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Cognition, Diagnosis, and Treatment of Alzheimer's Disease: A Review. 阿尔茨海默病的认知、诊断和治疗:综述
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-06-18 DOI: 10.2174/0118722083358924250606173812
Yuping Qin, Xiangxia Deng, Shuang Zhang

As the global population ages, the health of older adults has become a growing concern. Alzheimer's disease (AD) is a common ailment affecting older adults, but the diagnosis and treatment of AD are difficult given our insufficient understanding of the disease. This review aims to provide reliable information for patients and their families by presenting a detailed overview of the pathogenic factors, diagnostic methods, and clinical manifestation of AD, as well as advances in drug and physical therapies. The information presented here should help provide a more comprehensive understanding of AD for patients and their families and encourage family- or self-screening based on clinical manifestations, thus improving early AD detection. In addition, the current treatment methods for AD are summarized. Although a gold-standard treatment for AD is yet to be developed, controlled-release therapies and medications that slow disease progression or improve cognitive function are available. The appropriate treatment method depends on the patient's diagnosis and the local medical level, and the effectiveness of the treatments may vary. Therefore, improving our understanding of AD and cognition-related symptoms in the public is necessary to improve early AD diagnoses. This review provides information that will facilitate self-screening for AD based on clinical manifestations, which can improve the early clinical diagnosis rate.

随着全球人口老龄化,老年人的健康问题日益受到关注。阿尔茨海默病(AD)是一种影响老年人的常见疾病,但由于我们对这种疾病的了解不足,诊断和治疗是困难的。本文就阿尔茨海默病的发病因素、诊断方法、临床表现以及药物和物理治疗方面的进展作一综述,旨在为阿尔茨海默病患者及其家属提供可靠的信息。本文提供的信息有助于患者及其家属更全面地了解阿尔茨海默病,并鼓励家庭或根据临床表现进行自我筛查,从而提高阿尔茨海默病的早期发现。此外,对目前AD的治疗方法进行了总结。虽然阿尔茨海默病的黄金标准治疗方法尚未开发,但控制释放疗法和减缓疾病进展或改善认知功能的药物是可用的。适当的治疗方法取决于患者的诊断和当地的医疗水平,治疗的效果可能会有所不同。因此,提高我们对阿尔茨海默病和公众认知相关症状的认识对于提高阿尔茨海默病的早期诊断是必要的。本综述为基于临床表现的AD自我筛查提供信息,提高临床早期诊断率。
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引用次数: 0
Preface. 前言。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-06-11 DOI: 10.2174/0118722083417806250605092351
Nikolaos E Labrou
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引用次数: 0
Optimized Protocol for Sorghum Regeneration: Enhancing Embryogenic Callus Formation from Immature Inflorescences. 高粱再生优化方案:促进未成熟花序胚性愈伤组织形成。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-05-30 DOI: 10.2174/0118722083362270250116101522
Bangaru Naidu Thaddi

Aim: This study aims to develop an efficient and reproducible in vitro protocol for high-frequency embryogenic callus induction and subsequent plant regeneration in multiple sorghum (Sorghum bicolor L. Moench) cultivars, thereby establishing a foundation for genetic transformation, mutation breeding, and other biotechnological applications aimed at enhancing sorghum crop improvement and productivity.

Background: Sorghum (Sorghum bicolor (L.) Moench) is an important cereal crop known for its adaptability to harsh environments and nutritional value. Despite its significance, sorghum remains challenging for in vitro propagation due to difficulties in regenerating callus tissue, especially from monocotyledonous explants. Callus induction and regeneration protocols are crucial for genetic transformation, mutation breeding, and biotechnological applications in sorghum improvement.

Objective: To establish an effective in vitro protocol for callus induction and subsequent plant regeneration using different sorghum cultivars, optimizing conditions for highfrequency embryogenic callus formation and plant regeneration.

Methods: Six sorghum cultivars (IS 3477, IS 33095, IS 7155, IS 2898, IS 7005, and IS 1202) were selected. Immature inflorescence explants were cultured on a modified Murashige and Skoog's (MS) medium with 3% sucrose, 0.8% agar, and 2.0 mg/l 2,4-D for callus induction. After 14 days, embryogenic and non-embryogenic calli were distinguished. Regeneration media were optimized using embryogenic calli, with 1.5 mg/l 6- benzylaminopurine (BAP) for shoot development and 1 mg/l NAA (1-naphthaleneacetic acid) in a half-strength MS medium for root development.

Results: Two distinct forms of calli were observed: a non-embryogenic light yellow callus and a white, granular embryogenic callus. Embryogenic callus induction frequency varied from 40% to 96% among the cultivars, with IS 3477 and IS 33095 exhibiting the highest frequencies (96% and 88%, respectively), while IS 1202 showed the lowest (40%). Regenerated shoots were successfully developed within 6-18 days and later transferred to a rooting medium, resulting in healthy plantlets. Transplanted plantlets showed normal growth and no morphological abnormalities in the field.

Conclusion: This study provides a reliable protocol for efficient callus induction and plant regeneration in multiple sorghum cultivars. The optimized conditions can be utilized for genetic studies, crop improvement, and biotechnological applications, thus contributing to the advancement of sorghum breeding and biotechnology research.

目的:建立高效、可重复的高粱(sorghum bicolor L. Moench)多品种高频胚性愈伤组织诱导及后续植株再生的离体方法,为提高高粱作物改良和产量的遗传转化、突变育种等生物技术应用奠定基础。背景:高粱(Sorghum bicolor (L.))是一种重要的谷类作物,以其对恶劣环境的适应性和营养价值而闻名。尽管具有重要意义,但由于愈伤组织再生困难,特别是单子叶外植体愈伤组织再生困难,高粱的离体繁殖仍然具有挑战性。愈伤组织诱导和再生方案是高粱遗传转化、突变育种和生物技术改良应用的关键。目的:建立不同高粱品种愈伤组织诱导和植株再生的有效离体方案,优化高频胚性愈伤组织形成和植株再生的条件。方法:选取6个高粱品种(IS 3477、IS 33095、IS 7155、IS 2898、IS 7005和IS 1202)。未成熟花序外植体在添加3%蔗糖、0.8%琼脂和2.0 mg/l 2,4- d的改良MS培养基上培养愈伤组织。14 d后,分化出胚性愈伤组织和非胚性愈伤组织。以胚性愈伤组织为再生培养基,以1.5 mg/l 6-苄基氨基嘌呤(BAP)促进芽部发育,1 mg/l NAA(1-萘乙酸)在半强度MS培养基中促进根发育。结果:观察到两种不同形式的愈伤组织:非胚性淡黄色愈伤组织和白色颗粒状胚性愈伤组织。不同品种胚性愈伤组织诱导率在40% ~ 96%之间,其中IS 3477和IS 33095的诱导率最高(分别为96%和88%),而IS 1202的诱导率最低(40%)。再生芽在6-18天内发育成功,然后转移到生根培养基上,形成健康的植株。移栽植株生长正常,田间无形态异常。结论:本研究为高粱多品种愈伤组织诱导和植株再生提供了可靠的方案。优化后的条件可用于遗传研究、作物改良和生物技术应用,从而促进高粱育种和生物技术研究的发展。
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引用次数: 0
Biosynthesis, Characterization, Antibacterial and Anti-Biofilm Activity of CuO Nanoparticles using Ephedra major Plant Extract against Pseudomonas aeruginosa. 麻黄主要植物提取物制备CuO纳米颗粒抗铜绿假单胞菌的生物合成、表征及抗菌抗生物膜活性
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-05-09 DOI: 10.2174/0118722083375049250507052242
Pegah Shakib, Zahra Yari Talib, Asadullah Asadi, Zahra Najafi

Introduction: Nanoparticles are nanometer-sized particles that have unique properties and are used in various fields such as medicine, environment, and technology. The Ephedra major plant, with its medicinal properties, is a rich source for extracting molecules that can be used as agents for the biosynthesis of nanoparticles and improve their properties. The aim of the current study was the biosynthesis of copper oxide nanoparticles (CuONPs) using Ephedra major extracts, as well as the evaluation of their antibacterial and anti-biofilm activity against Pseudomonas aeruginosa.

Materials and methods: The synthesis of CuO nanoparticles was performed using the aqueous extract of the leaves of Ephedra major plant .The synthesized nanoparticles were evaluated by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The well diffusion method investigated the antimicrobial activity of CuO-NPs synthesized against Pseudomonas aeruginosa. Then, the MIC and MBC of the synthesized nanoparticles were determined in 96-well microplates with different concentrations of CuO-NPs, aqueous extract, and chloramphenicol. The inhibition of Pseudomonas aeruginosa biofilm was investigated by staining with 1% crystal violet.

Results: The results of the UV-Vis analysis showed that the absorption at the wavelength of 385 nm was the highest, which confirmed the formation of CuO-NPs. SEM and EDX results indicated that the nanoparticles formed in a spherical shape with an average size of 30 to 80 nm. Also, EDX analysis showed the presence of copper, carbon, and oxygen elements in nanoparticles. The CuO-PNs at the concentration of 2000 μg/ml exhibited a significant inhibitory effect against P. aeruginosa. Also, the Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) of nanoparticles were 312 μg/ml. In addition, the results showed that CuO-NPs have an effect in inhibiting biofilm formation.The inhibitory effect against biofilm was greater with increasing concentration.

Conclusion: The results of this study prove that CuO-NPs synthesized from the aqueous extract of Ephedra major plant can be used as an effective option in treating infections caused by P. aeruginosa.

纳米粒子是一种纳米大小的粒子,具有独特的性能,应用于医学、环境和技术等各个领域。麻黄属主要植物具有药用特性,是提取分子的丰富来源,可作为纳米颗粒生物合成剂并改善其性能。本研究的目的是利用麻黄主要提取物生物合成氧化铜纳米颗粒(CuONPs),并评价其对铜绿假单胞菌的抗菌和抗生物膜活性。材料与方法:以麻黄叶水提液为原料合成CuO纳米颗粒,采用扫描电镜(SEM)和傅里叶变换红外光谱(FTIR)对合成的纳米颗粒进行表征。孔扩散法研究了合成的CuO-NPs对铜绿假单胞菌的抑菌活性。然后用不同浓度的CuO-NPs、水提物和氯霉素分别在96孔微孔板上测定合成纳米颗粒的MIC和MBC。用1%结晶紫染色研究了铜绿假单胞菌生物膜的抑菌作用。结果:紫外-可见光谱分析结果表明,在385 nm处吸收最高,证实了CuO-NPs的形成。SEM和EDX结果表明,纳米颗粒呈球形,平均尺寸为30 ~ 80 nm。此外,EDX分析显示纳米颗粒中存在铜、碳和氧元素。浓度为2000 μg/ml的cuo - pn对铜绿假单胞菌有明显的抑制作用。最小抑菌浓度(MIC)和最小杀菌浓度(MBC)均为312 μg/ml。此外,结果表明,CuO-NPs具有抑制生物膜形成的作用。对生物膜的抑制作用随浓度的增加而增强。结论:以麻黄为主要植物的水提物合成的CuO-NPs可作为治疗铜绿假单胞菌感染的有效选择。
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引用次数: 0
Total Phenolic and Flavonoid Contents and Antioxidant Activity of Dactylorhiza hatagirea (D. Don) Soo. 牛蹄草总酚和类黄酮含量及抗氧化活性研究
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-05-08 DOI: 10.2174/0118722083369496250502071714
Megha Sharma, Kumud Saklani, G K Dhingra, Sumit Purohit, Subhash Chandra

Objectives: Plant secondary metabolites include chemical compounds like flavonoids and phenolic acids. The use of these ingredients in traditional medicine to prevent or treat diabetes and cancer is becoming more prevalent because of their capacity to function as antioxidant agents. The objective of the research was to estimate the quantities of total phenols and flavonoids, together with the antioxidant capacity of various Dactylorhiza hatagirea extracts.

Methods: Total flavonoid and phenolic contents were determined by aluminum chloride and Folin-Ciocalteu techniques, respectively. Diphenyl-picrylhydrazyl (DPPH) and ABTS approaches were used for assessing the scavenging of free radicals. Employing standard methods, the preliminary phytochemical activity of the extract was assessed, and its reducing power was tested in the presence of potassium hexacyanoferrate.

Results: A maximum concentration of 58.88 ± 0.32 of gallic acid was identified per gram of methanolic extract as phenolic content. Quercetin, at 85.51 ± 0.40 mg/gram, had the most flavonoid content. The strongest reducing power output measured was 1.968 ± 0.01 g. In comparison, the IC50 values for DPPH and ABTS assays were 162.79 ± 0.24 and 39.75 ± 0.20 µg/ml, respectively. Thus, this plant differs from others in that it has potent antioxidant capabilities.

Conclusion: The methanolic crude extract of D. hatagirea and the estimated contents of phenols and flavonoids exhibited potent antioxidant action, particularly against DPPH and ABTS assays. Due to its relatively high phenolic and flavonoid contents, this plant is an exciting option for treating diseases. Therefore, secondary metabolites can be found and employed as low-resistance, multi-target antioxidant drugs for treating a variety of cancers, cardiovascular and neurodegenerative disorders, as well as other chronic diseases that are resistant to existing antibiotics.

目的:植物次生代谢产物包括类黄酮和酚酸等化合物。在传统医学中使用这些成分来预防或治疗糖尿病和癌症正变得越来越普遍,因为它们具有抗氧化剂的功能。本研究的目的是测定不同成分的总酚和总黄酮含量以及抗氧化能力。方法:采用氯化铝法测定总黄酮含量,采用福林法测定酚类含量。采用DPPH法和ABTS法测定自由基清除能力。采用标准方法,初步评估了提取物的植物化学活性,并在六氰高铁酸钾存在下测试了其还原能力。结果:每克甲醇提取物中未食子酸含量最高可达58.88±0.32。槲皮素类黄酮含量最高,为85.51±0.40 mg/g。测定的最强还原功率输出为1.968±0.01 g。相比之下,DPPH和ABTS的IC50值分别为162.79±0.24和39.75±0.20µg/ml。因此,这种植物与其他植物的不同之处在于它具有强大的抗氧化能力。结论:金丝桃甲醇粗提物及其所含酚类和黄酮类化合物具有较强的抗氧化作用,特别是抗DPPH和ABTS。由于其相对较高的酚类和类黄酮含量,这种植物是治疗疾病的令人兴奋的选择。因此,次级代谢物可以被发现并作为低耐药、多靶点抗氧化药物,用于治疗多种癌症、心血管和神经退行性疾病,以及其他对现有抗生素耐药的慢性疾病。
{"title":"Total Phenolic and Flavonoid Contents and Antioxidant Activity of Dactylorhiza hatagirea (D. Don) Soo.","authors":"Megha Sharma, Kumud Saklani, G K Dhingra, Sumit Purohit, Subhash Chandra","doi":"10.2174/0118722083369496250502071714","DOIUrl":"https://doi.org/10.2174/0118722083369496250502071714","url":null,"abstract":"<p><strong>Objectives: </strong>Plant secondary metabolites include chemical compounds like flavonoids and phenolic acids. The use of these ingredients in traditional medicine to prevent or treat diabetes and cancer is becoming more prevalent because of their capacity to function as antioxidant agents. The objective of the research was to estimate the quantities of total phenols and flavonoids, together with the antioxidant capacity of various Dactylorhiza hatagirea extracts.</p><p><strong>Methods: </strong>Total flavonoid and phenolic contents were determined by aluminum chloride and Folin-Ciocalteu techniques, respectively. Diphenyl-picrylhydrazyl (DPPH) and ABTS approaches were used for assessing the scavenging of free radicals. Employing standard methods, the preliminary phytochemical activity of the extract was assessed, and its reducing power was tested in the presence of potassium hexacyanoferrate.</p><p><strong>Results: </strong>A maximum concentration of 58.88 ± 0.32 of gallic acid was identified per gram of methanolic extract as phenolic content. Quercetin, at 85.51 ± 0.40 mg/gram, had the most flavonoid content. The strongest reducing power output measured was 1.968 ± 0.01 g. In comparison, the IC50 values for DPPH and ABTS assays were 162.79 ± 0.24 and 39.75 ± 0.20 µg/ml, respectively. Thus, this plant differs from others in that it has potent antioxidant capabilities.</p><p><strong>Conclusion: </strong>The methanolic crude extract of D. hatagirea and the estimated contents of phenols and flavonoids exhibited potent antioxidant action, particularly against DPPH and ABTS assays. Due to its relatively high phenolic and flavonoid contents, this plant is an exciting option for treating diseases. Therefore, secondary metabolites can be found and employed as low-resistance, multi-target antioxidant drugs for treating a variety of cancers, cardiovascular and neurodegenerative disorders, as well as other chronic diseases that are resistant to existing antibiotics.</p>","PeriodicalId":21064,"journal":{"name":"Recent patents on biotechnology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144014791","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
Synthesis and Biological Properties of Formulated Skin Serum Containing Coelomic Fluid of Earthworm Eisenia fetida/andrei. 含蚯蚓体腔液配方皮肤血清的合成及生物学特性研究。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-05-07 DOI: 10.2174/0118722083342120250426085714
Parisa Imeni, Mehdi Zarabi, Pegah Shakib, Ashkan Dirbaziyan

Background and objectives: In this study, the coelomic fluid of Eisenia fetida/ andrei species was used for the first time to prepare an anti-aging serum, and its antioxidant and antibacterial properties were investigated. In addition, its cytotoxicity on mouse fibroblast cells was measured as material for the production of natural anti-aging products.

Material and methods: This study investigates the antibacterial, antioxidant, and cytotoxic properties of coelomic fluid extracted from Eisenia fetida/andrei. Earthworms were cultured for a year, and their coelomic fluid was extracted using an electroshock method, sterilized, and lyophilized into powder. Antibacterial activity was tested against Escherichia coli and Staphylococcus aureus using MIC assays. Antioxidant properties were evaluated using the DPPH radical scavenging assay. Cytotoxicity effects on L929 and NHEK cell lines were assessed using MTT assays. Oxidative stress and enzymatic activities were analyzed by measuring malondialdehyde (MDA) levels and catalase activity in NHEK cells treated with coelomic fluid. A serum formulation incorporating coelomic fluid was prepared and subjected to stability tests, including pH, temperature, mechanical, and heavy metal residue analysis. Antibacterial and antioxidant properties of the serum were also evaluated. Statistical analyses were conducted using SPSS software (version 0.26). Results highlight the multifunctional potential of coelomic fluid for biomedical and cosmetic applications.

Results: Coelomic fluid exhibited antibacterial activity with MICs of 0.15 mg/mL for both E. coli and S. aureus, showing significant inhibition at higher concentrations. Ciprofloxacin and penicillin demonstrated stronger effects compared to the coelomic fluid. Antioxidant activity increased with concentration, achieving 77% inhibition at 10 mg/mL, with an IC50 of 10.67 mg/mL. Cytotoxicity analysis revealed no significant toxicity below 20 mg/mL, with enhanced cell viability at 2.5-5 mg/mL and restorative effects on fibroblasts at 10 mg/mL. Oxidative stress assays indicated reduced lipid peroxidation and increased catalase activity without inducing significant oxidative stress. Measurement of residues of mercury and lead in the sera showed that they were less than 0.01 ppm for mercury and less than 0.03 and 0.05 ppm for lead, respectively. These levels are below the U.S. Food and Drug Administration's approved limits for these metals. Aqueous serum containing coelomic fluid showed similar antibacterial and antioxidant properties, emphasizing its potential for cosmetic and pharmaceutical applications.

Conclusions: These results show that the use of earthworm coelomic fluid in skin care serum slows the aging process and restores damaged cells.

背景与目的:本研究首次利用飞天Eisenia fetida/ andrei种属的体腔液制备抗衰老血清,并对其抗氧化和抗菌性能进行研究。此外,还测定了其对小鼠成纤维细胞的细胞毒性,作为制备天然抗衰老产品的材料。材料与方法:本实验研究了鸡Eisenia fetida/andrei体腔液的抑菌、抗氧化和细胞毒性。蚯蚓培养一年,用电击法提取体腔液,消毒,冻干成粉末。采用MIC法测定其对大肠杆菌和金黄色葡萄球菌的抑菌活性。采用DPPH自由基清除法评价其抗氧化性能。采用MTT法评价对L929和NHEK细胞株的细胞毒性作用。通过测定经体腔液处理的NHEK细胞丙二醛(MDA)水平和过氧化氢酶活性,分析氧化应激和酶活性。制备了含有体腔液的血清配方,并进行了稳定性测试,包括pH值、温度、机械和重金属残留分析。并对血清的抗菌和抗氧化性能进行了评价。采用SPSS软件(0.26版)进行统计学分析。结果强调了体腔液在生物医学和美容应用方面的多功能潜力。结果:体腔液对大肠杆菌和金黄色葡萄球菌的抑菌活性均为0.15 mg/mL,且浓度越高抑菌效果越明显。环丙沙星和盘尼西林的效果比体腔液更强。抗氧化活性随浓度增加而增加,在10 mg/mL时达到77%的抑制作用,IC50为10.67 mg/mL。细胞毒性分析显示,低于20 mg/mL时无明显毒性,2.5-5 mg/mL时细胞活力增强,10 mg/mL时对成纤维细胞有恢复作用。氧化应激试验表明,在不诱导显著氧化应激的情况下,脂质过氧化降低,过氧化氢酶活性增加。测定血清中汞和铅的残留量表明,汞的残留量小于0.01 ppm,铅的残留量分别小于0.03和0.05 ppm。这些水平低于美国食品和药物管理局批准的这些金属的限量。含有体腔液的水血清显示出类似的抗菌和抗氧化性能,强调了其在化妆品和制药方面的应用潜力。结论:使用蚯蚓体腔液护肤血清可延缓衰老过程,修复受损细胞。
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引用次数: 0
Molecular Variation of Methicillin-resistant Staphylococcus haemolyticus Isolated from Patients in Ramadi City, Iraq. 伊拉克拉马迪市耐甲氧西林溶血葡萄球菌分离株的分子变异
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-04-30 DOI: 10.2174/0118722083348921250420012437
Omar Salih Shallal Al-Heeti, Safaa Abed Lateef Almeani, Samah Al Tawil, Yasir Merie Nayyef, Mohammed Mukhles Ahmed

Background: The increasing prevalence of Staphylococcus haemolyticus infections in community and hospital settings presents a significant health challenge due to growing antibiotic resistance and biofilm formation.

Objective: This study aims to:(1) perform a molecular analysis of prevalent native strains in Anbar, Iraq, (2) differentiate between various pathogenic strains using multilocus sequence typing (MLST) to enhance epidemiological and surveillance efforts. The objective is to trace the origins of these strains and distinguish between invasive and indigenous strains. While S. haemolyticus is generally part of the normal human microbiota, it can lead to serious infections in individuals with prior injuries or surgical procedures. It is particularly skilled at developing antibiotic resistance, making it a leading cause of hospital-acquired infections, largely through the staphylococcal cassette chromosome mec (SCCmec). Methicillin-resistant S. haemolyticus (MRSH) has developed resistance to oxacillin/cefoxitin through SCCmec acquisition, and hospital-associated MRSH strains are increasingly resistant to multiple antibiotics.

Methodology: The preparation of blood agar medium followed the manufacturer's guidelines. After autoclaving at 121ºC for 15 minutes, the medium was cooled to 50ºC. The mixture was then thoroughly mixed and poured into sterile Petri dishes. This medium is used for isolating and cultivating bacteria, as well as for detecting hemolytic activity and identifying the type of hemolysis. Genomic extraction and molecular screening of multidrug- resistant (MDR) isolates were performed, followed by MLST analysis. Data were processed using the University of Nebraska Medical Center's pubMLST website.

Results: To explore the genetic relationships among S. haemolyticus strains, their genomic DNA was analyzed using MLST typing based on the protocol from the MLST Institute database. All S. haemolyticus isolates in the study underwent MLST gene screening through PCR to verify the presence of housekeeping genes (arc, SH1200, hemH, leuB, SH1341, cfxE, and ribose ABC). PCR electrophoresis results demonstrated successful amplification of all target genes, confirming their appropriateness for MLST analysis. Three isolates were recognized as novel global strains, designated ST153, ST154, and ST155. In addition, five other strains were previously registered as ST3, ST9, ST29, ST123, and ST124.

Conclusion: The findings diverge from the established global understanding of type distribution in Asia. To combat the spread of highly resistant strains, it is crucial to monitor virulence factors and antibiotic resistance closely.

背景:由于抗生素耐药性和生物膜的形成,社区和医院溶血葡萄球菌感染的流行率不断上升,对健康构成了重大挑战。目的:本研究旨在:(1)对伊拉克安巴尔省流行的本地菌株进行分子分析;(2)利用多位点序列分型(MLST)对不同致病菌株进行区分,以加强流行病学和监测工作。目的是追踪这些菌株的起源,并区分入侵菌株和本地菌株。虽然溶血链球菌通常是正常人类微生物群的一部分,但它可导致先前受伤或手术过的个体严重感染。它特别擅长产生抗生素耐药性,使其成为医院获得性感染的主要原因,主要是通过葡萄球菌盒式染色体mec (SCCmec)。耐甲氧西林溶血链球菌(MRSH)通过SCCmec获得对oxacillin/头孢西丁产生耐药性,并且医院相关的MRSH菌株对多种抗生素的耐药性越来越强。方法:血琼脂培养基的制备遵循制造商的指导方针。在121ºC高压灭菌15分钟后,将培养基冷却至50ºC。然后将混合物彻底混合并倒入无菌培养皿中。这种培养基用于分离和培养细菌,以及检测溶血活性和确定溶血类型。对多药耐药(MDR)菌株进行基因组提取和分子筛选,并进行MLST分析。数据通过内布拉斯加大学医学中心的pubMLST网站进行处理。结果:根据MLST研究所数据库的方案,采用MLST分型方法分析了溶血链球菌的基因组DNA,探讨了溶血链球菌的遗传关系。本研究中所有溶血链球菌分离株均通过PCR进行MLST基因筛选,以验证内参基因(arc、SH1200、hemH、leuB、SH1341、cfxE和核糖ABC)的存在。PCR电泳结果显示,所有目标基因均扩增成功,证实其适合MLST分析。三个分离株被确定为新的全球菌株,命名为ST153, ST154和ST155。此外,另外5个毒株此前被登记为ST3、ST9、ST29、ST123和ST124。结论:这一发现与全球对亚洲类型分布的认识有所不同。为了对抗高耐药菌株的传播,密切监测毒力因素和抗生素耐药性至关重要。
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引用次数: 0
Exploring the Two-Way Role: Biological and Anti-Epileptic Properties of Imidazole and 2-Mercaptobenzimidazole Derivatives. 探索咪唑和2-巯基苯并咪唑衍生物的生物学和抗癫痫特性的双向作用。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-04-25 DOI: 10.2174/0118722083345879250403115017
Geetika Goel, Jannat Ul Firdous

Imidazole and 2-mercapto benzimidazole analogues are a group of molecules that have various biological activities and good therapeutic potential in the treatment of epilepsy. This review explores their dual role, focusing on their biological properties and anti-epileptic effects. A spectrum of biological activities is displayed by imidazole derivatives and 2- mercaptobenzimidazole, such as antifungal, antioxidant, anti-inflammatory, and antimicrobial actions, leading to their therapeutic flexibility apart from epilepsy treatment. Imidazole derivatives mechanistically modulate Gamma-Aminobutyric Acid (GABA) receptors, inhibit ion channels, and exert neuroprotective effects, enabling them to be used for seizure control. Their mechanisms of action involve modulation of oxidative stress pathways as well as providing neuroprotective effects against epilepsy. In terms of structure, both imidazole and 2-mercaptobenzimidazole derivatives have gone through extensive structure-activity relationship studies to enhance their biological and pharmacological aspects. However, numerous concerns, such as bioavailability, selectivity, and side effects, hinder their effective application in the treatment of various diseases. Looking forward, further research into novel derivatives and formulation strategies holds promise for enhancing efficacy and reducing adverse effects. This review consolidates current knowledge, emphasizing the multifaceted roles of imidazole and 2-mercapto benzimidazole derivatives in biological systems and their potential as anti-epileptic agents, thus providing insights for future research and clinical applications.

咪唑和2-巯基苯并咪唑类似物是一类具有多种生物活性的分子,在治疗癫痫方面具有良好的治疗潜力。本文就其生物学特性和抗癫痫作用作一综述。咪唑衍生物和2-巯基苯并咪唑具有一系列的生物活性,如抗真菌、抗氧化、抗炎和抗菌作用,除了治疗癫痫外,还具有治疗灵活性。咪唑衍生物通过机制调节γ -氨基丁酸(GABA)受体,抑制离子通道,并发挥神经保护作用,使其能够用于控制癫痫发作。它们的作用机制包括调节氧化应激途径以及提供抗癫痫的神经保护作用。在结构方面,咪唑和2-巯基苯并咪唑衍生物都经过了广泛的构效关系研究,以增强其生物学和药理学意义。然而,许多问题,如生物利用度、选择性和副作用,阻碍了它们在治疗各种疾病中的有效应用。展望未来,进一步研究新的衍生物和配方策略有望提高疗效和减少不良反应。本综述整合了现有的知识,强调咪唑和2-巯基苯并咪唑衍生物在生物系统中的多方面作用及其作为抗癫痫药物的潜力,从而为未来的研究和临床应用提供见解。
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引用次数: 0
Intellectual Property Rights Effects on India's Pharmaceutical Industry. 知识产权对印度制药业的影响。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-04-21 DOI: 10.2174/0118722083344893250411032817
Virendra S Gomase, Suchita P Dhamane, Swati C Jagdale

The Indian pharmaceutical industry took full advantage of the "process patent regime". It aggressively pursued the expansion of its market share by offering the most reasonably priced generic versions of pharmaceuticals to emerging and developing nations. The Indian government remained neutral over the implementation of the TRIPS agreement until 2005. Indian pharmaceutical patent law is distinct from legislation in other nations in several ways, some of which are among the most critical intellectual property issues in the nation. Over the past thirty years, the lack of product patent protection has been a significant setback for the Indian pharmaceutical business. "Molecules" that were patented and protected internationally but which India failed to protect. The Act's ambiguity makes it common for opponents of pharmaceutical patents to file unreasonable serial pre-grant oppositions. In addition, the number of pre-grant opposition filings is surging exponentially. The potential for revocation, oppositions before and after the grant, and counterclaims in cases of infringement are just a few of the challenges that may arise during the process of a patent. The TRIPS Agreement compliance of the Indian patent system will be guaranteed by the Patents (Amendment) Rules, 2005, and the Patents (Amendment) Ordinance, 2004. Nonetheless, another notable accomplishment of the Ordinance and the Rules is the progressive change of the Indian patent prosecution system. In keeping with its international obligations, the Indian government is working to create a patent system that encourages technical development. Additionally, India is working to alleviate concerns about the inadequate enforcement of its current intellectual property rules.

印度制药业充分利用了“工艺专利制度”。它通过向新兴国家和发展中国家提供价格最合理的仿制药,积极扩大其市场份额。2005年之前,印度政府对TRIPS协议的实施一直保持中立。印度药品专利法在几个方面不同于其他国家的立法,其中一些是该国最关键的知识产权问题。在过去的30年里,缺乏产品专利保护一直是印度制药业的一个重大挫折。“分子”在国际上获得了专利和保护,但印度没有保护。该法案的模糊性使得药品专利的反对者在授权前提出不合理的一系列反对意见很常见。此外,批准前反对申请的数量呈指数级增长。潜在的撤销、授权前后的反对以及侵权案件中的反诉只是专利过程中可能出现的一些挑战。《2005年专利(修订)规则》和《2004年专利(修订)条例》将保证印度专利制度符合《与贸易有关的知识产权协定》。尽管如此,《条例》和《规则》的另一个显著成就是印度专利审查制度的逐步变化。为了履行其国际义务,印度政府正在努力建立一个鼓励技术发展的专利制度。此外,印度正在努力减轻人们对其现行知识产权法规执行不力的担忧。
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引用次数: 0
A Review on Adaption of Microbiomes to Polynuclear Aromatic Hydrocarbons: An Alternate Approach to Environment Sustainability. 微生物群对多核芳烃的适应:环境可持续性的另一种途径
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-04-16 DOI: 10.2174/0118722083343885250326070617
Ruchika Garg, Kiran Dobhal, Sayantan Mukhopadhyay

Polycyclic aromatic hydrocarbons (PAHs) have been identified as catastrophic pollutants that can damage both the environment and human health. To restore a healthy surrounding, an environmental expert targeted the PAH contamination reduction strategy. Bioremediation techniques are overruling the conventional techniques due to their high disbursement and inefficient outcomes. Several PAHs, including Pyrene (PYR), Chrysene (CHY), Benz[a]anthracene (BaA), Benzo[a]pyrene (BaP), Fluoranthene (FLU) Indenol [1,2,3-cd] pyrene (INP), Benzo[ghi]perylene (BghiP), and, Dibenz [a, h] anthracene (DBA) have been identified by the International Agency for Research on Cancer (IARC) as carcinogenic, mutagenic, and teratogenic. Since PAHs are less hydrophilic and have more lipophilic properties, they are readily absorbed from the GIT of mammals. Grilled beef and chicken meat that had been charcoal-grilled contained Anthracene (ANT), BaP, Benzo[k]fluoranthene (BkF), Phenanthrene (PHE), and PYR. The highest dietary daily intake of BkF was reported to be 1.09 μg/ day in the intestine of grilled beef and 23.22μg/day in the stomach of grilled chicken. A number of bacterial species have been identified in the biodegradation of PAHs, including Mycobacterium gilvum (M. gilvum), Sphingobium chlorophenolicum (S. chlorophenolicum), Bacillus halotolerant, Mycobacterium flavescens (M. flavescens), Micrococcus luteus, Crassostrea gigas, Crassostrea gasar, and Crassostrea rhizosphere, Pseudomonas Putida, Rhodococcus wratislaviensis, and Kocuria rosea. Numerous fungi, including Arbuscular mycorrhiza, Aspergillus ficuum, Aspergillus flavus, and Aspergillus fumigatus, use PAHs as the source of carbon and energy for survival. To a certain extent, algae such as Selenastrum capricornutum and Chlamydomonas reinhardtii (C. Reinhardtian) also depend on PAHs to survive. This review aims to highlight the calamitous effect of high molecular weight PAHs on the surrounding, and humankind, as well as the advancement in bioremediation approaches in recent years. The authors also addressed the newly isolated microbiomes, including bacteria, fungi, algae, and others, as promising candidates for using PAHs as a source of carbon and energy.

多环芳烃(PAHs)已被确定为危害环境和人类健康的灾难性污染物。为了恢复健康的环境,一位环境专家提出了减少多环芳烃污染的战略。生物修复技术由于其高支出和低效率的结果,正在取代传统技术。几种多环芳烃,包括芘(PYR)、芘(CHY)、苯并[a]蒽(BaA)、苯并[a]芘(BaP)、氟蒽(FLU)、吲哚[1,2,3-cd]芘(INP)、苯并[hi]苝(bhip)和二苯并[a, h]蒽(DBA),已被国际癌症研究机构(IARC)鉴定为具有致癌性、诱变性和致畸性。由于多环芳烃的亲水性较差,而亲脂性较强,因此很容易从哺乳动物的胃肠道中吸收。炭烤牛肉和鸡肉中含有蒽(ANT)、BaP、苯并[k]荧光蒽(BkF)、菲(PHE)和PYR。烤牛肉肠中BkF日摄入量最高,为1.09 μg/d,烤鸡胃中为23.22μg/d。在多环芳烃的生物降解中,已经发现了许多细菌物种,包括gilvum分枝杆菌(M. gilvum)、chlorophenolicum Sphingobium (S. chlorophenolicum)、耐盐芽孢杆菌、黄分枝杆菌(M. flavescens)、黄体微球菌、长牡蛎、粗牡蛎和根际牡蛎、恶臭假单胞菌、wratislaviensis红球菌和玫瑰红球菌。许多真菌,包括丛枝菌根、曲霉、黄曲霉和烟曲霉,都使用多环芳烃作为生存的碳和能量来源。在一定程度上,像Selenastrum capricornutum和Chlamydomonas reinhardtii (C. Reinhardtian)等藻类也依赖多环芳烃生存。本文综述了高分子量多环芳烃对环境和人类的危害,以及近年来生物修复方法的进展。作者还提到了新分离的微生物组,包括细菌、真菌、藻类等,它们是利用多环芳烃作为碳和能源来源的有希望的候选者。
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引用次数: 0
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Recent patents on biotechnology
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