ABSTRACT
PURPOSE: Galactose mutarotase (GALM) deficiency was first reported in 2019 as the fourth type of galactosemia. This study aimed to investigate the clinical and genotypic spectra of GALM deficiency. METHODS: This was a questionnaire-based retrospective survey conducted in Japan between February 2022 and March 2023. RESULTS: We identified 40 patients with GALM deficiency in Japan (estimated prevalence: 1:181,835). Four of 38 patients (10.5%) developed cataracts, which resolved with lactose restriction in 3 out of 4 patients. Transient transaminitis was the most common symptom (23.1%). All of the patients followed lactose restriction; discontinuation of the restriction after infancy did not cause any complications. Moreover, none of the participants experienced long-term complications. Two variants, GALM NM_138801.3: c.294del and c.424G>A, accounted for 72.5% of the identified pathogenic variants. The patients showed moderately elevated blood galactose levels with lactose intake; however, the elevation was lower than that observed in galactokinase deficiency. CONCLUSION: GALM deficiency is characterized by a similar but milder phenotype and lower blood galactose elevation than in galactokinase deficiency. Diagnosis and initiation of lactose restriction in early infancy should be essential for prevention of cataracts, especially in cases of irreversible opacity.
Subject(s)
Galactose , Galactosemias , Phenotype , Humans , Japan/epidemiology , Galactosemias/genetics , Galactosemias/epidemiology , Female , Male , Child, Preschool , Infant , Retrospective Studies , Child , Adolescent , Adult , Surveys and Questionnaires , Mutation/genetics , Genotype , Cataract/genetics , Cataract/epidemiology , Cataract/bloodABSTRACT
Krabbe disease (KD) is a rare inherited demyelinating disorder caused by a deficiency in the lysosomal enzyme galactosylceramide (GalCer) ß-galactosidase. Most patients with KD exhibit fatal cerebral demyelination with apoptotic oligodendrocyte (OL) death and die before the age of 2-4 years. We have previously reported that primary OLs isolated from the brains of twitcher (twi) mice, an authentic mouse model of KD, have cell-autonomous developmental defects and undergo apoptotic death accompanied by abnormal accumulation of psychosine, an endogenous cytotoxic lyso-derivative of GalCer. In this study, we aimed to investigate the effects of the preclinical promyelinating drugs clemastine and Sob-AM2 on KD OL pathologies using primary OLs isolated from the brains of twi mice. Both agents specifically prevented the apoptotic death observed in twi OLs. However, while Sob-AM2 showed higher efficacy in restoring the impaired differentiation and maturation of twi OLs, clemastine more potently reduced the endogenous psychosine levels. These results present the first preclinical in vitro data, suggesting that clemastine and Sob-AM2 can act directly and distinctly on OLs in KD and ameliorate their cellular pathologies associated with myelin degeneration.
Subject(s)
Apoptosis , Clemastine , Disease Models, Animal , Leukodystrophy, Globoid Cell , Oligodendroglia , Psychosine , Animals , Leukodystrophy, Globoid Cell/pathology , Leukodystrophy, Globoid Cell/genetics , Leukodystrophy, Globoid Cell/drug therapy , Oligodendroglia/pathology , Oligodendroglia/metabolism , Oligodendroglia/drug effects , Mice , Clemastine/pharmacology , Apoptosis/drug effects , Psychosine/analogs & derivatives , Psychosine/metabolism , Cell Differentiation/drug effects , Myelin Sheath/metabolism , Myelin Sheath/pathology , Brain/pathology , Brain/metabolism , Brain/drug effects , Cells, CulturedABSTRACT
Hydrogen is attracting attention as an energy carrier for realizing a low-carbon society, because it can directly convert the energy obtained from chemical reactions into electrical energy without carbon dioxide emissions. This paper presents in situ transmission electron microscopy (TEM) observations related to hydrogen storage in metal and metal hydrides, hydrogen embrittlement of metallic materials used for storing and transporting hydrogen in containers and pipes, and fuel cells and water electrolysis using metal catalysts and oxides as electrode materials. All of these processes are important for practical applications of hydrogen. Numerous in situ TEM studies have revealed the microscopic structural changes when hydrogen reacts with the materials, when hydrogen is solidly dissolved in the materials and during the operation of the material. This review is expected to facilitate further development of TEM operando observations of hydrogen-related materials.
ABSTRACT
The paddlewheel-type dimetal core ([M2]) is a ubiquitous motif in the nodes in coordination polymers (CPs) and metal-organic frameworks (MOFs). However, their preparation has relied on ligand-substitution-labile metal ions owing to challenges associated with crystallization. Consequently, examples featuring ligand-substitution-inert metal ions, such as Ru or Rh, are scarce. This study presents the synthesis of novel reticular imine-linked CPs incorporating the paddlewheel-type diruthenium(II, II) ([Ru2II,II]; 1-Ru) or dirhodium(II, II) ([Rh2II,II]; 1-Rh) subunits. The synthetic approach involved a Schiff base dehydration condensation reaction between p-formylbenzoate-bridged [Ru2II,II] or [Rh2II,II] precursors (i.e., CHO-Ru and CHO-Rh, respectively) and 2,5-dimethyl-1,4-phenylenediamine in a 1:2 ratio. The catalytic activities of 1-Ru and 1-Rh for the photochemical reduction of CO2 in a heterogeneous system depended on the metal site. The 1-Rusystem exhibited exceptional selectivity, generating 3.0 ´ 104 mmol g-1 of CO after 24 h of irradiation, whereas the 1-Rhsystem generated a lower amount of CO (3.2 ´ 103 mmol g-1). The catalytic activity of 1-Ru ranked with that of all relevant catalytic systems. This study paves the way for the exploration of [Ru2II,II]- or [Rh2II,II]-based polymers with open metal site-dependent functional properties.