GR15 peptide of S-adenosylmethionine synthase SAMe from Arthrospira platensis demonstrated antioxidant mechanism against H2O2 induced oxidative stress in in-vitro MDCK cells and in-vivo zebrafish larvae model

GR15 is a short molecule or peptide composed of aliphatic amino acids and possesses to have antioxidant properties. The GR15, 1GGGAFSGKDPTKVDR15 was identified from the protein S-adenosylmethionine synthase (SAMe) expressed during the sulfur departed state of Arthrospira platensis (spirulina or cyanobacteria). The in-silico assessment and the structural features of GR15 showed its antioxidant potency. Real-time PCR analysis found the up-regulation of ApSAMe expression on day 15 against oxidative stress due to 10 mM H2O2 treatment in A. platensis (Ap). The antioxidant activity of GR15 was accessed by the cell-free antioxidant assays such as ABTS, SARS, HRAS and NO; the results showed dose-dependent antioxidant activity. The toxicity assay was performed in both in vitro and in vivo models, in which peptide does not exhibit any toxicity in MDCK cell and zebrafish embryos. The intercellular ROS reduction potential of GR15 peptide was also investigated in both in vitro and in vivo models including LDH assay, antioxidant enzymes (SOD and CAT), and fluorescent staining assay (DCFDA, Hochest and Acridine orange sting) was performed; the results showed that the GR15 peptide was effectively reduced the ROS level. Further, RT-PCR demonstrated that GR15 enhanced the antioxidant property and also up-regulated the antioxidant gene, thus reduced the ROS level in both in vitro and in vivo models. Based on the results obtained from this study, we propose that GR15 has the potential antioxidant ability; hence further research can be directed towards the therapeutic product or drug development against disease caused by oxidative stress

Signet cell rectal carcinoma with prostatic involvement detected by FAPI-04 PET-MRI fusion

Abstract A 60-year-old male patient diagnosed with mucinous adenocarcinoma of lower third of rectum underwent abdominoperineal resection and permanent colostomy followed by adjuvant chemotherapy. Response evaluation with F-18 FDG PET-CT showed a complete metabolic response. After 6 months, CEA levels started increasing and clinically a recurrence was suspected. A restaging FDG PET-CT showed no obvious malignant disease. Patient presented again within a month with complaints of urinary retention and haematuria. CEA levels were further elevated, and Ga-68 FAPI-04 (FAPI) PET-CT was performed. FAPI PET-CT revealed prostatic and seminal vesicle disease involvement. Additionally, an MRI of pelvis was done and fused with FAPI PET for confirmation of prostatic involvement

Molecular mechanism of down-regulating adipogenic transcription factors in 3T3-L1 adipocyte cells by bioactive anti-adipogenic compounds

Obesity is growing at an alarming rate, which is characterized by increased adipose tissue. It increases the probability of many health complications, such as diabetes, arthritis, cardiac disease, and cancer. In modern society, with a growing population of obese patients, several individuals have increased insulin resistance. Herbal medicines are known as the oldest method of health care treatment for obesity-related secondary health issues. Several traditional medicinal plants and their effective phytoconstituents have shown anti-diabetic and anti adipogenic activity. Adipose tissue is a major site for lipid accumulation as well as the whole-body insulin sensitivity region. 3T3-L1 cell line model can achieve adipogenesis. Adipocyte characteristics features such as expression of adipocyte markers and aggregation of lipids are chemically induced in the 3T3-L1 fibroblast cell line. Differentiation of 3T3-L1 is an efficient and convenient way to obtain adipocyte like cells in experimental studies. Peroxisome proliferation activated receptor γ (PPARγ) and Cytosine-Cytosine-Adenosine Adenosine-Thymidine/Enhancer-binding protein α (CCAAT/Enhancer-binding protein α or C/EBPα) are considered to be regulating adipogenesis at the early stage, while adiponectin and fatty acid synthase (FAS) is responsible for the mature adipocyte formation. Excess accumulation of these adipose tissues and lipids leads to obesity. Thus, investigating adipose tissue development and the underlying molecular mechanism is important in the therapeutical approach. This review describes the cellular mechanism of 3T3-L1 fibroblast cells on potential anti-adipogenic herbal bioactive compounds

Electrodeposition of vanadium pentoxide on carbon fiber cloth as a binder-free electrode for high-performance asymmetric supercapacitor

Electrodeposition technique is a convenient and robust approach for the development of transition metal oxides as electrodes, particularly for supercapacitor applications. However, achieving uniform coating is difficult and relies on the constrained deposition parameters. Herein, we fabricated the binder-free spiral rope-like structured V2O5 on carbon fiber cloth (CFC) by simple and versatile electrodeposition method for high performance asymmetric supercapacitors. The deposition rate of V2O5 nanostructures on CFC was controlled by varying the electrodeposition duration. The resultant optimum duration (30 min) of the binder-free V2O5@CFC-30 electrode showed an excellent performance with a high areal capacitance of 354 mF/cm2 in 1 M Na2SO4 aqueous electrolyte. Furthermore, the asymmetric supercapacitor (ASC) was developed using V2O5@CFC-30 as a positive electrode and O, N, S enriched activated carbon (O, N, S@AC) as a negative electrode. The ASC demonstrated a maximum device-specific capacitance of 57 F/g, excellent cyclic stability (~94%) even after 10,000 cycles and maximum specific energy (17.7 Wh/kg) and power (2728 W/kg). Furthermore, the flexible supercapacitor delivered maximum specific energy (13 Wh/kg) and power (3871 W/kg) with an outstanding capacity retention of 91% over 4000 cycles. This research makes the electrodeposition of V2O5 ideally suited for a binder-free, high performance supercapacitor applications

Synergetic effect induced/tuned bimetallic nanoparticles (Pt-Ni) anchored graphene as a catalyst for oxygen reduction reaction and scalable SS-314L serpentine flow field proton exchange membrane fuel cells (PEMFCs)

© 2022 Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/A simple design of electroactive and cost-effective electrocatalysts for oxygen reduction reaction (ORR) activity is crucial towards energy conversion in the commercialization of proton exchange membrane fuel cells (PEMFCs). Herein, we synthesized a stable electroactive bimetallic catalyst of Ni anchored with low loading of Pt nanoparticles, and graphene used as a supportive material for catalyst integration (Pt3-Ni/G). It exhibited maximum electrochemical surface area (ECSA, 108.56 m2/gPt), mass activity (2.2 A mgPt) and specific activity (3.47 mA cm-2), signifying an excellent ORR activity. In addition, a scalable PEMFC fabrication through 0.2 mgPtcm-2 Pt3-Ni/G as cathode with an active area of 25 cm2 and stainless steel-314L (SS-314L) used as a serpentine flow field. This strategy provides a maximum power output of 71.25 W mgPt-1 at current density 1.59 A cm-2. In addition, Pt3-Ni/C//Pt/C, based PEMFC system delivered a constant power output (68.75 W mgPt-1) even after 4 h of continuous cycling.This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF-2014R1A6A1030419). This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (No. 2020112382). The authors also wish to acknowledge the support and facilities offered by the PSG management, PSG Institute of Advanced Studies, PSG Sons & Charities, Coimbatore, India.Peer ReviewedPostprint (published version

Engineering redox active sites enriched 3D-on-2D bimetallic double layered hydroxide electrode for supercapatteries

DOI link format: http://dx.doi.org/10.1016/j.mtener.2022.101182 © 2022 Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/The functionalization of structural nanoengineered battery-type electrodes has aided the emergence of supercapattery (SCp) subclass, which enables a wide range of applications. Herein, our research work provides a platform for two-step fabrication of nanoengineered 3D-on-2D structure as a promising approach to obtain high-performance battery-type electrodes. The hierarchical 2D NiCo bimetallic LDH NC(12)40 electrode was fabricated using electrodeposition, while the nanoengineered 3D ZIF-67 on 2D LDH electrode was achieved via pseudomorphic replication techniques. The fabricated 3D-on-2D NC(12)40-30 electrode reveals a maximum areal capacity of 1044 mC cm-2 at a current density of 4 mA cm-2 in 6 M KOH electrolyte. Furthermore, NC(12)40-30//AC was integrated as a SCp device, achieving a maximum specific capacitance of 63 F/g and maximum specific energy and power of 20.5 W/h/kg and 8522.7 W/kg, respectively, with improved capacitance retention (85%) even after 10,000 cycles. Thus, the assembled SCp coin cell displays 18-LED illumination in four different commercial LED colors, indicating the viability of the battery-type electrode for SCp development.This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF-2014R1A6A1030419) and by the National Research Foundation of Korea (NRF) Grant funded by the Korean government (MSIT) (No. 2020112382). This work has been partially supported by the Spanish government under project PID2019-109215RB-C41 (SCALED).Peer ReviewedPostprint (author's final draft

Selenium enriched hybrid metal chalcogenides with enhanced redox kinetics for high-energy density supercapacitors

© 2021 Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/Rational design and synergistic interactions between the electrode and electroactive materials have a huge impact on elevating the energy storage performance of supercapacitor devices. Herein, selenium enriched hybrid NiSe2@Fe3Se4 (NFS) nanocomposites have been facilely deposited on Ni-foam using chemical bath deposition (CBD) technique. The NiSe2@Fe3Se4 hybrid composites exhibited better electrochemical performance than that of monometallic selenides (NiSe2 and Fe3Se4), which can be attributed to the synergy effect and improved conductivity of polymetallic ions over the Ni foam substrate. The effect of NFS deposition time on Ni foam was studied and it greatly influences the morphological and electrochemical performances. Specifically, the NFS deposited for 36 h (NFS@36 h) provides a maximum areal capacity of 6.05 C cm-2 at 6 mA cm-2, which is almost four-fold higher than that of pure NiSe2 (0.168 C cm-2) and Fe3Se4 (1.46 C cm-2). Furthermore, a hybrid supercapacitor (HSC) is assembled utilizing the NFS@36 h as a positive electrode and biomass derived O, N enriched activated carbon as a negative electrode with an aqueous electrolyte. With a high-mass loading of 21.5 mg cm-2, the device demonstrates superior specific energy of 52 W h kg-1 at 398 W kg-1 specific power and even maintained 19 W h kg-1 at a maximum specific 8000 W kg-1. Furthermore, the device exhibited excellent cycling durability with ~ 92% of specific capacitance retention for 10,000 charge/discharge cycles at 5 A g-1. Besides, the HSCs have been successfully illuminated several light emitting diodes (LEDs) and portable displays demonstrating superior energy storage performance.Peer ReviewedPostprint (author's final draft

Anti-Cancer and Anti-Inflammatory Activities of a Short Molecule, PS14 Derived from the Virulent Cellulose Binding Domain of Aphanomyces invadans, on Human Laryngeal Epithelial Cells and an In Vivo Zebrafish Embryo Model

In this study, the anti-cancer and anti-inflammatory activities of PS14, a short peptide derived from the cellulase binding domain of pathogenic fungus, Aphanomyces invadans, have been evaluated, in vitro and in vivo. Bioinformatics analysis of PS14 revealed the physicochemical properties and the web-based predictions, which indicate that PS14 is non-toxic, and it has the potential to elicit anti-cancer and anti-inflammatory activities. These in silico results were experimentally validated through in vitro (L6 or Hep-2 cells) and in vivo (zebrafish embryo or larvae) models. Experimental results showed that PS14 is non-toxic in L6 cells and the zebrafish embryo, and it elicits an antitumor effect Hep-2 cells and zebrafish embryos. Anticancer activity assays, in terms of MTT, trypan blue and LDH assays, showed a dose-dependent inhibitory effect on cell proliferation. Moreover, in the epithelial cancer cells and zebrafish embryos, the peptide challenge (i) caused significant changes in the cytomorphology and induced apoptosis; (ii) triggered ROS generation; and (iii) showed a significant up-regulation of anti-cancer genes including BAX, Caspase 3, Caspase 9 and down-regulation of Bcl-2, in vitro. The anti-inflammatory activity of PS14 was observed in the cell-free in vitro assays for the inhibition of proteinase and lipoxygenase, and heat-induced hemolysis and hypotonicity-induced hemolysis. Together, this study has identified that PS14 has anti-cancer and anti-inflammatory activities, while being non-toxic, in vitro and in vivo. Future experiments can focus on the clinical or pharmacodynamics aspects of PS14

A synthetic antioxidant molecule, GP13 derived from cysteine desulfurase of spirulina, Arthrospira platensis exhibited anti-diabetic activity on L6 rat skeletal muscle cells through GLUT-4 pathway

Objectives: Diabetes creates oxidative stress, which damages several organs and causes various problems including hyperglycemia, hyperlipidemia, hypertension, and maybe iron dyshomeostasis. Consequently, antioxidant therapy may be a promising strategy to avoid diabetes and diabetic complications. In the current study, we investigated the activity of the antioxidant GP13 peptide in an in-vitro diabetic model. Methods: All anti-diabetic and antioxidant in-vitro tests were performed on differentiated L6 myotubes cells. MTT assay was used to analyze the cytotoxic effect of the GP13 at different concentrations (10 μM to 80 μM) in the L6 cells. The DCFDA fluorescence was performed to confirm the radical scavenging effect of GP13 in the myotubule cells. The cells were treated with different concentrations of GP13 peptide before the enzyme assay was conducted. The differentiated L6 myotubes were kept for serum deprivation for 8 h before being treated with GP13 peptide. The RNA extraction from the L6 myotubes was performed using the Trizol reagent. Results: Cell viability analysis exhibited the non-toxic nature of GP13 in a dose-dependent manner (10 μM to 80 μM). Antioxidant enzyme, superoxide dismutase activity was 23.25 U/mL in the untreated group, whereas it was only 11.75 U/mL in the group that was exposed to GP13 at 80 μM. The catalase activity at 40 μM was slightly altered in the cells, while the hydrogen peroxide inhibition activity was higher (91.2%) compared to the control group. Additionally, GP13 showed anti-diabetic effects through a dose-dependent increase in glycogen storage (6.1 mM). It was discovered that 40 μM was the ideal concentration for the highest level of activity. Additionally, the genes involved in diabetes-related to antioxidants and the insulin signalling system were investigated. Conclusion: It is concluded that the GP13 peptide from A. platensis is a promising agent for anti-diabetic and antioxidant activities. To treat diabetes and its consequences, we thus propose that GP13 be regarded as a natural lead. The animal model design of this study has limitations, and further research is needed to draw conclusions about its therapeutic relevance to people

Aquatic Peptide: The Potential Anti-Cancer and Anti-Microbial Activity of GE18 Derived from Pathogenic Fungus <i>Aphanomyces invadans</i>

Small molecules as well as peptide-based therapeutic approaches have attracted global interest due to their lower or no toxicity in nature, and their potential in addressing several health complications including immune diseases, cardiovascular diseases, metabolic disorders, osteoporosis and cancer. This study proposed a peptide, GE18 of subtilisin-like peptidase from the virulence factor of aquatic pathogenic fungus Aphanomyces invadans, which elicits anti-cancer and anti-microbial activities. To understand the potential GE18 peptide-induced biological effects, an in silico analysis, in vitro (L6 cells) and in vivo toxicity assays (using zebrafish embryo), in vitro anti-cancer assays and anti-microbial assays were performed. The outcomes of the in silico analyses demonstrated that the GE18 peptide has potent anti-cancer and anti-microbial activities. GE18 is non-toxic to in vitro non-cancerous cells and in vivo zebrafish larvae. However, the peptide showed significant anti-cancer properties against MCF-7 cells with an IC50 value of 35.34 µM, at 24 h. Besides the anti-proliferative effect on cancer cells, the peptide exposure does promote the ROS concentration, mitochondrial membrane potential and the subsequent upregulation of anti-cancer genes. On the other hand, GE18 elicits significant anti-microbial activity against P. aeruginosa, wherein GE18 significantly inhibits bacterial biofilm formation. Since the peptide has positively charged amino acid residues, it targets the cell membrane, as is evident in the FESEM analysis. Based on these outcomes, it is possible that the GE18 peptide is a significant anti-cancer and anti-microbial molecule