KR20220162669A - Composition for preventing or treating inflammatory diseases comprising extracts of Acorus gramineus and Dendropanax morbifera - Google Patents
Composition for preventing or treating inflammatory diseases comprising extracts of Acorus gramineus and Dendropanax morbifera Download PDFInfo
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- KR20220162669A KR20220162669A KR1020220158373A KR20220158373A KR20220162669A KR 20220162669 A KR20220162669 A KR 20220162669A KR 1020220158373 A KR1020220158373 A KR 1020220158373A KR 20220158373 A KR20220158373 A KR 20220158373A KR 20220162669 A KR20220162669 A KR 20220162669A
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Abstract
Description
본 발명은 석창포 추출물 및 황칠 추출물을 포함하는 염증성 질환 예방 또는 치료용 조성물에 관한 것으로, 보다 상세하게는 석창포 추출물 및 황칠 추출물 혼합에 따라 항염증 효능이 상승된 염증성 질환의 예방 또는 치료용 약학적 조성물에 관한 것이다.The present invention relates to a composition for preventing or treating inflammatory diseases comprising an extract of Irispo and Hwangchil extract, and more particularly, a pharmaceutical composition for preventing or treating inflammatory diseases with increased anti-inflammatory efficacy according to a mixture of extract of Irispo and Hwangchil extract. It is about.
염증은 손상에 대한 살아있는 조직의 반응으로 염증 반응은 면역계를 동원 하는 생체의 방어와 치유에 핵심적인 역할을 하고 있을 뿐 아니라 많은 질병의 병리작용에 관련되어 있는 대단히 중요한 과정이다. 염증을 일으키는 원인은 무수히 많으나 세균, 진균, 바이러스와 같은 생물성 원인도 그 중 하나이다. 또한, 염증 반응 시, 면역세포인 마크로파지(macrophage)는 인터루킨(interleukin-1β, IL-1β)이나 종양괴사인자(tumor necrosis factor-α; TNF-α)와 같은 사이토카인(cytokine)류 또는 일산화질소(nitric oxide, NO)나 프로스타글란딘(prostaglandin, PG)등의 다른 염증 매개체(inflammatory mediator)를 생산함으로써 반응 진행과정에서 중요한 역할을 수행한다. 마크로파지(Macrophage)에 의한 이런 매개체의 생산은 많은 염증성 조직에서 발견된다. Inflammation is a response of living tissue to damage, and the inflammatory response not only plays a key role in defense and healing of the living body by mobilizing the immune system, but also is a very important process involved in the pathology of many diseases. There are countless causes of inflammation, but biological causes such as bacteria, fungi, and viruses are one of them. In addition, during the inflammatory response, macrophages, which are immune cells, produce cytokines such as interleukin-1β (IL-1β) or tumor necrosis factor-α (TNF-α) or nitric oxide. It plays an important role in the reaction process by producing other inflammatory mediators such as nitric oxide (NO) and prostaglandin (PG). Production of these mediators by macrophages is found in many inflammatory tissues.
예를 들어 생체가 세균 내독소(bacterial endotoxin)인 리포폴리싸카라이드(lipopolysaccharide, LPS)와 같은 외부 면역 자극 물질에 노출되면 생체신호전달 경로를 거쳐 면역세포들이 활성화되며 동시에 이들 세포에 의한 염증 유발 인자들의 발현이 증가하게 되는데, 이 과정의 첫 단계로 해당 인자의 mRNA 발현이 증가하게 된다. 또한, 증가된 IL-1β, IL-6, TNF-α 등과 같은 사이토카인, iNOS, COX-2 등과 같은 염증 매개인자 및 생체 효소들은 염증(inflammation), 통증조절 (pain control), 세포사멸(apoptosis), 종양생성(tumorigenesis), 자가면역반응(autoimmune response)등의 약리학적 또는 생리학적 생체반응에서 중요한 역할을 수행한다.For example, when a living body is exposed to an external immune stimulating substance such as lipopolysaccharide (LPS), a bacterial endotoxin, immune cells are activated through a biological signal transduction pathway, and at the same time, inflammation-inducing factors by these cells As the first step in this process, the mRNA expression of the factor increases. In addition, increased cytokines such as IL-1β, IL-6, and TNF-α, inflammatory mediators such as iNOS and COX-2, and biological enzymes promote inflammation, pain control, and apoptosis. ), tumorigenesis, autoimmune response, etc., and plays an important role in pharmacological or physiological biological reactions.
염증 매개 인자의 과생산은 류마티스성 관절염, 아테롬성 동맥경화증, 만성 간염, 폐섬유화증 등과 같은 많은 염증성 질환에서 쉽게 발견되며 이들 질환의 병리현상에 대한 주요인이 된다. 따라서, 이러한 염증 유발 매개 인자에 대한 유전자 발현의 저해방법은 다양한 염증성 질환을 예방하거나 억제할 수 있는 치료원리 및 방법이 될 수 있다. Overproduction of inflammatory mediators is easily found in many inflammatory diseases, such as rheumatoid arthritis, atherosclerosis, chronic hepatitis, and pulmonary fibrosis, and is a major factor in the pathology of these diseases. Therefore, the inhibition of gene expression for these inflammatory mediators can be a treatment principle and method capable of preventing or suppressing various inflammatory diseases.
염증성 질환은 감염, 외상, 면역학적 반응을 포함한 인체 내의 반응으로, 발열, 홍조, 부종, 통증 등의 급성 염증 증후가 있으며, 염증 과정의 후반에는 염증부위로의 백혈구의 이주 및 사이토카인(cytokine), 변성 효소(degradative enzyme), 일과성 활성산소(transient reactive oxygen species), 민감림프구(sensitized lmphocyte)의 생성 등 세포 내의 변화가 일어난다. 만성적인 염증질환에서는 백혈구의 침윤에 의해 세포 활성화 및 세포사멸이 일어난다. Inflammatory disease is a response within the body including infection, trauma, and immunological response, and has acute inflammatory symptoms such as fever, flushing, swelling, and pain. Intracellular changes such as generation of degradative enzymes, transient reactive oxygen species, and sensitized lmphocytes occur. In chronic inflammatory diseases, cell activation and apoptosis occur due to infiltration of leukocytes.
한편, 황칠나무(Dendropanax morbifera)는 두릅나무과에 속하는 식물이다. 세계에서 오직 한국의 해남, 완도와 같은 남부 해안 지역과 제주도에서만 자생하는 상록 활엽교목으로 수피에 상처를 주면 황색의 수지액이 나오는데 이것을 황칠(黃漆)이라고 한다. 본초 강목에서는 황칠나무가 번열을 제거하고, 안질 및 화상치료에 효과가 있다고 알려져 있다. 종래의 황칠나무에 관한 관련 기술로는 한국 특허공개 제2000-0004499호에 항암활성을 가지는 황칠나무 추출물이 기재되어 있고, 간세포 보호효과를 갖는 황칠 추출물, 황칠 분획물 및 이들을 함유한 약학 조성물이 기재되어 있으나, 고농도의 황칠 추출물은 세포 독성을 보이는 것으로 확인되었다.On the other hand, hwangchil tree ( Dendropanax morbifera ) is a plant belonging to the Aralia family. It is an evergreen broad-leaved arboreous tree that grows only in southern coastal areas such as Haenam and Wando in Korea and Jeju Island in the world. Hwangchil tree is known to be effective in removing burns and treating eye problems and burns. As a related technology related to Hwangchil tree, Korean Patent Publication No. 2000-0004499 describes Hwangchil tree extract having anticancer activity, Hwangchil extract having hepatocellular protective effect, Hwangchil fraction, and pharmaceutical compositions containing them. However, it was confirmed that a high concentration of hwangchil extract showed cytotoxicity.
석창포(Acorus gramineus)는 한국, 일본, 중국 및 다른 아시안 국가에서, 소화 문제, 우울증, 뇌전증 및 중추신경계 질환과 같은 다양한 질병을 치료하는데 사용되는 전통적인 약물로 오랫동안 알려져 왔다 (Koo, BS, et al., Biological & Pharmaceutical Bulletin, 26:978-982, 2000). 약물학적으로, 석창포는 항진균성, 항균성, 살충력 및 신경보호력을 가지고 있으며, 석창포를 배양된 쥐의 뉴런에 처리하였을 때, 글루타메이트에 의한 세포독성으로부터 보호한다는 보고가 있었다. 또한, 뉴런의 죽음에 의한 약화된 허혈과 억제된 메탐프타민에 의해 유발된 과다활동으로부터 보호하며, 알츠하이머 질환의 예방 및 치료에 사용된다고 보고되었다 (Lee, HS, et al., Bioresource Technology, 98:1324-1328, 2007; Cho, J, et al., Journal of Ethnopharmacology, 73:31-37, 2000; Kwon, YS, et al., Biological and Pharmaceutical Bulletin, 27:906-909, 2004). Acorus gramineus has long been known as a traditional drug used in Korea, Japan, China and other Asian countries to treat various diseases such as digestive problems, depression, epilepsy and central nervous system diseases (Koo, BS, et al. , Biological & Pharmaceutical Bulletin, 26:978-982, 2000). Pharmacologically, seokchangpo has antifungal, antibacterial, insecticidal and neuroprotective powers, and it has been reported that when seokchangpo is treated with cultured rat neurons, it protects against glutamate-induced cytotoxicity. In addition, it has been reported that it protects from attenuated ischemia due to neuronal death and hyperactivity induced by suppressed methamphetamine, and is used for the prevention and treatment of Alzheimer's disease (Lee, HS, et al. , Bioresource Technology , 98 :1324-1328, 2007; Cho, J, et al. , Journal of Ethnopharmacology , 73:31-37, 2000; Kwon, YS, et al. , Biological and Pharmaceutical Bulletin , 27:906-909, 2004).
이에, 본 발명에서는 황칠 추출물의 독성을 감소시키고 항염증 효과를 증대시키기 위해 예의 노력한 결과, 석창포 추출물 및 황칠 추출물 혼합 사용시에 세포 독성은 감소한 반면, 항염증 효과에 대해 상승효과를 보이는 것을 확인하고, 본 발명을 완성하였다.Therefore, in the present invention, as a result of diligent efforts to reduce the toxicity of Hwangchil extract and increase the anti-inflammatory effect, the cytotoxicity was reduced when the mixture of Seokchangpo extract and Hwangchil extract was used, while synergistic effect on the anti-inflammatory effect was confirmed. completed the present invention.
본 발명의 목적은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 염증성 질환의 예방 또는 치료용 약학적 조성물을 제공하는 데 있다. An object of the present invention is to provide a pharmaceutical composition for preventing or treating inflammatory diseases comprising seokchangpo extract and hwangchil extract as an active ingredient.
본 발명의 다른 목적은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 염증성 질환의 예방 또는 개선용 건강기능성 식품 조성물을 제공하는 데 있다.Another object of the present invention is to provide a health functional food composition for preventing or improving inflammatory diseases comprising seokchangpo extract and hwangchil extract as an active ingredient.
본 발명의 또 다른 목적은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 항염용 화장료 조성물을 제공하는 데 있다.Another object of the present invention is to provide a cosmetic composition for anti-inflammatory comprising seokchangpo extract and hwangchil extract as an active ingredient.
상술한 문제를 해결하기 위해, In order to solve the above problems,
본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 염증성 질환의 예방 또는 치료용 약학조성물을 제공한다. The present invention provides a pharmaceutical composition for preventing or treating inflammatory diseases comprising seokchangpo extract and hwangchil extract as an active ingredient.
본 발명의 바람직한 일실시예에 있어서, 상기 석창포 추출물 및 황칠 추출물은 물, 탄소수 1 내지 4의 저급 알코올, 에틸아세테이트, 메틸렌클로라이드 및 이들의 혼합용매로 이루어지는 군에서 선택되는 1종 이상의 용매에 의해 추출될 수 있다. In a preferred embodiment of the present invention, the seokchangpo extract and hwangchil extract are extracted by one or more solvents selected from the group consisting of water, lower alcohol having 1 to 4 carbon atoms, ethyl acetate, methylene chloride, and mixed solvents thereof It can be.
본 발명의 바람직한 다른 일실시예에 있어서, 상기 석창포 추출물 및 황칠 추출물은 물에 의해 추출될 수 있다. In another preferred embodiment of the present invention, the seokchangpo extract and hwangchil extract may be extracted by water.
본 발명의 바람직한 또 다른 일실시예에 있어서, 상기 석창포 추출물은 석창포의 뿌리줄기에서 추출되며, 황칠 추출물은 황칠의 잎, 가지 또는 수피에서 추출될 수 있다. In another preferred embodiment of the present invention, the seokchangpo extract is extracted from the rhizome of seokchangpo, hwangchil extract can be extracted from the leaves, branches or bark of hwangchil.
본 발명의 바람직한 또 다른 일실시예에 있어서, 상기 석창포 추출물 및 황칠 추출물은 9 : 1(w/w) 내지 8 : 2(w/w) 비율로, 바람직하게는 7 : 1(w/w) 비율로 혼합될 수 있다. In another preferred embodiment of the present invention, the seokchangpo extract and hwangchil extract are 9: 1 (w / w) to 8: 2 (w / w) ratio, preferably 7: 1 (w / w) They can be mixed in any proportion.
본 발명의 바람직한 또 다른 일실시예에 있어서, 상기 석창포 추출물 및 황칠 추출물은 NO, iNOS 및 COX-2를 포함하는 염증반응 매개인자(inflammatory mediators) 생성 및 TNF-α, IL-1β 및 IL-6를 포함하는 염증성 사이토카인 생성을 억제할 수 있다.In another preferred embodiment of the present invention, the seokchangpo extract and hwangchil extract produce inflammatory mediators including NO, iNOS and COX-2 and TNF-α, IL-1β and IL-6 It can inhibit the production of inflammatory cytokines, including.
본 발명의 바람직한 또 다른 일실시예에 있어서, 상기 염증성 질환은 피부염, 알레르기, 아토피, 천식, 결막염, 백내장, 치주염, 비염, 중이염, 인후염, 편도염, 폐렴, 폐혈증, 위궤양, 위염, 크론병, 치질, 강직성 척추염, 루푸스, 섬유근통, 건선, 관절염, 골관절염, 류마티스 관절염, 견관절주위염, 건염, 건초염, 근육염, 간염, 방광염, 신장염, 다발성 경화증, 당뇨병, 피부경화증, 통풍, 퇴행성 신경변성 질환, 신경염증 질환, 규폐증, 죽상동맥경화증 및 허혈 중 선택된 어느 하나 이상일 수 있다. In another preferred embodiment of the present invention, the inflammatory disease is dermatitis, allergy, atopy, asthma, conjunctivitis, cataract, periodontitis, rhinitis, otitis media, sore throat, tonsillitis, pneumonia, sepsis, gastric ulcer, gastritis, Crohn's disease, hemorrhoids , ankylosing spondylitis, lupus, fibromyalgia, psoriasis, arthritis, osteoarthritis, rheumatoid arthritis, periarthritis, tendinitis, tenosynovitis, myositis, hepatitis, cystitis, nephritis, multiple sclerosis, diabetes, scleroderma, gout, degenerative neurodegenerative diseases, neuroinflammatory diseases , silicosis, atherosclerosis, and ischemia may be any one or more selected.
본 발명의 바람직한 또 다른 일실시예에 있어서, 상기 염증성 질환은 다발성 경화증, 신경모세포종, 뇌졸중, 알츠하이머 병, 파킨슨 병, 루게릭 병, 헌팅턴 병, 크로이츠펠트야콥병, 외상 후 스트레스 장애, 우울증, 학습장애, 인지장애, 기억력손상, 정신분열증, 및 근위축성측색경화증으로 이루어진 군에서 선택되는 신경 염증성 질환일 수 있다.In another preferred embodiment of the present invention, the inflammatory disease is multiple sclerosis, neuroblastoma, stroke, Alzheimer's disease, Parkinson's disease, Lou Gehrig's disease, Huntington's disease, Creutzfeldt-Jakob disease, post-traumatic stress disorder, depression, learning disability, It may be a neuroinflammatory disease selected from the group consisting of cognitive impairment, memory impairment, schizophrenia, and amyotrophic lateral sclerosis.
또한, 본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 염증성 질환의 예방 또는 개선용 건강기능식품 조성물을 제공한다.In addition, the present invention provides a health functional food composition for preventing or improving inflammatory diseases comprising seokchangpo extract and hwangchil extract as an active ingredient.
또한, 본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 항염용 화장료 조성물을 제공한다.In addition, the present invention provides an anti-inflammatory cosmetic composition comprising an extract of seokchangpo and hwangchil extract as an active ingredient.
또한, 본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 인지 기능 증진용 조성물을 제공한다.In addition, the present invention provides a composition for enhancing cognitive function comprising seokchangpo extract and hwangchil extract as an active ingredient.
또한, 본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 인지 장애 질환 예방 또는 치료용 약학적 조성물, 인지 장애 질환 또는 기억력 개선용 건강기능식품 조성물을 제공한다.In addition, the present invention provides a pharmaceutical composition for preventing or treating cognitive disorder disease, a functional food composition for improving cognitive disorder disease or memory, comprising an extract of seokchangpo and hwangchil extract as an active ingredient.
본 발명에서는 석창포 추출물 및 황칠 추출물 혼합 사용시에 항염증 효능은 현저하게 상승한 반면, 세포 독성은 오히려 감소한 것을 확인하였으므로, 본 발명의 석창포 추출물 및 황칠 추출물은 염증성 질환의 치료 및 예방용 약학적 조성물 또는 건강기능성 식품뿐만 아니라 항염증용 화장료 조성물에 유용하게 이용할 수 있다.In the present invention, anti-inflammatory efficacy was remarkably increased when using a mixture of extract and hwangchil extract, whereas it was confirmed that the cytotoxicity rather decreased, the extract of seokchangpo and hwangchil extract of the present invention is a pharmaceutical composition for the treatment and prevention of inflammatory diseases or health It can be usefully used in cosmetic compositions for anti-inflammatory as well as functional foods.
도 1은 석창포 추출물 및 황칠 추출물 단독 처리시 항염증 효과 및 세포 독성을 확인한 데이터이다 (A: 황칠 추출물 처리에 따른 NO 발생, B: 황칠 추출물 처리에 따른 세포 생존율, C: 석창포 추출물 처리에 따른 NO 발생, D: 석창포 추출물 처리에 따른 세포 생존율).
도 2는 석창포 추출물 및 황칠 추출물 혼합 처리시 항염증 효과 및 세포 독성을 확인한 데이터이다 (A: NO 발생, B: 세포 생존율).
도 3은 석창포 추출물 및 황칠 추출물 혼합 처리시 iNOS 및 COX-2를 포함하는 염증반응 매개인자(inflammatory mediators)의 mRNA 발현 정도를 확인한 데이터이다 (A: PCR에 따른 전기영동 밴드, B: GAPDH 대비 iNOS mRNA 발현량, C: GAPDH 대비 COX-2 mRNA 발현량).
도 4는 석창포 추출물 및 황칠 추출물 혼합 처리시 TNF-α, IL-1β 및 IL-6를 포함하는 염증성 사이토카인의 mRNA 발현 정도를 확인한 데이터이다 (A: PCR에 따른 전기영동 밴드, B: GAPDH 대비 TNF-α mRNA 발현량, C: GAPDH 대비 IL-1β mRNA 발현량, D: GAPDH 대비 IL-6 mRNA 발현량).
도 5는 석창포 추출물 및 황칠 추출물 혼합 처리시 iNOS 및 COX-2를 포함하는 염증반응 매개인자(inflammatory mediators)의 단백질 발현 정도를 확인한 데이터이다 (A: 웨스턴 블랏 밴드, B: β-actin 대비 iNOS 단백질 발현량, C: β-actin 대비 COX-2 단백질 발현량).Figure 1 is data confirming the anti-inflammatory effect and cytotoxicity when the extract and hwangchil extract alone were treated (A: NO generation according to hwangchil extract treatment, B: cell viability according to hwangchil extract treatment, C: NO according to hwangchil extract treatment Occurrence, D: cell viability according to the treatment with the extract of Iris Iris).
Figure 2 is the data confirming the anti-inflammatory effect and cytotoxicity of the seokchangpo extract and Hwangchil extract mixed treatment (A: NO generation, B: cell viability).
Figure 3 is data confirming the mRNA expression level of inflammatory mediators including iNOS and COX-2 during the mixed treatment of seokchangpo extract and hwangchil extract (A: electrophoretic band according to PCR, B: iNOS compared to GAPDH mRNA expression level, C: COX-2 mRNA expression level relative to GAPDH).
Figure 4 is data confirming the mRNA expression level of inflammatory cytokines including TNF-α, IL-1β and IL-6 during the treatment of seokchangpo extract and hwangchil extract mixture (A: electrophoretic band according to PCR, B: GAPDH contrast TNF-α mRNA expression level, C: GAPDH versus IL-1β mRNA expression level, D: GAPDH versus IL-6 mRNA expression level).
Figure 5 is data confirming the protein expression level of inflammatory mediators including iNOS and COX-2 during the mixed treatment of seokchangpo extract and hwangchil extract (A: Western blot band, B: iNOS protein compared to β-actin Expression level, C: COX-2 protein expression level relative to β-actin).
상술한 바와 같이, 고농도의 황칠 추출물을 세포 독성을 보이는 문제점이 있다. 이에, 본 발명에서는 황칠 추출물의 독성을 감소시키고 항염증 효과를 증대시키기 위해 세포 독성 없이 항염증 효과가 우수한 물질을 선별하고자 예의 노력한 결과, 석창포 추출물 및 황칠 추출물 혼합 사용시에 세포 독성은 감소한 반면, 항염증 효과에 대해 상승효과를 보이는 것을 확인하였다.As described above, there is a problem in that high concentrations of hwangchil extract show cytotoxicity. Therefore, in the present invention, as a result of diligent efforts to select a substance having excellent anti-inflammatory effect without cytotoxicity in order to reduce the toxicity of Hwangchil extract and increase the anti-inflammatory effect, the cytotoxicity is reduced when using a mixture of Seokchangpo extract and Hwangchil extract, while anti-inflammatory It was confirmed that it showed a synergistic effect on the inflammatory effect.
따라서, 본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 염증성 질환의 예방 또는 치료용 약학조성물에 관한 것이다.Therefore, the present invention relates to a pharmaceutical composition for the prevention or treatment of inflammatory diseases comprising an extract of seokchangpo and hwangchil extract as an active ingredient.
본 발명에 있어서, 상기 석창포 추출물 및 황칠 추출물은 물, 탄소수 1 내지 4의 저급 알코올, 에틸아세테이트, 메틸렌클로라이드 및 이들의 혼합용매로 이루어지는 군에서 선택되는 1종 이상의 용매에 의해 추출될 수 있다. 또한 추출방법으로는 상온추출법, 열수추출법, 냉침추출법, 환류추출법, 용매추출법, 수증기증류법, 초음파추출법, 용출법, 압착법 등의 방법이 사용될 수 있다. 본 발명의 석창포 추출물 및 황칠 추출물은 바람직하게는 열수추출법을 이용하여 각각 추출하는 것을 특징으로 할 수 있다. In the present invention, the seokchangpo extract and hwangchil extract may be extracted by one or more solvents selected from the group consisting of water, lower alcohols having 1 to 4 carbon atoms, ethyl acetate, methylene chloride, and mixed solvents thereof. In addition, as the extraction method, methods such as room temperature extraction, hot water extraction, cold brew extraction, reflux extraction, solvent extraction, steam distillation, ultrasonic extraction, elution, and compression may be used. Seokchangpo extract and hwangchil extract of the present invention may be characterized in that each extraction is preferably performed using a hot water extraction method.
본 발명에 있어서, 상기 석창포 추출물은 석창포의 뿌리줄기에서 추출되며, 황칠 추출물은 황칠의 잎, 가지 또는 수피에서 추출되는 것을 특징으로 한다. In the present invention, the seokchangpo extract is extracted from the rhizome of seokchangpo, hwangchil extract is characterized in that extracted from the leaves, branches or bark of hwangchil.
본 발명에 있어서, 상기 석창포 추출물 및 황칠 추출물은 9 : 1(w/w) 내지 8 : 2(w/w) 비율로, 바람직하게는 7 : 1(w/w) (또는, 8.75 : 1.25 (w/w)) 비율로 혼합될 수 있다. In the present invention, the seokchangpo extract and hwangchil extract are 9: 1 (w / w) to 8: 2 (w / w) ratio, preferably 7: 1 (w / w) (or, 8.75: 1.25 ( w/w)) ratio.
상기 석창포 추출물 및 황칠 추출물을 중량비로 나타내면 100 중량부당 석창포 추출물은 85 ~ 90 중량부, 바람직하게는 87.5 중량부로 포함될 수 있으며, 황칠 추출물은 10 ~ 15 중량부, 바람직하게는 12.5 중량부로 포함될 수 있다.When the seokchangpo extract and hwangchil extract are expressed in weight ratio, the seokchangpo extract per 100 parts by weight may be included in 85 to 90 parts by weight, preferably 87.5 parts by weight, and the hwangchil extract may be included in 10 to 15 parts by weight, preferably 12.5 parts by weight. .
본 발명에 있어서, 상기 석창포 추출물 및 황칠 추출물은 NO, iNOS 및 COX-2를 포함하는 염증반응 매개인자(inflammatory mediators) 생성을 억제하는 것을 특징으로 할 수 있다. 또한, 상기 석창포 추출물 및 황칠 추출물은 IL-1β, IL-6 및 TNF-α를 포함하는 염증성 사이토카인(cytokines) 생성을 억제하는 것을 특징으로 할 수 있다.In the present invention, the seokchangpo extract and hwangchil extract may be characterized by inhibiting the production of inflammatory mediators including NO, iNOS and COX-2. In addition, the seokchangpo extract and hwangchil extract may be characterized by inhibiting the production of inflammatory cytokines (cytokines) including IL-1β, IL-6 and TNF-α.
본 발명의 구체적인 일구현예에서, 황칠 열수 추출물 및 석창포 열수 추출물을 추출한 다음 각각의 추출물에 대한 세포 독성 및 항염증 활성을 확인하였다. 그 결과, 도 1에 나타난 바와 같이, 황칠 열수 추출물은 농도 의존적으로 NO 발생을 억제하나, 고농도에서는 세포 독성을 보이는 것을 확인하였다. 반면, 석창포 열수 추출물은 세포독성이 없는 것을 확인하였으며, 황칠 추출물 보다 항염증 활성은 낮으나 농도 의존적으로 NO 발생을 억제하는 것을 확인하였다.In a specific embodiment of the present invention, Hwangchil hot water extract and seokchangpo hot water extract were extracted, and then the cytotoxicity and anti-inflammatory activity of each extract was confirmed. As a result, as shown in FIG. 1, it was confirmed that Hwangchil hot water extract suppressed NO generation in a concentration-dependent manner, but exhibited cytotoxicity at high concentrations. On the other hand, it was confirmed that the hot water extract of Seokchangpo was not cytotoxic, and it was confirmed that the anti-inflammatory activity was lower than that of Hwangchil extract, but it inhibited NO generation in a concentration-dependent manner.
본 발명의 구체적인 다른 일구현예에서, 석창포 열수 추출물 및 황칠 열수 추출물을 혼합하였을 때, 항염증 효능에 대한 상승효과(synergy effect)를 보이는지 확인하기 위해, NO 발생 억제 효능에 대한 IC50 농도 값을 기준으로 두 추출물을 배합하였다. 황칠 열수 추출물의 IC50 값은 100 ㎍/㎖, 석창포 추출물의 IC50 값은 700 ㎍/㎖으로 확인되었으므로, 이를 참고로 석창포 추출물 및 황칠 추출물이 7 : 1(w/w) 비율로 배합하였다. 도 2에 나타난 바와 같이 석창포 추출물 및 황칠 추출물이 7 : 1(w/w) 비율로 배합된 경우, 세포독성 없이 높은 항염증 효능을 보이는 것을 확인하였다. 또한, 석창포 열수 추출물 및 황칠 열수 추출물의 총합이 800 ㎍인 경우에는 NO 발생이 억제율이 가장 높았으며, 세포 독성은 전혀 보이지 않는 것을 확인하였다. In another specific embodiment of the present invention, when the hot water extract of Seokchangpo and the hot water extract of Hwangchil were mixed, in order to determine whether a synergy effect on the anti-inflammatory effect was observed, the IC 50 concentration value for the NO generation inhibitory effect was measured. Two extracts were combined as a basis. Since the IC 50 value of hwangchil hot water extract was 100 μg/ml and the IC 50 value of seokchangpo extract was confirmed to be 700 μg/ml, with reference to this, the seokchangpo extract and hwangchil extract were blended at a 7: 1 (w/w) ratio. As shown in Figure 2, it was confirmed that when the seokchangpo extract and hwangchil extract were combined in a 7: 1 (w / w) ratio, high anti-inflammatory efficacy without cytotoxicity. In addition, when the total amount of the hot water extract of Seokchangpo and the hot water Hwangchil extract was 800 μg, the NO generation inhibition rate was the highest, and it was confirmed that no cytotoxicity was observed.
나아가, 석창포 추출물 및 황칠 추출물의 혼합에 대한 상승 효과를 추가적으로 검증하기 위해 콜비(Colby)식을 사용하여 측정한 결과, 콜비식으로 계산된 이론값에 비해, 석창포 추출물 및 황칠 추출물이 7 : 1(w/w) 비율로 혼합된 경우(실측값)이 더 높은 것을 확인하였으며, 이는 석창포 추출물 및 황칠 추출물을 혼합할 경우 두 물질의 혼합에 따른 상승효과로 인해 항염증 활성이 증가한 것을 의미한다.Furthermore, in order to additionally verify the synergistic effect of the mixture of the extract of Irispo and Hwangchil extract, the results measured using the Colby formula, compared to the theoretical value calculated by the Colby formula, the extract of Seokchangpo and Hwangchil extract were 7: 1 ( w / w) it was confirmed that the ratio (measured value) was higher, which means that the anti-inflammatory activity increased due to the synergistic effect of the mixing of the two substances when the seokchangpo extract and hwangchil extract were mixed.
*본 발명의 구체적인 또 다른 일구현예에서, 석창포 추출물 및 황칠 추출물 혼합하였을 때, iNOS 및 COX-2를 포함하는 염증반응 매개인자(inflammatory mediators)의 mRNA 및 단백질 발현 정도를 확인하였다. 그 결과, 도 3 및 도 5에 나타난 바와 같이, 석창포 및 황칠 혼합 추출물에 의해 염증반응 매개인자(inflammatory mediators)인 iNOS 및 COX-2 mRNA 및 단백질 발현이 감소하는 것을 확인하였다. 또한, 석창포 추출물 및 황칠 추출물 단독 처리군 보다 석창포 및 황칠 추출물을 혼합하였을 때, iNOS 및 COX-2 단백질 발현이 효과적으로 억제되는 것을 확인하였다.* In another specific embodiment of the present invention, when seokchangpo extract and hwangchil extract were mixed, the mRNA and protein expression levels of inflammatory mediators including iNOS and COX-2 were confirmed. As a result, as shown in Figures 3 and 5, it was confirmed that the expression of iNOS and COX-2 mRNA and protein, which are inflammatory mediators, was reduced by the mixed extract of seokchangpo and hwangchil. In addition, it was confirmed that the iNOS and COX-2 protein expression was effectively suppressed when the mixture of seokchangpo and hwangchil extracts than the seokchangpo extract and hwangchil extract alone treatment group.
또한, 석창포 추출물 및 황칠 추출물 혼합하였을 때, TNF-α, IL-1β 및 IL-6를 포함하는 염증성 사이토카인의 mRNA 발현 정도를 확인한 결과, 도 4에 나타난 바와 같이, TNF-α, IL-1β 및 IL-6 생성이 감소하였으며, 특히 TNF-α및 IL-1β의 경우 단독 처리군에 비해 석창포 및 황칠 혼합 추출물 처리군에서 생성이 현저하게 감소하는 것을 확인하였다. In addition, as a result of confirming the mRNA expression level of inflammatory cytokines including TNF-α, IL-1β and IL-6, as shown in Figure 4, TNF-α, IL-1β when the extract of Seokchangpo and Hwangchil extract were mixed. And IL-6 production was reduced, in particular, in the case of TNF-α and IL-1β, it was confirmed that the production was significantly reduced in the seokchangpo and Hwangchil mixed extract treatment group compared to the single treatment group.
즉, 본 발명에서는 석창포 추출물 및 황칠 추출물 혼합 사용시에 항염증 효과에 대해 상승효과를 보이며, 세포 독성은 감소한 것을 확인하였으므로, 염증성 질환의 치료 및 예방에 활용될 수 있음을 확인하였다.That is, in the present invention, it was confirmed that it can be used for the treatment and prevention of inflammatory diseases, since it was confirmed that the anti-inflammatory effect was synergistic and the cytotoxicity was reduced when using a mixture of seokchangpo extract and hwangchil extract.
본 발명에 있어서, 상기 염증성 질환은 피부염, 알레르기, 아토피, 천식, 결막염, 백내장, 치주염, 비염, 중이염, 인후염, 편도염, 폐렴, 폐혈증, 위궤양, 위염, 크론병, 치질, 강직성 척추염, 루푸스, 섬유근통, 건선, 관절염, 골관절염, 류마티스 관절염, 견관절주위염, 건염, 건초염, 근육염, 간염, 방광염, 신장염, 다발성 경화증, 당뇨병, 피부경화증, 통풍, 퇴행성 신경변성질환, 규폐증, 죽상동맥경화증 및 허혈 중 선택된 어느 하나 이상일 수 있다. In the present invention, the inflammatory disease is dermatitis, allergy, atopy, asthma, conjunctivitis, cataract, periodontitis, rhinitis, otitis media, sore throat, tonsillitis, pneumonia, sepsis, gastric ulcer, gastritis, Crohn's disease, hemorrhoids, ankylosing spondylitis, lupus, fibromyalgia , Psoriasis, arthritis, osteoarthritis, rheumatoid arthritis, periarthritis, tendonitis, tenosynovitis, myositis, hepatitis, cystitis, nephritis, multiple sclerosis, diabetes, scleroderma, gout, neurodegenerative disease, silicosis, atherosclerosis and ischemia There can be more than one.
또한, 상기 염증성 질환은 상기 염증성 질환은 다발성 경화증, 신경모세포종, 뇌졸중, 알츠하이머 병, 파킨슨 병, 루게릭 병, 헌팅턴 병, 크로이츠펠트야콥병, 외상 후 스트레스 장애, 우울증, 학습장애, 인지장애, 기억력손상, 정신분열증, 및 근위축성측색경화증으로 이루어진 군에서 선택되는 신경 염증성 질환일 수 있다.In addition, the inflammatory diseases include multiple sclerosis, neuroblastoma, stroke, Alzheimer's disease, Parkinson's disease, Lou Gehrig's disease, Huntington's disease, Creutzfeldt-Jakob disease, post-traumatic stress disorder, depression, learning disability, cognitive impairment, memory impairment, It may be a neuroinflammatory disease selected from the group consisting of schizophrenia and amyotrophic lateral sclerosis.
본 발명의 약학적 조성물 100 중량부에 포함된 석창포 및 황칠 혼합 추출물은 0.01 중량부 내지 50 중량부, 바람직하게는 0.01 중량부 내지 25 중량부로 포함될 수 있으나, 이에 제한되지 않고 황칠 추출물에 의한 세포 독성을 보이지 않으며, 높은 항염증 효능을 보이는 범위 내로 포함될 수 있다.The mixed extract of Seokchangpo and Hwangchil contained in 100 parts by weight of the pharmaceutical composition of the present invention may be included in 0.01 part by weight to 50 parts by weight, preferably 0.01 part by weight to 25 parts by weight, but is not limited thereto, and the cytotoxicity of Hwangchil extract is not limited thereto. It does not show, and can be included within the range showing high anti-inflammatory efficacy.
본 발명의 약학 조성물은 각각 통상의 방법에 따라 다양한 형태로 제형화하여 사용될 수 있다. 예컨대, 산제, 과립제, 정제, 캡슐제, 현탁액, 에멀젼, 시럽 등의 경구형 제형으로 제형화할 수 있고, 외용제, 좌제 및 멸균 주사용액의 형태로 제형화하여 사용될 수 있다. 또한, 액제, 연고제, 크림제, 로션제, 스프레이제, 패취제, 겔제 또는 에어로졸제 등의 피부외용제의 형태로 사용될 수 있다.The pharmaceutical composition of the present invention may be formulated and used in various forms according to conventional methods. For example, it can be formulated into oral formulations such as powders, granules, tablets, capsules, suspensions, emulsions and syrups, and can be formulated and used in the form of external preparations, suppositories and sterile injection solutions. In addition, it may be used in the form of an external skin preparation such as a solution, ointment, cream, lotion, spray, patch, gel or aerosol.
각각의 제형에 따라 약학적으로 허용가능한 담체, 부형제 및 희석제를 더 포함할 수 있다. 또한 통상의 방법에 따라 산제, 과립제, 정제, 캡슐제, 현탁액, 에멀젼, 시럽, 에어로졸 등의 외용제 및 멸균 주사용액의 형태로 제형화하여 사용될 수 있으며, 바람직하게는 크림, 젤, 패취, 분무제, 연고제, 경구제, 로션제, 리니멘트제, 파스타제 또는 카타플라스마제 제형을 가질 수 있다. 예컨대, 해당 부위에 국부적으로 사용되는 피부외용제인 경우에는 통상적인 첨가제, 예를 들어 보존제, 의약 침투를 보조하는 용매, 연고 및 크림의 경우 연화제 등을 포함할 수 있으며, 에탄올 또는 올레일 알코올과 같은 통상적 담체를 함유할 수 있다.Depending on each formulation, pharmaceutically acceptable carriers, excipients and diluents may be further included. In addition, it can be formulated and used in the form of external preparations such as powders, granules, tablets, capsules, suspensions, emulsions, syrups, aerosols, and sterile injection solutions according to conventional methods, and preferably creams, gels, patches, sprays, It may have a formulation of an ointment, an oral agent, a lotion, a liniment agent, a pasta agent, or a cataplasma agent. For example, in the case of external skin preparations used locally on the corresponding area, conventional additives such as preservatives, solvents to aid drug penetration, ointments and creams may include softeners, etc., and ethanol or oleyl alcohol It may contain conventional carriers.
상기 담체, 부형제 및 희석제로는 락토즈, 덱스트로즈, 수크로스, 올리고당, 솔비톨, 만니톨, 자일리톨, 에리스리톨, 말티톨, 전분, 아카시아 고무, 알지네이트, 젤라틴, 칼슘 포스페이트, 칼슘 실리케이트, 셀룰로오스, 메틸 셀룰로오스, 미정질 셀룰로오스, 폴리비닐 피롤리돈, 물, 메틸히드록시 벤조에이트, 프로필히드록시 벤조에이트, 탈크, 마그네슘 스테아레이트, 광물유 등이 있다. 상기 약학 조성물을 제제화나 제형화할 경우에는 보통 사용하는 충진제, 증량제, 결합제, 습윤제, 붕해제, 계면활성제 등의 희석제 또는 부형제를 사용하여 조제된다.The carriers, excipients and diluents include lactose, dextrose, sucrose, oligosaccharides, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, gum acacia, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methyl cellulose, Microcrystalline cellulose, polyvinyl pyrrolidone, water, methylhydroxy benzoate, propylhydroxy benzoate, talc, magnesium stearate, mineral oil and the like. When formulating or formulating the pharmaceutical composition, it is prepared using diluents or excipients such as commonly used fillers, extenders, binders, wetting agents, disintegrants, and surfactants.
경구투여를 위한 고형제제에는 정제, 환제, 산제, 과립제, 캡슐제 등이 포함되며, 이러한 고형제제는 상기 조성물에 적어도 하나 이상의 부형제, 예를 들면 전분, 칼슘 카보네이트(calcium carbonate), 수크로오스(sucrose), 락토오스(lactose), 젤라틴 등을 섞어 조제된다. 또한 단순한 부형제 이외에 마그네슘 스티레이트 탈크 같은 윤활제들도 사용된다. 경구를 위한 액상제제로는 현탁제, 내용액제, 유제, 시럽제 등이 해당되는데, 흔히 사용되는 단순 희석제인 물, 리퀴드 파라핀 이외에 여러 가지 부형제, 예를 들면 습윤제, 감미제, 방향제, 보존제 등이 포함될 수 있다. 비경구 투여를 위한 제제에는 멸균된 수용액, 비수성용제, 현탁제, 유제, 동결건조 제제, 좌제 등이 포함된다. 비수성용제, 현탁제로는 프로필렌글리콜(propylene glycol), 폴리에틸렌글리콜, 올리브 오일과 같은 식물성 기름, 에틸올레이트와 같은 주사 가능한 에스테르 등이 사용될 수 있다. 좌제의 기제로는 위텝솔(witepsol), 마크로골, 트윈(tween) 61, 카카오지, 라우린지, 글리세로제라틴 등이 사용될 수 있다.Solid preparations for oral administration include tablets, pills, powders, granules, capsules, etc., and these solid preparations contain at least one excipient such as starch, calcium carbonate, sucrose, etc. It is prepared by mixing lactose, gelatin, etc. In addition to simple excipients, lubricants such as magnesium stearate and talc are also used. Liquid preparations for oral use include suspensions, solutions for oral use, emulsions, and syrups. In addition to water and liquid paraffin, which are commonly used simple diluents, various excipients such as wetting agents, sweeteners, aromatics, and preservatives may be included. have. Preparations for parenteral administration include sterilized aqueous solutions, non-aqueous solvents, suspensions, emulsions, freeze-dried preparations, suppositories, and the like. Propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable esters such as ethyl oleate may be used as non-aqueous solvents and suspending agents. As a base for the suppository, witepsol, macrogol, tween 61, cacao butter, laurin paper, glycerogeratin and the like may be used.
본 발명에서 사용되는 용어 "투여"는 임의의 적절한 방법으로 개체에게 본 발명의 약학 조성물을 제공하는 것을 의미한다. 본 발명은 약학 조성물은 연구자, 수의사, 의사 또는 기타 임상에 의해 생각되는 조직계, 동물 또는 인간에서 생물학적 또는 의학적 반응을 유도하는 유효 성분 또는 약학적 조성물의 양, 즉 치료되는 질환 또는 장애의 증상의 완화를 유도하는 양인 치료상 유효량으로 투여할 수 있다. 본 발명의 약학 조성물에 대한 치료상 유효 투여량 및 투여횟수는 원하는 효과에 따라 변화될 것임은 당업자에게 자명하다. 그러므로, 투여될 최적의 투여량은 당업자에 의해 쉽게 결정될 수 있으며, 질환의 종류, 질환의 중증도, 조성물에 함유된 유효성분 및 다른 성분의 함량, 제형의 종류, 환자의 연령, 체중, 일반 건강 상태, 성별 및 식이, 투여시간, 투여 경로 및 조성물의분비율, 치료기간, 동시 사용되는 약물을 비롯한 다양한 인자 등에 따라 조절될 수 있다. 본 발명의 약학 조성물은 개체에게 다양한 경로로 투여될 수 있다. 예를 들어, 정맥내, 복강내, 근육내, 동맥내, 구강, 심장내, 골수내, 경막내, 경피, 장관, 피하, 설하 또는 국소 투여할 수 있으나, 이에 제한되지 않는다. 본 발명의 약학 조성물은 1~10,000㎎/㎏/일의 양으로 투여할 수 있으며, 하루에 한번 투여할 수도 있고, 수 회에 나누어 투여할 수도 있다.As used herein, the term "administration" means providing the pharmaceutical composition of the present invention to a subject by any suitable method. The pharmaceutical composition of the present invention is the amount of an active ingredient or pharmaceutical composition that induces a biological or medical response in a tissue system, animal or human thought by a researcher, veterinarian, physician or other clinician, that is, alleviation of the symptoms of the disease or disorder being treated It can be administered in a therapeutically effective amount, which is an amount that induces It is apparent to those skilled in the art that the therapeutically effective dosage and frequency of administration of the pharmaceutical composition of the present invention will vary depending on the desired effect. Therefore, the optimal dosage to be administered can be easily determined by those skilled in the art, and the type of disease, the severity of the disease, the content of the active ingredient and other ingredients contained in the composition, the type of dosage form, the patient's age, weight, and general health condition , gender and diet, administration time, route of administration and secretion rate of the composition, treatment period, can be adjusted according to various factors including drugs used simultaneously. The pharmaceutical composition of the present invention can be administered to a subject by various routes. For example, intravenous, intraperitoneal, intramuscular, intraarterial, buccal, intracardiac, intramedullary, intrathecal, transdermal, intestinal, subcutaneous, sublingual or topical administration may be administered, but is not limited thereto. The pharmaceutical composition of the present invention may be administered in an amount of 1 to 10,000 mg/kg/day, and may be administered once a day or divided into several times.
또한, 본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 염증성 질환의 예방 또는 개선용 건강기능식품 조성물에 관한 것이다.In addition, the present invention relates to a health functional food composition for preventing or improving inflammatory diseases comprising seokchangpo extract and hwangchil extract as an active ingredient.
본 발명에 있어서, 상기 석창포 추출물 및 황칠 추출물은 9 : 1(w/w) 내지 8 : 2(w/w) 비율로, 바람직하게는 7 : 1(w/w) 비율로 혼합될 수 있으며, 구체적인 내용은 상기 염증성 질환의 예방 또는 치료용 약학적 조성물과 동일하다. In the present invention, the seokchangpo extract and hwangchil extract may be mixed in a ratio of 9: 1 (w / w) to 8: 2 (w / w), preferably in a ratio of 7: 1 (w / w), The specific details are the same as the pharmaceutical composition for preventing or treating inflammatory diseases.
본 발명의 석창포 추출물 및 황칠 추출물은 건강기능식품, 식품 첨가제 또는 식이보조제로 사용될 수 있다. 본 발명의 추출물이 식품 첨가제로 사용할 경우, 추출물을 그대로 첨가하거나, 다른 식품 또는 식품 성분과 함께 혼합하여 사용되는 등 통상적인 방법에 따라 적절하게 사용될 수 있다.Seokchangpo extract and hwangchil extract of the present invention can be used as a health functional food, food additive or dietary supplement. When the extract of the present invention is used as a food additive, it may be appropriately used according to a conventional method, such as adding the extract as it is or mixing it with other foods or food ingredients.
또한 상기 석창포 추출물 및 황칠 추출물의 혼합양은 사용 목적(예방, 건강 또는 치료적 처치)에 따라 적합하게 변경될 수 있다. 구체적인 예로, 식품 또는 음료의 제조 시에는 본 발명의 추출물은 원료에 대하여 15중량% 이하, 바람직하게는 10중량% 이하의 양으로 첨가된다. 그러나 건강 및 위생을 목적으로 하거나 또는 건강 조절을 목적으로 하여 장기간 섭취할 경우에는 상기 범위 이하의 양으로 첨가될 수 있으며, 안전성 면에서 아무런 문제가 없기 때문에 유효성분은 상기 범위 이상의 양으로도 사용될 수 있다.In addition, the mixed amount of the seokchangpo extract and hwangchil extract may be appropriately changed according to the purpose of use (prevention, health or therapeutic treatment). As a specific example, when preparing food or beverage, the extract of the present invention is added in an amount of 15% by weight or less, preferably 10% by weight or less, based on the raw material. However, for long-term intake for health and hygiene purposes or health control purposes, it may be added in an amount below the above range, and since there is no problem in terms of safety, the active ingredient may be used in an amount above the above range. have.
상기 식품의 종류에는 특별한 제한은 없으나, 본 발명의 추출물을 첨가할 수 있는 식품의 예로는 육류, 소시지, 빵, 초콜릿, 캔디류, 스낵류, 과자류, 피자, 라면, 기타 면류, 껌류, 아이스크림류를 포함한 낙농제품, 각종 수프, 음료수, 차, 드링크제, 알코올 음료, 비타민 복합제 등이 있으며, 통상적인 의미에서의 건강식품을 모두 포함한다.There is no particular limitation on the type of food, but examples of food to which the extract of the present invention can be added include meat, sausage, bread, chocolate, candy, snacks, confectionery, pizza, ramen, other noodles, chewing gum, and ice cream. Dairy products, various soups, beverages, tea, drinks, alcoholic beverages, vitamin complexes, etc., include all health foods in a conventional sense.
본 발명의 식품 조성물이 음료로 제조될 경우 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등의 추가 성분을 포함할 수 있다. 상기 천연 탄수화물로는 포도당, 과당 등의 모노사카라이드; 말토오스, 수크로오스 등의 디사카라이드; 덱스트린, 사이클로덱스트린 등의 천연 감미제; 사카린, 아스파르탐 등의 합성 감미제 등이 사용될 수 있다. 상기 천연 탄수화물은 본 발명의 식품 조성물 총 중량에 대하여 0.01 ~ 10중량%, 바람직하 게는 0.01 ~ 0.1중량%로 포함된다.When the food composition of the present invention is prepared as a beverage, it may contain additional ingredients such as various flavoring agents or natural carbohydrates, like conventional beverages. Examples of the natural carbohydrate include monosaccharides such as glucose and fructose; disaccharides such as maltose and sucrose; natural sweeteners such as dextrins and cyclodextrins; Synthetic sweeteners such as saccharin and aspartame may be used. The natural carbohydrate is included in an amount of 0.01 to 10% by weight, preferably 0.01 to 0.1% by weight, based on the total weight of the food composition of the present invention.
본 발명의 식품 조성물은 여러 가지 영양제, 비타민, 전해질, 풍미제, 착색제, 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알코올, 탄산음료에 사용되는 탄산화제 등을 포함할 수 있으며, 천연 과일주스, 과일주스 음료 및 야채 음료의 제조를 위한 과육을 포함 할 수 있으나 이에 제한되지 않는다. 이러한 성분은 독립적으로 또는 조합하여 사용할 수 있다. 상기의 첨가제 비율은 크게 제한되지는 않으나, 본 발명의 식품 조성물 총 중량에 대하여 0.01 ~ 0.1중량% 범위내로 포함되는 것이 바람직하다.The food composition of the present invention contains various nutrients, vitamins, electrolytes, flavors, colorants, pectic acid and its salts, alginic acid and its salts, organic acids, protective colloidal thickeners, pH adjusters, stabilizers, preservatives, glycerin, alcohols, carbonic acid It may include carbonation agents used in beverages, etc., and may include fruit flesh for the manufacture of natural fruit juice, fruit juice beverages, and vegetable beverages, but is not limited thereto. These components may be used independently or in combination. The proportion of the above additives is not particularly limited, but is preferably included within the range of 0.01 to 0.1% by weight based on the total weight of the food composition of the present invention.
또한, 본 발명은 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 항염용 화장료 조성물에 관한 것이다.In addition, the present invention relates to an anti-inflammatory cosmetic composition comprising an extract of seokchangpo and hwangchil extract as an active ingredient.
본 발명의 화장료 조성물은 상기 유효성분 이외에 화장료 조성물에 통상적으로 사용되는 항산화제, 안정화제, 용해화제, 비타민, 안료, 향료 등과 같은 통상적인 보조제 및 담체가 더 포함될 수 있다. 예를 들어, 상기 화장료 조성물에는 글리세린, 부틸렌 글라이콜, 폴리옥시에칠렌 경화피마자유, 토코페릴 아세테이트, 시트릭산, 판테놀, 스쿠알란, 소듐 시트레이트, 알란토인 등의 보조성분이 추가로 더 포함될 수 있다.The cosmetic composition of the present invention may further include conventional adjuvants and carriers such as antioxidants, stabilizers, solubilizers, vitamins, pigments, fragrances, etc., which are commonly used in cosmetic compositions, in addition to the above active ingredients. For example, the cosmetic composition may further include auxiliary ingredients such as glycerin, butylene glycol, polyoxyethylene hydrogenated castor oil, tocopheryl acetate, citric acid, panthenol, squalane, sodium citrate, and allantoin. .
본 발명의 화장료 조성물은 기본적으로 피부에 도포되는 것이므로, 당업계의 화장료 조성물을 참조하여 통상적으로 제조되는 어떠한 제형으로도 제조될 수 있다. 예를 들어, 용액, 현탁액, 유탁액, 페이스트, 겔, 크림, 로션, 파우더, 비누, 계면활성제-함유 클린싱, 오일, 분말 파운데이션, 유탁액 파운데이션, 왁스 파운데이션 및 스프레이 등으로 제형화될 수 있으나, 이에 한정되는 것은 아니다. 보다 상세하게는, 유연 화장수, 영양 화장수, 영양크림, 마사지크림, 에센스, 아이크림, 클렌징크림, 클렌징폼, 클렌징워터, 마스크팩, 스프레이 또는 파우더의 제형으로 제조될 수 있다.Since the cosmetic composition of the present invention is basically applied to the skin, it may be prepared in any formulation conventionally prepared with reference to cosmetic compositions in the art. For example, it may be formulated into solutions, suspensions, emulsions, pastes, gels, creams, lotions, powders, soaps, surfactant-containing cleansers, oils, powder foundations, emulsion foundations, wax foundations and sprays, It is not limited to this. More specifically, it may be prepared in the form of flexible lotion, nourishing lotion, nourishing cream, massage cream, essence, eye cream, cleansing cream, cleansing foam, cleansing water, mask pack, spray or powder.
나아가, 본 발명의 석창포 추출물 및 황칠 추출물을 유효성분으로 포함하는 인지 기능 증진용 조성물에 관한 것이다. 상기 인지 기능은 학습 능력, 기억 능력 및 집중력으로 이루어진 어느 하나 이상인 것을 특징으로 한다.Furthermore, it relates to a composition for enhancing cognitive function comprising the extract of Seokchangpo and Hwangchil extract of the present invention as an active ingredient. The cognitive function is characterized in that any one or more consisting of learning ability, memory ability, and concentration.
이하, 실시예를 통하여 본 발명을 더욱 상세히 설명하고자 한다.Hereinafter, the present invention will be described in more detail through examples.
이들 실시예는 오로지 본 발명을 예시하기 위한 것으로서, 본 발명의 범위가 이들 실시예에 의해 제한되는 것으로 해석되지 않는 것은 당업계에서 통상의 지식을 가진 자에게 있어서 자명할 것이다.These examples are only for exemplifying the present invention, and it will be apparent to those skilled in the art that the scope of the present invention is not to be construed as being limited by these examples.
석창포 추출물 및 황칠 추출물 제조Manufacture of seokchangpo extract and hwangchil extract
1-1 : 석창포 추출물 제조1-1: Manufacture of Iris extract
석창포(Acorus gramineus, AG) 의 뿌리줄기(rhizome) 부분은 제주 산야초 Co(Jeju, Korea) 에서 구입한 것을 사용하였다. 건조된 석창포 뿌리줄기 150 g에 증류수를 넣고 100℃ 에서 4시간 동안 끓여서 추출물을 추출한 후, 상기 추출물을 동결건조시킨 다음, 4℃ 냉장고에 보관하였다 (수율 152g). 상기 동결건조된 샘플은 사용 전에 PBS에 재현탁한 다음, 0.22 μM 필터로 필터링하였다.The rhizome part of Acorus gramineus (AG) was purchased from Jeju Sanyacho Co (Jeju, Korea). Distilled water was added to 150 g of the dried rhizome of Iris Iris, boiled at 100 ° C for 4 hours to extract an extract, and then the extract was freeze-dried and stored in a refrigerator at 4 ° C (yield 152 g). The lyophilized samples were resuspended in PBS before use and then filtered with a 0.22 μM filter.
1-2 : 황칠 추출물 제조1-2: Manufacture of hwangchil extract
황칠(Dendropanax morbiferus)의 잎을 3 ~ 5일간 50℃ ~ 60℃의 온도를 유지하여 건조시켜 준비하였다. 건조된 황칠 잎 1kg 당 5ℓ의 물을 첨가한 다음, 90℃ 에서 8 시간동안 끓여서 추출물을 추출하였다. 열수 추출과정은 2회 수행하였으며, 추출한 황칠 잎 열수 추출물을 60℃ ~ 70℃에서 진공 농축 후 동결건조 하여 보관하였다.The leaves of Hwangchil ( Dendropanax morbiferus ) were prepared by drying by maintaining a temperature of 50 ° C to 60 ° C for 3 to 5 days. After adding 5 liters of water per 1 kg of dried hwangchil leaves, the extract was extracted by boiling at 90 ° C. for 8 hours. The hot water extraction process was performed twice, and the extracted Hwangchil leaf hot water extract was vacuum-concentrated at 60 ° C to 70 ° C, then freeze-dried and stored.
석창포 추출물 및 황칠 추출물의 항염증 효능 확인Confirmation of anti-inflammatory efficacy of seokchangpo extract and hwangchil extract
2-1 : 세포 독성 확인2-1: Confirmation of cytotoxicity
본 발명에서는 상기 실시예 1에서 수득한 석창포 열수 추출물 및 황칠 열수 추출물 각각에 대한 세포 독성 정도를 측정하였다. BV-2 세포 생존율은 공지된 방법(Kim, J J, et al., Journal of Ethnopharmacology, 140:213-221, 2012)을 사용하여 측정하였다.In the present invention, the degree of cytotoxicity of each of the hot water extract Seokchangpo and the hot water Hwangchil extract obtained in Example 1 was measured. BV-2 cell viability was measured using a known method (Kim, JJ, et al. , Journal of Ethnopharmacology , 140:213-221, 2012).
먼저, 뮤린 미세아교세포(microglia) 세포주(Murine microglia cell line) BV-2를 실험에 사용하였으며, BV-2 세포는 열로 비활성화시킨 10% FBS와 항생제(페니실린 100 U/㎖, 스트렙토마이신 100 ㎍/㎖)가 포함된 DMEM 배지를 사용하여 배양하여 준비하였다 (37.0℃, 5% CO2 및 95% 공기).First, murine microglia cell line BV-2 was used in the experiment, and BV-2 cells were inactivated by heat with 10% FBS and antibiotics (penicillin 100 U/ml,
그 다음, BV-2 세포를 96 웰 플레이트에 1×104 세포/웰로 도말(plating)한 다음, 농도를 달리한 시료를 처리하였다. 1시간 후에 신경염증 유발 인자인 LPS(200 ng/㎖)로 처리한 다음, 24시간 동안 BV-2 세포를 자극하였으며, 처리 후에는 배지를 버리고, MTT(500 ㎍/㎖)을 포함한 100 ㎕ DMEM 배지를 각 웰에 첨가하여 37℃에서 4시간 배양하였다. 배양 후, 배지는 버리고 DMSO를 각 웰에 첨가하여 포마잔(formazan)을 용해하였다. 광학농도(OD)는 552 ㎚에서 측정하여 대조구와 비교하였다.Then, the BV-2 cells were plated in a 96-well plate at 1×10 4 cells/well, and samples having different concentrations were treated. After 1 hour, it was treated with neuroinflammatory factor LPS (200 ng/ml), and then BV-2 cells were stimulated for 24 hours. After the treatment, the medium was discarded and 100 μl DMEM containing MTT (500 μg/ml) A medium was added to each well and cultured at 37°C for 4 hours. After culturing, the medium was discarded and DMSO was added to each well to dissolve formazan. Optical density (OD) was measured at 552 nm and compared with the control.
그 결과, 도 1에 나타난 바와 같이, 고농도의 황칠 열수 추출물에서는 세포 독성을 보이는 것을 확인한 반면, 석창포 추출물은 세포 독성이 거의 없는 것을 확인하였다.As a result, as shown in Figure 1, it was confirmed that the high-concentration hwangchil hot water extract showed cytotoxicity, whereas the seokchangpo extract was confirmed to have little cytotoxicity.
2-2 : NO 생성 측정2-2: NO production measurement
본 발명에서는 상기 실시예 1에서 수득한 석창포 열수 추출물 및 황칠 열수 추출물 각각에 대한 항염증 효능을 확인하기 위해, 아질산염(NO) 방출 저해 작용효능을 측정하였으며, 아질산염 농도에 측정은 공지된 방법(Kim, JJ, et al., Journal of Ethnopharmacology, 140:213-221, 2012)을 사용하여 측정하였다.In the present invention, in order to confirm the anti-inflammatory efficacy of each of the hot water extract of Seokchangpo and the hot water extract of Hwangchil obtained in Example 1, the nitrite (NO) release inhibitory effect was measured, and the nitrite concentration was measured by a known method (Kim , JJ, et al. , Journal of Ethnopharmacology , 140:213-221, 2012).
구체적으로, BV-2 세포를 96 웰 플레이트에 1×104 세포/웰로 도말(plating)한 다음, 항염증 효능을 분석하기 위하여 석창포 열수 추출물 및 황칠 열수 추출물을 농도별로 처리하였다. 1시간 후에 신경염증 유발 인자인 LPS(200ng/㎖)로 처리한 다음, 24시간 동안 BV-2 세포를 자극하였으며, 이 때 생산되는 아질산염(NO)가 농도 의존적으로 저해효능을 보이는지 분석하였다.Specifically, BV-2 cells were plated at 1×10 4 cells/well in a 96-well plate, and then treated with seokchangpo hot water extract and hwangchil hot water extract at each concentration in order to analyze anti-inflammatory efficacy. After 1 hour, the cells were treated with LPS (200 ng/ml), a neuroinflammatory inducer, and then stimulated for 24 hours, and nitrite (NO) produced at this time was analyzed to have inhibitory effects in a concentration-dependent manner.
아질산염(NO)의 측정은 그리스(Griess) 시약을 이용한 NO 어세이 키트(NO assay kit; Abcam)를 사용하였으며, 측정 방법은 키트의 사용설명서에 따라 진행하였다. 세포배양액 100 ㎕ 및 그리스 시약을 혼합한 후 10분간 반응시키고 540 nm의 흡광도에서 관찰하였으며, 농도는 표준곡선(standard curve)을 이용하여 최종 확인하였다.Nitrite (NO) was measured using a NO assay kit (Abcam) using a Griess reagent, and the measurement method was performed according to the kit's instructions. After mixing 100 μl of the cell culture medium and the grease reagent, the mixture was reacted for 10 minutes and observed at 540 nm absorbance, and the concentration was finally confirmed using a standard curve.
그 결과, 도 1에 나타난 바와 같이, 황칠 열수 추출물 및 석창포 열수 추출물 모두 농도 의존적으로 NO 발생을 억제시키는 것을 확인하였다. As a result, as shown in Figure 1, it was confirmed that both hwangchil hot water extract and seokchangpo hot water extract inhibit NO generation in a concentration-dependent manner.
석창포 추출물 및 황칠 추출물의 혼합 사용으로 인한 상승효과 확인Confirmation of synergistic effect due to mixed use of seokchangpo extract and hwangchil extract
3-1 : 세포 독성 확인3-1: Confirmation of cytotoxicity
본 발명에서는 황칠 열수 추출물 및 석창포 열수 추출물을 혼합하였을 때, 세포 독성 정도를 상기 실시예 2-1과 동일한 방법으로 수행하였다.In the present invention, when Hwangchil hot water extract and Seokchangpo hot water extract were mixed, the degree of cytotoxicity was performed in the same manner as in Example 2-1.
석창포 추출물 및 황칠 추출물의 NO 발생 억제 효능에 대한 IC50 농도 값을 기준으로 두 추출물을 배합하였다. 황칠 열수 추출물의 IC50 값은 100 ㎍/㎖, 석창포 추출물의 IC50 값은 700 ㎍/㎖으로 나타났으며, 하기 표 3과 같은 농도로 처리하였다.The two extracts were combined based on the IC 50 concentration value for the NO generation inhibitory effect of the seokchangpo extract and hwangchil extract. The IC 50 value of the hwangchil hot water extract was 100 μg/ml and the IC 50 value of the extract of Seokchangpo was 700 μg/ml, and the treatment was performed at the concentration shown in Table 3 below.
그 결과, 도 2에 나타난 바와 같이, 석창포 열수 추출물 및 황칠 열수 추출물을 7 : 1(w/w) 비율로 혼합하였을 때, 단독 처리군보다 세포 독성이 감소한 것을 확인하였다.As a result, as shown in Figure 2, when the seokchangpo hot water extract and hwangchil hot water extract were mixed at a ratio of 7: 1 (w / w), it was confirmed that the cytotoxicity was reduced compared to the single treatment group.
3-2 : NO 생성 측정3-2: Measurement of NO production
본 발명에서는 석창포 열수 추출물 및 황칠 열수 추출물을 혼합하였을 때, 상승효과를 확인하기 위해 NO 발생 억제 정도를 상기 실시예 2-2와 동일한 방법으로 수행하였다.In the present invention, when the hot-water extract of Seokchangpo and the hot-water Hwangchil extract were mixed, the degree of NO generation inhibition was performed in the same manner as in Example 2-2 to confirm the synergistic effect.
그 결과, 도 2에 나타난 바와 같이, 석창포 열수 추출물 및 황칠 열수 추출물을 혼합하였을 때, 단독 처리군보다 NO 발생이 효과적으로 억제되는 것을 확인하였다.2 종의 추출물을 조합한 경우의 항염 활성이, 추출물 각각의 항염 활성의 단순한 합계(기대되는 활성) 보다 커지는 경우, 이것을 상승효과라고 한다. 석창포 추출물 및 황칠 추출물의 혼합에 대한 상승 예측 작용은 하기 수학식 1의 콜비(Colby)식을 사용하여 다음과 같이 산출될 수 있다 (S.R, Colby, "Calculating Synergistic and Antagonistic Responses of Herbicide Combinations", Weeds 1967, 15, 20-22).As a result, as shown in Figure 2, it was confirmed that NO generation was more effectively suppressed than the single treatment group when the hot water extract of Seokchangpo and the hot water extract of Hwangchil were mixed. The anti-inflammatory activity when the two extracts were combined was If it is greater than the simple sum (expected activity) of each anti-inflammatory activity, this is called a synergistic effect. The synergistic predictive action for the mixture of seokchangpo extract and hwangchil extract can be calculated as follows using Colby's formula in Equation 1 (S.R, Colby, "Calculating Synergistic and Antagonistic Responses of Herbicide Combinations",
[수학식 1][Equation 1]
E = α + β-(α × β÷ 100)E = α + β - (α × β÷ 100)
α 및 β는 추출물을 각각 단독 처리할 경우의 항염 활성 측정값이며, E는 예측치로 α 및 β가 혼합되었을 경우의 예측되는 항염 활성이다. 본 발명에서는 NO 발생 억제율을 상기 콜비식에 대입하여 황칠 추출물 및 석창포 추출물의 혼합사용에 따른 예측값을 측정하였다. 실측값이 예측값 보다 크면 상승효과가 있는 것으로 판단 할 수 있으며, 본 발명에서는 혼합처리의 상승효과를 추가적으로 검증하기 위하여 콜비식으로 계산된 이론값과 실측값을 비교하였다.α and β are anti-inflammatory activity measurements when the extract is treated alone, and E is the predicted anti-inflammatory activity when α and β are mixed as predicted values. In the present invention, the predicted value according to the mixed use of Hwangchil extract and Seokchangpo extract was measured by substituting the NO generation inhibition rate into the Colby formula. If the measured value is greater than the predicted value, it can be determined that there is a synergistic effect. In the present invention, in order to additionally verify the synergistic effect of the mixing treatment, the theoretical value calculated by the Colby formula and the actual value were compared.
상기 표 4에 나타난 바와 같이, 석창포 추출물 700 ㎍/㎖ 및 황칠 추출물 100 ㎍/㎖를 혼합하였을 때 콜비식에 대한 NO 발생 억제율에 대한 예측값은 80.73%으로 계산되었으며, 실제 NO 발생 억제율은 81.44%인 것으로 확인되었다. As shown in Table 4, when 700 μg/ml of seokchangpo extract and 100 μg/ml of hwangchil extract were mixed, the predicted value for the NO generation inhibition rate for the Colby formula was calculated to be 80.73%, and the actual NO generation inhibition rate was 81.44%. confirmed to be
즉, 실측값이 예측값 보다 큰 것으로 확인되었음므로, 본 발명에서는 석창포 추출물 및 황칠 추출물 혼합 사용에 따른 항염증 효능의 상승효과를 확인하였다.That is, since the measured value was confirmed to be greater than the predicted value, in the present invention, the synergistic effect of anti-inflammatory efficacy according to the mixed use of seokchangpo extract and hwangchil extract was confirmed.
석창포 및 황칠 혼합 추출물에 따른 염증반응 매개인자 및 염증성 사이토 카인 발현 변화 확인Confirmation of inflammatory response mediators and inflammatory cytokine expression changes according to seokchangpo and hwangchil mixed extracts
4-1 : 염증반응 매개인자 및 염증성 사이토 카인 mRNA 발현 억제능 확인4-1: Confirmation of inflammatory response mediator and inflammatory cytokine mRNA expression suppression ability
본 발명에서는 LPS로 자극된 BV-2 세포에 석창포 및 황칠 혼합 추출물을 처리하였을 때 iNOS, COX-2를 포함하는 염증반응 매개인자(inflammatory mediators) 및 IL-1β, IL-6, TNF-α를 포함하는 염증성 사이토카인(cytokines)의 mRNA 발현이 억제되는지 확인하였다. In the present invention, when LPS-stimulated BV-2 cells were treated with the mixed extract of Irispo and Hwangchil, inflammatory mediators including iNOS and COX-2, IL-1β, IL-6, and TNF-α were inhibited. It was confirmed whether the mRNA expression of inflammatory cytokines (cytokines) including the inhibition was confirmed.
먼저, BV-2 세포를 각 웰당 5 × 105 세포/웰이 되도록 6-웰 플레이트에 분주한 다음, 석창포 열수 추출물 및 황칠 열수 추출물을 농도별로 처리한 후, 1시간 후에 신경염증 유발 인자인 LPS(200 ng/㎖)로 처리하여 배앵하였다. 6시간 후 TRIzol 시약을 사용하여 전체 RNA를 분리하였다. RNA 2 ㎍을 이용하여 역전사시킨 다음, Oligo (dT) 18 프라이머와 AccuPowerTM RT Premix를 이용하여 cDNA를 제조하였다. 유전자 특이적 프라이머와 반응조건을 하기 표 5와 같이 하여 PCR을 수행하였으며, 각각의 mRNA 발현 정도를 대조군인 GAPDH에 대한 상대적 발현량으로 나타내었다.First, the BV-2 cells were dispensed into a 6-well plate to be 5 × 10 5 cells/well per well, and then treated with hot water extract of Seokchangpo and hot water extract from Hwangchil by concentration, and then 1 hour later, LPS, a neuroinflammation factor. (200 ng/ml) and cultured. After 6 hours, total RNA was isolated using TRIzol reagent. After reverse transcription using 2 μg of RNA, cDNA was prepared using Oligo (dT) 18 primer and AccuPower™ RT Premix. PCR was performed using gene-specific primers and reaction conditions as shown in Table 5 below, and the expression level of each mRNA was expressed as a relative expression level relative to GAPDH as a control group.
번호order
number
온도(℃)annealing
Temperature (℃)
도 3에 나타난 바와 같이, 석창포 및 황칠 혼합 추출물에 의해 염증반응 매개인자인 iNOS 및 COX-2 mRNA 발현이 감소하는 것을 확인하였다. 또한, 도 4에 나타난 바와 같이, 석창포 및 황칠 혼합 추출물에 의해 IL-1β, IL-6, TNF-α를 포함하는 염증성 사이토카인의 mRNA 발현이 감소하는 것을 확인하였다. 특히 TNF-α및 IL-1β의 경우 단독 처리군에 비해 석창포 및 황칠 혼합 추출물 처리군에서 생성이 현저하게 감소하는 것을 확인하였다.As shown in Figure 3, it was confirmed that the expression of iNOS and COX-2 mRNA, which are inflammatory response mediators, was reduced by the mixed extract of seokchangpo and hwangchil. In addition, as shown in Figure 4, it was confirmed that the mRNA expression of inflammatory cytokines including IL-1β, IL-6, TNF-α decreased by the seokchangpo and hwangchil mixed extract. In particular, in the case of TNF-α and IL-1β, it was confirmed that the production was significantly reduced in the mixed extract treatment group Seokchangpo and Hwangchil compared to the single treatment group.
4-2 : 염증반응 매개 인자 발현 억제능 확인4-2: Confirmation of the ability to suppress the expression of inflammatory response mediators
본 발명에서는 LPS로 자극된 BV-2 세포에 석창포 및 황칠 혼합 추출물을 처리하였을 때 염증반응 매개인자인 iNOS 및 COX-2 단백질 발현이 억제되는지 확인하였다. In the present invention, it was confirmed that the expression of iNOS and COX-2 proteins, which are inflammatory response mediators, was inhibited when BV-2 cells stimulated with LPS were treated with a mixed extract of Irispo and Hwangchil.
*먼저, BV-2 세포를 각 웰당 5 × 105 세포/웰이 되도록 6-웰 플레이트에 분주한 다음, 석창포 열수 추출물 및 황칠 열수 추출물을 농도별로 처리한 후, 1시간 후에 신경염증 유발 인자인 LPS(200 ng/㎖)로 처리하여 배앵하였다*First, the BV-2 cells were dispensed into a 6-well plate to be 5 × 10 5 cells/well per well, and then treated with hot water extract of Seokchangpo and hot water extract from Hwangchil by concentration, and after 1 hour, the neuroinflammation-inducing factor, Incubated by treatment with LPS (200 ng/ml)
24시간 후, 세포를 차가운 PBS(ice cold PBS)로 2회 세척한 다음, RIPA 버퍼(PBS, 1% NP-40, 0.5% sodium deoxycholate, and 0.1% SDS, containing fresh protease inhibitor cocktail) 50 ㎖ 또는 100 ㎖를 첨가하여 전체 세포 용해물을 수득하였다. 바이오-라드 DC 단백질 어세이(Bio-Rad DC Protein Assay)는 단백질 농도를 결정하는데 사용하였다.After 24 hours, the cells were washed twice with ice cold PBS, and then RIPA buffer (PBS, 1% NP-40, 0.5% sodium deoxycholate, and 0.1% SDS, containing fresh protease inhibitor cocktail) 50 ml or 100 ml was added to obtain whole cell lysate. A Bio-Rad DC Protein Assay was used to determine protein concentration.
전체 세포 용해물 40 ㎍을 10% SDS-PAGE 겔로 전기영동 한 다음, 분리된 단백질을 PVDF막(Millipore; 미국)으로 트랜스퍼 시켰다. 비특이적 결합을 차단하기 위해 PVDF막을 5% 스킴밀크가 포함된 PBS로 1시간 동안 반응시켰다. PVDF막은 항-iNOS 항체 (1:1000), 항-COX-2 항체 (1:1000), 항-β-actin 항체 (1:2000)를 처리하여 4℃에서 하룻밤 동안 반응시킨 다음, 2차 항체(horseradish peroxidase-conjugated secondary antibody; 1:1000-2000)를 처리하여 1시간 동안 반응시켰다. 40 μg of the whole cell lysate was electrophoresed on a 10% SDS-PAGE gel, and then the separated proteins were transferred to a PVDF membrane (Millipore; USA). In order to block non-specific binding, the PVDF membrane was reacted with PBS containing 5% skim milk for 1 hour. The PVDF membrane was treated with anti-iNOS antibody (1:1000), anti-COX-2 antibody (1:1000), and anti-β-actin antibody (1:2000) overnight at 4°C, followed by secondary antibody (horseradish peroxidase-conjugated secondary antibody; 1:1000-2000) and reacted for 1 hour.
그 다음, ECL 검출 키트(detection kit)와 발광 영상 분석기(Luminescent Image Analyzer; LAS-3000, Fujifilm, 일본)를 사용하여 항체 특이적 밴드를 관찰하였다. 각각의 단백질 발현 정도는 대조군인 β-actin에 대한 상대적 발현량으로 나타내었다.Then, antibody-specific bands were observed using an ECL detection kit and a luminescent image analyzer (LAS-3000, Fujifilm, Japan). The level of expression of each protein was expressed as a relative expression level of β-actin as a control group.
그 결과, 도 5에 나타난 바와 같이, 석창포 및 황칠 혼합 추출물에 의해 염증반응 매개인자(inflammatory mediators)인 iNOS 및 COX-2 단백질 발현이 감소하는 것을 확인하였다. As a result, as shown in Figure 5, it was confirmed that the expression of iNOS and COX-2 proteins, which are inflammatory mediators, was reduced by the mixed extract of seokchangpo and hwangchil.
또한, 석창포 추출물 및 황칠 추출물 단독 처리군 보다 석창포 및 황칠 추출물을 혼합하였을 때, iNOS 및 COX-2 단백질 발현이 효과적으로 억제되는 것을 확인하였다.In addition, it was confirmed that iNOS and COX-2 protein expression was effectively suppressed when the mixture of seokchangpo and hwangchil extracts than the seokchangpo extract and hwangchil extract alone treatment group.
<110> GLOCAL Industry-Academic Cooperation Foundation Konkuk University <120> Composition for preventing or treating inflammatory diseases comprising extracts of Acorus gramineus and Dendropanax morbifera <130> 1067838 <160> 12 <170> KoPatentIn 3.0 <210> 1 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> iNOS_F <400> 1 gaggtactca gcgtgctcca 20 <210> 2 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> iNOS_R <400> 2 agggaggaaa gggagagagg 20 <210> 3 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> COX-2_F <400> 3 tgagtggtag ccagcaaagc 20 <210> 4 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> COX-2_R <400> 4 ctgcagtcca ggttcatgg 19 <210> 5 <211> 21 <212> DNA <213> Artificial Sequence <220> <223> IL-6_F <400> 5 ggaggcttaa ttacacatgt t 21 <210> 6 <211> 21 <212> DNA <213> Artificial Sequence <220> <223> IL-6_R <400> 6 tgatttcaag atgaattgga t 21 <210> 7 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> IL-1b_F <400> 7 caaggagaac caagcaacga 20 <210> 8 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> IL-1b_R <400> 8 ttggccgagg actaaggagt 20 <210> 9 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> TNFa_F <400> 9 agggagagtg gtcaggttgc 20 <210> 10 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> TNFa_R <400> 10 cagcctggtc accaaatcag 20 <210> 11 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> GAPDH_F <400> 11 accacagtcc atgccatcac 20 <210> 12 <211> 20 <212> DNA <213> Artificial Sequence <220> <223> GAPDH_R <400> 12 ccaccaccct gttgctgtag 20 <110> GLOCAL Industry-Academic Cooperation Foundation Konkuk University <120> Composition for preventing or treating inflammatory diseases comprising extracts of Acorus gramineus and Dendropanax morbifera <130> 1067838 <160> 12 <170> KoPatentIn 3.0 <210> 1 <211> 20 <212> DNA <213> artificial sequence <220> <223> iNOS_F <400> 1 gaggtactca gcgtgctcca 20 <210> 2 <211> 20 <212> DNA <213> artificial sequence <220> <223> iNOS_R <400> 2 agggaggaaa gggagagagg 20 <210> 3 <211> 20 <212> DNA <213> artificial sequence <220> <223> COX-2_F <400> 3 tgagtggtag ccagcaaagc 20 <210> 4 <211> 19 <212> DNA <213> artificial sequence <220> <223> COX-2_R <400> 4 ctgcagtcca ggttcatgg 19 <210> 5 <211> 21 <212> DNA <213> artificial sequence <220> <223> IL-6_F <400> 5 ggaggcttaa ttacacatgt t 21 <210> 6 <211> 21 <212> DNA <213> artificial sequence <220> <223> IL-6_R <400> 6 tgatttcaag atgaattgga t 21 <210> 7 <211> 20 <212> DNA <213> artificial sequence <220> <223> IL-1b_F <400> 7 caaggaac caagcaacga 20 <210> 8 <211> 20 <212> DNA <213> artificial sequence <220> <223> IL-1b_R <400> 8 ttggccgagg actaaggagt 20 <210> 9 <211> 20 <212> DNA <213> artificial sequence <220> <223> TNFa_F <400> 9 aggggagagtg gtcaggttgc 20 <210> 10 <211> 20 <212> DNA <213> artificial sequence <220> <223> TNFa_R <400> 10 cagcctggtc accaaatcag 20 <210> 11 <211> 20 <212> DNA <213> artificial sequence <220> <223> GAPDH_F <400> 11 accacagtcc atgccatcac 20 <210> 12 <211> 20 <212> DNA <213> artificial sequence <220> <223> GAPDH_R <400> 12 ccaccaccct gttgctgtag 20
Claims (4)
상기 신경 염증성 질환은 알츠하이머 병, 파킨슨 병, 인지장애, 기억력손상 및 퇴행성 신경질환으로 이루어진 군에서 선택되는 신경 염증성 질환인 것을 특징으로 하는 신경 염증성 질환의 예방 또는 치료용 약학조성물.
7: As a pharmaceutical composition for the prevention or treatment of neuroinflammatory diseases comprising seokchangpo extract and hwangchil extract mixed at a ratio of 1 (w / w) as active ingredients,
The neuroinflammatory disease is Alzheimer's disease, Parkinson's disease, cognitive disorders, memory impairment and neuroinflammatory disease selected from the group consisting of neurodegenerative diseases characterized in that for preventing or treating a pharmaceutical composition for the prevention of neuroinflammatory diseases.
According to claim 1, characterized in that the seokchangpo extract and hwangchil extract are extracted by one or more solvents selected from the group consisting of water, lower alcohols having 1 to 4 carbon atoms, ethyl acetate, methylene chloride and mixed solvents thereof A pharmaceutical composition for the prevention or treatment of neuroinflammatory diseases to be.
상기 신경 염증성 질환은 알츠하이머 병, 파킨슨 병, 인지장애, 기억력손상 및 퇴행성 신경질환으로 이루어진 군에서 선택되는 신경 염증성 질환인 것을 특징으로 하는 신경 염증성 질환의 예방 또는 개선용 건강기능식품 조성물.
7: 1 (w / w) as a health functional food composition for the prevention or improvement of neuroinflammatory diseases containing the extract and Hwangchil extract mixed in a ratio of active ingredients,
The neuroinflammatory disease is a neuroinflammatory disease selected from the group consisting of Alzheimer's disease, Parkinson's disease, cognitive impairment, memory impairment, and neurodegenerative diseases.
상기 석창포 추출물 및 황칠 추출물은 물, 탄소수 1 내지 4의 저급 알코올, 에틸아세테이트, 메틸렌클로라이드 및 이들의 혼합용매로 이루어지는 군에서 선택되는 1종 이상의 용매에 의해 추출되는 것을 특징으로 하는 신경 염증성 질환의 예방 또는 개선용 건강기능식품 조성물.
According to claim 3,
The seokchangpo extract and hwangchil extract are extracted by one or more solvents selected from the group consisting of water, lower alcohols having 1 to 4 carbon atoms, ethyl acetate, methylene chloride and mixed solvents thereof Prevention of neuroinflammatory diseases, characterized in that Or health functional food composition for improvement.
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KR1020220057375A KR102471629B1 (en) | 2020-07-16 | 2022-05-10 | Composition for preventing or treating inflammatory diseases comprising extracts of Acorus gramineus and Dendropanax morbifera |
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KR1020220057375A KR102471629B1 (en) | 2020-07-16 | 2022-05-10 | Composition for preventing or treating inflammatory diseases comprising extracts of Acorus gramineus and Dendropanax morbifera |
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