Biometals最新文献

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Lead-induced changes in plant cell ultrastructure: an overview. 铅诱导的植物细胞超微结构变化:概述
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-26 DOI: 10.1007/s10534-024-00639-5
Oumaima El Khattabi, Youssef Lamwati, Fatima Henkrar, Blanche Collin, Clement Levard, Fabrice Colin, Abdelaziz Smouni, Mouna Fahr
{"title":"Lead-induced changes in plant cell ultrastructure: an overview.","authors":"Oumaima El Khattabi, Youssef Lamwati, Fatima Henkrar, Blanche Collin, Clement Levard, Fabrice Colin, Abdelaziz Smouni, Mouna Fahr","doi":"10.1007/s10534-024-00639-5","DOIUrl":"https://doi.org/10.1007/s10534-024-00639-5","url":null,"abstract":"<p><p>Lead (Pb) is one of the most harmful toxic metals and causes severe damage to plants even at low concentrations. Pb inhibits plant development, reduces photosynthesis rates, and causes metabolic disfunctions. Plant cells display these alterations in the form of abnormal morphological modifications resulting from ultrastructural changes in the cell wall, plasma membrane, chloroplast, endoplasmic reticulum, mitochondria, and nuclei. Depending on plant tolerance capacity, the ultrastructural changes could be either a sign of toxicity that limits plant development or an adaptive strategy to cope with Pb stress. This paper gathers data on Pb-induced changes in cell ultrastructure observed in many tolerant and hyperaccumulator plants and describes the ultrastructural changes that appear to be mechanisms to alleviate Pb toxicity. The different modifications caused by Pb in cell organelles are summarized and reinforced with hypotheses that provide an overview of plant responses to Pb stress and explain the physiological and morphological changes that occur in tolerant plants. These ultrastructural modifications could help assess the potential of plants for use in phytoremediation.</p>","PeriodicalId":491,"journal":{"name":"Biometals","volume":" ","pages":""},"PeriodicalIF":4.1,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142338779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cytotoxic and ROS generation activity of anthraquinones chelate complexes with metal ions 蒽醌类化合物与金属离子的螯合物的细胞毒性和 ROS 生成活性。
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-21 DOI: 10.1007/s10534-024-00632-y
Viktor A. Timoshnikov, Irina A. Slepneva, Olga A. Chinak, Olga Yu Selyutina, Nikolay E. Polyakov
{"title":"Cytotoxic and ROS generation activity of anthraquinones chelate complexes with metal ions","authors":"Viktor A. Timoshnikov,&nbsp;Irina A. Slepneva,&nbsp;Olga A. Chinak,&nbsp;Olga Yu Selyutina,&nbsp;Nikolay E. Polyakov","doi":"10.1007/s10534-024-00632-y","DOIUrl":"10.1007/s10534-024-00632-y","url":null,"abstract":"<div><p>Anthraquinones (AQs) are very effective chemotherapeutic agent, however their fundamental shortcoming is high cardiotoxicity caused by reactive oxygen species (ROS). Therefore, development of improved antitumor drugs with enhanced efficacy but reduced side effects remains a high priority. In the present study we evaluated the cytotoxicity and ROS generation activity of chelate complex of redox-active anthraquinone 2-phenyl-4-(butylamino)naphtho[2,3-h]quinoline-7,12-dione (Q1) with iron and copper ions. Cytotoxicity study was performed using the lung cancer cell line A549 and breast cancer cell line MDA-MB-231. Q1 and Cu-Q1 complex demonstrate high activity in these experiments, but Fe-Q1 complex inactive. The ROS generation activity has been studied by EPR spin trapping technique using A549, MDA-MB-231 cell lines, and T lymphoblast cell line MOLT-4. It was shown that Q1 is able to penetrate into these cells and participate in redox reactions with the formation of a semiquinone radical. Fe(III) chelate complex formation results in much slower kinetics of ROS generation compared with pure Q1, which could be connected with a lower penetration through the cell membrane.</p><h3>Graphical abstract</h3>\u0000<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 6","pages":"1643 - 1656"},"PeriodicalIF":4.1,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142278431","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Leptospira interrogans proteome’s response to zinc highlights the potential involvement of this metal in translational—machinery and virulence 讯号钩端螺旋体蛋白质组对锌的反应突显了这种金属在翻译机械和毒力方面的潜在参与。
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-21 DOI: 10.1007/s10534-024-00634-w
Amanda Silva Hecktheuer, Cassia Moreira Santos, Fabienne Antunes Ferreira, Angela Silva Barbosa, Lourdes Isaac, Marilis Valle Marques, Ricardo Ruiz Mazzon
{"title":"The Leptospira interrogans proteome’s response to zinc highlights the potential involvement of this metal in translational—machinery and virulence","authors":"Amanda Silva Hecktheuer,&nbsp;Cassia Moreira Santos,&nbsp;Fabienne Antunes Ferreira,&nbsp;Angela Silva Barbosa,&nbsp;Lourdes Isaac,&nbsp;Marilis Valle Marques,&nbsp;Ricardo Ruiz Mazzon","doi":"10.1007/s10534-024-00634-w","DOIUrl":"10.1007/s10534-024-00634-w","url":null,"abstract":"<div><p>Leptospires, as motile Gram-negative bacteria, employ sophisticated strategies for efficient invasion and dissemination within their hosts. In response, hosts counteract pathogens through nutritional immunity, a concept involving the deprivation of essential metals such as zinc. Zinc, pivotal in modulating pathogen-host interactions, influences proteins structural, catalytic, and regulatory functions. A comprehensive understanding of how leptospires regulate intracellular zinc availability is crucial for deciphering their survival mechanisms. This study explores the proteomic profile of <i>Leptospira interrogans</i> sv. Copenhageni str. 10A cultivated in Ellinghausen-McCullough-Johnson-Harris medium supplemented with the zinc chelator TPA or ZnCl<sub>2</sub>. Among the 2161 proteins identified, 488 were subjected to scrutiny, revealing 102 less abundant and 81 more abundant in response to TPA. Of these 488 proteins, 164 were exclusive to the presence of TPA and 141 were exclusive to the zinc-enriched conditions. Differentially expressed proteins were classified into clusters of orthologous groups (COGs) with a distribution in metabolic functions (37.8%), information storage/processing (21.08%), cellular processes/signaling (28.04%), and poorly characterized proteins (10.65%). Differentially expressed proteins are putatively involved in processes like 1-carbon compound metabolism, folate biosynthesis, and amino acid/nucleotide synthesis. Zinc availability significantly impacted key processes putatively related to leptospires’ interactions with their host, such as motility, biofilm formation, and immune escape. Under conditions of higher zinc concentration, ribosomal proteins, chaperones and components of transport systems were observed, highlighting interactions between regulatory networks responsive to zinc and iron in <i>L. interrogans</i>. This study not only revealed hypothetical proteins potentially related to zinc homeostasis, but also identified possible virulence mechanisms and pathogen-host adaptation strategies influenced by the availability of this metal. There is an urgent need, based on these data, for further in-depth studies aimed at detailing the role of zinc in these pathways and mechanisms, which may ultimately determine more effective therapeutic approaches to combat <i>Leptospira</i> infections.</p></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 6","pages":"1677 - 1698"},"PeriodicalIF":4.1,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142278432","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Experimental and computational evaluation of anti-malarial and antioxidant potential of transition metal (II) complexes with tridentate schiff base derived from pyrrolopyrimidine 过渡金属 (II) 与源自吡咯并嘧啶的三叉片基配合物的抗疟疾和抗氧化潜力的实验和计算评估
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-13 DOI: 10.1007/s10534-024-00636-8
Abhay D. Bagul, Manish Kumar, Amer M. Alanazi, Aisha Tufail, Nasir Tufail, Digamber D. Gaikwad, Amit Dubey
{"title":"Experimental and computational evaluation of anti-malarial and antioxidant potential of transition metal (II) complexes with tridentate schiff base derived from pyrrolopyrimidine","authors":"Abhay D. Bagul,&nbsp;Manish Kumar,&nbsp;Amer M. Alanazi,&nbsp;Aisha Tufail,&nbsp;Nasir Tufail,&nbsp;Digamber D. Gaikwad,&nbsp;Amit Dubey","doi":"10.1007/s10534-024-00636-8","DOIUrl":"10.1007/s10534-024-00636-8","url":null,"abstract":"<div><p>In the twenty-first century, we are experiencing persistent waves of diverse pathogen variations, contributing significantly to global illness and death rates. Within this varied spectrum of illnesses, malaria and oxidative damage emerge as prominent obstacles that have persistently affected human health. The motivation for exploring the antioxidant potential of transition metal (II) complexes with tridentate Schiff base ligands is driven by the need for effective treatments against malaria and oxidative stress-related conditions. Both malaria and oxidative damage are significant global health concerns. Transition metal complexes can potentially offer enhanced anti-malarial and antioxidant activities, providing a dual benefit. To explore the aforementioned facts and examine the therapeutic potential, the previously synthesized pyrrolopyrimidinehydrazide-3-chlorobenzaldehyde, such as HPPHmCB ligand(1)andtheirMn(II),Fe(II),Co(II),Ni(II), Pd(II),Cu(II),Zn(II),Cd(II),Hg(II)complexes(2–10) of benzaldehydes and pyrrolopyrimidinehydrazide were proposed for in vitro anti-malarial and antioxidant investigation. These compounds were assessed for their anti-malarial efficacy against <i>Plasmodium falciparum</i> using a micro assay protocol, with IC<sub>50</sub> values indicating the concentration required to inhibit parasite maturation by 50%. The Hg(II) complex displays pronounced antimalarial activity with an IC<sub>50</sub> value of 1.98 ± 0.08 µM, closely aligning with the efficacy of quinine, whereas Zn(II), Cu(II), Pd(II) complexes demonstrates most significant anti-malarial activity, with IC<sub>50</sub> values close to the reference compound quinine. The antioxidant activity of the compounds was evaluated using the DPPH assay, with several metal complexes such as Cu(II)and Zn(II) showing strong potential in neutralizing oxidative stress. Furthermore, molecular docking simulations were conducted to explore the binding interactions of the compounds with PfNDH2, providing insights into their pharmacological potential. The study also examined the electronic properties, solubility, and potential hepatotoxicity of the compounds. The findings suggest that the metal complexes could be promising candidates for further development as anti-malarial agents, offering enhanced potency compared to the base compound.</p></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 6","pages":"1713 - 1737"},"PeriodicalIF":4.1,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142255450","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Insoluble HIFa protein aggregates by cadmium disrupt hypoxia-prolyl hydroxylase (PHD)-hypoxia inducible factor (HIFa) signaling in renal epithelial (NRK-52E) and interstitial (FAIK3-5) cells 镉的不溶性HIFa蛋白聚集体破坏了肾上皮细胞(NRK-52E)和肾间质细胞(FAIK3-5)中的缺氧-脯氨酰羟化酶(PHD)-缺氧诱导因子(HIFa)信号传导
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-10 DOI: 10.1007/s10534-024-00631-z
Timm Schreiber, Bettina Scharner, Frank Thévenod
{"title":"Insoluble HIFa protein aggregates by cadmium disrupt hypoxia-prolyl hydroxylase (PHD)-hypoxia inducible factor (HIFa) signaling in renal epithelial (NRK-52E) and interstitial (FAIK3-5) cells","authors":"Timm Schreiber,&nbsp;Bettina Scharner,&nbsp;Frank Thévenod","doi":"10.1007/s10534-024-00631-z","DOIUrl":"10.1007/s10534-024-00631-z","url":null,"abstract":"<div><p>The kidney is the main organ that senses changes in systemic O<sub>2</sub> pressure by hypoxia-PHD-HIFa (HPH) signaling, resulting in adaptive target gene activation, including erythropoietin (EPO). The non-essential transition metal cadmium (Cd) is nephrotoxic and disrupts the renal HPH pathway, which may promote Cd-associated chronic renal disease (CKD). A deeper molecular understanding of Cd interference with renal HPH signaling is missing, and no data with renal cell lines are available. In rat kidney NRK-52E cells, which model the proximal tubule, and murine fibroblastoid atypical interstitial kidney (FAIK3-5) cells, which mimic renal EPO-producing cells, the chemical hypoxia mimetic dimethyloxalylglycine (DMOG; 1 mmol/l) or hypoxia (1% O<sub>2</sub>) activated HPH signaling. Cd<sup>2+</sup> (2.5–20 µmol/l for ≤ 24 h) preferentially induced necrosis (trypan blue uptake) of FAIK3-5 cells at high Cd whereas NRK-52E cells specially developed apoptosis (PARP-1 cleavage) at all Cd concentrations. Cd (12.5 µmol/l) abolished HIFa stabilization and prevented upregulation of target genes (quantitative real-time polymerase chain reaction and immunoblotting) induced by DMOG or hypoxia in both cell lines, which was caused by the formation of insoluble HIFa aggregates. Strikingly, hypoxic preconditioning (1% O<sub>2</sub> for 18 h) reduced apoptosis of FAIK3-5 and NRK-52E cells at low Cd concentrations and decreased insoluble HIFa proteins. Hence, drugs mimicking hypoxic preconditioning could reduce CKD induced by chronic low Cd exposure.</p></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 6","pages":"1629 - 1642"},"PeriodicalIF":4.1,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10534-024-00631-z.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142209897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
New solvated Mo(VI) complexes of isatin based asymmetric bisthiocarbohydrazones as potent bioactive agent: synthesis, DFT-molecular docking studies, biological activity evaluation and crystal structures 作为强效生物活性剂的异靛基不对称双硫代羧酰肼的新溶解钼(VI)配合物:合成、DFT-分子对接研究、生物活性评价和晶体结构。
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-06 DOI: 10.1007/s10534-024-00633-x
Yeliz Kaya, Ayşe Erçağ, Savaş Kaya, Avni Berisha, Birnur Akkaya, Yunus Zorlu
{"title":"New solvated Mo(VI) complexes of isatin based asymmetric bisthiocarbohydrazones as potent bioactive agent: synthesis, DFT-molecular docking studies, biological activity evaluation and crystal structures","authors":"Yeliz Kaya,&nbsp;Ayşe Erçağ,&nbsp;Savaş Kaya,&nbsp;Avni Berisha,&nbsp;Birnur Akkaya,&nbsp;Yunus Zorlu","doi":"10.1007/s10534-024-00633-x","DOIUrl":"10.1007/s10534-024-00633-x","url":null,"abstract":"<div><p>New solvated Mo(VI) complexes were isolated from the reaction of [MoO<sub>2</sub>(acac)<sub>2</sub>] with asymmetric isatin bisthiocarbohydrazone ligands. The ligands were obtained from the reaction of isatin monothiocarbohydrazone with 3,5-dibromo salicylaldehyde (L1), 3,5-dichloro salicylaldehyde (L2) and 3-chloro-5-bromo salicylaldehyde (L3), respectively. In the complexes, the ligands serve as ONS donors and coordinate to the [MoO<sub>2</sub>]<sup>2+</sup> nucleus. The bonding sites are azomethine nitrogen atom, phenolic oxygen atom and thiol sulfur atom. The sixth coordination site is completed by an oxygen atom from an ethanol solvent. The ethanol-coordinated Mo(VI) complexes, C1–C3, [MoO<sub>2</sub>L(EtOH)] (L: L1–L3), were characterized using elemental analysis, IR and <sup>1</sup>H NMR spectroscopies, and conductivity measurements. By crystallizing ethanol-solvated solid complexes from an EtOH/DMSO mixture, DMSO-solvated complexes (C4–C6) suitable for X-ray crystallography were obtained. Crystal structure analysis supports the proposed complex structures and geometries, but the ethanol in the sixth coordination site has been replaced by DMSO. When the anticarcinogenic effects of the ligands and complexes (C1–C3) on the C6 cell line were examined, it was found that the complexes showed higher activity than the ligands. The C3 complex appears to have the best anti-cancer activity compared to doxorubicin. Additionally, all compounds were determined to have high total antioxidant capacity. Data obtained from theoretical studies (DFT and docking) support experimental studies.</p></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 6","pages":"1657 - 1675"},"PeriodicalIF":4.1,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142138930","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Iron oxide nanoparticles derived from Polyalthia korintii (Dunal) Benth. & Hook. F leaves extract exhibits biological and dye degradation potentials 从 Polyalthia korintii (Dunal) Benth. & Hook.F 叶提取物具有生物和染料降解潜力。
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-05 DOI: 10.1007/s10534-024-00610-4
K. E. Hana Mol, Tancia Rosalin, K. K. Elyas
{"title":"Iron oxide nanoparticles derived from Polyalthia korintii (Dunal) Benth. & Hook. F leaves extract exhibits biological and dye degradation potentials","authors":"K. E. Hana Mol,&nbsp;Tancia Rosalin,&nbsp;K. K. Elyas","doi":"10.1007/s10534-024-00610-4","DOIUrl":"10.1007/s10534-024-00610-4","url":null,"abstract":"<div><p>Green synthesis of iron oxide nanoparticles using plant extracts is of tremendous interest owing to its cost effectiveness, ecofriendly and high efficiency compared to physical and chemical approaches. In the current study, we describe a green approach for producing iron oxide nanoparticles utilizing <i>Polyalthia korintii</i> aqueous leaf extract (PINPs). The prepared PINPs were assessed of their biological and dye degradation potentials. The physico-chemical characterization of PINPs using UV–Visible spectrophotometer, Fourier Transform Infrared Spectroscopy, X-Ray Diffraction studies, Field emission Scanning Electron Microscopy and Energy Dispersive X-ray spectroscopy analysis confirmed the synthesized sample comprised of iron oxide entity, predominantly spherical with the size range of 40–60 nm. Total Phenolic Content of PINPs is 59.36 ± 1.64 µg GAE/mg. The PINPs exhibited 89.78 ± 0.07% DPPH free radical scavenging and 28.7 ± 0.21% ABTS cation scavenging activities. The antibacterial activities were tested against different gram-positive and gram-negative bacteria and PINPs were more effective against <i>Enterococcus faecalis</i> and <i>Klebsiella pneumoniae</i>. Cytotoxicity of PINPs against K562 and HCT116 were measured and IC50 values were found to be 84.99 ± 4.3 µg/ml and 79.70 ± 6.2 µg/ml for 48 h respectively. The selective toxicity of PINPs was demonstrated by their lowest activity on lymphocytes, HEK293 cells, and erythrocytes. The toxicity (LC 50 values) against first, second, third and fourth instar larvae of <i>Culex quinquefasciatus</i> was 40 ± 1.5 mg/mL, 45 ± 0.8 mg/mL, 99 ± 2.1 mg/mL and 120 ± 3.5 mg/mL respectively. Finally, PINPs were utilized to as a catalyst for removal of textile dyes like Methylene blue and methyl orange in a fenton-like reaction. The results showed 100% dye degradation efficiency in a fenton like reaction within 35 min. Thus, the green synthesized PINPs exhibit antioxidant, antibacterial, antiproliferative, larvicidal and dye degradation potentials, indicating their suitability for biological and environmental applications.</p></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 5","pages":"1289 - 1303"},"PeriodicalIF":4.1,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142131557","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Adjuvant therapy with zinc supplementation; anti-inflammatory and anti-oxidative role in multiple myeloma patients receiving autologous hematopoietic stem cell transplantation: a randomized controlled clinical trial 补充锌的辅助治疗;在接受自体造血干细胞移植的多发性骨髓瘤患者中的抗炎和抗氧化作用:随机对照临床试验。
IF 4.1 3区 生物学
Biometals Pub Date : 2024-09-01 DOI: 10.1007/s10534-024-00630-0
Kasra Jahankhani, Niloofar Taghipour, Maryam Nikoonezhad, Hossein Behboudi, Mahshid Mehdizadeh, Dariush Kadkhoda, Abbas Hajifathali, Nariman Mosaffa
{"title":"Adjuvant therapy with zinc supplementation; anti-inflammatory and anti-oxidative role in multiple myeloma patients receiving autologous hematopoietic stem cell transplantation: a randomized controlled clinical trial","authors":"Kasra Jahankhani,&nbsp;Niloofar Taghipour,&nbsp;Maryam Nikoonezhad,&nbsp;Hossein Behboudi,&nbsp;Mahshid Mehdizadeh,&nbsp;Dariush Kadkhoda,&nbsp;Abbas Hajifathali,&nbsp;Nariman Mosaffa","doi":"10.1007/s10534-024-00630-0","DOIUrl":"10.1007/s10534-024-00630-0","url":null,"abstract":"<div><p>Multiple myeloma (MM) patients are often accompanied by heightened levels of oxidative stress, even following bone marrow transplantation. Trace mineral supplements have been found to regulate and inhibit the activity of oxidative radicals and inflammatory factors, which are involved in the pathogenesis of MM. The study sought to evaluate the effectiveness of the supplementation by analyzing changes in oxidative, anti-oxidative, and inflammation markers. Patients were randomly assigned to a zinc or placebo group, with the former receiving 30 mg of zinc or placebo tablets daily for 1 month. Blood samples were collected from the patients on the day of transplantation, 15 days, and 30 days post-transplantation. Real-time PCR was employed to measure the expression of oxidative/antioxidative genes. Furthermore, the protein level of oxidative markers in serum samples was assessed. Finally, serum TNF-α concentrations were measured using the ELISA technique. The expression levels of SOD1, SOD2, and NRF2 genes were significantly higher on days 15 and 30 compared to the control group (P &lt; 0.05), with a greater increase on day 30 (P &lt; 0.05). Conversely, the expression levels of Keap1 and NOX2 genes were lower on day 30 than those of the control group (P &lt; 0.05), with a further decrease from day 15 to day 30 (P &lt; 0.05). The experimental group exhibited a notable reduction in TNF-α cytokine levels on day 30 compared to the control and placebo groups (P &lt; 0.05). All findings were coordinated according to the nutritional questionnaire. Our findings suggest a potential benefit of zinc supplementation in managing the adverse effects of chemotherapy in MM patients, warranting further investigation.</p></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 6","pages":"1609 - 1627"},"PeriodicalIF":4.1,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142103130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Levodopa-induced dyskinesia: brain iron deposition as a new hypothesis 左旋多巴诱发的运动障碍:作为新假说的脑铁沉积。
IF 4.1 3区 生物学
Biometals Pub Date : 2024-08-30 DOI: 10.1007/s10534-024-00628-8
Fanshi Zhang, Zhuofan Ye, Yuanyang Xie, Mei Liu, Li Zhang, Jun Zhang, Zucai Xu
{"title":"Levodopa-induced dyskinesia: brain iron deposition as a new hypothesis","authors":"Fanshi Zhang,&nbsp;Zhuofan Ye,&nbsp;Yuanyang Xie,&nbsp;Mei Liu,&nbsp;Li Zhang,&nbsp;Jun Zhang,&nbsp;Zucai Xu","doi":"10.1007/s10534-024-00628-8","DOIUrl":"10.1007/s10534-024-00628-8","url":null,"abstract":"<div><p>Parkinson’s disease (PD) is a common neurodegenerative disease in the older adults. The main pathological change in PD is the degenerative death of dopamine (DA) neurons in the midbrain substantia nigra, which causes a significant decrease in the DA content of the striatum. However, the exact etiology of this pathological change remains unclear. Genetic factors, environmental factors, aging, and oxidative stress may be involved in the degenerative death of dopaminergic neurons in PD. Pharmacological treatment using levodopa (<span>l</span>-DOPA) remains the main treatment for PD. Most patients with PD consuming <span>l</span>-DOPA for a long time usually develop levodopa-induced dyskinesia (LID) after 6.5 years of use, and LID seriously affects the quality of life and increases the risk of disability. Recently, studies have revealed that cerebral iron deposition may be involved in LID development and that iron deposition has neurotoxic effects and accelerates disease onset. However, the relationship between cerebral iron deposition and LID remains unclear. Herein, we reviewed the mechanisms by which iron deposition may be associated with LID development, which are mainly related to oxidative stress, neuroinflammation, and mitochondrial and lysosomal dysfunction. Using iron as an important target, the search and development of safe and effective brain iron scavengers, and thus the alleviation and treatment of LID, has a very important scientific and clinical value, as well as a good application prospect.</p></div>","PeriodicalId":491,"journal":{"name":"Biometals","volume":"37 6","pages":"1307 - 1323"},"PeriodicalIF":4.1,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142103131","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stability of metal ion complexes with the synthetic phytosiderophore proline-2′-deoxymugineic acid 金属离子与合成植物苷酸脯氨酸-2'-脱氧木精酸复合物的稳定性。
IF 4.1 3区 生物学
Biometals Pub Date : 2024-08-28 DOI: 10.1007/s10534-024-00629-7
Anna Evers, Jackson Kohn, Oliver Baars, James M. Harrington, Kosuke Namba, Owen W. Duckworth
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