CN116585438A - 经前舒颗粒在制备治疗更年期综合征的产品中的应用 - Google Patents
经前舒颗粒在制备治疗更年期综合征的产品中的应用 Download PDFInfo
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Abstract
本发明属于医药技术领域,尤其涉及一种经前舒颗粒在制备治疗更年期综合征的产品中的应用。本发明提供了经前舒颗粒在制备治疗更年期综合征的产品中的应用,实验表明经前舒颗粒可以增加雌激素水平,有效治疗因雌激素减少而引起的妇女更年期综合症。同时发现,当经前舒颗粒与文冠果油配合使用时,在提高雌激素水平(E2)方面可以发挥协同增效作用。
Description
技术领域
本发明属于医药技术领域,具体为一种经前舒颗粒在制备治疗更年期综合征的产品中的应用。
背景技术
更年期综合征是由雌激素水平下降而引起的一系列症状。更年期妇女,由于卵巢功能减退,垂体功能亢进,分泌过多的促性腺激素,引起植物神经功能紊乱,从而出现一系列程度不同的症状,如月经变化、面色潮红、心悸、失眠、乏力、抑郁、多虑、情绪不稳定,易激动,注意力难于集中等,称为“更年期综合征”。有研究表明,更年期妇女其中约有1/3妇女能顺利度过而无自觉症状,而2/3妇女出现或轻或重或长或短的症状。轻则表现为心烦易怒、情绪波动,往往影响家庭生活和谐;重则合并其他疾病导致卧床不起,丧失生活自理能力,给家人增加无尽的烦恼和生活负担。近年来,由于生活、工作压力的增大,其发病年龄有所提前,且发病率呈逐年升高的趋势,随着社会老龄化的进程,这一问题越来越受到医学界的重视。
中医认为,妇女更年期发病是年龄的增长、操劳、产于、体弱多病等因素,使肾气逐衰,冲任脉虚,天癸将竭,脏腑功能紊乱,阴阳平衡失调所致。肾虚是主要病机,肾为先天之本,肾衰必然影响心、肝、脾使其功能失调,发生多种病理改变。西医则认为,雌激素水平过度降低引起下丘脑-垂体-卵巢轴或肾上腺功能紊乱所致的神经递质、激素、细胞因子等产生失衡是更年期发病的主要原因。因此,神经内分泌免疫与更年期综合征的关系最密切。临床和实验研究表明:更年期综合征组血FSH、LH水平高于正常更年期组,而E2水平较正常更年期组显著下降,说明雌激素的过度减少是更年期综合征的基础。
目前治疗更年期综合征的研究很多,如CN103356962A公开了一种治疗更年期综合症的中药组合物,其中药原料及重量份配比为:牡丹皮5-20份、栀子5-25份、柴胡5-25份、当归10-30份、白术10-40份、白芍10-40份、云苓10-30份、桔梗5-20份、木香5-20份、青皮5-25份、陈皮5-25份、半夏5-20份、莱菔子5-20份、砂仁5-20份、八月炸5-25份、枳实5-20份、巴戟天5-20份、淫羊藿10-40份、郁金5-25份、香附5-20份、薄荷5-20份、丝瓜络5-20份、疾藜5-20份、川芎10-30份、元胡10-30份和甘草5-15份。该发明的中药组合物具有疏肝理气、健脾补肾、养血活血、清心解郁的功效,可用于治疗更年期综合症。CN112618656A公开了一种治疗妇女更年期综合征的中药组合物,所述中药组合物由如下原料药制成:枸杞25-45重量份、人参9-15重量份、黄芪5-8重量份、黄精5-8重量份、肉桂1-4重量份、丁香1-4重量份和甘草1-4重量份。该发明的中药组合物能够治疗妇女更年期综合征,有效改善更年期各种症状。
新药研发的成本高,近年来,老药新用的研究策略已成为药物研发的热点。经前舒颗粒是目前市售的中成药,由当归、炒白芍、柴胡、麸炒白术、牡丹皮、香附、陈皮、郁金、砂仁、人参和甘草组成,具有养肝解郁,理气止痛的功能,可用于经前期综合征属肝气郁结、脾运失调证,可缓解经前情绪低落,郁闷不乐、头疼、心烦、经前乳房胀痛、腹部胀满,食欲不振等症状。目前,尚未发现经前舒颗粒在治疗更年期综合征方面的新用途。
发明内容
本发明的目的在于提供了一种经前舒颗粒在制备治疗更年期综合征的产品中的应用,实验发现经前舒颗粒可以增加雌激素水平,有效治疗因雌激素减少而引起的妇女更年期综合症。
为了实现上述目的,本发明采用以下技术方案:
本发明提供了一种经前舒颗粒在制备治疗更年期综合征的产品中的应用。
本发明中所述经前舒颗粒,包括当归、炒白芍、柴胡、麸炒白术、牡丹皮、香附、陈皮、郁金、砂仁、人参和甘草。
优选地,所述经前舒颗粒为当归、炒白芍、柴胡、麸炒白术、牡丹皮、香附、陈皮、郁金、砂仁、人参和甘草经水提制备而成。
本发明中所述的更年期综合征为围绝经期、更年期和绝经后期中由雌激素减少而引起的雌激素降低而引起的各种更年期症状。
优选地,所述更年期症状包括月经变化、面色潮红、心悸、失眠、乏力、抑郁、多虑、情绪不稳定,易激动和注意力难于集中。
进一步优选地,所述更年期症状还包括骨质疏松和体重增加。
所述产品包括经前舒颗粒。
优选地,所述产品还包括制药学上可接受的载体。
所述产品的剂型为颗粒剂、片剂、粉剂、丸剂、混悬剂或胶囊剂。
本发明还提供了一种治疗更年期综合征的药剂,包括经前舒颗粒。
优选地,所述药剂的剂型为颗粒剂、片剂、粉剂、丸剂、混悬剂或胶囊剂。
本发明还提供了另一种治疗更年期综合征的药剂,包括经前舒颗粒和文冠果油。
所述药剂中的经前舒颗粒和文冠果油可以为独立包装,也可以混合制备成颗粒剂、片剂、粉剂、丸剂、混悬剂或胶囊剂。
本发明还提供了上述治疗更年期综合征的药剂在制备治疗更年期综合征的产品中的应用。
本发明的有益效果为:
实验证明,本发明的经前舒颗粒可以提高雌激素水平,有效治疗因雌激素减少而引起的妇女更年期综合症。
同时发现,当经前舒颗粒与文冠果油配合使用时,在提高雌激素水平(E2)方面可以发挥协同增效作用。
具体实施方式
本发明提供了经前舒颗粒在制备治疗更年期综合征的产品中的应用,本领域技术人员可以借鉴本文内容,适当改进工艺参数实现。特别需要指出的是,所有类似的替换和改动对本领域技术人员来说是显而易见的,它们都被视为包括在本发明。本发明的方法及应用已经通过较佳实施例进行了描述,相关人员明显能在不脱离本发明内容、精神和范围内对本文的方法和应用进行改动或适当变更与组合,来实现和应用本发明技术。
本发明采用的试剂皆为普通市售品,皆可于市场购得。
药效评价
1、实验材料
1.1试验药物
(1)经前舒颗粒;由秦皇岛市山海关药业有限责任公司提供,批准文号:国药准字号Z20053087。临用时以等量蒸馏水分散开,用时摇匀,4℃保存;
(2)阳性对照:参照CN112618656A实施例1制备得到的中药组合物,临用时以等量蒸馏水分散开,用时摇匀,4℃保存。
(3)文冠果油,由文冠果压榨而得,神经酸(C24:1)不低于3.2%。
1.2实验动物
更年期综合征(MS)模型大鼠,雌性,体重220-240g,购自上海英拜生物科技。
1.3试剂
大鼠雌二醇(E2)ELISA酶联免疫试剂盒,购自于上海一研生物科技有限公司。
2、实验方法
2.1实验动物分组和给药
将MS大鼠随机分为:空白组、经前舒颗粒组、复配组、阳性对照组和文冠果油组,每组8只,自大鼠第3天起,灌胃给药,20μL/只,1日3次,给药30天。
给药剂量:经前舒颗粒组、复配组和阳性对照组:1000mg/kg;空白组给予相同剂量的蒸馏水,其中,复配组的灌胃药物为经前舒颗粒和文冠果油的混合物,具体为:6g经前舒颗粒+5ml文冠果油。
文冠果油组,灌胃文冠果油,25μL/只,1日3次,给药30天。
第30天后,MS大鼠眼眶取血,待血液凝固后,离心取血清,-20℃保存。
2.2检测大鼠血清中雌二醇的含量
取MS大鼠血清,采用ELISA试剂盒检测各组大鼠血清中雌二醇(E2)的含量。
3、统计学方法
采用Graphpad PrismV6.0进行统计分析实验结果以“平均值±s”表示;s为标准差,首先检测数据的方差齐性及正态分布情况,然后应用t检验进行分析。P>0.05,显示无统计学差异;P<0.05显示具有统计学差异,P<0.01显示统计学差异显著。
4、实验结果
给药后,经前舒颗粒组、复配组和阳性对照组的血清E2水平明显升高,与空白组相比,经前舒颗粒组、复配组有极显著差异(P<0.01),阳性对照组有显著性差异(P<0.05);复配组的血清E2水平,与经前舒颗粒组相比有显著差异(P<0.05);而文冠果油组的血清E2水平,与空白组相比无显著性差异(P>0.05);结果见表1。
表明:经前舒颗粒较现有技术,其具有更好的提高雌激素水平的效果,同时发现,当经前舒颗粒与文冠果油配合使用时,在提高雌激素水平(E2)方面可以发挥协同增效作用。
表1MS大鼠血清E2水平变化(单位为pg/mL)
注:*表示与空白组相比,有显著性差异即P<0.05;**表示与空白组相比,有极显著性差异即P<0.01;#表示与经前舒颗粒组相比有显著性差异,即P<0.05。
以上是结合具体实施例对本发明进一步的描述,但这些实施例仅仅是范例性的,并不对本发明的范围构成任何限制。本领域技术人员应该理解的是,在不偏离本发明的精神和范围下可以对本发明技术方案的细节和形式进行修改或替换,但这些修改和替换均落入本发明的保护范围内。
Claims (10)
1.经前舒颗粒在制备治疗更年期综合征的产品中的应用。
2.根据权利要求1所述的应用,其特征在于,所述经前舒颗粒,包括当归、炒白芍、柴胡、麸炒白术、牡丹皮、香附、陈皮、郁金、砂仁、人参和甘草。
3.根据权利要求1所述的应用,其特征在于,所述经前舒颗粒为当归、炒白芍、柴胡、麸炒白术、牡丹皮、香附、陈皮、郁金、砂仁、人参和甘草经水提制备而成。
4.根据权利要求1所述的应用,其特征在于,所述的更年期综合征为围绝经期、更年期和绝经后期中由雌激素减少而引起的雌激素降低而引起的更年期症状。
5.根据权利要求4所述的应用,其特征在于,所述更年期症状包括月经变化、面色潮红、心悸、失眠、乏力、抑郁、多虑、情绪不稳定,易激动、注意力难于集中、骨质疏松和体重增加。
6.根据权利要求1所述的应用,其特征在于,所述产品包括经前舒颗粒。
7.根据权利要求1所述的应用,其特征在于,所述产品的剂型为颗粒剂、片剂、粉剂、丸剂、混悬剂或胶囊剂。
8.一种治疗更年期综合征的药剂,其特征在于,包括经前舒颗粒。
9.根据权利要求8所述的药剂,其特征在于,包括文冠果油。
10.权利要求8或9所述的药剂在制备治疗更年期综合征产品中的应用。
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