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1.
Aquat Toxicol ; 266: 106791, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38070396

ABSTRACT

Selenium, a trace mineral, is essential for several physiological processes in humans and animals. It is an antioxidant vital for the immunological response, DNA synthesis, thyroid hormone metabolism, and antioxidant defense enzymes. Zebrafish embryos and larvae were exposed to different concentrations of sodium selenite (SodSe) and selenium nanoparticles (SeNs) at various developmental stages. The study evaluated the impact of SodSe and SeNs on larvae survival, hatching rate, and morphological abnormalities. Also, acridine orange staining was used to analyze the apoptotic cell death, and behavioral tests were conducted to assess anxiety-like behaviors. The results showed that both SodSe and SeNs influence the development and neurobehavior of zebrafish larvae in a concentration-dependent manner. SodSe at high concentration causes low survival rates, delayed hatching, and increased morphological defects in zebrafish larvae. In addition, exposure to SodSe resulted in elevated apoptosis in different larval tissues. Zebrafish larvae treated with SodSe and SeNs exhibited anxiety-like behaviour, increased thigmotaxis, less exploratory behaviour, and less swimming patterns. The nerve conductions and stimuli responses evaluated through acetylcholine esterase (AChE) and cortisol assays, revealed a decrease in the activity in a dose-dependent manner of SodSe and SeNs. Interestingly, the effects of SeNs were lower even at higher concentrations when compared with SodSe at lower concentrations on zebrafish embryos. This shows that SeNs synthesized through biological methods may be less toxic and may have lower effect on the development and neurobehavior of zebrafish larvae. Thus, our study confirms the cytotoxic and neurobehavioral effects of SodSe and suggests the use of SeNs at lower concentration to provide insights into better understanding of developmental stages and metabolic pathways in zebrafish larvae.


Subject(s)
Nanoparticles , Selenium , Water Pollutants, Chemical , Humans , Animals , Selenium/toxicity , Zebrafish/physiology , Sodium Selenite/toxicity , Antioxidants/pharmacology , Water Pollutants, Chemical/toxicity , Nanoparticles/toxicity , Larva , Embryo, Nonmammalian
2.
Appl Biochem Biotechnol ; 195(10): 5823-5837, 2023 Oct.
Article in English | MEDLINE | ID: mdl-36708493

ABSTRACT

Selenium in the form of selenoproteins is formed through a unique translocation recoding pathway and plays a vital role in human metabolism. Selenium nanoparticles (SeNPs) when synthesized using green synthesis from plant extract offer more advantages than physical and chemical methods. Previous studies have synthesized selenium nanoparticles from green tea and white tea; here, we report the synthesis of selenium nanoparticles from Camillia sinensis (L) Kuntze leaves (black tea) by green synthesis. Moreover, we have tested the antimicrobial and antioxidant activity of the plant extract, SeNPs, and combination of plant extract and SeNPs which have not been previously studied. The antimicrobial efficacy of SeNPs was tested against Klebsiella pneumonia, Candida albicans, and Staphylococcus aureus. They showed inhibitory effects against these organisms individually and in combination with Camellia sinensis leaf extract. The antioxidant properties of SeNPs were checked using FRAP and DPPH assays, where high radical scavenging activity was exhibited by SeNPs and in combination with the plant extract. Furthermore, synthesized SeNPs were examined for cytotoxicity tolerance against Vero cells and their IC50 values determine that plant-mediated SeNPs showed high cytotoxicity at minimal concentrations. If explored further, the reducing, capping, and stabilizing capabilities of SeNPs may demonstrate other inhibitory effects and could be explored for understanding the role of selenium in cellular metabolism.


Subject(s)
Anti-Infective Agents , Camellia sinensis , Nanoparticles , Selenium , Animals , Chlorocebus aethiops , Humans , Selenium/pharmacology , Selenium/chemistry , Camellia sinensis/metabolism , Vero Cells , Antioxidants/pharmacology , Antioxidants/chemistry , Nanoparticles/chemistry , Plant Extracts/pharmacology , Plant Extracts/chemistry , Anti-Infective Agents/chemistry
4.
Chemosphere ; 272: 129601, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33497928

ABSTRACT

Recently, the COVID-19 disease spread has emerged as a worldwide pandemic and cause severe threats to humanity. The World Health Organisation (WHO) releases guidelines to help the countries to reduce the spread of this virus to the public, like wearing masks, hand hygiene, social distancing, shutting down all types of public transports, etc. These conditions led to a worldwide economic fall drastically, and on the other hand, indirect environmental benefits like global air quality improvement and decreased water pollution are also pictured. Currently, use of face masks is part of a comprehensive package of the prevention and control measures that can limit the spread of COVID-19 since there is no clinically proven drugs or vaccine available for COVID-19. Mostly, face masks are made of petroleum-based non-renewable polymers that are non-biodegradable, hazardous to the environment and create health issues. This study demonstrates the extensive use of the face mask and how it affects human health and the marine ecosystem. It has become a great challenge for the government sectors to impose strict regulations for the proper disposal of the masks as medical waste by the public. Neglecting the seriousness of this issue may lead to the release of large tonnes of micro-plastics to the landfill as well as to the marine environment where mostly end-up and thereby affecting their fauna and flora population vastly. Besides, this study highlights the COVID-19 spread, its evolutionary importance, taxonomy, genomic structure, transmission to humans, prevention, and treatment.


Subject(s)
COVID-19 , Pandemics , Ecosystem , Humans , Masks , SARS-CoV-2
5.
Exp Hematol ; 89: 43-54.e2, 2020 09.
Article in English | MEDLINE | ID: mdl-32750404

ABSTRACT

Steady-state erythropoiesis generates new erythrocytes at a constant rate, and it has enormous productive capacity. This production is balanced by the removal of senescent erythrocytes by macrophages in the spleen and liver. Erythroid homeostasis is highly regulated to maintain sufficient erythrocytes for efficient oxygen delivery to the tissues, while avoiding viscosity problems associated with overproduction. However, there are times when this constant production of erythrocytes is inhibited or is inadequate; at these times, erythroid output is increased to compensate for the loss of production. In some cases, increased steady-state erythropoiesis can offset the loss of erythrocytes but, in response to inflammation caused by infection or tissue damage, steady-state erythropoiesis is inhibited. To maintain homeostasis under these conditions, an alternative stress erythropoiesis pathway is activated. Emerging data suggest that the bone morphogenetic protein 4 (BMP4)-dependent stress erythropoiesis pathway is integrated into the inflammatory response and generates a bolus of new erythrocytes that maintain homeostasis until steady-state erythropoiesis can resume. In this perspective, we define the mechanisms that generate new erythrocytes when steady-state erythropoiesis is impaired and discuss experimental models to study human stress erythropoiesis.


Subject(s)
Bone Morphogenetic Protein 4/genetics , Erythrocytes/cytology , Erythroid Precursor Cells/cytology , Erythropoiesis/genetics , Macrophages/cytology , Stress, Physiological/genetics , Animals , Bone Morphogenetic Protein 4/immunology , Cellular Senescence/immunology , Cytokines/genetics , Cytokines/immunology , Erythrocytes/immunology , Erythroid Precursor Cells/immunology , Erythropoiesis/immunology , Gene Expression Regulation , Humans , Inflammation , Liver/cytology , Liver/immunology , Macrophages/immunology , Mice , Models, Biological , Phagocytosis , Spleen/cytology , Spleen/immunology , Stress, Physiological/immunology
6.
Inflammopharmacology ; 28(3): 667-695, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32144521

ABSTRACT

Selenium is an essential immunonutrient which holds the human's metabolic activity with its chemical bonds. The organic forms of selenium naturally present in human body are selenocysteine and selenoproteins. These forms have a unique way of synthesis and translational coding. Selenoproteins act as antioxidant warriors for thyroid regulation, male-fertility enhancement, and anti-inflammatory actions. They also participate indirectly in the mechanism of wound healing as oxidative stress reducers. Glutathione peroxidase (GPX) is the major selenoprotein present in the human body, which assists in the control of excessive production of free radical at the site of inflammation. Other than GPX, other selenoproteins include selenoprotein-S that regulates the inflammatory cytokines and selenoprotein-P that serves as an inducer of homeostasis. Previously, reports were mainly focused on the cellular and molecular mechanism of wound healing with reference to various animal models and cell lines. In this review, the role of selenium and its possible routes in translational decoding of selenocysteine, synthesis of selenoproteins, systemic action of selenoproteins and their indirect assimilation in the process of wound healing are explained in detail. Some of the selenium containing compounds which can acts as cancer preventive and therapeutics are also discussed. These compounds directly or indirectly exhibit antioxidant properties which can sustain the intracellular redox status and these activities protect the healthy cells from reactive oxygen species induced oxidative damage. Although the review covers the importance of selenium/selenoproteins in wound healing process, still some unresolved mystery persists which may be resolved in near future.


Subject(s)
Inflammation/drug therapy , Inflammation/metabolism , Selenium/pharmacology , Selenium/therapeutic use , Selenoproteins/metabolism , Animals , Antioxidants/pharmacology , Antioxidants/therapeutic use , Humans , Oxidation-Reduction/drug effects , Reactive Oxygen Species/metabolism
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