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Hepatoprotective effect of flavonoid rich fraction of Sesbania grandiflora: Results of In vivo, in vitro, and molecular docking studies 大叶芝麻富含黄酮类成分的肝保护作用:体内、体外和分子对接研究的结果。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.101036
Anitha Kuttiappan , Santenna Chenchula , Murugesan Vanangamudi , Shvetank Bhatt , Radhika Chikatipalli , P Shaila Bhanu , Nagaraju Bandaru
<div><h3>Background</h3><p>Phytochemicals and their derivatives are promising target drugs for various ailments and have served as therapeutic agents for several decades. Using <em>in vivo</em> and <em>in vitro</em> models and molecular docking, this study investigated the pharmacological potential of a flavonoid-rich fraction of the ethanolic extract of <em>Sesbania grandiflora</em> (SG).</p></div><div><h3>Objectives</h3><p>This research aimed to determine whether flavonoid-rich whole-plant extracts of SGs have any cytoprotective or <em>in vivo</em> hepatoprotective effects. Additionally, the study was intended to elucidate the molecular connections between the discovered flavonoid flavonols and PPARα target proteins linked to liver problems, for which an in silico molecular docking investigation was performed.</p></div><div><h3>Materials and methods</h3><p>To separate the flavonoid components, the entire <em>Sesbania grandiflora</em> plant was first extracted using ethanol as a solvent by soxhlet extraction. The resulting ethanolic extract was then fractionated. The cytoprotective and hepatoprotective properties were evaluated via <em>in vitro</em> and <em>in vivo</em> experiments. SGOT, SGPT, triglyceride, bilirubin, and total protein levels were used to evaluate hepatotoxicity in animal models. <em>In vitro</em> studies on Hepatocellular Carcinoma G2 (HepG2) cell lines have examined their cytotoxic effects and antioxidant activity. The most promising flavonoid-flavanol compounds were identified by conducting molecular docking studies against PPARα target protein (PDB ID: <span><span>3VI8</span><svg><path></path></svg></span>) using MOE software.</p></div><div><h3>Results</h3><p><em>In vivo</em>, the serum levels of SGOT, SGPT, total triglyceride and total bilirubin were measured in experimental animals treated with the flavonoid-rich ethanolic extract of SG. Significant reductions in the levels of these hepatic injury markers were observed, indicating the hepatoprotective potential of the extract. Elevated levels of liver biomarkers in the untreated group indicated liver injury or dysfunction. The treated groups showed significant restoration of these biomarkers, suggesting the hepatoprotective potential of <em>SG</em>. The IC<sub>50</sub> value for the total flavonoid content of SG was 190.28 μg/ml, indicating its safety in inhibiting HepG2 cell growth. Flavonoid treatment decreased cell viability but did not affect antioxidant parameters in hepatocytes. In addition, SG restored the damaged hepatocyte architecture. Molecular docking studies revealed the binding affinities of flavonoids for PPARα. These findings suggest that a promising lead candidate for the development of therapeutic medicines against anti-TB drug-induced hepatotoxicity has been identified.</p></div><div><h3>Conclusion</h3><p>Our findings demonstrate the hepatoprotective potential of the flavonoid-rich fraction of <em>Sesbania grandiflora</em> both <em>in vivo</em> and <em>
背景:几十年来,植物化学物质及其衍生物一直是治疗各种疾病的有前途的靶向药物。本研究利用体内和体外模型以及分子对接,研究了大叶芝麻(SG)乙醇提取物中富含黄酮类成分的药理潜力:本研究旨在确定富含黄酮类化合物的 SG 全植物提取物是否具有细胞保护或体内肝脏保护作用。此外,该研究还旨在阐明已发现的类黄酮黄酮醇与与肝脏问题有关的 PPARα 靶蛋白之间的分子联系,并为此进行了硅学分子对接调查:为了分离黄酮类成分,首先使用乙醇作为溶剂,通过索氏提取法提取整株大叶芝麻。然后对得到的乙醇提取物进行分馏。通过体外和体内实验对其细胞保护和肝脏保护特性进行了评估。采用 SGOT、SGPT、甘油三酯、胆红素和总蛋白水平来评估动物模型的肝毒性。对肝细胞癌 G2(HepG2)细胞系进行的体外研究检验了它们的细胞毒性作用和抗氧化活性。通过使用 MOE 软件对 PPARα 靶蛋白(PDB ID:3VI8)进行分子对接研究,确定了最有前景的黄酮-黄烷醇化合物:用富含黄酮的 SG 乙醇提取物对实验动物进行体内血清 SGOT、SGPT、总甘油三酯和总胆红素水平的测定。结果表明,这些肝损伤标志物的水平明显降低,表明萃取物具有保护肝脏的潜力。未处理组的肝脏生物标志物水平升高表明肝脏损伤或功能障碍。治疗组的这些生物标志物水平明显恢复,表明 SG 具有保护肝脏的潜力。SG 总黄酮含量的 IC50 值为 190.28 μg/ml,表明其在抑制 HepG2 细胞生长方面具有安全性。类黄酮处理可降低细胞活力,但不会影响肝细胞的抗氧化参数。此外,SG 还能恢复受损的肝细胞结构。分子对接研究揭示了类黄酮与 PPARα 的结合亲和力。这些研究结果表明,我们已经找到了一种很有希望的候选药物,可用于开发抗结核药物引起的肝毒性的治疗药物:我们的研究结果表明,富含黄酮类成分的大叶芝麻在体内和体外都具有保肝潜力。这项研究对其作用机制提供了宝贵的见解,突出了其在治疗肝脏疾病方面的应用前景。本研究强调了五加科植物总黄酮富集部分的保肝和细胞保护潜力。
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引用次数: 0
Cross-cultural study on the uses of traditional herbal medicine to treat various women's health issues in Northeast India 关于印度东北部地区使用传统草药治疗各种妇女健康问题的跨文化研究。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.101024
Klaret Kropi, K.P. Jastone, Sweety Angelirie Kharumnuid, Hemanta Kumar Das, Moses M. Naga
<div><h3>Background</h3><div>This cross-cultural study conducted in the diverse regions of Assam, Meghalaya, and Manipur sheds light on the common utilization of five specific medicinal plants among indigenous communities residing in these areas.</div></div><div><h3>Objectives</h3><div>The main focus of this study is to document and compare the traditional medicinal plant used and the knowledge and practices related to women's health issues in different cultures; to identify commonalities and differences in the use of medicinal plants across cultures and various medicinal plants used traditionally by the indigenous communities to treat women's health problems according to their indigenous name, scientific name.</div></div><div><h3>Materials and methods</h3><div>The study used a survey method and a pre-structured interview schedule through one-on-one interactive communication and field observation. The authors collected data from three different states, i.e., Assam (Karbi Anglong district & Udalguri district), Meghalaya (East Khasi Hills district), and Manipur (Senapati district) by personally meeting and interacting with traditional herbal medicinal practitioners. For this study, 10 practitioners from each area of study were interviewed. During the data collection process, the vernacular name of the medicinal plant, methods of preparation, mode of application, and probable dosage were compiled and documented involving practitioners belonging to four different communities, i.e, Bodo, Karbi, Khasi, and Poumai Naga of the selected states.</div></div><div><h3>Results</h3><div>A total of 39 plant species were meticulously collected and documented across the Karbi Anglong district and Udalguri district in Assam, East Khasi Hills district in Meghalaya, and Senapati district in Manipur. Turmeric (<em>Curcuma longa</em>), ginger (<em>Zingiber officinale</em>), gooseberry (<em>Emblica officinalis</em>), papaya (<em>Carica papaya</em>), and passion fruit (<em>Passiflora edulis)</em> have emerged as common medicinal resources within these communities. Poaceae, represented by 5 species, emerged as the dominant family among the collected plants, highlighting the diversity and significance of these botanical remedies. <em>Zingiber officinale</em> Roscoe " has the highest usage report of 18 with an RFC (Relative frequency citation) of 0.45.</div></div><div><h3>Conclusion</h3><div>The study's findings reveal a rich repository of traditional herbal knowledge in the northeast regions of India. Notably, the indigenous communities of these regions use plant resources to cure a wide range of ailments. This study emphasizes the necessity of documenting, preserving, and transmitting traditional herbal medicinal knowledge for both cultural and practical reasons. It also provides vital insights into the importance of cross-cultural study in promoting different cultures, the richness of traditional medicinal knowledge by engaging with diverse cultures and demonstrates
背景:这项在阿萨姆邦、梅加拉亚邦和曼尼普尔邦不同地区进行的跨文化研究揭示了居住在这些地区的土著社区对五种特定药用植物的共同利用:这项在阿萨姆邦、梅加拉亚邦和曼尼普尔邦不同地区进行的跨文化研究揭示了居住在这些地区的土著社区对五种特定药用植物的共同利用:本研究的主要重点是记录和比较不同文化中使用的传统药用植物以及与妇女健康问题相关的知识和做法;确定不同文化中使用药用植物的共性和差异,以及土著社区根据其土著名称和学名传统上用于治疗妇女健康问题的各种药用植物:本研究采用了调查法和预设的访谈表,通过一对一的互动交流和实地观察进行。作者在三个不同的邦,即阿萨姆邦(卡比昂隆县和乌达尔古里县)、梅加拉亚邦(东卡西山县)和曼尼普尔邦(塞纳帕蒂县),通过与传统草药从业者的亲自会面和交流收集数据。在这项研究中,每个研究地区都采访了 10 名从业人员。在数据收集过程中,对药用植物的方言名称、制备方法、应用方式和可能的用量进行了汇编和记录,参与人员来自四个不同的社区,即所选邦的博多、卡比、卡西和普迈那加:在阿萨姆邦的卡比安格隆地区和乌达尔古里地区、梅加拉亚邦的东卡西山地区以及曼尼普尔邦的塞纳帕蒂地区,共精心收集并记录了 39 种植物。姜黄(Curcuma longa)、生姜(Zingiber officinale)、鹅掌楸(Emblica officinalis)、木瓜(Carica papaya)和西番莲(Passiflora edulis)已成为这些社区的常见药用资源。在采集的植物中,以 5 个物种为代表的草本植物科(Poaceae)是最主要的科,这突出了这些植物疗法的多样性和重要性。Zingiber officinale Roscoe "的使用率最高,有 18 种,RFC(相对频率引用)为 0.45:研究结果揭示了印度东北部地区丰富的传统草药知识宝库。值得注意的是,这些地区的原住民社区利用植物资源治疗各种疾病。这项研究强调,出于文化和实用的原因,有必要记录、保存和传播传统草药知识。它还就跨文化研究在促进不同文化方面的重要性、通过与不同文化接触而获得的丰富传统医药知识提供了重要见解,并展示了将传统医药纳入现代医疗保健系统的可能性,特别是在治疗这些文化多元地区妇女的健康问题方面。
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引用次数: 0
Management of post-hysterectomy urinary incontinence with composite Ayurveda treatment – A case report 用阿育吠陀复合疗法治疗子宫切除术后尿失禁--病例报告
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.100961
Ranjani Karthik Pandit
This is a case report of a patient who developed urinary incontinence after undergoing abdominal hysterectomy. This was successfully treated with Ayurvedic treatment procedures. A 63-year-old lady was suffering from urinary incontinence, which developed after hysterectomy. It did not subside even after undergoing trans vaginal taping. She was treated with Ayurvedic procedures and medicines for a period of 2 and a half months from 4th of March 2016 to 26th of May 2016. Matrabasti (medicated enema) and Madhutailika basti (enema treatment with honey and oil), along with other palliative medicines – Sukumara ghrita, Chandraprabha vati, Shilajatu, Mahakalyanaka kashaya, Mamsapachaka ghana vati and Mahatiktaka ghrita were given to the patient. Urinary incontinence reduced to dribbling of urine after Matra basti and after the second course of Basti (medicated enema), that is after one and half months, patient stopped using diapers and was relieved from incontinence. This case report summarises the effective management of urinary incontinence by adopting basti (enema) treatment along with other palliative ayurvedic medicine.
本病例报告了一名患者在接受腹部子宫切除术后出现尿失禁的情况。采用阿育吠陀治疗程序成功治疗了该病。一位 63 岁的女士在子宫切除术后出现尿失禁。即使接受了经阴道粘贴术,尿失禁症状仍未缓解。从 2016 年 3 月 4 日至 2016 年 5 月 26 日,她接受了为期两个半月的阿育吠陀疗法和药物治疗。患者接受了 Matrabasti(药物灌肠)和 Madhutailika basti(用蜂蜜和油进行灌肠治疗)以及其他缓和药物 - Sukumara ghrita、Chandraprabha vati、Shilajatu、Mahakalyanaka kashaya、Mamsapachaka ghana vati 和 Mahatiktaka ghrita。在 Matra basti 之后,尿失禁症状减轻为滴尿,在第二个 Basti 疗程(药物灌肠)之后,即一个半月之后,患者停止使用尿布,尿失禁症状得到缓解。本病例报告总结了通过采用巴斯提(灌肠)疗法和其他缓解性阿育吠陀疗法有效治疗尿失禁的情况。
{"title":"Management of post-hysterectomy urinary incontinence with composite Ayurveda treatment – A case report","authors":"Ranjani Karthik Pandit","doi":"10.1016/j.jaim.2024.100961","DOIUrl":"10.1016/j.jaim.2024.100961","url":null,"abstract":"<div><div>This is a case report of a patient who developed urinary incontinence after undergoing abdominal hysterectomy. This was successfully treated with Ayurvedic treatment procedures. A 63-year-old lady was suffering from urinary incontinence, which developed after hysterectomy. It did not subside even after undergoing trans vaginal taping. She was treated with Ayurvedic procedures and medicines for a period of 2 and a half months from 4<sup>th</sup> of March 2016 to 26<sup>th</sup> of May 2016. <em>Matrabasti</em> (medicated enema) and <em>Madhutailika</em> <em>basti</em> (enema treatment with honey and oil), along with other palliative medicines – <em>S</em><em>ukumara ghrita, Chandraprabha vati,</em> <em>S</em><em>hilajatu,</em> <em>M</em><em>ahakalyanaka kashaya,</em> <em>M</em><em>amsapachaka ghana vati and Mahatiktaka ghrita</em> were given to the patient. Urinary incontinence reduced to dribbling of urine after Matra basti and after the second course of <em>B</em><em>asti</em> (medicated enema), that is after one and half months, patient stopped using diapers and was relieved from incontinence. This case report summarises the effective management of urinary incontinence by adopting basti (enema) treatment along with other palliative ayurvedic medicine.</div></div>","PeriodicalId":15150,"journal":{"name":"Journal of Ayurveda and Integrative Medicine","volume":"15 5","pages":"Article 100961"},"PeriodicalIF":1.7,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142323999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy of Berberis vulgaris and Berberis integerrima on glycemic indices and weight profile in type 2 diabetic patients: A systematic review and meta-analysis of randomized controlled trials 小檗和非洲小檗对 2 型糖尿病患者血糖指数和体重状况的疗效:随机对照试验的系统回顾和荟萃分析
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.101039
Hassan ul Hussain , Eman Ali , Areesha Tanveer , Syed Muhammad Ismail , Humam Furqan , Muhammad Nadeem Ahsan , Sadia Iqbal , Muhammad Sohaib Asghar
Type 2 diabetes mellitus (T2DM) is a multifactorial lifelong condition. Berberis vulgaris (BV) and Berberis integerrima (BI) regulate glucose levels with minimal adverse effects. In this systematic review and meta-analysis, we evaluate the effect of BV and BI on glycemic indices, weight, and body mass index (BMI) against placebo.
Four electronic databases were searched till September 24, 2023. Inclusion criteria for studies were: (a) T2DM patients; (b) berberis (vulgaris/integerrima) therapy as intervention; (c) control group of placebo or metformin; (d) outcomes including fasting blood glucose (FBG) levels, glycated hemoglobin (HbA1c%), Homeostatic Model Assessment for Insulin Resistance (HOMA-IR), fasting serum insulin (FSI), 2-h postprandial glucose (2hPPG), fructosamine, weight, and BMI; (e) randomized controlled trials (RCTs). Data was pooled using a random-effects analysis model on Review Manager. The inverse variance statistical method was applied keeping weighted mean difference (WMD) as the effect measure. The Cochrane risk of bias tool evaluated the risk of bias. A p-value of less than 0.05 was considered significant.
Nine RCTs comprising 547 patients were included. Significant reduction was noted with berberis therapy in FBG (WMD: −14.52; 95% CI = −22.97, −6.07; P = 0.0008); HbA1c % (WMD: −0.30; 95% CI = −0.53, −0.07; P = 0.01); HOMA-IR (WMD: −0.97; 95% CI = −1.56, 0.37; P = 0.001). No significant differences were noted between the two groups in 2hPPG (WMD: 6.52; 95% CI = −21.57, 34.61; P = 0.65); FSI (WMD: −0.79; 95% CI = −1.80, 0.22, P = 0.13); Fructosamine (WMD: −12.57; 95% CI = −40.74, 15.60; P = 0.38); Weight (WMD: −1.89; 95% CI = −4.55, 0.76; P = 0.16) and BMI (WMD: −0.12; 95% CI = −0.90, 0.65; P = 0.76).
The data showed significant reduction in FBG and improved insulin levels but limited effects were observed in other glycemic indexes. More extensive RCTs are required globally to achieve a holistic comprehension of the connection between berberis and T2DM.
2 型糖尿病(T2DM)是一种多因素的终身疾病。小檗(BV)和非洲小檗(BI)可调节血糖水平,且不良影响极小。在本系统综述和荟萃分析中,我们评估了 BV 和 BI 与安慰剂相比对血糖指数、体重和体重指数(BMI)的影响。研究的纳入标准为(a) T2DM 患者;(b) 以小檗(庸俗草/integerrima)疗法作为干预措施;(c) 对照组为安慰剂或二甲双胍;(d) 结果包括空腹血糖 (FBG)水平、糖化血红蛋白 (HbA1c%)、胰岛素抵抗静态模型评估 (HOMA-IR)、空腹血清胰岛素 (FSI)、餐后 2 小时血糖 (2hPPG)、果糖胺、体重和体重指数 (BMI); (e) 随机对照试验 (RCT)。数据采用《综述管理器》上的随机效应分析模型进行汇总。采用反方差统计方法,将加权平均差(WMD)作为效果测量指标。科克伦偏倚风险工具对偏倚风险进行了评估。九项研究纳入了 547 名患者。小檗治疗显著降低了FBG(WMD:-14.52;95% CI = -22.97,-6.07;P = 0.0008);HbA1c %(WMD:-0.30;95% CI = -0.53,-0.07;P = 0.01);HOMA-IR(WMD:-0.97;95% CI = -1.56,0.37;P = 0.001)。两组在 2hPPG (WMD:6.52;95% CI = -21.57,34.61;P = 0.65);FSI(WMD:-0.79;95% CI =-1.80,0.22,P = 0.13);果糖胺(WMD:-12.57;95% CI =-40.74,15.60;P = 0.数据显示,FBG 显著降低,胰岛素水平得到改善,但对其他血糖指数的影响有限。要全面了解小檗与 T2DM 之间的关系,还需要在全球范围内开展更广泛的 RCT 研究。
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引用次数: 0
Analysis of quality parameters and preservative concentrations in Sahacharadi Kwatha: A comparative study of three commercial brands Sahacharadi Kwatha 的质量参数和防腐剂浓度分析:三种商业品牌的比较研究
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.101029
Sangeetha Gopal, Leon Ittiachen

Background

Sahacharadi Kwatha is traditionally employed in Ayurvedic therapy for "vata" related conditions such as back pain, herniated disc, palsy, sciatica, and paralysis. Classical Ayurvedic texts recommend the use of freshly prepared Kwatha for optimal patient benefits. However, in response to the commercialization of Ayurveda and the demand for convenient over-the-counter (OTC) formulations, various commercial preservatives have been incorporated by Ayurvedic manufacturers to facilitate OTC preparation and prolong shelf life.

Objectives

This study aims to comprehensively analyse and compare the quality parameters and preservative content in three prominent brands of Sahacharadi Kwatha available in the Indian market.

Materials and methods

Organoleptic and physicochemical properties, phytochemical content, and microbial load of the samples were analyzed following standardized procedures. Sodium benzoate levels in the samples were determined using both titrimetric and High-Performance Liquid Chromatography (HPLC) methods. High-Performance Thin-Layer Chromatography (HPTLC) profiles were compared to discern differences among the samples.

Results

The study revealed significant variations in organoleptic and physicochemical properties, HPTLC profiles, and microbial load among the tested samples. Sodium benzoate levels in all samples exceeded the FDA and API-approved limit. Additionally, substantial variations were noted in the phytochemical content of the samples.

Conclusion

This investigation underscores noteworthy disparities in quality parameters and preservative content within the tested market variants of Sahacharadi Kwatha. The findings emphasize the existence of unregulated standards in the preparation of Ayurvedic medicines available in the market, highlighting the imperative for standardization and validation of Ayurvedic formulations. Such measures are essential for enhancing consumer acceptability and fostering the overall development and growth of the Ayurveda industry.
背景Sahacharadi Kwatha 传统上用于阿育吠陀疗法,治疗与 "瓦塔 "有关的疾病,如背痛、椎间盘突出、麻痹、坐骨神经痛和瘫痪。经典的阿育吠陀经文建议使用新鲜制备的 Kwatha,以使患者获得最佳疗效。然而,随着阿育吠陀的商业化和对方便的非处方药(OTC)配方的需求,阿育吠陀制造商加入了各种商业防腐剂,以方便非处方药的制备并延长保质期。本研究旨在全面分析和比较印度市场上三种著名品牌的 Sahacharadi Kwatha 的质量参数和防腐剂含量。使用滴定法和高效液相色谱法测定了样品中的苯甲酸钠含量。研究结果表明,被测样品在感官和理化特性、HPTLC 图谱以及微生物量方面存在显著差异。所有样品中的苯甲酸钠含量都超过了 FDA 和 API 批准的限值。此外,样品中的植物化学成分含量也存在很大差异。调查结果表明,市场上阿育吠陀药物的制备标准不规范,因此必须对阿育吠陀配方进行标准化和验证。这些措施对于提高消费者的接受度、促进阿育吠陀产业的整体发展和增长至关重要。
{"title":"Analysis of quality parameters and preservative concentrations in Sahacharadi Kwatha: A comparative study of three commercial brands","authors":"Sangeetha Gopal,&nbsp;Leon Ittiachen","doi":"10.1016/j.jaim.2024.101029","DOIUrl":"10.1016/j.jaim.2024.101029","url":null,"abstract":"<div><h3>Background</h3><div><em>Sahacharadi Kwatha</em> is traditionally employed in Ayurvedic therapy for \"vata\" related conditions such as back pain, herniated disc, palsy, sciatica, and paralysis. Classical Ayurvedic texts recommend the use of freshly prepared Kwatha for optimal patient benefits. However, in response to the commercialization of Ayurveda and the demand for convenient over-the-counter (OTC) formulations, various commercial preservatives have been incorporated by Ayurvedic manufacturers to facilitate OTC preparation and prolong shelf life.</div></div><div><h3>Objectives</h3><div>This study aims to comprehensively analyse and compare the quality parameters and preservative content in three prominent brands of <em>Sahacharadi Kwatha</em> available in the Indian market.</div></div><div><h3>Materials and methods</h3><div>Organoleptic and physicochemical properties, phytochemical content, and microbial load of the samples were analyzed following standardized procedures. Sodium benzoate levels in the samples were determined using both titrimetric and High-Performance Liquid Chromatography (HPLC) methods. High-Performance Thin-Layer Chromatography (HPTLC) profiles were compared to discern differences among the samples.</div></div><div><h3>Results</h3><div>The study revealed significant variations in organoleptic and physicochemical properties, HPTLC profiles, and microbial load among the tested samples. Sodium benzoate levels in all samples exceeded the FDA and API-approved limit. Additionally, substantial variations were noted in the phytochemical content of the samples.</div></div><div><h3>Conclusion</h3><div>This investigation underscores noteworthy disparities in quality parameters and preservative content within the tested market variants of <em>Sahacharadi Kwatha</em>. The findings emphasize the existence of unregulated standards in the preparation of Ayurvedic medicines available in the market, highlighting the imperative for standardization and validation of Ayurvedic formulations. Such measures are essential for enhancing consumer acceptability and fostering the overall development and growth of the Ayurveda industry.</div></div>","PeriodicalId":15150,"journal":{"name":"Journal of Ayurveda and Integrative Medicine","volume":"15 5","pages":"Article 101029"},"PeriodicalIF":1.7,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142446553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of the best plant ratios for a polyherbal tea mix to obtain optimum antioxidant, antidiabetic, and β-glucuronidase inhibition activities 确定多草药茶混合物的最佳植物配比,以获得最佳抗氧化、抗糖尿病和β-葡萄糖醛酸酶抑制活性
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.101053
P. Gayani I. Dias , R.A. Upul J. Marapana , R.M. Udaya S.K. Rathnayaka , S.M.D. Sadhana Gayathri , N.G. Darshana Anuradha , Thilini C. Kananke , R.M. Kapila T. Rathnayaka , M.G.A. Namal Perera , Rasangani S. Sabaragamuwa , M. Nirmali Wickramaratne

Background

The influence of plant types and their ratios on the effectiveness of polyherbal formulations is a crucial yet underexplored area of research.

Objectives

This study aimed to identify the optimal ratios of Phylanthus debilis (PW), Osbeckia octrandra (HB), and Artrocarpus heterophyllus (WR) leaf powders for a polyherbal tea to achieve the best functional properties.

Material and methods

A three-level factorial design was used to examine the combined effect of three independent variables (PW, WR, and HB) on antioxidant, antidiabetic, and β-glucuronidase inhibitory activities. The variables were coded at three levels (−1, 0, +1), resulting in 10 experimental runs, with responses tested in triplicates.

Results

The highest antioxidant activity was observed in mixture 4 (PW: WR: HB = 4:1:1) for most assays. P. debilis exhibited the lowest IC50 values for α-glucosidase and β-glucuronidase inhibition, while O. octandra showed the lowest IC50 value for α-amylase inhibition compared to the mixtures. ANOVA indicated that the models and model terms of the mixture design are statistically significant (P ≤ 0.05) and the responses are well-fitted to the models (R2 = 0.8484 to 0.9993). The aqueous extractability of the polyherbal mixtures was higher than that of the individual herbs.

Conclusions

These study revealed that polyherbal formulations exhibit both synergistic and antagonistic effects on therapeutic efficacy. Mixtures 4 (PW: WR: HB = 4:1:1), 5 (PW: HB = 1:1), and 7 (PW: WR: HB = 1:1:1) were screened as the polyherbal mixtures having optimum values for selected functional properties. These combinations, along with individual herbal extracts, will undergo further testing to develop a tri-herbal tea formulation.
背景植物类型及其配比对多草药配方功效的影响是一个重要的研究领域,但尚未得到充分的探索。本研究旨在确定多草药茶中Pyylanthus debilis(PW)、Osbeckia octrandra(HB)和Artrocarpus heterophyllus(WR)叶粉的最佳配比,以实现最佳的功能特性。材料与方法采用三水平因子设计,考察三个自变量(PW、WR 和 HB)对抗氧化、抗糖尿病和β-葡萄糖醛酸酶抑制活性的综合影响。结果在大多数试验中,混合物 4(PW: WR: HB = 4:1:1)的抗氧化活性最高。与混合物相比,P. debilis 对α-葡萄糖苷酶和β-葡萄糖醛酸酶抑制作用的 IC50 值最低,而 O. octandra 对α-淀粉酶抑制作用的 IC50 值最低。方差分析表明,混合物设计的模型和模型项具有统计学意义(P ≤ 0.05),反应与模型拟合良好(R2 = 0.8484 至 0.9993)。多草药混合物的水萃取率高于单个草药的水萃取率。经筛选,混合物 4(PW:WR:HB = 4:1:1)、5(PW:HB = 1:1)和 7(PW:WR:HB = 1:1:1)是在选定功能特性方面具有最佳值的多草药混合物。这些组合以及单个草药提取物将接受进一步测试,以开发三草药茶配方。
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引用次数: 0
Virtual screening and network pharmacology-based synergistic coagulation mechanism identification of multiple components contained in compound Kushen Injection against hepatocellular carcinoma 基于虚拟筛选和网络药理学的复方苦参注射液抗肝癌多成分协同凝血机制鉴定
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.101055
Kejun Zhou , Mengyi Xie , Yu Liu , Lei Zheng , Juan Pu , Cheng Wang

Background

Hepatocellular carcinoma (HCC) is a primary liver malignancy commonly encountered in the setting of chronic liver disease and cirrhosis. Compound Kushen Injection (CKI) has been widely used in HCC, however, the underlying mechanisms are scarce.

Objective

To explore the molecular mechanisms of CKI for HCC.To explore the molecular mechanisms of CKI for HCC.

Materials and Methods

The chemical ingredients of CKI were reviewed from published articles and the potential targets were got from Herbal Ingredients’ Targets Platform. Coagulation-related targets were from Kyoto Encyclopedia of Genes and Genomes and HCC-related targets were from Therapeutic Target Database, Gene Expression Omnibus, and The Cancer Genome Atlas. Then the CKI-Herb-Target and CKI-Herb-Target-HCC networks were built. The shared targets between CKI and HCC were used for functional enrichment through Metascape and the shared coagulation-related target was used for molecular docking and survival analysis.

Results

A total of 23 chemical ingredients and 41 potential targets shared between CKI and HCC were obtained. The results of functional enrichment indicated that several canonical pathways of CKI mostly participated in the treatment of HCC. Furthermore, a chemical ingredient of CKI formed a stable hydrogen bond link with the ASN-189 on PLG, with a best binding energy of −4.7 kcal/mol. Finally, PLG was confirmed as the shared coagulation-related target and interrelated with the prognosis of HCC.

Conclusion

CKI probably improves HCC prognosis through PLG. Our research undoubtedly deepened the understanding of the molecular mechanism of CKI anti-HCC.
背景:肝细胞癌(HCC)是一种原发性肝脏恶性肿瘤,常见于慢性肝病和肝硬化。复方苦参注射液(CKI)已被广泛用于治疗 HCC,但其潜在机制尚不清楚:探索复方苦参注射液治疗 HCC 的分子机制:从已发表的文章中查阅CKI的化学成分,从中药成分靶点平台中获取潜在靶点。凝血相关靶点来自京都基因组百科全书,HCC相关靶点来自治疗靶点数据库、基因表达总库和癌症基因组图谱。然后建立了 CKI-Herb-Target 和 CKI-Herb-Target-HCC 网络。通过 Metascape 对 CKI 和 HCC 的共享靶点进行功能富集,并对凝血相关的共享靶点进行分子对接和生存分析:结果:共获得 23 种化学成分和 41 个潜在靶点。功能富集结果表明,CKI 的几条典型通路大多参与了 HCC 的治疗。此外,CKI的一种化学成分与PLG上的ASN-189形成了稳定的氢键连接,最佳结合能为-4.7 kcal/mol。最后,PLG被证实是凝血相关的共有靶点,并与HCC的预后相关:结论:CKI 可通过 PLG 改善 HCC 的预后。我们的研究无疑加深了对CKI抗HCC分子机制的理解。
{"title":"Virtual screening and network pharmacology-based synergistic coagulation mechanism identification of multiple components contained in compound Kushen Injection against hepatocellular carcinoma","authors":"Kejun Zhou ,&nbsp;Mengyi Xie ,&nbsp;Yu Liu ,&nbsp;Lei Zheng ,&nbsp;Juan Pu ,&nbsp;Cheng Wang","doi":"10.1016/j.jaim.2024.101055","DOIUrl":"10.1016/j.jaim.2024.101055","url":null,"abstract":"<div><h3>Background</h3><div>Hepatocellular carcinoma (HCC) is a primary liver malignancy commonly encountered in the setting of chronic liver disease and cirrhosis. Compound Kushen Injection (CKI) has been widely used in HCC, however, the underlying mechanisms are scarce.</div></div><div><h3>Objective</h3><div>To explore the molecular mechanisms of CKI for HCC.To explore the molecular mechanisms of CKI for HCC.</div></div><div><h3>Materials and Methods</h3><div>The chemical ingredients of CKI were reviewed from published articles and the potential targets were got from Herbal Ingredients’ Targets Platform. Coagulation-related targets were from Kyoto Encyclopedia of Genes and Genomes and HCC-related targets were from Therapeutic Target Database, Gene Expression Omnibus, and The Cancer Genome Atlas. Then the CKI-Herb-Target and CKI-Herb-Target-HCC networks were built. The shared targets between CKI and HCC were used for functional enrichment through Metascape and the shared coagulation-related target was used for molecular docking and survival analysis.</div></div><div><h3>Results</h3><div>A total of 23 chemical ingredients and 41 potential targets shared between CKI and HCC were obtained. The results of functional enrichment indicated that several canonical pathways of CKI mostly participated in the treatment of HCC. Furthermore, a chemical ingredient of CKI formed a stable hydrogen bond link with the ASN-189 on PLG, with a best binding energy of −4.7 kcal/mol. Finally, PLG was confirmed as the shared coagulation-related target and interrelated with the prognosis of HCC.</div></div><div><h3>Conclusion</h3><div>CKI probably improves HCC prognosis through PLG. Our research undoubtedly deepened the understanding of the molecular mechanism of CKI anti-HCC.</div></div>","PeriodicalId":15150,"journal":{"name":"Journal of Ayurveda and Integrative Medicine","volume":"15 5","pages":"Article 101055"},"PeriodicalIF":1.7,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142466222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of Withania somnifera based supplement for immunomodulatory and antiviral properties against viral infection 评估基于睡茄的补充剂对病毒感染的免疫调节和抗病毒特性。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.100955
Dileep Kumar Verma , Abdul Hasan , Manickavasagam Rengaraju , Shree Devi , Geetika Sharma , Vimal Narayanan , Sathiyarajeswaran Parameswaran , Thirumal Kumar D , Kanakavalli Kadarkarai , Sujatha Sunil

Background

Viral mediated diseases are continuously posing potent threat to human health. Nutraceuticals are being employed as novel therapeutics during viral outbreaks. MAM granules consist of Curcuma longa, Withania somnifera, and Piper nigrum, is one such patented Siddha nutraceutical supplement that has been proposed to be a therapeutic agent against viral diseases.

Objective

We characterised MAM for their phytochemical and physicochemical properties and evaluated its cytotoxicity via in vivo acute toxicity studies using Wistar rats and by cell-based MTT assays.

Materials and Methods

The antiviral properties of the aqueous extract of MAM were investigated against SARS-CoV-2 and chikungunya virus (CHIKV). Further, using ABTS radical scavenging, SOD enzymatic assays and measurement of intracellular ROS, we investigated the antioxidant potential of MAM extract and its ingredients in RAW264.7 cells. Additionally, production of inflammatory mediators was evaluated via NO release, PGE2 production and release of pro-inflammatory cytokines (IL-1β and TNFα).

Results

The MAM granules and aqueous extracts demonstrated no significant toxicity and demonstrated potent antiviral activity during co-incubation assay with SARS-CoV-2 and CHIKV. Moreover, we observed potent antioxidant and anti-inflammatory activity of MAM extract in a dose dependent manner. Further investigations on the individual ingredients with respect to their antioxidant and anti-inflammatory activities showed that all ingredients contributed synergistically and Withania somnifera showed most potent anti-oxidant activity.

Conclusion

The overall in vitro, and in vivo analysis demonstrated that MAM granules were non-toxic and possessed potent antiviral activity. Additionally, observed significant anti-oxidant and anti-inflammatory properties of MAM suggested the modulation of innate immune response in the host validating its use as an effective nutraceutical during viral outbreaks.
背景:病毒介导的疾病不断对人类健康构成严重威胁。在病毒爆发期间,保健食品被用作新型疗法。由莪术、睡莲和胡椒组成的 MAM 颗粒就是这样一种获得专利的 Siddha 营养保健品,已被建议用作病毒性疾病的治疗剂:我们研究了 MAM 的植物化学和物理化学特性,并通过使用 Wistar 大鼠进行体内急性毒性研究和基于细胞的 MTT 试验评估了其细胞毒性:研究了 MAM 水提取物对 SARS-CoV-2 和基孔肯雅病毒 (CHIKV) 的抗病毒特性。此外,我们还使用 ABTS 自由基清除、SOD 酶测定和细胞内 ROS 测量方法,研究了 MAM 提取物及其成分在 RAW264.7 细胞中的抗氧化潜力。此外,还通过 NO 释放、PGE2 产生和促炎细胞因子(IL-1β 和 TNFα)释放评估了炎症介质的产生:结果:在与 SARS-CoV-2 和 CHIKV 的共孵育试验中,MAM 颗粒和水提取物没有显示出明显的毒性,并表现出了强大的抗病毒活性。此外,我们还观察到 MAM 提取物具有很强的抗氧化和抗炎活性,其活性与剂量有关。对各种成分的抗氧化和抗炎活性的进一步研究表明,所有成分都具有协同作用,而睡茄的抗氧化活性最强:体外和体内的总体分析表明,MAM 颗粒无毒,具有强大的抗病毒活性。此外,还观察到 MAM 具有明显的抗氧化和抗炎特性,这表明它能调节宿主的先天免疫反应,因此可在病毒爆发时用作有效的营养保健品。
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引用次数: 0
An exploratory single-arm open-label clinical study to evaluate the combined effect of Vamana and Sarasvata Churna in reducing excessive daytime sleepiness 一项探索性单臂开放标签临床研究,旨在评估 Vamana 和 Sarasvata Churna 在减少白天过度嗜睡方面的综合效果
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.100960
Arathy Menon , Devipriya Soman , James Chacko , P.V. Anandaraman , Mahesh C. Kundagol , K. Sreejith
<div><h3>Background</h3><p>Excessive Daytime Sleepiness (EDS) is inferred as persistent sleepiness and often a general lack of energy during the day even after apparently adequate or even prolonged nighttime sleep. The subjects may not be identifying excessive daytime sleepiness but may present as feeling tired, lack of energy etc. They may seem apparently healthy and without any other systemic illness. The prevalence was found to be as high as 18 % in 2012 in United Kingdom. Also, it is a risk factor for diseases like Alzheimer's disease, Parkinson's disease and other neurodegenerative diseases. Conventional management (Modafinil, Sodium Oxybate and Stimulants) addresses only the subjective condition in EDS and is associated with adverse effects compromising the quality of life. In the current health scenario there is a need for alternative interventions to manage this disease. On analyzing this condition through <em>Ayurveda</em>, we could understand it as <em>Nidradhikya</em> (Excessive daytime sleepiness) which is caused due to vitiated <em>Kapha Dosha</em> along with <em>Vriddha Tamoguna</em> (increased <em>Tamoguna</em>) that can be managed by <em>Shodhana</em> (biopurification) followed <em>Shamana</em> (pacification) therapies.</p></div><div><h3>Objective</h3><p>This study was aimed to assess the combined effect of <em>Vamana</em> (therapeutic vomiting) and <em>Sarasvata Churna</em> in reducing Excessive Daytime Sleepiness.</p></div><div><h3>Materials and methods</h3><p>This was a single-arm exploratory open-label clinical trial. 10 subjects having EDS diagnosed using Modified Epworth Sleepiness Scale (MESS) with a score of 10–24 with proper exclusion were recruited from OPD and IPD, Department of <em>Kāyacikitsa</em>, Amrita School of Ayurveda. All the participants were clinically examined, sought for medical history and further checked biochemically to exclude any other systemic illness that may lead to this condition. Only healthy subjects with quality night sleep (assessed by PSQI) and without any other systemic illness were selected. The treatment protocol adopted was <em>Vamana Karma</em> followed by 30 days of <em>Sarasvata Churna</em> as <em>Shamana Aushadha</em> (medicine for pacification). Assessment was done using MESS on 0<sup>th</sup> day and after 30 days of <em>Shamana Aushadha Sevana.</em> After completion of treatment, the results were statistically analysed using Wilcoxon Signed Rank Test and final conclusion was drawn.</p></div><div><h3>Results</h3><p>On analysis of the symptoms using Modified Epworth Sleepiness Scale, the mean total score reduced from 14.8 to 2.8 with 81.08 % relief in these 10 subjects and a significant p value < 0.05 after <em>Vamana</em> followed by 30 days of <em>Shamana Aushadha Sevana</em>.</p></div><div><h3>Discussion</h3><p><em>Vamana</em> helps in <em>Kapha Nirharana</em> (expelling) which removes the <em>Avarana</em> (occlusion) of <em>Manas</em> seen in <em>Nidradhikya</em>. This results
背景白天过度嗜睡(EDS)被推断为持续性嗜睡,即使在夜间睡眠明显充足甚至较长的时间后,白天仍经常出现全身乏力。受试者可能无法识别白天过度嗜睡,但可能表现为感到疲倦、乏力等。他们可能看起来很健康,没有任何其他系统疾病。2012 年,英国的发病率高达 18%。此外,它还是阿尔茨海默病、帕金森病和其他神经退行性疾病的风险因素。传统的治疗方法(莫达非尼、羟基酸钠和兴奋剂)只能解决 EDS 患者的主观症状,而且会产生不良反应,影响生活质量。在当前的健康状况下,有必要采取其他干预措施来控制这种疾病。通过阿育吠陀对这种疾病进行分析,我们可以将其理解为Nidradhikya(白天过度嗜睡),它是由于Kapha Dosha受损以及Vriddha Tamoguna(Tamoguna增加)引起的,可以通过Shodhana(生物净化)和Shamana(安抚)疗法来控制。材料和方法这是一项单臂探索性开放标签临床试验。研究人员从阿姆利塔阿育吠陀学院 Kāyacikitsa 系的门诊部和住院部招募了 10 名使用改良埃普沃思嗜睡量表 (MESS) 诊断为 10-24 分的 EDS 受试者,并进行了适当的排除。所有受试者都接受了临床检查、病史询问和进一步的生化检查,以排除任何可能导致这种情况的其他系统疾病。只有夜间睡眠质量良好(通过 PSQI 评估)且无任何其他系统疾病的健康受试者才被选中。采用的治疗方案是 Vamana Karma,然后服用 30 天 Sarasvata Churna 作为 Shamana Aushadha(安神药)。在服用 Shamana Aushadha Sevana 的第 0 天和 30 天后,使用 MESS 进行评估。治疗结束后,使用 Wilcoxon Signed Rank Test 对结果进行统计分析,并得出最终结论。讨论Vamana 有助于 Kapha Nirharana(驱逐),从而消除 Nidradhikya 中 Manas 的 Avarana(闭塞)。这就产生了 Hrit Shuddhi(心灵的纯净),有助于实现 Mano Gunas(心灵的特质)(Satvoudaryam Tamojayaha)的平衡,从而形成管理路线。作为 Shamana Aushadha 而施用的 Sarasvata Churna 具有 Medhya(促智药)、Buddhi Smriti Dhriti Vardhaka(促进智力、记忆力和耐心)的特性,目前正用于 Vicetas。Sarasvata Churna 中的大多数药物都是 Rasayana(恢复活力),通过 Rasa Dhatu 的 Prinana(滋养)给 Manas 带来 Indriya Bala(增强感官)和 Priti(蔑视)。
{"title":"An exploratory single-arm open-label clinical study to evaluate the combined effect of Vamana and Sarasvata Churna in reducing excessive daytime sleepiness","authors":"Arathy Menon ,&nbsp;Devipriya Soman ,&nbsp;James Chacko ,&nbsp;P.V. Anandaraman ,&nbsp;Mahesh C. Kundagol ,&nbsp;K. Sreejith","doi":"10.1016/j.jaim.2024.100960","DOIUrl":"10.1016/j.jaim.2024.100960","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;p&gt;Excessive Daytime Sleepiness (EDS) is inferred as persistent sleepiness and often a general lack of energy during the day even after apparently adequate or even prolonged nighttime sleep. The subjects may not be identifying excessive daytime sleepiness but may present as feeling tired, lack of energy etc. They may seem apparently healthy and without any other systemic illness. The prevalence was found to be as high as 18 % in 2012 in United Kingdom. Also, it is a risk factor for diseases like Alzheimer's disease, Parkinson's disease and other neurodegenerative diseases. Conventional management (Modafinil, Sodium Oxybate and Stimulants) addresses only the subjective condition in EDS and is associated with adverse effects compromising the quality of life. In the current health scenario there is a need for alternative interventions to manage this disease. On analyzing this condition through &lt;em&gt;Ayurveda&lt;/em&gt;, we could understand it as &lt;em&gt;Nidradhikya&lt;/em&gt; (Excessive daytime sleepiness) which is caused due to vitiated &lt;em&gt;Kapha Dosha&lt;/em&gt; along with &lt;em&gt;Vriddha Tamoguna&lt;/em&gt; (increased &lt;em&gt;Tamoguna&lt;/em&gt;) that can be managed by &lt;em&gt;Shodhana&lt;/em&gt; (biopurification) followed &lt;em&gt;Shamana&lt;/em&gt; (pacification) therapies.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objective&lt;/h3&gt;&lt;p&gt;This study was aimed to assess the combined effect of &lt;em&gt;Vamana&lt;/em&gt; (therapeutic vomiting) and &lt;em&gt;Sarasvata Churna&lt;/em&gt; in reducing Excessive Daytime Sleepiness.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Materials and methods&lt;/h3&gt;&lt;p&gt;This was a single-arm exploratory open-label clinical trial. 10 subjects having EDS diagnosed using Modified Epworth Sleepiness Scale (MESS) with a score of 10–24 with proper exclusion were recruited from OPD and IPD, Department of &lt;em&gt;Kāyacikitsa&lt;/em&gt;, Amrita School of Ayurveda. All the participants were clinically examined, sought for medical history and further checked biochemically to exclude any other systemic illness that may lead to this condition. Only healthy subjects with quality night sleep (assessed by PSQI) and without any other systemic illness were selected. The treatment protocol adopted was &lt;em&gt;Vamana Karma&lt;/em&gt; followed by 30 days of &lt;em&gt;Sarasvata Churna&lt;/em&gt; as &lt;em&gt;Shamana Aushadha&lt;/em&gt; (medicine for pacification). Assessment was done using MESS on 0&lt;sup&gt;th&lt;/sup&gt; day and after 30 days of &lt;em&gt;Shamana Aushadha Sevana.&lt;/em&gt; After completion of treatment, the results were statistically analysed using Wilcoxon Signed Rank Test and final conclusion was drawn.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;p&gt;On analysis of the symptoms using Modified Epworth Sleepiness Scale, the mean total score reduced from 14.8 to 2.8 with 81.08 % relief in these 10 subjects and a significant p value &lt; 0.05 after &lt;em&gt;Vamana&lt;/em&gt; followed by 30 days of &lt;em&gt;Shamana Aushadha Sevana&lt;/em&gt;.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Discussion&lt;/h3&gt;&lt;p&gt;&lt;em&gt;Vamana&lt;/em&gt; helps in &lt;em&gt;Kapha Nirharana&lt;/em&gt; (expelling) which removes the &lt;em&gt;Avarana&lt;/em&gt; (occlusion) of &lt;em&gt;Manas&lt;/em&gt; seen in &lt;em&gt;Nidradhikya&lt;/em&gt;. This results ","PeriodicalId":15150,"journal":{"name":"Journal of Ayurveda and Integrative Medicine","volume":"15 5","pages":"Article 100960"},"PeriodicalIF":1.7,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0975947624000755/pdfft?md5=614cdfc87ae8f05c98f54c92c8646586&pid=1-s2.0-S0975947624000755-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142270913","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A consensus guideline on preferred items for reporting case series in homeopathy: The PITCH statement 顺势疗法病例系列报告首选项目共识指南:PITCH 声明
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-09-01 DOI: 10.1016/j.jaim.2024.101023
Abhijit Dutta

Background

Case series is a valuable tool for sharing clinical experiences and generating research questions in the field of medicine. However, there is a lack of standardized reporting guideline for case series in homeopathy, which limits their utility and comparability. The aim of this study is to develop a reporting guideline for case series in homeopathy using a Delphi consensus process.

Method

A group of 21 experts, with experience in reviewing, publishing, or editing case reports or series in homeopathy, were participated in the study. A modified Delphi consensus process was conducted with three rounds of electronic surveys to gather feedback and opinions on the items to be included in the reporting guideline. The GRADE group's nine-point Likert scale was used to rate each item's importance and criticality.

Result

The Delphi process resulted in a consensus-based reporting guideline for case series in homeopathy, which includes recommendations for reporting case series in eleven sections, including 'Title,' 'Abstract,' 'Keywords,' 'Introduction,' 'Methods,' 'Results,' 'Discussion,' 'Conclusion,' 'Patient Perspectives,' 'References,' and 'Additional Information.' PITCH comprises a total of 59 items that achieved consensus agreement. Of these, 13 are optional items and 14 items are exclusively applicable for prospective type of case series.

Conclusion

The PITCH reporting guideline provides a structured and standardized approach for reporting case series in homeopathy. The authors, journal editors, reviewers, and educators are encouraged to adopt and implement the guideline to enhance the quality of case series in homeopathic publications.
背景病例系列是医学领域分享临床经验和提出研究问题的重要工具。然而,顺势疗法缺乏标准化的病例系列报告指南,这限制了其实用性和可比性。本研究的目的是采用德尔菲共识程序,为顺势疗法的系列病例制定报告指南。研究方法21位具有顺势疗法病例报告或系列病例审核、出版或编辑经验的专家参与了本研究。研究采用改良的德尔菲共识流程,通过三轮电子调查收集反馈意见和对报告指南中应包含项目的看法。结果德尔菲过程产生了以共识为基础的顺势疗法病例系列报告指南,其中包括11个部分的病例系列报告建议,包括 "标题"、"摘要"、"关键词"、"引言"、"方法"、"结果"、"讨论"、"结论"、"患者观点"、"参考文献 "和 "附加信息"。PITCH 共有 59 个达成共识的项目。结论PITCH报告指南为顺势疗法病例系列报告提供了结构化和标准化的方法。我们鼓励作者、期刊编辑、审稿人和教育工作者采用并执行该指南,以提高顺势疗法出版物中病例系列的质量。
{"title":"A consensus guideline on preferred items for reporting case series in homeopathy: The PITCH statement","authors":"Abhijit Dutta","doi":"10.1016/j.jaim.2024.101023","DOIUrl":"10.1016/j.jaim.2024.101023","url":null,"abstract":"<div><h3>Background</h3><div>Case series is a valuable tool for sharing clinical experiences and generating research questions in the field of medicine. However, there is a lack of standardized reporting guideline for case series in homeopathy, which limits their utility and comparability. The aim of this study is to develop a reporting guideline for case series in homeopathy using a Delphi consensus process.</div></div><div><h3>Method</h3><div>A group of 21 experts, with experience in reviewing, publishing, or editing case reports or series in homeopathy, were participated in the study. A modified Delphi consensus process was conducted with three rounds of electronic surveys to gather feedback and opinions on the items to be included in the reporting guideline. The GRADE group's nine-point Likert scale was used to rate each item's importance and criticality.</div></div><div><h3>Result</h3><div>The Delphi process resulted in a consensus-based reporting guideline for case series in homeopathy, which includes recommendations for reporting case series in eleven sections, including 'Title,' 'Abstract,' 'Keywords,' 'Introduction,' 'Methods,' 'Results,' 'Discussion,' 'Conclusion,' 'Patient Perspectives,' 'References,' and 'Additional Information.' PITCH comprises a total of 59 items that achieved consensus agreement. Of these, 13 are optional items and 14 items are exclusively applicable for prospective type of case series.</div></div><div><h3>Conclusion</h3><div>The PITCH reporting guideline provides a structured and standardized approach for reporting case series in homeopathy. The authors, journal editors, reviewers, and educators are encouraged to adopt and implement the guideline to enhance the quality of case series in homeopathic publications.</div></div>","PeriodicalId":15150,"journal":{"name":"Journal of Ayurveda and Integrative Medicine","volume":"15 5","pages":"Article 101023"},"PeriodicalIF":1.7,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142421108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Journal of Ayurveda and Integrative Medicine
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