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May Traditional Chinese Medicine Reduce the Risk of Developing Rheumatoid Arthritis? An One-armed Prospective Study 中医药能否降低类风湿关节炎的患病风险?单臂前瞻性研究
Pub Date : 2024-03-01 Epub Date: 2024-01-14 DOI: 10.1016/j.ccmp.2023.100127
Kaixin Gao , Qi Liang , Dongyun Li , Chuanning Li , Maojie Wang , Xiumin Chen , Qingchun Huang , Zehuai Wen , Per-Johan Jakobsson , Runyue Huang

Background

Rheumatoid arthritis (RA) is a worldwide public health problem. Intervention and prevention before the onset of rheumatic diseases is a new direction in current research.

Objective

The aim of this study was to evaluate the potential and feasibility of traditional Chinese medicine (TCM) in the prevention of RA.

Methods

This was a single-armed prospective clinical trial. All participants were recruited from a single center in Guangdong, China. Adults who were tested positive for anti-cyclic citrullinated peptide antibody (anti-CCP) and/or rheumatoid factor (RF), had no synovitis and had never been treated with disease-modifying anti-rheumatic drugs (DMARDs), were enrolled to take the Huayu-Qiangshen-Tongbi (HQT) decoction orally twice daily, 200 mL each time for 24 weeks. Primary outcome was the proportion of patients who met 2010 ACR(American College of Rheumatology)/EULAR(European League Against Rheumatism) classification criteria of RA during observation. Secondary outcomes included levels of anti-CCP, RF, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), assessment of signs and symptoms, and radiographic progression by magnetic resonance imaging (MRI).

Results

19 individuals were enrolled in the study, 4 of which withdrew because of the epidemic of COVID-19. During the observation period, 3 individuals (20%) developed RA and they had longer morning stiffness (P = 0.009) and more obvious synovial enhancement in MRI (P = 0.041) at baseline when compared with those who did not develop RA. After 24 weeks of intervention, there were improvements in 28-swollen joint count (SJC28) (P = 0.046), Visual Analog Scale (VAS) (P = 0.019), Patient's Global Assessment (PtGA) (P = 0.019) and Physician's Global Assessment (PGA) (P = 0.031), but no statistical significance was observed in the levels of anti-CCP, RF, ESR, CRP, morning stiffness, 28-tender joint count (TJC28), Health Assessment Questionnaire (HAQ) and magnetic resonance imaging (MRI) analysis (P > 0.05).

Conclusion

The HQT formula is safe and could improve joint symptoms and signs in these at-risk individuals, but it remains to be investigated in futher study to see if it might potentially reduce the risk of developing RA. Besides, for individuals at high risk to develop RA, morning stiffness and synovial enhancement in MRI might be predictive factors and warning signs.

背景类风湿性关节炎(RA)是一个世界性的公共卫生问题。本研究旨在评估传统中医药在预防类风湿关节炎方面的潜力和可行性。所有参与者均来自中国广东的一个中心。参与者均为抗环瓜氨酸肽抗体(抗CCP)和/或类风湿因子(RF)检测呈阳性、无滑膜炎且从未接受过改善病情抗风湿药物(DMARDs)治疗的成年人,每天口服两次化瘀羌活汤(HQT),每次200毫升,共24周。主要结果是观察期间符合2010年ACR(美国风湿病学会)/EULAR(欧洲抗风湿病联盟)RA分类标准的患者比例。次要结果包括抗CCP、RF、红细胞沉降率(ESR)、C反应蛋白(CRP)水平,体征和症状评估,以及磁共振成像(MRI)的影像学进展。在观察期间,有3人(20%)患上了RA,与未患上RA的人相比,他们在基线时的晨僵时间更长(P = 0.009),核磁共振成像中的滑膜强化更明显(P = 0.041)。干预 24 周后,28 个关节肿胀计数(SJC28)(P = 0.046)、视觉模拟量表(VAS)(P = 0.019)、患者总体评估(PtGA)(P = 0.019)和医生总体评估(PGA)(P = 0.结论 HQT 配方是安全的,可以改善这些高危人群的关节症状和体征,但是否有可能降低患 RA 的风险仍有待进一步研究。此外,对于罹患 RA 的高危人群来说,磁共振成像中的晨僵和滑膜强化可能是预测因素和警示信号。
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引用次数: 0
Electroacupuncture Alleviates HIF1-α-mediated Early Mitophagy in Spinal Cord Injury 电针可减轻HIF1-α-介导的脊髓损伤早期有丝分裂
Pub Date : 2024-03-01 Epub Date: 2023-07-05 DOI: 10.1016/j.ccmp.2023.100103
Rong Hu , Xingying Wu , Kelin He , Mengting Shi , Haipeng Xu , Yi Chen , Bowen Chen , Lei Wu , Ruijie Ma , Kang Liang

Background

The inhibitory microenvironment around spinal cord injury (SCI) severely restricted functional repair after injury. Mitophagy was one of the important measures to maintain cellular homeostasis and ensure the harmonious nerve cell microenvironment. Hypoxia-inducible factor1α (HIF1-α) can mediate mitochondrial autophagy in neurodegenerative diseases, but the mechanisms are complex and diverse, which need to be further elucidated. Electroacupuncture plays a significant role in improving the neural microenvironment after spinal cord injury, promote long-term neurological function recovery in SCI patients, but whether electroacupuncture can participate in HIF1-α mediated mitophagy remains unknown.

Objective

Investigated the effects of HIF1-α on mitochondrial autophagy in rats with spinal cord contusion and the potential mechanism of electroacupuncture.

Methods

Following the successful construction of an SCI model of Sprague-Dawley rat utilizing a modified Allen method, electroacupuncture intervention was performed at T9 and T11 Jiaji acupoint (EX-B2), with further molecular biology and morphology examined by perfusion. To observe the effect of HIF1-α on local damage repair, the stereotypic injection of Hif1a knockdown virus was performed, and the changes of mitophagy in damaged local area was detected employing Western blotting, real-time fluorescence quantitative PCR, immunofluorescence, transmission electron microscopy and Nissl staining.

Results

HIF1-α as well as its mitophagy receptor BNIP3 and NIX are upregulated after spinal cord injury. Electroacupuncture treatment or local inhibition of HIF1-α expression can reverse the early autophagy state after spinal cord injury, reduce cell apoptosis and injury area, promote neuronal survival.

Conclusion

Electroacupuncture may serve as a promising strategy for spinal cord injury treatment, by alleviating HIF1-α mediated early mitochondrial autophagy.

背景脊髓损伤周围的抑制微环境严重限制了损伤后的功能修复。线粒体自噬是维持细胞内稳态、保证神经细胞微环境和谐的重要措施之一。缺氧诱导因子1α (hypoxia inducible factor1α, HIF1-α)可介导神经退行性疾病的线粒体自噬,但其机制复杂多样,有待进一步阐明。电针在改善脊髓损伤后神经微环境,促进脊髓损伤患者长期神经功能恢复方面具有显著作用,但电针是否参与HIF1-α介导的有丝分裂尚不清楚。目的探讨HIF1-α对脊髓挫伤大鼠线粒体自噬的影响及电针作用的可能机制。方法采用改良Allen法成功构建Sprague-Dawley大鼠脊髓损伤模型后,采用电针干预T9、T11夹脊穴(EX-B2),灌注观察分子生物学和形态学变化。为观察HIF1-α对局部损伤修复的影响,采用Hif1a敲低病毒模型注射,采用Western blotting、实时荧光定量PCR、免疫荧光、透射电镜和尼氏染色检测损伤局部有丝分裂的变化。结果脊髓损伤后,shif1 -α及其线粒体自噬受体BNIP3和NIX表达上调。电针治疗或局部抑制HIF1-α表达可逆转脊髓损伤后早期自噬状态,减少细胞凋亡和损伤面积,促进神经元存活。结论电针可减轻HIF1-α介导的早期线粒体自噬,是一种治疗脊髓损伤的有效方法。
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引用次数: 0
Anti-aging Related Activities and Health Benefits of Licochalcone A: A Review 李可查尔酮 A 的抗衰老相关活性和对健康的益处:综述
Pub Date : 2024-03-01 Epub Date: 2023-12-02 DOI: 10.1016/j.ccmp.2023.100125
Iffat Ara , Rita Turcio , Tasmia Islam , Md. Sabbir Hossain , Md. Kamrul Hasan

Background

Licochalcone A (LCA) is a flavonoid derived from the roots of Glycyrrhiza uralensis Fisch. ex DC and other related plants. Its natural source has been extensively used in complementary medicine, especially traditional Chinese medicine, to treat various ailments. Identified as a phenolic chalcone compound, LCA has gained significant attention in recent years due to its various pharmacological properties.

Objective

The objective of this review article is to assess the auti-aging ralated pharmacological properties of licochalcone A.

Method

An exhaustive search of several scientific databases was conducted using various relevant keywords to write this review article on LCA, focusing on its therapeutic applications and anti-aging-related pharmacological activities. Some inclusion and exclusion criteria were strictly followed to retrieve updated relevant articles.

Results

A collection of 292 papers were screened, and 131 were included in this review for an in-depth analysis of Licochalcone A, focusing on its anti-aging-related pharmacological activities and relevant mechanisms, and its toxicity and side effects. Moreover, the potential of LCA as a pharmacological product is discussed, emphasizing its health benefits and potential as a pharmaceutical product.

Conclusion

These findings indicate that Licochalcone A is a promising natural therapeutic agent for anti-aging therapy and other ailments.

背景甘草查耳酮 A(Licochalcone A,LCA)是一种黄酮类化合物,提取自甘草(Glycyrrhiza uralensis Fisch.它的天然来源已被广泛用于辅助医学,特别是传统中医学,以治疗各种疾病。本综述文章的目的是评估甘草查耳酮 A 的抗衰老药理特性。方法:为了撰写这篇关于甘草查耳酮的综述文章,我们使用各种相关关键词对多个科学数据库进行了详尽的检索,重点关注其治疗应用和抗衰老相关的药理活性。结果 筛选出 292 篇论文,其中 131 篇被纳入本综述,对李可查酮 A 进行了深入分析,重点关注其抗衰老相关药理活性和相关机制,以及其毒性和副作用。结论这些研究结果表明,李可查酮 A 是一种很有前景的天然治疗剂,可用于抗衰老治疗和其他疾病的治疗。
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引用次数: 0
GSZ Formula Enhances Sleep Quality: Exploring Its Active Ingredients and Mechanism Using a Network Medicine Approach GSZ配方提高睡眠质量:运用网络医学方法探讨其活性成分和作用机制
Pub Date : 2024-03-01 Epub Date: 2023-08-26 DOI: 10.1016/j.ccmp.2023.100107
Airong Ren , Mingxuan Ma , Yongyin Liang , Yarong Wang , Zhengkun Li , Yahui Liu , Qing Fan , Guozhen Cui

Background

Sleep is essential for maintaining human health, and insomnia is a widespread problem. Traditional Chinese medicine (TCM) has been used for centuries to treat sleep disorders, with fewer reported side effects compared to conventional treatments.

Objective

This study seeks to investigate the sleep-promoting effects of the GSZ formula, which comprises γ-aminobutyric acid (GABA), Schisandrae Chinensis Fructus (Wuweizi in Chinese), and Ziziphi Spinosae Semen (Suanzaoren in Chinese). In addition, we aim to explore the active ingredients and potential mechanisms underlying the sleep-enhancing effects of the formula.

Methods

The impact of GSZ on sleep was evaluated using two models, the complete sleep model and the subthreshold sleep model. Mice were randomly divided into five groups and orally administered GSZ solution (0.33 g/kg/day or 0.99 g/kg/day), positive drug diazepam (2.50 mg/kg) or a control solution for 30 days. Hypnosis model was established in mice using pentobarbital sodium. Sleep duration and incidence were measured by recording when the righting reflex of mice disappeared for more than 1 min. GABA and dopamine (DA) levels in mouse brain tissue were measured using ELISA kits. The ingredients of the GSZ formula were identified using mass spectrometry, and the targets of these ingredients and disease-related genes were retrieved from public databases. A network medicine approach was used to calculate the shortest path between ingredient targets and disease-related proteins. The expression levels of potential proteins, such as Akt, p-Akt, GSK-3β, and p-GSK-3β, were analyzed using Western blotting based on the predicted results.

Results

GSZ significantly prolonged sleep duration and enhanced the sleep rate in mice (P < 0.05). Furthermore, it elevated GABA levels and reduced DA levels in the mouse brain (P < 0.05). Network medicine analysis suggested that GABA, stearic acid, genistin, and coumestrol may be the most crucial active ingredients for sleep improvement. Western blotting analysis demonstrated that GSZ modulated the protein expression levels of p-Akt/Akt and p-GSK-3β/GSK-3β (P < 0.05).

Conclusion

Our study demonstrated that the GSZ formula could improve sleep, with key ingredients likely being GABA, stearic acid, genistin, and coumestrol. The mechanism might involve the regulation of the Akt/GSK-3β pathway, as revealed by the network medicine analysis and experimental validation. Our current new findings shed light on the potential mechanisms underlying the sleep-enhancing effects of the GSZ formula, which could provide experimental evidence to develop innovative treatments for insomnia.

睡眠对维持人体健康至关重要,而失眠是一个普遍存在的问题。几个世纪以来,中医一直被用于治疗睡眠障碍,与传统疗法相比,据报道其副作用更少。目的探讨由γ-氨基丁酸(GABA)、五味子、酸枣仁组成的GSZ方对睡眠的促进作用。此外,我们的目标是探索有效成分和潜在的机制下的睡眠增强效果的配方。方法采用完全睡眠模型和阈下睡眠模型评价GSZ对睡眠的影响。将小鼠随机分为5组,分别口服GSZ溶液(0.33 g/kg/d或0.99 g/kg/d)、阳性药物地西泮(2.50 mg/kg)或对照溶液30 d。采用戊巴比妥钠建立小鼠催眠模型。记录小鼠翻正反射消失1 min以上时的睡眠持续时间和睡眠发生率。ELISA试剂盒检测小鼠脑组织中GABA和多巴胺(DA)水平。采用质谱法鉴定GSZ配方的成分,并从公共数据库中检索这些成分的靶点和疾病相关基因。采用网络医学方法计算成分靶点与疾病相关蛋白之间的最短路径。根据预测结果,采用Western blotting分析Akt、p-Akt、GSK-3β、p-GSK-3β等潜在蛋白的表达水平。结果gsz显著延长小鼠睡眠时间,提高睡眠率(P <0.05)。此外,它提高了小鼠大脑中GABA水平,降低了DA水平(P <0.05)。网络医学分析表明,GABA、硬脂酸、genistin和coumestrol可能是改善睡眠最重要的活性成分。Western blotting分析表明,GSZ可调节P -Akt/Akt和P -GSK-3β/GSK-3β的蛋白表达水平(P <0.05)。结论GSZ配方具有改善睡眠的作用,其主要成分可能是GABA、硬脂酸、genistin和coumestrol。网络医学分析和实验验证表明,其机制可能与Akt/GSK-3β通路的调控有关。我们目前的新发现揭示了GSZ配方增强睡眠效果的潜在机制,这可能为开发创新的失眠治疗方法提供实验证据。
{"title":"GSZ Formula Enhances Sleep Quality: Exploring Its Active Ingredients and Mechanism Using a Network Medicine Approach","authors":"Airong Ren ,&nbsp;Mingxuan Ma ,&nbsp;Yongyin Liang ,&nbsp;Yarong Wang ,&nbsp;Zhengkun Li ,&nbsp;Yahui Liu ,&nbsp;Qing Fan ,&nbsp;Guozhen Cui","doi":"10.1016/j.ccmp.2023.100107","DOIUrl":"10.1016/j.ccmp.2023.100107","url":null,"abstract":"<div><h3>Background</h3><p>Sleep is essential for maintaining human health, and insomnia is a widespread problem. Traditional Chinese medicine (TCM) has been used for centuries to treat sleep disorders, with fewer reported side effects compared to conventional treatments.</p></div><div><h3>Objective</h3><p>This study seeks to investigate the sleep-promoting effects of the GSZ formula, which comprises <em>γ</em>-aminobutyric acid (GABA), Schisandrae Chinensis Fructus (Wuweizi in Chinese), and Ziziphi Spinosae Semen (Suanzaoren in Chinese). In addition, we aim to explore the active ingredients and potential mechanisms underlying the sleep-enhancing effects of the formula.</p></div><div><h3>Methods</h3><p>The impact of GSZ on sleep was evaluated using two models, the complete sleep model and the subthreshold sleep model. Mice were randomly divided into five groups and orally administered GSZ solution (0.33 g/kg/day or 0.99 g/kg/day), positive drug diazepam (2.50 mg/kg) or a control solution for 30 days. Hypnosis model was established in mice using pentobarbital sodium. Sleep duration and incidence were measured by recording when the righting reflex of mice disappeared for more than 1 min. GABA and dopamine (DA) levels in mouse brain tissue were measured using ELISA kits. The ingredients of the GSZ formula were identified using mass spectrometry, and the targets of these ingredients and disease-related genes were retrieved from public databases. A network medicine approach was used to calculate the shortest path between ingredient targets and disease-related proteins. The expression levels of potential proteins, such as Akt, p-Akt, GSK-3β, and p-GSK-3β, were analyzed using Western blotting based on the predicted results.</p></div><div><h3>Results</h3><p>GSZ significantly prolonged sleep duration and enhanced the sleep rate in mice (<em>P</em> &lt; 0.05). Furthermore, it elevated GABA levels and reduced DA levels in the mouse brain (<em>P</em> &lt; 0.05). Network medicine analysis suggested that GABA, stearic acid, genistin, and coumestrol may be the most crucial active ingredients for sleep improvement. Western blotting analysis demonstrated that GSZ modulated the protein expression levels of p-Akt/Akt and p-GSK-3β/GSK-3β (<em>P</em> &lt; 0.05).</p></div><div><h3>Conclusion</h3><p>Our study demonstrated that the GSZ formula could improve sleep, with key ingredients likely being GABA, stearic acid, genistin, and coumestrol. The mechanism might involve the regulation of the Akt/GSK-3β pathway, as revealed by the network medicine analysis and experimental validation. Our current new findings shed light on the potential mechanisms underlying the sleep-enhancing effects of the GSZ formula, which could provide experimental evidence to develop innovative treatments for insomnia.</p></div>","PeriodicalId":72608,"journal":{"name":"Clinical complementary medicine and pharmacology","volume":"4 1","pages":"Article 100107"},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41517972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Therapeutic Benefits of Vernonia amygdalina in the Treatment of Inflammation and Its Associated Diseases 杏仁蕨在治疗炎症及其相关疾病中的疗效
Pub Date : 2024-03-01 Epub Date: 2023-11-15 DOI: 10.1016/j.ccmp.2023.100122
Du-Bois Asante , Gideon Akuamoah Wiafe , Korantema Mawuena Tsegah , Nelson Kwabla Domey

Background

In the presence of a stimulus that disrupts homeostasis, the body elicits a response known as inflammation. The inflammatory response is expected to restore the normal functioning of the body and initiate healing where necessary. However, the persistent activity of acute inflammation results in chronic inflammation which causes adverse consequences associated with diseases such as diabetes and arthritis. In traditional medical practice, Vernonia amygdalina is used to treat several ailments such as malaria, fever, diabetes, and inflammatory conditions such as those related to pain and swelling.

Objective

This review seeks to explore and discuss the therapeutic benefits of V. amygdalina in the treatment of inflammation and its associated diseases.

Methods

We reviewed the scientific literature indexed in PubMed, ScienceDirect and Springer, and discussed the reported anti-inflammatory properties of V. amygdalina and its curative activity in inflammation-associated diseases.

Results

A total of 30 published articles were identified describing the therapeutic effect of V. amygdalina in predominately experimental models. The anti-inflammatory properties of V. amygdalina have been linked to the presence of bioactive phytoconstituents predominantly present in the leaves of the plant.

Conclusions

Multiple studies have demonstrated that the aqueous and ethanolic extracts of V. amygdalina can inhibit the production of proinflammatory cytokines and enzymes in inflammatory cells, reducing inflammation and its associated complications. We critically appraise the current evidence, and discuss the potential use of this medicinal plant in the treatment of inflammatory conditions.

背景 在受到破坏机体平衡的刺激时,机体会产生一种称为炎症的反应。炎症反应可望恢复机体的正常功能,并在必要时启动愈合。然而,急性炎症的持续活动会导致慢性炎症,造成与糖尿病和关节炎等疾病相关的不良后果。在传统医学实践中,杏仁蕨可用于治疗多种疾病,如疟疾、发烧、糖尿病以及与疼痛和肿胀有关的炎症。方法我们查阅了 PubMed、ScienceDirect 和 Springer 中索引的科学文献,并讨论了所报道的杏仁酸橙的抗炎特性及其对炎症相关疾病的治疗活性。结论多项研究表明,苦杏仁水提取物和乙醇提取物可抑制炎症细胞中促炎细胞因子和酶的产生,从而减轻炎症及其相关并发症。我们对目前的证据进行了批判性评估,并讨论了这种药用植物在治疗炎症方面的潜在用途。
{"title":"Therapeutic Benefits of Vernonia amygdalina in the Treatment of Inflammation and Its Associated Diseases","authors":"Du-Bois Asante ,&nbsp;Gideon Akuamoah Wiafe ,&nbsp;Korantema Mawuena Tsegah ,&nbsp;Nelson Kwabla Domey","doi":"10.1016/j.ccmp.2023.100122","DOIUrl":"10.1016/j.ccmp.2023.100122","url":null,"abstract":"<div><h3>Background</h3><p>In the presence of a stimulus that disrupts homeostasis, the body elicits a response known as inflammation. The inflammatory response is expected to restore the normal functioning of the body and initiate healing where necessary. However, the persistent activity of acute inflammation results in chronic inflammation which causes adverse consequences associated with diseases such as diabetes and arthritis. In traditional medical practice, <em>Vernonia amygdalina</em> is used to treat several ailments such as malaria, fever, diabetes, and inflammatory conditions such as those related to pain and swelling.</p></div><div><h3>Objective</h3><p>This review seeks to explore and discuss the therapeutic benefits of <em>V. amygdalina</em> in the treatment of inflammation and its associated diseases.</p></div><div><h3>Methods</h3><p>We reviewed the scientific literature indexed in PubMed, ScienceDirect and Springer, and discussed the reported anti-inflammatory properties of <em>V. amygdalina</em> and its curative activity in inflammation-associated diseases.</p></div><div><h3>Results</h3><p>A total of 30 published articles were identified describing the therapeutic effect of <em>V. amygdalina</em> in predominately experimental models. The anti-inflammatory properties of <em>V. amygdalina</em> have been linked to the presence of bioactive phytoconstituents predominantly present in the leaves of the plant.</p></div><div><h3>Conclusions</h3><p>Multiple studies have demonstrated that the aqueous and ethanolic extracts of <em>V. amygdalina</em> can inhibit the production of proinflammatory cytokines and enzymes in inflammatory cells, reducing inflammation and its associated complications. We critically appraise the current evidence, and discuss the potential use of this medicinal plant in the treatment of inflammatory conditions.</p></div>","PeriodicalId":72608,"journal":{"name":"Clinical complementary medicine and pharmacology","volume":"4 1","pages":"Article 100122"},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S277237122300044X/pdfft?md5=d13fc61925d0578c34d556bf71082e49&pid=1-s2.0-S277237122300044X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139303756","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
Reviving Fertility: Phytochemicals as Natural Allies in the Fight against Non-genetic Male Infertility 恢复生育能力:植物化学物质是对抗非遗传性男性不育症的天然盟友
Pub Date : 2024-03-01 Epub Date: 2024-01-17 DOI: 10.1016/j.ccmp.2024.100128
Vivek P. Chavda , Shreya S Sonak , Pankti C. Balar , Krupa Vyas , Pranali Palandurkar , Komal Mule , Krishna Patel , Vivek Hala , Dixa A. Vaghela , Devarshi Acharya , Akta Vaishnav , Jimil Gandhi , Vasso Apostolopoulos

Background

Male infertility poses a growing challenge to the healthcare system, with its prevalence on the rise. Unhealthy lifestyle, food, and addictions such as smoking, alcoholism, etc. accelerate the occurrence. While several approaches are being investigated to prevent and treat this condition, each therapeutic approach has its drawbacks. Traditional medications continue to play a crucial role in the healthcare system. In recent years, there has been a shift towards determining the efficacy of phytochemicals (or, herbal drugs) as remedies.

Objective

To evaluate the effect of various herbs, plant, metabolites, or a part of plant in management of non-genetic male infertility.

Methods

The male infertility-associated keywords were searched in PubMed, excluding those non-English writen papers. A total of 146 pertinent and closely connected records were included for full reading and inclusion in the systemic evaluation.

Results

The manuscript focuses on individual herbal drug components, their active ingredients, their role in improving the condition and quality of life, and decreasing the prevalence of male infertility.

Conclusion

Herbal medicinal plants show promising outcomes to treat male infertility. Herbal alternatives are appealing and have regained popularity. The future holds promise for some of these herbal treatments to advance with many showing improved outcomes in males with infertility issues.

背景男性不育症对医疗系统构成了日益严峻的挑战,其发病率呈上升趋势。不健康的生活方式、食物以及吸烟、酗酒等不良嗜好加速了不育症的发生。虽然目前正在研究多种方法来预防和治疗这种疾病,但每种治疗方法都有其缺点。传统药物仍然在医疗保健系统中发挥着重要作用。目的 评价各种草药、植物、代谢物或植物的一部分在治疗非遗传性男性不育症中的效果。方法 在 PubMed 上搜索与男性不育症相关的关键词,排除非英文撰写的论文。结果手稿重点关注了单个草药成分、其有效成分、在改善病情和生活质量以及降低男性不育症发病率方面的作用。草药替代品很有吸引力,并重新受到欢迎。未来,其中一些草药疗法有望取得进展,许多草药疗法显示出对男性不育症患者有更好的疗效。
{"title":"Reviving Fertility: Phytochemicals as Natural Allies in the Fight against Non-genetic Male Infertility","authors":"Vivek P. Chavda ,&nbsp;Shreya S Sonak ,&nbsp;Pankti C. Balar ,&nbsp;Krupa Vyas ,&nbsp;Pranali Palandurkar ,&nbsp;Komal Mule ,&nbsp;Krishna Patel ,&nbsp;Vivek Hala ,&nbsp;Dixa A. Vaghela ,&nbsp;Devarshi Acharya ,&nbsp;Akta Vaishnav ,&nbsp;Jimil Gandhi ,&nbsp;Vasso Apostolopoulos","doi":"10.1016/j.ccmp.2024.100128","DOIUrl":"10.1016/j.ccmp.2024.100128","url":null,"abstract":"<div><h3>Background</h3><p>Male infertility poses a growing challenge to the healthcare system, with its prevalence on the rise. Unhealthy lifestyle, food, and addictions such as smoking, alcoholism, etc. accelerate the occurrence. While several approaches are being investigated to prevent and treat this condition, each therapeutic approach has its drawbacks. Traditional medications continue to play a crucial role in the healthcare system. In recent years, there has been a shift towards determining the efficacy of phytochemicals (or, herbal drugs) as remedies.</p></div><div><h3>Objective</h3><p>To evaluate the effect of various herbs, plant, metabolites, or a part of plant in management of non-genetic male infertility.</p></div><div><h3>Methods</h3><p>The male infertility-associated keywords were searched in PubMed, excluding those non-English writen papers. A total of 146 pertinent and closely connected records were included for full reading and inclusion in the systemic evaluation.</p></div><div><h3>Results</h3><p>The manuscript focuses on individual herbal drug components, their active ingredients, their role in improving the condition and quality of life, and decreasing the prevalence of male infertility.</p></div><div><h3>Conclusion</h3><p>Herbal medicinal plants show promising outcomes to treat male infertility. Herbal alternatives are appealing and have regained popularity. The future holds promise for some of these herbal treatments to advance with many showing improved outcomes in males with infertility issues.</p></div>","PeriodicalId":72608,"journal":{"name":"Clinical complementary medicine and pharmacology","volume":"4 1","pages":"Article 100128"},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772371224000019/pdfft?md5=083ee448ca43e6b94fc8fdf1b3b9c542&pid=1-s2.0-S2772371224000019-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139632996","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
The Effect of Xu's Influenza Decoction Combined with Oseltamivir on Influenza A: A Propensity Score Matching Study 徐流感汤联合奥司他韦治疗甲型流感疗效的倾向性评分匹配研究。
Pub Date : 2024-03-01 Epub Date: 2023-08-31 DOI: 10.1016/j.ccmp.2023.100113
Tianxi Chen , Shuyan Fu , Fengyuan Tian , Qiushuang Li , Hongyu Ling , Yijie Lou , Jun Tang , Hong Zheng

Background

The resurgence of seasonal influenza virus circulation has been seen in 2021–2022 after the temporary suppression in 2020–2021. Neuraminidase inhibitors (NAIs) are widely applied in the clinical treatment of influenza A despite several limitations.

Objective

To access the efficacy of Xu's influenza decoction (XID) in combination therapy with oseltamivir for the treatment of influenza A.

Methods

In this retrospective cohort study, the eligible participants were diagnosed with influenza A between June 1, 2018, and May 30, 2022, in the First Affiliated Hospital of Zhejiang Chinese Medical University. According to whether Xu's influenza decoction was applied, patients were divided into two groups: treated with or without XID. Propensity score matching (PSM) was used to further adjust the covariates between groups. The primary outcome was to compare time to defervescence via K-M curves, Breslow tests, and Cox regression analysis. In Cox proportional hazards model, a univariate analysis was performed to obtain preliminary results, while a further multivariate analysis was conducted to study the independent factors that influence defervescence. Subgroup analysis was conducted according to body temperature and time from onset to admission. The secondary outcome consisted of routine blood and C-reactive protein (CRP), length of stay, and medical costs.

Results

A total of 336 patients with influenza A were enrolled in this study (i.e., 163 patients in the XID+oseltamivir group; 173 patients in the oseltamivir group). After 1:1 matching via PSM, 230 patients meeting the criteria were included in the analysis, with 115 in each arm. The XID+oseltamivir group had shorter time to defervescence (36 h vs 44 h, P = 0.011), shorter length of stay (3 days vs 4 days, P = 0.018), and higher defervescence possibility (HR=1.384, 95%CI: 1.054–1.818). Subgroup analysis indicated that for patients during non-window period (≥ 48 h) with medium-grade fever (38.1℃–39℃), the XID+oseltamivir combination therapy reduced time to defervescence (P = 0.04995/0.004) with a higher defervescence possibility (HR=1.524/1.683). Meanwhile, there's no statistical significance but observable trends of the XID+oseltamivir group in the lower medical costs (3068.07 yuan vs 3120.68 yuan), the lower neutrophils% (48.53% vs 51.00%) and the higher lymphocyte% (39.83% vs 37.72%).

Conclusion

The combination of XID and oseltamivir can shorten the time to defervescence and length of stay in influenza A. Its antipyretic effect is mainly reflected in the medium-grade and non-window periods.

背景:在2020-2021年短暂抑制之后,2021-2022年季节性流感病毒传播再次抬头。神经氨酸酶抑制剂(NAIs)广泛应用于甲型流感的临床治疗,尽管存在一些局限性。目的探讨徐氏流感汤联合奥司他韦治疗甲型流感的疗效。方法本回顾性队列研究纳入2018年6月1日至2022年5月30日在浙江中医药大学第一附属医院确诊的甲型流感患者。根据是否应用徐氏流感汤,将患者分为两组:加用和不加用。采用倾向得分匹配(PSM)进一步调整组间协变量。主要结局是通过K-M曲线、Breslow检验和Cox回归分析比较时间与退热。在Cox比例风险模型中,单因素分析获得初步结果,并进一步进行多因素分析,研究影响退热的独立因素。根据患者体温及发病至入院时间进行亚组分析。次要结果包括常规血和c反应蛋白(CRP)、住院时间和医疗费用。结果共有336例甲型流感患者入组,其中XID+奥司他韦组163例;奥司他韦组173例患者)。经PSM 1:1匹配后,230例符合标准的患者纳入分析,每组115例。XID+奥司他韦组退热时间较短(36 h vs 44 h, P = 0.011),住院时间较短(3 d vs 4 d, P = 0.018),退热可能性较高(HR=1.384, 95%CI: 1.054 ~ 1.818)。亚组分析显示,对于中度发热(38.1℃~ 39℃)的非窗口期(≥48 h)患者,XID+奥司他韦联合治疗可缩短退热时间(P = 0.04995/0.004),退热可能性更高(HR=1.524/1.683)。同时,XID+奥司他韦组在较低的医疗费用(3068.07元对320.68元)、较低的中性粒细胞百分比(48.53%对51.00%)和较高的淋巴细胞百分比(39.83%对37.72%)方面无统计学意义,但有明显的趋势。结论XID联合奥司他韦可缩短甲流退热时间和住院时间,其退热作用主要体现在中度和非窗口期。
{"title":"The Effect of Xu's Influenza Decoction Combined with Oseltamivir on Influenza A: A Propensity Score Matching Study","authors":"Tianxi Chen ,&nbsp;Shuyan Fu ,&nbsp;Fengyuan Tian ,&nbsp;Qiushuang Li ,&nbsp;Hongyu Ling ,&nbsp;Yijie Lou ,&nbsp;Jun Tang ,&nbsp;Hong Zheng","doi":"10.1016/j.ccmp.2023.100113","DOIUrl":"10.1016/j.ccmp.2023.100113","url":null,"abstract":"<div><h3>Background</h3><p>The resurgence of seasonal influenza virus circulation has been seen in 2021–2022 after the temporary suppression in 2020–2021. Neuraminidase inhibitors (NAIs) are widely applied in the clinical treatment of influenza A despite several limitations.</p></div><div><h3>Objective</h3><p>To access the efficacy of Xu's influenza decoction (XID) in combination therapy with oseltamivir for the treatment of influenza A.</p></div><div><h3>Methods</h3><p>In this retrospective cohort study, the eligible participants were diagnosed with influenza A between June 1, 2018, and May 30, 2022, in the First Affiliated Hospital of Zhejiang Chinese Medical University. According to whether Xu's influenza decoction was applied, patients were divided into two groups: treated with or without XID. Propensity score matching (PSM) was used to further adjust the covariates between groups. The primary outcome was to compare time to defervescence via K-M curves, Breslow tests, and Cox regression analysis. In Cox proportional hazards model, a univariate analysis was performed to obtain preliminary results, while a further multivariate analysis was conducted to study the independent factors that influence defervescence. Subgroup analysis was conducted according to body temperature and time from onset to admission. The secondary outcome consisted of routine blood and C-reactive protein (CRP), length of stay, and medical costs.</p></div><div><h3>Results</h3><p>A total of 336 patients with influenza A were enrolled in this study (i.e., 163 patients in the XID+oseltamivir group; 173 patients in the oseltamivir group). After 1:1 matching via PSM, 230 patients meeting the criteria were included in the analysis, with 115 in each arm. The XID+oseltamivir group had shorter time to defervescence (36 h <em>vs</em> 44 h, <em>P</em> = 0.011), shorter length of stay (3 days <em>vs</em> 4 days, <em>P</em> = 0.018), and higher defervescence possibility (HR=1.384, 95%CI: 1.054–1.818). Subgroup analysis indicated that for patients during non-window period (≥ 48 h) with medium-grade fever (38.1℃–39℃), the XID+oseltamivir combination therapy reduced time to defervescence (<em>P</em> = 0.04995/0.004) with a higher defervescence possibility (HR=1.524/1.683). Meanwhile, there's no statistical significance but observable trends of the XID+oseltamivir group in the lower medical costs (3068.07 yuan <em>vs</em> 3120.68 yuan), the lower neutrophils% (48.53% <em>vs</em> 51.00%) and the higher lymphocyte% (39.83% <em>vs</em> 37.72%).</p></div><div><h3>Conclusion</h3><p>The combination of XID and oseltamivir can shorten the time to defervescence and length of stay in influenza A. Its antipyretic effect is mainly reflected in the medium-grade and non-window periods.</p></div>","PeriodicalId":72608,"journal":{"name":"Clinical complementary medicine and pharmacology","volume":"4 1","pages":"Article 100113"},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47324579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An in vitro Anti-urolithiasis Activity of a Herbal Formulation: Spinacia oleracea L. and Coriandrum sativum L. 一种草药配方的体外抗尿路结石活性:菠菜(Spinacia oleracea L.)和芫荽(Coriandrum sativum L.
Pub Date : 2024-03-01 Epub Date: 2023-11-18 DOI: 10.1016/j.ccmp.2023.100124
Sumathy Raj , Monica Shree Gnana Soundara Rajan , Suganthi Ramasamy , Rimal Isaac Rajamony Suthies Goldy , Ramathilaga Ariyamuthu , Monisha Sudhagar , Sakthivel Gandhi , Prakash Shoba , Manikandan Gurusamy

Background

Hard mineral and acid salt deposits that clump together in concentrated urine are known as kidney stones. A complicated chain of physicochemical events, including hyper saturation, nucleation, growth, aggregation, and retention in the urinary tract, leads to urolithiasis, the third most prevalent urinary tract issue. Numerous traditional medications and therapies are less successful in treating urolithiasis and frequently cause recurrences.

Objective

The present study is focused on evaluating the anti-urolithiasis activities of the polyherbal formulation prepared from Spinacia oleracea L. and Coriandrum sativum L. seeds.

Methods

To evaluating the anti-urolithiasis activities of the polyherbal formulation prepared from S. oleracea and C. sativum seeds against oxalate crystals by employing an in vitro inhibition, aggregation, and nucleation assay, employing a spectrophotometer followed by microscopic observation, and further monitored by egg semipermeable membrane model, using cystone as a standard drug.

Results

In the present work, the alkaloids, glycosides, flavonoids, glycosides, phenols, saponins, steroids, tannins, terpenoids, and triterpenoids were found in the extracts of S. oleracea and C. sativum. The in vitro assays in the present study clearly indicated that all the mixture extracts readily prevented crystal nucleation, growth and aggregation. The aqueous extract of the mixture inhibited significant inhibitory potential against the crystallization process.

Conclusion

It can be said that the phyto-constituents enriched homemade preparation possibly will be used as a medication for the management of kidney stones by dissolving the oxalate stone in the kidney.

背景在浓缩尿液中凝结成块的坚硬矿物质和酸性盐沉淀物被称为肾结石。一连串复杂的物理化学过程,包括高饱和度、成核、生长、聚集以及在尿路中的滞留,导致了尿路结石这一第三大泌尿系统疾病。许多传统药物和疗法在治疗尿路结石方面都不太成功,而且经常导致复发。采用体外抑制、聚集和成核试验,使用分光光度计,然后进行显微镜观察,并以鸡蛋半透膜模型为标准药物,进一步监测其抗草酸盐结晶的活性。结果在本研究中,发现 S. oleracea 和 C. sativum 的提取物中含有生物碱、苷类、黄酮类、糖苷类、酚类、皂苷类、甾体类、单宁酸、萜类和三萜类化合物。本研究中的体外试验清楚地表明,所有混合物提取物都能很容易地阻止晶体成核、生长和聚集。结论可以说,富含植物成分的自制制剂可以通过溶解肾脏中的草酸盐结石来治疗肾结石。
{"title":"An in vitro Anti-urolithiasis Activity of a Herbal Formulation: Spinacia oleracea L. and Coriandrum sativum L.","authors":"Sumathy Raj ,&nbsp;Monica Shree Gnana Soundara Rajan ,&nbsp;Suganthi Ramasamy ,&nbsp;Rimal Isaac Rajamony Suthies Goldy ,&nbsp;Ramathilaga Ariyamuthu ,&nbsp;Monisha Sudhagar ,&nbsp;Sakthivel Gandhi ,&nbsp;Prakash Shoba ,&nbsp;Manikandan Gurusamy","doi":"10.1016/j.ccmp.2023.100124","DOIUrl":"https://doi.org/10.1016/j.ccmp.2023.100124","url":null,"abstract":"<div><h3>Background</h3><p>Hard mineral and acid salt deposits that clump together in concentrated urine are known as kidney stones. A complicated chain of physicochemical events, including hyper saturation, nucleation, growth, aggregation, and retention in the urinary tract, leads to urolithiasis, the third most prevalent urinary tract issue. Numerous traditional medications and therapies are less successful in treating urolithiasis and frequently cause recurrences.</p></div><div><h3>Objective</h3><p>The present study is focused on evaluating the anti-urolithiasis activities of the polyherbal formulation prepared from <em>Spinacia oleracea</em> L<em>.</em> and <em>Coriandrum sativum</em> L. seeds.</p></div><div><h3>Methods</h3><p>To evaluating the anti-urolithiasis activities of the polyherbal formulation prepared from <em>S. oleracea</em> and <em>C. sativum</em> seeds against oxalate crystals by employing an <em>in vitro</em> inhibition, aggregation, and nucleation assay, employing a spectrophotometer followed by microscopic observation, and further monitored by egg semipermeable membrane model, using cystone as a standard drug.</p></div><div><h3>Results</h3><p>In the present work, the alkaloids, glycosides, flavonoids, glycosides, phenols, saponins, steroids, tannins, terpenoids, and triterpenoids were found in the extracts of <em>S. oleracea</em> and <em>C. sativum</em>. The <em>in vitro</em> assays in the present study clearly indicated that all the mixture extracts readily prevented crystal nucleation, growth and aggregation. The aqueous extract of the mixture inhibited significant inhibitory potential against the crystallization process.</p></div><div><h3>Conclusion</h3><p>It can be said that the phyto-constituents enriched homemade preparation possibly will be used as a medication for the management of kidney stones by dissolving the oxalate stone in the kidney.</p></div>","PeriodicalId":72608,"journal":{"name":"Clinical complementary medicine and pharmacology","volume":"4 1","pages":"Article 100124"},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772371223000463/pdfft?md5=046c7ab340a7c93285826e0964d3a469&pid=1-s2.0-S2772371223000463-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139548979","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
Diuretic Activity of Ethanol Extract of Piper attenuatum Leaves Might Be Due to the Inhibition of Carbonic Anhydrase Enzyme: An in vivo and in silico Investigation 胡椒叶乙醇提取物的利尿活性可能与抑制碳酸酐酶有关:体内和体外研究
Pub Date : 2024-03-01 Epub Date: 2023-10-17 DOI: 10.1016/j.ccmp.2023.100117
Shikha Sharma , Gaurav Kumar , Nitin Kumar , Neeraj K. Sethiya , Dheeraj Bisht

Background

Ayurvedic system of medicine is well established for prevention and treatment of renal problems. There are vast number of medicinal plants mentioned in Ayurvedic system of medicine, including Piper attenuatum Buch.-Ham. ex Miq., are known to exhibits diuretic properties.

Objective

To investigate possible mechanism and diuretic activity of ethanol extract of P. attenuatum leaves.

Methods

Present study reports an in vivo diuretic activity of ethanol extracts of P. attenuatum leaves.Twenty-four Sprague-Dawley male rats were deprived from food and water for 20 h, followed by being divided into four groups to receive normal saline, Furosemide, and two doses of the ethanol extract, respectively. Further, the ethanol extract were subjected for prelimnary phytochemical screening test, and analytical investigation was performed via high-performance thin-layer chromatography (HPTLC), followed by effectiveness exploration of putative bioactive compounds from P. attenuatum against human carbonic anhydrase (hCA) enzyme using molecular docking tool.

Results

During phytochemicals screening, several groups of compounds such as amides, terpenoids, proteins, flavonoids, and glycosides have been identified. Further, HPTLC reveals presence of carbohydrates, proteins, amino acids, steroids, alkaloids, flavonoids, tannins, glycosides, and terpenoids. Significant diuretic action was revealed for both 200 mg/kg bw and 400 mg/kg bw of ethanol extract of P. attenuatum leaves. Interestingly, molecular docking analysis demonstrated greater binding affinity of compounds such as Cepharadione A, Norcepharadione B, Galbelgin, Crotepoxide, and Pipoxide chlorohydrin out of total 23 studied compounds against hCA isoforms (a key biomarker for diuretic) and score is comparable with standard drug Acetazolamide.

Conclusion

It was concluded from the present studies that ethanol extract of P. attenuatum leaves exhibits significant diuretic activity. The activity may be correlated due to the presence of Cepharadione A, Norcepharadione B, Galbelgin, Crotepoxide, and Pipoxide chlorohydrin as key component responsible for inhibition of hCA isoforms.

吠陀医学体系在预防和治疗肾脏问题方面已经建立了良好的体系。在阿育吠陀医学体系中,有大量的药用植物被提及,其中包括风笛草(Piper attenuatum)。进行筛选。已知具有利尿作用。目的探讨黄菖蒲叶乙醇提取物的利尿作用及其可能机制。方法本研究报道了黄菖蒲叶乙醇提取物的体内利尿作用。24只雄性Sprague-Dawley大鼠不食不水20小时,然后分为四组,分别给予生理盐水、速尿和两剂乙醇提取物。此外,对乙醇提取物进行初步的植物化学筛选试验,并通过高效薄层色谱(HPTLC)进行分析研究,然后利用分子对接工具对推定的垂穗藤抗人碳酸酐酶(hCA)酶活性化合物进行有效性探索。结果在植物化学物质筛选过程中,已鉴定出酰胺类、萜类、蛋白质类、黄酮类和苷类等化合物。此外,HPTLC还显示了碳水化合物、蛋白质、氨基酸、类固醇、生物碱、类黄酮、单宁、糖苷和萜类化合物的存在。200 mg/kg bw和400 mg/kg bw的乙醇提取物均有显著的利尿作用。有趣的是,分子对接分析表明,在所研究的23种化合物中,Cepharadione A、Norcepharadione B、Galbelgin、Crotepoxide和Pipoxide氯醇等化合物对hCA异构体(利尿剂的关键生物标志物)的结合亲和力更高,得分与标准药物Acetazolamide相当。结论从本研究可以看出,黄精叶乙醇提取物具有明显的利尿作用。该活性可能与头孢地酮A、去甲头孢地酮B、Galbelgin、Crotepoxide和Pipoxide氯醇作为抑制hCA亚型的关键成分的存在有关。
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引用次数: 0
Phytochemical Screening and Evaluation of Pharmacological Potential of Baliospermum solanifolium Leaf Extract 秃杉叶提取物的植物化学筛选和药理潜力评估
Pub Date : 2024-03-01 Epub Date: 2023-11-22 DOI: 10.1016/j.ccmp.2023.100123
Amit Mazumder, Rabindra Nath Acharyya, Milton Kumar Kundu, Pritam Kundu, Md. Amirul Islam, Md. Mustafizur Rahman

Background

Baliospermum solanifolium is a traditional medicinal plant, locally known as “dantigaacha” from Euphorbiaceae family, and has been used in different diseases treatments likes helminthiasis, skin diseases, diabetes, snake-bite, and leukoderma.

Objectives

Depending on the traditional uses of B. solanifolium and the lack of scientific works, we aimed to conduct some pharmacological tests on its leaves.

Methods

Active constituents of B. solanifolium were assessed by qualitative screening. DPPH (2,2-diphenyl-1-picrylhydrazyl) was used for free radical scavenging assay. Behavioral change and mortality rate were used as indicators to assess the toxicity of B. solanifolium. The antidiabetic potential was evaluated by oral glucose tolerance test (OGTT) and alpha-glucosidase enzyme inhibitory activity. In antidiarrheal activity, castor oil-induced mice were used. Antibacterial test was carried out by disk diffusion assay and MIC determination. Furthermore, analgesic activity was done by acetic acid-induced writhing method.

Results

B. solanifolium contains alkaloids, carbohydrates, glycosides, flavonoids, tannis, phenolics etc. Acute toxicity test ensured the safety of the extract. In DPPH, the extract showed antioxidant activity with an IC50 (concentration needed to scavenge 50% DPPH) value of 61.65 µg/mL. Total phenolic, flavonoid and tannin contents were determined as 124 mg GAE/g, 440 mg QE/g and 344 mg GAE/g dried extract, respectively. In OGTT, the extract reduced the blood glucose level significantly. In the alpha-glucosidase inhibitory activity, the plant showed a concentration-dependent reduction of the enzyme at IC50 of 8.53 mg/mL. In the antidiarrheal test, B. solanifolium inhibit defecation 30.69% and 53.41% at dose 250 mg/kg and 500 mg/kg, respectively. The extract also showed antibacterial activity against four bacterial strains in the disk diffusion method and minimum inhibitory concentration (MIC) values were 62.5 µg/mL, 62.5 µg/mL, 125 µg/mL and 62.5 µg/mL against four bacterial strains, independently. In analgesic activity test, the extract reduced the writhing impulse up to 48.51% at 500 mg/kg dose.

Conclusion

B. solanifolium contains many active phytoconstituents which may be the possible candidates for targeting diabetes, microbial infection, diarrhea and pain in the future.

背景大戟科植物大戟(Baliospermum solanifolium)是一种传统的药用植物,在当地被称为 "dantigaacha",被用于治疗各种疾病,如蠕虫病、皮肤病、糖尿病、蛇咬伤和白皮病等。采用 DPPH(2,2-二苯基-1-苦基肼)进行自由基清除试验。行为变化和死亡率是评估 B. solanifolium 毒性的指标。抗糖尿病潜力通过口服葡萄糖耐量试验(OGTT)和α-葡萄糖苷酶抑制活性进行评估。在止泻活性方面,使用了蓖麻油诱导的小鼠。抗菌试验是通过盘扩散试验和 MIC 测定进行的。此外,镇痛活性是通过醋酸诱导蠕动法进行的。急性毒性试验确保了提取物的安全性。在 DPPH 试验中,提取物显示出抗氧化活性,IC50(清除 50% DPPH 所需的浓度)值为 61.65 µg/mL。总酚、类黄酮和单宁的含量分别为 124 毫克 GAE/克、440 毫克 QE/ 克和 344 毫克 GAE/克。在 OGTT 试验中,提取物能显著降低血糖水平。在α-葡萄糖苷酶抑制活性中,该植物显示出浓度依赖性的酶抑制作用,IC50 为 8.53 毫克/毫升。在止泻试验中,当剂量为 250 毫克/千克和 500 毫克/千克时,B. solanifolium 对排便的抑制率分别为 30.69% 和 53.41%。在盘扩散法中,该提取物还对四种细菌菌株具有抗菌活性,对四种细菌菌株的最小抑菌浓度(MIC)分别为 62.5 µg/mL、62.5 µg/mL、125 µg/mL和 62.5 µg/mL。在镇痛活性测试中,500 毫克/千克剂量的提取物可降低 48.51% 的蠕动冲动。
{"title":"Phytochemical Screening and Evaluation of Pharmacological Potential of Baliospermum solanifolium Leaf Extract","authors":"Amit Mazumder,&nbsp;Rabindra Nath Acharyya,&nbsp;Milton Kumar Kundu,&nbsp;Pritam Kundu,&nbsp;Md. Amirul Islam,&nbsp;Md. Mustafizur Rahman","doi":"10.1016/j.ccmp.2023.100123","DOIUrl":"10.1016/j.ccmp.2023.100123","url":null,"abstract":"<div><h3>Background</h3><p><em>Baliospermum solanifolium</em> is a traditional medicinal plant, locally known as “dantigaacha” from Euphorbiaceae family, and has been used in different diseases treatments likes helminthiasis, skin diseases, diabetes, snake-bite, and leukoderma.</p></div><div><h3>Objectives</h3><p>Depending on the traditional uses of <em>B. solanifolium</em> and the lack of scientific works<em>,</em> we aimed to conduct some pharmacological tests on its leaves.</p></div><div><h3>Methods</h3><p>Active constituents of <em>B. solanifolium</em> were assessed by qualitative screening. DPPH (2,2-diphenyl-1-picrylhydrazyl) was used for free radical scavenging assay. Behavioral change and mortality rate were used as indicators to assess the toxicity of <em>B. solanifolium</em>. The antidiabetic potential was evaluated by oral glucose tolerance test (OGTT) and alpha-glucosidase enzyme inhibitory activity. In antidiarrheal activity, castor oil-induced mice were used. Antibacterial test was carried out by disk diffusion assay and MIC determination. Furthermore, analgesic activity was done by acetic acid-induced writhing method.</p></div><div><h3>Results</h3><p><em>B. solanifolium</em> contains alkaloids, carbohydrates, glycosides, flavonoids, tannis, phenolics etc. Acute toxicity test ensured the safety of the extract. In DPPH, the extract showed antioxidant activity with an IC<sub>50</sub> (concentration needed to scavenge 50% DPPH) value of 61.65 µg/mL. Total phenolic, flavonoid and tannin contents were determined as 124 mg GAE/g, 440 mg QE/g and 344 mg GAE/g dried extract, respectively. In OGTT, the extract reduced the blood glucose level significantly. In the alpha-glucosidase inhibitory activity, the plant showed a concentration-dependent reduction of the enzyme at IC<sub>50</sub> of 8.53 mg/mL. In the antidiarrheal test, <em>B. solanifolium</em> inhibit defecation 30.69% and 53.41% at dose 250 mg/kg and 500 mg/kg, respectively. The extract also showed antibacterial activity against four bacterial strains in the disk diffusion method and minimum inhibitory concentration (MIC) values were 62.5 µg/mL, 62.5 µg/mL, 125 µg/mL and 62.5 µg/mL against four bacterial strains, independently. In analgesic activity test, the extract reduced the writhing impulse up to 48.51% at 500 mg/kg dose.</p></div><div><h3>Conclusion</h3><p><em>B. solanifolium</em> contains many active phytoconstituents which may be the possible candidates for targeting diabetes, microbial infection, diarrhea and pain in the future.</p></div>","PeriodicalId":72608,"journal":{"name":"Clinical complementary medicine and pharmacology","volume":"4 1","pages":"Article 100123"},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772371223000451/pdfft?md5=0e5098eb8f5de5fafb318b7a58dbc7fb&pid=1-s2.0-S2772371223000451-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139292065","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
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Clinical complementary medicine and pharmacology
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