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Maclura tinctoria (L.) D. Don ex Steud. (Moraceae): a review of the advances in ethnobotanical knowledge, phytochemical composition, and pharmacological potential Maclura tinctoria (L.)Don ex Steud。(桑科):民族植物学知识,植物化学成分和药理潜力的进展综述
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-06-20 DOI: 10.1007/s13596-024-00764-z
Patricia Quintero-Rincón, Yina Pájaro-González, Fredyc Diaz-Castillo

Maclura tinctoria (Moraceae), commonly known as dinde, is a lactescent tree of significant economic importance with extensive ethnomedicinal and ethnobotanical applications. Among native populations in the Neotropics, dinde is used to address diverse forms of inflammatory arthritis, along with ailments stemming from viral, bacterial, or fungal origins. Its efficacy stands out notably in the treatment of conditions affecting the buccal cavity, respiratory tract, and venereal infections. These medicinal attributes have spurred investigations into their potential for developing nutraceuticals and pharmacological agents. Also, dinde has a commercial appeal intertwined with the remarkable qualities of its wood, which include the resistance to moisture and termites. This review consolidates information encompassing peer-reviewed articles from major scientific databases such as Science Direct, Scopus, Springer, PubMed, and Google Scholar. The review spans fifty-four phytocompounds, characterized by remarkable structural complexity and identified from the year 2000 onward. These compounds are categorized into flavones, isoflavones, flavonols, flavanols, flavanones, chalcones, and xanthones, where a significant portion exhibiting glycosylation or prenylation. Additionally, phenolic acids and condensed tannins contribute to the chemical diversity of this species. This comprehensive review offers updated insights into the potential bioactivity of chemical constituents identified in this plant, elucidating findings derived from different studies employing both in vitro and in vivo assays.

Graphical abstract

moruca tinctoria (Moraceae),通常被称为dinde,是一种具有重要经济意义的乳龄树,具有广泛的民族医学和民族植物学应用。在新热带地区的土著居民中,丁丁被用来治疗各种形式的炎症性关节炎,以及由病毒、细菌或真菌引起的疾病。其疗效突出,特别是在治疗条件影响口腔,呼吸道和性病感染。这些药用特性促使人们对其开发营养保健品和药理学制剂的潜力进行了研究。此外,dinde具有商业吸引力,其木材的卓越品质交织在一起,包括防潮和抗白蚁。本综述整合了来自主要科学数据库(如Science Direct、Scopus、施普林格、PubMed和谷歌Scholar)的同行评议文章的信息。回顾了54种植物化合物,其特点是结构复杂,并从2000年开始鉴定。这些化合物可分为黄酮类、异黄酮类、黄酮醇类、黄烷醇类、黄烷酮类、查尔酮类和山酮类,其中大部分发生糖基化或烯酰化。此外,酚酸和浓缩单宁有助于该物种的化学多样性。这篇全面的综述为这种植物中鉴定的化学成分的潜在生物活性提供了最新的见解,阐明了来自体外和体内试验的不同研究结果。图形抽象
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引用次数: 0
Larvicidal and antiplasmodial studies of Eucalyptus camaldulensis (Myrtaceae) Leaf 桉树(桃金娘科)叶的杀幼虫剂和抗疟研究
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-06-18 DOI: 10.1007/s13596-024-00765-y
Stephen A. Adesida, Samuel A. Oguntimehin, Funmilayo G. Famuyiwa, Kolade O. Faloye, Seun B. Ogundele, Oyenike I. Bello, Oluyemi J. Oladiran, Ayobami J. Olusola, Adetola H. Adewole, Praise A. Adebayo, Maryam O. Oredola

Eucalyptus camaldulensis is a medicinal plant used as insect repellant and antimalarial agent in ethnomedicine. This study examined the antiplasmodial and larvicidal potential of E. camaldulensis leaf extract and also identified the plant extract's most active fraction(s). The acute oral toxicity test of the methanol extract was evaluated using Lorke’s method. The larvicidal assay was performed on the extract and partitioned fractions according to the 2005 World Health Organization guidelines, while the 4-day chemosuppressive and curative antimalarial assays were carried out against Plasmodium bergei bergei. Endosulphan and chloroquine (10 mg/kg) was used as the positive controls for the larvicidal and antiplasmodial assays, respectively, while tween 80 in normal saline (1%) was the negative control. The methanol leaf extract of EC showed good larvicidal activity across all tested concentrations (LC50 3.79 ± 0.64 mg/mL), while the aqueous fraction with LC50 of 2.80 ± 0.14 mg/mL was the most active. Its acute toxicity test showed it was safe up to 5000 mg/kg. The extract significantly increased dose-dependent antiplasmodial activity for the chemosuppressive and curative models (p < 0.05) than the negative control. At 800 mg/kg, EC gave chemosuppressive (53.69 ± 1.62%) and curative (81.26 ± 1.87%) activities, which was significantly lower than that of 10 mg/kg chloroquine (82.00 ± 0.57% and 92.51 ± 0.22% respectively). The aqueous partitioned fraction gave the highest chemosuppression (73.84 ± 2.73%) at 80 mg/kg, which was comparable to the positive control. The methanol extract of E. camaldulensis leaf is a promising larvicidal and antimalarial agent that could proffer a solution to vector control and the prevalence of malaria.

桉树是一种药用植物,在民族医药中被用作驱虫剂和抗疟药。本研究考察了喀麦隆桉叶提取物的抗疟和杀幼虫剂潜力,并确定了该植物提取物中最具活性的部分。采用 Lorke 法评估了甲醇提取物的急性口服毒性试验。根据 2005 年世界卫生组织指南,对萃取物和分配馏分进行了杀幼虫试验,并对贝氏疟原虫进行了为期 4 天的化学抑制和治疗性抗疟试验。杀幼虫剂和抗疟药物试验分别使用内吸磷和氯喹(10 毫克/千克)作为阳性对照,而正常生理盐水(1%)中的吐温 80 则作为阴性对照。氨基甲酸乙酯的甲醇叶提取物在所有测试浓度下都显示出良好的杀幼虫活性(半数致死浓度为 3.79 ± 0.64 毫克/毫升),而水提取物的半数致死浓度为 2.80 ± 0.14 毫克/毫升,活性最高。急性毒性测试表明,该提取物在 5000 毫克/千克以下是安全的。与阴性对照组相比,该提取物在化学抑制和治疗模型中的剂量依赖性抗疟活性明显提高(p < 0.05)。在 800 毫克/千克的剂量下,氨基甲酸乙酯具有化学抑制(53.69 ± 1.62%)和治疗(81.26 ± 1.87%)活性,明显低于 10 毫克/千克氯喹(分别为 82.00 ± 0.57% 和 92.51 ± 0.22%)。在 80 毫克/千克的剂量下,水分配馏分的化学抑制率最高(73.84 ± 2.73%),与阳性对照组相当。E.camaldulensis叶片的甲醇提取物是一种很有前景的杀幼虫剂和抗疟药剂,可为病媒控制和疟疾流行提供解决方案。
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引用次数: 0
Cecropia obtusifolia: phytopharmacology and its potential use in the treatment of diseases Cecropia obtusifolia:植物药理学及其在疾病治疗中的潜在用途
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-06-13 DOI: 10.1007/s13596-024-00756-z
Yolotl Moreno-Hernandez, Zendy Evelyn Olivo-Vidal, Xariss Miryam Sánchez-Chino, Angel Betanzos-Reyes, Benito Salvatierra-Izaba

Chronic non-communicable diseases are the primary cause of death globally, with infectious diseases following closely behind. Therefore, efforts are being made worldwide to combat and manage these diseases through the discovery of new treatments, including the exploration of natural products. Cecropia obtusifolia has gained attention due to its pharmacological properties, including hypotensive, hypoglycemic, hypolipidemic, and antimalarial effects. These properties have been attributed to the secondary metabolites present, such as chlorogenic acid, isoorientin, and flavonolignans. The plant has demonstrated the ability to lower blood glucose and lipids, reduce blood pressure, and exhibit antiplasmodial activity. Therefore, this report comprehensively reviews the pharmacological effects and potential applications in treating various illnesses. It aims to serve as a reference for further research and the use of this compound as a therapeutic agent.

Graphical abstract

慢性非传染性疾病是全球死亡的主要原因,传染病紧随其后。因此,全世界正在努力通过发现新的治疗方法,包括探索天然产物,来防治和管理这些疾病。由于其药理特性,包括降压、降血糖、降血脂和抗疟疾的作用,斜眼已经引起了人们的关注。这些特性归因于次生代谢物的存在,如绿原酸、异荭草苷和黄酮木质素。该植物已被证明具有降低血糖和血脂、降低血压和抗疟原虫活性的能力。因此,本文就其药理作用及其在治疗各种疾病中的潜在应用作一综述。旨在为进一步研究和使用该化合物作为治疗剂提供参考。图形抽象
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引用次数: 0
Unveiling the potential antibacterial mechanism of Melaleuca cajuputi leaf extract by cell morphology studies and molecular docking analysis 通过细胞形态学研究和分子对接分析揭示 Melaleuca cajuputi 叶提取物的潜在抗菌机制
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-06-04 DOI: 10.1007/s13596-024-00763-0
Musa Isah, Wan-Nor-Amilah Wan Abdul Wahab, Hasmah Abdullah, Shajarahtunnur Jamil, Mohd Dasuki Sul’ain, Abdullahi Ibrahim Uba, Gokhan Zengin, Dibyajit Lahiri, Hisham Atan Edinur, Wan Rosli Wan Ishak

The antimicrobial properties of the Melaleuca cajuputi plant have been documented. However, the underlying antimicrobial mechanisms remain relatively unexplored. Thus, this study aimed to investigate the antibacterial effects of M. cajuputi leaf extract against selected bacterial strains and unveil the potential antibacterial mechanisms of the most potent sub-fraction through time-kill assay, cell morphology studies, and molecular docking analysis. The fractions and sub-fractions were obtained from the methanolic extract of M. cajuputi leaf by bioassay-guided fractionation. The antibacterial activity was tested against Staphylococcus aureus, Streptococcus agalactiae, Klebsiella pneumoniae, and Escherichia coli using broth microdilution assay. The most potent sub-fraction, Melaleuca fraction 2d (MF2d), demonstrated remarkable antibacterial activity with MIC values ranging from 0.063 to 0.25 mg/mL and induced significant cellular damage against the tested bacteria. The chemical characterization of the most potent sub-fraction (MF2d) from methanolic extract of M. cajuputi leaf identified five (5) compounds with 2-isopropyl-10-methyl phenanthrene (83.09%) as the major component. In-silico molecular docking analysis revealed that all the docked ligands showed strong binding propensity towards target bacterial proteins, including DNA gyrase (PDB ID: 1ZI0), dihydropteroate synthase (PDB ID: 1AD1), and D-alanyl transferase (PDB ID: 6O93) with the binding energy ranging from − 6.0 to − 8.4 kcal/mol. The overall findings demonstrated the potential of the M. cajuputi plant as a valuable source of novel antibacterial agents.

Melaleuca cajuputi 植物的抗菌特性已有文献记载。然而,其潜在的抗菌机制相对来说仍有待探索。因此,本研究旨在通过时间致死试验、细胞形态学研究和分子对接分析,研究 M. cajuputi 叶提取物对所选细菌菌株的抗菌效果,并揭示最强亚馏分的潜在抗菌机制。通过生物测定指导下的分馏,从 M. cajuputi 叶的甲醇提取物中获得了馏分和子馏分。采用肉汤微量稀释法对金黄色葡萄球菌、无乳链球菌、肺炎克雷伯氏菌和大肠杆菌进行了抗菌活性测试。功效最强的子馏分,即白千层馏分 2d(MF2d),具有显著的抗菌活性,其 MIC 值介于 0.063 至 0.25 毫克/毫升之间,并能对受试细菌造成明显的细胞损伤。从 M. cajuputi 叶甲醇提取物中提取的最有效亚馏分(MF2d)的化学特征鉴定发现了五(5)种化合物,其中 2-异丙基-10-甲基菲(83.09%)是主要成分。硅内分子对接分析表明,所有对接配体都显示出与目标细菌蛋白的强烈结合倾向,包括 DNA 回旋酶(PDB ID:1ZI0)、二氢吡咯酸合成酶(PDB ID:1AD1)和 D-丙氨酰转移酶(PDB ID:6O93),结合能在 - 6.0 至 - 8.4 kcal/mol 之间。总体研究结果表明,M. cajuputi 植物具有作为新型抗菌剂宝贵来源的潜力。
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引用次数: 0
Survey the change of skin surface temperature at the face when using tonifying or dispersing acupuncture manipulations at dazhui acupoint in healthy volunteers 调查健康志愿者在大椎穴使用补法或散法针刺时面部皮肤表面温度的变化
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-06-03 DOI: 10.1007/s13596-024-00762-1
Dieu-Thuong Thi Trinh, Phuong-Quynh Ngoc Le, Minh-Man Pham Bui, Nguyen Lam Vuong

In addition to stimulating specific acupoints, acupuncture uses manipulations with varying effects. For Dazhui acupoint, tonifying acupuncture clears heat, while dispersing acupuncture dissipates it. This study aims to compare changes in facial skin temperature caused by these techniques in healthy volunteers. The single-blinded, randomized controlled trial involved 57 healthy volunteers aged 18–30, undergoing three sessions of acupuncture with a one-week interval. Participants were randomly assigned to three groups with different acupuncture sequences: sham-tonifying-dispersing, tonifying-dispersing-sham, and dispersing-sham-tonifying. Acupuncture sessions lasted 30 min, and facial skin temperatures were measured at five time points using a FLIR C5 thermal camera. We recorded that tonifying acupuncture at the Dazhui acupoint led to a significant increase from 34.30 °C (33.65–35.20 °C) to 35.40 °C (34.85–35.85 °C) in facial skin temperature while dispersing acupuncture led to a significant decrease from 34.90 °C (33.95–35.65 °C) to 34.00 °C (33.00–34.75 °C). Compared to the sham group, both tonifying and dispersing acupuncture showed significant differences in skin temperature. The variation in skin temperature between tonifying and dispersing acupuncture was also statistically significant. These results show that acupuncture at the Dazhui acupoint can influence facial skin temperature, establishing a relationship between this acupoint and facial physiology. Moreover, the contrasting skin temperature responses to tonifying and dispersing acupuncture techniques at Dazhui validate their distinct physiological effects.

除了刺激特定穴位外,针灸还使用具有不同效果的手法。对于大椎穴,补针可以清热,而散针可以散热。本研究旨在比较这些手法对健康志愿者面部皮肤温度的影响。这项单盲随机对照试验涉及 57 名 18-30 岁的健康志愿者,他们接受了三次针灸治疗,每次间隔一周。参与者被随机分配到三组,针刺顺序各不相同:假-补-散、补-散-咸和散-咸-补。针灸过程持续 30 分钟,使用 FLIR C5 热像仪在五个时间点测量面部皮肤温度。根据我们的记录,针刺大椎穴后,面部皮肤温度从34.30 °C(33.65-35.20 °C)显著升高至35.40 °C(34.85-35.85 °C),而针刺散寒穴后,面部皮肤温度从34.90 °C(33.95-35.65 °C)显著下降至34.00 °C(33.00-34.75 °C)。与假针刺组相比,补法和散法针刺组的皮肤温度均有显著差异。补针和散针之间的皮温差异也具有统计学意义。这些结果表明,针刺大椎穴可影响面部皮肤温度,从而确立了该穴位与面部生理之间的关系。此外,补法和散法针刺大椎穴时皮肤温度反应的对比也验证了其不同的生理效应。
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引用次数: 0
In vitro and in silico assessment of anti-cholinesterase potential of Ricinus communis L. (Euphorbiaceae): furnished with network pharmacology 大戟科植物蓖麻抗胆碱酯酶潜力的体外和硅学评估:网络药理学的应用
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-05-27 DOI: 10.1007/s13596-024-00749-y
Isaac Karimi, Layth Jasim Mohammad, Namdar Yousofvand, Jasim Mohammed Abdulhussein, Baydaa Abed Hussein

Searching for cholinesterase (ChE) inhibitory small molecules will open a new horizon to design eco-friendly antiinsectants and anti-Alzheimer’s disease agents since we encounter to drug resistance against available drugs/toxins. Here, the ChE inhibitory activity of methyl alcohol extracts of Ricinus communis L. (RC) has been investigated in vitro and its mechanism was mined computationally. The beans of RC showed anti-ChE properties for acetyl-ChE (AChE) of 65.33% and for butyryl-ChE (BChE) of 49.00%. The methyl alcohol extract of RC leaves showed lesser inhibitory effects of 27.67% for AChE than 5.67% for BChE. In silico findings showed that among phytochemicals found in RC, stigmasterol oleate, fucosterol, trachylobane, lupeol, casbene, and alpha-amyrin have a trustful binding affinity (BA) of − 12.2, − 11.9, − 10.6, − 10.4, − 10.2, and − 9.9 kcal/mol with AChE, respectively, while beta-tocopherol, beyerene and kaurene have same negative BA − 9.8 kcal/mol. Alpha-tocopherol and gamma-tocopherol showed identical BA of − 9.6 kcal/mol. In this regard, delta-tocopherol and beta-amyrin showed BA of − 9.5 (kcal/mol), therefore all phytochemicals may be considered putative binders of AChE. In this line, alpha- and beta-amyrin, lupeol, stigmasterol oleate, fucosterol, casbene, beyerene, and catechin found in RC showed greater BA of − 11.3, − 11, − 10.7, − 9.6, − 9.6, − 9.5, − 9.3, and − 9 kcal/mol while alpha-tocopherol, kaurene, and trachylobane have identical BA at − 8.8 kcal/mol, therefore, they may inhibit BChE. In sum, RC can be considered as a natural factory of anti-ChE lead-like molecules that was gifted by Mesopotamian medicine and Kurdish ethnomedicine to the modern biopharmaceuticals.

由于我们会遇到对现有药物/毒素的耐药性,因此寻找胆碱酯酶(ChE)抑制小分子将为设计环保型抗昆虫剂和抗阿尔茨海默病药物开辟一片新天地。在此,我们对蓖麻(Ricinus communis L.,RC)甲醇提取物的胆碱酯酶抑制活性进行了体外研究,并对其机理进行了计算挖掘。蓖麻豆对乙酰胆碱酯酶(AChE)的抗胆碱酯酶活性为 65.33%,对丁酰胆碱酯酶(BChE)的抗胆碱酯酶活性为 49.00%。RC 叶子的甲醇提取物对乙酰胆碱酯酶(AChE)的抑制率为 27.67%,对丁酰胆碱酯酶(BChE)的抑制率为 5.67%。硅学研究结果表明,在 RC 中发现的植物化学物质中,豆固醇油酸酯、褐藻甾醇、三羟甲基氨基甲烷、羽扇豆醇、卡丝烯和 alpha-amyrin 与 AChE 的可信结合亲和力(BA)分别为 - 12.2、 - 11.9、 - 10.6、 - 10.4、 - 10.2 和 - 9.9 千卡/摩尔,而 beta-生育酚、贝烯和高岭烯与 AChE 的负结合亲和力(BA)同样为 - 9.8 千卡/摩尔。α-生育酚和γ-生育酚的负 BA 值相同,均为-9.6 kcal/mol。在这方面,δ-生育酚和β-amyrin 的 BA 值为-9.5(kcal/mol),因此所有植物化学物质都可被视为 AChE 的推定结合剂。在此基础上,RC 中的α-和β-阿米林、羽扇豆醇、豆甾醇油酸酯、褐藻甾醇、卡西烯、贝瑞烯和儿茶素的 BA 值分别为-11.3、-11、-10.7、-9.6、-9.6、-9.5、-9.3 和-9 kcal/mol,而α-生育酚、高岭烯和三羟甲基氨基甲烷的 BA 值相同,均为-8.8 kcal/mol,因此它们可能会抑制 BChE。总之,RC 可被视为美索不达米亚医学和库尔德民族医学为现代生物制药提供的抗胆碱酯酶铅样分子的天然工厂。
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引用次数: 0
Deciphering the historical tapestry of medicinal plants and remedies in Brazil: an analysis of sales records from the Botica Real between 1806 and 1818 解密巴西药用植物和药方的历史织锦:对 1806 至 1818 年间皇家植物园销售记录的分析
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-05-27 DOI: 10.1007/s13596-024-00759-w
Leonardo de Souza Carvalho, Lorraynne Oliveira de Souza, Ygor Jessé Ramos, Nina Cláudia Barboza da Silva

This study aims to explore previously overlooked facets of the commercialization and utilization of medicinal plants and their derivatives in the "Botica Real" (Royal Apothecary) from 1806 to 1818. Using primary sources from the National Library of Brazil, the National Archives, the Brazilian Historical and Geographic Institute, and online newspaper libraries, a thorough document analysis was conducted. Key documents include the "Regimento dos preços dos medicamentos símplices, preparados e compostos", lists of shipments from the “Botica Real” in Minas Gerais and Rio de Janeiro (Brazilian states), "Post-mortem Inventories" of merchants, and the "Pharmacopoeia Geral para o Reino e Domínios de Portugal". The examination of these documents unveiled terms related to medicinal species, their scientific names, parts used, and application methods. These terms were categorized by their origin (animal, vegetable, or mineral), with a particular focus on plant species, where botanical nomenclature was updated. The research highlighted an evolution in the number of terms associated with medicinal plants, increasing from 219 in 1806 to 303 in 1818, with a total of 156 identified species across 58 botanical families. Notably, Lamiaceae had 15 species, followed by Asteraceae (14) and Fabaceae (12). Exotic species constituted 85%, while naturalized and native Brazilian species comprised 9% and 5%, respectively. The study documented various pharmaceutical preparations, predominantly in solid, liquid, and semi-solid forms, with spirits, elixirs, and solutions being the most common, along with tinctures, fluid extracts, and compounded powders. This historical survey not only sheds light on past pharmaceutical practices with medicinal plants but also offers valuable insights for contemporary phytotherapy.

Graphical abstract

本研究旨在探讨 1806 年至 1818 年期间 "皇家药房"(Botica Real)中药用植物及其衍生物的商业化和利用方面以前被忽视的问题。利用巴西国家图书馆、国家档案馆、巴西历史和地理研究所以及在线报纸图书馆的原始资料,进行了全面的文献分析。主要文件包括 "Regimento dos preços dos medicamentos símplices, preparados e compostos"、巴西米纳斯吉拉斯州和里约热内卢州 "Botica Real "的货物清单、商人的 "死后清单 "以及 "Pharmacopoeia Geral para o Reino e Domínios de Portugal"。对这些文献的研究揭示了与药用物种、其学名、使用部位和应用方法有关的术语。这些术语按其来源(动物、植物或矿物)进行了分类,尤其侧重于植物物种,其中植物学术语得到了更新。研究强调了与药用植物相关的术语数量的演变,从 1806 年的 219 个增加到 1818 年的 303 个,58 个植物科中共有 156 个已确定的物种。值得注意的是,唇形科有 15 个物种,其次是菊科(14 个)和豆科(12 个)。外来物种占 85%,归化物种和巴西本地物种分别占 9% 和 5%。研究记录了各种药物制剂,主要以固体、液体和半固体形式存在,其中最常见的是烈性酒、酏剂和溶液,此外还有酊剂、液体提取物和复方粉末。这项历史调查不仅揭示了过去药用植物的制药方法,还为当代植物疗法提供了宝贵的启示。
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引用次数: 0
Inhibition of phosphodiesterase 4 attenuates myocardial ischemia/reperfusion injury by inhibiting cardiomyocytes apoptosis 抑制磷酸二酯酶 4 可通过抑制心肌细胞凋亡减轻心肌缺血再灌注损伤
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-05-26 DOI: 10.1007/s13596-024-00755-0
Hyun Jeong Kwak

The effects of selective inhibitors of phosphodiesterase type 4 (PDE4), rolipram on gastric and brain ischemia/reperfusion injuries were investigated. However, the effects of rolipram on myocardial ischemic/reperfusion (I/R) are not fully understood. Here, it was investigated whether rolipram has protective effects on in vitro and in vivo myocardial I/R. Treatment with rolipram on H9c2 cells significantly inhibited cell death during I/R in a concentration-dependent manner. Rolipram also exerted a profound protective effect on apoptosis by decreasing the apoptosis-induced protein Bax and increasing the inhibitory protein Bcl-2 during I/R. Furthermore, rolipram suppressed the caspase-3 activity in cardiomyocytes exposed to I/R. To further investigate the role of rolipram on in vivo myocardial I/R, in vivo myocardial I/R model was established by ligating left anterior descending artery (LAD) for 1 h followed by 1 h of reperfusion. Compared to ischemic control group, administration of rolipram reduced infarct size and lactate dehydrogenase (LDH) level against myocardial I/R injury model. These findings indicate that rolipram has protective effect against I/R injury in cardiomyocytes. This beneficial effect is partly dependent on decreased Bax, caspase-3 as well as increased Bcl-2.

研究人员研究了 4 型磷酸二酯酶(PDE4)选择性抑制剂罗利普仑对胃和脑缺血再灌注损伤的影响。然而,罗利普仑对心肌缺血再灌注(I/R)的影响还不完全清楚。本文研究了罗利普仑对体外和体内心肌缺血再灌注是否具有保护作用。使用罗利普仑治疗 H9c2 细胞能以浓度依赖性的方式显著抑制 I/R 过程中的细胞死亡。同时,罗利普仑还通过降低诱导细胞凋亡的蛋白Bax和增加抑制蛋白Bcl-2,在I/R过程中对细胞凋亡产生深远的保护作用。此外,罗利普仑还能抑制暴露于 I/R 的心肌细胞中的 caspase-3 活性。为了进一步研究罗利普兰对体内心肌I/R的作用,研究人员通过结扎左前降支动脉(LAD)1小时,然后再灌注1小时,建立了体内心肌I/R模型。与缺血对照组相比,服用罗利普仑可减少心肌梗死面积,降低乳酸脱氢酶(LDH)水平,从而减轻心肌I/R损伤。这些研究结果表明,罗利普仑对心肌细胞的I/R损伤具有保护作用。这种益处部分取决于 Bax、caspase-3 的减少和 Bcl-2 的增加。
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引用次数: 0
Nanoform of curcumin: expansion in therapeutic applications 纳米形式的姜黄素:在治疗应用的扩展
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-05-25 DOI: 10.1007/s13596-024-00760-3
Harshita Mohanty, Raman P. Yadav

Curcumin is a well-known natural compound for therapeutic applications. Despite being a promising candidate, its poor water solubility, physicochemical instability, rapid degradation, poor bioactive absorption, low pharmacokinetics, low penetration and targeting efficacy, alkaline sensitivity, heat and light sensitivity limits its usage. Continuous efforts are being carried out to improve the properties of native curcumin into nanocurcumin preparation with change in structural organisation with improved properties. Several nanoformulations such as nanotube, nanopolymer, nanogel, micelle, liposome, dendrimer, quantum dot based nanocurcumin has been constructed and their potential applications explored. This has led to opening of new avenue in therapeutics domain for combating various diseases such as anti-microbial, anti-cancer, anti-diabetes, neuroprotective effect, immunomodulatory effect etc. Further, nanoform of curcumin is highlighted in reference to reversal of drug resistance and drug sensitivity enhancement. Apart from these, the review also summarizes about some clinical trials conducted using nanocurcumin in various disease domain.

姜黄素是一种众所周知的用于治疗的天然化合物。但其水溶性差、理化不稳定、降解快、生物活性吸收差、药代动力学性能差、渗透和靶向效果差、碱敏性、热敏性和光敏性等限制了其应用。人们一直在努力改善天然姜黄素的性能,通过改变结构组织来改善纳米姜黄素的性能。构建了基于纳米管、纳米聚合物、纳米凝胶、胶束、脂质体、树突、量子点的纳米姜黄素等纳米配方,并探索了其潜在的应用前景。这为抗微生物、抗癌、抗糖尿病、神经保护作用、免疫调节作用等治疗领域开辟了新的途径。此外,纳米形式的姜黄素在逆转耐药和增强药物敏感性方面得到了强调。除此之外,本文还对纳米姜黄素在不同疾病领域的临床试验进行了综述。
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引用次数: 0
The association between brain temperament and anxiety in mothers with premature infants hospitalized in the neonatal intensive care unit (NICU) based on Persian medicine 基于波斯医学的新生儿重症监护室(NICU)住院早产儿母亲的大脑气质与焦虑之间的关系
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-05-19 DOI: 10.1007/s13596-024-00757-y
Fatemeh Hashemi, Ghazaleh Heydarirad, Fatemeh Asadollah, Lida Nikfarid

During the postpartum period, anxiety emerges as a significant health concern for women, particularly among mothers whose infants are born prematurely. According to Persian Medicine, also known as Traditional Iranian Medicine (PM), anxiety disorders are caused by an imbalance in the brain’s temperament. Recent studies have found a strong connection between one's temperament and overall happiness. Our research aims to explore the link between brain temperament and anxiety levels in mothers of premature infants receiving care in NICUs, drawing upon the principles of PM. In this particular study, 105 mothers with premature infants admitted to NICUs were enrolled based on meeting specific inclusion criteria. The assessment utilized both the “State-Trait Anxiety Inventory” and the “Brain Mizaj Temperament Questionnaire.” The results showed that there was a significant difference in the mean scores of state (overt) anxiety (P = 0.009) and trait (hidden) anxiety (P = 0.006) based on the mothers’ brain temperament, and mothers with a hotter brain temperament had higher levels of overt and hidden anxiety. Consequently, the study’s outcomes suggest a correlation between brain temperament and anxiety levels among mothers with preterm infants hospitalized in NICUs.

在产后期间,焦虑成为妇女,尤其是婴儿早产的母亲的一个重要健康问题。波斯医学(又称伊朗传统医学)认为,焦虑症是由大脑气质失衡引起的。最近的研究发现,一个人的气质与整体幸福感之间存在密切联系。我们的研究旨在借鉴 PM 的原理,探索在新生儿重症监护室接受护理的早产儿母亲的大脑气质与焦虑水平之间的联系。在这项研究中,有 105 名早产儿母亲被纳入新生儿重症监护室,她们均符合特定的纳入标准。评估采用了 "状态-特质焦虑量表 "和 "脑米扎伊气质问卷"。结果显示,根据母亲的大脑气质,状态(显性)焦虑(P = 0.009)和特质(隐性)焦虑(P = 0.006)的平均得分存在显著差异,大脑气质较热的母亲显性焦虑和隐性焦虑水平较高。因此,研究结果表明,在新生儿重症监护室住院的早产儿母亲的大脑气质与焦虑水平之间存在相关性。
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引用次数: 0
期刊
Advances in Traditional Medicine
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