Unilateral nephrectomy for young infants with congenital nephrotic syndrome of the Finnish type

Clinical and Experimental Nephrology - The management of congenital nephrotic syndrome of the Finnish type (CNF) is challenging. It is difficult to withdraw intravenous albumin infusions, resulting...     

Occipital neuralgia as a presenting symptom of cervicomedullary dural arteriovenous fistula

Dural arteriovenous fistulas (DAVFs) at the cervicomedullary junction are rare and have a wide variation in presentation. We report a case of occipital neuralgia (ON) as a rare presenting symptom of cervicomedullary DAVF causing intramedullary hemorrhage at the C1 level. It is important to consider the underlying causes of ON, and precise neurological examinations and radiological evaluations are needed.     

(GγAγδβ)0$({}^{\rm G}{\gamma}{}^{\rm A}{\gamma}\delta\beta)^0$-Thalassemia: Report of two cases in a family

Case 1 presented with severe anemia and received an intrauterine blood cell transfusion at 33 weeks of gestation. The anemia spontaneously improved in early infancy. Case 2, the father of Case 1, had an uneventful birth with no evidence of anemia, though microcytic anemia was observed during childhood. The genetic analysis of the β-globin gene cluster identified a novel heterozygous deletion of DNA extending from the Gγ-globin gene downstream to the β-globin gene, confirming a diagnosis of (^Gγ^Aγδβ)⁰-thalassemia. In cases where thalassemia is suspected based on blood tests, a genetic diagnosis should be performed for the sake of the offspring.     

Contractile response of guinea pig ileum by repetitive application of morphine.

1. The repetitive application of morphine gradually induced a contracture in the isolated guinea pig ileum. 2. The optimum conditions for induction of the contracture were as follows: the concentration, incubation time and washout time of morphine were 1 or 10 microM, 2 and 3 min, respectively. 3. Preincubation with naloxone or TTX blocked this morphine-induced contracture. 4. Among twitch-inhibiting drugs, only clonidine induced a contracture similar to that induced by morphine, while tetrodotoxin (TTX) and adenosine did not. 5. The contracture was also observed in the longitudinal muscle-myenteric plexus preparations. 6. These findings indicate that morphine has a dual inhibitory and excitatory action on the guinea pig ileum and that its repetitive application preferentially diminish the inhibitory one.     

A case of solitary bone cyst in the skull increasing in size after trivial head injury

A 12-year-old boy had been known to have a small swelling in the left high vertex for several years. After a trivial head hit to the site of the swelling, the swelling enlarged gradually. A bone window CT scan showed a lesion having bubble-like lytic change in the left parietal bone. Similar changes, but small, were able to be pointed out in a CT scan taken seven years previously. In the following 13 months CT scans eventually revealed sequential increases to 3.5 cm in diameter. Surgical exploratory resection of the mass was performed. Intraoperatively, partial destruction of the outer skull table and a simple cyst with serous yellowish brown colored fluid were identified. There was no finding adherent to the diploic structure. The bone defect after excision was reconstructed by using a titanium plate. The patient was followed up for 2 years after the surgery. Bone window CT showed bony development of normal appearance. Histological examination showed the cyst wall consisted of fibrous connective tissue but there were neither epithelial nor endothelial cells. The histopathological diagnosis of SBC was most likely. SBC is relatively common in long bones, but rarely in flat bones. Only several cases of the SBC of cranial bone have been reported. Although a craniectomy for total excision followed by cranioplasty by resin was common, in cases of children, cyst removal with titanium plate application would be an alterative. SBC increasing in size after head injury is extremely rare, but clinicians may need to be aware of cystic skull bone tumors increasing in size after head injury.     

Rapid detection of donor-dependent photocatalytic hydrogen evolution by NMR spectroscopy

Understanding molecular processes at nanoparticle surfaces is essential for designing active photocatalytic materials. Here, we utilize nuclear magnetic resonance (NMR) spectroscopy to track photocatalytic hydrogen evolution using donor molecules and water isotopologues. Pt–TiO₂ catalysts were prepared and used for isotopic hydrogen evolution reactions using alcohols as electron donors. ¹H NMR monitoring revealed that evolution of the H₂ and HD species is accompanied by the oxidation of donor molecules. The isotopic selectivity in the hydrogen evolution reaction gives rise to formal overpotential. Based on a comparison of the rates of hydrogen evolution and donor oxidation, we propose the use of ethanol as an efficient electron donor for the hydrogen evolution reaction without re-oxidation of radical intermediates.

Isotopic molecule processes at photocatalytic hydrogen evolution reactions observed by NMR clarify the importance of the choice of electron donors for efficient chemical energy conversions at electrified interfaces.

The conversion of light energy to chemical energy requires a combination of electronic excitation and sequential electron transfer.^1–3 Efficient electronic excitation is achieved by choosing materials with suitable optical properties, while efficient electron transfer can be achieved by rational design of catalytically active surface sites.⁴ To achieve high catalytic performance, an understanding of the molecular processes occurring at the catalyst surface is required.Photocatalytic hydrogen evolution is accompanied by oxidation of the electron donor. Most studies on this reaction have been conducted using in-line mass spectrometry measurements⁵ or oxygen-quenching methods.⁶ However, monitoring the whole reaction cycle using one methodology remains challenging.Nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for observing chemical reactions. This method is mainly used to confirm small-molecule conversions in organic synthesis. However, NMR spectroscopy can also be used to gain information of nanoparticle surfaces⁷ or even for the detection of photocatalytic reactions.^8–10 Furthermore, NMR spectroscopy can be used to determine the nuclear spin states of product molecules.¹¹ Nevertheless, there are very few reported studies on the in situ observation of photocatalytic hydrogen evolution using NMR spectroscopy.Accordingly, in the present study, we utilized NMR spectroscopy to observe the photocatalytic hydrogen evolution reaction. We employed Pt–TiO₂, which is frequently used for the photocatalytic hydrogen evolution reaction, as a model catalyst for this study. NMR spectroscopy enabled sub-micromole-scale detection of reaction products within one minute. We investigated the dependence of isotopic hydrogen evolution reactions on the donor molecules. The effects of efficient donors on the photocatalytic hydrogen evolution reaction are discussed.Pt–TiO₂ nanoparticles were prepared by a typical chemical reduction method (see ESI^†). The morphologies of TiO₂ and Pt–TiO₂ nanoparticles were characterized by transmission electron microscopy, as shown in Fig. S1 and S2.^† The average size of the Pt nanoparticles is approximately 5 nm. The average size of the TiO₂ nanoparticles is within the range 20–30 nm. Typically, 5 mg of catalysts and 0.6 mL of reaction mixture were introduced to an NMR tube under Ar for observation of the photocatalytic hydrogen evolution reaction by NMR spectroscopy. Fig. 1a shows the ¹H NMR spectra of Pt–TiO₂/2-propanol/D₂O before and after light irradiation. Before light irradiation, three peaks are observed (Fig. 1a, black). The single peak observed at 4.81 ppm is assigned to HDO.¹²¹H signals from the methine and methyl groups of 2-propanol are observed at 4.01 and 1.20 ppm, respectively.Open in a separate windowFig. 1 ¹H NMR spectra of Pt–TiO₂/2-propanol/D₂O. The black lines are the ¹H NMR spectra before light irradiation. The red lines are the ¹H NMR spectra after light irradiation for 15 min. (a) Full spectrum. (b) Enlargement of the oxidation product. (c) Enlargement of the area for the H₂ and HD species.After light irradiation, additional species are observed (Fig. 1a, red). We confirmed the photocatalytic response of the Pt–TiO₂ nanoparticles from ON–OFF experiments (Fig. S3^†). The oxidation product is acetone resulting from two-electron and two-proton oxidation of 2-propanol. The signal at 2.25 ppm is assigned to the methyl group in the acetone (Fig. 1b).¹² Hydrogen evolution is observed as a reduction reaction. Four peaks are observed between 4.5 and 4.7 ppm (Fig. 1c). The single peak at 4.63 ppm can be assigned to H₂ dissolved in the solvent.¹³ Other peaks at 4.66, 4.59, and 4.52 ppm are assigned to the HD.^14–16 The observed coupling constant for HD is 43 Hz, which is a typical value for HD.^14–16 The difference in the chemical shifts of H₂ and HD is due to variation of the nuclear magnetic screening constants with interatomic separation as a consequence of the zero-point energy in vibration.^17,18Importantly, NMR spectroscopy can detect H₂ and HD species from the photocatalytic hydrogen evolution reaction. The observed peak splitting of the three peaks is due to the heteronuclear coupling between hydrogen and deuterium atoms.^14–16 The observed chemical shift for H₂ in methanol/D₂O is 4.56 ppm. The observed chemical shifts of HD in methanol/D₂O are 4.60, 4.53, and 4.46 ppm (Fig. S4^†). These values are similar to those for 2-propanol/D₂O. The observed chemical shift of H₂ in ethanol/D₂O is 4.61 ppm. Those for HD in ethanol/D₂O are 4.65, 4.57, and 4.50 ppm (Fig. S5^†). The slight shift in the H₂ and HD signals is due to the difference in the shielding effect depending on the solvation environment.^19–21 The coupling constant between hydrogen and deuterium in HD is 43 Hz, and it is 43 Hz in methanol/D₂O and ethanol/D₂O. The similarity in the coupling constants for the different solvents indicates that the chemical bonding between hydrogen and deuterium is consistent.^14–16 Interestingly, the fullwidth at half maximum (FWHM) values for the H₂ and HD signals are dependent on the solvent. The FWHM values for the H₂ signal are 1.48, 2.24, and 3.51 Hz in methanol/D₂O, ethanol/D₂O, and 2-propanol/D₂O, respectively. The FWHM values for the HD signal are 1.59, 2.00, and 3.32 Hz for methanol/D₂O, ethanol/D₂O, and 2-propanol/D₂O, respectively. H₂ and HD show similar FWHM values in the same solvent. However, the FWHM value is solvent-dependent. In general, a wider peak indicates lower mobility.¹⁶ Therefore, it is expected that 2-propanol induces lower mobility for the hydrogen, probably because of the rotation or diffusional freedom of hydrogen molecules. The solvation environment of hydrogen influences the molecular mobility of hydrogen species in the photocatalytic hydrogen evolution reaction.Oxidation products of the donor molecules are observed in the NMR spectra, as shown in Fig. S4 and S5.^† The number of product molecules is quantified on the basis of the hydrogen atoms in the alkyl chain groups in 2-propanol, ethanol, and methanol as reactants. For methanol, the signals for methylene glycol, 1-methoxymethanol, and methyl formate are observed as shown in Fig. S4.^† For ethanol, acetaldehyde and acetic acid are observed as the products, as shown in Fig. S5.^† As described above, the oxidation product of 2-propanol is limited to acetone. This is due to the unstable intermediate formed in the oxidation of 2-propanol.²² Conversely, the reaction products of methanol^23–26 and ethanol²⁷ are complicated owing to the sequential oxidation and/or hydration reactions.We evaluated the isotopic selectivity of the hydrogen evolution reaction depending on the donor molecules. Fig. 2 shows the typical isotopic selectivity of the hydrogen evolution reaction. The amounts of H₂ and HD were quantified from the NMR spectra. The HD/H₂ ratios were calculated to be 4.1, 3.4, and 1.9 for 2-propanol, ethanol, and methanol, respectively, where the mixture ratio of D₂O and alcohol is 1 : 1. In both cases, attenuation of the hydrogen evolution reaction is specifically observed for methanol. This is probably due to poisoning of the Pt surface with carbon monoxide molecules evolved from the oxidation of methanol at the TiO₂ surface.²⁸Open in a separate windowFig. 2Isotopic selectivity for HD (black) and H₂ (red) from the photocatalytic hydrogen evolution reaction using a 1 : 1 mixture of D₂O and the corresponding alcohol upon light irradiation for 15 min.H₂ is classified as o-H₂ or p-H₂ depending on the nuclear spin isomer.^29,30o-H₂ is observable and p-H₂ is not by NMR because of the Zeeman splitting of the nucleus spin momentum. Because of the spin statistic, the ratio of o-H₂ and p-H₂ is 3 : 1.^29,30 D₂ is not included in the observation because of the low sensitivity to D atoms, even in ²H NMR spectroscopy measurements. Similarly, we observed an increase in the oxidation products of methanol and ethanol. Importantly, the selectivity for the oxidation and hydrogen evolution reaction were continuously monitored, as shown in Fig. S6–S11.^† In addition, the maximum concentration of H₂ in this photocatalytic reaction is approximately 1 mmol L⁻¹, which is below the solubility limits of water and alcohol.^31–34 These results suggest that a robust photocatalytic process continues throughout the catalytic cycle.Isotopic hydrogen evolution provides information about the reaction mechanism at the metal surface.^35–39 The reaction follows an electrochemical adsorption and desorption cycle. The adsorption of atomic hydrogen from the proton donor (Volmer step)⁴⁰ is followed by either desorption via recombination of adsorbed hydrogens (Tafel step)⁴¹ or desorption of atomic hydrogen with a proton donor (Heyrovsky step).⁴² The enrichment of hydrogen over deuterium is observed for the Heyrovsky, Tafel, and Volmer step sequence.^40–42 Generally, the Tafel step is rate-limiting in the hydrogen evolution process for Pt surfaces. Therefore, isotopic selectivity is not dependent on electrochemical potential.As shown in Fig. 2, the isotopic selectivity is similar for the reactions using 2-propanol and ethanol. This suggests that the formal potential of the hydrogen evolution reaction is similar for these two conditions. Additionally, we evaluated self-diffusion of water molecules and each alcohol molecule as shown in Table S1.^† We determined diffusion coefficients for the alcohols and HDO. These results suggest that the diffusion of the reactant in the hydrogen evolution reaction is not the rate-determining step in the photocatalytic reaction cycle.⁴³Interestingly, the efficiency of the multi-electron transfer is dependent on the donor molecule. Fig. S12^† shows the time-course of the oxidation and reduction reactions obtained by accounting for the half-reaction. Linearity in the time-course plot is observed, indicating stable photocatalysis. Therefore, the reaction rate was calculated from the slope of each reaction. Fig. 3 and S12^† show the rates of oxidation and reduction obtained by accounting for the number of electrons in the half-reaction, defined as r_ox and r_red. For a 3 : 1 ratio of D₂O and alcohol, r_red is nominally low. This is probably due to the small number of donor molecules in the catalytic reaction. Importantly, r_red shows the highest value of 0.26 μmol min⁻¹ for the combination of 2-propanol/D₂O (1 : 1). This value is comparable with that for ethanol/D₂O (1 : 1), which is 0.22 μmol min⁻¹. Conversely, the r_ox values for 2-propanol and ethanol are not comparable. Indeed, r_ox for 2-propanol is seven times higher than that for ethanol.Open in a separate windowFig. 3Rates of the oxidation reaction (black) and hydrogen evolution reaction (red) using a 1 : 1 mixture of D₂O and the corresponding alcohol.Finally, we discuss the effect of donor molecules on the efficiency of the photocatalytic hydrogen evolution reaction. The stability of the radical derived from the alcohol plays an important role in the reaction efficiency. 2-Propanol is oxidized to the tertiary carbocation radical intermediate, which is consumed by spontaneous oxidation at the TiO₂ surface (Fig. 4a).^44–47 For ethanol (Fig. 4b), the oxidized carbocation radical species is expected to be unstable compared with that for 2-propanol. Therefore, the rate of the hydrogen evolution reaction is comparable with the rate of the oxidation reaction. For methanol (Fig. 4c), the carbon monoxide evolved is expected to attenuate the hydrogen evolution reaction.²⁸ Thus, the efficiency of the redox reaction can be evaluated from the NMR spectroscopy results.Open in a separate windowFig. 4Schematic representations of photocatalytic hydrogen evolution reactions over Pt–TiO₂ using (a) 2-propanol, (b) ethanol, and (c) methanol.In conclusion, we used NMR spectroscopy to track the photocatalytic hydrogen evolution reaction using Pt–TiO₂ as a model catalyst. We performed rapid detection of dissolved hydrogen molecules in the solvent and the oxidized product at the sub-micromole scale by ¹H NMR. The method is useful for observation of the dynamic state of molecules in solution and product-based determination of the reaction mechanism. This method is also applicable to the screening of photocatalysts under given conditions. In addition, we found that an efficient multi-electron-transfer photocatalytic reaction is possible using ethanol as the donor molecule. This study demonstrates the utility of NMR for the clarification of the hydrogen evolution reaction mechanism as a means to evaluate potential catalysts, from organic molecular catalysts to inorganic nanocrystals.     

Modified SH2 domain to phototrap and identify phosphotyrosine proteins from subcellular sites within cells

Spatial regulation of tyrosine phosphorylation is important for many aspects of cell biology. However, phosphotyrosine accounts for less than 1% of all phosphorylated substrates, and it is typically a very transient event in vivo. These factors complicate the identification of key tyrosine kinase substrates, especially in the context of their extraordinary spatial organization. Here, we describe an approach to identify tyrosine kinase substrates based on their subcellular distribution from within cells. This method uses an unnatural amino acid-modified Src homology 2 (SH2) domain that is expressed within cells and can covalently trap phosphotyrosine proteins on exposure to light. This SH2 domain-based photoprobe was targeted to cellular structures, such as the actin cytoskeleton, mitochondria, and cellular membranes, to capture tyrosine kinase substrates unique to each cellular region. We demonstrate that RhoA, one of the proteins associated with actin, can be phosphorylated on two tyrosine residues within the switch regions, suggesting that phosphorylation of these residues might modulate RhoA signaling to the actin cytoskeleton. We conclude that expression of SH2 domains within cellular compartments that are capable of covalent phototrapping can reveal the spatial organization of tyrosine kinase substrates that are likely to be important for the regulation of subcellular structures.