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1.
Neurosci Biobehav Rev ; 142: 104849, 2022 11.
Article in English | MEDLINE | ID: mdl-36116576

ABSTRACT

Two-thirds of individuals experience adversity during childhood such as neglect, abuse or highly-stressful events. Early-life adversity (ELA) increases the life-long risk of developing mood and substance use disorders. Reward-related deficits has emerged as a key endophenotype of such psychiatric disorders. Animal models are invaluable for studying how ELA leads to reward deficits. However, the existing literature is heterogenous with difficult to reconcile findings. To create an overview, we conducted a systematic review containing multiple meta-analyses regarding the effects of ELA on reward processes overall and on specific aspects of reward processing in animal models. A comprehensive search identified 120 studies. Most studies omitted key details resulting in unclear risk of bias. Overall meta-analysis showed that ELA significantly reduced reward behaviors (SMD: -0.42 [-0.60; -0.24]). The magnitude of ELA effects significantly increased with longer exposure. When reward domains were analyzed separately, ELA only significantly dampened reward responsiveness (SMD: -0.525[-0.786; -0.264]) and social reward processing (SMD: -0.374 [-0.663; -0.084]), suggesting that ELA might lead to deficits in specific reward domains.


Subject(s)
Reward , Stress, Psychological , Animals , Affect , Stress, Psychological/psychology
2.
Environ Sci Pollut Res Int ; 28(12): 14372-14385, 2021 Mar.
Article in English | MEDLINE | ID: mdl-33210250

ABSTRACT

This study examines the impact of foreign direct investments on ecological footprint along with other explanatory variables of 92 countries from the year 2001 to 2016. Here, we applied the panel quantile regression model to meet the purpose of our study as it considers unobserved country heterogeneity, unlike other statistical methods. The study reveals that foreign direct investment has a positive relationship with the ecological footprint in each quantile except one, which proves the constancy of the pollution haven hypothesis. Moreover, we also tried to detect the impact of economic growth, manufacturing value-added, the percentage of world exports, and institutional quality on the ecological footprint in this study. The findings of this study also reveal that economic growth and manufacturing value-added are negatively associated with the ecological footprint. With respect to the percentage of world exports and institutional quality, we found a positive relationship with the ecological footprint. From the result of our study, different policy implications have been proposed for host countries and foreign investors on improving the economy through foreign direct investment with minimal ecological footprint.


Subject(s)
Carbon Dioxide , Economic Development , Carbon Dioxide/analysis , Environmental Pollution/analysis , Internationality , Investments
3.
J Inherit Metab Dis ; 41(4): 719-729, 2018 07.
Article in English | MEDLINE | ID: mdl-29560582

ABSTRACT

Primary CoQ10 deficiency is a clinically and genetically heterogeneous, autosomal recessive disorder resulting from mutations in genes involved in the synthesis of coenzyme Q10 (CoQ10). To date, mutations in nine proteins required for the biosynthesis of CoQ10 cause CoQ10 deficiency with varying clinical presentations. In 2009 the first patient with mutations in COQ9 was reported in an infant with a neonatal-onset, primary CoQ10 deficiency with multi-system disease. Here we describe four siblings with a previously undiagnosed lethal disorder characterized by oligohydramnios and intrauterine growth restriction, variable cardiomyopathy, anemia, and renal anomalies. The first and third pregnancy resulted in live born babies with abnormal tone who developed severe, treatment unresponsive lactic acidosis after birth and died hours later. Autopsy on one of the siblings demonstrated brain changes suggestive of the subacute necrotizing encephalopathy of Leigh disease. Whole-exome sequencing (WES) revealed the siblings shared compound heterozygous mutations in the COQ9 gene with both variants predicted to affect splicing. RT-PCR on RNA from patient fibroblasts revealed that the c.521 + 2 T > C variant resulted in splicing out of exons 4-5 and the c.711 + 3G > C variant spliced out exon 6, resulting in undetectable levels of COQ9 protein in patient fibroblasts. The biochemical profile of patient fibroblasts demonstrated a drastic reduction in CoQ10 levels. An additional peak on the chromatogram may represent accumulation of demethoxy coenzyme Q (DMQ), which was shown previously to accumulate as a result of a defect in COQ9. This family expands our understanding of this rare metabolic disease and highlights the prenatal onset, clinical variability, severity, and biochemical profile associated with COQ9-related CoQ10 deficiencies.


Subject(s)
Ataxia/genetics , Leigh Disease/pathology , Mitochondrial Diseases/genetics , Muscle Weakness/genetics , Mutation , Ubiquinone/deficiency , Acidosis, Lactic/etiology , Autopsy , Female , Humans , Infant, Newborn , Male , Pregnancy , Siblings , Ubiquinone/genetics , Exome Sequencing
4.
Langmuir ; 30(48): 14621-30, 2014 Dec 09.
Article in English | MEDLINE | ID: mdl-25380407

ABSTRACT

Molecular simulation techniques have revealed that the incorporation of fullerenes within porous aromatic frameworks (PAFs) remarkably enhances methanol uptake while inhibiting water uptake. The highest selectivity of methanol over water is found to be 1540 at low pressure (1 kPa) and decreases gradually with increasing pressure. The adsorption of water is very small compared to methanol, a useful material property for membrane and adsorbent-based separations. Grand canonical Monte Carlo (GCMC) simulations are utilized to calculate the pure component and mixture adsorption isotherms. The water and methanol mixture simulations show that water uptake is further inhibited above the pure component results because of the dominant methanol adsorption. Molecular dynamics (MD) simulations confirm that water diffusivity is also inhibited by strong methanol adsorption in the mixture. Overall, this study reveals profound hydrophobicity in C60@PAF materials and recommends C60@PAFs as suitable applicants for adsorbent and membrane-based separations of methanol/water mixtures and other alcohol/water separation applications.

5.
J Med Genet ; 51(7): 470-4, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24706940

ABSTRACT

BACKGROUND: Sedaghatian-type spondylometaphyseal dysplasia (SSMD) is a neonatal lethal form of spondylometaphyseal dysplasia characterised by severe metaphyseal chondrodysplasia with mild limb shortening, platyspondyly, cardiac conduction defects, and central nervous system abnormalities. As part of the FORGE Canada Consortium we studied two unrelated families to identify the genetic aetiology of this rare disease. METHODS AND RESULTS: Whole exome sequencing of a child affected with SSMD and her unaffected parents identified two rare variants in GPX4. The first (c.587+5G>A) was inherited from the mother, and the second (c.588-8_588-4del) was de novo (NM_001039848.1); both were predicted to impact splicing of GPX4. In vitro studies confirmed the mutations spliced out part of exon 4 and skipped exon 5, respectively, with both resulting in a frameshift and premature truncation of GPX4. Subsequently, a second child with SSMD was identified; although DNA from the child was not available, the two unaffected parents were found by Sanger sequencing to each carry the same heterozygous stop mutation in exon 3 of GPX4, c.381C>A, p.Tyr127* (NM_001039848.1). CONCLUSIONS: Our identification of truncating mutations in GPX4 in two families affected with SSMD supports the pathogenic role of mutated GPX4 in this very rare disease. GPX4 is a member of the glutathione peroxidase family of antioxidant defence enzymes and protects cells against membrane lipid peroxidation. GPX4 is essential for early embryo development, regulating anti-oxidative and anti-apoptotic activities. Our findings highlight the importance of this enzyme in development of the cardiac, nervous, and skeletal systems.


Subject(s)
Frameshift Mutation , Glutathione Peroxidase/genetics , Osteochondrodysplasias/diagnostic imaging , Osteochondrodysplasias/genetics , Amino Acid Sequence , Base Sequence , Codon, Nonsense , Consanguinity , DNA Mutational Analysis , Fatal Outcome , Female , Genetic Association Studies , Genetic Predisposition to Disease , HEK293 Cells , Humans , Infant, Newborn , Male , Molecular Sequence Data , Osteochondrodysplasias/enzymology , Pedigree , Phospholipid Hydroperoxide Glutathione Peroxidase , Polymorphism, Single Nucleotide , Radiography
6.
Langmuir ; 29(50): 15689-97, 2013 Dec 17.
Article in English | MEDLINE | ID: mdl-24283466

ABSTRACT

The volumetric hydrogen capacity remains one of the most challenging criteria for on-board hydrogen storage system requirements. Here a new concept for hydrogen storage of porous aromatic frameworks (PAFs) impregnated with lithium-decorated fullerenes (Li6C60) is described. The loading of Li6C60 and the effect on the adsorption of hydrogen (H2) has been investigated by molecular simulation. It is shown that the incorporation of Li6C60 can enhance the volumetric capacity of H2 from 12 to 44 g L(-1), a 260% increase at 10 bar and 77 K. The impregnation of Li6C60 increases the heat of adsorption and surface area at the cost of the available pore volume. However, the increase in adsorbed hydrogen outweighs any pore volume loss under optimized Li6C60 loading and operating conditions. In addition, the H2 volumetric uptake is shown to correlate with the volumetric surface area at all pressures whereas the H2 gravimetric uptake correlates with the heat of adsorption at low pressures, surface area at moderate pressures, and pore volume at high pressures.

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