KR20170090362A - Composition having sleep-improving effect comprising an extract of herbal combination, and uses thereof - Google Patents
Composition having sleep-improving effect comprising an extract of herbal combination, and uses thereof Download PDFInfo
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- KR20170090362A KR20170090362A KR1020170011986A KR20170011986A KR20170090362A KR 20170090362 A KR20170090362 A KR 20170090362A KR 1020170011986 A KR1020170011986 A KR 1020170011986A KR 20170011986 A KR20170011986 A KR 20170011986A KR 20170090362 A KR20170090362 A KR 20170090362A
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Abstract
Description
본 발명은 수면 증진 또는 개선용 조성물 및 이의 용도에 관한 것으로서, 보다 구체적으로는 복합 생약 추출물을 함유하는 수면 증진 또는 개선용 조성물, 수면장애 또는 불면증 예방, 개선 또는 치료용 조성물에 관한 것이다.More particularly, the present invention relates to a composition for enhancing or improving sleeping ability containing a herbal extract, a composition for preventing, ameliorating or treating sleep disorders or insomnia.
현대 사회에서 많은 사람들은 스트레스와 불안, 초조 때문에 수면장애를 겪고 있다. 통계에 의하면 성인의 약 15%가 불안증상에 의한 불면증 때문에 약물 치료가 필요하다고 알려져 있으며, 불면의 원인으로는 스트레스, 긴장, 공포 등 다양하며, 치료 약물로는 벤조다이아제핀 계열의 약물과 세로토닌 효능약 등이 사용되고 있으나, 이러한 약물들은 장기간 사용하였을 때 내성 및 의존성이 형성되는 부작용이 심한 문제점이 있다.Many people in the modern world suffer from sleep disturbance because of stress, anxiety, and agitation. According to the statistics, about 15% of adults are known to need medication due to insomnia due to anxiety symptoms. Insomnia is caused by stress, tension, and fear. Therapeutic drugs include benzodiazepines and serotonin Drugs, etc., are used. However, these drugs have a serious side effect of being formed with tolerance and dependency when they are used for a long period of time.
따라서, 수면제 장기복용자 및 제한자의 경우 이를 대체할 수 있는 수단으로 천연 보조제의 필요성이 높아지고 있으며, 수면 증진 건강기능식품에 대한 수요가 증대되고 있는 실정인바, 이에 대한 연구가 진행되고 있으나(국내등록특허 10-1333982), 아직 미미한 실정이다.Accordingly, the need for natural supplements is increasing as a means of replacing long-term sleepers and restaurateurs, and there is a growing demand for functional foods for sleep enhancement, 10-1333982), but it is still small.
한편, 산약(山藥)은 마과(Dioscoreaeaceae)에 속하는 참마(Dioscorea japonica Thunb) 또는 마(Dioscorea batatas Thunb)의 뿌리 줄기로서, 맛은 달고 성질은 따듯하다. 산약은 항암작용, 항산화 작용, 면역증가작용, 및 스트레스에 대한 방어 작용에 관한 연구 등이 보고되고 있다.On the other hand, Yam (山藥) is a rhizome of yam (Dioscorea japonica Thunb) or village (Dioscorea batatas Thunb) belonging to magwa (Dioscoreaeaceae), the taste is sweet nature is warm. Studies on anticancer, antioxidant, immunity increasing, and defense against stress have been reported.
어성초(魚腥草)는 삼백초과의 약모밀(Houttuynia cordata Thunberg)의 개화기의 지상부를 말하며, 맛은 맵고 성질은 약간 차다. 어성초는 항염효과, 항암효과 및 면역증진효과 등이 보고되고 있다.Hwaseongcho (魚 腥草) is the top part of the flowering period of the Hwangtimnyeong ( Houttuynia cordata Thunberg), and the taste is spicy and the quality is a bit cold. Anti-inflammatory, anti-cancer, and immunity-enhancing effects of Hwasungcho have been reported.
용안육(龍眼肉)은 무환자나무과의 용안(Dimocarpus longan Lour.:龍眼)의 가종피를 말하며, 맛은 달고 성질은 따듯하다. 용안육은 기억력 증진, 스트레스 억제 효과가 있는 것으로 보고된 바 있다.The dragon eye meat (dragon eye meat) refers to the seed coat of the dragon eye ( Dimocarpus longan Lour .: dragon eye), and the taste is sweet and the quality is warm. Ryeonggak has been reported to improve memory and stress.
본 발명자들은, 부작용 없이 수면 증진 또는 개선 효과가 뛰어난 천연 약물을 개발하기 위하여 예의 연구한 결과, 산약(Dioscoreae batatas Decaisne), 어성초(Houttuynia cordata THUNB), 용안육(Euphoria longana STEUD)의 복합 생약추출물이 우수한 수면 증진 또는 개선효과가 있음을 확인함으로써 본 발명을 완성하였다.The present inventors, as a result of intensive studies in order to promote sleep or develop an excellent natural substance improving effect without side effects, Yam (Dioscoreae batatas Decaisne), by ensuring that the Houttuynia cordata (Houttuynia cordata THUNB), combined herbal extracts having excellent promotion or improvement of sleep yonganyuk (Euphoria longana STEUD) effect and completed the present invention.
이에, 본 발명의 목적은 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는, 수면 증진 또는 개선용 조성물을 제공하는 것이다.Accordingly, an object of the present invention is to provide a composition for enhancing or improving sleep quality, which comprises an extract of a complex herbal medicine of Lycopersicon esculentum, Lycopersicon esculentum, and Pigmentosa as an active ingredient.
또한, 본 발명의 또 다른 목적은 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는, 수면장애 또는 불면증 예방, 개선 또는 치료용 조성물을 제공하는 것이다.It is still another object of the present invention to provide a composition for preventing, ameliorating or treating sleep disorders or insomnia, which comprises an extract of a complex herbal medicine of Acanthopanax senticosus, Acanthopanax senticosus and Pigmentosa as an active ingredient.
그러나 본 발명이 이루고자 하는 기술적 과제는 이상에서 언급한 과제에 제한되지 않으며, 언급되지 않은 또 다른 과제들은 아래의 기재로부터 당업자에게 명확하게 이해될 수 있을 것이다.However, the technical problem to be solved by the present invention is not limited to the above-mentioned problems, and other matters not mentioned can be clearly understood by those skilled in the art from the following description.
상기 목적을 달성하기 위하여, 본 발명은 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는, 수면 증진 또는 개선용 조성물을 제공한다.In order to achieve the above object, the present invention provides a composition for enhancing or improving sleep quality, which comprises an extract of a complex herbal medicine consisting of Acanthopanax senticosus, Acanthopanax senticosus and Pigmentosae as active ingredients.
또한, 본 발명은 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는, 수면장애 또는 불면증 예방 또는 치료용 약학적 조성물을 제공한다.In addition, the present invention provides a pharmaceutical composition for preventing or treating sleep disorder or insomnia, which comprises, as an active ingredient, a complex herbal medicine extract of Acanthopanax senticosus, Acanthopanax senticosus and Pigmentosa.
또한, 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는, 수면장애 또는 불면증 개선용 건강기능식품 조성물을 제공한다.The present invention also provides a health functional food composition for improving sleeping disorder or insomnia, which comprises, as an active ingredient, a complex herbal medicine extract of lily of the valley, lily of the valley and yin yang.
본 발명의 일 구현예로, 상기 추출물은 물, C1 내지 C4의 저급알코올 또는 이들의 혼합용매를 사용하여 추출될 수 있다.In one embodiment of the present invention, the extract can be extracted using water, a C 1 to C 4 lower alcohol, or a mixed solvent thereof.
본 발명의 다른 구현예로, 상기 저급알코올은 에탄올일 수 있다.In another embodiment of the present invention, the lower alcohol may be ethanol.
본 발명의 또 다른 구현예로, 상기 추출물은 산약, 어성초 및 용안육이 1: 0.1 내지 10: 0.1 내지 10의 중량비로 혼합되어 추출될 수 있다.In another embodiment of the present invention, the extract may be mixed and extracted at a weight ratio of 1: 0.1 to 10: 0.1 to 10 in the range of 1: 0.1 to 10: 1.
본 발명의 또 다른 구현예로, 상기 중량비는 1: 1: 1일 수 있다.In another embodiment of the present invention, the weight ratio may be 1: 1: 1.
또한, 본 발명은 상기 조성물을 개체에 투여하는 단계를 포함하는, 수면장애 또는 불면증 예방 또는 치료방법을 제공한다.The present invention also provides a method for preventing or treating sleep disorders or insomnia comprising the step of administering the composition to a subject.
본 발명은 상기 조성물의 수면장애 또는 불면증 예방 또는 치료 용도를 제공한다.The present invention provides a composition for preventing or treating sleep disorders or insomnia.
본 발명의 복합 생약 추출물은 부작용이 거의 없고, 수면 증진, 증대 및 개선 효과가 뛰어나기 때문에, 수면 장애 또는 불면증의 예방, 개선 및 치료용 약학적 조성물 및 건강기능식품으로 유용하게 이용될 수 있다. 또한, 본 발명에 의하면 기존의 천연 항불면증제를 뛰어넘는 새로운 치료제 및 치료법을 제공할 수 있다.The complex herbal medicine extract of the present invention has little side effects and is excellent in the effect of enhancing, increasing and improving sleeping. Therefore, it can be effectively used as a pharmaceutical composition and health functional food for preventing, ameliorating and treating sleep disorder or insomnia. In addition, according to the present invention, a new therapeutic agent and a therapeutic method that exceed the existing natural antihypertensive agents can be provided.
도 1 및 도 2는 복합 생약 추출물의 수면 증진 및 개선 효과를 확인하기 위해, 상기 복합 생약 추출물 투여 후 뇌파를 측정한 결과를 나타낸 것이다.
도 3은 복합 생약 추출물에 의한 초파리의 운동 활성 변화에 대하여 확인한 결과를 나타낸 것이다.FIG. 1 and FIG. 2 show the results of measurement of brain waves after administration of the herbal medicine extract to confirm the effect of improving the sleepiness of the herbal medicine extracts.
FIG. 3 shows the result of confirming the change of the movement activity of Drosophila by the herbal extract of the complex herb.
본 발명은 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는, 수면 증진 또는 개선용 조성물을 제공한다.The present invention provides a composition for enhancing or improving sleepiness, which comprises an extract of a complex herbal medicine of lily of the sea, herringbone and eyelid as an active ingredient.
상기 수면 증진 또는 개선은 수면 잠재기(sleep latency)가 감소하고 수면지속기간(sleep duration)이 증가하는 효과일 수 있으나, 이에 제한되지 않는다.The sleep enhancement or improvement may be an effect of reducing the sleep latency and increasing the sleep duration, but is not limited thereto.
본 발명의 조성물에서 유효성분인 복합생약 추출물은 통상적인 추출 방법에 의해 얻을 수 있고, 시판되는 것을 구입하여 사용할 수 있다. 통상적인 추출 방법은 열수 추출, 냉침 추출, 환류 추출, 초음파 추출 등을 포함할 수 있으나, 이에 한정되지 않는다.In the composition of the present invention, the herbal extract of the present invention may be obtained by a conventional extraction method, and a commercially available herbal extract may be used. Typical extraction methods include, but are not limited to, hot water extraction, cold extraction, reflux extraction, ultrasonic extraction, and the like.
보다 구체적으로, 본 발명의 복합생약 추출물은 생약 재료인 산약(Dioscoreae batatas Decaisne), 어성초(Houttuynia cordata THUNB), 용안육(Euphoria longana STEUD)을 물로 세척하여 음건 후, 모두 마쇄하여 상기 생약재료 중량의 약 1 내지 20배, 바람직하게는 약 2 내지 10배에 달하는 부피의 물, C1 내지 C4의 저급알코올 또는 이들의 혼합용매, 바람직하게는 30% 에탄올로 0 내지 120℃ 온도에서 약 1시간 내지 1일 동안, 열수 추출, 냉침 추출, 환류 냉각 추출, 초음파 추출 또는 초임계 추출 등의 추출방법으로 추출한 후, 추출액을 냉각 후에 여과하고 여과액을 동결 건조하여 본 발명의 복합생약 추출물을 얻을 수 있다.More specifically, the herbal extract of the present invention is prepared by washing the herbal materials Dioscoreae batatas Decaisne, Houttuynia cordata THUNB, and Euphoria longana STEUD with water, 1 to 20 times, preferably about 2 to 10 times the volume of water, a C1 to C4 lower alcohol or a mixture thereof, preferably 30% ethanol at a temperature of 0 to 120 DEG C for about 1 hour to 1 day The extract may be filtered after cooling, and the filtrate may be lyophilized to obtain the herbal extract of the present invention.
상기 추출물은 산약, 어성초 및 용안육이 1: 0.1 내지 10: 0.1 내지 10의 중량비로 혼합되어 추출되는 것이 바람직하고, 1: 1: 1의 중량비로 혼합되어 추출되는 것이 가장 바람직하다.Preferably, the extract is mixed and extracted at a weight ratio of 1: 0.1 to 10: 0.1 to 10, and most preferably mixed at a weight ratio of 1: 1: 1.
본 발명의 일 실시예서는, 산약, 어성초 및 용안육의 복합 생약 추출물의 수면 증진 및 개선효과를 확인한 결과, 상기 복합 생약 추출물을 투여한 군의 wake와 rem 에서 TUKEY HSD와 LSD 모두 유의미한 결과가 나타남을 확인하였고, 초파리 치매모델에서 대조군에 비해 상기 복합 생약 추출물 처리군에서 밤 운동성이 유의하게 감소하였으며, 낮 운동성이 유의하게 증가한 것을 확인하였다 (실시예 2 참조).In one embodiment of the present invention, it was found that the combination of herbal extracts of Sanskrit, Hwasungcho, and Yongcheng resulted in improvement of sleeping and improving effects of both herb extracts and TUKEY HSD and LSD in wake and rem . In the Drosophila dementia model, the night mobility was significantly lowered in the herbal extract-treated group than in the control group, and the low mobility was significantly increased (see Example 2).
따라서, 본 발명의 복합생약 추출물은 수면을 증진, 증대 또는 개선함으로써 수면 장애 또는 불면증의 예방, 개선, 억제 또는 치료에 유용한 의약품 및 건강기능식품으로 사용될 수 있다. Therefore, the compound herbal medicine extract of the present invention can be used as medicines and health functional foods useful for preventing, ameliorating, inhibiting or treating sleep disorder or insomnia by improving, increasing or improving sleeping surface.
이에, 본 발명의 다른 양태로서, 본 발명은 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는, 수면장애 또는 불면증 예방 또는 치료용 약학적 조성물을 제공한다.Accordingly, as another aspect of the present invention, the present invention provides a pharmaceutical composition for preventing or treating sleep disorder or insomnia, which comprises, as an active ingredient, a complex herbal medicine extract of lily of the valley,
본 발명의 약학적 조성물은 복합 생약 추출물과 함께 수면 장애 또는 불면증에 치료 효과를 갖는 공지의 유효성분을 1종 이상 더 함유할 수 있다.The pharmaceutical composition of the present invention may contain at least one known active ingredient having a therapeutic effect on sleep disorder or insomnia together with the herbal extract of the present invention.
본 발명의 조성물은 약학적 조성물의 제조에 통상적으로 사용하는 적절한 담체, 부형제 및 희석제를 더 포함할 수 있다. 또한 통상의 방법에 따라 산제, 과립제, 정제, 캡슐제, 현탁액, 에멀젼, 시럽, 에어로졸 등의 경구형 제형, 외용제, 좌제 및 멸균 주사용액의 형태로 제형화하여 사용될 수 있다.The compositions of the present invention may further comprise suitable carriers, excipients and diluents conventionally used in the manufacture of pharmaceutical compositions. In addition, it can be formulated in the form of powders, granules, tablets, capsules, suspensions, emulsions, oral preparations such as syrups and aerosols, external preparations, suppositories and sterilized injection solutions according to a conventional method.
상기 조성물에 포함될 수 있는 담체, 부형제 및 희석제로는 락토오스, 덱스트로오스, 수크로오스, 소르비톨, 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 및 광물유 등이 있다. 상기 조성물을 제제화할 경우에는 보통 사용하는 충진제, 증량제, 결합제, 습윤제, 붕해제, 계면활성제 등의 희석제 또는 부형제를 사용하여 조제된다.Examples of carriers, excipients and diluents that can be included in the composition include lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methylcellulose , Microcrystalline cellulose, polyvinylpyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate and mineral oil. When the composition is formulated, it is prepared using a diluent such as a filler, an extender, a binder, a wetting agent, a disintegrant, a surfactant, or an excipient usually used.
본 발명의 약학적 조성물은 목적하는 방법에 따라 경구 투여하거나 비경구투여(예를 들어, 정맥 내, 피하, 복강 내 또는 국소에 적용)할 수 있으며, 투여량은 환자의 상태 및 체중, 질병의 정도, 약물형태, 투여경로 및 시간에 따라 다르지만, 당업자에 의해 적절하게 선택될 수 있다.The pharmaceutical composition of the present invention may be administered orally or parenterally (for example, intravenously, subcutaneously, intraperitoneally or topically) depending on the intended method, and the dose may vary depending on the condition and the weight of the patient, The mode of administration, the route of administration, and the time, but may be appropriately selected by those skilled in the art.
본 발명의 약학적 조성물은 약학적으로 유효한 양으로 투여한다. 본 발명에 있어서, "약학적으로 유효한 양"은 의학적 치료에 적용 가능한 합리적인 수혜/위험 비율로 질환을 치료하기에 충분한 양을 의미하며, 유효용량 수준은 환자의 질환의 종류, 중증도, 약물의 활성, 약물에 대한 민감도, 투여 시간, 투여 경로 및 배출 비율, 치료기간, 동시 사용되는 약물을 포함한 요소 및 기타 의학 분야에 잘 알려진 요소에 따라 결정될 수 있다. 본 발명의 약학적 조성물은 개별 치료제로 투여하거나 다른 치료제와 병용하여 투여될 수 있고 종래의 치료제와는 순차적 또는 동시에 투여될 수 있으며, 단일 또는 다중 투여될 수 있다. 상기한 요소들을 모두 고려하여 부작용 없이 최소한의 양으로 최대 효과를 얻을 수 있는 양을 투여하는 것이 중요하며, 이는 당업자에 의해 용이하게 결정될 수 있다.The pharmaceutical composition of the present invention is administered in a pharmaceutically effective amount. In the present invention, "pharmaceutically effective amount" means an amount sufficient to treat a disease at a reasonable benefit / risk ratio applicable to medical treatment, and an effective dosage level is determined depending on the type of disease, severity, , Sensitivity to the drug, time of administration, route of administration and rate of release, duration of treatment, factors including co-administered drugs, and other factors well known in the medical arts. The pharmaceutical composition of the present invention can be administered as an individual therapeutic agent or in combination with other therapeutic agents, and can be administered sequentially or simultaneously with conventional therapeutic agents, and can be administered singly or in multiple doses. It is important to take into account all of the above factors and to administer the amount in which the maximum effect can be obtained in a minimal amount without side effects, which can be easily determined by those skilled in the art.
구체적으로, 본 발명의 약학적 조성물의 유효량은 환자의 연령, 성별, 상태, 체중, 체내에서 활성 성분의 흡수도, 불활성율 및 배설속도, 질병종류, 병용되는 약물에 따라 달라질 수 있으며, 일반적으로는 체중 1㎏ 당 0.0001 내지 150 mg, 바람직하게는 0.001 내지 100 mg을 매일 또는 격일 투여하거나 1일 1 내지 3회로 나누어 투여할 수 있다. 그러나 투여 경로, 비만의 중증도, 성별, 체중, 연령 등에 따라서 증감될 수 있으므로 상기 투여량이 어떠한 방법으로도 본 발명의 범위를 한정하는 것은 아니다.Specifically, the effective amount of the pharmaceutical composition of the present invention may vary depending on the age, sex, condition, body weight, the degree of absorption of the active ingredient in the body, the rate of inactivation and excretion, the type of disease, May be administered in a daily dose of 0.0001 to 150 mg, preferably 0.001 to 100 mg, per 1 kg of body weight or one to three divided doses per day. However, the dosage may be varied depending on the route of administration, the severity of obesity, sex, weight, age, etc. Therefore, the dosage is not limited to the scope of the present invention by any means.
또한, 본 발명의 또 다른 양태로서, 본 발명은 산약, 어성초 및 용안육의 복합 생약 추출물을 유효성분으로 함유하는 수면 장애 또는 불면증 개선용 건강기능식품 조성물을 제공한다.According to still another aspect of the present invention, there is provided a health functional food composition for improving sleeping disorder or insomnia, which comprises, as an active ingredient, a complex herbal extract of lily of the valley,
본 발명에서 사용되는 용어 "개선"이란 치료되는 상태와 관련된 파라미터, 예를 들면 증상의 정도를 적어도 감소시키는 모든 행위를 의미한다. The term "improvement" as used in the present invention means all actions that at least reduce the degree of symptom associated with the condition being treated.
본 발명의 조성물은 수면 장애 또는 불면증의 예방 또는 개선을 목적으로 건강기능식품에 첨가될 수 있다. 본 발명의 복합 생약 추출물을 식품 첨가물로 사용할 경우, 상기 복합 생약 추출물을 그대로 첨가하거나 다른 식품 또는 식품 성분과 함께 사용할 수 있고, 통상적인 방법에 따라 적절하게 사용할 수 있다. 유효성분의 혼합양은 사용 목적(예방, 건강 또는 치료적 처치)에 따라 적합하게 결정될 수 있다. 일반적으로, 식품 또는 음료의 제조시 본 발명의 복합 생약 추출물은 원료에 대하여 15 중량% 이하, 바람직하게는 10 중량% 이하의 양으로 첨가된다. 그러나, 건강 및 위생을 목적으로 하거나 또는 건강 조절을 목적으로 하는 장기간의 섭취의 경우 상기 양은 상기 범위 이하일 수 있으며, 안전성 면에서 아무런 문제가 없기 때문에 유효성분은 상기 범위 이상의 양으로도 사용될 수 있다.The composition of the present invention may be added to health functional foods for the purpose of preventing or ameliorating sleep disorders or insomnia. When the complex herbal medicine extract of the present invention is used as a food additive, the herbal medicine extract may be added as it is or may be used together with other food or food ingredients, and may be appropriately used according to a conventional method. The amount of the active ingredient to be mixed can be suitably determined according to the intended use (prevention, health or therapeutic treatment). In general, the herbal extract of the present invention is added in an amount of not more than 15% by weight, preferably not more than 10% by weight based on the raw material. However, in the case of long-term intake for the purpose of health and hygiene or for the purpose of health control, the amount may be less than the above range, and since there is no problem in terms of safety, the active ingredient may be used in an amount exceeding the above range.
상기 식품의 종류에는 특별한 제한은 없다. 상기 물질을 첨가할 수 있는 식품의 예로는 육류, 소세지, 빵, 쵸코렛, 캔디류, 스넥류, 과자류, 피자, 라면, 기타 면류, 껌류, 아이스크림류를 포함한 낙농제품, 각종 스프, 음료수, 차, 드링크제, 알콜 음료 및 비타민 복합제 등이 있으며, 통상적인 의미에서의 건강기능식품을 모두 포함한다.There is no particular limitation on the kind of the food. Examples of the food to which the above substances can be added include dairy products including meat, sausage, bread, chocolate, candy, snack, confectionery, pizza, ramen, other noodles, gums, ice cream, various soups, drinks, tea, Alcoholic beverages, and vitamin complexes, all of which include health functional foods in a conventional sense.
본 발명의 건강음료 조성물은 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다. 상술한 천연 탄수화물은 포도당 및 과당과 같은 모노사카라이드, 말토오스 및 수크로오스와 같은 디사카라이드, 덱스트린 및 시클로덱스트린과 같은 폴리사카라이드, 및 자일리톨, 소르비톨 및 에리트리톨 등의 당알콜이다. 감미제로서는 타우마틴, 스테비아 추출물과 같은 천연 감미제나, 사카린, 아스파르탐과 같은 합성 감미제 등을 사용할 수 있다. 상기 천연 탄수화물의 비율은 본 발명의 조성물 100㎖당 일반적으로 약 0.01~0.20g, 바람직하게는 약 0.04~0.10g 이다.The health beverage composition of the present invention may contain various flavors or natural carbohydrates as an additional ingredient such as ordinary beverages. The above-mentioned natural carbohydrates are monosaccharides such as glucose and fructose, polysaccharides such as disaccharides such as maltose and sucrose, dextrin and cyclodextrin, and sugar alcohols such as xylitol, sorbitol and erythritol. Examples of sweeteners include natural sweeteners such as tau martin and stevia extract, synthetic sweeteners such as saccharin and aspartame, and the like. The ratio of the natural carbohydrate is generally about 0.01 to 0.20 g, preferably about 0.04 to 0.10 g per 100 ml of the composition of the present invention.
상기 외에 본 발명의 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, 알콜, 탄산 음료에 사용되는 탄산화제 등을 함유할 수 있다. 그 밖에 본 발명의 조성물은 천연 과일쥬스, 과일쥬스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 조합하여 사용할 수 있다. 이러한 첨가제의 비율은 크게 중요하진 않지만 본 발명의 조성물 100 중량부 당 0.01~0.20 중량부의 범위에서 선택되는 것이 일반적이다.In addition to the above, the composition of the present invention may further contain various nutrients, vitamins, electrolytes, flavors, colorants, pectic acids and salts thereof, alginic acid and its salts, organic acids, protective colloid thickeners, pH adjusting agents, stabilizers, preservatives, A carbonating agent used in a carbonated beverage, and the like. In addition, the composition of the present invention may contain flesh for the production of natural fruit juices, fruit juice drinks and vegetable drinks. These components may be used independently or in combination. Although the ratio of such additives is not critical, it is generally selected in the range of 0.01 to 0.20 parts by weight per 100 parts by weight of the composition of the present invention.
또한, 본 발명의 또 다른 양태로서, 본 발명은 산약, 어성초 및 용안육의 복합 생약 추출물을 개체에게 투여하는 단계를 포함하는 수면 장애 또는 불면증의 예방 또는 치료 방법을 제공한다. 상기 개체는 인간 또는 비-인간을 포함하는 포유류이며, 비-인간 포유류는 마우스, 랫트, 개, 고양이, 말, 소, 양, 염소, 돼지, 토끼 등을 포함하나 이에 한정되지 않는다.Further, as another embodiment of the present invention, the present invention provides a method for preventing or treating sleep disorder or insomnia comprising the step of administering to a subject a complex herbal extract of lily of the valley, herringbone and eyedropper. The subject is a mammal including a human or non-human, and non-human mammals include, but are not limited to, mice, rats, dogs, cats, horses, cows, sheep, goats, pigs, rabbits and the like.
이하, 본 발명의 이해를 돕기 위하여 바람직한 실시예를 제시한다. 그러나 하기의 실시예는 본 발명을 보다 쉽게 이해하기 위하여 제공되는 것일 뿐, 하기 실시예에 의해 본 발명의 내용이 한정되는 것은 아니다.Hereinafter, preferred embodiments of the present invention will be described in order to facilitate understanding of the present invention. However, the following examples are provided only for the purpose of easier understanding of the present invention, and the present invention is not limited by the following examples.
[실시예] [Example]
실시예 1. 실험준비 및 실험방법Example 1. Experimental Preparation and Experimental Method
1-1. 복합 생약 추출물의 제조1-1. Preparation of complex herbal medicine extract
본 실험에 사용한 생약들은 ㈜동양허브에서 구입하여 정선한 것을 사용하였다. 먼저 산약, 어성초, 용안육을 음건 및 분쇄한 후, 산약 33g, 어성초 33g, 용안육 33g을 혼합하여 30% 에탄올 1ℓ에 넣고 약탕기를 이용해 열수 추출물을 얻은 후 동결건조하였다. 동결건조한 시료 100mg을 1ml의 30% 에탄올에 넣고 녹인 후 0.2um 필터로 불순물을 제거한 후 시료로 사용하였다. The herbal medicine used in this experiment was purchased from Dongyang Hub Co., Ltd. First, the shiitake mushroom, shiitake mushroom, and yongcunmyk were shredded and shredded, mixed with 33 g of acid moss, 33 g of mushroom and 33 g of yongsanmyeol, and the mixture was added to 1 L of 30% ethanol, followed by lyophilization. 100 mg of the lyophilized sample was dissolved in 1 ml of 30% ethanol, and the impurities were removed with a 0.2-μm filter and used as a sample.
체중이 60kg인 성인이 복용하는 복합 생약(산약, 어성초, 용안육을 1:1:1의 중량비로 혼합)을 1000mg, 3000mg로 정하고, 이를 마우스에 적용하기 위해 하기 공식을 이용하여 사료를 제조하였다.1000 mg, and 3000 mg of the complex medicines (mixed with liquorice, horseradish, and yogurts at a weight ratio of 1: 1: 1), which are taken by an adult having a body weight of 60 kg, were prepared.
HED (mg/kg)=Animal dose (mg/kg) X Animal Km/Human Km HED (mg / kg) = Animal dose (mg / kg) X Animal Km / Human Km
1-2. 실험동물1-2. Experimental animal
250g 내외의 Sprague-Dawley종 수컷 흰쥐(샘타코, 한국)를 사용하였으며, 수술 전 동물을 사육실의 사육상자에 2마리씩 넣고 동물이 물과 먹이를 자유롭게 먹을 수 있도록 하였다. 사육실의 환경은 12시간(08:00-20:00에 조명켜짐) 명암주기가 조절되고 온도가 20~25℃, 습도는 45~65% 정도로 유지하였다.Sprague-Dawley male rats (Samtaco, Korea) were used at a dose of 250 g. Pre-operative animals were placed in a breeding box in the breeding room to allow the animals to freely eat water and food. The environment of the breeding room was controlled by 12 hours (lighting at 08: 00-20: 00), the temperature was 20 ~ 25 ℃ and the humidity was 45 ~ 65%.
1-3. 수술(surgery)1-3. Surgery
수술을 총 3그룹(normal, A200; 200mg/kg, A400; 400mg/kg) 으로 나누어 수술을 진행하였고 각 그룹당 6마리씩 총 18마리로 진행하였다. 수술을 위해 Pentobarbital(40mg/kg)을 동물의 복강 내 주사하여 마취하였다. 마취된 쥐를 입체 고정기(stereotaxic instrument, Stoelting CO, USA)에 위치시키고 정수리점(bregma) 및 시옷점(lambda)이 수평이 되게 고정하였다. 두피 하에 출혈을 억제한 다음, 털을 깎고 두피를 절개하고 집게로 절개된 피부를 잡아 벌려 두개골 면이 노출되게 하여 골막(periosteum)을 제거하고 뼈를 노출시켰다. 염증이 생기는 것을 방지하기 위해 두개골 면의 골막 등의 조직 및 혈액을 깨끗이 제거하고 70% 소독용 알콜로 닦았다. Paxinos 및 Watson의 해부도에 따라 드릴로 구멍을 내고 electrode를 경막에 닿도록 삽입하였다. 근전도 기록을 위해 목 근육에 두 가닥의 은선 전극을 삽입 하였다. 뇌파 기록전극 및 근전도 기록전극의 연결된 핀들을 소뇌상부 두개골 위에 위치시키고 치과용 시멘트를 발라서 두개골 상부에 고정하였다. 수술이 끝난 동물을 사육실의 사육상자에 1마리씩 넣고 1주일간 회복시켰다. 회복기에도 12시간 명암주기를 적용하고 물과 먹이를 자유로이 섭취하도록 하였다.The operation was divided into 3 groups (normal, A200; 200 mg / kg, A400; 400 mg / kg) Pentobarbital (40 mg / kg) was anesthetized by intraperitoneal injection of the animals for surgery. The anesthetized rats were placed on a stereotaxic instrument (Stoelting CO, USA) and the bregma and lambda points were leveled. After curbing the bleeding under the scalp, the hair was cut, the scalp was incised, and the incised skin was opened to expose the skull surface to remove the periosteum and expose the bones. To prevent inflammation, tissues such as the periosteum of the skull surface and blood were cleaned and wiped with 70% alcohol for disinfection. Drill holes were made according to the dissection of Paxinos and Watson, and the electrode was inserted into contact with the dura. Two electrodes were inserted into the neck muscles for EMG recording. Electroencephalogram recording electrodes and connected electrodes of EMG recording electrodes were placed on the upper cerebellum of the cerebellum and fixed on the upper part of the skull by applying dental cement. The animals were placed in a breeding box in the breeding room and were restored for 1 week. During the recovery phase, 12-hour light cycle was applied and water and food were freely consumed.
1-4. 1-4. 뇌파검사EEG (( ElectroencephalographyElectroencephalography ; EEG); EEG)
수술회복 후, 쥐를 실험조건에 적응하도록 하였다. 경구투여로 각각의 약물을 투여하고 10분 후 EEG 레코딩(8:00pm부터 12시간 동안)을 진행하였다. 각성(Wake), REM(rapid eye movement), NREM(non-REM) 수면의 시간은 동물수면 전문분석 프로그램인 SleepSign Ver. 3 software (Kissei Comtec, Nagano, Japan)로 기록하였다.After recovery, the mice were adapted to the experimental conditions. Each drug was administered orally and 10 minutes later EEG recording (from 8:00 pm for 12 hours) was performed. Sleep, rapid eye movement, and non-REM sleep were measured using SleepSign Ver. 3 software (Kissei Comtec, Nagano, Japan).
수면 잠재기(sleep latency)는 샘플 투여와 적어도 2분간 지속되는 첫번째 연속적인 NREM 수면 삽화(sleep episode) 사이의 경과시간으로써 정의되며, six 4-s 시기이상 연속되고, NREM 수면으로 기록되지는 않는다. EEG 파워 스펙트럼은 0.5Hz 간격으로 계산되고 이를 통합하여 평균을 산출하였다. 이를 통해 델타파 활성 (0.65-4 Hz), 쎄타파 활성 (6-10 Hz) 및 알파파 활성 (12-14 Hz)의 3개의 주파수 영역으로 나누었다. NREM 수면의 EEG 파워 밀도(EEG power density)는 개별 랫트들의 총 EEG 파워 (0-20 Hz)로부터 각 간격의 퍼센트를 계산함으로써 한 그룹으로 표준화되었다. 한편, 수면-각성 상태는 일반적으로 다음과 같이 특정한다: Sleep latency is defined as the elapsed time between sample administration and the first consecutive NREM sleep episode lasting at least 2 minutes, continuing for more than six 4-s periods, and not recorded as NREM sleep. The EEG power spectra were calculated at 0.5 Hz intervals and integrated to calculate the mean. This was divided into three frequency regions: delta wave activity (0.65-4 Hz), theta wave activity (6-10 Hz) and alpha wave activity (12-14 Hz). The EEG power density of NREM sleep was normalized to one group by calculating the percentage of each interval from the total EEG power (0-20 Hz) of the individual rats. On the other hand, the sleep-wake state is generally specified as follows:
각성 : 저-진폭 EEG 및 고-전압 EMG 활성; Arousal: low-amplitude EEG and high-voltage EMG activity;
NREM 수면 : 고-진폭의 slow 또는 spindle EEG 및 저-전압 EMG 활성; NREM sleep: high-amplitude slow or spindle EEG and low-voltage EMG activity;
REM 수면 : 저-전압 EEG 및 EMG 활성.REM sleep: low-voltage EEG and EMG activity.
실시예Example 2. 복합 생약 추출물의 수면 증진 및 개선 효과 확인 2. Identification of improvement of sleep and improvement effect of herbal medicine extract
2-1. 복합 생약 추출물에 따른 동물모델에서의 수면 증진 효과 확인2-1. Identification of the effect of sleeping on animal models by herbal extracts
상기 실시예 1-3에 기재된 방법에 의해 수술을 진행한 실험동물을 상기 실시예 1-4에 기재된 방법으로 뇌파를 측정하였다.The animals subjected to the surgery by the method described in the above Example 1-3 were measured for brain waves by the method described in Examples 1-4.
그 결과, 도 1 및 도 2에 나타낸 바와 같이, 복합 생약 추출물을 400mg/kg의 농도로 투여한 군(A400)에서 wake와 rem 에서 TUKEY HSD와 LSD 모두 유의미한 결과가 나타남을 확인하였다. 또한, 약물농도가 증가함에 따라 wake 감소 / rem 증가의 경향성이 존재함을 알 수 있었다.As a result, as shown in FIG. 1 and FIG. 2, it was confirmed that both TUKEY HSD and LSD showed significant results in wake and rem in the group (A400) in which the herbal extract was administered at a concentration of 400 mg / kg. Also, there was a tendency of wake reduction / rem increase with increasing drug concentration.
2-2. 복합 생약 추출물에 따른 Aß42 형질전환 초파리 치매모델에서의 수면 증진 효과 확인2-2. Identification of effect of sleep enhancement on Aß42 transgenic Drosophila dementia model by combination herbal medicine extract
본 발명에 따른 복합 생약 추출물이 초파리의 운동 활성에 끼치는 영향을 확인하기 위해서, 상기 실시예 1-1을 통해 제조된 복합 생약 추출물 (산약, 어성초, 용안육을 1:1:1의 중량비로 혼합; HED)을 5% 자당 (sucrose) 및 1% 한천 (agar)배지에 100㎎/㎖의 농도로 배합한 후, 초파리 행동 조사 분석 시스템 (Drosophila Activity Monitoring system, DAM; TriKinetics, Waltham, MA, USA)을 이용하여 운동 활성 수준을 평가하였다.In order to confirm the effects of the herbal extracts of the present invention on the locomotor activity of the fruit flies, the herbal extracts prepared in Example 1-1 were mixed at a weight ratio of 1: 1: 1; (Drosophila Activity Monitoring System, DAM; Tri- kinetics, Waltham, MA, USA) was added to a 5% sucrose and 1% agar medium at a concentration of 100 mg / Was used to evaluate the level of locomotor activity.
보다 구체적으로, 상기 DAM 시스템은 4일 동안 (3일 정상식이에 적응, 4일 수크로오스 한천 배지에서 아미노산을 처리한 실험) 어두운 환경에서 수행하였으며, 이 때, 실험군으로는 대조군, 복합 생약 추출물 처리군 (HED), 산약 처리군 및 용안육 처리군 그룹으로 나누어, 각 그룹당 10마리씩 튜브에서 24시간 적응시킨 다음, 1분 간격으로 4일 동안 활동량을 기록하고, 4일 동안의 평균 활동량을 계산하였다.More specifically, the DAM system was performed in a dark environment for 4 days (3 days of normal diet, 4 days of treatment with an amino acid in a sucrose agar medium), and the experimental group was a control group, a complex herbal extract treatment group (HED), acid treatment group, and luciferase treatment group. The animals were adapted for 24 hours in a tube of 10 animals per group, and the activity was recorded for 4 days at 1 minute intervals and the average activity for 4 days was calculated.
이 때, 상기 결과값은 평균 ± 표준편차 (SEM)로 나타내었으며, 유의성 수준은 *p < 0.05 vs elav > Aß42 및 #p < 0.05 vs elav > Aß42 + 산약으로 하였다.The results were expressed as mean ± standard deviation (SEM), and significance level was defined as p <0.05 vs. elav> Aß42 and #p <0.05 vs elav> Aß42 +
그 결과, 도 3에 나타낸 바와 같이, 복합 생약 추출물 처리군 (HED)의 밤 운동성이 대조군에 비해 유의성 있게 감소한 것을 확인하였으며, 낮 운동성이 대조군에 비해 유의성 있게 증가한 것을 확인하였다.As a result, as shown in FIG. 3, it was confirmed that the night mobility of the herbal extract-treated group (HED) was significantly lower than that of the control group, and the low mobility was significantly increased compared with the control group.
전술한 본 발명의 설명은 예시를 위한 것이며, 본 발명이 속하는 기술분야의 통상의 지식을 가진 자는 본 발명의 기술적 사상이나 필수적인 특징을 변경하지 않고서 다른 구체적인 형태로 쉽게 변형이 가능하다는 것을 이해할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적이 아닌 것으로 이해해야만 한다.It will be understood by those skilled in the art that the foregoing description of the present invention is for illustrative purposes only and that those of ordinary skill in the art can readily understand that various changes and modifications may be made without departing from the spirit or essential characteristics of the present invention. will be. It is therefore to be understood that the above-described embodiments are illustrative in all aspects and not restrictive.
Claims (11)
A composition for enhancing or improving sleep quality, comprising an extract of a complex herbal medicine of Lilium, Liliaceae, and Yongcheng as an active ingredient.
A pharmaceutical composition for the prevention or treatment of sleep disorders or insomnia, which comprises as an active ingredient, a herbal medicine extract of a combination of lupine, lupine, and lupine.
The pharmaceutical composition according to claim 2, wherein the extract is extracted using water, a C 1 to C 4 lower alcohol, or a mixed solvent thereof.
The pharmaceutical composition according to claim 3, wherein the lower alcohol is ethanol.
[Claim 3] The pharmaceutical composition according to claim 2, wherein the extract is a mixture of scutellaria baicalensis, horsetail, and canola oil mixed in a weight ratio of 1: 0.1 to 10: 0.1 to 10.
6. The pharmaceutical composition according to claim 5, wherein the weight ratio is 1: 1: 1.
A composition for health functional food for improving sleeping disorder or insomnia, which comprises as an active ingredient, a herbal medicine extract of a combination of lupus erythematosus, lupus erythematosus, and lupus erythematosus.
The health functional food composition according to claim 7, wherein the extract is extracted with water, a C 1 to C 4 lower alcohol, or a mixed solvent thereof.
The health functional food composition according to claim 8, wherein the lower alcohol is ethanol.
[Claim 7] The health functional food composition according to claim 7, wherein the extract is prepared by mixing the fish extracts, the herbal extracts, and the yogurts at a weight ratio of 1: 0.1 to 10: 0.1 to 10.
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CN108143913A (en) * | 2018-02-10 | 2018-06-12 | 武汉立芳华科技有限公司 | A kind of bluish dogbane goes tired sleeping cream and production method |
CN108721448A (en) * | 2018-07-30 | 2018-11-02 | 佛山科学技术学院 | A kind of sleeping health Chinese medicine and preparation method thereof |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0838124A (en) * | 1994-07-28 | 1996-02-13 | Nikku Ind Co Ltd | Medicinal herb tea containing longanae arillus and production thereof |
KR20020015540A (en) * | 2000-08-22 | 2002-02-28 | 김상근 | Food materials for preventing dementia and foods using the same |
JP2005060357A (en) * | 2003-08-12 | 2005-03-10 | ▲張▼ ▲書▼廷 | Health food for promoting sleep and tranquirizing by using plant as raw material and method for producing the same |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006327970A (en) * | 2005-05-25 | 2006-12-07 | Daicho Kikaku:Kk | Digestive apparatus agent and anti-stress agent |
KR101041044B1 (en) * | 2008-09-10 | 2011-06-13 | 우석대학교 산학협력단 | A composition for reducing sleep induction time and prolonging sleeping time, and a method for preparing the same |
KR20110101648A (en) * | 2010-03-09 | 2011-09-16 | 김동환 | Composition for inducing sleep |
KR101470241B1 (en) * | 2013-11-14 | 2014-12-08 | 동국대학교 경주캠퍼스 산학협력단 | Pharmaceutical composition for the prevention or treatment of depression |
-
2017
- 2017-01-25 KR KR1020170011986A patent/KR101875307B1/en active IP Right Grant
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0838124A (en) * | 1994-07-28 | 1996-02-13 | Nikku Ind Co Ltd | Medicinal herb tea containing longanae arillus and production thereof |
KR20020015540A (en) * | 2000-08-22 | 2002-02-28 | 김상근 | Food materials for preventing dementia and foods using the same |
JP2005060357A (en) * | 2003-08-12 | 2005-03-10 | ▲張▼ ▲書▼廷 | Health food for promoting sleep and tranquirizing by using plant as raw material and method for producing the same |
Non-Patent Citations (2)
Title |
---|
LC Chen 외 3명. Drug-use pattern of Chinese herbal medicines in insomnia: a 4-year survey in Taiwan. Neuroscience Letters. Volume 34, Issue 5, 2009, pp. 555-560 * |
왕덕중 외 6명. 수면장애를 동반한 당뇨병성 소양증 환자에 대한 육미지황탕가미방(六味地黃湯加味方) 투여 1례. 대한한방내과학회지. Volume 26, Issue 3, 2005, pp. 725-732 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108143913A (en) * | 2018-02-10 | 2018-06-12 | 武汉立芳华科技有限公司 | A kind of bluish dogbane goes tired sleeping cream and production method |
CN108721448A (en) * | 2018-07-30 | 2018-11-02 | 佛山科学技术学院 | A kind of sleeping health Chinese medicine and preparation method thereof |
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