The stacking order of graphite layers in mesocarbon microbeads (MCMB5) heat-treated between 700 and 3000°C was examined by analyses of x-ray diffraction measurements, and lithium insertion into the MCMBs has been observed using solid-state ti-nuclear magnetic resonance (7Li-NMR) spectroscopy. In MCMTBs heat-treated above 2000°C, the fully lithiated MCMBs showed two bands at ca. 45 ppm (vs. LiC1) and ca. 27 ppm in their 7Li-NMR spectra. The profile of the band at 45 ppm was very close to that for the first-stage lithium graphite intercalation compound (Li-GIC), though the other band at 27 ppm could not be assigned to any phases of Li-GICs. From these results, it is suggested that the structures of the MCMBs heat-treated above 2000°C for lithium insertion are classified as graphitic structure, which has the AB stacking order of graphite layers, and turbostratic structure with a random stacking sequence of graphite layers; the fully lithiated compositions of both structures were estimated as LiC6 and ca. Li,2C6, respectively. Although MCMB heat-treated at 700°C gave a higher capacity than LiC6, the line shift in the 7Li-NMR spectra indicated that lithium stored in the MCMB displayed an ionic character. Capacity change of the MCMBs during charge-discharge cycling up to 20 cycles and capacity loss at higher current densities (< 200 mA g') were also examined.) unless CC License in place (see abstract). ecsdl.org/site/terms_use address. Redistribution subject to ECS terms of use (see 128.122.253.228 Downloaded on 2015-02-06 to IP
1. Diabetic neuropathy is one of the most frequent complications of diabetes mellitus. However, the mechanisms underlying these disorders are not yet well defined and it has been reported that currently available analgesics have hardly any ameliorating effect on painful diabetic neuropathy. 2. The purpose of the present study was to evaluate the antinociceptive effect of oxcarbazepine (OCBZ), a keto derivative of carbamazepine (CBZ), in animal models generally used in pain research and in rats and mice with streptozotocin (STZ)-induced diabetes. In addition, we compared the effect of OCBZ with those of CBZ, mexiletine and morphine. 3. Diabetes was induced by injection of STZ at a dose of 300 mg/kg (i.p.) in mice and 50 mg/kg (i.v.) in rats. Experiments were conducted 2 weeks after STZ injection and those animals with a serum glucose level above 400 mg/dL were used for data analysis. Antinociceptive effects of the drugs were evaluated by the paw withdrawal test (normal, STZ-induced diabetic and carrageenin-injected rats), tail-flick test (normal and STZ-induced diabetic mice) and nociceptive behaviour (formalin-injected mice). 4. In the present study, diabetic mice showed thermal hyperalgesia and diabetic rats exhibited mechanical hyperalgesia. From these results, the STZ-induced diabetic animals used in the present study were found to be suitable for research on painful diabetic neuropathy. In STZ-induced diabetic animals, the antinociceptive effects of OCBZ, CBZ and mexiletine were facilitated, whereas the effect of morphine was attenuated, compared with effects in normal animals. 5. Oxcarbazepine inhibited the formalin-induced biphasic pain responses and increased the nociceptive threshold in the case of carrageenin-induced hyperalgesia. In view of these results, inhibition of substance P-mediated pain transmission may be involved in the antinociceptive action of OCBZ. 6. These results indicate that OCBZ has an analgesic action and is a possible therapeutic agent for the treatment of neuropathic pain, such as occurs in painful diabetic neuropathy.
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