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2.
J Acupunct Meridian Stud ; 17(1): 38-43, 2024 Feb 29.
Article in English | MEDLINE | ID: mdl-38409813

ABSTRACT

Background: : Osteoarthritis of the knee (OAK) is a chronic degenerative musculoskeletal disorder that strongly affects the elderly population and decreases their quality of life. Pain, stiffness, and restricted knee movements are the major characteristic features of OAK. There are no studies available on the effect of the liver 7 (LR 7) acupuncture point on pain and range of motion. Objectives: : To study the effectiveness of the LR 7 acupuncture point on pain and range of motion in chronic OAK patients. Methods: : Thirty-five subjects aged between 40 and 65 years were recruited from Government Yoga and Naturopathy Medical College, Chennai. Participants were included in the study after they fulfilled the eligibility criteria. The duration of acupuncture was 20 minutes (5 days/week) for 2 weeks. Baseline and post-intervention assessments were performed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and the degree of knee flexion and extension was measured using a goniometer. Results: : Pre- and post-trial outcomes were compared using paired t-tests. LR 7 acupuncture reduced the WOMAC score from 49 to 30 (p < 0.001), indicating that pain was alleviated. Treatment increased the range of knee flexion from 110 to 115 degrees and reduced knee extension (p < 0.01) from 16 to 9 degrees (p < 0.001). These findings indicate that acupuncture treatment improved the range of knee movement. Conclusion: : The present study showed that 10 sessions of LR 7 acupuncture for people with OAK significantly reduced pain and increased range of motion. We conclude that LR 7 acupuncture is an adjuvant therapy for alleviating pain and managing OAK.


Subject(s)
Acupuncture Therapy , Osteoarthritis, Knee , Adult , Aged , Humans , Middle Aged , Acupuncture Points , India , Liver , Osteoarthritis, Knee/therapy , Pain , Quality of Life , Range of Motion, Articular , Treatment Outcome
3.
Diabetes Metab Syndr ; 14(6): 2245-2249, 2020.
Article in English | MEDLINE | ID: mdl-33395786

ABSTRACT

BACKGROUND AND AIMS: COVID-19 is a multi-system disease, with coagulation abnormalities. D-dimer levels are increased in this disease. We aimed to determine the association of D-dimer levels and mortality and to establish its optimal cut off values in predicting mortality. Association of D-dimer levels with diabetes mellitus has also been established. METHODS: Information on 483 patients with confirmed COVID-19 was retrospectively collected and analyzed. The optimal D-dimer cutoff point and C-statistic of routine tests both on admission and during hospital stay were evaluated by receiver operator characteristic (ROC) curve. RESULTS: D-dimer elevation (≥0.50 µg/mL) was seen in 80.1% of the hospitalized patients. D-dimer level ≥2.01 µg/mL was a significant predictor of subsequent deaths (P < 0.01; HR, 3.165; 95% CI, 2.013-4.977). High D-dimer values (≥0.50 µg/mL) were observed in 72 of the 75 (96%) cases with a fatal outcome. Median D-dimer value among non-survivors was 6.34 µg/mL and among survivors it was 0.94 µg/mL. A higher proportion of fatal outcomes occurred in patients with underlying disease (89.0%), most prominent of which was diabetes mellitus (66%). The median D-dimer value was found to be significantly high in diabetic patients (1.68 µg/mL). CONCLUSIONS: Among the measured coagulation parameters, D-dimer during hospital stay had the highest C-index to predict in-hospital mortality in COVID-19 patients. D-dimer value ≥ 2.01 µg/mL can effectively predict in-hospital mortality in patients with COVID-19. A significant association of increased D-dimer level has been found with diabetes mellitus and elderly age.


Subject(s)
COVID-19/blood , COVID-19/mortality , Fibrin Fibrinogen Degradation Products/metabolism , Adult , Aged , Biomarkers/blood , Female , Humans , Male , Middle Aged , Mortality/trends , Predictive Value of Tests , Retrospective Studies , Young Adult
4.
J Antimicrob Chemother ; 74(6): 1618-1626, 2019 06 01.
Article in English | MEDLINE | ID: mdl-30863862

ABSTRACT

BACKGROUND: MDR Staphylococcus aureus is a major aetiological agent of catheter-associated infections. A quorum sensing targeted drug development approach proves to be an effective alternative strategy to combat such infections. METHODS: Intravenous catheters were coated with polymethacrylate copolymers loaded with the antivirulent compound 2-[(methylamino)methyl]phenol (2MAMP). The in vitro drug release profile and kinetics were established. The anti-biofilm effect of the coated catheters was tested against clinical isolates of MDR S. aureus. The in vivo studies were carried out using adult male Wistar rats by implanting coated catheters in subcutaneous pockets. Histopathological analysis was done to understand the immunological reactions induced by 2MAMP. RESULTS: A uniform catheter coating of thickness 0.1 mm was achieved with linear sustained release of 2MAMP for 6 h. The coating formulation was cytocompatible. The in vitro and in vivo anti-adherence studies showed reduced bacterial accumulation in coated catheters after 48 h. The histopathological results confirmed that the coated catheter did not bring about any adverse inflammatory response. CONCLUSIONS: The developed anti-quorum-coated catheter that is non-toxic and biocompatible has the potential to be used in other medical devices, thereby preventing catheter-associated infections.


Subject(s)
Catheter-Related Infections/microbiology , Catheters , Coated Materials, Biocompatible , Polymers , Quorum Sensing/drug effects , Staphylococcal Infections/microbiology , Staphylococcus aureus/drug effects , Animals , Biofilms/drug effects , Catheter-Related Infections/drug therapy , Catheters/microbiology , Coated Materials, Biocompatible/pharmacology , Disease Models, Animal , Microbial Sensitivity Tests , Polymers/chemistry , Rats , Spectrum Analysis , Staphylococcal Infections/drug therapy , Staphylococcal Infections/pathology
5.
Diabetes Metab ; 45(3): 276-285, 2019 06.
Article in English | MEDLINE | ID: mdl-30165157

ABSTRACT

AIMS: MicroRNAs (miRNAs) from extracellular vesicles (EVs) have been proposed as promising biomarkers for a number of diseases. In this study, their potential as urine-based biomarkers of diabetic nephropathy (DN) was assessed. METHODS: MiRNAs were profiled in urinary EVs from 160 fasting subjects with normal glucose tolerance (NGT) and in T2DM patients with either microalbumininuria (MIC) or macroalbuminuria (MAC). RESULTS: A total of 73 miRNAs detected in urinary EVs (NGT) were predicted to target important functions for kidney homoeostasis, thereby validating their use as indicators of kidney dysfunction. Indeed, a urinary EV miRNA signature was found to comprise increased levels of let-7i-3p, miR-24-3p and miR-27b-3p, and decreased levels of miR-15b-5p, to identify patients with MIC. ROC curve analysis confirmed this ability to identify MIC in normo-albuminuria T2DM (T2DM-NA) patients and to differentiate between MAC and T2DM patients. These miRNAs were also predicted to target protein networks involved in the Wnt/ß-catenin signalling cascade, activin receptor signalling and cell differentiation/proliferation, and correlated with eGRF, HbA1c, serum creatinine, urea, albumin and blood pressure. Concentrations of miR-30a-5p were specifically modified in urinary EVs from patients with MAC, but not MIC, suggesting that miR-30a-5p could be related to severe kidney damage. CONCLUSION: Urinary EV miRNAs correlate with the degree of MIC. As they are also thought to regulate pathways that are targets of pharmacological agents to prevent DN (reticulum stress, activin receptors), they may also serve as non-invasive 'liquid biopsies' to stratify patients at risk of developing MAC and to monitor treatment efficacy.


Subject(s)
Albuminuria/diagnosis , Diabetes Mellitus, Type 2/urine , Diabetic Nephropathies/diagnosis , Extracellular Vesicles/metabolism , MicroRNAs/metabolism , Adult , Albuminuria/urine , Asian People , Biomarkers/urine , Diabetic Nephropathies/urine , Female , Humans , Male , MicroRNAs/genetics , Middle Aged , Phenotype
6.
Environ Monit Assess ; 190(8): 445, 2018 Jul 02.
Article in English | MEDLINE | ID: mdl-29968022

ABSTRACT

The purpose of the present study was to explain land-use/cover changes in Coimbatore City Corporation using Landsat ETM+ and Landsat 8 Operational Land Imager (OLI) and Thermal Infrared Sensor (TIRS) data for the period of 2003-2014. Two Landsat images from years 2003 and 2014 were downloaded from USGS Earth Explorer. Maximum likelihood method was used to classify the images into five classes: urban fabric, vegetation, water bodies, agriculture lands, and barren lands. Overall kappa accuracy measure is about to 87.60 and 86.15% for the years 2003 and 2014, respectively. The change detection analysis has been performed for years 2003 and 2014 postclassified images. The results of the study have indicated that Coimbatore City has experienced rapid modifications in LULC, particularly in terms of urban/built-up area. Over the past 11 years, urban/built-up areas have increased by 94.5 km2, resulting in a significant drop in the area of agricultural land and vegetation cover. It is found that (1) urban areas are increased 200% due to population growth cum rapid economic progress. (2) Vegetation cover decreased 38.76% due to conversion into urban features. (3) Water bodies in area increased to 15.78% due to eradication of encroachment. (4) There is loss of 1.89% of agricultural lands due to demand for construction activities. (5) About 85.24% of barren lands were converted into other uses, particularly 57.33% to urban areas. (6) Urban growth has accelerated towards north-eastern, northern, and eastern parts, where national highways exist. The built-up areas were dropped from 85.32 to 22.28%, within 5-km distance from the city center.


Subject(s)
Conservation of Natural Resources , Environmental Monitoring/methods , Geographic Information Systems , Remote Sensing Technology , Agriculture , Cities , India , Population Growth , Urbanization
7.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-700162

ABSTRACT

Objective: To synthesize bio-inspired gold nanoparticles (AuNPs) using the leaf extract of Justicia adhatoda and evaluate the anti-cancer activity on human lung cancer cell line (A549). Methods: Synthesis of AuNPs was done using an aqueous leaf extract of Justicia adhatoda as a green route. The bio-synthesized AuNPs were confirmed and characterized by using various spectral studies such as UV-Vis spectrum, Scanning Electron Microscope with EDAX, Transmission Electron Microscope, Fourier Transmission Infrared Spectroscope analysis and Surface Enhanced Raman Spectroscopy. The cell viability was determined by MTT reduction assay. In addition, cytomorphology and the nuclear morphological study of A549 cell line was observed under fluorescence microscope. Results: UV-Vis spectrum showed surface plasmon resonance peak at 547 nm, scanning electron microscope and transmission electron microscope studies showed the monodispersed spherical shape and its average size in the range of 40.1 nm was noticed. Fourier Transmission Infrared Spectroscope analysis confirmed that the C=O group of amino acids of proteins had strong ability to bind with the surface of nanoparticle. Interestingly, our results also demonstrated inhibited proliferation of A549 cell line by MTT (IC50 value: 80 μg/mL). Cell morphology was observed and cell death was caused by apoptosis as revealed by propidium iodide staining. Conclusions: The current study proves the anticancer potential of bio-synthesized AuNPs. Thus, synthesized AuNPs can be used for the treatment of human lung cancer cell (A549) and it can be exploited for drug delivery in future.

9.
Mol Cell Biochem ; 423(1-2): 93-104, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27699590

ABSTRACT

In the context of high human consumption of fructose diets, there is an imperative need to understand how dietary fructose intake influence cellular and molecular mechanisms and thereby affect ß-cell dysfunction and insulin resistance. While evidence exists for a relationship between high-fat-induced insulin resistance and metabolic disorders, there is lack of studies in relation to high-fructose diet. Therefore, we attempted to study the effect of different diets viz., high-fat diet (HFD), high-fructose diet (HFS), and a combination (HFS + HFD) diet on glucose homeostasis and insulin sensitivity in male Wistar rats compared to control animals fed with normal pellet diet. Investigations include oral glucose tolerance test, insulin tolerance test, histopathology by H&E and Masson's trichrome staining, mRNA expression by real-time PCR, protein expression by Western blot, and caspase-3 activity by colorimetry. Rats subjected to high-fat/fructose diets became glucose intolerant, insulin-resistant, and dyslipidemic. Compared to control animals, rats subjected to different combination of fat/fructose diets showed increased mRNA and protein expression of a battery of ER stress markers both in pancreas and liver. Transcription factors of ß-cell function (INSIG1, SREBP1c and PDX1) as well as hepatic gluconeogenesis (FOXO1 and PEPCK) were adversely affected in diet-induced insulin-resistant rats. The convergence of chronic ER stress towards apoptosis in pancreas/liver was also indicated by increased levels of CHOP mRNA & increased activity of both JNK and Caspase-3 in rats subjected to high-fat/fructose diets. Our study exposes the experimental support in that high-fructose diet is equally detrimental in causing metabolic disorders.


Subject(s)
Diabetes Mellitus, Experimental/metabolism , Dietary Carbohydrates/adverse effects , Dietary Fats/adverse effects , Endoplasmic Reticulum Stress/drug effects , Fructose/adverse effects , Insulin Resistance , Liver/metabolism , Pancreas/metabolism , Animals , Diabetes Mellitus, Experimental/pathology , Dietary Carbohydrates/pharmacology , Dietary Fats/pharmacology , Fructose/pharmacology , Humans , Liver/pathology , Male , Pancreas/pathology , Rats , Rats, Wistar
10.
Biomed Pharmacother ; 82: 72-9, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27470341

ABSTRACT

Activation of the IL-6 mediated JAK-STAT (Janus associated kinase-signal transducer and activator of transcription) oncogenic signalling plays a major role in hepatocellular carcinoma pathogenesis. The aim of this study is to assess the anti-tumour, anti-proliferative and apoptotic potential of artesunate and its capacity to modulate JAK-STAT pathway in a nitrosodiethylamine mediated experimental hepatocellular carcinoma model. Administration of nitrosodiethylamine (200mg/kg body weight by i.p. Injections) to rats resulted in alterations of liver pathophysiological parameters such as increased relative liver weight, and increased tumour nodule occurrence. It also increased the levels of serum marker enzymes (AST, ALT, ALP, LDH, and γGT) and tumour biomarker (AFP) levels suggestive of its capacity to cause liver tumourigenesis. Additionally, the immunohistochemistry of liver sections pertaining to nitrosodiethylamine administered animals showed increased detection of AgNOR, PCNA, and GST-Pi positive cells suggestive of its capacity to promote liver proliferation associated tumourigenesis. On the contrary, artesunate (25mg/kg bodyweight) supplementation to nitrosodiethylamine administered animals decreased all the above mentioned pathophysiological, biochemical, and immunohistochemistry parameters suggesting its anti-tumour and anti-proliferative potential. Furthermore, immunoblot analysis showed significant up-regulation of IL-6, GP130, JAK-2, STAT-3 (pY705), Bcl-xL, Bcl-2 and simultaneous down-regulation of Caspase-3, PARP and SOCS-3 in nitrosodiethylamine administered animals. Nevertheless, the immunoblot analysis revealed vice-versa on artesunate supplementation to nitrosodiethylamine administered animals, indicating promotion of the feedback loop inhibition mechanism through SOCS3 up-regulation thereby leading to suppression of JAK-STAT signalling. Overall all these findings substantiate that artesunate promotes anti-tumour, anti-proliferation and apoptosis against nitrosodiethylamine mediated hepatocellular carcinoma.


Subject(s)
Artemisinins/therapeutic use , Carcinoma, Hepatocellular/drug therapy , Interleukin-6/metabolism , Janus Kinases/metabolism , Liver Neoplasms, Experimental/drug therapy , STAT3 Transcription Factor/metabolism , Signal Transduction , Animals , Artemisinins/pharmacology , Artesunate , Biomarkers, Tumor/blood , Blotting, Western , Body Weight/drug effects , Carcinoma, Hepatocellular/pathology , DNA Fragmentation/drug effects , Immunoblotting , Immunohistochemistry , Liver/drug effects , Liver/enzymology , Liver/pathology , Liver Neoplasms, Experimental/pathology , Male , Organ Size/drug effects , Proliferating Cell Nuclear Antigen/metabolism , Rats, Wistar , Signal Transduction/drug effects , Silver Staining , alpha-Fetoproteins/metabolism
11.
Int. braz. j. urol ; 41(6): 1116-1125, Nov.-Dec. 2015. tab, graf
Article in English | LILACS | ID: lil-769752

ABSTRACT

Purpose: Sodium thiosulfate (STS) is clinically reported to be a promising drug in preventing nephrolithiasis. However, its mechanism of action remains unclear. In the present study, we investigated the role of mitochondrial KATP channel in the renal protection mediated by STS. Materials and Methods: Nephrolithiasis was induced in Wistar rats by administrating 0.4% ethylene glycol (EG) along with 1% ammonium chloride for one week in drinking water followed by only 0.75% EG for two weeks. Treatment groups received STS, mitochondrial KATP channel opener and closer exclusively or in combination with STS for two weeks. Results: Animals treated with STS showed normal renal tissue architecture, supported by near normal serum creatinine, urea and ALP activity. Diazoxide (mitochondria KATP channel opening) treatment to the animal also showed normal renal tissue histology and improved serum chemistry. However, an opposite result was shown by glibenclamide (mitochondria KATP channel closer) treated rats. STS administered along with diazoxide negated the renal protection rendered by diazoxide alone, while it imparted protection to the glibenclamide treated rats, formulating a mitochondria modulated STS action. Conclusion: The present study confirmed that STS render renal protection not only through chelation and antioxidant effect but also by modulating the mitochondrial KATP channel for preventing urolithiasis.


Subject(s)
Animals , Male , Antioxidants/pharmacokinetics , Chelating Agents/pharmacology , Ethylene Glycol , Nephrolithiasis/prevention & control , Potassium Channels/pharmacology , Thiosulfates/pharmacology , Antioxidants/therapeutic use , Calcium Oxalate/metabolism , Chelating Agents/therapeutic use , Disease Models, Animal , Electrophoresis, Agar Gel , Kidney/drug effects , Kidney/pathology , Lipid Peroxidation/drug effects , Nephrolithiasis/pathology , Potassium Channels/therapeutic use , Random Allocation , Rats, Wistar , Reproducibility of Results , Treatment Outcome , Thiosulfates/therapeutic use
12.
Front Microbiol ; 6: 832, 2015.
Article in English | MEDLINE | ID: mdl-26322037

ABSTRACT

Urinary Tract Infection (UTI) is a globally widespread human infection caused by an infestation of uropathogens. Eventhough, Escherichia coli is often quoted as being the chief among them, Staphylococcus aureus involvement in UTI especially in gestational UTI is often understated. Staphylococcal accessory regulator A (SarA) is a quorum regulator of S. aureus that controls the expression of various virulence and biofilm phenotypes. Since SarA had been a focussed target for antibiofilm agent development, the study aims to develop a potential drug molecule targeting the SarA of S. aureus to combat biofilm associated infections in which it is involved. In our previous studies, we have reported the antibiofilm activity of SarA based biofilm inhibitor, (SarABI) with a 50% minimum biofilm inhibitory concentration (MBIC50) value of 200 µg/mL against S. aureus associated with vascular graft infections and also the antibiofilm activity of the root ethanolic extracts of Melia dubia against uropathogenic E. coli. In the present study, in silico design of a hybrid molecule composed of a molecule screened from M. dubia root ethanolic extracts and a modified SarA based inhibitor (SarABI(M)) was undertaken. SarABI(M) is a modified form of SarABI where the fluorine groups are absent in SarABI(M). Chemical synthesis of the hybrid molecule, 4-(Benzylamino)cyclohexyl 2-hydroxycinnamate (henceforth referred to as UTI Quorum-Quencher, UTI(QQ)) was then performed, followed by in vitro and in vivo validation. The MBIC50 and MBIC90 of UTI(QQ) were found to be 15 and 65 µg/mL, respectively. Confocal laser scanning microscopy (CLSM) images witnessed biofilm reduction and bacterial killing in either UTI(QQ) or in combined use of antibiotic gentamicin and UTI (QQ) . Similar results were observed with in vivo studies of experimental UTI in rat model. So, we propose that the drug UTI(QQ) would be a promising candidate when used alone or, in combination with an antibiotic for staphylococcal associated UTI.

13.
ScientificWorldJournal ; 2015: 926249, 2015.
Article in English | MEDLINE | ID: mdl-26413565

ABSTRACT

This paper presents the detailed simulation of two-dimensional incompressible laminar wall jet flow over a shallow cavity. The flow characteristics of wall jet with respect to aspect ratio (AR), step length (X u), and Reynolds number (Re) of the shallow cavity are expressed. For higher accuracy, third-order discretization is applied for momentum equation which is solved using QUICK scheme with SIMPLE algorithm for pressure-velocity coupling. Low Reynolds numbers 25, 50, 100, 200, 400, and 600 are assigned for simulation. Results are presented for streamline contour, velocity contour, and vorticity formation at wall and also velocity profiles are reported. The detailed study of vortex formation on shallow cavity region is presented for various AR, X u , and Re conditions which led to key findings as Re increases and vortex formation moves from leading edge to trailing edge of the wall. Distance between vortices increases when the step length (X u) increases. When Re increases, the maximum temperature contour distributions take place in shallow cavity region and highest convection heat transfer is obtained in heated walls. The finite volume code (FLUENT) is used for solving Navier-Stokes equations and GAMBIT for modeling and meshing.

14.
Drug Chem Toxicol ; 38(3): 328-36, 2015.
Article in English | MEDLINE | ID: mdl-25308553

ABSTRACT

CONTEXT: Neonicotinoid insecticides are synthetic analogues of nicotine that acts on the central nervous system of insects by blocking post synaptic acetylcholine receptor. Acetamiprid is one of the widely used neonicotinoid class of insecticide used to control sucking insects like aphids, bees, mosquitoes, on crops. Data on the possible immunotoxic nature of acetamiprid are lacking. OBJECTIVE: The present study was conducted in Wistar rats with the objective of evaluating the immunotoxic potential of acetamiprid administered orally at the dose levels of 27.5, 55 and 110 mg/kg b.w. (equivalent to 5.5, 11 and 22 mg/kg b.w.) for a period of 90 days. MATERIALS AND METHODS: In experiment 1, general toxicity testing including the evaluation of clinical signs, hemato-biochemical changes, response of the lymphocytes towards T and B cell mitogens, macrophage function, gross and histopathology of the lymphoid organs (spleen, thymus, lymph nodes, etc.) were performed. In the second experiment, humoral and cell-mediated responses during immunological challenges were evaluated. RESULTS: Significant decreases were observed in the stimulation index of lymphocyte proliferation to B cell mitogen and in the nitrite production of macrophages of rats treated with 110 mg/kg of acetamiprid. Significant decrease in the lymphoproliferative response towards the B cell mitogen indicated the inability of the B lymphocytes to respond on stimulation that might increase the chances of susceptibility to infections. Acetamiprid also caused 15-28% reduction in nitrite production, an important signal for efficient inflammatory response of macrophages. The functional impairment of macrophages may involve aberrations in the enzymatic degradation of microbes, oxidative burst, generation of free radicals, phagocytosis, release of proinflammatory cytokines and thereby, may hamper host defence causing susceptibility to diseases. No significant changes over hematology, biochemistry, organ weights, histopathology of major immune organs, delayed type hypersensitivity test, response to sRBCs and lymphoproliferation assay for T cell mitogen were observed. CONCLUSION: In conclusion, the results demonstrate for the first time that the subchronic administration of acetamiprid (20% SP-soluble powder) cause significant decreases in the lymphocyte proliferation as well as the macrophage function at the dose level of 110 mg/kg. Considering the chronic population adjusted dose (0.023 mg/kg/day) through dietary exposure for acetamiprid, judicious use of acetamiprid is highly essential. Indiscriminate use of acetamiprid exceeding the doses advised might pose a hazard.


Subject(s)
B-Lymphocytes/drug effects , Insecticides/toxicity , Macrophages/drug effects , Pyridines/toxicity , T-Lymphocytes/drug effects , Administration, Oral , Animals , B-Lymphocytes/immunology , B-Lymphocytes/metabolism , Cell Proliferation/drug effects , Cells, Cultured , Dose-Response Relationship, Drug , Female , Hemagglutination/drug effects , Hemagglutination Tests , Hypersensitivity, Delayed/chemically induced , Hypersensitivity, Delayed/immunology , Immunity, Cellular/drug effects , Immunity, Humoral/drug effects , Insecticides/administration & dosage , Lymphocyte Activation/drug effects , Macrophage Activation/drug effects , Macrophages/immunology , Macrophages/metabolism , Male , Neonicotinoids , Pyridines/administration & dosage , Rats, Wistar , T-Lymphocytes/immunology , T-Lymphocytes/metabolism , Time Factors , Toxicity Tests, Subchronic
15.
Int Braz J Urol ; 41(6): 1116-25, 2015.
Article in English | MEDLINE | ID: mdl-26742969

ABSTRACT

PURPOSE: Sodium thiosulfate (STS) is clinically reported to be a promising drug in preventing nephrolithiasis. However, its mechanism of action remains unclear. In the present study, we investigated the role of mitochondrial KATP channel in the renal protection mediated by STS. MATERIALS AND METHODS: Nephrolithiasis was induced in Wistar rats by administrating 0.4% ethylene glycol (EG) along with 1% ammonium chloride for one week in drinking water followed by only 0.75% EG for two weeks. Treatment groups received STS, mitochondrial KATP channel opener and closer exclusively or in combination with STS for two weeks. RESULTS: Animals treated with STS showed normal renal tissue architecture, supported by near normal serum creatinine, urea and ALP activity. Diazoxide (mitochondria KATP channel opening) treatment to the animal also showed normal renal tissue histology and improved serum chemistry. However, an opposite result was shown by glibenclamide (mitochondria KATP channel closer) treated rats. STS administered along with diazoxide negated the renal protection rendered by diazoxide alone, while it imparted protection to the glibenclamide treated rats, formulating a mitochondria modulated STS action. CONCLUSION: The present study confirmed that STS render renal protection not only through chelation and antioxidant effect but also by modulating the mitochondrial KATP channel for preventing urolithiasis.


Subject(s)
Antioxidants/pharmacokinetics , Chelating Agents/pharmacology , Ethylene Glycol , Nephrolithiasis/prevention & control , Potassium Channels/pharmacology , Thiosulfates/pharmacology , Animals , Antioxidants/therapeutic use , Calcium Oxalate/metabolism , Chelating Agents/therapeutic use , Disease Models, Animal , Electrophoresis, Agar Gel , Kidney/drug effects , Kidney/pathology , Lipid Peroxidation/drug effects , Male , Nephrolithiasis/pathology , Potassium Channels/therapeutic use , Random Allocation , Rats, Wistar , Reproducibility of Results , Thiosulfates/therapeutic use , Treatment Outcome
16.
Spectrochim Acta A Mol Biomol Spectrosc ; 138: 314-20, 2015 Mar 05.
Article in English | MEDLINE | ID: mdl-25506648

ABSTRACT

Synthesis of titanium dioxide (TiO2) nanoparticles and TiO2 loaded cashew nut shell activated carbon (TiO2/CNSAC) had been undertaken using sol-gel method and their application in BG and MB dyes removal under sunlight radiation has been investigated. The synthesized photocatalysts were characterized by X-ray diffraction analysis (XRD), Fourier infra-red spectroscopy (FT-IR), UV-Vis-diffuse reflectance spectroscopy (DRS) and scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDX). The various experimental parameters like amount of catalyst, contact time for efficient dyes degradation of BG and MB were concerned in this study. Activity measurements performed under solar irradiation has shown good results for the photodegradation of BG and MB in aqueous solution. It was concluded that the higher photocatalytic activity in TiO2/CNSAC was due to parameters like band-gap, number of hydroxyl groups, surface area and porosity of the catalyst. The kinetic data were also described by the pseudo-first-order and pseudo-second-order kinetic models.


Subject(s)
Anacardium , Carbon/chemistry , Coloring Agents/chemistry , Methylene Blue/chemistry , Quaternary Ammonium Compounds/chemistry , Titanium/chemistry , Adsorption , Catalysis , Crystallization , Food Analysis/methods , Microscopy, Electron, Scanning , Phase Transition , Porosity , Spectrophotometry, Ultraviolet , Spectroscopy, Fourier Transform Infrared , Sunlight , X-Ray Diffraction
17.
Drug Chem Toxicol ; 38(1): 50-6, 2015 Jan.
Article in English | MEDLINE | ID: mdl-24649920

ABSTRACT

CONTEXT: Withania somnifera (L) Dunal (Solanaceae) is an important traditional herbal medicine used for thousands of years and is considered as the Indian ginseng. Reports on the effect of Withania somnifera root (WSR) extract on the developing foetus of pregnant rats including mortality, structural abnormalities, changes in growth and effects on dams are not available. OBJECTIVE: The present study was performed to evaluate the prenatal developmental toxicity potential of WSR extract in rats. MATERIALS AND METHODS: WSR extract was given orally to pregnant rats during the period of major organogenesis and histogenesis (days 5 to 19 of gestation) at the dose levels of 500, 1000 and 2000 mg/kg/day. Clinical observations including mortality, moribundity, behavioural changes, signs of overt toxicity, body weight, gross pathological changes of dams and foetal analyses including external malformations, skeletal and soft tissue malformations were evaluated. RESULTS: No evidence of maternal or foetal toxicity was observed. WSR extract caused no changes (p < 0.05) in body weight of parental females, number of corpora lutea, implantations, viable foetuses, external, skeletal and visceral malformations. DISCUSSION AND CONCLUSION: Under the conditions of the study, the no-observed-effect level (NOEL) of WSR extract for maternal and developmental toxicity was concluded to be at least 2000 mg/kg/day.


Subject(s)
Abnormalities, Drug-Induced/etiology , Embryonic Development/drug effects , Maternal Exposure/adverse effects , Plant Extracts/toxicity , Withania/chemistry , Abnormalities, Drug-Induced/embryology , Administration, Oral , Animals , Dose-Response Relationship, Drug , Female , No-Observed-Adverse-Effect Level , Plant Extracts/isolation & purification , Plant Roots/chemistry , Pregnancy , Rats, Wistar , Toxicity Tests
18.
Chem Biol Interact ; 219: 175-83, 2014 Aug 05.
Article in English | MEDLINE | ID: mdl-24954034

ABSTRACT

The salubrious effects of 3-Formylchromone (3-FC) against nitrosodiethylamine (NDEA) mediated early hepatocellular carcinogenesis was investigated in vivo by this study. Male Wistar rats were administered three interspersed intraperitoneal injections of NDEA (200 mg/kg body weight) until sixth week, followed by, thrice a week oral dose of 3-FC (25 mg/kg body weight) from the seventh week to eleventh week. Oral supplementation of Wistar rats with 3-FC prevented the increase in serum marker enzymes (AST, ALT, LDH) and serum pre-neoplastic marker (γ-GT) induced by NDEA. Biochemical observations were found to be further correlated with histological studies, indicating the potential of 3-FC to mediate suppression of hepatic damage/pre-neoplastic lesions. Argyrophilic nucleolar organizer region (AgNOR) staining was done in histology sections to confirm the anti-proliferative potential of 3-FC against NDEA-induced early hepatocellular carcinogenesis. RT-PCR and immunoblot analysis was done to find the modulations in the gene transcript/protein level expression of pre-neoplastic marker (GST-pi), proliferation marker (PCNA), apoptotic mediators (PPARγ, NFκB-p65 and p53). 3-FC was found to favorably modulate the expressions of GST-pi, PCNA, PPARγ, NFκB-p65, p53 clearly confirming the anti-proliferative and apoptotic potential of 3-FC. Further, the apoptotic effect of 3-FC against NDEA-induced early hepatocellular carcinogenesis was confirmed by caspase-3 activity assay and DNA fragmentation analysis. Based on these findings, it is concluded that 3-FC possesses hepatoprotective, anti-pre-neoplastic, anti-proliferative and apoptosis inducing capability against NDEA-induced early hepatocellular carcinogenesis.


Subject(s)
Apoptosis/physiology , Carcinoma, Hepatocellular/chemically induced , Chromones/pharmacology , Liver Neoplasms/chemically induced , Alanine Transaminase/blood , Animals , Apoptosis/drug effects , Aspartate Aminotransferases/blood , Carcinoma, Hepatocellular/drug therapy , Carcinoma, Hepatocellular/pathology , Chromones/administration & dosage , Chromones/therapeutic use , Diethylnitrosamine/metabolism , Diethylnitrosamine/toxicity , Glutathione S-Transferase pi/genetics , Glutathione S-Transferase pi/metabolism , Histocytochemistry , L-Lactate Dehydrogenase/blood , Liver Neoplasms/drug therapy , Liver Neoplasms/pathology , Male , PPAR gamma/genetics , PPAR gamma/metabolism , Proliferating Cell Nuclear Antigen/genetics , Proliferating Cell Nuclear Antigen/metabolism , RNA/chemistry , RNA/genetics , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction , Transcription Factor RelA/genetics , Transcription Factor RelA/metabolism , gamma-Glutamyltransferase/blood
19.
Colloids Surf B Biointerfaces ; 113: 207-12, 2014 Jan 01.
Article in English | MEDLINE | ID: mdl-24096157

ABSTRACT

Application of plant extracts for the burn/wound treatment is followed over the decades as a common practice and it is an important aspect in clinical management. In this study porous collagen sponges (CS) were prepared using fish scales and were incorporated with mupirocin (CSM) and extracts of Macrotyloma uniflorum (CSPE) separately to impart antimicrobial activity to the sponges. The results showed that the addition of plant extract increased the tensile strength of CSPE and stability against collagenase enzyme. FTIR studies have shown the incorporation of plant extract in CSPE, SEM studies have revealed the porous nature of the sponges and XRD patterns have shown the retention of collagen triple helical structure even after the addition of plant extract. CSPE and CSM have exhibited antimicrobial properties. The sponges prepared were analysed for their in vitro biocompatibility studies using fibroblasts and keratinocyte cell lines and the results have shown their biocompatible nature. Based on the results obtained, CS, CSM and CSPE may be tried as a burn/wound dressing materials, initially, in small animals in vivo.


Subject(s)
Burns , Collagen/chemistry , Fabaceae/chemistry , Plant Extracts/pharmacology , Wound Healing/drug effects , Animals , Anti-Infective Agents/chemistry , Anti-Infective Agents/pharmacology , Bacillus subtilis/drug effects , Biocompatible Materials/chemistry , Cell Survival/drug effects , Collagenases/metabolism , Fishes , Mice , Mupirocin/chemistry , NIH 3T3 Cells , Plant Extracts/chemistry , Porosity , Spectroscopy, Fourier Transform Infrared , Staphylococcus aureus/drug effects , Tensile Strength , X-Ray Diffraction
20.
J Nanosci Nanotechnol ; 13(6): 4017-24, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23862442

ABSTRACT

In this present investigation, the colloidal silica and nano ZrO2 embedded silica solution were prepared using sol-gel method followed by the sonication process. The particle size was measured for the prepared silica sol with and without ZrO2 nanoparticles. The prepared nanoparticles were coated on the cotton fabric through pad dry method. The phase and functional group analysis of the cotton fabrics after coating reveals the presence of metal oxides on the surface. The surface morphology of the coated fabrics analysed using SEM shows that the nanoparticles were in spherical morphology with slight agglomerations. The element analysis confirms the presence of silica (SiO2) and ZrO2/SiO2 nanoparticles along with cellulose on the surface. The washing durability of the coated fabrics after 5th and 10th wash indicates that the nanoparticles were strongly adhered on the fabric surface. The burning performance of coated fabrics is in the order of ZrO2/SiO2 (19.5 s) > SiO2 (11.3 s) before and after wash; UV resistance of fabric was in the order of ZrO2/SiO2 > SiO2 > uncoated fabric. Cotton fabrics coated with ZrO2/SiO2 particles show better UV and flammability protection for textile applications.

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