeze-dried. To determine the anti-oxidative properties, we tested DPPH-free radical-scavenging activity and xanthine oxidase inhibitory activity. To determine anti-inflammatory and analgesic potential, we investigated acetic acid-induced vascular permeability and writhing test in ICR mice. For anti-pyretic activities, an LPS-induced pyrexia study was conducted in rabbits. To evaluate the anti-histamine activity, we examined compound 48/80-induced systemic anaphylaxis in ICR mice and the release of β-hexosaminidase on rat basophilic leukemia (RBL-2H3) cells. Results: Ephedrae herba, Forsythiae fructus, Cinnamomi ramulus, and Cimicifugae rhizome showed potent free-radical scavenging activities. Gentianae macrophyllae radix inhibited acetic acid-induced vascular permeability. Schizonepetae spica and Cimicifugae rhizome inhibited acetic acid. Cinnamomi ramulus and Angelicae decursivae radix inhibited LPS-induced pyrexia. Angeliace dahuricae radix and Asari radix inhibited compound 48/80. Scutellariae radix, Cinnamomi ramulus, Ephedrae herba, and Zingiberis rhizoma crudus potently inhibited the release of β-hexosaminidase. Conclusions: We examined the anti-inflammatory, analgesic, anti-pyretic and anti-histamine activities of 20 herbal medicines;We examined the anti-inflammatory, analgesic, anti-pyretic and anti-histamine activities of 20 herbal medicines Codonopsis pilosulae radix, Zingiberis rhizoma crudus, and Cinnamomi ramulus showed novel efficacy. These results suggest that some of herbal medicines may be very effective in treating common cold.

• 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.

• 한국식품영양과학회지
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• 제34권9호
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• pp.1330-1335
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• 2005

붉은 갈색계통 염색제 성분 중의 하나인 p-phenylenediamine(PPD)는 일반적으로 여성들이 사용하는 염색제의 주요 성분으로 시야 흐림 및 구토와 같은 전신적 아나필락시스, 피부염 또는 방광암 등이 유발된다고 한다. 그러나 PPD의 피부 독성과 유해산소와 관련된 연구는 아직까지 미흡한 실정이다. 본 실험에서는 체중 $230\pm20g$의 Sprague-Dawley 종의 흰쥐의 피부에 PPD을 도포하였을 때 조직의 손상정도를 상호비교하고 조직의 손상 원인을 구명하고자 실험동물에 PPD($2.5\%$ PPD in $2\%\;NH_{4}OH$)을 표면적 $25 mg/16.5\;cm^2$씩 2일 간격으로 3회 및 5회 도포하였다. PPD 3회보다 5회 도포군에서 피부조직 의 표피 및 케라틴 층의 비후, glucose 5-phosphatase 활성의 감소 및 acid phosphatase 활성의 증가 정도가 높게 나타났다. 또한 유해산소의 생성계 및 해독계와 관련하여 피부조직의 손상정도를 확인한 결과, 유해산소 생성계인 xanthine oxidase의 활성은 PPD 3회 보다5회 도포군에서 유의하게 증가하였다. 그러나 유해산소 해독계인 superoxide dismutase, catalase, glutathione S-transferase 활성 및 reduced glutathione 함량은 대조군보다 PPD 도포군에서 감소하였다. 한편, xanthine oxidase의 활성이 3회 PPD 도포군에서는 별다른 변동이 없음에도 불구하고 oxygen free radical system의 감소와 피부조직의 손상이 나타난 것은 흰쥐의 피부조직 에서 PPD를 대사하는 동안 생성된 대사산물에 의한 것으로 생각된다. 이상의 실험 결과를 종합해 볼 때 PPD 도포에 의한 피부조직의 손상은 PPD 도포 횟수에 비례하여 유해산소 생성율이 증가하여 나타난 결과로 생각된다.