CN117223741A - Traditional Chinese medicine diet for improving constipation and preparation method thereof - Google Patents

Traditional Chinese medicine diet for improving constipation and preparation method thereof Download PDF

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CN117223741A
CN117223741A CN202311145170.4A CN202311145170A CN117223741A CN 117223741 A CN117223741 A CN 117223741A CN 202311145170 A CN202311145170 A CN 202311145170A CN 117223741 A CN117223741 A CN 117223741A
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何红艳
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Jishi Hanfang Ningbo Medical Technology Co ltd
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Abstract

本发明属于中药药膳技术领域,公开了一种改善便秘的中药药膳及其制备方法。本发明改善便秘的中药药膳中包含杏仁、佛手、桔梗、麦芽、山药、山楂、鸡内金、郁李仁、紫苏籽、火麻仁、圆苞车前子壳和秋葵粉作为有效成分。本发明的中药药膳是基于中医十余年慢性便秘的临床诊疗经验,结合扎实的中医理论基础研究完善而得,对慢性便秘的预防及治疗的安全性、有效性久经临床验证。The invention belongs to the technical field of traditional Chinese medicinal diet and discloses a traditional Chinese medicinal diet for improving constipation and a preparation method thereof. The traditional Chinese medicinal diet for improving constipation of the present invention contains almonds, bergamot, platycodon, malt, yam, hawthorn, Gallus gallus gallus gallus gallinae, Yu Liren, perilla seeds, hemp seeds, plantain husk and okra powder as active ingredients. The traditional Chinese medicinal diet of the present invention is based on more than ten years of clinical diagnosis and treatment experience of chronic constipation in traditional Chinese medicine, combined with solid theoretical basic research of traditional Chinese medicine. Its safety and effectiveness in the prevention and treatment of chronic constipation have been clinically verified for a long time.

Description

一种改善便秘的中药药膳及其制备方法A kind of traditional Chinese medicinal diet for improving constipation and its preparation method

技术领域Technical field

本发明涉及中药技术领域,具体是涉及一种改善便秘的中药药膳及其制备方法。The present invention relates to the technical field of traditional Chinese medicine, and specifically relates to a traditional Chinese medicinal diet for improving constipation and a preparation method thereof.

背景技术Background technique

慢性便秘发病率高,危害大,会给患者带来巨大的痛苦。饮食结构及饮食习惯的改变加上不科学的生活方式,致使慢性便秘的发病率越来越高,成为影响现代人生活质量的常见病、多发病,而且慢性便秘还导致其他肛肠疾病、泌尿系统疾病和心脑血管疾病的恶化,引起焦虑症、抑郁症等精神心理疾病。然而,市场上治疗慢性便秘的药物多是含有蒽醌类物质的刺激性泻药,起效快但副作用明显,极易导致顽固性泻剂依赖性便秘、结肠黑变病,还会增加肿瘤、息肉的发病率。Chronic constipation has a high incidence rate and great harm, and can cause great pain to patients. Changes in dietary structure and eating habits coupled with unscientific lifestyles have led to an increasing incidence of chronic constipation, which has become a common and frequently-occurring disease that affects the quality of life of modern people. Chronic constipation also leads to other anorectal diseases and urinary system diseases. The exacerbation of diseases and cardiovascular and cerebrovascular diseases can cause mental illness such as anxiety and depression. However, most of the drugs on the market for the treatment of chronic constipation are stimulant laxatives containing anthraquinones, which have quick effects but significant side effects. They can easily lead to intractable laxative-dependent constipation, colonic melanosis, and an increase in tumors and polyps. incidence rate.

近年来“圆运动”理论越来越受到中医学者的重视,基于气机圆理论,可分析便秘的中医病机。气机是人体生命活动的关键,气机升降出入正常则人体各项生理活动有序、协调进行。若气机升降出入失调则人体生理机能被打乱,百病丛生。升、降、浮、沉是人体气机的“圆运动”形式,人体的生理机制和病理变化以气机的“圆运动”形式统摄起来,即可以理解为人体生命活动就是一个微型的气机圆运动。“圆运动”的生理即“轴运轮行,轮运轴灵”,“圆运动”的病理即“轴不旋转,轮不升降”。饮食积滞而损害脾胃,脾胃运化功能失职,而至脾胃之轴不旋转,并出现脾阳不升、胃气不降。同时现代人容易因情志不遂而出现肝气不舒讨伐脾胃,肺失宣降而津液不能下达,会出现肠燥秘结,肾气亏虚,不能温煦脾阳,推动脾胃运化及脾升胃降,脾胃升清降浊失职、肠燥秘结。In recent years, the "circular motion" theory has received more and more attention from traditional Chinese medicine scholars. Based on the circular theory of qi movement, the traditional Chinese medicine pathogenesis of constipation can be analyzed. Qi movement is the key to human life activities. If the movement of Qi movement is normal, all physiological activities of the human body will proceed in an orderly and coordinated manner. If the movement of Qi is out of balance, the physiological functions of the human body will be disrupted and all kinds of diseases will arise. Rising, falling, floating and sinking are the "circular movements" of the human body's qi. The physiological mechanisms and pathological changes of the human body are unified by the "circular movement" of the qi. That is to say, the life activities of the human body are just a miniature qi. circular motion. The physiology of "circular motion" is that "the axis moves and the wheel moves, and the wheel moves the axis." The pathology of "circular motion" is that "the axis does not rotate, and the wheel does not rise or fall." The stagnant diet will damage the spleen and stomach, and the spleen and stomach's transportation and transformation functions will fail. As a result, the axis of the spleen and stomach will not rotate, and spleen yang will not rise and stomach qi will not fall. At the same time, modern people are prone to have liver qi that attacks the spleen and stomach due to poor emotions, and the lungs are ineffective and body fluids cannot be discharged. They may suffer from intestinal dryness and constipation, and kidney qi deficiency, which cannot warm the spleen yang, promote the transportation and transformation of the spleen and stomach, and promote the spleen and stomach. Descending, spleen and stomach ascend clear and descend turbidity, constipation due to constipation of intestinal dryness.

中药药膳是以中国传统医学为理论基础,以药物(中药)和食物为主要原料,以中国烹饪工艺为基本手段,以养生健身、防病治病为根本目的的美味食品。中医药历来重视食补、药膳和食疗,我国现存最早的中医理论经典《黄帝内经》中就提出了食养的概念,唐代孙思邈的《备急千金要方》、宋代陈直的《养老奉亲书》、元代忽思慧的《饮膳正要》等专著中都有关于食疗的记载,而《神农本草经》、《本草纲目》等记载的动植物药材中,很多都是药食两用的日常食品。针对慢性便秘的中药药膳验方众多,但由于缺乏传统中医理论的指导,存在滥用、误用的情况,无法满足人们的需求。因此,需要开发符合我国国情、安全有效的中药药膳改善慢性便秘。Traditional Chinese medicinal diet is a delicious food based on traditional Chinese medicine as the theoretical basis, using drugs (TCM) and food as the main raw materials, using Chinese cooking techniques as the basic means, and with the fundamental purpose of maintaining health and fitness, preventing and curing diseases. Traditional Chinese medicine has always attached great importance to dietary supplements, medicated diets and dietary therapies. The earliest extant traditional Chinese medicine theory classic in my country, the Huangdi Neijing, puts forward the concept of dietary nourishment. There are records of dietary therapy in monographs such as "Book" and "Yinshan Zhengyao" written by Hu Sihui of the Yuan Dynasty. Many of the animal and plant medicinal materials recorded in "Shen Nong's Materia Medica" and "Compendium of Materia Medica" are both medicinal and dietary. daily food. There are many traditional Chinese medicine and dietary prescriptions for chronic constipation, but due to the lack of guidance from traditional Chinese medicine theory, there are cases of abuse and misuse, and they cannot meet people's needs. Therefore, it is necessary to develop safe and effective traditional Chinese medicine diet to improve chronic constipation that is consistent with my country's national conditions.

发明内容Contents of the invention

本发明的目的是为了克服上述背景技术的不足,结合气机圆理论,提供一种改善便秘的中药药膳及其制备方法。本发明改善便秘的中药药膳是中医十余年慢性便秘的临床诊疗经验结合扎实的中医理论基础研究完善而得,不含大黄、番泻叶、芦荟、决明子、何首乌等富含蒽醌类物质的刺激性泻药成分,对慢性便秘的预防及治疗的安全性、有效性久经临床验证。The purpose of the present invention is to overcome the above-mentioned deficiencies in the background technology and provide a Chinese medicinal diet for improving constipation and a preparation method thereof in combination with the theory of qi movement and circle. The traditional Chinese medicinal diet for improving constipation of the present invention is obtained from more than ten years of clinical diagnosis and treatment experience of chronic constipation combined with solid theoretical basic research of traditional Chinese medicine. It does not contain rhubarb, senna, aloe, cassia, polygonum multiflorum and other anthraquinone-rich substances. The stimulant laxative ingredient has long been clinically proven to be safe and effective in preventing and treating chronic constipation.

为达到本发明的目的,本发明改善便秘的中药药膳中包含杏仁、佛手、桔梗、麦芽、山药、山楂、鸡内金、郁李仁、紫苏籽、火麻仁、圆苞车前子壳和秋葵粉作为有效成分。In order to achieve the purpose of the present invention, the traditional Chinese medicinal diet for improving constipation of the present invention contains almonds, bergamot, platycodon, malt, yam, hawthorn, gallinaceae, Yuliren, perilla seeds, hemp seeds, plantain husk and autumn leaves. Sunflower powder as active ingredient.

上述中药药膳在现有药膳饼干的基础上,去掉了较为滋腻的黄精以避免防碍脾胃的运化功能,不含水溶性膳食纤含量相对较低的奇亚籽、香菇、银耳、芹菜、低聚果糖,加入了杏仁、紫苏籽,以加强宽肺润肠,另外还加入了郁李仁、火麻仁润肠通便。The above-mentioned traditional Chinese medicinal diet is based on the existing medicated dietary biscuits. The relatively greasy Polygonatum japonica has been removed to avoid hindering the transportation function of the spleen and stomach. It does not contain chia seeds, shiitake mushrooms, white fungus, celery, and low water-soluble dietary fiber content. Polyfructose is added with almonds and perilla seeds to strengthen the lungs and moisturize the intestines. In addition, plum kernels and hemp seeds are added to moisturize the intestines and relieve constipation.

本发明中药药膳的成分都是依据气机圆理论的生理病理状态和改善方案而选择。其中,山楂、鸡内金、麦芽消食健脾,以复轴旋。佛手、麦芽疏肝解郁,以调木轮升降。山药补脾养胃,生津益肺,补肾益气生津,脾肺肾三脏通条,气机推动有力,以复轴旋轮动。桔梗宣肺,杏仁、紫苏籽降气,亦升亦降,津液得布,肠道得以滋养润滑。杏仁、火麻仁、郁李仁滋润肠道。这些药物共同作用,已达到轴旋轮动。此外、圆苞车前子壳、秋葵粉含有丰富的膳食纤维及微量元素,增加大便体积,软化粪便,刺激肠道蠕动,改善肠道菌群环境,从而增强人体排便功能。The ingredients of the traditional Chinese medicine diet of the present invention are selected based on the physiological and pathological conditions and improvement plans of the Qi Yuan theory. Among them, hawthorn, Gallus gallus gallus gallinae, malt are used for digestion and spleen strengthening, and for complex axis rotation. Bergamot and malt soothe the liver and relieve depression, and regulate the rise and fall of the wood chakra. Yams nourish the spleen and stomach, promote the production of body fluids and lungs, nourish the kidneys and replenish qi and promote the production of body fluids. The three internal organs of the spleen, lungs and kidneys are unblocked, and the qi machine drives powerfully and rotates in a double axis. Platycodon calms the lungs, while almonds and perilla seeds lower qi, both rising and falling. Body fluids are distributed and the intestines are nourished and lubricated. Almonds, hemp seeds, and plum blossoms nourish the intestines. These drugs work together to achieve a rotational movement. In addition, psyllium husk and okra powder are rich in dietary fiber and trace elements, which can increase stool volume, soften stool, stimulate intestinal peristalsis, improve the intestinal flora environment, thereby enhancing human defecation function.

进一步地,在本发明的一些实施例中,所述改善便秘的中药药膳中按重量份数计包含杏仁6-18份、佛手6-18份、山药15-45份、山楂6-18份、鸡内金6-18份、桔梗6-18份、麦芽6-18份、郁李仁2-18份、紫苏籽2-18份、火麻仁2-18份、圆苞车前子壳粉1-45份、秋葵粉1-18份。Further, in some embodiments of the present invention, the traditional Chinese medicinal diet for improving constipation includes 6-18 parts by weight of almonds, 6-18 parts of bergamot, 15-45 parts of yam, 6-18 parts of hawthorn, 6-18 parts of Gallus gallus gallus L., 6-18 parts of Platycodon grandiflorum, 6-18 parts of malt, 2-18 parts of Yuliren, 2-18 parts of Perilla seeds, 2-18 parts of Hemp seeds, 1 part of Psyllium husk powder -45 parts, okra powder 1-18 parts.

进一步地,在本发明的一些实施例中,所述改善便秘的中药药膳是饼干。Further, in some embodiments of the present invention, the Chinese medicinal diet for improving constipation is biscuits.

进一步地,在本发明的一些实施例中,所述饼干中按重量份数计包含杏仁6-18份、佛手6-18份、山药15-45份、山楂6-18份、鸡内金6-18份、桔梗6-18份、麦芽6-18份、郁李仁2-18份、紫苏籽2-18份、火麻仁2-18份、圆苞车前子壳粉1-45份、秋葵粉1-18份、面粉610份。Further, in some embodiments of the present invention, the biscuit contains 6-18 parts by weight of almonds, 6-18 parts of bergamot, 15-45 parts of yam, 6-18 parts of hawthorn, and 6 parts of Gallus gallus gallus L. -18 parts, platycodon 6-18 parts, malt 6-18 parts, plum kernels 2-18 parts, perilla seeds 2-18 parts, hemp seeds 2-18 parts, psyllium husk powder 1-45 parts, Okra powder 1-18 parts, flour 610 parts.

进一步地,本发明还提供了一种前述改善便秘的中药药膳饼干的制备方法,所述方法包含以下步骤:Further, the present invention also provides a method for preparing the aforementioned traditional Chinese medicine biscuits for improving constipation, which method includes the following steps:

(1)准备药粉:将杏仁、佛手、山药、山楂、鸡内金、桔梗、麦芽、郁李仁、紫苏籽、火麻仁经过超微粉碎,再与圆苞车前子壳粉、秋葵粉混合均匀;(1) Prepare medicinal powder: ultrafinely crush almonds, bergamot, yam, hawthorn, Gallus gallus gallus L., Platycodon grandiflorum, malt, plum kernels, perilla seeds, and hemp seeds, and then mix with plantain husk powder and okra powder. well mixed;

(2)配粉和面:依次在药粉中加入水、棕榈油、白砂糖,搅拌,加入面粉,搅拌调制至无干粉,面团不起筋;(2) Mix flour and dough: Add water, palm oil, and white sugar to the powder in sequence, stir, add flour, and mix until there is no dry powder and the dough has no gluten;

(3)成型:使用模具制成各种形状的饼干坯;(3) Forming: Use molds to make biscuit blanks of various shapes;

(4)烘烤:控制好温度进行烘烤;(4) Baking: control the temperature for baking;

(5)喷油:均匀喷淋棕榈油;(5) Oil spray: spray palm oil evenly;

(6)冷却整理:烘烤后饼干冷却至室温,转入包装间;(6) Cooling and finishing: After baking, the biscuits are cooled to room temperature and transferred to the packaging room;

(7)包装。(7) Packaging.

进一步地,在本发明的一些实施例中,所述步骤(1)中经过超微粉碎后达到200-400目的细度。Further, in some embodiments of the present invention, the fineness of 200-400 mesh is achieved after ultrafine grinding in step (1).

进一步地,在本发明的一些实施例中,所述步骤(4)中温度控制为上火170-260℃,下火160-240℃。Further, in some embodiments of the present invention, the temperature control in step (4) is 170-260°C for upper heat and 160-240°C for lower heat.

进一步地,在本发明的一些实施例中,所述步骤(5)中喷油的量控制标准为:称量喷前喷后各10片饼干,重量增加10-20%,喷油量即达标要求。Further, in some embodiments of the present invention, the control standard for the amount of oil injected in step (5) is: weigh 10 biscuits before and after spraying, and if the weight increases by 10-20%, the amount of oil injected reaches the standard. Require.

与现有技术相比,本发明的优点如下:Compared with the prior art, the advantages of the present invention are as follows:

(1)本发明中杏仁、佛手、桔梗、麦芽、山药、山楂、鸡内金、郁李仁、紫苏籽、火麻仁、圆苞车前子壳、秋葵粉等中药合用,具有补脾养胃,宽肠下气,生津、润肠通便之功效,可用于脾气虚则大肠传导无力,津枯不能滋润大肠,气机郁滞,通降失常,大肠传导失职,产生便秘、腹胀、嗳气、胸胁痞满,大便时努挣无力,便后疲乏不适等症的辅助或替代药物治疗。(1) In the present invention, traditional Chinese medicines such as almonds, bergamot, platycodon, malt, yam, hawthorn, Gallus gallus gallus gallinae, Yuliren, perilla seeds, hemp seeds, plantain husk, okra powder and other traditional Chinese medicines are used in combination to nourish the spleen and nourish the body. It has the effect of widening the intestines and lowering Qi, producing body fluids, moistening the intestines and laxative. It can be used to treat weak spleen-spleen conduction in the large intestine, dry body fluid unable to moisten the large intestine, stagnation of Qi, abnormal circulation, failure of large intestine conduction, resulting in constipation, bloating, and belching. Supplementary or alternative drug treatment for symptoms such as fullness in the chest and flanks, weakness during defecation, and fatigue and discomfort after defecation.

(2)本发明前期完成的省级中医药管理局难治疾病临床研究项目“一种中药药膳治疗慢传输型便秘的临床研究”,研究病例185人,临床治愈率67.75%,显效率91.68%,有效率100%。(2) The clinical research project for refractory diseases of the Provincial Administration of Traditional Chinese Medicine completed in the early stage of this invention, "Clinical Research on a Traditional Chinese Medicinal Diet for the Treatment of Slow Transit Constipation", studied 185 cases, the clinical cure rate was 67.75%, and the effective rate was 91.68% , 100% effective.

(3)本发明改善便秘的中药药膳主要针对于慢性便秘人群,充分发扬了中医药食疗、食养健康的服务特色,提高了习惯性便秘人群生活质量,同时也为社会减少了医疗开销,促进了中药保健食品的不断发展。(3) The traditional Chinese medicinal diet for improving constipation of the present invention is mainly aimed at people with chronic constipation, fully develops the service characteristics of traditional Chinese medicine diet therapy and food maintenance, improves the quality of life of people with habitual constipation, and at the same time reduces medical expenses for the society and promotes The continuous development of traditional Chinese medicine health food.

具体实施方式Detailed ways

为了使本发明的目的、技术方案及优点更加清楚明白,以下结合实施例,对本发明进行进一步详细说明。本发明的附加方面和优点将在下面的描述中部分给出,部分将从下面的描述中变得明显,或通过本发明的实践了解到。应当理解,以下描述仅仅用以解释本发明,并不用于限定本发明。In order to make the purpose, technical solutions and advantages of the present invention clearer, the present invention will be further described in detail below in conjunction with examples. Additional aspects and advantages of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention. It should be understood that the following description is only used to explain the present invention and is not intended to limit the present invention.

本文中所用的术语“包含”、“包括”、“具有”、“含有”或其任何其它变形,意在覆盖非排它性的包括。例如,包含所列要素的组合物、步骤、方法、制品或装置不必仅限于那些要素,而是可以包括未明确列出的其它要素或此种组合物、步骤、方法、制品或装置所固有的要素。As used herein, the terms "includes," "includes," "has," "contains," or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a composition, step, method, article, or device that includes listed elements need not be limited to those elements, but may include other elements not expressly listed or inherent to such composition, step, method, article, or device. elements.

当量、浓度、或者其它值或参数以范围、优选范围、或一系列上限优选值和下限优选值限定的范围表示时,这应当被理解为具体公开了由任何范围上限或优选值与任何范围下限或优选值的任一配对所形成的所有范围,而不论该范围是否单独公开了。例如,当公开了范围“1至5”时,所描述的范围应被解释为包括范围“1至4”、“1至3”、“1至2”、“1至2和4至5”、“1至3和5”等。当数值范围在本文中被描述时,除非另外说明,否则该范围意图包括其端值和在该范围内的所有整数和分数。When an amount, concentration, or other value or parameter is expressed in terms of a range, a preferred range, or a range defined by a series of upper preferred values and lower preferred values, this should be understood to specifically disclose any upper range limit or preferred value and any lower range limit. or any pairing of preferred values, whether or not that range is individually disclosed. For example, when the range "1 to 5" is disclosed, the described range should be interpreted to include the ranges "1 to 4," "1 to 3," "1 to 2," "1 to 2, and 4 to 5." , "1 to 3 and 5" etc. When a numerical range is described herein, unless otherwise stated, the range is intended to include the endpoints thereof and all integers and fractions within the range.

本发明要素或组分前的不定冠词“一种”和“一个”对要素或组分的数量要求(即出现次数)无限制性。因此“一个”或“一种”应被解读为包括一个或至少一个,并且单数形式的要素或组分也包括复数形式,除非所述数量明显只指单数形式。The indefinite articles "a" and "an" before the elements or components of the present invention do not limit the quantity requirements (ie, the number of occurrences) of the elements or components. Therefore "a" or "an" should be read to include one or at least one, and the singular form of an element or component also includes the plural form, unless it is obvious that the stated number refers to the singular form only.

此外,下面所描述的术语“一个实施例”、“一些实施例”、“示例”、“具体示例”、或“一些示例”等的描述意指结合该实施例或示例描述的具体特征、结构、材料或者特点包含于本发明的至少一个实施例或示例中。在本说明书中,对上述术语的示意性表述不是必须针对相同的实施例或示例。而且,本发明各个实施方式中所涉及到的技术特征只要彼此之间未构成冲突就可以相互组合。In addition, the following description of the terms "one embodiment", "some embodiments", "example", "specific examples", or "some examples" means specific features, structures described in connection with the embodiment or examples. , materials or features are included in at least one embodiment or example of the invention. In this specification, the schematic expressions of the above terms are not necessarily directed to the same embodiment or example. Moreover, the technical features involved in the various embodiments of the present invention can be combined with each other as long as they do not conflict with each other.

实施例1Example 1

便秘药膳对慢传输型便秘动物的药效作用研究Study on the efficacy of constipation medicinal diet on animals with slow transit constipation

试剂:血清NO及eNOS检测试剂盒购自南京建成生物工程研究所;印度墨水(北京诺博莱德科技有限公司,批号:20160217);水合氯醛(天津市科密欧化学试剂有限公司,批号:20140629);钙检测试剂盒(罗氏诊断产品上海有限公司,批号:20161201);苏木素、伊红(Bioswamp有限公司);药膳由实验室自制。Reagents: Serum NO and eNOS detection kits were purchased from Nanjing Jiancheng Bioengineering Institute; India ink (Beijing Nobleled Technology Co., Ltd., batch number: 20160217); chloral hydrate (Tianjin Comio Chemical Reagent Co., Ltd., batch number : 20140629); calcium detection kit (Roche Diagnostic Products Shanghai Co., Ltd., batch number: 20161201); hematoxylin and eosin (Bioswamp Co., Ltd.); medicated diet was made by the laboratory.

实验动物:SPF级健康昆明大鼠,体重(200±20)g,雌性40只,雄性40只,均饲养在条件可控(室温维持在22±2℃、湿度维持在50%-70%)的动物房。Experimental animals: SPF grade healthy Kunming rats, weighing (200±20) g, 40 females and 40 males, all kept under controllable conditions (room temperature maintained at 22±2°C, humidity maintained at 50%-70%) animal room.

STC模型制备:根据文献方法,采用大黄致泻结肠法造模,除正常组外,其余大鼠按150mg/(kg·d)给予大黄灌胃,随后灌胃剂量以150mg/(kg·d)递增,直到50%大鼠出现腹泻,维持该剂量直到80%的大鼠稀便消失,然后再以150mg/(kg·d)递增,直到50%大鼠出现腹泻并维持剂量再次至80%大鼠便秘,然后再加量,如此循环3次。直到第3次出现80%的大鼠稀便消失,维持该剂量继续灌胃1周,发现大鼠毛发枯燥,易激怒,粪便量明显减少,质地偏硬,粪便含水量明显降低,表明慢传输性便秘模型复制成功。Preparation of STC model: According to the method in the literature, the rhubarb-induced diarrhea colon model was used to model the colon. Except for the normal group, the other rats were given rhubarb at a dose of 150 mg/(kg·d) by gavage, and then the gavage dose was 150 mg/(kg·d). Incrementally increase until 50% of the rats have diarrhea, maintain this dose until 80% of the rats have loose stools disappear, and then increase by 150 mg/(kg·d) until 50% of the rats have diarrhea and maintain the dose again to 80% of the rats. If the rat is constipated, then increase the dose, and repeat this cycle 3 times. Until the third time when 80% of the rats' loose stools disappeared, the dose was maintained and continued for 1 week. It was found that the rats' hair was dry and irritable, the amount of feces was significantly reduced, the texture was hard, and the water content of the feces was significantly reduced, indicating slow transmission. The sexual constipation model was successfully replicated.

造模成功标准:大鼠精神状态较差,性情急躁易怒,外形瘦小,被毛发黄疏松、欠光泽,甚者竖毛,皮肤松软,部分拱背、脱肛,活动减少,食纳减少,造模前期大便溏稀,次频,后期大便逐渐成形、变硬,次数减少,颗粒变小。大鼠消化道解剖显示,大便主要聚集在结肠,呈串珠状,空肠和回肠无明显粪便残留,检测大鼠肠道推进率和血清D-木糖含量较正常小鼠均明显降低,标志着造模成功。Success criteria for modeling: Rats have poor mental state, irritable and irritable temperament, thin appearance, yellow and loose hair, lack of luster, and even piloerection, soft skin, partial arched back, prolapse of the anus, reduced activity, reduced food intake, and constipation. In the early stage of the mold, the stool is loose and frequent. In the later stage, the stool gradually takes shape and becomes hard, the frequency decreases, and the particles become smaller. The anatomy of the digestive tract of rats showed that feces mainly gathered in the colon and were in the shape of beads. There were no obvious fecal residues in the jejunum and ileum. The intestinal propulsion rate and serum D-xylose content of rats were significantly lower than those of normal mice, indicating that The model was successful.

实施例2Example 2

按以下工艺流程制备本发明实验用改善便秘的中药药膳及现有技术中改善便秘的中药药膳(简称原药膳):The traditional Chinese medicinal diet for improving constipation in experiments of the present invention and the traditional Chinese medicinal diet for improving constipation in the prior art are prepared according to the following process flow:

1.原辅料验收:产品质量合格,提供有效验证资料,纳入生产许可证的原辅料须提供产品生产许可证;其中,本发明药膳配方的有效组分配比为:将杏仁6g、佛手6g、山药15g、山楂6g、鸡内金6g、桔梗6g、麦芽6g、郁李仁2g、紫苏籽2g、火麻仁2g经过超微粉碎,达到200-400目的细度,与圆苞车前子壳粉3g、秋葵粉3g混合均匀;原药膳配方的有效组成分配比为:将黄精10g、佛手6g、山药15g、山楂6g、鸡内金6g、桔梗6g、麦芽6g、奇亚籽1g经过超微粉碎,达到200-400目的细度,与圆苞车前子壳粉1g、秋葵粉1g、香菇粉1g、银耳粉1g、芹菜粉1g、低聚果糖1g混合均匀。1. Acceptance of raw and auxiliary materials: the product quality is qualified and valid verification data is provided. The raw and auxiliary materials included in the production license must provide a product production license; among them, the effective component ratio of the medicated dietary formula of the present invention is: 6g almond, 6g bergamot, yam 15g, hawthorn 6g, Gallus gallus gallus L. 6g, platycodon 6g, malt 6g, plum blossom kernel 2g, perilla seed 2g, hemp seed 2g are ultrafinely crushed to a fineness of 200-400 mesh, and 3g of plantain husk powder , 3g okra powder and mix evenly; the effective composition distribution ratio of the original medicinal formula is: 10g polygonatum, 6g bergamot, 15g yam, 6g hawthorn, 6g gallinaceus, 6g platycodon, 6g malt, 1g chia seeds through ultra-fine grinding , to a fineness of 200-400 mesh, mix evenly with 1g of plantain husk powder, 1g of okra powder, 1g of shiitake mushroom powder, 1g of tremella powder, 1g of celery powder, and 1g of fructooligosaccharide.

2.配粉和面:在药膳中,依次加入水、棕榈油、白砂糖等配料,搅拌10分钟左右,后加入面粉610g,搅拌3-5分钟调制至无干粉,面团不起筋即可。水温要求28℃左右,补水或水量稍多于配料比、温度高于控制要求、搅拌时间稍长等都能破坏酥性的结构。2. Mix flour and dough: In the medicinal diet, add water, palm oil, white sugar and other ingredients in sequence, stir for about 10 minutes, then add 610g of flour, stir for 3-5 minutes until there is no dry powder and the dough has no gluten. The water temperature is required to be around 28°C. Replenishing water or the amount of water is slightly more than the ingredient ratio, the temperature is higher than the control requirement, and the mixing time is slightly longer, etc., which can destroy the crispy structure.

3.成型:将面团放入料斗,经各种型号的成型机模具制成各种形状的饼干坯。3. Forming: Put the dough into the hopper and use various types of molding machines to make biscuit blanks of various shapes.

4.烘烤:烘烤炉的温度和饼干坯烘烤的时间,炉温一区设定为上火:170℃左右,下火160℃左右,二区设定为上火:230℃左右,下火210℃左右,三区设定为上火:260℃左右,下火240℃左右,四区设定为上火:250℃左右,下火230℃左右,五区设定为上火:240℃左右,下火220℃左右,六区设定为上火:220℃左右,下火210℃左右,履带带速600~900,成品含水率为≤4%。4. Baking: The temperature of the baking oven and the baking time of the biscuit dough. The first zone of the oven temperature is set to upper heat: about 170°C, and the lower heat is about 160°C. The second zone is set to upper heat: about 230°C. The lower fire is about 210℃, the third zone is set to upper fire: about 260℃, the lower fire is about 240℃, the fourth zone is set to upper fire: about 250℃, the lower fire is about 230℃, the fifth zone is set to upper fire: The temperature is about 240℃, the lower fire is about 220℃, the six zones are set to the upper fire: about 220℃, the lower fire is about 210℃, the crawler speed is 600~900, and the moisture content of the finished product is ≤4%.

5.喷油:本发明药膳采用棕榈油预先加热,并控制在35℃左右,喷油量由喷油机上下阀门控制,称量喷前喷后各10片饼干,重量增加15%左右,喷油量达标要求。原药膳采用棕榈油、紫苏籽油、火麻仁油混合物预先加热,并控制在35℃左右,喷油量由喷油机上下阀门控制,称量喷前喷后各10片饼干,重量增加15%左右,喷油量达标要求。5. Oil injection: The medicated diet of the present invention is preheated with palm oil and controlled at about 35°C. The amount of oil injection is controlled by the upper and lower valves of the oil injection machine. Weigh 10 biscuits before and after spraying, and the weight will increase by about 15%. The oil quantity meets the standard requirements. The original medicinal diet uses a mixture of palm oil, perilla seed oil, and hemp seed oil to be preheated and controlled at about 35°C. The amount of oil injection is controlled by the upper and lower valves of the oil injection machine. Weigh 10 biscuits before and after spraying, and the weight increases. About 15%, the fuel injection volume meets the standard requirements.

6.冷却整理:烘烤后饼干经冷却至室温,经输送带运输冷却后转入内包装间。6. Cooling and finishing: After baking, the biscuits are cooled to room temperature, transported by the conveyor belt, cooled, and then transferred to the inner packaging room.

7.包装。7. Packaging.

实施例3Example 3

分组给药:将大鼠雌雄分开,适应性喂养7天,按随机数字表法分为正常组(10只)和造模组(60只),随后将造模成功的60只大鼠随机分为模型组(STC,10只),莫沙必利组(2.5mg/kg/d,10只),原药膳低剂量组(饼干:10g/kg/d,10只),原药膳高剂量组(饼干:30g/kg/d,10只),本发明药膳低剂量组(饼干:10g/kg/d,10只),本发明药膳高剂量组(饼干:30g/kg/d,10只)。STC组大鼠每天给予等体积生理盐水灌胃,连续给药14d,每天2次。Group administration: Male and female rats were separated and adaptively fed for 7 days. They were divided into a normal group (10 rats) and a modeling group (60 rats) according to a random number table. Then, the 60 rats that were successfully modeled were randomly divided into They are the model group (STC, 10 animals), the mosapride group (2.5 mg/kg/d, 10 animals), the original medicated diet low-dose group (biscuits: 10g/kg/d, 10 animals), and the original medicated diet high-dose group. (biscuits: 30g/kg/d, 10 pieces), the medicated diet low-dose group of the present invention (biscuits: 10g/kg/d, 10 pieces), the medicated diet high-dose group of the invention (biscuits: 30g/kg/d, 10 pieces) . Rats in the STC group were given an equal volume of normal saline by gavage every day for 14 days, twice a day.

观察评价指标Observe evaluation indicators

一般行为学:造模至取材期间,每天观察各组大鼠的精神状态、反应性、皮毛、进食情况,大便质、量的改变。General Behavior: During the period from modeling to material collection, the mental state, reactivity, fur, eating conditions, and changes in stool quality and quantity of rats in each group were observed every day.

24h粪便总量与粪便含水量:收集造模后和给药后各组大鼠24h粪便总量,记录颗粒数,称湿质(A),将粪便放入干燥箱中干燥3h,称干质(B),计算粪便含水量=(A-B)/A×100%。24h total feces volume and fecal moisture content: Collect the total 24h feces volume of rats in each group after modeling and administration, record the number of particles, and call it wet mass (A). Put the feces into a drying box to dry for 3 hours, and call it dry mass. (B), calculate fecal water content = (A-B)/A×100%.

排便情况:大鼠禁食不禁水24h,将印度墨水经口灌入大鼠胃中(2ml/只),灌胃结束后立即开始计时,持续观察大鼠6h,记录每只大鼠从灌胃到首粒粪便排出的时间,并记录6h内大鼠排便的粒数和质量。Defecation situation: The rats were fasted and water-free for 24 hours. India ink was orally poured into the stomachs of the rats (2ml/rat). The timing started immediately after the end of the gastric administration. The rats were continuously observed for 6 hours, and each rat was recorded from the time of gastric administration. The time until the first feces is excreted, and the number and quality of the rat's feces within 6 hours are recorded.

小肠推进检测:实验结束时,大鼠禁食12h,然后对大鼠灌胃10%活性炭混悬液,每只灌胃2mL。30min后,麻醉处死大鼠并暴露腹腔,将幽门至回盲部的小肠管取出并轻柔拉直,测量碳末推进长度(cm)和小肠管的总长度(cm)。炭末推进率(%)=炭末推进长度/小肠管总长度×100%。Small intestinal propulsion test: At the end of the experiment, the rats were fasted for 12 hours, and then 10% activated carbon suspension was administered to the rats, 2 mL of which was administered to each rat. After 30 minutes, the rats were anesthetized and the abdominal cavity was exposed. The small intestinal tube from the pylorus to the ileocecal part was taken out and gently straightened. The length of carbon powder advancement (cm) and the total length of the small intestinal tube (cm) were measured. Carbon powder advancement rate (%) = Carbon powder advancement length/total length of small intestine × 100%.

ELISA测定:ELISA法检测大鼠结肠NO、cGMP、PKG的表达,取各组大鼠距肛门11cm处结肠1.5cm,用生理盐水冲洗干净后用匀浆器将标本匀浆充分,2500r/min离心20min,收集上清。采用ELISA法测定小鼠结肠组织中NO、cGMP、PKG水平,具体方法按试剂盒说明进行。ELISA measurement: ELISA method was used to detect the expression of NO, cGMP, and PKG in the colon of rats. Take 1.5cm of the colon from the rats in each group 11cm away from the anus, rinse it with physiological saline, homogenize the specimen fully with a homogenizer, and centrifuge at 2500r/min. 20min, collect the supernatant. The ELISA method was used to measure the levels of NO, cGMP, and PKG in mouse colon tissue. The specific method was carried out according to the instructions of the kit.

ELISA法检测血清中P物质(SP)、血管活性肠肽(VIP)、生长抑素(SS)含量,取各组大鼠血清,解冻后稀释成适宜浓度,每孔加样50μL,按照ELISA试剂盒法测定。ELISA method was used to detect the contents of substance P (SP), vasoactive intestinal peptide (VIP), and somatostatin (SS) in serum. Take the serum of rats from each group, thaw it and dilute it to an appropriate concentration. Add 50 μL to each well, and follow the ELISA reagents. Box method determination.

实施例4Example 4

采用SPSS18.0统计软件进行处理分析,计量资料以(x±s)表示,首先检验方差齐性,各组间比较采用单因素方差分析,两组间比较采用LSD法,P<0.05为差异有统计学意义。SPSS18.0 statistical software was used for processing and analysis. The measurement data were expressed as (x±s). First, the homogeneity of variances was tested. One-way analysis of variance was used for comparison between each group. LSD method was used for comparison between two groups. P<0.05 was considered a difference. Statistical significance.

各组STC大鼠24h粪便总量、粪便含水量比较:造模后,模型组大鼠24h粪便总量、粪便含水量均明显低于正常组,差异有统计学意义(P<0.05);给药后,本发明药膳高低剂量组、原药膳高低剂量组、莫沙必利组大鼠情况均有所好转;药膳高、低剂量组和莫沙必利组大鼠粪便质地变软,24h粪便总量、粪便含水量均高于模型组,差异有统计学意义(P<0.05),提示药膳能增加STC大鼠的粪便总量与含水量,改善便秘症状。同时,本发明药膳高剂量组大鼠24h粪便总量高于原药膳高剂量组,本发明药膳低剂量组大鼠24h粪便总量高于原药膳低剂量组,因此本发明药膳较原药膳更能增加STC大鼠的粪便总量。Comparison of the total 24-hour feces volume and fecal water content of STC rats in each group: After modeling, the 24-hour total feces volume and fecal water content of rats in the model group were significantly lower than those of the normal group, and the difference was statistically significant (P<0.05); After taking the medicine, the conditions of the rats in the high and low dose groups of the medicated diet of the present invention, the high and low dose groups of the original medicated diet, and the mosapride group all improved; the texture of the feces of the rats in the high and low dose groups of the medicated diet and the mosapride group became softer, and their feces after 24 hours became softer. The total volume and fecal water content were higher than those of the model group, and the difference was statistically significant (P<0.05), suggesting that medicated diet can increase the total volume and water content of feces in STC rats and improve constipation symptoms. At the same time, the total 24-hour feces of rats in the high-dose medicated diet group of the present invention is higher than that of the original medicated diet high-dose group, and the total 24-hour feces of rats in the low-dose medicated diet group of the present invention is higher than that of the original medicated diet low-dose group. Therefore, the medicated diet of the present invention is more efficient than the original medicated diet. Can increase the total amount of feces in STC rats.

表1各组STC大鼠24h粪便总量比较Table 1 Comparison of the total feces volume of STC rats in each group in 24 hours

注:模型组与正常组比较,▲P<0.05;给药组与模型组比较,*P<0.05Note: Comparing the model group with the normal group, ▲P<0.05; Comparing the drug administration group with the model group, *P<0.05

表2各组STC大鼠粪便含水量比较Table 2 Comparison of fecal water content of STC rats in each group

注:模型组与正常组比较,▲P<0.05;给药组与模型组比较,*P<0.05Note: Comparing the model group with the normal group, ▲P<0.05; Comparing the drug administration group with the model group, *P<0.05

药膳对STC大鼠肠道推进功能的影响:结果显示,模型组大鼠首次排黑便时间明显长于正常组,炭末推进率明显低于正常组(P<0.05),说明STC模型造成大鼠肠道推进功能减弱;药膳高、低剂量组、莫沙必利组首次排黑便时间明显短于模型组,各给药组大鼠炭末推进率均明显高于模型组,差异有统计学意义(P<0.05),提示该药膳能增强STC大鼠肠道传输功能。同时,本发明药膳高剂量组大鼠首次排黑便时间、炭末推进率均优于原药膳高剂量组,本发明药膳低剂量组大鼠首次排黑便时间、炭末推进率均优于原药膳低剂量组,因此提示本发明药膳更能增强STC大鼠肠道传输功能。Effect of medicated diet on intestinal propulsion function of STC rats: The results showed that the first urinary defecation time of rats in the model group was significantly longer than that of the normal group, and the charcoal propulsion rate was significantly lower than that of the normal group (P<0.05), indicating that the STC model caused rats The intestinal propulsion function is weakened; the time to first defecation of black stool in the high- and low-dose medicated diet groups and the mosapride group is significantly shorter than that in the model group. The charcoal propulsion rate of rats in each administration group is significantly higher than that in the model group, and the difference is statistically significant. Significance (P<0.05), suggesting that the medicated diet can enhance the intestinal transmission function of STC rats. At the same time, the time for the first black stool and the charcoal propelling rate of the rats in the high-dose medicated diet group of the present invention were better than those of the original medicated high-dose group. The time and the charcoal propelling rate of the rats in the low-dose medicated diet group of the present invention were both better than The original medicated diet low-dose group, therefore, it is suggested that the medicated diet of the present invention can better enhance the intestinal transmission function of STC rats.

表3各组STC大鼠肠道传输功能比较Table 3 Comparison of intestinal transmission function of STC rats in each group

注:模型组与正常组比较,▲P<0.05;给药组与模型组比较,*P<0.05Note: Comparing the model group with the normal group, ▲P<0.05; Comparing the drug administration group with the model group, *P<0.05

药膳对STC大鼠结肠组织NO、cGMP、PKG表达的影响:有研究认为慢传输型便秘与肠神经系统失调有关,肠神经系统通过释放神经递质直接控制肠道平滑肌的运动,其中抑制性神经递质一氧化氮(NO)起重要作用。NO合成增加能导致慢传输型便秘的发生,主要原因是NO可与鸟苷酸环化酶(GC)相结合,使得cGMP生成增加,而cGMP作为第二信使,是该信号通路的中心环节,可以作用于下游蛋白,其中PKG参与生物信号传递,细胞增殖凋亡、抑制肠道蠕动等多种生物效应。Effects of medicinal diet on the expression of NO, cGMP and PKG in the colon tissue of STC rats: Some studies believe that slow transit constipation is related to the disorder of the enteric nervous system. The enteric nervous system directly controls the movement of intestinal smooth muscles by releasing neurotransmitters, among which inhibitory nerves The transmitter nitric oxide (NO) plays an important role. Increased NO synthesis can lead to the occurrence of slow transit constipation. The main reason is that NO can combine with guanylyl cyclase (GC) to increase the production of cGMP. As a second messenger, cGMP is the central link of this signaling pathway. It can act on downstream proteins, among which PKG is involved in biological signal transmission, cell proliferation and apoptosis, inhibition of intestinal peristalsis and other biological effects.

本发明研究结果显示,模型组大鼠结肠NO、cGMP、PKG的表达明显高于正常组,差异有统计学意义(P<0.05);给药2周后,药膳高、低剂量组和莫沙必利组大鼠结肠NO、cGMP、PKG的表达均低于模型组,差异有统计学意义(P<0.05)。同时本发明药膳高剂量组大鼠结肠NO、cGMP、PKG的表达均低于原药膳高剂量组,本发明药膳低剂量组大鼠结肠NO、cGMP、PKG的表达均低于原药膳低剂量组。The research results of the present invention show that the expressions of NO, cGMP and PKG in the colon of rats in the model group are significantly higher than those in the normal group, and the difference is statistically significant (P<0.05); after 2 weeks of administration, the expression of NO, cGMP and PKG in the colon of rats in the model group was significantly higher than that of the moxa group. The expressions of NO, cGMP and PKG in the colon of rats in the Bili group were lower than those in the model group, and the differences were statistically significant (P<0.05). At the same time, the expressions of NO, cGMP and PKG in the colon of rats in the high-dose medicated diet group of the present invention are all lower than those in the original medicated diet high-dose group. The expressions of NO, cGMP and PKG in the colon of rats in the low-dose medicated diet group of the present invention are all lower than those in the original medicated diet low-dose group. .

表4各组STC大鼠结肠组织生化因子表达比较Table 4 Comparison of the expression of biochemical factors in colon tissue of STC rats in each group

注:模型组与正常组比较,▲P<0.05;给药组与模型组比较,*P<0.05Note: Comparing the model group with the normal group, ▲P<0.05; Comparing the drug administration group with the model group, *P<0.05

药膳对STC大鼠血清中SP、VIP、SS表达的影响:SP是主要的胃肠激素,能够直接加快结肠的收缩运动和刺激消化道平滑肌的收缩;VIP能够抑制肠道松弛、抑制结肠和直肠的紧张性,直接影响便秘的产生;SS作为肠神经系统的抑制性神经递质,可以调节肠肽类激素的分泌释放及抑制胃肠蠕动。与空白组相比,模型组大鼠血清中SP含量明显降低,VIP、SS含量明显升高;给药治疗2周后,与模型组相比,莫沙必利组、药膳膏高、中剂量组SP含量明显升高,VIP、SS含量显著降低。同时本发明药膳高剂量组相对原药膳高剂量组大鼠SP含量稍有升高,VIP、SS含量稍著降低。本发明药膳低剂量组相对原药膳高剂量组大鼠SP含量稍有升高,VIP、SS含量稍著降低。Effect of medicated diet on the expression of SP, VIP, and SS in the serum of STC rats: SP is the main gastrointestinal hormone, which can directly accelerate the contraction movement of the colon and stimulate the contraction of the smooth muscle of the digestive tract; VIP can inhibit intestinal relaxation, inhibit colon and rectum The tension directly affects the occurrence of constipation; SS, as an inhibitory neurotransmitter in the enteric nervous system, can regulate the secretion and release of intestinal peptide hormones and inhibit gastrointestinal motility. Compared with the blank group, the SP content in the serum of rats in the model group was significantly reduced, and the VIP and SS contents were significantly increased; after 2 weeks of treatment, compared with the model group, the mosapride group, high- and medium-dose medicated ointment The SP content in the group was significantly increased, and the VIP and SS contents were significantly reduced. At the same time, compared with the high-dose medicated diet group of the present invention, the SP content of rats in the high-dose medicated diet group was slightly increased, and the VIP and SS contents were slightly reduced. Compared with the high-dose group of the original medicated diet, the SP content of rats in the low-dose medicated diet group of the present invention was slightly increased, and the VIP and SS contents were slightly reduced.

表5各组STC大鼠血清中SP、VIP、SS表达的比较Table 5 Comparison of SP, VIP and SS expression in serum of STC rats in each group

组别Group SP(pg/mL)SP(pg/mL) VIP(pg/mL)VIP(pg/mL) SS(pg/mL)SS(pg/mL) 正常组normal group 16.01±2.2116.01±2.21 93.51±11.9693.51±11.96 52.93±8.1252.93±8.12 模型组model group 6.12±1.10▲6.12±1.10▲ 185.29±20.15▲185.29±20.15▲ 137.65±15.61▲137.65±15.61▲ 原药膳高剂量组Original medicinal diet high dose group 11.33±1.25*11.33±1.25* 126.7±16.84*126.7±16.84* 72.24±9.43*72.24±9.43* 原药膳低剂量组Original medicated diet low-dose group 8.56±1.03*8.56±1.03* 153.2±18.53*153.2±18.53* 112.52±11.37*112.52±11.37* 本发明药膳高剂量组Medicinal diet high-dose group of the present invention 14.31±1.35*14.31±1.35* 105.31±15.14*105.31±15.14* 65.21±9.81*65.21±9.81* 本发明药膳低剂量组Medicinal diet low-dose group of the present invention 10.12±1.05*10.12±1.05* 119.32±15.62*119.32±15.62* 78.51±12.47*78.51±12.47* 莫沙必利组Mosapride group 11.62±1.73*11.62±1.73* 136.3±15.85*136.3±15.85* 118.32±14.32*118.32±14.32*

通过药效实验研究发现,给予药膳治疗2周后,STC大鼠便秘现象有明显改善,肠蠕动功能增强,两款药膳均能明显提高血液中SP含量,降低VIP、SS含量,降低大鼠结肠组织NO、cGMP、PKG表达,进而调节大鼠胃肠道功能,促进肠道蠕动,改善便秘;本发明药膳组优于原药膳组。Through drug efficacy experiments, it was found that after 2 weeks of medicated diet treatment, the constipation of STC rats was significantly improved, and the intestinal peristalsis function was enhanced. Both medicated diets could significantly increase the SP content in the blood, reduce the VIP and SS content, and reduce the intestinal motility of the rats. tissue NO, cGMP, and PKG expression, thereby regulating the gastrointestinal function of rats, promoting intestinal peristalsis, and improving constipation; the medicated diet group of the present invention is better than the original medicated diet group.

本领域的技术人员容易理解,以上所述仅为本发明的实施例而已,并不用以限制本发明,凡在本发明的精神和原则之内所作的任何修改、等同替换和改进等,均应包含在本发明的保护范围之内。It is easy for those skilled in the art to understand that the above are only examples of the present invention and are not intended to limit the present invention. Any modifications, equivalent substitutions and improvements made within the spirit and principles of the present invention shall be included within the protection scope of the present invention.

Claims (10)

1.一种改善便秘的中药药膳,其特征在于,所述改善便秘的中药药膳中药物包含杏仁、佛手、桔梗、麦芽、山药、山楂、鸡内金、郁李仁、紫苏籽、火麻仁、圆苞车前子壳和秋葵粉作为有效成分。1. A kind of traditional Chinese medicinal diet for improving constipation, characterized in that the medicines in the traditional Chinese medicinal diet for improving constipation include almonds, bergamot, platycodon, malt, yam, hawthorn, Gallus gallus gallus gallinae, Yu Liren, perilla seeds, hemp seeds, Psyllium husk and okra powder are used as active ingredients. 2.根据权利要求1所述的改善便秘的中药药膳,其特征在于,所述改善便秘的中药药膳中药物按重量份数计包含杏仁6-18份、佛手6-18份、山药15-45份、山楂6-18份、鸡内金6-18份、桔梗6-18份、麦芽6-18份、郁李仁2-18份、紫苏籽2-18份、火麻仁2-18份、圆苞车前子壳粉1-45份、秋葵粉1-18份。2. The traditional Chinese medicinal diet for improving constipation according to claim 1, characterized in that the medicines in the traditional Chinese medicinal diet for improving constipation include 6-18 parts by weight of almonds, 6-18 parts of bergamot, and 15-45 parts of yam. 6-18 parts of hawthorn, 6-18 parts of Gallus gallus gallus L., 6-18 parts of Platycodon grandiflorum, 6-18 parts of malt, 2-18 parts of Yuliren, 2-18 parts of perilla seeds, 2-18 parts of hemp seeds, 1-45 parts of plantain husk powder and 1-18 parts of okra powder. 3.根据权利要求1所述的改善便秘的中药药膳,其特征在于,所述改善便秘的中药药膳中药物按重量份数计包含杏仁6-10份、佛手6-10份、山药15-25份、山楂6-10份、鸡内金6-10份、桔梗6-10份、麦芽6-10份、郁李仁2-6份、紫苏籽2-6份、火麻仁2-6份、圆苞车前子壳粉1-6份、秋葵粉1-6份。3. The traditional Chinese medicinal diet for improving constipation according to claim 1, characterized in that the medicines in the traditional Chinese medicinal diet for improving constipation include 6-10 parts by weight of almonds, 6-10 parts of bergamot, and 15-25 parts of yam. 6-10 parts of hawthorn, 6-10 parts of Gallus gallus gallus L., 6-10 parts of platycodon, 6-10 parts of malt, 2-6 parts of Yuliren, 2-6 parts of perilla seeds, 2-6 parts of hemp seeds, 1-6 parts of psyllium husk powder and 1-6 parts of okra powder. 4.根据权利要求1所述的改善便秘的中药药膳,其特征在于,所述改善便秘的中药药膳是饼干。4. The Chinese medicinal diet for improving constipation according to claim 1, characterized in that the Chinese medicinal diet for improving constipation is biscuits. 5.根据权利要求1所述的改善便秘的中药药膳,其特征在于,所述改善便秘的中药药膳中有效成分含量为8-30%。5. The traditional Chinese medicinal diet for improving constipation according to claim 1, characterized in that the content of active ingredients in the traditional Chinese medicinal diet for improving constipation is 8-30%. 6.根据权利要求1所述的改善便秘的中药药膳,其特征在于,所述改善便秘的中药药膳中按重量份数计包含杏仁6-18份、佛手6-18份、山药15-45份、山楂6-18份、鸡内金6-18份、桔梗6-18份、麦芽6-18份、郁李仁2-18份、紫苏籽2-18份、火麻仁2-18份、圆苞车前子壳粉1-45份、秋葵粉1-18份、面粉550-660份。6. The traditional Chinese medicinal diet for improving constipation according to claim 1, characterized in that the traditional Chinese medicinal diet for improving constipation contains 6-18 parts by weight of almonds, 6-18 parts of bergamot, and 15-45 parts of yam. , 6-18 parts of hawthorn, 6-18 parts of Gallus gallus gallus L., 6-18 parts of platycodon, 6-18 parts of malt, 2-18 parts of Yuliren, 2-18 parts of perilla seeds, 2-18 parts of hemp seeds, round 1-45 parts of psyllium husk powder, 1-18 parts of okra powder, 550-660 parts of flour. 7.权利要求1-6任一项所述改善便秘的中药药膳的制备方法,其特征在于,所述方法包含以下步骤:7. The preparation method of the traditional Chinese medicinal diet for improving constipation according to any one of claims 1-6, characterized in that the method comprises the following steps: (1)准备药粉:将杏仁、佛手、山药、山楂、鸡内金、桔梗、麦芽、郁李仁、紫苏籽、火麻仁经过超微粉碎,再与圆苞车前子壳粉、秋葵粉混合均匀;(1) Prepare medicinal powder: ultrafinely crush almonds, bergamot, yam, hawthorn, Gallus gallus gallus L., Platycodon grandiflorum, malt, plum kernels, perilla seeds, and hemp seeds, and then mix with plantain husk powder and okra powder. well mixed; (2)配粉和面:依次在药粉中加入水、棕榈油、白砂糖,搅拌,加入面粉,搅拌调制至无干粉,面团不起筋;(2) Mix flour and dough: Add water, palm oil, and white sugar to the powder in sequence, stir, add flour, and mix until there is no dry powder and the dough has no gluten; (3)成型:使用模具制成各种形状的饼干坯;(3) Forming: Use molds to make biscuit blanks of various shapes; (4)烘烤:控制好温度进行烘烤;(4) Baking: control the temperature for baking; (5)喷油:均匀喷淋棕榈油;(5) Oil spray: spray palm oil evenly; (6)冷却整理:烘烤后饼干冷却至室温,转入包装间;(6) Cooling and finishing: After baking, the biscuits are cooled to room temperature and transferred to the packaging room; (7)包装。(7) Packaging. 8.根据权利要求7所述改善便秘的中药药膳的制备方法,其特征在于,所述步骤(1)中经过超微粉碎后达到200-400目的细度。8. The preparation method of traditional Chinese medicine for improving constipation according to claim 7, characterized in that, in step (1), the fineness is 200-400 mesh after ultrafine grinding. 9.根据权利要求7所述改善便秘的中药药膳的制备方法,其特征在于,所述步骤(4)中温度控制为上火170-260℃,下火160-240℃。9. The preparation method of traditional Chinese medicine for improving constipation according to claim 7, characterized in that in the step (4), the temperature is controlled to 170-260°C for upper heat and 160-240°C for lower heat. 10.根据权利要求7所述改善便秘的中药药膳的制备方法,其特征在于,所述步骤(5)中喷油的量控制标准为:称量喷前喷后各10片饼干,重量增加10-20%,喷油量即达标要求。10. The preparation method of Chinese herbal medicine for improving constipation according to claim 7, characterized in that the amount control standard of oil spraying in step (5) is: weigh 10 biscuits before and after spraying, and the weight is increased by 10 -20%, the fuel injection amount meets the standard requirements.
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CN105106588A (en) * 2015-07-16 2015-12-02 朱新华 Traditional Chinese medicinal composition for effectively treating constipation
CN113170848A (en) * 2021-05-08 2021-07-27 深圳市老年医学研究所 Precise medicinal dietary therapy product for preventing and treating senile functional constipation and preparation method thereof
CN115804397A (en) * 2022-12-12 2023-03-17 何红艳 Medicated food for improving constipation and preparation method thereof

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102511823A (en) * 2012-01-09 2012-06-27 金景华 Spleen-warming and stomach-benefiting food therapy traditional Chinese medicine composition, spleen-warming and stomach-benefiting food therapy grilled chicken or food therapy meat and manufacture method thereof
CN105106588A (en) * 2015-07-16 2015-12-02 朱新华 Traditional Chinese medicinal composition for effectively treating constipation
CN113170848A (en) * 2021-05-08 2021-07-27 深圳市老年医学研究所 Precise medicinal dietary therapy product for preventing and treating senile functional constipation and preparation method thereof
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