INVESTIGATION OF HEAVY METAL ADSORPTION ON MICROPLASTICS

Microplastics and heavy metals represent two pollutant classes which have adverse impacts on aquatic ecosystems. This study has investigated the adsorption of two heavy metals [Lead (Pb)II and Aluminum (Al)III] on three different types of microplastics [polyethylene terephthalate (PET), polyamide (PA), ethylene vinyl acetate (EVA)]. The Scanning Electron Microscope (SEM) analysis has shown that microplastics have different surface characteristics. The effects of parameters such as the pH of solution, duration of contact, initial concentration and temperature on adsorption capacity have been examined Experimental results have been applied to the adsorption isotherm models of Langmuir and Freundlich and it has been seen that the Freundlich model has been seen as more suitable than the Langmuir model. Moreover, the pseudo-second kinetic has been found to be more appropriate than the pseudo-first kinetic model. Adsorption percentages have changed according to the type of microplastic and working conditions. Finally, the study has investigated the potential of microplastics to act as an instrument of transport for heavy metals to the food chain and for their bioaccumulation

A localization method for the measurement of fast relaxing 13C NMR signals in humans at high magnetic fields

Nuclear magnetic resonance (NMR) signals with short T1 and T2, such as the 13C signal of glycogen, are difficult to localize in three dimensions without major signal loss. A pulse sequence that accomplishes the spatial localization of 1H-decoupled 13C NMR signals on a whole-body scanner within the Food and Drug Administration guidelines for specific absorption rates was designed. The method uses an optimized three-dimensional outer volume suppression scheme combined with one-dimensional image-selected in vivo spectroscopy and surface coil detection. The localization performance of the sequence was validated at 4 T with double chambered phantoms and 13C magnetic resonance imaging. Localized 13C spectra were acquired from human brain and muscle. © Springer-Verlag 2005

Uptake, accumulation and some biochemical responses in Raphanus sativus L. to zinc stress

The responses of radish (Raphanus sativus L.) to increasing concentrations of ZnCl2 (1, 5 and 10 mM) in Hoagland nutrient medium were studied. Under the conditions of these increasing zinc concentrations, the highest zinc accumulation was obtained in the roots of the plants treated with 10 mM applications. The zinc concentration in the vegetative parts, was highest in the root and was lowest in the cotyledons. The highest bioconcentration factor (BCF) value was detected in the roots in 5 mM zinc applications. When compared with the control, total zinc uptake was observed to increase in 1, 5 and 10 mM ZnCl2 treatments. The total accumulation rate (TAR) for zinc was highest in 10 mM ZnCl2 treatment, while the lowest TAR was observed in radish plants exposed to 1 mM ZnCl2. Plants treated with 5, 10 mM ZnCl2 showed significant decreases in chlorophyll (Chl a, Chl b, Chl a/b) and carotenoid content compared with the control. Peroxidase (POD) activity especially in radish roots increased significantly with increasing concentrations of ZnCl2 (5 and 10 mM) while the total protein amount decreased when compared with the control. The results of this study showed that, radish plants could tolerate the negative effects of zinc stress up to 1 mM ZnCl2 concentration and that in zinc concentrations of 5 mM and above toxic effects were existent.Key words: Radish, Raphanus sativus, zinc, metal toxicity, uptake, accumulation, peroxidase, pigment

In vivo 1H NMR spectroscopy of the human brain at high magnetic fields: Metabolite quantification at 4T vs. 7T

A comprehensive comparative study of metabolite quantification from the human brain was performed on the same 10 subjects at 4T and 7T using MR scanners with identical consoles, the same type of RF coils, and identical pulse sequences and data analysis. Signal-to-noise ratio (SNR) was increased by a factor of 2 at 7T relative to 4T in a volume of interest selected in the occipital cortex using half-volume quadrature radio frequency (RF) coils. Spectral linewidth was increased by 50% at 7T, which resulted in a 14% increase in spectral resolution at 7T relative to 4T. Seventeen brain metabolites were reliably quantified at both field strengths. Metabolite quantification at 7T was less sensitive to reduced SNR than at 4T. The precision of metabolite quantification and detectability of weakly represented metabolites were substantially increased at 7T relative to 4T. Because of the increased spectral resolution at 7T, only one-half of the SNR of a 4T spectrum was required to obtain the same quantification precision. The Cramé r-Rao lower bounds (CRLB), a measure of quantification precision, of several metabolites were lower at both field strengths than the intersubject variation in metabolite concentrations, which resulted in a strong correlation between metabolite concentrations of individual subjects measured at 4T and 7T. © 2009 Wiley-Liss, Inc

In Vivo Molecular Signatures of Cerebellar Pathology in Spinocerebellar Ataxia Type 3

BackgroundNo treatment exists for the most common dominantly inherited ataxia Machado‐Joseph disease, or spinocerebellar ataxia type 3 (SCA3). Successful evaluation of candidate therapeutics will be facilitated by validated noninvasive biomarkers of disease pathology recapitulated by animal models.ObjectiveWe sought to identify shared in vivo neurochemical signatures in two mouse models of SCA3 that reflect the human disease pathology.MethodsCerebellar neurochemical concentrations in homozygous YACMJD84.2 (Q84/Q84) and hemizygous CMVMJD135 (Q135) mice were measured by in vivo magnetic resonance spectroscopy at 9.4 tesla. To validate the neurochemical biomarkers, levels of neurofilament medium (NFL; indicator of neuroaxonal integrity) and myelin basic protein (MBP; indicator of myelination) were measured in cerebellar lysates from a subset of mice and patients with SCA3. Finally, NFL and MBP levels were measured in the cerebellar extracts of Q84/Q84 mice upon silencing of the mutant ATXN3 gene.ResultsBoth Q84/Q84 and Q135 mice displayed lower N‐acetylaspartate than wild‐type littermates, indicating neuroaxonal loss/dysfunction, and lower myo‐inositol and total choline, indicating disturbances in phospholipid membrane metabolism and demyelination. Cerebellar NFL and MBP levels were accordingly lower in both models as well as in the cerebellar cortex of patients with SCA3 than controls. Importantly, N‐acetylaspartate and total choline correlated with NFL and MPB, respectively, in Q135 mice. Long‐term sustained RNA interference (RNAi)‐mediated reduction of ATXN3 levels increased NFL and MBP in Q84/Q84 cerebella.ConclusionsN‐acetylaspartate, myo‐inositol, and total choline levels in the cerebellum are candidate biomarkers of neuroaxonal and oligodendrocyte pathology in SCA3, aspects of pathology that are reversible by RNAi therapy. © 2020 International Parkinson and Movement Disorder SocietyPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/163456/2/mds28140.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/163456/1/mds28140_am.pd

Human neutrophil development and functionality are enabled in a humanized mouse model

Mice with a functional human immune system serve as an invaluable tool to study the development and function of the human immune system in vivo. A major technological limitation of all current humanized mouse models is the lack of mature and functional human neutrophils in circulation and tissues. To overcome this, we generated a humanized mouse model named MISTRGGR, in which the mouse granulocyte colony-stimulating factor (G-CSF) was replaced with human G-CSF and the mouse G-CSF receptor gene was deleted in existing MISTRG mice. By targeting the G-CSF cytokine-receptor axis, we dramatically improved the reconstitution of mature circulating and tissue-infiltrating human neutrophils in MISTRGGR mice. Moreover, these functional human neutrophils in MISTRGGR are recruited upon inflammatory and infectious challenges and help reduce bacterial burden. MISTRGGR mice represent a unique mouse model that finally permits the study of human neutrophils in health and disease

Proton MRS of the unilateral substantia nigra in the human brain at 4 tesla: Detection of high GABA concentrations

Parkinson's disease (PD) is characterized by loss of dopaminergic neurons in the substantia nigra (SN), the cause of which is unknown. Characterization of early SN pathology could prove beneficial in the treatment and diagnosis of PD. The present study shows that with the use of short-echo (5 ms) Stimulated-Echo Acquisition Mode (STEAM) spectroscopy and LCModel, a neurochemical profile consisting of 10 metabolites, including γ-aminobutyric acid (GABA), glutamate (Glu), and glutathione (GSH), can be measured from the unilateral SN at 4 tesla. The neurochemical profile of the SN is unique and characterized by a fourfold higher GABA/Glu ratio compared to the cortex, in excellent agreement with established neurochemistry. The presence of elevated GABA levels in SN was validated with the use of editing, suggesting that partial volume effects were greatly reduced. These findings establish the feasibility of obtaining a neurochemical profile of the unilateral human SN by single-voxel spectroscopy in small volumes. © 2006 Wiley-Liss, Inc